Next Article in Journal
Can the Caper (Capparis spinosa L.) Still Be Considered a Difficult-to-Propagate Crop?
Previous Article in Journal
A Reliable Regeneration Method in Genome-Editable Bell Pepper ‘Dempsey’
 
 
Font Type:
Arial Georgia Verdana
Font Size:
Aa Aa Aa
Line Spacing:
Column Width:
Background:
Article

Leaf Morpho-Colorimetric Characterization of Different Grapevine Varieties through Changes on Plant Water Status

by
Gastón Gutiérrez-Gamboa
1,
Nicolás Torres-Huerta
2,
Miguel Araya-Alman
3,*,
Nicolás Verdugo-Vásquez
4,
Yerko Moreno-Simunovic
5,
Héctor Valdés-Gómez
6 and
César Acevedo-Opazo
5,*
1
Escuela de Agronomía, Facultad de Ciencias, Universidad Mayor, Huechuraba 8580000, Chile
2
Stoller Chile SA, Ruta 5 Sur, KM 192, Curicó 3340000, Chile
3
Departamento de Ciencias Agrarias, Universidad Católica del Maule, km 6 Camino Los Niches, Curicó 3340000, Chile
4
Centro de Investigación Intihuasi, Instituto de Investigaciones Agropecuarias (INIA), Colina San Joaquín s/n, La Serena 1700000, Chile
5
Facultad de Ciencias Agrarias, Universidad de Talca, 2 Norte 685, Casilla 747, Talca 346000, Chile
6
Departamento de Fruticultura y Enología, Pontificia Universidad Católica de Chile, Av. Vicuña Mackenna 4860, Macul 7810000, Chile
*
Authors to whom correspondence should be addressed.
Horticulturae 2021, 7(9), 315; https://doi.org/10.3390/horticulturae7090315
Submission received: 6 August 2021 / Revised: 1 September 2021 / Accepted: 14 September 2021 / Published: 16 September 2021
(This article belongs to the Section Viticulture)

Abstract

:
(1) Background: Currently, some ampelographic methods are developing in order to identify grapevine varieties. For this purpose, morpho-colorimetric parameters in leaves have been analyzed by digital imagen analysis, but some environmental conditions may affect their determinations. (2) Methods: A research study was conducted to characterize leaf morpho-colorimetric parameters in five grapevine varieties growing under different plant water status and to discriminate them under these conditions. Leaves were collected in vines, and twelve leaf morpho-colorimetric and fractal dimension variables were assessed. (3) Results: Merlot presented the highest values of perimeter and area to perimeter ratio in leaves and higher leaf area than Chardonnay in both plant water conditions. Most of the leaf morpho-colorimetric variables allowed discriminating the grapevine varieties under the contrasted hydric conditions. Under non-water stress, Carmenère was not related to any measured parameters. Merlot was positively related to most of the leaf morphometric parameters, whereas Chardonnay presented the opposite behavior. RGB color system variables allowed discriminating the grapevine varieties under water stress conditions, and Sauvignon Blanc was not related to any measured parameter. Chardonnay and Pinot Noir were positively related to green color and negatively related to most of the leaf morphometric parameters, whereas Merlot showed the opposite behavior. (4) Conclusions: Leaf morpho-colorimetric and fractal dimension parameters were affected by plant water stress and more variables should be incorporated into the new ampelographic methods in order to characterize leaf morpho-colorimetric parameters of the different grapevine varieties more clearly.

1. Introduction

Ampelography is the field of botany concerning the identification and classification of grapevine varieties that includes several parameters or descriptors that are measured on leaves, shoots, clusters and berries [1,2]. The main descriptors involved in ampelographic characterization comprises types of hair, color, shape and size, textures and appearance [3]. Based on this, ampelography provides relevant morphological and agronomical information for varietal characterization studies, breeding programs and conservation purposes [4,5].
Ampelography remains a problem of concern since the wide number of grapevine varieties and the variability within them cause difficulty in their identification and recognition [6]. More than 6000 varieties have been identified based on ampelographic descriptors, but only a small number of varieties are used for the vineyard establishment [7]. Currently, there is great interest within the wine industry to explore the potential of minority grapevine varieties as adaptation strategies to face global warming [8]. Based on this, there is a need to ensure trueness of plant and to avoid planting wrong material, which may result in significant financial losses to viticulturists.
A more objective classification of grapevine varieties has been developed in the last decades by chemical, spectroradiometry and genetic fingerprinting techniques, including recently digital photography methods [2,6,7]. Based on empirical knowledge, leaf shape and shoot-tip pubescence are the best ampelographic descriptors for variety identification [1,9]. Therefore, leaf morphology provides distinctive traits for reaching this goal [1,9]. In recent years, some authors reported that plant water stress may affect leaf morphological characteristics, affecting varietal identification [2,10]. By digital photography and image analysis algorithms, it is possible to obtain a range of leaf morphological parameters that may solve the above-mentioned problems [11]. In a preliminary study, Fuentes et al. [6] reported that the automatic extraction of morpho-colorimetric data, NIR chemical fingerprinting and machine learning modelling rendered rapid, accurate and non-destructive methods for variety classification. However, it is possible that leaf morpho-colorimetric characteristics of the vines could be affected by plant water status. Therefore, the aim of this work was to characterize morpho-colorimetric and fractal dimension parameters from scanned mature leaves of vines managed under different soil water status by image analysis and to discriminate them under these contrasting conditions.

