Review articles

Recent advancements in understanding the terroir effect on aromas in grapes and wines This article is published in cooperation with the XIIIth International Terroir Congress November 17-18 2020, Adelaide, Australia. Guest editors: Cassandra Collins and Roberta De Bei


Terroir is about the link between wine and its origin. It has long been understood by sensory evaluation that the taste of wine from a given variety can be related to its origins. Specific organoleptic characteristics of wine are influenced by environmental factors such as soil and climate. By deconstructing the effect of measurable soil and climate parameters on grape and wine aroma compounds, the terroir effect on wine typicity can be better understood. Climate influences on vine development and grape ripening are mainly associated with temperature, radiation and rainfall, while soil influences are primarily associated with water availability and nitrogen supply. Significant advances have been made over recent years in understanding wine aromas and their molecular basis and influences of climate and soil on a wide range of molecules responsible for wine aroma expression. This article aims to review these recent research advances to obtain a more comprehensive understanding of how terroir influences wine typicity. The effect of terroir on wine quality and typicity is sometimes considered intangible and difficult to explain on a scientific basis. By combining agronomic, analytical and sensory approaches, however, this review shows that the terroir effect is mediated by measurable factors that can easily be monitored in the vineyard. Assessment of the results compiled by this review allows the suggestion that terroir expression at specific sites might be maximized by choosing appropriate plant material in relation to soil and climate, by acting on manageable parameters like vine water and nitrogen status, or by implementing canopy management to modify microclimate in the bunch zone.


1. Understanding the effect of terroir on wine typicity

The quality and style of wine are influenced by the place where the vines grow (Jackson and Lombard, 1993). It is acknowledged that particular local soil and climate conditions have a major influence on wine sensory attributes (Seguin, 1988; van Leeuwen et al., 2004). The winegrower is also of importance in shaping this so-called terroir effect by choosing plant material and vineyard management practices adapted to local soil and climate conditions (van Leeuwen and Seguin, 2006) and the winemaker needs to translate berry composition into optimum wine quality by the use of appropriate winemaking techniques. Climate has long been considered as a major factor in wine production (Winkler, 1965; Jones and Davis, 2000). The influence of soil on grape ripening and wine quality has been investigated by many authors (Seguin, 1969; Bodin and Morlat, 2006; Morlat and Bodin, 2006; Renouf et al., 2010; van Leeuwen et al., 2018). However, to go beyond a descriptive link between wine typicity, soil and climate, it is necessary to break these down into measurable parameters (van Leeuwen et al., 2018). The climate acts primarily through the influence of air temperatures, rainfall and radiation. Temperature acts on phenology (Duchêne and Schneider, 2005; Parker et al., 2011) and grape ripening (Coombe, 1986). Solar radiation influences photosynthesis (Zufferey et al., 2000) and secondary metabolites in grapes (Spayd et al., 2002; Alonso et al., 2016). Soil provides nutrients to the vines. Among these, nitrogen (N) is of major importance, because it influences yield, vigour and grape composition at ripeness (Spayd et al., 1993; Hilbert et al., 2003; Trégoat et al., 2002). Vine water status is determined both by soil type and rooting depth (through their effect on soil water holding capacity) and climate (through rainfall and reference evapotranspiration). Vine water status influences shoot development (Pellegrino et al., 2005), yield (Matthews and Anderson, 1989), grape ripening (van Leeuwen et al., 2009) and fruit composition (Matthews and Anderson, 1988). Hence, the terroir effect can be assessed through the measurement of air temperatures, radiation, rainfall, soil water holding capacity and vine nitrogen status. Comprehensive databases are published on air temperatures in winegrowing regions (Gladstones, 2011) and temperature zoning within winegrowing regions is accessible at an increasingly finer scale (Santos et al., 2012; Bois et al., 2018; de Rességuier et al., 2020). Radiation can be easily quantified as well (Smart, 1986). Many indicators have been validated to assess vine nitrogen status (Spayd et al., 1993; van Leeuwen et al., 2000; Hilbert et al., 2003) and vine water status (Cifre et al., 2005; van Leeuwen et al., 2009; Rienth and Scholasch, 2019). Today, major parameters determining terroir expression can be quantified and even spatialized at vineyard scale (van Leeuwen et al., 2018; de Rességuier et al., 2020).

2. Aromas in grapes and wines

Aroma expression in wine is of major importance (Peynaud and Blouin, 2013) and aromas can be classified as primary (produced during grape ripening), secondary (produced during fermentation) and tertiary (produced during wine ageing) (Ribéreau-Gayon et al., 2020). The odorous compounds associated with primary aromas can either be free (volatile compounds) or bound (conjugated) initially to other molecules in grapes and revealed later, during fermentation, or ageing (Rapp, 1988). Although classified as secondary aromas, ester compounds produced during fermentation are more or less abundant depending on wine composition. Hundreds of odorous compounds have been identified in wines and these can be grouped in specific families (Ferreira, 2010; Ribéreau-Gayon et al., 2020).

2.1. Green and peppery flavours

One family includes several compounds involved in green aromas. Major contributors are methoxypyrazines, in particular 2-methoxy-3-isobutylpyrazine (IBMP) (Allen et al., 1991; Lacey et al., 1991). IBMP is responsible for the odour of green (bell) pepper. C6 compounds are also involved in green aromas (González-Barreiro et al., 2015). The abundance of C6 compounds in wines is modulated by winemaking processes (Ferreira et al., 1995a). The literature is, however, scarce about a possible impact of environmental factors on their presence in grapes and wines. 1,8-cineole is a monoterpene providing minty flavours to wine (Capone et al., 2011; Poitou et al., 2017). (-)-rotundone is a sesquiterpene that is an important aroma compound of Syrah and some other varieties, responsible for peppery notes (Wood et al., 2008).

2.2. Other monoterpenes

Terpenes are an important family of grape and wine aromas that can be found as free compounds or glycosidated forms in grapes (Marais, 1983). They have been identified for their involvement in the Muscat aromas of many grapevine varieties (Muscat, Gewürztraminer, Riesling) (Park and Noble, 1993).

2.3. Volatile thiols and C13-norisoprenoids

Volatile thiols are an aroma family first identified in Sauvignon blanc but also present in numerous other varieties (Darriet et al., 2012). They are present in grapes as non-odorant glutathione or cysteine bound precursors that are released during alcoholic fermentation by the yeast (Peyrot des Gachons et al., 2000). The most important volatile thiols are 3-sulfanylhexanol (3SH, grapefruit), 3-Sulfanylhexyl acetate (3SHA, passion fruit) and 4-methyl-4-sulfanylpentan-2-one (4MSP, boxwood) (Tominaga et al., 1998). C13-norisoprenoids, are another family of major compounds involved in wine aroma (Lee et al., 2007). Among these, β-damascenone is described by fruity-flowery or baked apple nuances (Kotseridis et al., 1999, Pineau et al., 2007), while 1,1,6-trimethyl-1,2-dihydronaphtalene (TDN) recalls kerosene-like notes (Marais et al., 1992). The latter is particularly present in older Riesling wines (Simpson, 1978; Simpson, 1979; Sacks et al., 2012; Ziegler et al., 2019). Megastigmatrienone is a C13-norisopreniod with the smell of spices and tobacco (Slaghenaufi et al., 2016). Hence, this compound is often referred to as “tabanone”.

2.4. Dried fruit aromas

Recently, several compounds involved in dried fruit aromas in must and red wines have been identified, including massoia lactone (Pons et al., 2017a), γ-nonalactone and furaneol (Pons et al., 2008), 3-methyl-2,4-nonanedione (MND, Pons et al., 2011) and (Z)-1, 5-octadien-3-one (Allamy et al., 2017). The aromatic expression of this family of compounds is specific to the phenomenon of over-ripening in grapes and is detected in wines resulting from their vinification.

2.5. Substitutes esters and qualitative fruit aromas

Substituted esters are another important family of compounds with several studies demonstrating their particular sensory impact on fruity expression in red wines, even when these compounds were present at concentrations below their olfactory thresholds. Numerous synergistic effects between fruity compounds have been described in the past, highlighting the fact that these esters increased the perception of fruity aromas (Cameleyre et al., 2015).

2.6. Other aroma compounds and complementary observations

Dimethyl sulphide (DMS) is an aroma compound in wine reminiscent of blackcurrant at low concentration, truffle or undergrowth at medium concentration and green olive or asparagus at high concentration (Spedding and Raut, 1982; Anocibar-Beloqui et al., 1996). DMS concentration is positively correlated to ageing bouquet complexity of great Bordeaux red wines (Picard et al., 2015). Although DMS does not present fruity aromas, it has an indirect impact on fruity aroma expression, enhancing, at low concentrations, blackcurrant aroma (Lytra et al., 2014). Aromatic N,S-heterocycles form a large family of compounds involved in wine aroma with a broad spectrum of odours from meat to cooked potatoes, roasted coffee or hazelnut (Marchand et al., 2000). Finally, o-aminoacetophenone (AAP) is associated with the untypical ageing flavour in white wines, in particular from Riesling (Rapp et al., 1993). Wines with high levels of AAP recall naphthalene, floor polish acacia blossom or mothballs and displaying a metallic bitterness on the palate (Schneider, 2014).

Volatile odorous compounds are not variety specific, but rather their concentration generally varies with the cultivar. For instance, Riesling wines contain more TDN compared to wine from Chardonnay or Gewürztraminer (Sacks et al., 2012) and wines from Cabernet-Sauvignon or Carmenère contain more IBMP than wine from Merlot (Roujou de Boubée et al., 2000). Aroma compounds in wine can also vary to a large extent with environmental conditions like soil or climate (Dunlevy et al., 2009; Pons et al., 2017b). The influence of variety, soil and climatic conditions on the taste of wine is referred to as the “terroir effect” (van Leeuwen and Seguin, 2006). To quantify the effect of soil and climate, they need to be broken down into measurable parameters, such as air temperature, radiation, vine water status and vine nitrogen status (van Leeuwen et al., 2018). This article aims to review the impact of these soil and climate parameters on major aroma compounds expressed in wine, to better understand how terroir shapes wine typicity. The interplay between climate, soil, grapevine variety and management techniques (including winemaking) is, however, complex and wine typicity cannot be totally predicted beforehand. Additionally, this review highlights gaps in the existing literature where more research is needed to improve our understanding of the terroir effect.

Effect of major terroir factors on aroma expression in grapes and wines

1. Effect of air temperature

1.1. Green and peppery flavours

Methoxypyrazines are particularly odorant green flavours in grapes and wines. They are present as free aromas in grapes and their concentration does not vary during wine ageing (Roujou de Boubée et al., 2000). IBMP is the most impacting methoxypyrazine in wine, mainly present in Sauvignon blanc or Cabernet-Sauvignon wines. During maturation, methoxypyrazines, and in particular, IBMP, decrease in grapes with increasing temperatures. This decrease is similar in magnitude compared to the effect of light (Koch et al., 2012). Falcão et al. (2007) showed that IBMP increased with the altitude of the vineyard, which can be attributed to lower temperatures. This observation is important because at higher altitudes light intensity is generally higher compared to low altitudes, which shows that in this study the effect of temperature is independent of the effect of light. In most studies where leaf removal is considered, the effect of temperature and sunlight cannot be separated (Roujou de Boubée et al., 2000). In an experiment where grapes were heated by 1.5 °C average over the season without modifying radiation, Cabernet-Sauvignon contained less IBMP at bunch closure while at this stage there was no difference with the control in Sauvignon blanc grapes (Wu et al., 2019). 1,8-cineole is a monoterpene with a menthol/eucalyptus flavour, particularly present in wines from Cabernet-Sauvignon. Its concentration decreases with temperature (Antalick et al., 2015; Poitou et al., 2017). However, in these studies, the effect of temperature and vine water status were not totally differentiated: vintages with lower 1,8-cineole content in wines were also dryer. Rotundone is a peppery flavour present in grapes and wines from Syrah and some other varieties. It has been highlighted that cool vintages were favourable to obtaining high levels of (-)-rotundone in wines (Caputi et al., 2011). Notably, high temperatures during the ripening period expressed in degree hours above 25 °C or 30 °C decrease (-)-rotundone in grapes and wines (Zhang et al., 2015a; Zhang et al., 2015b; Harner et al., 2019). Delayed fruit ripening by pre-véraison treatment of Syrah grapes with 1-naphthaleneacetic acid (NAA) increased (-)-rotundone in grapes and wines (Davies et al., 2015).

