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Improving the identification, handling and storage of “difficult” seeds ...

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- Low Constant temperature oven method, particularly used for oil crops. To attain <strong>the</strong><br />

required moisture content, samples are kept at 101 – 103 °C for 17 hours.<br />

- High constant temperature oven method – This method is used to determine <strong>the</strong> moisture<br />

content in cereal <strong>seeds</strong>, samples are kept at 130–133 °C for 4 hours for large seeded cereals<br />

(like maize) <strong>and</strong> for 2 hrs for o<strong>the</strong>r cereals <strong>and</strong> also 1 hr for o<strong>the</strong>r species.<br />

Storage containers<br />

Seeds being kept in <strong>the</strong> long- <strong>and</strong> medium-term are sealed in laminated aluminum foil bags. Paper<br />

bags are used for those <strong>seeds</strong> that are stored under short-term <strong>storage</strong> condition.<br />

Viability monitoring (question 5.5)<br />

The Institute performs viability monitoring on ex-situ collections. Monitoring is usually done every<br />

7-10 years from <strong>the</strong> date stored. Different substrates are used for germination testing:<br />

▪ S<strong>and</strong> for large <strong>seeds</strong> (100 <strong>seeds</strong> per Petri dish with 2 replications)<br />

▪ Filter paper for small <strong>and</strong> medium sized <strong>seeds</strong> (50 <strong>seeds</strong> per Petri dish with 4 replications)<br />

Species that demonstrate low level <strong>of</strong> viability during initial tests<br />

Sorghum sp.<br />

Oryza sp.<br />

As studies that focus on <strong>the</strong> effect <strong>of</strong> <strong>storage</strong> age on species under conservation are lacking, it is<br />

difficult to generalize about species that show a significant increase or decrease in % germination or<br />

no significant change.<br />

Constraints (question 5.10) <strong>and</strong> possible solutions<br />

▪ Drying room facility – <strong>the</strong> old drying room has been working for 30 yrs (1976-2006), <strong>the</strong><br />

equipments <strong>of</strong> <strong>the</strong> dry room are so old , <strong>the</strong> dehumidifier is not working properly, causing a<br />

reduction in viability<br />

▪ Lack <strong>of</strong> trained manpower to maintain gene bank facilities (high dependency on<br />

experts/technicians from abroad)<br />

▪ Lack <strong>of</strong> proper data base management<br />

▪ Lack <strong>of</strong> duplicate gene bank<br />

Possible solutions to <strong>the</strong> constraints<br />

▪ Installation <strong>of</strong> new drying room facilities<br />

▪ Build human capacity through training & streng<strong>the</strong>n facilities for study <strong>and</strong> data management.<br />

▪ Establish a duplicate gene bank <strong>and</strong> o<strong>the</strong>r mini-gene banks elsewhere in <strong>the</strong> country.

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