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Increasing Efficiencies in Propagation - Workpackage 2 Details

Start date :0

Completion date :45

(Month 0 marking the start of the project.)

Partner responsible:Dr. Andreas Meier Dinkel

Nos. of other partners involved:1, 3, 8, 9, 10, 11, 13.

Objectives

  1. To develop systems for large scale vegetative propagation of selected genotypes of Fraxinus by cuttings, micropropagation, and their low temperature storage in vitro.
  2. To determine the best physiological treatments to mother donor plants which will give : a) controllable flowering, b) viable shoot cultures c) rooting in cuttings (cascade grafting, timing, temperature, pruning, water regimes).
  3. Determine which shifts in fundamental metabolism are indicative of healthy cultures, good rooting, and apparent rejuvenation.
  4. To find indicators of juvenile and mature states by quantifying the expression of "late embryogenic abundant proteins "(LEAPs), using antibodies in : shoot cultures with different states of rejuvenation and ages; adventitious shoots, & somatic and zygotic embryos.
  5. Transfer the micropropagation technology to SMEs; evaluate: the effects of the propagation regimes on the quality and growth potential of propagated material; the optimal mycorrhizal associations and the best nursery practices which ensures normal shoot, root and plant development in all material produced for clonal field tests.
  6. Determine the best methods for rooting in cuttings derived from micropropagated plants.

Deliverables

(Month 0 marking the start of the project with all delivery dates being relative to this start date.)

Deliverable
No14
Deliverable Title Delivery
date

15
Nature
16
Dissemination level
17
PU = to public
RE = contractors
D14 Plus trees of Fraxinus selected from provenance & progeny trials, grafted and conserved in the field and nursery 12 R RE
D15 Proliferating shoot cultures of selected genotypes ( 10 Genotypes in 2001;
and 30-40 in 2003)
12,
34
O RE
D16 A treatment programme for initiation of cultures from mature lines, rooting in cuttings 38 R RE
D17 Protocols on media, culture period, explant, and environmental conditions for optimal micropropagation 24 R RE
D18 Marker proteins for health, rooting competences & juvenility 36 R RE
D19 Somatic embryogenesis & adventitious regeneration assayed 36 R PU
D20 Technology & selected lines transferred to SMEs & mycorrhization., cutting propagated & evaluated in the nursery 42 R RE
D21 Protocol for plant treatments for flower induction & seed setting 46 R RE