1.2. Other monoterpenes

Contradictory results are reported about the effect of temperature on terpenols. A negative effect of higher temperatures was shown on monoterpene concentrations and in particular linalool and geraniol (Duchêne et al., 2016). This decrease was correlated with a decrease of linalool synthase gene expression. Belancic et al. (1997) also suggested that high berry temperature negatively affects monoterpene concentrations in berries. Conversely, other studies showed a positive effect of increased growing degree days on monoterpenes, and in particular linalool, in Riesling and other varieties (Marais et al., 1992; Reynolds et al., 1995; Schüttler et al., 2013). The distribution pattern of single monoterpenes is temperature-dependant (Marais et al., 1992). All of these studies did not allow, however, to decouple the effect of sun-exposure/radiation from temperature.

1.3. Volatile thiols and C13-norisoprenoids

The impact of temperature on volatile thiols is not fully understood, although 4MSP seems to decrease under high temperatures in wines from Sauvignon blanc (Darriet et al., 2019). In a field experiment where grapes were heated by 1.5 °C on average without modifying incoming radiation, the aldehydic glutathionylated precursor of 3SH (Glut-3SH-Al) was much lower in grapes from Cabernet-Sauvignon and Sauvignon blanc compared to the control (Wu et al., 2019). Marais et al. (1992) showed that cool climate Riesling from Germany contained less TDN compared to warm-climate Riesling from South-Africa. In leaf removal trials, warmer grapes produce wines with higher TDN levels, although these experimental designs do not allow separating the effect of temperature from the effect of sunlight (Kwasniewski et al., 2010). No relation was found with altitude (temperature) for α-ionone, β-ionone and β-damascenone (Falcão et al., 2007). Tabanone levels are higher in Bordeaux wines produced from warmer vintages (Le Menn et al., 2019). This observation, however, does not exclude possible interference of other factors like water deficit, because warm vintages are often (but not always) dryer vintages.

1.4. Dried fruit aromas

There is a clear effect of temperature on compounds involved in dried fruit aromas. The concentration of aroma-impact compounds like γ-nonalactone (coconut, cooked peaches) (Pons et al., 2008), massoia lactone (dried figs), furaneol (caramel) or MND (anis, fruit pit) (Pons et al., 2017a) were higher is must and wine samples marked by this aroma. Field experiments as well as those conducted in the laboratory demonstrated that Merlot was much more likely to develop these aroma compounds than Cabernet-Sauvignon. It is also worth mentioning that (Z)-1,5-octadien-3-one, reminiscent of dried figs at low concentrations (<100 ng/L), increased in dried grapes in a warm incubator (Allamy et al., 2018). Precursors of these compounds were not clearly identified, but high temperatures at the end of maturation likely enhance in situ oxidation mechanisms leading to fatty acid family cleavage as well as to Maillard chemical reactions, which explains the formation of these compounds in grapes. It is likely that the temperature effect is independent of vine water status because γ-nonalactone and massoia lactone content in wines from a Pomerol estate (Bordeaux) were high in warm vintages, whether they were dry (2003) or wet (2007) (Pons et al., 2017a).

1.5. Other aroma compounds and complementary observations

Le Menn et al. (2019) observed particularly high DMS levels in Bordeaux wines of the very warm 2003 vintage, perhaps due to either a high production of the precursors of DMS (pDMS) in the berries or to the increased transformation of pDMS into DMS associated with high yeast-available nitrogen as reported by De Royer Dupré et al. (2014). Le Menn et al. (2019) also observed that aromatic heterocycles seemed to be higher in aged wines from warm vintages. Several hypotheses, such as production in the berries by Maillard-like reactions, presence of high cysteine concentrations in wine acting like a precursor, or high pH need to be explored. Although not an aroma compound, glutathione is of particular importance in aroma expression in wines, because it acts as a preserving agent for white and rosé wine aromas (in particular for volatile thiols) during wine production and ageing. Wines produced in the Bordeaux area showed lower levels of glutathione in warm years, but this effect was not independent of a possible effect of water deficit (Pons et al., 2015; Pons et al., 2017). There is, however, scientific evidence for a temperature effect on glutathione, whereby antioxidant compounds like glutathione and ascorbate tend to decrease in plants under high temperatures (Szymańska et al., 2017). Moreover, such grapes contain higher levels of polyphenols, which increases their sensitivity to oxidation mechanisms, resulting in a quick decrease of glutathione in grape must during crushing and pressing (Nikolantonaki et al., 2012). An in-depth review on the effect of temperature on wine composition, including aroma compounds was published by Drappier et al. (2017).

2. Effect of radiation

2.1. Green and peppery flavours

Hashizume and Samuta (1999) observed lower levels of IBMP in grapes under high radiation. Most studies on the impact of light on methoxypyrazines are conducted in leaf removal trials, where the effect of sunlight and temperature cannot be separated (Ryona et al., 2008). In one of the rare studies where light and temperature could be separated, Koch et al. (2012) concluded that the effect of light in decreasing IBMP concentrations in grapes acts prior to véraison. Varying light conditions after véraison did not modify IBMP content in grape berries. These authors showed that the depressing effect of high temperature and high light intensity on methoxypyrazines was similar in magnitude. There seems to be no impact of UV-B intensity on IBMP (Grega et al., 2012). C6 compounds are lower in sun-exposed bunches compared to shaded bunches (Bureau et al., 2000). The effect of light on (-)-rotundone has not been formally investigated but there is evidence suggesting a stimulating effect. Indeed, mean irradiation, hours of sunshine and cumulative solar exposure (CSEv) over the maturation showed a positive contribution to prediction models for (-)-rotundone concentrations in wine (Geffroy et al., 2019a; Harner et al., 2019). These observations are in accordance with studies showing that defoliation can enhance (-)-rotundone when implemented in cool-climate vineyards, where the increasing effect on berry surface temperature is limited (Homich et al., 2017, Geffroy et al., 2019b).

2.2. Other monoterpenes

Terpenols were decreased in artificially shaded bunches of Muscat de Frontignan compared to the control, while they were not in naturally shaded bunches. This could be, however, an indirect effect, because the temperature was higher in artificially shaded bunches, but much lower in naturally shaded bunches compared to the control (Bureau et al., 2000). Exposure to full sunlight increased terpenol content in Traminette (Skinkis et al., 2010). In an experiment where the effect of light and temperature were well separated, Friedel et al. (2016) showed that exposure to light increased monoterpenes in Riesling grape berries. Terpene synthase genes responded positively to light. Total substituted esters slightly increased with higher radiation, while linalool increased with exposure to light and UV-B (Šuklje et al., 2014). However, in this research project, an interference with temperature cannot be excluded, the light-exposed treatments being slightly warmer.

2.3. Volatile thiols and C13-norisoprenoids

3SH increases with the exposure to sunlight and UV-B, while 3SHA increases with the exposure to sunlight, but not with UV-B (Šuklje et al., 2014). In this leaf removal experiment, the effect of sunlight was, however, not well separated from the effect of temperature. The effect of UV-B on 3SH is consistent with Kobayashi et al. (2011), who showed that UV-B radiation increases the production of precursors of this thiol. C13-norisoprenoids increase under higher sunlight (Marais et al., 1999), probably because of an increase in their precursors, which are carotenoids (Kwasniewski et al., 2010). Schultz et al. (1998) demonstrated that carotenoid levels in Riesling decreased by eliminating UV-B radiation at controlled temperatures. Kwasniewski et al. (2010), Schüttler et al. (2013) and Schüttler et al. (2016) showed higher TDN levels in Riesling wines from sun-exposed grapes, with greater impact of early leaf removal (Schüttler et al., 2013), but in this trial, the effect of light and temperature were not well separated. In another leaf removal experiment, Riesling grapes shaded by cloth showed lower TDN concentrations than naturally shaded grapes (Gerdes et al., 2001), indicating the importance of radiation quality. Schüttler et al. (2013) showed that sun exposure on grapes increased TDN levels in young wines (12 months after bottling), but this effect disappeared after 22 months of ageing.

2.4. Dried fruit aromas

Dried fruit aromas (furaneol, homofuraneol and γ-nonalactone) increased post-harvest under light exposure but not carbonyl compounds such as MND and (Z)-1,5-octadien-3-one (Allamy et al., 2018). Regarding the latter, it is not excluded that under the experimental conditions the effect of dehydration overruled a possible radiation effect.

2.5. Other aroma compounds and complementary observations

High UV-B levels are associated with increased AAP content in white wines (Hühn et al., 1999; Schultz, 2000). Under high radiation antioxidant compounds like glutathione and ascorbate tend to decrease in plants (Szymańska et al., 2017). Total phenolics increase with exposure of grapes to light (Alonso et al., 2016) and UV-B (Gregan et al., 2012), which may negatively impact volatile thiols in white wine production during pre-fermentation processes.

3. Effect of vine nitrogen status

3.1. Green and peppery flavours

Many studies found an increase of IBMP in wine produced from vines with high nitrogen status. Nitrogen status does not, however, directly affect IBMP content in grapes but does so indirectly. High N vines are often vigorous and more prone to bunch shading, which decreases both the temperature of the grapes and their exposure to sunlight (Mendez-Costabel et al., 2014). In an experiment where vine N status was decoupled from vine water status and where no marked differences in vigour were recorded between the control and vines with high N status, IBMP content in grapes was not affected (Helwi et al., 2015). It can thus be concluded that high nitrogen status does not affect directly IBMP content in grapes but indirectly, through an altered bunch microclimate. In a nitrogen fertilization trial (30 vs. 60 kg N/ha/year), Mendez-Costabel et al. (2014) found no effect on C6 compounds. No research was found studying the effect of vine nitrogen status on (-)-rotundone. However, as with IBMP, an indirect increase through a cooler bunch microclimate as a consequence of higher plant vigour can be expected.

3.2. Other monoterpenes

Few studies are dedicated to the effect of vine nitrogen status on monoterpenes. Terpenes are reported to decrease with nitrogen fertilisation (Garde-Cerdán et al., 2015).

3.3. Volatile thiols and C13-norisoprenoids

Many studies report a consistent effect of vine nitrogen status on volatile thiols. Volatile thiols are higher in wines produced from vines which are naturally high in nitrogen (due to soil type and climatic condition, Peyrot des Gachons et al., 2005). In a fertilisation trial, Choné et al. (2006) managed to produce grapes with much-increased content in volatile thiol precursors due to fertilisation with 60 kg N/ha/year. Nitrogen was applied to the soil around bloom, to limit a possible impact on vine vigour. Similar results were obtained by Lacroux et al. (2008). In their experiment nitrogen fertilisation was also applied late in the season, through foliar applications. They observed that the addition of sulphur to the foliar nitrogen application increased the effect on volatile thiols. Helwi et al. (2016) showed a positive effect of nitrogen on the glutathionylated precursor of 3SH (glut-3SH), while it did not affect the cysteinylated precursor (cys-3SH). TDN was shown to decrease in Riesling wines with high nitrogen fertilization in a long-term trial, while other C13-norisoprenoids were not affected (Linsenmeier and Löhnertz, 2007). In another nitrogen fertilisation experiment performed on Pinot noir, Yuan et al. (2018) observed that low nitrogen status was associated with low β-damascenone content in wine.