2. Materials and Methods

2.1. Site of Study and Plant Material

An experimental vineyard (cv. Sauvignon Blanc, Chardonnay, Carmenère, Merlot and Pinot Noir) was used for this field trial during the 2011–2012 growing season. The experimental vineyard is in Panguilemo, Talca, Chile (Maule Valley) (Talca, WGS84 datum, 35°22.2′ S; 71°35.39′ W, at 121 m.a.s.l.). The vineyard was established in 2006, and the vines were trained to a vertical shoot position trellis system and pruned into two bilateral spur cordons. The vine density was about 5000 vines ha−1, spaced at 2.00 m × 1.00 m between rows and within the row, respectively, with an east–west orientation. The vineyard was drip irrigated using two lines of 2 L h−1 with self-compensating emitters spaced every 0.5 m.

2.2. Soil and Climate Conditions

The vineyard soil presents a clay loam texture with a depth root of 1.50 m. Soil bulk density, field capacity, wilting point and available water were 1.36 g cm−3, 0.31 m3 m−3, 0.13 m3 m−3 and 0.18 m3 m−3, respectively. The reports published by Pañitrur-De la Fuente et al. [12] and Gutierrez-Gamboa et al. [13] present more information concerning soil data and viticultural management performed in the vineyard.
An automatic weather station (Adcon Telemetry, A730, Klosterneuburg, Austria) located close to the experimental vineyard (around 50 m from the field trial) was used to obtain climatic data [13]. Briefly, average, maximum and minimum temperature in the growth season were 16.9, 34.6 °C and 0.0 °C, respectively, whereas precipitations registered for the same period was 31.8 mm, which was concentrated in the spring months. In the winter, 1438 chilling hours were accumulated. In the growth season, degree days accumulation was 1375 °C, vapor-pressure deficit reached 1.05 kPa and the reference evapotranspiration was 1037 mm. The climatic characteristics mentioned are characteristic of the Maule valley [14].

2.3. Experimental Design

The experimental design was a randomized complete block divided into two treatments (blocks) in which five grapevine varieties, such as Sauvignon Blanc, Chardonnay, Carmenère, Merlot and Pinot Noir, were arranged. One of the two blocks was managed under no water stress (without irrigation restriction), while the other was managed following a progressive water restriction until reaching severe water stress (leaf water potential <−1.4 MPa), according to the stress classification stated by van Leeuwen et al. [15]. A total of ten treatments (variety × water condition) were arranged in the vineyard, considering five plants per treatment in which eight mature leaves per plant were collected to determine leaf morpho-colorimetric variables. The selected vines evidenced good phytosanitary conditions and were homogeneous in vegetative growth, productivity and climatic conditions.

2.4. Leaf Collection Process and Leaf Morpho-Colorimetric and Fractal Dimension Analysis

Leaf collection protocol was carried out following the methodology stated by Fuentes et al. [6]. Briefly, eight mature leaf samples by plant were collected from the vineyard, stored in plastic bags and then transported in a cooler with ice blocks to avoid leaf dehydration. Healthy, fully expanded and mature leaves (including petiole) were collected from the fifth position of each vine shoot with the aim of attaining uniform physiological maturity of leaves for modelling purposes.
The collected leaves were scanned using a Hewlett Packard Scanjet G3010 (Hewlett-Packard Software Company, Palo Alto, CA, USA) scanner (Figure 1).
The obtained images were analyzed by using a customized code written in Matlab® ver. R2010a (Mathworks Inc., Natick, MA, USA). The blue band of the image was then post-processed to identify the leaf morpho-colorimetric and fractal dimension variables (Figure 1). As described by Fuentes et al. [6], an initial calibration for the scanner was made using black squares as references of known dimensions to relate pixel count in the x and y coordinates to dimensions and area using metric units (cm and cm2). Scanner calibration allowed automatic analysis of leaf images, extracting morphometric and color parameters and the fractal dimensions of each leaf sample [6]. These variables were analyzed according to the protocols stated by Fuentes et al. [6]. The parameters obtained from this process are presented in Table 1.

2.5. Plant Water Status and Gas Exchange Measurements

The leaf water potential (Ψleaf) was measured to define the treatments. This parameter was determined by using a pressure chamber (PMS Instrument Co., model 600, Corvallis, OR, USA), according to the methods stated by Acevedo-Opazo et al. [16] and by Jara-Rojas et al. [17].
An infrared gas analyzer model LI 6400 (Li-cor, Lincoln, NV, USA) was used to determine stomatal conductance (gs), transpiration (E) and net CO2 assimilation (AN) in Sauvignon Blanc, Chardonnay, Merlot and Pinot Noir and not for Carmenère. Based on some of these variables, the intrinsic water use efficiency (AN gs−1) was calculated as the ratio between AN and gs according to the report published by Medrano et al. [18]. The gas exchange measurements were performed according to the steps reported by Gutiérrez-Gamboa et al. [13]. Three determinations were made between 12:00 and 14:00 h in the north side of the canopy at the middle zone (sixth leaf from the tip on fruit-bearing shoots) on 20 December 2011, 27 December 2011 and 21 January 2012. Measurements were performed in five different vines per treatment on fully sunny days without changing the original position of the selected leaves in the canopy and maintaining the same light regime, ensuring that the leaves were exposed to full sunlight (PAR > 800 μmol m−2 s−1).

