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Ipomoea (Sweetpotato/Kumara) Post-Entry Quarantine Testing Manual

Ipomoea (Sweetpotato/Kumara) Post-Entry Quarantine Testing Manual

Ipomoea (Sweetpotato/Kumara) Post-Entry Quarantine Testing Manual

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Whole plants should be planted into sufficiently sized pots (eg 3 L minimum) containing<br />

50:50 (v/v) pasteurised peat:pumice planting media and a few grams of slow-release fertiliser<br />

with trace elements (e.g. Osmocote ® ). Nodal cuttings should be taken from growing vines to<br />

maintain the clone and facilitate quarantine examination and testing. Cuttings with one or<br />

two leaves and at least two nodes can be rooted directly in pasteurised pumice sand or perlite<br />

before transferring to planting media. It would be worth preserving clonal material in tissue<br />

culture as a back-up resource, and to preserve any established virus-free status.<br />

Plants in tissue culture<br />

Tissue culture plantlets can be sub-cultured after arrival by cutting into nodal sections and<br />

placing into new tissue culture vessels with fresh nutrient media (e.g. Murashige and Skoog<br />

media).<br />

Plantlets to be tested are carefully excised from the tissue culture vessel and washed to<br />

remove any remaining agar and planted into pots of planting media containing 50:50 (v/v)<br />

pasturised peat:perlite or 50:50 (v/v) peat:vermiculite. The plantlets must be protected from<br />

desiccation for approximately three weeks by covering initially with a vented plastic tub or<br />

bag. Alternatively, the plants can be misted regularly to keep the planting media moist, and<br />

to maintain a high relative humidity. Pots should be placed in bright light, but not direct<br />

sunlight during the three weeks. After this period, any coverings should be removed and the<br />

plants moved to higher light intensity.<br />

5.3 Pollen<br />

Anthers can be collected from mature but unopened flowers and dried in warm, light<br />

conditions. Following this drying period, pollen should be collected into a centrifuge vial or<br />

into gel capsules and stored at 4°C in a sealed container in the presence of a strong desiccant<br />

such as calcium chloride.<br />

6. INSPECTION<br />

The inspection requirements for the operator of the facility are set out in the “MPI<br />

Biosecurity Authority Standard PBC-NZ-TRA-PQCON”<br />

(http://www.biosecurity.govt.nz/files/regs/stds/pbc-nz-tra-pqcon.pdf )<br />

Photographs of symptoms caused by significant regulated diseases can be found in Appendix<br />

1. However, please note that pot-grown sweetpotato plants can be prone to nutrient<br />

deficiencies if not adequately fertilised and nutrient deficiencies can resemble virus infection,<br />

e.g. chlorosis and necrosis. Symptoms related to nutrient deficiencies can be found in<br />

Appendix 2. Further information on nutrient deficiencies is described in Clark & Moyer<br />

(1988).<br />

<strong>Ipomoea</strong> <strong>Post</strong>-<strong>Entry</strong> <strong>Quarantine</strong> <strong>Testing</strong> <strong>Manual</strong> · November 2012<br />

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