3.4. Dried fruit aromas

To the knowledge of the authors, there is no evidence of any effect of vine nitrogen status on dried fruit aromas in wines.

3.5. Substituted esters and qualitative fruit aromas

Nitrogen levels in must are related to vine nitrogen status (Bell and Henschke, 2005). The effect of yeast-available nitrogen and amino acid content in must on substituted esters and their corresponding acids formation during alcoholic fermentation has been the subject of several studies. Foliar N fertilisation increased the levels of ethyl hexanoate and ethyl octanoate in Tempranillo, while it decreased the concentration of isoamyl acetate (Ancín‐Azpilicueta et al., 2013). A recent study assessed the influence of must yeast-available nitrogen content on fruity aroma variation during alcoholic and malolactic fermentation in red wine (Lytra et al., 2020). Higher yeast-available nitrogen content significantly increased concentrations of short- and substituted alkyl fatty acid ethyl esters produced during alcoholic fermentation (up to a 67 % increase in samples with the highest nitrogen content) and hydroxycarboxylic acid ethyl esters generated during malolactic fermentation (up to a 58 % increase in samples with the highest nitrogen content). Sensory profiles showed that malolactic fermentation led to a significant increase in black-berry and jammy-fruit notes, thus revealing the role of substituted esters as natural fruity-note enhancers.

3.6. Other aroma compounds and complementary observations

DMS potential in grapes (pDMS) increases with vine nitrogen status (De Royer Dupré et al., 2014). In this research, however, the effect of nitrogen cannot clearly be separated from the effect of vine water status: vines with high yeast-available amino acids had also undergone more severe water deficits. However, an effect of vine nitrogen status on DMS content in wine is highly likely, because the formation of pDMS in berries is related to the abundance of amino acids, in particular S-methylmethionine (Segurel et al., 2005). Similarly, the levels of several N,S-heterocycles are positively correlated with the amount of amino acids in aged Champagne reserve wines (Le Menn et al., 2017), which is in agreement with the fact that amino acids are precursors of heterocycles (Marchand et al., 2000). In red wine only three N,S-heterocycles were reported to be correlated to vine nitrogen status (Le Menn et al., 2019).

Low vine nitrogen status is associated with higher levels of AAP in white wines (Hühn et al., 1999; Schneider, 2014).

Low vine N-status increases the levels of skin polyphenols and decreases glutathione content in grapes (Choné et al., 2006; Pons et al., 2017b). During pre-fermentation manipulations of grapes, polyphenols are transformed into quinones which are highly reactive with the precursors of volatile thiols, while glutathione acts as a preservative of these compounds. Hence, vines with low nitrogen status produce wine with low levels of volatile thiols, not only because grapes contain less precursors but also because the high concentrations in polyphenols and low concentrations in glutathione provoke increased loss of these precursors.

4. Effect of vine water status

4.1. Green and peppery flavours

Deficit irrigation decreases IBMP content in wines (Chapman et al., 2005; Mendez-Costabel et al., 2014). However, this effect may be, indirect because of an increased bunch shading in fully irrigated vines which are generally more vigorous. Roujou de Boubée et al. (2000) reported an effect of water deficit on decreasing IBMP content in wines independently from radiation. No effect of irrigation treatment on C6 compounds was reported by Mendez-Costabel et al. (2014). 1,8-cineole was lower in wines produced from vines which had undergone water deficits, although this effect was not completely independent from a possible temperature effect (Antalick et al., 2015; Poitou et al., 2017). Wines made from vines irrigated just prior to véraison had a greater (-)-rotundone concentration than those made from non-irrigated vines (Geffroy et al., 2014; Geffroy et al., 2016). As no differences in berry surface temperature were observed between the two treatments (Geffroy et al., 2016), the effect induced by irrigation is likely to be direct rather than indirect through a modification of bunch microclimate (Geffroy et al., 2016). The importance of water supply was also emphasized in another study showing that calcium concentration in leaf petioles, a variable that correlated with δ13C, had a strong influence on (-)-rotundone accumulation (Harner et al., 2019). At an intra-block scale, a similar correlation was observed between δ13C measured on grape sugar at harvest and (-)-rotundone concentrations in wine (Geffroy et al., 2014).

4.2. Other monoterpenes

Monoterpene concentrations were found to increase with the intensity of water deficits (Schüttler et al., 2013; Savoi et al., 2016) while Giordano et al. (2013) reported higher terpineol levels in irrigated vines compared to the dry control.

4.3. Volatile thiols and C13-norisoprenoids

Volatile thiols increase under mild water deficit and decrease under severe water deficit (Peyrot des Gachons et al., 2005; Schüttler et al., 2013). Schüttler et al. (2013) observed a tendency toward lower TDN levels in wines from vines facing strong water deficits. Water deficit increased tabanones in wines after ageing (Le Menn et al., 2019), with wines from severely water-stressed vines showing remarkably high tabanone content after several years of bottle ageing. In a study conducted in Nemea on Agiorgitiko (Peloponesos, Geece) C13-norisoprenoids were high in wines produced by microvinification from parcels where vines were facing water deficits (Koundouras et al., 2006). This is also consistent with results from an irrigation trial reported by Bindon et al. (2007), where water deficit induced by partial rootzone drying (PRD) caused increases in the concentration of hydrolytically released C13-norisoprenoids β-damascenone, β-ionone, and TDN. This study also found carotenoids, which are precursors of C13-norisoprenoids, increased in PRD grapes when the fruit approached maturity.

4.4. Dried fruit aromas

There is no clear evidence of an effect of water deficit on dried fruit aromas when it occurs at the beginning of the ripening process. However, when severe water deficit during the last days before harvest triggers dehydration, there can be a profound effect on berry composition. A threshold of 10 % desiccation was determined, above which dried fruit aromas begin to appear (Allamy et al., 2018).

4.5. Other aroma compounds and complementary observations

De Royer Dupré et al. (2014) reported increased pDMS in water deficit vines, but no clear separation could be established from a possible nitrogen effect, due to water deficit vines also having higher yeast-available amino acids. This observation is consistent with Picard et al. (2017) who observed enhanced ageing bouquet in wines produced from water deficit vines. DMS plays a direct role in the ageing bouquet of wine by producing intense truffle-like aromas (Picard et al., 2015) and an indirect role by enhancing fruity flavours (Lytra et al., 2016). In the study of Picard et al. (2017), the ageing bouquet of matured red Bordeaux wines was compared against the water status of the vines as assessed by δ13C measured on wine (Guyon et al., 2015). Ageing bouquet typicity was significantly correlated to δ13C (Figure 1). Another study found water deficit increased fruity characters in wine and reduced green flavours (Chapman et al., 2005). In this study, the increased fruity character in deficit irrigated vines was attributed to esters, although no aroma compounds were measured. It is not clear either whether the differences were due to a direct effect of water deficit or an indirect effect through differences in bunch microclimate (vigour) or yield. Water stress in vines is associated with higher levels of AAP in white wines (Hühn et al., 1999), especially in combination with low vine nitrogen status (Schneider, 2014). Levels of glutathione in wines from the Bordeaux area were lower in dry years, but this effect was not independent of a possible effect of temperature, because dry years were also warm years in this study (Pons et al., 2015; 2017). Water deficit increases polyphenols in grapes and wines. These may react with volatile thiol precursors during pre-fermentation operation and reduce subsequent thiol expression in wine (Pons et al., 2017b).

Figure 1. Ageing bouquet typicity score as a function of δ13C measured on wine representing vine water status.

Sensory and chemical analyses were performed on a series of 29 red Bordeaux wines, which were subsequently classified according to their ageing bouquet representativeness (i.e., low typicity in black squares; high typicity in red circles).

How terroir shapes the aroma profile of grapes and wines

1. Hierarchy of terroir factors and variety choice

Predominant terroir factors are climate, soil and the grapevine variety (van Leeuwen et al., 2004). It can be considered that the influence of climate and soil is expressed through the grapevine variety. Although there are some general trends across varieties, each one has a specific aromatic composition. Hence, the terroir effect needs to be considered for each variety separately, with the focus in this article on some major varieties: Cabernet-Sauvignon, Merlot, Syrah, Sauvignon blanc and Riesling. Cabernet-Sauvignon is the most widely planted red variety in the world followed by Merlot, while Syrah is fourth (Anderson and Aryal, 2013). Sauvignon blanc is the third most widely planted white variety while Riesling is number six. The compounds responsible for the aromatic expression of these varieties are well known. Other major varieties in terms of planted acreage according to Anderson and Ayral (2013) were discarded in this analysis, either because their aroma structure is less well known (Tempranillo and Chardonnay), because they are only of local importance (Aíren, Rkatsitelli), or because they are mainly used for spirit production (Trebbiano, also called Ugni blanc).

2. The climate component: temperature and radiation

The temperature regime during grape ripening is of major importance in aroma typicity in wine. Temperature can be considered at a broad scale with winegrowing regions characterized from cool to warm by means of agroclimatic indicators (Winkler, 1965; Gladstones, 2011). Recently, the temperature structure inside winegrowing regions was explored, showing that considerable variability in temperature can exist at the mesoscale (Bois et al., 2018) or even at the microscale (de Rességuier et al., 2020). Radiation varies with cloud cover and increases with altitude. High radiation levels are received in vineyards planted in the Andes of Argentina, where the effect of low cloud cover is combined with the effect of high altitude. The temperature during grape ripening is impacted by the phenology, with early phenology causing grapes to ripen during the warmest part of the summer. At a given location, temperature and radiation vary from year-to-year (so-called “vintage-effect”) and, as a result of climate change, may be increasing in most winegrowing regions over time (Garcia de Cortazar et al., 2017).

Cool temperatures during grape ripening will increase green flavours, like IBMP or 1,8-cineole (Falcão et al., 2007; Koch et al., 2012; Poitou et al., 2017). Excessive levels of IBMP are detrimental to red wine quality, but concentrations close to the perception threshold presumably provide freshness, as does the presence of 1,8-cineole. In Sauvignon blanc, IBMP is important for the perceived freshness, and the finest wines from this variety are obtained when the presence of IBMP and volatile thiols is balanced. High radiation has a similar effect to temperature in decreasing IBMP levels in grapes and wines. Low temperatures induce higher levels of (-)-rotundone in Syrah, which is generally an appreciated character of this variety (Zhang et al., 2015a, Zhang et al., 2015b; Caputi et al., 2011). High temperatures increase dried fruit aromas in red wine which may lead to decreased aroma complexity and premature ageing (Pons et al., 2017a; Pons et al., 2017b), in particular for Merlot (Allamy et al., 2017; 2018). Some compounds which play an important role in the ageing bouquet of fine red wines, such as DMS and possibly tabanones, are more abundant in wines from Cabernet-Sauvignon and Merlot when grapes ripen in warm conditions (Le Menn et al., 2019). Sauvignon blanc produced in warm locations express more tropical fruit aromas and less asparagus and boxwood aromas. Riesling produced in warm climates is more prone to express kerosene-like and ripe fruit flavours induced by the presence of TDN and rearrangement of linalool towards oxide forms or α-terpineol (Marais et al., 1992; Ziegler et al., 2020).

Aroma expression in grapes and wines is positively related to radiation. High radiation reduces green flavours (methoxypyrzaines and C6 compounds; Koch et al., 2012) and increases fruity flavours induced by monoterpenes (Friedel et al., 2016), volatile thiols, esters (Suklje et al., 2014), C13-norisoprenoids (Marais et al., 1999) and peppery notes from (-)-rotundone (Geffroy et al, 2019a,b).