2.6. Statistical Analysis

The measured variables were analyzed by principal component analysis (PCA) to classify the leaves by variety using The Unscrambler® X ver. 10.1 (CAMO Software, Oslo, Norway). PCA was performed to identify the main relationships among the measured variables and to relate them to the quality of characterization (prediction) of the different grapevine varieties. Following this assumption, the proposed method considers that the first and second principal components of the PCA (PC 1 and PC 2) should represent the leaf morpho-colorimetric characterization at each observation (variety) if a significant amount of variance is explained by PC1 and PC2. If so, the score of both components can be used to rank all the observations according to the leaf morpho-colorimetric parameter values observed at these sites. In addition, the significant differences for the measured parameters were assessed using analysis of variance (ANOVA), and the Tukey test (p ≤ 0.05) was used for mean separation using the Statgraphics Centurion XVI.I statistical package (Warrento, VA, USA). Finally, the contribution of each variable to each principal component was added as Supplementary Materials.

3. Results

3.1. Leaf Morpho-Colorimetric Variables Analyzed in Grapevine Varieties Cultivated under No Water Stress Conditions

Leaf morpho-colorimetric parameters such as eccentricity, blue color, red and green index and fractal dimension were statistically similar among the varieties (Table 2). Merlot presented the highest values of leaf perimeter, maximum length of leaf and area to perimeter ratio (Table 2). In contrast, Pinot Noir exhibited the lowest value of this last parameter (Table 2). Merlot showed higher leaf area than Chardonnay and Sauvignon Blanc and higher red and green index than Carmenère and Chardonnay (Table 2). Maximum length of petiole was higher in Carmenère, Merlot and Sauvignon Blanc than in Chardonnay (Table 2). Regarding color parameters, Carmenère and Sauvignon Blanc presented higher red and green color than Merlot and Pinot Noir (Table 2).

3.2. Leaf Morpho-Colorimetric Variables Analyzed in Grapevine Varieties Cultivated under Water Stress Conditions

Fractal dimensions did not vary among the varieties cultivated under water stress and no water stress conditions (Table 2). Merlot presented the highest leaf perimeter, minimum length of leaf and area to perimeter ratio and the lowest red color (Table 2). Merlot showed higher leaf area and maximum length of leaf than Carmenère, Chardonnay and Pinot Noir (Table 2). Carmenère presented lower eccentricity than Chardonnay and Pinot Noir, while this last one showed lower maximum length of petiole than Carmenère, Merlot and Sauvignon Blanc (Table 2). Regarding color parameters, Chardonnay presented higher green color than Merlot and Sauvignon Blanc (Table 2). Carmenère showed lower blue color than Chardonnay and Pinot Noir and lower red and green index than Merlot, Pinot Noir and Sauvignon Blanc (Table 2).

3.3. Leaf Gas Exchange Parameters and Intrinsic Water Use Efficiency in Grapevine Varieties Managed under Different Water Supply

Leaf gas exchange parameters were not affected in grapevine varieties managed under stress water conditions (Table 3). Only the grapevine varieties cultivated under no water stress conditions presented statistical differences on transpiration (E), stomatal conductance (gs) and intrinsic water-use efficiency (AN gs−1) (Table 3). Based on this, Pinot Noir presented lower transpiration than Merlot and Sauvignon Blanc (Table 3). Sauvignon Blanc showed higher stomatal conductance and lower intrinsic water-use efficiency than Merlot and Pinot Noir (Table 3).

3.4. Multivariate Analysis to Discriminate the Different Grapevine Varieties

In order to discriminate the different varieties and assess the effects of treatments on leaf a morpho-colorimetric characteristics, PCA was performed (Figure 2), including all available data. Principal component 1 (PC 1) explained 61.8% of the variance and principal component 2 (PC 2) explained 21.6%, representing an 83.4% of all the variance. PC 1 was strongly correlated with leaf area (A), leaf perimeter (P), perimeter to area ratio of leaf (P2/A), maximum length of leaf (LMax), minimum length of leaf (LMin), maximum length of petiole (LMax P) and red color, while PC 2 was strongly correlated only with red and green index (RG). Both components allowed discriminating the different grapevine varieties except Sauvignon Blanc, which was not related to any ampelographic parameter. Pinot Noir was positively related to eccentricity (Ex) and negatively related to LMax P. Carmenère was positively related to fractal dimension (FR) and negatively related to blue color. Merlot was positively related to most of the leaf morphometric parameters, such as A, LMax and LMin, whereas Chardonnay showed the opposite behavior, and it was negatively correlated to leaf morphometric characteristics.
In order to discriminate the different varieties and assess the effects of water stress conditions (leaf water potential <−1.4 MPa) on leaf a morpho-colorimetric characteristics, PCA was performed (Figure 3a). PC 1 (PC 1) explained 64.1% of the variance and principal component 2 (PC 2) explained 20.2%, representing 84.4% of all the variance. PC 1 was strongly correlated to A, P, P2/A, LMax, LMin, LMax P and red color, while PC 2 was only strongly correlated with RG. Both components allowed discriminating the different grapevine varieties except for Sauvignon Blanc, which was not related to any morpho-colorimetric parameter. Under water stress conditions, Chardonnay and Pinot Noir were positively related to green color and negatively related to most of the leaf morphometric parameters such as A, LMax, LMin and P2/A, whereas Merlot showed the opposite behavior. Carmenère was negatively related to Ex and blue color.
In order to discriminate the different varieties and assess the effects of no water stress (without irrigation restriction) on leaf morpho-colorimetric characteristics, PCA was performed (Figure 3b). Principal component 1 (PC 1) explained 60.0% of the variance, and principal component 2 (PC 2) explained 23.0%, representing 83.0% of all the variance. PC 1 was strongly correlated to A, P, LMax, LMin and red and green index, while PC 2 was only strongly correlated with FR. Both components allowed discriminating different grapevine varieties except Carmenère, which was not related to any ampelographic parameter. Pinot Noir was positively related to Ex and negatively related to FR, whereas Sauvignon Blanc was negatively related to RG. Merlot was positively related to some leaf morphometric parameters such as A, LMax and LMin, whereas Chardonnay presented the opposite behavior.

