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PHASE 3
This is the stage in which berries mature and are
harvested for winemaking purposes, although its
onset is highly dependent on the successful
completion of the previous two phases. Many
processes are taking place at this time.
Berry growth
Cell expansion proceeds at a high rate and berries
obviously increase in size during Phase 3, but this
strongly depends on sugar and water availability in
the vine.
SUGAR ACCUMULATION
Hormones activate the relevant genes and these
synthesize the enzymes for sugar import into the
berry. Generally, sugar accumulation is more rapid
in the weeks following veraison and becomes
slower afterwards, although this may be less so in
cooler climates.
In Australia sugar accumulation is often considered
to be fast relative to phenolic and aroma
development. This is likely due to the high
evaporative loss of water from berry surfaces under
the dry conditions experienced in many grape
growing regions (grape skins are not 100% water
tight). Berries can therefore have high sugar levels
early in the ripening process This may have
implications for management of some diseases
such as the fungus Botrytis whose growth is
favoured by sugar accumulation in berries.
ACID DEPLETION
During this phase, berries cannot derive energy for
metabolic processes from sugars. Instead, for most
requirements, the malic acid content of the berry is
drawn on and broken down to provide energy.
During hot night time conditions, malic acid is further
depleted in the respiratory process. In conditions
above 35°C, tartaric acid provides the energy source.
When the energy needs of berries is low (when
temperatures are either very high or very low so
that metabolic processes are minimised) some malic
acid is transformed to sugar rather than being
broken down to release energy. This maintains the
UNDERSTANDING GRAPEVINE GROWTH NUMBER 5:
Viti-Noteswww.crcv.com.au 2005
The berry development process – Phase 3
Current Vitinote titles in this
Understanding grapevine
growth series include:
1. Dormancy and budburst
2. Spring shoot
and root growth
3. Flowering
4. The berry development
process – Phases 1 and 2
5. The berry development
process – Phase 3
6. Defining berry ripeness
7. Site factors influencing
berry ripening processes
and rates of ripening PHASE 3 IS THE PERIOD OF RAPID CELL
EXPANSION AND SUGAR
ACCUMULATION. POTASSIUM, AMINO
ACIDS AND PHENOLIC COMPOUNDS
INCREASE, MALIC ACID IS DEGRADED,
AND MOST FLAVOURS ARE DEVELOPED
www.crcv.com.au
pH inside cells and generally accounts for about 5% of sugar
accumulation in berries. The presence of abscisic acid (ABA) in berries
increases this activity resulting in a faster ripening process.
AROMA DEVELOPMENT
The methoxypyrazines responsible for the capsicum/asparagus aromas of
some wines decrease as berries mature, in proportion to malic acid
depletion, so that it is possible for viticulturists and winemakers to
monitor isobutyl-methoxypyrazine decline by monitoring malic acid.
Conversely, the terpenoids which give floral or citrus aromas increase.
The production of some terpenoids post-veraison is related to the sugar
content of berries, however their final concentration will vary according
to the interaction between rates of production and degradation of these
compounds.
PHENOLICS
Anthocyanins begin to accumulate in the skins of red varieties about two
weeks before the colour is visible.
In red varieties the levels of tannins in grape skins are already relatively
high at veraison and remain essentially constant thereafter.
In white grapes, phenolic compounds diminish to minimal concentrations
as berries mature.
Anthocyanins are an end product of sugar metabolism, but require only
a minimum amount of sugar to develop, so that their accumulation is
independent of the sugar content of berries. Tannins evolve changing
mouth feel characteristics over time, and their concentrations in berries
are more independent of climatic conditions than are anthocyanins. The
ability to extract seed tannins decreases after veraison.
NITROGENOUS COMPOUNDS
Nitrogen comes in a number of chemical forms and is an essential
component of amino acids which are the building blocks for the more
complex proteins that often act as hormones and enzymes in metabolic
processes in the vine.
During Phase 3 of berry development, 80% of the nitrogen in berries is
in the skins and seeds, while the juice contains barely 20% of the total
berry nitrogen. Over the period of maturation, the ammonium
concentration in berries decreases after veraison and the protein fraction
increases, as ammonium is gradually incorporated into more complex
compounds within the berry. The protein fraction is very small, however,
with the majority of nitrogen occurring in amino acids - at maturity 50-
90% of the total nitrogen in grape juice exists as a component of amino
acids.The soluble protein concentration in the berry reaches a maximum
before maturation and then decreases. The concentration of proteins in
grape juice at harvest can vary between 1.5-100mg/L.