3. The soil component: vine nitrogen status

Among nutrients that vines assimilate from the soil, nitrogen (N) has the greatest impact on vine development, yield and fruit composition (Bell and Henschke, 2005). The soil effect in terroir expression is partly mediated through soil nitrogen availability (van Leeuwen et al., 2018). The latter depends on soil organic matter content and several factors involved in its turnover by soil microorganisms (soil temperature, humidity, aeration, pH, lime content, organic matter and C/N content) (van Leeuwen et al., 2000). Vine nitrogen status has a major impact on aroma compounds in grapes and wines. This effect can be either direct or indirect. The indirect effect is mediated through increased vigour, which alters the microclimate in the bunch zone, making it cooler, and less exposed to radiation. High vine nitrogen status increases often green flavours particularly IBMP in Sauvignon blanc, Cabernet-Sauvignon and, to a lesser extent Merlot wines. However, Helwi et al. (2015) have shown that this effect is indirect and induced by higher vigour and more shaded microclimate in the bunch zone. A strong, direct effect of nitrogen has been shown on volatile thiols, or more precisely their precursors (Choné et al., 2006; Helwi et al., 2016). Volatile thiols are involved in the fruity character of Cabernet-Sauvignon wines and the boxwood/tropical fruit aromas of Sauvignon blanc. They are also involved in the typicity of Riesling wine (Schüttler et al., 2015). In Sauvignon blanc, high N status increases glutathione content in grapes and wines and reduces the amount of phenolic compounds in berry skin, leading to better conservation of thiol derived aromas. A moderately high N status can be considered as favourable to the typicity of Sauvignon blanc wines because for this variety the combination of volatile thiols and IBMP is appreciated by consumers. Excessively high vine N-status can reduce the quality of wines from Cabernet-Sauvignon due to an excess of green aromas, while high N-status contributes to lower TDN levels in Riesling wines (Linsenmeier and Löhnertz, 2007). A balanced nitrogen status of the vines is considered being preventive against the formation of undesirable AAP (Schneider, 2014). In aged Merlot and Cabernet-Sauvignon wines, unlimited nitrogen uptake by the vines favours the development of DMS during ageing, which is a positive contributor to the bouquet appreciated by wine experts (Le Menn et al., 2019).

4. The combined effect of soil and climate: vine water status

Vine water status is a major driver of terroir expression (Seguin, 1969). It depends on climatic conditions (rainfall and reference evapotranspiration) and soil type (soil water holding capacity, SWHC) (van Leeuwen et al., 2009). Wine aromatic typicity is much impacted by vine water status.

The wines produced from vines which undergo water deficit, may present a reduction in green aromas (Cabernet-Sauvignon, Merlot, Sauvignon blanc) and contain less (-)-rotundone (Syrah). It is not well established if this effect is direct, or indirect, as mediated by lower vigour and more exposed fruit to sunlight (Chapman et al., 2005; Mendez-Costabel et al., 2014). Wines from water deficit vines are more fruity (Chapman et al., 2005) and contain more C13-norisoprenoids (Koundouras et al., 2006; Bindon et al., 2007). After bottle ageing, these wines contain more DMS (De Royer Dupré et al., 2014) and display an improved ageing bouquet (Picard et al., 2017). Mild water deficit increases thiol expression in Sauvignon blanc, although this becomes detrimental with severe water deficit (Peyrot des Gachons et al., 2005). Riesling wines from grapes grown under water deficit are more prone to develop AAP during bottle ageing (Schneider, 2014).

5. Predicting aroma typicity from different terroirs

Major drivers of terroir expression are air temperature, radiation, vine water status and vine nitrogen status. Temperature and radiation can be measured in a classical weather station. Vine water status can be assessed by measuring stem water potential or δ13C (van Leeuwen et al., 2009). Vine nitrogen status can be assessed by measuring yeast-available nitrogen in grapes (van Leeuwen et al., 2018). Once these four terroir factors are adequately characterized, aroma expression can be predicted (Figure 2) using published data from the literature (Table 1). The interplay between environmental factors (climate and soil) plant material (in particular the grapevine variety), management practices and winemaking techniques is, however, complex and more research is needed to obtain a complete understanding of flavour typicity in relation to terroir. In many experiments, terroir factors (in particular light and temperature, but also vine water and nitrogen status) are not well separated. References in which the impact of one terroir factor on a specific aroma compound or family was investigated without possible interference of other factors are mentioned in bold in Table 1. Unfortunately, they are a minority among the studies consulted for this review. White cells in Table 1 highlight topics where more research is needed. It appears that the effect of water deficit on aroma compounds is relatively well understood, but that progress can be made on the understanding of the effects of vine nitrogen status, for instance on 1,8 cineole, (-)-rotundone or dried fruit aromas. This should be relatively easy to do, because several reliable plant-based indicators, like yeast-available nitrogen, or petiole nitrogen content, are available to assess vine N status.

Figure 2. Overview of the terroir effect on aromas in grapes and wines.

Terroir expression is mainly mediated through (1) air temperature (climate), (2) radiation (climate), (3) vine nitrogen status and vine water status which results from (A) soil water holding capacity (soil), (B) reference evapotranspiration (climate) and (C) rainfall (climate). These four components related to soil and climate impact aroma composition and expression in grapes and wines. By connecting recent advances in the understanding of the impact of environmental factors on aroma expression, wine typicity in relation to terroir can be better understood.

Table 1. Effect of four terroir factors (air temperature, radiation, vine nitrogen status, vine water deficit) on aroma compounds in grapes and wines.



Terroir factor


Aroma compound or family

Air temperature


Vine nitrogen status

Vine water deficit

Green and peppery flavours


Koch et al., 2012; Falçao et al., 2007; Wu et al., 2919

Hazizume et Samuta, 1999; Ryona et al., 2008; Koch et al., 2012

Helwi et al., 2015

Roujou de Boubée et al., 2000; Mendez-Costabel et al., 2014

C6 compounds


Bureau et al., 2000

Mendez-Costabel et al., 2014

Mendez-Costabel et al., 2014


Antalick et al., 2015; Poitou et al., 2017



Antalick et al., 2015; Poitou et al., 2017


Caputi et al., 2011, Zhang et al., 2015a et b; Harner et al., 2019

Homich et al., 2017; Geffroy et al., 2019a et b; Harner et al., 2019

Not investigated but indirect increase expected

Geffroy et al., 2014; 2016; Harner et al., 2019

Other monoterpenes

Other monoterpenes

Marais et al., 1992; Reynolds et al., 1995; Belancic et al., 1997; Schüttler et al., 2013; Duchêne et al., 2016

Bureau et al., 2000; Skinkis et al., 2010; Suklje et al., 2014; Friedel et al., 2016

Garde-Cerdan et al., 2015

Schüttler et al., 2013; Giordano et al., 2013; Savoi et al., 2016

Volatile thiols and C13-norisoprenoids

Volatile thiols

Darriet et al., 2019; Wu et al., 2019

Suklje et al., 2014

Peyrot des Gachons et al., 2005; Choné et al., 2006; Lacroux et al., 208; Helwi et al., 2016

Peyrot des Gachons et al., 2005; Schuttler et al., 2013


Marais et al., 1992; Kwasniewsky et al., 2010; Ziegler et al., 2019

Schultz et al., 1998; Gerdes et al., 2001 ; Kwasniewsky et al., 2010

Linsenmeier et al., 2007

Bindon et al., 2007; Schüttler et al., 2013


Le Menn et al., 2019



Le Menn et al., 2019

Other C13-norisoprenoids

Falçao et al., 2007

Marais et al., 1999

Yuan et al., 2018 (β-damascenone)

Koundouras et al., 2006

Dried fruit aromas

Dried fruit aromas

Pons et al., 2008; Pons et al., 2017a; Pons et al., 217b; Allamy et al., 2018

Allamy et al., 2018


Possible increasing effect when late water deficit leads to dehydration




Suklje et al., 2014

Ancin-Azpilicueta et al., 2013; Lytra et al., 2020

Chapman et al., 2005

Orher compounds


Le Menn et al., 2019


Le Menn et al., 2019

De Royer Dupré et al., 2014

Red wine aging bouquet




Picard et al., 2017

Aromatic heterocycles

Le Menn et al., 2019


Le Menn et al., 2017




Hühn et al., 1999; Schultz et al., 2000

Hühn et al., 1999

Hühn et al., 1999


Pons et al., 2015; 2017; Szymanski et al., 2017

Szymanski et al., 2017

Choné et al., 2006; Pons et al., 2017

Pons et al., 2017b



Alonso et al., 2016

Choné et al., 2006

Pons et al., 2015

Red colour indicates that the aroma compound (or family) increases with increasing terroir factor, blue colour that aroma compound (or family) decreases with increasing terroir factor. Grey colour indicates no effect was shown. In references in bold the terroir factor was investigated without interference from other factors. In references not printed in bold the effect of several factors cannot be easily disentangled (e.g., light and temperature in a leaf removal trial).

6. Examples of typical aroma profiles related to specific terroirs

Sauvignon blanc is grown under a wide range of climatic conditions and soil types. Typical cool climate Sauvignon blanc is produced in Marlborough, New Zealand, and Sancerre, France. In brief, the typical aroma of cool climate Sauvignon blanc is shaped by a delicate balance between green aromas (bell pepper induced by IBMP and boxwood by 4MSP) and fruity aromas (grapefruit induced by 3SH and passion fruit by 3SHA). In very cool climates, like the Awatere Valley in New Zealand (a sub-region of Marlborough), the green aromas of asparagus and bell pepper can dominate the fruity character related to varietal odorous thiols. However, sensory perception is a complex, multi-odour component blend and these observations can sometimes be modulated by the abundance of other volatile compounds. Examples of warm climate Sauvignon blanc can be found in the USA, Australia and Chili. The aroma profile of these is dominated by passion fruit. Bordeaux is a major winegrowing area for Sauvignon blanc where the climate is temperate. The most expressive Sauvignon blanc is produced in the cooler parts of the Bordeaux area, on soils with medium to high water holding capacity and medium to high in nitrogen supply due to moderately high organic matter content. Severe water deficits and low vine nitrogen status are factors which are clearly negatively impacting aromatic typicity of Sauvignon blanc wines. High radiation reduces IBMP in Sauvignon blanc grapes and increases volatile thiols.

Merlot and Cabernet-Sauvignon grown in cool climates, or with low radiation, can be green, because of the presence of IBMP, although this is fairly rare for Merlot, which is more early ripening. An excess of IBMP is generally not appreciated, although some green aromas, like 1,8-cineole, can provide some minty freshness in the aroma expression. Merlot and Cabernet-Sauvignon grown in temperate climates express fruity flavours and develop a complex ageing bouquet after a few years of bottle storage. These positive characters are induced by a wide range of compounds, including substituted esters, volatile thiols (in particular 3SH) and DMS. Aroma expression after bottle ageing is enhanced when wines are produced by vines facing water deficits. It has been shown that these wines contain more DMS and tabanones. Under warm climates, wines from the above mentioned varieties can express dried fruit aromas, in particular when produced from Merlot. Some of the finest wines from Cabernet-Sauvignon are produced in Margaux, Saint-Julien, Pauillac and Saint-Estèphe (Bordeaux, France). In the Bordeaux area, Cabernet-Sauvignon ripens late in the season, when temperatures are decreasing, eliminating any possible risk of dried fruit aromas. The gravel soils of these appellations induce an interesting combination of moderate to severe water deficit and unlimited nitrogen supply to the vines. This combination of cool climate, water deficit, and unlimited nitrogen can shape beautiful ageing bouquets.

Syrah can express different typicities depending on the climate. In cool climate vineyards, such as those from the northern Rhone valley in France, the Victoria's Grampians region in Australia, or the Hawke's Bay area is New Zealand, Syrah expresses very intense peppery aromas, induced by the presence of (-)-rotundone. The combination of cool temperatures and high light is positive for (-)-rotundone expression in Syrah grapes and wines. In warmer climates (i.e., Languedoc area or southern Rhone valley in France, Barossa valley in Australia), Syrah is rather marked by the expression of ripe and dried fruit, and black olive aromas. DMS has been identified as a major contributor to these notes (Segurel et al., 2004).

