Many a Cabernet Sauvignon vine have been planted worldwide but the two poles of excellence, if one considers production volume and consumer spend, are definitively Napa and Bordeaux. In this exercise I examine the use of Cabernet Sauvignon clones in the two regions to determine whether there are any appreciable differences in type and/or application and, if so, how it manifests. But first, some background on clones.
Early vineyards were planted/replanted with cuttings sourced from successful vines in a vineyard, a process which is referred to as massal selection. The advantage of this method is that all the good qualities of the parent plants can be passed on to these new vines but the same is also true for negative characteristics. The more modern practice is to use clonal selections as the source for these new plantings and, in so doing, pass on the desirable characteristics while eliminating those that provide negative effects. Areas of potential clonal differentiation are shown in the table below.
Component Characters | Manifestations |
Vine | Upright Weeping High yield Low yield |
Leaf | More lobed Less lobed |
Cluster | Compact Loose |
Berry | Color Size Shape Maturity pH |
Flavor | Anthocyanin levels Color Muscat character |
Wine | Sensory perception |
In the case of clonal selection, the source material has undergone a number of procedures "designed to isolate and provide premium stock to grape growers" (Jackson, Wine Science). The key objective of any clonal selection program is to improve crop yield and grape quality by providing virus-free (or impact-neutral) rootstock and scions to the grower. Viruses can negatively impact the vine in the following areas (Bisson):
- Vine
- Pruning weight
- Shoot numbers
- Yield
- Cluster numbers
- Berry
- Berry weight
- Sugar levels
- Titratable acidity
- pH
- Other measures
- Shoot weight
- Cluster weight
- Berries/cluster
Source: Modified from Deborah Golino presentation on source of Cabernet Sauvignon clones, UCD course, 5/15/2008 |
The heat therapy identified in the Disease Elimination Phase involves exposing dormant cuttings to high temperatures (~ 38℃) for several weeks. This approach has been supplanted by shoot-tip culture, "a disease elimination technique whereby pieces of the apical growing point are excised from a plant and cultured in a sterile growth media apart from the plant. In microshoot tip therapy, as practiced at FPS, a growing tip that is less than 0.5mm is excised from the shoot tip. Many pathogens, including viruses and the crown gall bacterium, are eliminated by this technique" (http://iv.ucdavis.edu/files/72924.pdf).
The body responsible for certification of clones in France is the Institut Francais de la Vigne et du Vin (IFV; formerly ENTAV) and its regional vine selection partners (INRA Bordeaux, Chambre d'agriculture de Gironde, and Chambre d'agriculture des Pyrenees-Atlantiques for Cabernet Sauvignon). This organization began its work in the 1960s and has traversed two generations of clones with a third generation in its future (See figure immediately below). The IFV clone-certification process is illustrated in the second figure.
Jackson recommends that more than one clone be planted in a vineyard as a mechanism for increasing the variability and complexity of flavors in the finished wine. Boulton, et al. (Principles and Practices of Winemaking), suggests at least two clones should be planted in small plots and up to five or six in larger vineyards in order to avoid problems that may arise due to limited genetic variation in a single clone.
I will continue with the specifics of the Cabernet Sauvignon clones in my next post.
©Wine -- Mise en abyme
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