The range of amino acids and proteins formed is to some extent
characteristic of the variety and environmental influences under which
individual vines grow. Generally, however a small number of amino acids
predominates. Many amino acids can be transformed to fulfill a need by
the vine, eg. to manage stress due to drought conditions. This is of use
to the vine, but some of these ‘defence’ proteins can be problematic. For
example, some cannot be utilised by yeasts in the winemaking process,
and a high concentration of the amino acid arginine may produce
urethane (a carcinogen) in wine. Some amino acids can be transformed
to malic acid and into sugars to provide energy for the berry if needed.
CELL WALLS
The maturing process of berries is accompanied by a gradual
‘weakening’ of berry cell walls.
Pectin, a compound which acts to strengthen the rigid cellulose walls
which characterise all higher plants, is gradually dissolved as berries
ripen. The rate of degradation is further exacerbated if the vine has
access to high levels of potassium, which moves readily into berries and
compounds this process.These more fragile cell walls increase the berry’s
susceptibility to attack by bunch rotting fungi such as Botrytis.
High potassium levels in juice can be a factor of the type of rootstock, eg.
Schwarzman,or result from shading in the canopy.Potassium affects quality
of red wine by increasing pH and impacting on anthocyanin development.
THE CRC for Viticulture is a joint venture between the following core participants, working with a wide range of supporting partners.
FURTHER INFORMATION
Product or service information is provided to inform the viticulture industry
about available resources,and should not be interpreted as an endorsement.
USEFUL REFERENCES:
• Biology of the grapevine, 1992 by MG Mullins, A Bouquet and E
Williams published by Cambridge University Press.
• Soil, irrigation and nutrition, Grape Production Series No. 2, 2003
edited by P Nicholas.
• Viticulture and Environment, 1992 by J Gladstones.
• Viticulture, 1992 by BG Coombe and PR Dry.
Information in this Vitinote has been adapted from the CRCV Winegrape
quality management: Research to Practice® workshop manual. The
Viticulture Research to Practice®
workshops are training programs
whose delivery can be fine-tuned to suit each region.
• Enquiries to Peter Mansfield at Winetac on (08) 8373 7090 or visit
www.crcv.com.au for more information.
Visit the web site at www.crcv.com.au/viticare/vitinotes/ for updates and
more Vitinote titles.
©2005 Cooperative Research Centre for Viticulture

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berry-development-process-iii

  • 1. PHASE 3 This is the stage in which berries mature and are harvested for winemaking purposes, although its onset is highly dependent on the successful completion of the previous two phases. Many processes are taking place at this time. Berry growth Cell expansion proceeds at a high rate and berries obviously increase in size during Phase 3, but this strongly depends on sugar and water availability in the vine. SUGAR ACCUMULATION Hormones activate the relevant genes and these synthesize the enzymes for sugar import into the berry. Generally, sugar accumulation is more rapid in the weeks following veraison and becomes slower afterwards, although this may be less so in cooler climates. In Australia sugar accumulation is often considered to be fast relative to phenolic and aroma development. This is likely due to the high evaporative loss of water from berry surfaces under the dry conditions experienced in many grape growing regions (grape skins are not 100% water tight). Berries can therefore have high sugar levels early in the ripening process This may have implications for management of some diseases such as the fungus Botrytis whose growth is favoured by sugar accumulation in berries. ACID DEPLETION During this phase, berries cannot derive energy for metabolic processes from sugars. Instead, for most requirements, the malic acid content of the berry is drawn on and broken down to provide energy. During hot night time conditions, malic acid is further depleted in the respiratory process. In conditions above 35°C, tartaric acid provides the energy source. When the energy needs of berries is low (when temperatures are either very high or very low so that metabolic processes are minimised) some malic acid is transformed to sugar rather than being broken down to release energy. This maintains the UNDERSTANDING GRAPEVINE GROWTH NUMBER 5: Viti-Noteswww.crcv.com.au 2005 The berry development process – Phase 3 Current Vitinote titles in this Understanding grapevine growth series include: 1. Dormancy and budburst 2. Spring shoot and root growth 3. Flowering 4. The berry development process – Phases 1 and 2 5. The berry development process – Phase 3 6. Defining berry ripeness 7. Site factors influencing berry ripening processes and rates of ripening PHASE 3 IS THE PERIOD OF RAPID CELL EXPANSION AND SUGAR ACCUMULATION. POTASSIUM, AMINO ACIDS AND PHENOLIC COMPOUNDS INCREASE, MALIC ACID IS DEGRADED, AND MOST FLAVOURS ARE DEVELOPED
