Development of Storage Techniques for Thampakam (Hopea Parviflora Bedd) Seeds
By: Shaji M.
Contributor(s): Sudhakara K (Guide).
Material type:
BookPublisher: Vellanikkara Department of Silviculture and Agroforestry,College of Forestry, 2002DDC classification: 634.9 Online resources: Click here to access online Dissertation note: MSc Abstract: A detailed study was conducted at College of Forestry, Kerala
Agricultural University, Vellanikkara, Thrissur, Kerala during 1999-2001 to
develop a suitable storage technique for the seeds of Hopea parviflora Bedd.
species through synthetic seed and cryopreservation technology. Moisture content
of intact seeds/ seeds without seed coat/: excised embryonic axes decreased with
increase in intensity and duration of desiccation levels and only the seeds without
seed coat showed significant difference in moisture content due to maturity levels.
Leachate conductivity was not significantly affected due to maturity levels of intact
seeds and excised embryonic axes. But seeds without seed coat showed significant
difference in leachate conductivity due to maturity levels and it was higher at seven
weeks after anthesis. Increasing the duration of desiccation significantly increased
the leachate conductivity of intact seeds/ seeds without seed coat! embryonic axes.
Germination parameters of intact seeds and seeds without seed coat were not
affected significantly by increased desiccation. However, excised embryonic axes
showed significant difference in germination parameters when the intensity and
duration of desiccation was increased. The synthetic seeds developed from these
desiccated axes also showed significant difference in their germination parameters.
Synthetic seeds stored at 4°C retained maximum viability after four weeks,
compared to those stored at 200 C and 27 0 C. When stored at 27 0 C, the synthetic
seeds developed from six weeks mature embryos retained viability up to three
weeks whereas those at seven weeks after anthesis retained viability up to two
weeks only. After cryopreservation, the propagules invariably failed to regenerate
but could retain green colour for two to three days.
| Item type | Current location | Call number | Status | Date due | Barcode |
|---|---|---|---|---|---|
Theses
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KAU Central Library, Thrissur Theses | 634.9 SHA/DE PG (Browse shelf) | Available | 172062 |
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MSc
A detailed study was conducted at College of Forestry, Kerala
Agricultural University, Vellanikkara, Thrissur, Kerala during 1999-2001 to
develop a suitable storage technique for the seeds of Hopea parviflora Bedd.
species through synthetic seed and cryopreservation technology. Moisture content
of intact seeds/ seeds without seed coat/: excised embryonic axes decreased with
increase in intensity and duration of desiccation levels and only the seeds without
seed coat showed significant difference in moisture content due to maturity levels.
Leachate conductivity was not significantly affected due to maturity levels of intact
seeds and excised embryonic axes. But seeds without seed coat showed significant
difference in leachate conductivity due to maturity levels and it was higher at seven
weeks after anthesis. Increasing the duration of desiccation significantly increased
the leachate conductivity of intact seeds/ seeds without seed coat! embryonic axes.
Germination parameters of intact seeds and seeds without seed coat were not
affected significantly by increased desiccation. However, excised embryonic axes
showed significant difference in germination parameters when the intensity and
duration of desiccation was increased. The synthetic seeds developed from these
desiccated axes also showed significant difference in their germination parameters.
Synthetic seeds stored at 4°C retained maximum viability after four weeks,
compared to those stored at 200 C and 27 0 C. When stored at 27 0 C, the synthetic
seeds developed from six weeks mature embryos retained viability up to three
weeks whereas those at seven weeks after anthesis retained viability up to two
weeks only. After cryopreservation, the propagules invariably failed to regenerate
but could retain green colour for two to three days.
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