The typicity of Riesling wines is shaped by various aromatic nuances, which reflect growing conditions, in particular temperature and vine water status. Typical cool climate Riesling wines, as they are grown in Europe (e.g., Germany, Alsace, Austria), are marked by the fruity aromas induced by volatile thiols and terpenols. These fruity aromas can range from fresh citrus, green apple, pear, peach and apricot, to ripe and sweet fruit character accompanied by floral, mineral, spicy and honey like aroma (Schüttler et al., 2015). They are enhanced under high light (Friedel et al., 2016). Wines from steep slope vineyards with low water holding capacity often show distinctive floral nuances and lack citrus or grapefruit character in years with water deficit, caused by elevated linalool concentrations and lower volatile thiol concentrations. Bottle aged bouquet, especially in Riesling wines from warmer climates, like Australia or South Africa, but also from United States, Canada or New Zealand contains more kerosene-like aromas as a result of the presence of TDN (Ziegler et al., 2019). Riesling wines from warmer climatic zones also tend to be characterised more by ripe fruit aromas, which can be related to a change in monoterpene pattern through acidic catalyzed rearrangements of terpenols towards their oxide forms or a-terpineol (Marais et al., 1992). When Riesling vines face severe stress (high UV-B radiation, water stress or nitrogen deficiency) AAP can develop in the wine and give yield to untypical (premature) ageing.

7. Managing aromatic typicity related to terroirs

Terroir factors (temperature, radiation, water, nitrogen) induce specific aromatic typicities. The choice of plant material and management factors can, however, modulate this expression. The excessive presence of green aromas is generally not appreciated in red wines. They are often the result of low temperatures during grape ripening, low light intensity, unlimited water supply and/or unlimited nitrogen supply. The presence of green flavours can be reduced by planting early ripening varieties (Merlot instead of Cabernet-Sauvignon). Another option is reducing nitrogen availability by planting cover crop or increasing exposure to light by leaf removal (which will also increase the temperature in the bunch zone). It should be mentioned that 1,8 cineole in grapes and wines can be induced by the presence of the invasive plant Artemisia verlotiorum in vineyards (Poitou et al., 2017). Under warm climates there is a risk to produce red wines that are excessively marked by overriding and “trivial” dried fruit aromas, which reduces freshness and aromatic complexity. These can be limited by planting later ripening varieties (Cabernet-Sauvignon instead of Merlot). Other options are earlier harvest dates or increased vigour to expose bunches to less direct sunlight. In Sauvignon blanc grape fruit expression can easily be enhanced by nitrogen fertilization (when soil N supply is limited). In warm climates, or on soils inducing moderate to severe water deficits, red varieties should be preferred over Sauvignon blanc for the production of high-quality wines. Berry temperature and light can be manipulated through canopy management and leaf removal. An extensive review on the effect of management practices on aroma compounds in grapes and wines can be found in Alem et al., 2019. The effect of plant material (rootstock and clone) on aroma compounds in Riesling is addressed in Ziegler et al., 2020.

8. The impact of winemaking

Fermentation (alcoholic and malolactic) and ageing have a major impact on wine aromas (Lytra et al., 2020). Many wine flavours are either not detectable or present as non-odorous bound precursors in grapes and are shaped during the fermentation process. Among others, this applies to β-damanscenone (Lloyd et al., 2011), floral aromas including β-ionone (Loscos et al., 2007), volatile thiols (Murat et al., 2001), esters (Ferreira et al., 1995b; Lytra et al., 2020) and monoterpenes (Park and Noble, 1993). Other flavour compounds may increase wine ageing, like tabanones (Slaghenaufi and Ugliano, 2018) or barrel ageing (Cameleyre et al., 2020). Aroma compounds can also be lost during winemaking. Volatile thiols are reported to be particularly sensitive to oxidation during pre-fermentation processes (Blanchard et al., 2004). In contrast to substituted esters accumulated during ageing, most linear fatty acid esters produced during alcoholic fermentation decline with age (Lytra et al., 2020). It is obvious that winemaking techniques also have a major impact on aroma expression in wines. It is, however, out of the scope of this article to review these in detail.


Wine typicity in relation to terroir is largely shaped by odorous compounds. Over the past decades, a wide body of literature is published on the molecular basis of wine aromas. Many of these studies relate cultivar specific aroma profiles and how these are influenced by environmental factors and management practices. The effect of several environmental factors in these studies is, unfortunately, often not easy to disentangle. Many studies on the effect of light on aroma compounds are conducted by means of leaf removal trials, where generally bunch temperature is increased in the bunches exposed to more sunlight. In irrigation or nitrogen fertilisation trials vigour is often increased. In such situations, it is hard to know if the observed effect from the treatment is direct or indirect (i.e., mediated by modified bunch microclimate). There is clearly a need for improved experimental design, where the effect of each factor can be studied without interference with other factors. Major effects of terroir expression are air temperature, radiation, water supply to the vines and vine nitrogen status. In this article, the effect of these factors on aroma compounds is reviewed, to provide a better understanding of how terroir shapes aromatic typicity.


    The authors are grateful to Mark Gowdy for editing and English spelling corrections.


