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Grapevine Micropropagation for Production of Disease-Free Vines

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Presentation on theme: "Grapevine Micropropagation for Production of Disease-Free Vines"— Presentation transcript:

1 Grapevine Micropropagation for Production of Disease-Free Vines
Berva Brock Junior, Organizational Leadership Program University of Wyoming, Sheridan Research and Extension Center

2 Grape Production in United States
World’s most valuable fruit crop 10 – 12th most valuable agricultural crop in US 1.2 million workers in grape & wine industry National economic impact – $ 162 billion annually Wine America (National Association of Wines), 2008

3 Grapevine Propagation Techniques
Cutting – Softwood and hardwood Layering – Air, mound, serpentine Budding (sometimes described as bud grafting) Grafting – Softwood (green grafting), hardwood (bench, bridge, inarch-approach, exarch, cleft, whip, etc.) In vitro culture – Micropropagation

4 Commercial Grape Propagation
Double A Vineyards, NY 6 feet between rows, 12” between cutting rows and 2” between individual cuttings. 80,000 cuttings per acre (5,00000 – 8,00000 cuttings/yr.) Rooted cutting

5 Grapevine Propagation for the Homeowner
Growth Flowering Rooting Growth, flowering and rooting in canes after 5 weeks of exposure to light

6 Limitations of Conventional Propagation
Limited availability of elite planting material Problems with spreading insect, bacterial and viral diseases Insect – Phylloxera Bacteria – Agrobacterium, Pierce’s disease Viral – Leaf roll and fan leaf viruses

7 Pierce’s Disease Infection in Grapevines
PD infected vine Vines dead from PD Xylem infection Leaf symptoms Affected shoots Affected berries

8 Control – No cure for infected vines. Uproot and burn vines
Crown Gall Disease in Grape Control – No cure for infected vines. Uproot and burn vines

9 Viral Diseases Leaf roll infected vineyard Fan leaf infected vineyard
Leaf roll infected vines Fan leaf infected vineyard Infected berries

10 Grapevine Micropropagation
Micropropagation involves using apical meristems from actively growing shoots of field grown grapevines Shoot apical meristems are then placed onto plant growth medium with growth regulators for shoot proliferation Resulting shoots are then rooted, hardened under high humidity and then transferred outdoors

11 Micropropagation Protocol

12 Advantages of Micropropagation
Production of bacterial and virus-free plants Rapid propagation of elite varieties Plants arising from tissue culture are uniform in growth, vigor, yield and quality

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14 Source of Grape Germplasm

15 Grape Micropropagation Protocol
Obtain shoot tips Shoot apical meristem Meristem after excision Growth of shoot apical meristem Shoot proliferation Shoot culture maintenance

16 Grape Micropropagation Protocol
Rooting proliferated shoots Transfer to soil Acclimation Hardening Transfer to Green House

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19 Himrod Data on Shoot Proliferation 12-21-12 Start Date
Meristem after excision Proliferation after 4 weeks Himrod Start Date # of nodes in dish Date of Data # of shoots in 4 weeks # of shoots In 8 weeks 5 39 1028 33 478 29 346

20 Future Studies Optimizing micropropagation protocols for additional 25 varieties Study performance of tissue cultured produced plants under field conditions

21 Acknowledgements UW College of Agriculture (Special Problems Fellowship awarded to Berva Brock) UW Agricultural Experiment Station (SREC) Department of Plant Sciences Wyoming Department of Agriculture


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