  • 2. www.crcv.com.au pH inside cells and generally accounts for about 5% of sugar accumulation in berries. The presence of abscisic acid (ABA) in berries increases this activity resulting in a faster ripening process. AROMA DEVELOPMENT The methoxypyrazines responsible for the capsicum/asparagus aromas of some wines decrease as berries mature, in proportion to malic acid depletion, so that it is possible for viticulturists and winemakers to monitor isobutyl-methoxypyrazine decline by monitoring malic acid. Conversely, the terpenoids which give floral or citrus aromas increase. The production of some terpenoids post-veraison is related to the sugar content of berries, however their final concentration will vary according to the interaction between rates of production and degradation of these compounds. PHENOLICS Anthocyanins begin to accumulate in the skins of red varieties about two weeks before the colour is visible. In red varieties the levels of tannins in grape skins are already relatively high at veraison and remain essentially constant thereafter. In white grapes, phenolic compounds diminish to minimal concentrations as berries mature. Anthocyanins are an end product of sugar metabolism, but require only a minimum amount of sugar to develop, so that their accumulation is independent of the sugar content of berries. Tannins evolve changing mouth feel characteristics over time, and their concentrations in berries are more independent of climatic conditions than are anthocyanins. The ability to extract seed tannins decreases after veraison. NITROGENOUS COMPOUNDS Nitrogen comes in a number of chemical forms and is an essential component of amino acids which are the building blocks for the more complex proteins that often act as hormones and enzymes in metabolic processes in the vine. During Phase 3 of berry development, 80% of the nitrogen in berries is in the skins and seeds, while the juice contains barely 20% of the total berry nitrogen. Over the period of maturation, the ammonium concentration in berries decreases after veraison and the protein fraction increases, as ammonium is gradually incorporated into more complex compounds within the berry. The protein fraction is very small, however, with the majority of nitrogen occurring in amino acids - at maturity 50- 90% of the total nitrogen in grape juice exists as a component of amino acids.The soluble protein concentration in the berry reaches a maximum before maturation and then decreases. The concentration of proteins in grape juice at harvest can vary between 1.5-100mg/L. The range of amino acids and proteins formed is to some extent characteristic of the variety and environmental influences under which individual vines grow. Generally, however a small number of amino acids predominates. Many amino acids can be transformed to fulfill a need by the vine, eg. to manage stress due to drought conditions. This is of use to the vine, but some of these ‘defence’ proteins can be problematic. For example, some cannot be utilised by yeasts in the winemaking process, and a high concentration of the amino acid arginine may produce urethane (a carcinogen) in wine. Some amino acids can be transformed to malic acid and into sugars to provide energy for the berry if needed. CELL WALLS The maturing process of berries is accompanied by a gradual ‘weakening’ of berry cell walls. Pectin, a compound which acts to strengthen the rigid cellulose walls which characterise all higher plants, is gradually dissolved as berries ripen. The rate of degradation is further exacerbated if the vine has access to high levels of potassium, which moves readily into berries and compounds this process.These more fragile cell walls increase the berry’s susceptibility to attack by bunch rotting fungi such as Botrytis. High potassium levels in juice can be a factor of the type of rootstock, eg. Schwarzman,or result from shading in the canopy.Potassium affects quality of red wine by increasing pH and impacting on anthocyanin development.
  • 3. THE CRC for Viticulture is a joint venture between the following core participants, working with a wide range of supporting partners. FURTHER INFORMATION Product or service information is provided to inform the viticulture industry about available resources,and should not be interpreted as an endorsement. USEFUL REFERENCES: • Biology of the grapevine, 1992 by MG Mullins, A Bouquet and E Williams published by Cambridge University Press. • Soil, irrigation and nutrition, Grape Production Series No. 2, 2003 edited by P Nicholas. • Viticulture and Environment, 1992 by J Gladstones. • Viticulture, 1992 by BG Coombe and PR Dry. Information in this Vitinote has been adapted from the CRCV Winegrape quality management: Research to Practice® workshop manual. The Viticulture Research to Practice® workshops are training programs whose delivery can be fine-tuned to suit each region. • Enquiries to Peter Mansfield at Winetac on (08) 8373 7090 or visit www.crcv.com.au for more information. Visit the web site at www.crcv.com.au/viticare/vitinotes/ for updates and more Vitinote titles. ©2005 Cooperative Research Centre for Viticulture