4. Discussion

Since the beginning of the century, there is a new tendency within the wine industry to introduce varieties of different origins for wine diversification [19]. A correct ampelographic classification of grapevine varieties allows ensuring varietal authenticity and avoids planting material the wrong at a vineyard establishment. In the past, there have been varietal identification mistakes or confusion with grapevine material, both internationally and in the national wine industry. The Carmenère variety was improperly known as Merlot in Chile, and it was not until two decades ago that it was correctly identified by ampelography description [20]. Currently, Carmenère (7.87%) is the fifth most planted variety behind Cabernet Sauvignon (29.50%), Sauvignon Blanc (11.17%), Merlot (8.63%) and Chardonnay (8.16%) in Chile. Based on this, mistakes in grapevine identification potentially can result in significant financial costs associated with replants and in other aspects of the wine production chain.
Based on this, it is interesting that our results showed clear discrimination between Merlot and Carmenère using digital images and multivariate analysis (Figure 2 and Figure 3). Merlot was strongly related to high values of leaf morphometric parameters, while Carmenère was inversely related to blue color and positively related to fractal dimension. In spring, the young leaves of Carmenère variety present a characteristic orange color, while the leaves take on an anthocyanin pigmentation that gives them a characteristic blue-reddish color when close to harvest [21]. The fractal dimension shows a strong correlation with human perception of surface roughness [22], which could discriminate Carmenère from the rest of the studied grapevine varieties after its analysis under both plant water status (Figure 2). On the other hand, Pinot Noir was positively related to eccentricity (Figure 2). The eccentricity is the ratio of the distance between the foci of the ellipse and its major axis length, and its value ranges between 0 and 1 [23]. If the grapevine varieties leaves are viewed from the eccentricity point of view, a high value of this parameter results in an elongated shape of the leaf. Pinot Noir leaf is of medium size, orbicular, dark green, thick, funnel-shaped, generally entirely trilobed or weakly trilobed [9]. These results are very interesting since some techniques do not readily discriminate varieties with morphological differences due to mutations, as in the case among Pinot Noir, Pinot Blanc and Pinot Gris [24].
Severe water stress (leaf water potential <−1.4 MPa) affected grapevine variety discrimination (Figure 3). Chardonnay and Pinot Noir were strongly positively related to red color and negatively related to leaf morphometric parameters, which is opposite to Merlot (Figure 3). This grapevine variety reached non-significant high values of net CO2 assimilation compared to Chardonnay and Pinot Noir (Table 3). The red light is absorbed more strongly by photosynthetic pigments and is predominantly absorbed by the top few cell layers; consequently, red photons used less efficiency in terms of being dissipated [25]. Merlot presented non-significant higher intrinsic water-use efficiency (WUE) than the rest of the studied grapevine varieties. WUE reflects the balance between vine production (kg of biomass produced or moles of CO2 assimilated) and water costs (m3 of water used or moles of water transpired) [18,26]. Several reports showed that Merlot presents higher WUE compared to several grapevine varieties [13,26,27,28]. Therefore, the hydric behavior and gas exchange of Merlot vines grown under severe water stress could not affect their ability to develop a canopy with a high leaf area and, thus, is positively related to leaf morphometric parameters.
Non-water stress (without irrigation restriction) affected the discrimination of Sauvignon Blanc and Carmenère (Table 3). Sauvignon Blanc reached higher values of stomatal conductance and transpiration and lower values of WUE compared to some of the rest of the studied varieties (Table 3). In Carmenère, transpiration could be sustained, despite presenting a large leaf area through less sensitive stomata [17]. In this case, the hydraulic system needs high-water transport capacity in the soil-plant-atmosphere continuum, and this variety can be less sensitive to xylem embolisms [29].
To solve the problems of discrimination of grapevine varieties by digital images, the selected leaf morpho-colorimetric parameters must not be affected by the environmental factors and viticultural practices. The color of upper size of blade, area of leaf anthocyanin coloration, goffering of blade, shape of teeth, size of teeth in relation to blade, length of teeth compared with their width, degree of opening and overlapping of petiole sinus and shape of base of petiole sinus, among other descriptors, could be interesting parameters for ampelographic classification of the grapevine varieties using digital images.

5. Conclusions

Leaf morpho-colorimetric variables studied in this trial allowed discriminating grapevine varieties, except Sauvignon Blanc, after their analysis under contrasting hydric conditions. Merlot, Carmenère, Chardonnay and Pinot Noir were separated by using digital images and multivariate analysis. Merlot was strongly related to high values of leaf morphometric parameters contrary to Chardonnay, while Carmenère was inversely related to blue color and positively related to fractal dimension. On the other hand, Carmenère and Pinot Noir were related to fractal dimension and eccentricity, respectively. RGB color system variables allowed discriminating the grapevine varieties managed under water stress conditions. Chardonnay and Pinot Noir were positively related to red color and negatively related to leaf morphometric parameters, which is opposite to Merlot. Full irrigation affected the discrimination of Sauvignon Blanc and Carmenère. Thus, leaf morpho-colorimetric characteristics of the vines were modified by plant water status. Lastly, the digital image is an interesting method to classify grapevine varieties, but it is important to validate it in future studies, proposing new leaf morpho-colorimetric variables to more clearly separate the varieties that cannot be discriminated, such as Sauvignon Blanc in this study.