  • Alem, H., Rigou, P., Schneider, R., Ojeda, H., & Torregrosa, L. (2019). Impact of agronomic practices on grape aroma composition: a review. Journal of the Science of Food and Agriculture, 99(3), 975-985.
  • Allamy, L., Darriet, P., & Pons, A. (2017). Identification and organoleptic contribution of (Z)-1, 5-octadien-3-one to the flavor of Vitis vinifera cv. Merlot and Cabernet-Sauvignon musts. Journal of Agricultural and Food Chemistry, 65(9), 1915-1923.
  • Allamy, L., Darriet, P. and Pons, A. (2018). Molecular interpretation of dried-fruit aromas in Merlot and Cabernet-sauvignon musts and young wines : impact of over-ripening. Food Chemistry, 266, 245-253.
  • Allen, M. S., Lacey, M. J., Harris, R. L., & Brown, W. V. (1991). Contribution of methoxypyrazines to Sauvignon blanc wine aroma. American Journal of Enology and Viticulture, 42(2), 109-112.
  • Alonso, R., Berli, F. J., Fontana, A., Piccoli, P., & Bottini, R. (2016). Malbec grape (Vitis vinifera L.) responses to the environment: Berry phenolics as influenced by solar UV-B, water deficit and sprayed abscisic acid. Plant Physiology and Biochemistry, 109, 84-90.
  • Ancín‐Azpilicueta, C., Nieto‐Rojo, R., & Gómez‐Cordón, J. (2013). Effect of foliar urea fertilisation on volatile compounds in Tempranillo wine. Journal of the Science of Food and Agriculture, 93(6), 1485-1481.
  • Anderson, K., & Aryal, N. R. (2013). Which winegrape varieties are grown where?: a global empirical picture. University of Adelaide Press.
  • Anocibar-Beloqui, A., Kotseridis, Y., & Bertrand, A. (1996). Détermination de la teneur en sulfure de diméthyle DANS quelques vins rouges. Journal International des Sciences de la Vigne et du Vin, 30(3), 167-170.
  • Antalick, G., Tempère, S., Šuklje, K., Blackman, J. W., Deloire, A., de Revel, G., & Schmidtke, L. M. (2015). Investigation and sensory characterization of 1, 4-Cineole: a potential aromatic marker of Australian Cabernet-Sauvignon Wine. Journal of Agricultural and Food Chemistry, 63(41), 9103-9111.
  • Belancic, A., Agosin, E., Ibacache, A., Bordeu, E., Baumes, R., Razungles, A., & Bayonove, C. (1997). Influence of sun exposure on the aromatic composition of Chilean Muscat grape cultivars Moscatel de Alejandria and Moscatel rosada. American Journal of Enology and Viticulture, 48(2), 181-186.
  • Bell, S. J., & Henschke, P. A. (2005). Implications of nitrogen nutrition for grapes, fermentation and wine. Australian Journal of Grape and Wine Research, 11(3), 242-295.
  • Bindon, K. A., Dry, P. R., & Loveys, B. R. (2007). Influence of plant water status on the production of C13-norisoprenoid precursors in Vitis vinifera L. cv. Cabernet-Sauvignon grape berries. Journal of Agricultural and Food Chemistry, 55(11), 4493-4500.
  • Blanchard, L., Darriet, P., & Dubourdieu, D. (2004). Reactivity of 3-mercaptohexanol in red wine: Impact of oxygen, phenolic fractions, and sulfur dioxide. American Journal of Enology and Viticulture, 55(2), 115-120.
  • Bodin, F., & Morlat, R. (2006). Characterization of viticultural terroirs using a simple field model based on soil depth I. Validation of the water supply regime, phenology and vine vigour, in the Anjou vineyard (France). Plant and Soil, 281(1-2), 37-54.
  • Bois, B., Joly, D., Quenol, H., Pieri, P., Gaudillère, J. P., Guyon, D., Saur, E., & van Leeuwen, C. (2018). Temperature-based zoning of the Bordeaux wine region. OENO One, 52(4).
  • Bureau, S. M., Razungles, A. J., & Baumes, R. L. (2000). The aroma of Muscat of Frontignan grapes: effect of the light environment of vine or bunch on volatiles and glycoconjugates. Journal of the Science of Food and Agriculture, 80(14), 2012-2020.<2012::AID-JSFA738>3.0.CO;2-X
  • Cameleyre, M., Tempere, S., & Barbe, J. C. (2015). Distribution and organoleptic impact of ethyl 3-hydroxybutanoate enantiomers in wine. Journal of Agricultural and Food Chemistry, 63(48), 10484-10491.
  • Cameleyre, M., Lytra, G., Schütte, L., Vicard, J. C., & Barbe, J. C. (2020). Oak Wood Volatiles Impact on Red Wine Fruity Aroma Perception in Various Matrices. Journal of Agricultural and Food Chemistry.
  • Capone, D. L., Van Leeuwen, K., Taylor, D. K., Jeffery, D. W., Pardon, K. H., Elsey, G. M., & Sefton, M. A. (2011). Evolution and occurrence of 1, 8-cineole (Eucalyptol) in Australian wine. Journal of Agricultural and Food Chemistry, 59(3), 953-959.
  • Caputi, L., Carlin, S., Ghiglieno, I., Stefanini, M., Valenti, L., Vrhovsek, U. & Mattivi, F., (2011). Relationship of changes in rotundone content during grape ripening and winemaking to manipulation of the “peppery” character of wine. Journal of Agricultural and Food Chemistry, 59(10), 5565-5571.
  • Chapman, D. M., Roby, G., Ebeler, S. E., Guinard, J. X., & Matthews, M. A. (2005). Sensory attributes of Cabernet-Sauvignon wines made from vines with different water status. Australian Journal of Grape and Wine Research, 11(3), 339-347.
  • Choné, X., Lavigne-Cruège, V., Tominaga, T., van Leeuwen, C., Castagnède, C., Saucier, C., & Dubourdieu, D. (2006). Effect of vine nitrogen status on grape aromatic potential: flavor precursors (S-cysteine conjugates), glutathione and phenolic content in Vitis vinifera L. Cv Sauvignon blanc grape juice. Journal International des Sciences de la Vigne et du Vin, 40(1), 1-6.
  • Cifre, J., Bota, J., Escalona, J. M., Medrano, H., & Flexas, J. (2005). Physiological tools for irrigation scheduling in grapevine (Vitis vinifera L.): An open gate to improve water-use efficiency?. Agriculture, Ecosystems & Environment, 106(2-3), 159-170.
  • Coombe, B. G. (1986). Influence of temperature on composition and quality of grapes. In Symposium on Grapevine Canopy and Vigor Management, XXII IHC 206 (pp. 23-36).
  • Davies, C., Nicholson, E. L., Böttcher, C., Burbidge, C. A., Bastian, S. E., Harvey, K. E., Huang, A.-C, Taylor, D.K. & Boss, P. K. (2015). Shiraz wines made from grape berries (Vitis vinifera) delayed in ripening by plant growth regulator treatment have elevated rotundone concentrations and “pepper” flavor and aroma. Journal of Agricultural and Food Chemistry, 63(8), 2137-2144.
  • Darriet, P., Thibon, C. & Dubourdieu D. (2012) Aroma and aroma precursors in grape Berry in The Biochemistry of the Grape Berry, Geros H., Chaves M., Delrot S., Eds, Bentham Science Publisher pp 111-136.
  • Darriet, P., Pons, A., Thibon, C., Drappier, J., Andrée, M., Cholet, C., Redon P., Wu, J., Pieri, P. & Geny-Denis L. (2019). Climate change and varietal aromatic component : between expected impact and experimental observations. 8th OENOVITI International meeting, 13 May 2019, Athens, Greece.
  • De Royer Dupré, N., Schneider, R., Payan, J. C., Salançon, E., & Razungles, A. (2014). Effects of vine water status on dimethyl sulfur potential, ammonium, and amino acid contents in Grenache noir grapes (Vitis vinifera). Journal of Agricultural and Food Chemistry, 62(13), 2760-2766.
  • de Rességuier, L., Mary, S., Le Roux, R., Petitjean, T., Quénol, H., & van Leeuwen, C. (2020). Temperature variability at local scale in the Bordeaux area. Relations with environmental factors and impact on vine phenology. Frontiers in Plant Science, 11.
  • Drappier, J., Thibon, C., Rabot, A., & Geny-Denis, L. (2017). Relationship between wine composition and temperature: Impact on Bordeaux wine typicity in the context of global warming. Critical Reviews in Food Science and Nutrition, 59(1), 14-30.
  • Duchêne E. & Schneider C., 2005. Grapevine and climatic change : a glance at the situation in Alsace. Agronomy for. Sustainable Development, 25, 93-99.
  • Duchêne, E., Butterlin, G., Claudel, P. & Jaegli, N. (2016). Consequences of elevated temperatures during ripening on the biosynthesis of monoterpenols in grape berries. In: Climwine, sustainable grape and wine production in the context of climate change, 11-13 April 2016, Bordeaux.
  • Dunlevy, J. D., Kalua, C. M., Keyzers, R. A., & Boss, P. K. (2009). The production of flavour & aroma compounds in grape berries. In Grapevine molecular physiology & biotechnology (pp. 293-340). Springer, Dordrecht.
  • Falcão, L. D., de Revel, G., Perello, M. C., Moutsiou, A., Zanus, M. C., & Bordignon-Luiz, M. T. (2007). A survey of seasonal temperatures and vineyard altitude influences on 2-methoxy-3-isobutylpyrazine, C13-norisoprenoids, and the sensory profile of Brazilian Cabernet-Sauvignon wines. Journal of Agricultural and Food Chemistry, 55(9), 3605-3612.
  • Ferreira, B., Hory, C., Bard, M. H., Taisant, C., Olsson, A., & Le Fur, Y. (1995a). Effects of skin contact and settling on the level of the C18: 2, C18: 3 fatty acids and C6 compounds in Burgundy Chardonnay musts and wines. Food quality and preference, 6(1), 35-41.
  • Ferreira, V., Fernández, P., Peña, C., Escudero, A., & Cacho, J. F. (1995b). Investigation on the role played by fermentation esters in the aroma of young Spanish wines by multivariate analysis. Journal of the Science of Food and Agriculture, 67(3), 381-392.
  • Ferreira, V. (2010). Volatile aroma compounds and wine sensory attributes. In Managing wine quality (pp. 3-28). Woodhead Publishing.
  • Friedel, M., Frotscher, J., Nitsch, M., Hofmann, M., Bogs, J., Stoll, M., & Dietrich, H. (2016). Light promotes expression of monoterpene and flavonol metabolic genes and enhances flavour of winegrape berries (Vitis vinifera L. cv. Riesling). Australian Journal of Grape and Wine Research, 22(3), 409-421.
  • Garde-Cerdán, T., Santamaría, P., Rubio-Bretón, P., González-Arenzana, L., López-Alfaro, I., & López, R. (2015). Foliar application of proline, phenylalanine, and urea to Tempranillo vines: Effect on grape volatile composition and comparison with the use of commercial nitrogen fertilizers. LWT-Food Science and Technology, 60(2), 684-689.
  • Garcia de Cortazar, I. , Duchêne, É., Destrac, A., Barbeau, G., De Rességuier, L., Lacombe, T., Parker A., Saurin N. & van Leeuwen, C. (2017). Grapevine phenology in France: from past observations to future evolutions in the context of climate change, OENO One, 51, 115-126.
  • Geffroy, O., Dufourcq, T., Carcenac, D., Siebert, T., Herderich, M., & Serrano, E. (2014). Effect of ripeness and viticultural techniques on the rotundone concentration in red wine made from Vitis vinifera L. cv. Duras. Australian Journal of Grape and Wine Research, 20(3), 401-408.
  • Geffroy, O., Siebert, T., Herderich, M., Mille, B., & Serrano, E. (2016). On-vine grape drying combined with irrigation allows to produce red wines with enhanced phenolic and rotundone concentrations. Scientia horticulturae, 207, 208-217.
  • Geffroy, O., Descôtes, J., Levasseur-Garcia, C., Debord, C., Denux, J. P., & Dufourcq, T. (2019a). A 2-year multisite study of viticultural and environmental factors affecting rotundone concentration in Duras red wine. OENO One, 53(3).
  • Geffroy, O., Li Calzi, M., Ibpfelt, K., Yobregat, O., Feilhes, C. & Dufoucq, T., (2019b). Using common viticultural practices to modulate the rotundone and 3-isobutyl-2-methoxypyrazine composition of Vitis vinifera L. cv. Fer red wines from a temperate climate wine region with very cool nights. OENO One, 53(4).
  • Gerdes, S.M., Winterhalter, P., Ebeler, S.E. (2001). Effect of Sunlight Exposure on Norisoprenoid Formation in White Riesling Grapes, In Carotenoid-Derived Aroma Compounds, American Chemical Society. p. 262-272.
  • Giordano, M., Zecca, O., Belviso, S., Reinotti, M., Gerbi, V., & Rolle, L. (2013). Volatile fingerprint and physico-mechanical properties of Muscat blanc grapes grown in mountain area: a first evidence of the influence of water regimes. Italian Journal of Food Science, 25(3), 329.
  • Gladstones, J. (2011). Wine, terroir and climate change. Wakefield Press.
  • González-Barreiro, C., Rial-Otero, R., Cancho-Grande, B., & Simal-Gándara, J. (2015). Wine aroma compounds in grapes: A critical review. Critical Reviews in Food Science and Nutrition, 55(2), 202-218.
  • Gregan, S. M., Wargent, J. J., Liu, L., Shinkle, J., Hofmann, R., Winefield, C., Trought, M. & Jordan, B. (2012). Effects of solar ultraviolet radiation and canopy manipulation on the biochemical composition of Sauvignon Blanc grapes. Australian Journal of Grape and Wine Research, 18(2), 227-238.
  • Guyon, F., van Leeuwen, C., Gaillard, L., Grand, M., Akoka, S., Remaud, G. S., Sabathié, N. & Salagoïty, M. H. (2015). Comparative study of 13 C composition in ethanol and bulk dry wine using isotope ratio monitoring by mass spectrometry and by nuclear magnetic resonance as an indicator of vine water status. Analytical and Bioanalytical Chemistry, 407(30), 9053-9060.
  • Harner, A.D., Vanden Heuvel, J.E., Marini, R.P., Elias, R.J. & Centinari, M. (2019). Modeling the impacts of weather and cultural factors on rotundone concentration in cool-climate Noiret wine grapes. Frontiers in Plant Science, 10, 1255.
  • Hashizume, K., & Samuta, T. (1999). Grape maturity and light exposure affect berry methoxypyrazine concentration. American Journal of Enology and Viticulture, 50(2), 194-198.
  • Helwi, P., Habran, A., Guillaumie, S., Thibon, C., Hilbert, G., Gomes, E., Delrot, S., Darriet P. & van Leeuwen., C. (2015). Vine nitrogen status does not have a direct impact on 2-methoxy-3-isobutylpyrazine in grape berries and wines. Journal of agricultural and food chemistry, 63(44), 9789-9802.
  • Helwi, P., Guillaumie, S., Thibon, C., Keime, C., Habran, A., Hilbert, G., Gomes, E., Darriet, P., Delrot, S. & van Leeuwen, C. (2016). Vine nitrogen status and volatile thiols and their precursors from plot to transcriptome level. BMC plant biology, 16(1), 173.
  • Hilbert, G., Soyer, J. P., Molot, C., Giraudon, J., Milin, M., & Gaudillere, J. P. (2003). Effects of nitrogen supply on must quality and anthocyanin accumulation in berries of cv. Merlot. Vitis, 42(2), 69.
  • Homich, L. J., Elias, R. J., Heuvel, J. E. V., & Centinari, M. (2017). Impact of fruit-zone leaf removal on rotundone concentration in Noiret. American Journal of Enology and Viticulture, 68(4), 447-457.
  • Hühn, T., Sponholz, W. R., Bernath, K., Friedmann, A., Hess, G., Muno, H., & Fromm, W. (1999). The influence of high-energy shortwave radiation and other environmental factors on the genesis of compounds affecting the wine quality in Vitis vinifera L., cv. Mueller-Thurgau. Vitic. Enol. Sci, 54(4), 101-104.
  • Jackson, D. I., & Lombard, P. B. (1993). Environmental and management practices affecting grape composition and wine quality-a review. American Journal of Enology and Viticulture, 44(4), 409-430.
  • Jones, G. V., & Davis, R. E. (2000). Climate influences on grapevine phenology, grape composition, and wine production and quality for Bordeaux, France. American Journal of Enology and Viticulture, 51(3), 249-261.
  • Kobayashi, H., Takase, H., Suzuki, Y., Tanzawa, F., Takata, R., Fujita, K., Kohno, M., Mochizuki, M., Suzuki, S. & Konno, T. (2011). Environmental stress enhances biosynthesis of flavor precursors, S-3-(hexan-1-ol)-glutathione and S-3-(hexan-1-ol)-L-cysteine, in grapevine through glutathione S-transferase activation. Journal of Experimental Botany, 62(3), 1325-1336.
  • Koch, A., Ebeler, S. E., Williams, L. E., & Matthews, M. A. (2012). Fruit ripening in Vitis vinifera: light intensity before and not during ripening determines the concentration of 2‐methoxy‐3‐isobutylpyrazine in Cabernet-Sauvignon berries. Physiologia Plantarum, 145(2), 275-285.
  • Kotseridis, Y., Baumes, R. L., & Skouroumounis, G. K. (1999). Quantitative determination of free and hydrolytically liberated β-damascenone in red grapes and wines using a stable isotope dilution assay. Journal of Chromatography A, 849(1), 245-254.
  • Koundouras, S., Marinos, V., Gkoulioti, A., Kotseridis, Y., & van Leeuwen, C. (2006). Influence of vineyard location and vine water status on fruit maturation of nonirrigated cv. Agiorgitiko (Vitis vinifera L.). Effects on wine phenolic and aroma components. Journal of Agricultural and Food Chemistry, 54(14), 5077-5086.
  • Kwasniewski, M. T., Vanden Heuvel, J. E., Pan, B. S., & Sacks, G. L. (2010). Timing of cluster light environment manipulation during grape development affects C13 norisoprenoid and carotenoid concentrations in Riesling. Journal of Agricultural and Food Chemistry, 58(11), 6841-6849.
  • Lacey, M. J., Allen, M. S., Harris, R. L., & Brown, W. V. (1991). Methoxypyrazines in Sauvignon blanc grapes and wines. American Journal of Enology and Viticulture, 42(2), 103-108.
  • Lacroux, F., Trégoat, O., van Leeuwen, C., Pons, A., Tominaga, T., Lavigne-Cruège, V., & Dubourdieu, D. (2008). Effect of foliar nitrogen and sulphur application on aromatic expression of Vitis vinifera L. cv. Sauvignon blanc. Journal International des Sciences de la Vigne et du Vin, 42(3), 125-132.
  • Lee, S. H., Seo, M. J., Riu, M., Cotta, J. P., Block, D. E., Dokoozlian, N. K., & Ebeler, S. E. (2007). Vine microclimate and norisoprenoid concentration in Cabernet-Sauvignon grapes and wines. American Journal of Enology and Viticulture, 58(3), 291-301.
  • Le Menn, N., Marchand, S., de Revel, G., Demarville, D., Laborde, D., & Marchal, R. (2017). N, S, O-Heterocycles in aged champagne reserve wines and correlation with free amino acid concentrations. Journal of Agricultural and Food Chemistry, 65(11), 2345-2356.
  • Le Menn, N., van Leeuwen, C., Picard, M., Riquier, L., de Revel, G., & Marchand, S. (2019). Effect of vine water and nitrogen status, as well as temperature, on some aroma compounds of aged red Bordeaux wines. Journal of Agricultural and Food Chemistry, 67(25), 7098-7109.
  • Linsenmeier, A.W., Löhnertz, O. (2007). Changes in Norisoprenoid Levels with Long-term Nitrogen Fertilisation in different intages of Vitis vinifera var. Riesling Wines. South African Journal of Enology and Viticulture, 28(1), 17 – 24.
