The expression of dehydrin proteins in desiccation-sensitive (recalcitrant) seeds of temperate trees

Planta ◽  
1994 ◽  
Vol 193 (4) ◽  
pp. 478-485 ◽  
Author(s):  
W. E. Finch-Savage ◽  
S. K. Pramanik ◽  
J. D. Bewley
Keyword(s):  
Recalcitrant Seeds ◽  
Temperate Trees

Mitotic Activity Dynamics in Recalcitrant Seeds Acer sachharinum during Maturation and Germination

HortScience ◽  
1998 ◽  
Vol 33 (3) ◽  
pp. 479c-479
Author(s):  
L. Kozeko ◽  
V. Troyan ◽  
L. Musatenko
Keyword(s):  
Cell Division ◽  
Mitotic Activity ◽  
Quiescent State ◽  
Activity Levels ◽  
Recalcitrant Seeds ◽  
Mature Embryos ◽  
Before And After ◽  
Orthodox Seeds ◽  
Mature Seeds ◽  
Activity Dynamics

In orthodox seeds the cell division within the embryo meristems arrests during maturation at embryo moisture content (MC) 65% to 47%, and the maturation completion and transition of seeds to quiescent state occurs at MC about 10%. The arrest of cycling happens asynchronously in different meristematic tissues during desiccation: first in shoot and then in root. The aim of this work was to define a mitotic activity dynamics in recalcitrant seeds with the high MC at maturation end and the absence of quiescent state characteristic of it. The object was seeds of Acer saccharinum, using widely for planting of greenery in Kiev city. The mitotic activity was determined in 0.5 mm of the embryo root pole (RP) and 0.5 mm of the shoot pole with embryo leaves (SP). The A. sachharinum seeds completed them maturation at MC 53% (FW basis). During maturation the mitotic index (MI) in RP decreased from 3.2% in immature seeds (at embryos MC 80%) to 0 in mature seeds and in SP–from 5.4% to 3.3%, respectively. Cell division in SP arrested by dehydration of mature embryos to MC 46% by PEG 6000 (30%). The seeds lost viability by desiccation to MC 34%. The mature seeds were able to germinate immediately after abscission. During seed germination the cell division reactived in RP and increased in SP already before root protrusion. In plantlets 10–15 mm long the MI increased to 8% in RP and 12% in SP. Thus, the strategy of immediate germination of recalcitrant A. sachharinum seeds includes a preservation of cell division in SP of mature embryos, in contrast with orthodox seeds, and high mitotic activity levels in meristems of germinating embryos before and after root protrusion.

Preservation of Recalcitrant Seeds

Science ◽  
2013 ◽  
Vol 339 (6122) ◽  
pp. 915-916 ◽  
Author(s):  
C. Walters ◽  
P. Berjak ◽  
N. Pammenter ◽  
K. Kennedy ◽  
P. Raven
Keyword(s):  
Recalcitrant Seeds

scholarly journals Predicted Effects of Climate Change on Winter Chill Accumulation by Temperate Trees in South Korea

2018 ◽  
Vol 87 (2) ◽  
pp. 166-173 ◽  
Author(s):  
YoSup Park ◽  
ByulHaNa Lee ◽  
Hee-Seung Park
Keyword(s):  
Climate Change ◽  
South Korea ◽  
Winter Chill ◽  
Temperate Trees

Effects of differential drying rates on viability retention of recalcitrant seeds of Ekebergia capensis

1998 ◽  
Vol 8 (4) ◽  
pp. 463-471 ◽  
Author(s):  
N. W. Pammenter ◽  
Valerie Greggains ◽  
J. I. Kioko ◽  
J. Wesley-Smith ◽  
Patricia Berjak ◽  
...  
Keyword(s):  
Water Content ◽  
Exponential Function ◽  
Time Course ◽  
Drying Rate ◽  
Recalcitrant Seeds ◽  
Tissue Water ◽  
Initial Water ◽  
Viability Loss ◽  
Drying Rates ◽  
Water Contents

AbstractThe drying rate of whole seeds of Ekebergia capensis (Meliaceae) was shown to influence the response to desiccation, with rapidly dried seeds surviving to lower water contents. Short-term rapid drying (to water contents higher than those leading to viability loss) actually increased the rate of germination. The form of the time course of decline of axis water content varied with drying rate; slow drying could be described by an exponential function, whereas with rapid drying initial water loss was faster than predicted by an exponential function. These observations suggest that slow drying brought about homogeneous dehydration and that the rapid drying was uneven across the tissue. This raised the possibility that the different responses to dehydration were a function of different distributions of water in the axis tissue under the two drying regimes. However, ultrastructural observations indicated that different deleterious processes may be occurring under the different drying treatments. It was tentatively concluded that a major cause of viability loss in slowly dried material was likely to be a consequence of aqueous-based processes leading to considerable membrane degradation. Uneven distribution of tissue water could not be rejected as a contributory cause of the survival of rapidly dried seeds to low bulk water contents. The differential response to dehydration at different drying rates implies that it is not possible to determine a ‘critical water content’ for viability loss by recalcitrant seeds.

Storage of Recalcitrant Seeds

Seed Quality ◽  
2020 ◽  
pp. 209-222
Author(s):  
H. F. Chin
Keyword(s):  
Recalcitrant Seeds

scholarly journals A new approach towards the so-called recalcitrant seeds

2018 ◽  
Vol 40 (3) ◽  
pp. 221-236 ◽  
Author(s):  
Claudio José Barbedo
Keyword(s):  
Plant Conservation ◽  
Point Of View ◽  
Recalcitrant Seeds ◽  
New Approach ◽  
Recalcitrant Seed ◽  
Seed Conservation ◽  
Conservation Technology ◽  
Orthodox Seeds ◽  
Standard Life ◽  
Life Behavior

ABSTRACT: Water is essential, irreplaceable, and indispensable for any kind of carbon-based-life metabolic activity. Water-dependent living beings are the expected pattern in nature. However, some organisms can survive for some time at a minimum water content, such as seeds of some species (orthodox seeds). Nevertheless, the expected standard life behavior is found in seeds of another group of species, the so-called recalcitrant seeds, which are sensitive to desiccation. A huge range of different behaviors can be found between these two groups, leading authors to consider that orthodoxy and recalcitrance is not an all-or-nothing situation. Notwithstanding, we are still too far from understanding the differences and similarities between all these kinds of seeds and this has been a serious barrier to the development of plant conservation technologies. A new approach to understanding the differences between these seeds is presented here based on seed maturation, environmental influences, and evolution. From this point of view, all kinds of seed behavior are contemplated and, consequently, some new perspectives are considered for the recalcitrant seed conservation technology, the most intensely desired technology nowadays in this area.

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