Supplementary Materials

The following are available online at https://www.mdpi.com/article/10.3390/horticulturae7090315/s1, Table S1. Variable’s contribution in the PCA combined (Figure 2). Table S2. Variable’s contribution in the PCA grapevine varieties managed under stress water conditions (Figure 3a). Table S3. Variable’s contribution in the PCA grapevine varieties managed under no water stress (Figure 3b).

Author Contributions

Conceptualization, C.A.-O. and H.V.-G.; methodology, N.T.-H. and M.A.-A.; software, N.T.-H. and M.A.-A.; validation, N.V.-V., M.A.-A., C.A.-O. and H.V.-G.; formal analysis, N.T.-H., G.G.-G., N.V.-V. and M.A.-A.; investigation, C.A.-O., H.V.-G. and Y.M.-S.; resources, C.A.-O., H.V.-G. and Y.M.-S.; data curation, N.T.-H., N.V.-V., C.A.-O., H.V.-G. and M.A.-A.; writing—original draft preparation, N.T.-H., G.G.-G., N.V.-V. and M.A.-A.; writing—review and editing, C.A.-O., H.V.-G. and Y.M.-S.; visualization, C.A.-O., H.V.-G. and Y.M.-S.; supervision, C.A.-O., H.V.-G. and Y.M.-S.; project administration, C.A.-O. and H.V.-G.; funding acquisition, C.A.-O. and H.V.-G. All authors have read and agreed to the published version of the manuscript.

Funding

This research received no external funding.

Institutional Review Board Statement

Not applicable.

Informed Consent Statement

Not applicable.

Data Availability Statement

Not applicable.

Acknowledgments

The authors would like to thank K.-H. Schulze, Maribel Rojas, Claudio Verdugo and all the technical staff of Panguilemo Experimental Station for their invaluable role in the good course of the experiments.

Conflicts of Interest

The authors declare no conflict of interest.