  • Lloyd, N. D., Capone, D. L., Ugliano, M., Taylor, D. K., Skouroumounis, G. K., Sefton, M. A., & Elsey, G. M. (2011). Formation of damascenone under both commercial and model fermentation conditions. Journal of Agricultural and Food Chemistry, 59(4), 1338-1343.
  • Loscos, N., Hernandez-Orte, P., Cacho, J., & Ferreira, V. (2007). Release and formation of varietal aroma compounds during alcoholic fermentation from nonfloral grape odorless flavor precursors fractions. Journal of Agricultural and Food Chemistry, 55(16), 6674-6684.
  • Lytra, G., Tempere, S., Zhang, S., Marchand, S., de Revel, G., & Barbe, J. C. (2014). Olfactory impact of dimethyl sulfide on red wine fruity esters aroma expression in model solution. Journal International des Sciences de la Vigne et du Vin, 48(1), 75-85.
  • Lytra, G., Tempere, S., Marchand, S., de Revel, G., & Barbe, J. C. (2016). How do esters and dimethyl sulphide concentrations affect fruity aroma perception of red wine? Demonstration by dynamic sensory profile evaluation. Food Chemistry, 194, 196-200.
  • Lytra, G., Miot-Sertier, C., Moine, V., Coulon, J., & Barbe, J. C. (2020). Influence of must yeast-assimilable nitrogen content on fruity aroma variation during malolactic fermentation in red wine. Food Research International, 109294.
  • Marais, J., Van Wyk, C. J., & Rapp, A. (1992). Effect of Storage Time, Temperature and Region on the Levels of 1, l, 6-Trimethyl-1, 2-dihydronaphthalene and other Volatiles, and on Quality of Weisser Riesling Wines. South African Journal of Enology and Viticulture, 13, 23-32.
  • Marais, J. (1983). Terpenes in the aroma of grapes and wines: a review. South African Journal of Enology and Viticulture, 4(2), 49-58.
  • Marais, J., Hunter, J. J., & Haasbroek, P. D. (1999). Effect of canopy microclimate, season and region on Sauvignon blanc grape composition and wine quality. South African Journal of Enology and Viticulture, 20(1), 19-30.
  • Marchand, S., de Revel, G., & Bertrand, A. (2000). Approaches to wine aroma: release of aroma compounds from reactions between cysteine and carbonyl compounds in wine. Journal of Agricultural and Food Chemistry, 48(10), 4890-4895.
  • Matthews, M. A., & Anderson, M. M. (1988). Fruit ripening in Vitis vinifera L.: responses to seasonal water deficits. American Journal of Enology and Viticulture, 39(4), 313-320.
  • Matthews, M. A., & Anderson, M. M. (1989). Reproductive development in grape (Vitis vinifera L.): responses to seasonal water deficits. American Journal of Enology and Viticulture, 40(1), 52-60.
  • Mendez-Costabel, M. P., Wilkinson, K. L., Bastian, S. E. P., Jordans, C., McCarthy, M., Ford, C. M., & Dokoozlian, N. K. (2014). Effect of increased irrigation and additional nitrogen fertilisation on the concentration of green aroma compounds in Vitis vinifera L. Merlot fruit and wine. Australian Journal of Grape and Wine Research, 20(1), 80-90.
  • Morlat, R., & Bodin, F. (2006). Characterization of viticultural terroirs using a simple field model based on soil depth–II. Validation of the grape yield and berry quality in the Anjou vineyard (France). Plant and Soil, 281(1-2), 55-69.
  • Murat, M. L., Masneuf, I., Darriet, P., Lavigne, V., Tominaga, T., & Dubourdieu, D. (2001). Effect of Saccharomyces cerevisiae yeast strains on the liberation of volatile thiols in Sauvignon blanc wine. American Journal of Enology and Viticulture, 52(2), 136-139.
  • Nikolantonaki, M., Thibon, C., Shinoda, K., Teissedre P.-L. & Darriet P. (2012). Levels and influence of flavan-3-ols must contents on varietal aroma of young Sauvignon blanc wines: Effect of pressing conditions, grape origin and vintage. 9th Symposium International d’Oenologie Bordeaux, 15-17 Juin 201; In ŒNO 2011, Dunod, Paris pp 708-715.
  • Park, S. K., & Noble, A. C. (1993). Monoterpenes and monoterpene glycosides in wine aromas. In: Beer and wine production, American Chemical Society, 98-109. DOI: 10.1021/bk-1993-0536.ch006
  • Parker, A. K., de Cortázar‐Atauri, I. G., van Leeuwen, C., & Chuine, I. (2011). General phenological model to characterise the timing of flowering and veraison of Vitis vinifera L. Australian Journal of Grape and Wine Research, 17(2), 206-216.
  • Pellegrino, A., Lebon, E., Simonneau, T., & Wery, J. (2005). Towards a simple indicator of water stress in grapevine (Vitis vinifera L.) based on the differential sensitivities of vegetative growth components. Australian Journal of Grape and Wine Research, 11(3), 306-315.
  • Peynaud, É., & Blouin, J. (2013). Le goût du vin-5e Éd: Le grand livre de la dégustation. Dunod.
  • Peyrot des Gachons, C., Tominaga, T., & Dubourdieu, D. (2000). Measuring the aromatic potential of Vitis vinifera L. Cv. Sauvignon blanc grapes by assaying S-cysteine conjugates, precursors of the volatile thiols responsible for their varietal aroma. Journal of Agricultural and Food Chemistry, 48(8), 3387-3391.
  • Peyrot des Gachons, C., van Leeuwen, C., Tominaga, T., Soyer, J. P., Gaudillère, J. P., & Dubourdieu, D. (2005). Influence of water and nitrogen deficit on fruit ripening and aroma potential of Vitis vinifera L cv Sauvignon blanc in field conditions. Journal of the Science of Food and Agriculture, 85(1), 73-85.
  • Picard, M., Thibon, C., Redon, P., Darriet, P., de Revel, G., & Marchand, S. (2015). Involvement of dimethyl sulfide and several polyfunctional thiols in the aromatic expression of the aging bouquet of red Bordeaux wines. Journal of Agricultural and Food Chemistry, 63(40), 8879-8889.
  • Picard, M., van Leeuwen, C., Guyon, F., Gaillard, L., de Revel, G., & Marchand, S. (2017). Vine water deficit impacts aging bouquet in fine red Bordeaux wine. Frontiers in Chemistry, 5, 56.
  • Poitou, X., Thibon, C., & Darriet, P. (2017). 1, 8-Cineole in french red wines: evidence for a contribution related to its various origins. Journal of Agricultural and Food Chemistry, 65(2), 383-393.
  • Pons, A., Lavigne, V., Eric, F., Darriet, P., and Dubourdieu, D. (2008). Identification of volatile compounds responsible for prune aromas in prematurely aged red wines. J. Agric. Food Chem., 56(13) :5285-5294.
  • Pons, A., Lavigne, V., Darriet, P., & Dubourdieu, D. (2011). Determination of 3-methyl-2, 4-nonanedione in red wines using methanol chemical ionization ion trap mass spectrometry. Journal of Chromatography A, 1218(39), 7023-7030.
  • Pons, A., Lavigne, V., Darriet, P., & Dubourdieu, D. (2015). Glutathione preservation during winemaking with Vitis vinifera white varieties: Example of Sauvignon blanc grapes. American Journal of Enology and Viticulture, 66(2), 187-194.
  • Pons, A., Allamy, L., Lavigne, V., Dubourdieu, D., & Darriet, P. (2017a). Study of the contribution of massoia lactone to the aroma of Merlot and Cabernet-Sauvignon musts and wines. Food Chemistry, 232, 229-236.
  • Pons, A., Allamy, L., Schüttler, A., Rauhut, D., Thibon, C., & Darriet, P. (2017b). What is the expected impact of climate change on wine aroma compounds and their precursors in grape? OENO One, 51(2), 141-146.
  • Rapp, A. (1988). Wine aroma substances from gas chromatographic analysis. In Wine analysis (pp. 29-66). Springer, Berlin, Heidelberg.
  • Rapp, A., Versini, G., & Ullemeyer, H. (1993). 2-Aminoacetophenon: verursachende komponente der untypischen Alterungsnote (Naphthalinton, Hybridton) bei wein. Vitis, 32(1), 61-62.
  • Renouf, V., Trégoat, O., Roby, J. P., & van Leeuwen, C. (2010). Soils, rootstocks and grapevine varieties in prestigious Bordeaux vineyards and their impact on yield and quality. Journal International des Sciences de la Vigne et du Vin, 44(3), 127-134.
  • Reynolds, A. G., Wardle, D. A., Hall, J. W., & Dever, M. (1995). Fruit maturation of four Vitis vinifera cultivars in response to vineyard location and basal leaf removal. American Journal of Enology and Viticulture, 46(4), 542-558.
  • Ribéreau-Gayon, P., Dubourdieu, D., Doneche, B., & Lonvaud, A. (2020). Handbook of Enology, the Microbiology of Wine and Vinifications, Volume 1, Wiley.
  • Rienth, M., & Scholasch, T. (2019). State-of-the-art of tools and methods to assess vine water status. OENO One, 53(4)
  • Roujou de Boubée, D., van Leeuwen, C., & Dubourdieu, D. (2000). Organoleptic impact of 2-methoxy-3-isobutylpyrazine on red Bordeaux and Loire wines. Effect of environmental conditions on concentrations in grapes during ripening. Journal of Agricultural and Food Chemistry, 48(10), 4830-4834.
  • Ryona, I., Pan, B. S., Intrigliolo, D. S., Lakso, A. N., & Sacks, G. L. (2008). Effects of cluster light exposure on 3-isobutyl-2-methoxypyrazine accumulation and degradation patterns in red wine grapes (Vitis vinifera L. cv. Cabernet Franc). Journal of Agricultural and Food Chemistry, 56(22), 10838-10846.
  • Sacks, G. L., Gates, M. J., Ferry, F. X., Lavin, E. H., Kurtz, A. J., & Acree, T. E. (2012). Sensory threshold of 1, 1, 6-trimethyl-1, 2-dihydronaphthalene (TDN) and concentrations in young Riesling and non-Riesling wines. Journal of Agricultural and Food Chemistry, 60(12), 2998-3004.
  • Santos, J. A., Malheiro, A. C., Pinto, J. G., & Jones, G. V. (2012). Macroclimate and viticultural zoning in Europe: observed trends and atmospheric forcing. Climate Research, 51(1), 89-103.
  • Savoi, S., Wong, D. C., Arapitsas, P., Miculan, M., Bucchetti, B., Peterlunger, E., Fait, A., Mattivi, F. & Castellarin, S. D. (2016). Transcriptome and metabolite profiling reveals that prolonged drought modulates the phenylpropanoid and terpenoid pathway in white grapes (Vitis vinifera L.). BMC plant biology, 16(1), 67.
  • Schneider, V. (2014). Atypical Aging Defect: Sensory Discrimination, Viticultural Causes, and Enological Consequences. A Review. American Journal of Enology and Viticulture, 65(3), 277-284.
  • Schultz, H.R., Löhnertz, O., Bettner, W., Balo, B., Linsenmeier, A., Jähnisch, A., Müller, M., Gaubatz, B., & Varadi, G. (1998). Is grape composition affected by current levels of UV-B radiation ?. Vitis, 37(4), 191-192.
  • Schultz, H. (2000). Climate change and viticulture: a European perspective on climatology, carbon dioxide and UV‐B effects. Australian Journal of Grape and Wine Research, 6(1), 2-12.
  • Schüttler, A., Fritsch, S., Hoppe, J.E., Schüssler, C., Jung, R., Thibon, C., Gruber, B., Lafontaine, M., Stol, M., de Revel, G., Schultz, H., Rauhut, D. & Darriet, P. (2013). Facteurs influençant la typicité aromatique des vins du cépage Vitis vinifera cv. Riesling. Aspects sensoriels, chimiques et viticoles. Revue des Œnologues, 149S, 36-41.
  • Schüttler, A., Friedel, M., Jung, R., Rauhut, D., & Darriet, P. (2015). Characterizing aromatic typicality of Riesling wines: merging volatile compositional and sensory aspects. Food Research International, 69, 26-37.
  • Schüttler, A., Guthier, C., Stoll, M., Darriet, P., & Rauhut, D. (2016). Riesling: Impact of grape cluster zone defoliation, grape must clarification and yeast strain on TDN potential in cool climate wines. Wine & Viticulture Journal, 31(2), 51.
  • Seguin, G. (1969). L'alimentation en eau de la vigne dans des sols du Haut-Médoc. Journal International des Sciences de la Vigne et du Vin, 3(2), 93-141.
  • Seguin, G. (1988). Ecosystems of the great red wines produced in the maritime climate of Bordeaux. In Proceedings of the Symposium on Maritime Climate Winegrowing. L. Fuller-Perrine (Ed.) (pp. 36-53).
  • Segurel, M.A., Razungles, A.J., Riou, C., Salles, M. & Baumes R.L. (2004). Contribution of dimethyl sulfide to the aroma of Syrah and Grenache noir wines and estimation of its potential in grapes of these varieties. Journal of Agricultural and Food Chemistry, 52(23), 7084-7093.
  • Segurel, M. A., Razungles, A. J., Riou, C., Trigueiro, M. G., & Baumes, R. L. (2005). Ability of possible DMS precursors to release DMS during wine aging and in the conditions of heat-alkaline treatment. Journal of Agricultural and Food Chemistry, 53(7), 2637-2645.
  • Simpson, R. F. (1978). 1,1,6-Trimethyl-1,2-dihydronaphthalene: an important contributor to the bottle aged bouquet of wine. Chemistry and Industry 56, 1, 37.
  • Simpson, R. F. (1979). Aroma composition of bottle aged white wine. Vitis, 18(2), 148-154.
  • Skinkis, P. A., Bordelon, B. P., & Butz, E. M. (2010). Effects of sunlight exposure on berry and wine monoterpenes and sensory characteristics of Traminette. American Journal of Enology and Viticulture, 61(2), 147-156.
  • Slaghenaufi, D., Perello, M. C., Marchand, S., & de Revel, G. (2016). Quantification of megastigmatrienone, a potential contributor to tobacco aroma in spirits. Food Chemistry, 203, 41-48.
  • Slaghenaufi, D., & Ugliano, M. (2018). Norisoprenoids, sesquiterpenes and terpenoids content of Valpolicella wines during aging: Investigating aroma potential in relationship to evolution of tobacco and balsamic aroma in aged wine. Frontiers in chemistry, 6, 66.
  • Smart, R. E. (1986). Influence of light on composition and quality of grapes. In Symposium on Grapevine Canopy and Vigor Management, XXII IHC 206 (pp. 37-48).
  • Spayd, S. E., Wample, R. L., Stevens, R. G., Evans, R. G., & Kawakami, A. K. (1993). Nitrogen fertilization of White Riesling in Washington: effects on petiole nutrient concentration, yield, yield components, and vegetative growth. American Journal of Enology and Viticulture, 44(4), 378-386.
  • Spayd, S. E., Tarara, J. M., Mee, D. L., & Ferguson, J. C. (2002). Separation of sunlight and temperature effects on the composition of Vitis vinifera cv. Merlot berries. American Journal of Enology and Viticulture, 53(3), 171-182.
  • Spedding, D. J., & Raut, P. (1982). The influence of dimethyl sulphide and carbon disulphide in the bouquet of wines. Vitis, 21, 240-246. DOI:
  • Šuklje, K., Antalick, G., Coetzee, Z., Schmidtke, L. M., Baša Česnik, H., Brandt, J., du Toit W.J., Lisjak, K. & Deloire, A. (2014). Effect of leaf removal and ultraviolet radiation on the composition and sensory perception of Vitis vinifera L. cv. S auvignon B lanc wine. Australian Journal of Grape and Wine Research, 20(2), 223-233.
  • Szymańska, R., Ślesak, I., Orzechowska, A., & Kruk, J. (2017). Physiological and biochemical responses to high light and temperature stress in plants. Environmental and Experimental Botany, 139, 165-177.
  • Tominaga, T., Peyrot des Gachons, C., & Dubourdieu, D. (1998). A New Type of Flavor Precursors in Vitis vinifera L. cv. Sauvignon Blanc: S-Cysteine Conjugates. Journal of Agricultural and Food Chemistry, 46(12), 5215-5219.
  • Trégoat, O., van Leeuwen, C., Choné, X., & Gaudillere, J. P. (2002). Etude du régime hydrique et de la nutrition azotée de la vigne par des indicateurs physiologiques. Influence sur le comportement de la vigne et la maturation du raisin (Vitis vinifera L. cv Merlot, 2000, Bordeaux). Journal International des Sciences de la Vigne et du Vin, 36(3), 133-142.
  • van Leeuwen, C., Friant, P., Soyer, J. P., Molot, C., Choné, X., & Dubourdieu, D. (2000). Measurement of total nitrogen and assimilable nitrogen in grape juice to assess vine nitrogen status. Journal International des Sciences de la Vigne et du Vin, 34(2), 75-82.
  • van Leeuwen, C., & Seguin, G. (2006). The concept of terroir in viticulture. Journal of Wine Research, 17(1), 1-10.
  • van Leeuwen, C., Friant, P., Chone, X., Tregoat, O., Koundouras, S., & Dubourdieu, D. (2004). Influence of climate, soil, and cultivar on terroir. American Journal of Enology and Viticulture, 55(3), 207-217.
  • van Leeuwen, C., Trégoat, O., Choné, X., Bois, B., Pernet, D., & Gaudillère, J. P. (2009). Vine water status is a key factor in grape ripening and vintage quality for red Bordeaux wine. How can it be assessed for vineyard management purposes? Journal International des Sciences de la Vigne et du Vin, 43(3), 121-134.
  • van Leeuwen, C., Roby, J. P., & de Rességuier, L. (2018). Soil-related terroir factors: A review. OENO one, 52(2), 173-188.
  • Winkler, A. J. (1965). General viticulture. Univ of California Press.
  • Wood, C., Siebert, T. E., Parker, M., Capone, D. L., Elsey, G. M., Pollnitz, A. P. & Krammer, G. (2008). From wine to pepper: rotundone, an obscure sesquiterpene, is a potent spicy aroma compound. Journal of Agricultural and Food Chemistry, 56(10), 3738-3744.
  • Wu, J., Drappier, V., Hilbert, G., Guillaumie, S., Dai, Z., Geny, L., Delrot, S., Darriet, P., Thibon, C. & Pieri, P. (2019). The effects of a moderate grape temperature increase on berry secondary metabolites. OENO One, 53(2), 321-333.
  • Yuan, F., Schreiner, R.P., Osborne, J., Qian, M.C. (2018). Effects of Soil NPK Supply on Pinot noir Wine Phenolics and Aroma Composition. American Journal of Enology and Viticulture, 69, 371-385.
  • Zhang, P., Howell, K., Krstic, M., Herderich, M., Barlow, E. W. R., & Fuentes, S. (2015a). Environmental factors and seasonality affect the concentration of rotundone in Vitis vinifera L. cv. Shiraz wine. PloS One, 10(7).
  • Zhang, P., Barlow, S., Krstic, M., Herderich, M., Fuentes, S., & Howell, K. (2015b). Within-vineyard, within-vine, and within-bunch variability of the rotundone concentration in berries of Vitis vinifera L. cv. Shiraz. Journal of Agricultural and Food Chemistry, 63(17), 4276-4283.
  • Ziegler, M., Gök, R., Bechtloff, P., Winterhalter, P., Schmarr, H.-G., Fischer, U. (2019). Impact of matrix variables and expertise of panelists on sensory thresholds of 1,1,6-trimethyl-1,2- dihydronaphthalene known as petrol off-flavor compound in Riesling wines, Food Quality and Preference, 78, art. no. 103735.
  • Ziegler, M., Wegmann-Herr, P., Schmarr, H.-G., Gök, R., Winterhalter, P., & Fischer, U. (2020). Impact of Rootstock, Clonal Selection, and Berry Size of Vitis vinifera sp. Riesling on the formation of TDN, vitispiranes, and other volatile Compounds, Journal of Agricultural and Food Chemistry, 68, 3834 – 3849.
  • Zufferey, V., Murisier, F., & Schultz, H. R. (2000). A model analysis of the photosynthetic response of Vitis vinifera L. cvs Riesling and Chasselas leaves in the field: I. Interaction of age, light and temperature. Vitis, 39(1), 19-26.


