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A manual of rice seed health testing - IRRI books - International Rice ...

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3.2 Dry <strong>seed</strong><br />

inspection using a<br />

magnifying lens.<br />

3.3 Dry <strong>seed</strong><br />

inspection using a<br />

stereobinocular<br />

microscope.<br />

Data from the tests should be recorded<br />

on appropriate recording<br />

sheets and signed by the responsible<br />

analyst. The names <strong>of</strong> fungi<br />

should be recorded according to the<br />

state they are found during <strong>testing</strong>.<br />

If conidia are found, the conidial<br />

epithet is recorded; if the perfect<br />

stage is detected, the perfect stage<br />

epithet is recorded; if both are<br />

present, both epithets are recorded.<br />

For uniformity in recording, the<br />

currently accepted epithet should<br />

be used. (See Appendix 1 for sample<br />

recording sheets for dry <strong>seed</strong><br />

inspection, washing test, blotter and<br />

agar plate tests, and for<br />

Aphelenchoides besseyi.).<br />

Table 3.2. Methods and equipment used in <strong>rice</strong> <strong>seed</strong> <strong>health</strong> <strong>testing</strong>.<br />

Method<br />

Direct method<br />

For sclerotia,<br />

smut, malformed<br />

and moldy <strong>seed</strong>s<br />

Tilletia barclayana<br />

contamination<br />

Washing test<br />

Aphelenchoides<br />

besseyi sedimentation<br />

test<br />

Indirect method<br />

Blotter test<br />

Agar test for<br />

fungi and<br />

bacteria<br />

Test tube agar<br />

growing-on test<br />

Inoculation<br />

Other methods<br />

Serological<br />

test<br />

Preparation<br />

procedures<br />

Shake by hand<br />

or use automatic<br />

shaker; then<br />

centrifuge at low<br />

speed<br />

Use modified<br />

Baermann funnel<br />

In NUV incubation<br />

21 °C, with timer<br />

12 h NUV light/<br />

12 h darkness<br />

Seed surface<br />

sterilization in<br />

table top<br />

incubators (28 °C)<br />

In growth chamber + b<br />

(28 °C) 12 h light/<br />

day or on laboratory<br />

table top<br />

near window<br />

In growth chamber +<br />

(28 °C) 12 h light<br />

or in glasshouse<br />

As required<br />

Detection/identificatlon tools<br />

Hand Stereobinocular Compound Others<br />

lens microscope microscope<br />

+<br />

+ +<br />

+ +<br />

+ Haemocytometer<br />

Tally counter<br />

+ + Tally counter<br />

+ + Freezer for deep<br />

+ a + a freezing method<br />

Laminar flow<br />

cabinet<br />

Sterile sand/<br />

soil, light<br />

a To verify spores. b To magnify developing lesions. Equipment 15

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