References

  1. Soldavini, C.; Schneider, A.; Stefanini, M.; Dallaserra, M.; Policarpo, M. Super ampelo, a software for ampelometric and ampelographic descriptions in vitis. Acta Hortic. 2009, 827, 253–258. [Google Scholar] [CrossRef]
  2. Garcia-Muñoz, S.; Muñoz-Organero, G.; De Andrés, M.T.; Cabello, F. Ampelography-An old technique with future uses: The case of minor varieties of Vitis vinifera L. from the Balearic Islands. J. Int. Des Sci. La Vigne Du Vin 2011, 45, 125–137. [Google Scholar] [CrossRef]
  3. Zdunić, G.; Budić-Leto, I.; Vrhovsek, U.; Tomić-Potrebuješ, I.; Maletić, E. Ampelographic and oenological characterization of the ancient grapevine cv. Dobričić grown in the coastal region of Croatia. OENO One 2012, 46, 263–273. [Google Scholar] [CrossRef]
  4. Barth, S.; Forneck, A.; Verzeletti, F.; Blaich, R.; Schumann, F. Genotypes and phenotypes of an ex situ Vitis vinifera ssp. sylvestris (Gmel.) beger germplasm collection from the upper rhine valley. Genet. Resour. Crop Evol. 2009, 56, 1171–1181. [Google Scholar] [CrossRef]
  5. Khalil, S.; Tello, J.; Hamed, F.; Forneck, A. A multivariate approach for the ampelographic discrimination of grapevine (Vitis vinifera) cultivars: Application to local Syrian genetic resources. Genet. Resour. Crop Evol. 2017, 64, 1841–1851. [Google Scholar] [CrossRef] [Green Version]
  6. Fuentes, S.; Hernández-Montes, E.; Escalona, J.M.; Bota, J.; Gonzalez Viejo, C.; Poblete-Echeverría, C.; Tongson, E.; Medrano, H. Automated grapevine cultivar classification based on machine learning using leaf morpho-colorimetry, fractal dimension and near-infrared spectroscopy parameters. Comput. Electron. Agric. 2018, 151, 311–318. [Google Scholar] [CrossRef]
  7. Tessier, C.; David, J.; This, P.; Boursiquot, J.M.; Charrier, A. Optimization of the choice of molecular markers for varietal identification in Vitis vinifera L. Theor. Appl. Genet. 1999, 98, 171–177. [Google Scholar] [CrossRef]
  8. Gutiérrez-Gamboa, G.; Zheng, W.; Martínez de Toda, F. Current viticultural techniques to mitigate the effects of global warming on grape and wine quality: A comprehensive review. Food Res. Int. 2021, 139, 109946. [Google Scholar] [CrossRef] [PubMed]
  9. Galet, P. Précis D’ampélographie Pratique, 7th ed.; Éditions, L., Ed.; Impremerie JF Impression: Montpellier, France, 1998; ISBN 2-902771-08-8. [Google Scholar]
  10. Bowers, J.E.; Bandman, E.B.; Meredith, C.P. DNA fingerprint characterization of some wine grape cultivars. Am. J. Enol. Vitic. 1993, 44, 266–274. [Google Scholar]
  11. Bodor, P.; Baranyai, L.; Ladányi, M.; Bálo, B.; Strever, A.E.; Bisztray, G.D.; Hunter, J.J. Stability of ampelometric characteristics of Vitis vinifera L. cv. “Syrah” and ‘Sauvignon blanc” leaves: Impact of within-vineyard variability and pruning method/bud load. S. Afr. J. Enol. Vitic. 2016, 34, 129–137. [Google Scholar] [CrossRef] [Green Version]
  12. Paňitrur-De La Fuente, C.; Valdés-Gómez, H.; Roudet, J.; Acevedo-Opazo, C.; Verdugo-Vásquez, N.; Araya-Alman, M.; Lolas, M.; Moreno, Y.; Fermaud, M. Classification of winegrape cultivars in Chile and France according to their susceptibility to Botrytis cinerea related to fruit maturity. Aust. J. Grape Wine Res. 2018, 24, 145–157. [Google Scholar] [CrossRef]
  13. Gutiérrez-Gamboa, G.; Pérez-Donoso, A.G.; Pou-Mir, A.; Acevedo-Opazo, C.; Valdés-Gómez, H. Hydric behaviour and gas exchange in different grapevine varieties (Vitis vinifera L.) from the Maule Valley (Chile). S. Afr. J. Enol. Vitic. 2019, 40, 181–191. [Google Scholar] [CrossRef]
  14. Verdugo-Vásquez, N.; Acevedo-Opazo, C.; Valdés-Gómez, H.; Ingram, B.; De Cortázar-Atauri, I.G.; Tisseyre, B. Temporal stability of within-field variability of total soluble solids of grapevine under semi-arid conditions: A first step towards a spatial model. OENO One 2018, 52, 15–30. [Google Scholar] [CrossRef] [Green Version]
  15. Van Leeuwen, C.; Tregoat, O.; Choné, X.; Bois, B.; Pernet, D.; Gaudillére, J.P. 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? OENO One 2009, 43, 121–134. [Google Scholar] [CrossRef]
  16. Acevedo-Opazo, C.; Valdés-Gómez, H.; Taylor, J.A.; Avalo, A.; Verdugo-Vásquez, N.; Araya, M.; Jara-Rojas, F.; Tisseyre, B. Assessment of an empirical spatial prediction model of vine water status for irrigation management in a grapevine field. Agric. Water Manag. 2013, 124, 58–68. [Google Scholar] [CrossRef]
  17. Jara-Rojas, F.; Ortega-Farías, S.; Valdés-Gómez, H.; Acevedo-Opazo, C. Gas exchange relations of ungrafted grapevines (cv. Carménère) growing under irrigated field conditions. S. Afr. J. Enol. Vitic. 2015, 36, 231–242. [Google Scholar] [CrossRef] [Green Version]
  18. Medrano, H.; Tomás, M.; Martorell, S.; Escalona, J.M.; Pou, A.; Fuentes, S.; Flexas, J.; Bota, J. Improving water use efficiency of vineyards in semi-arid regions. A review. Agron. Sustain. Dev. 2015, 35, 499–517. [Google Scholar] [CrossRef] [Green Version]
  19. Gutiérrez-Gamboa, G.; Liu, S.; Pszczólkowski, P. Resurgence of minority and autochthonous grapevine varieties in South America: A review of their oenological potential. J. Sci. Food Agric. 2020, 100, 465–482. [Google Scholar] [CrossRef]
  20. Pszczólkowski, P. Sauvignon Blanc, Cabernet-Sauvignon y Carmenère, cepas claves de la viticultura actual de Chile. RIVAR 2015, 2, 1–16. [Google Scholar]
  21. Pszczólkowski, P. La invención del cv. Carménère (Vitis vinifera L) en Chile, desde la mirada de uno de sus actores. Universum 2004, 19, 150–165. [Google Scholar] [CrossRef]
  22. Backes, A.R.; Casanova, D.; Bruno, O.M. Color texture analysis based on fractal descriptors. Pattern Recognit. 2012, 45, 1984–1992. [Google Scholar] [CrossRef]
  23. Uluturk, C.; Ugur, A. Recognition of leaves based on morphological features derived from two half-regions. In Proceedings of the International Symposium on INnovations in Intelligent SysTems and Applications, Trabzon, Turkey, 2–4 July 2012; pp. 1–4. [Google Scholar]
  24. Tassie, L. Vine Identification-Knowing What You Have; Greenhill Road Wayville: Wayville, Australia, 2010. [Google Scholar]
  25. Yang, F.; Liu, Q.; Cheng, Y.; Feng, L.; Wu, X.; Fan, Y.; Raza, M.A.; Wang, X.; Yong, T.; Liu, W.; et al. Low red/far-red ratio as a signal promotes carbon assimilation of soybean seedlings by increasing the photosynthetic capacity. BMC Plant Biol. 2020, 20, 148. [Google Scholar] [CrossRef] [PubMed] [Green Version]
  26. Tomás, M.; Medrano, H.; Escalona, J.M.; Martorell, S.; Pou, A.; Ribas-Carbó, M.; Flexas, J. Variability of water use efficiency in grapevines. Environ. Exp. Bot. 2014, 103, 148–157. [Google Scholar] [CrossRef]
  27. Bota, J.; Tomás, M.; Flexas, J.; Medrano, H.; Escalona, J.M. Differences among grapevine cultivars in their stomatal behavior and water use efficiency under progressive water stress. Agric. Water Manag. 2016, 164, 91–99. [Google Scholar] [CrossRef]
  28. Pou, A.; Medrano, H.; Tomàs, M.; Martorell, S.; Ribas-Carbó, M.; Flexas, J. Anisohydric behaviour in grapevines results in better performance under moderate water stress and recovery than isohydric behaviour. Plant Soil 2012, 359, 335–349. [Google Scholar] [CrossRef]
