Sauvignon Blanc Grapevine Improvement Programme
Public Summary Reports
December 2021
This quarter marks the launch of the programme, which was announced by Agriculture Minister Hon Damien O’Connor and New Zealand Wine on 9th December.
March 2022
Over the January to March quarter the New Zealand wine industry’s attention turns to harvesting grapes for the current vintage. For the SB2.0 programme, the focus has been on setting up a new multi-institutional team to deliver the program’s objectives.
June 2022
Membership of the programme’s Commercial and Technical Advisory groups was determined this quarter, including highly experienced members of the New Zealand wine industry and international experts.
September 2022
New staff have joined BRI’s grapevine Improvement team to support the establishment of the young vines in the nursery and the identification of novel genetic traits with the potential to improve the resilience, productivity, and sustainability of Sauvignon Blanc viticulture.
December 2022
Establishing a large population of diverse Sauvignon Blanc vines is the key goal of the first half of this programme. Despite starting at a difficult time in the season, plant production is now ahead of schedule. Over the summer the aim is to grow the new plantlets into strong vines that are well-prepared for winter dormancy.
March 2023
After a very busy summer season, the programme has grown the collection of Sauvignon Blanc (SB) vines to 6,000 plantlets ahead of winter 2023. Leaf samples are now being collected from each plant for DNA extractions so that a database of known genetic diversity can be produced while the plants are dormant over winter.
June 2023
After the success of completing production of the project’s first 6,000 new vines ahead of schedule, we were notified of a failure by the plant production subcontractor, who had mistakenly produced and delivered vines that were of the wrong grapevine variety. This will result in a time delay. All other work is progressing on schedule, including plant selection work and DNA sequencing.
September 2023
As a result of the plant production failure identified last quarter, the Programme end date has been delayed by 18 months until April 2030. Plant and Food Research Ltd. have agreed to bear the cost of replacing the plants produced to date and have reached a financial settlement agreement that will ensure the programme funders are not asked to bear additional costs resulting from the delayed milestones. Production of replacement Sauvignon Blanc vines is now well underway.
December 2023
In November, industry representatives from eighteen grantor companies met at Bragato Research Institute in Blenheim for the second annual Programme Grantors’ Workshop. Over an interactive morning of presentations and conversation, the grantors reviewed the programme progress over the past year and discussed the approaches being used to develop and select New Zealand’s own future clones.
March 2024
The production rate of new Sauvignon Blanc clones over the summer has continued to increase, as plant growth media have been further optimised. At approximately 60 cm in height, the most mature vines are already demonstrating unique traits indicative of the underlined genetic changes among them. The new clones appear healthy and have been growing rapidly, with the bases of their stems beginning to show sufficient lignification ahead of autumn.
June 2024
Despite the slow regeneration of Sauvignon Blanc plantlets, increased resourcing to plant production and efforts to optimise the growth conditions for the plantlets has enabled the Programme to reach its target of 6,000 new plantlets by the end of June 2024. These new vines will continue to grow in a climate-controlled indoor environment throughout the winter until they can be planted out in a new research vineyard this spring.
September 2024
During the winter, DNA from new Sauvignon Blanc (SB) clones and commercial vines was analysed to identify the type of genetic changes that vary among individuals. The established sequencing and data analysis pipelines will be used to characterise the full scope of genetic variation produced during the Programme term.