Cornelis van Leeuwen

Affiliation : EGFV, Bordeaux Sciences Agro, INRAE, Univ. Bordeaux , ISVV, F-33882 Villenave d’Ornon, France
Country : France
Biography :

Kees (Cornelis van Leeuwen) is a professor of viticulture at Bordeaux Sciences Agro, which makes part of Bordeaux University’s Institut des Sciences de la Vigne et du Vin. Kees van Leeuwen conducts research on the concept of terroir in viticulture. His works are centred on environmental constraint in the expresssion of vine-growing terroir. This constraint is most often a limiting of water supply or a limiting of nitrogen nutrition in the vines. Kees van Leeuwen has taken part in the creation and evaluation of several indicators of water supply regime and nitrogen status in vines. Kees van Leeuwen has also worked on the climate’s effect on the expression of vine-growing terroir. The vine’s response is evaluated through the precocity of its vegetation, its growth and development and its grapes constituents at ripeness. Particular attention is paid to the grapes’ aromatic potential in relation to environmental factors. He participated in the creation of the Grapevine Flowering Veraison model (GFV model).
Kees van Leeuwen is a consultant for Château Cheval Blanc in Saint-Émilion. He has carried out or taken part in numerous studies to map the different soils of wine estates and appellations. Kees van Leeuwen was the editor-in-chief of the Journal International des Sciences de la Vigne et du Vin from 2001 to 2016. He writes on a regular basis for the Dutch magazine « Perswijn ».

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