  29. Zufferey, V.; Cochard, H.; Ameglio, T.; Spring, J.L.; Viret, O. Diurnal cycles of embolism formation and repair in petioles of grapevine (Vitis vinifera cv. Chasselas). J. Exp. Bot. 2011, 62, 3885–3894. [Google Scholar] [CrossRef] [Green Version]
Figure 1. Example of scanned leaves of the 5 cultivars for the classification study (up) and corresponding binary images for automatic shape recognition (down) to obtain morpho-colorimetric parameters from each leaf. Letter of each leaf corresponds to (a) Sauvignon Blanc, (b) Chardonnay, (c) Carmenère, (d) Merlot and (e) Pinot Noir. Leaf sizes in the Figure are not proportional to real values.
Figure 1. Example of scanned leaves of the 5 cultivars for the classification study (up) and corresponding binary images for automatic shape recognition (down) to obtain morpho-colorimetric parameters from each leaf. Letter of each leaf corresponds to (a) Sauvignon Blanc, (b) Chardonnay, (c) Carmenère, (d) Merlot and (e) Pinot Noir. Leaf sizes in the Figure are not proportional to real values.
Horticulturae 07 00315 g001aHorticulturae 07 00315 g001b
Figure 2. Principal component analysis (PCA) graph combining score plot and loadings for leaf morpho-colorimetric parameters obtained from five different grapevine varieties considering all data.
Figure 2. Principal component analysis (PCA) graph combining score plot and loadings for leaf morpho-colorimetric parameters obtained from five different grapevine varieties considering all data.
Horticulturae 07 00315 g002
Figure 3. Principal component analysis (PCA) graph combining score plot and loadings for leaf morpho-colorimetric parameters obtained from five different grapevine varieties managed under stress water conditions (left, a) and no water restriction (right, b).
Figure 3. Principal component analysis (PCA) graph combining score plot and loadings for leaf morpho-colorimetric parameters obtained from five different grapevine varieties managed under stress water conditions (left, a) and no water restriction (right, b).
Horticulturae 07 00315 g003
Table 1. Description of the leaf morpho-colorimetric features for variety characterization and discrimination.
Table 1. Description of the leaf morpho-colorimetric features for variety characterization and discrimination.
ParameterUnitDescription
Area (A)cm2Area of the leaf surface
Perimeter (L)cmPerimeter of the leaf surface
Maximum length (LMax)cmMaximum length of the leaf
Minimum length (LMin)cmMinimum length of the leaf
Maximum length of petiole (LMax P)cmLength of leaf vine petiole
Area to perimeter ratio (P2/A)UnitlessArea to perimeter ratio of leaf
Eccentricity (Ex)UnitlessLength: width ratio in which zero is given to a straight line and one represents a circle
RGB color scaleUnitlessRGB scale used to measure color: R = red, G = green, B = blue colors and
RG = red and green index
Fractal dimension (FR)UnitlessFractal dimension measured using the box-counting method
Table 2. Mean values for the leaf morpho-colorimetric features obtained by scanning leaves from five different grapevine varieties under stress and no stress treatments.
Table 2. Mean values for the leaf morpho-colorimetric features obtained by scanning leaves from five different grapevine varieties under stress and no stress treatments.
ParameterTreatmentVariety
CarmenèreChardonnayMerlotPinot NoirSauvignon Blanc
Area (cm2)No Stress161.37 ± 18.55 ab137.08 ± 6.58 a196.05 ± 14.85 b160.87 ± 5.71 ab152.22 ± 15.67 a
Stress143.92 ± 10.14 a129.74 ± 2.38 a180.87 ± 18.62 b121.15 ± 18.29 a147.21 ± 0.68 ab
Perimeter (cm)No Stress83.01 ± 6.10 a75.77 ± 2.30 a98.17 ± 4.23 b74.57 ± 1.78 a77.28 ± 3.70 a
Stress80.29 ± 3.11 a74.67 ± 1.09 a97.80 ± 9.54 b67.12 ± 5.55 a79.65 ± 3.22 a
Maximum length (cm)No Stress13.10 ± 0.74 a12.36 ± 0.24 a14.62 ± 0.46 b13.20 ± 0.28 a12.73 ± 0.71 a
Stress12.43 ± 0.44 a12.09 ± 0.06 a14.09 ± 0.71 b11.53 ± 0.91 a12.64 ± 0.42 ab
Minimum length (cm)No Stress12.30 ± 0.76 a11.31 ± 0.32 a13.76 ± 0.60 b12.24 ± 0.24 a11.86 ± 0.57 a
Stress11.62 ± 0.38 a11.01 ± 0.13 a13.08 ± 0.68 b10.55 ± 0.79 a11.64 ± 0.37 a
Maximum length of petiole (cm)No Stress11.78 ± 1.01 b9.00 ± 0.29 a11.80 ± 0.85 b10.12 ± 0.66 ab11.40 ± 1.25 b
Stress10.76 ± 0.43 b9.01 ± 0.23 ab11.05 ± 0.64 b7.93 ± 1.18 a10.45 ± 0.94 b
Area to perimeter ratioNo Stress42.76 ± 1.40 b41.89 ± 0.67 b49.23 ± 2.44 c34.57 ± 0.66 a39.32 ± 0.50 b
Stress44.88 ± 2.59 a42.98 ± 0.54 a52.90 ± 4.98 b37.33 ± 0.51 a43.19 ± 3.07 a
EccentricityNo Stress0.35 ± 0.01 a0.41 ± 0.00 a0.35 ± 0.04 a0.39 ± 0.03 a0.37 ± 0.03 a
Stress0.35 ± 0.01 a0.42 ± 0.02 b0.38 ± 0.02 ab0.41 ± 0.03 b0.40 ± 0.00 ab
Red colorNo Stress69.48 ± 2.28 c68.96 ± 0.63 bc63.58 ± 2.35 a64.37 ± 0.95 ab71.83 ± 1.80 c
Stress74.93 ± 2.50 b81.24 ± 2.49 b68.16 ± 1.09 a75.92 ± 3.47 b75.94 ± 2.44 b
Green colorNo Stress75.06 ± 3.05 c74.35 ± 1.73 bc65.39 ± 3.39 a67.72 ± 1.82 ab75.74 ± 1.96 c
Stress81.48 ± 2.74 bc85.36 ± 2.55 c70.91 ± 0.71 a78.97 ± 3.58 bc77.77 ± 1.72 b
Blue colorNo Stress46.54 ± 0.76 a46.86 ± 1.69 a48.53 ± 0.62 a47.53 ± 1.52 a49.06 ± 0.49 a
Stress45.78 ± 0.63 a50.34 ± 0.83 b47.81 ± 1.52 ab48.04 ± 1.40 ab49.49 ± 1.10 b
Fractal dimensionNo Stress1.65 ± 0.02 a1.52 ± 0.02 a1.64 ± 0.04 a1.65 ± 0.02 a1.60 ± 0.03 a
Stress1.67 ± 0.02 a1.67 ± 0.01 a1.63 ± 0.03 a1.49 ± 0.03 a1.64 ± 0.01 a
Red and green indexNo Stress−0.039 ± 0.005 a−0.037 ± 0.007 a−0.014 ± 0.009 b−0.025 ± 0.009 ab−0.027 ± 0.005 ab
Stress−0.042 ± 0.010 a−0.025 ± 0.004 ab−0.020 ± 0.010 b−0.020 ± 0.006 b−0.012 ± 0.005 b
For each variable and treatment, different letters in the same row show statistically significant differences assessed using the Tukey test (α = 0.05).
Table 3. Gas exchange variables and intrinsic water-use efficiency obtained in leaves from five different grapevine varieties under stress and no stress treatments.
Table 3. Gas exchange variables and intrinsic water-use efficiency obtained in leaves from five different grapevine varieties under stress and no stress treatments.
ParameterTreatmentVariety
ChardonnayMerlotPinot NoirSauvignon Blanc
Net CO2 assimilation (AN)No stress16.74 a16.36 a16.39 a17.39 a
Stress10.90 a11.04 a10.33 a13.30 a
Both13.82 a13.70 a13.36 a15.35 a
Transpiration (E)No stress11.01 ab11.81 b9.47 a12.23 b
Stress7.49 a7.37 a6.45 a7.79 a
Both9.25 a9.59 a7.97 a10.00 a
Stomatal conductance (gs)No stress0.42 ab0.40 a0.38 a0.54 b
Stress0.25 a0.22 a0.20 a0.30 a
Both0.33 a0.31 a0.34 a0.42 a
Intrinsic water-use efficiency (AN gs−1)No stress40.30 ab41.24 b48.06 b32.40 a
Stress68.02 a70.95 a65.69 a67.89 a
Both50.14 a56.09 a56.87 a50.14 a
For each variable and treatment, different letters in the same row show statistically significant differences assessed using the Tukey test (α = 0.05). Data correspond to the average of the three data of measurements.
Publisher’s Note: MDPI stays neutral with regard to jurisdictional claims in published maps and institutional affiliations.

Share and Cite

MDPI and ACS Style

Gutiérrez-Gamboa, G.; Torres-Huerta, N.; Araya-Alman, M.; Verdugo-Vásquez, N.; Moreno-Simunovic, Y.; Valdés-Gómez, H.; Acevedo-Opazo, C. Leaf Morpho-Colorimetric Characterization of Different Grapevine Varieties through Changes on Plant Water Status. Horticulturae 2021, 7, 315. https://doi.org/10.3390/horticulturae7090315

AMA Style

Gutiérrez-Gamboa G, Torres-Huerta N, Araya-Alman M, Verdugo-Vásquez N, Moreno-Simunovic Y, Valdés-Gómez H, Acevedo-Opazo C. Leaf Morpho-Colorimetric Characterization of Different Grapevine Varieties through Changes on Plant Water Status. Horticulturae. 2021; 7(9):315. https://doi.org/10.3390/horticulturae7090315

Chicago/Turabian Style

Gutiérrez-Gamboa, Gastón, Nicolás Torres-Huerta, Miguel Araya-Alman, Nicolás Verdugo-Vásquez, Yerko Moreno-Simunovic, Héctor Valdés-Gómez, and César Acevedo-Opazo. 2021. "Leaf Morpho-Colorimetric Characterization of Different Grapevine Varieties through Changes on Plant Water Status" Horticulturae 7, no. 9: 315. https://doi.org/10.3390/horticulturae7090315

APA Style

Gutiérrez-Gamboa, G., Torres-Huerta, N., Araya-Alman, M., Verdugo-Vásquez, N., Moreno-Simunovic, Y., Valdés-Gómez, H., & Acevedo-Opazo, C. (2021). Leaf Morpho-Colorimetric Characterization of Different Grapevine Varieties through Changes on Plant Water Status. Horticulturae, 7(9), 315. https://doi.org/10.3390/horticulturae7090315

Note that from the first issue of 2016, this journal uses article numbers instead of page numbers. See further details here.

Article Metrics

Back to TopTop