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. 2023 Dec 11;12(24):4444. doi: 10.3390/foods12244444

Sensory Determination of Peach and Nectarine Germplasms with Instrumental Analysis

Meng Sun 1,2, Julin Ma 1,2,3, Zhixiang Cai 1,2, Juan Yan 1,2, Ruijuan Ma 1,2, Mingliang Yu 1,2, Yinfeng Xie 3,*, Zhijun Shen 1,2,*
PMCID: PMC10743018  PMID: 38137247

Abstract

The flavour and mouthfeel of peaches are crucial qualities of peach germplasm resources that significantly influence consumer preferences. In this study, we utilized 212 peach germplasm resources from the Nanjing Peach Resource Repository, National Fruit Germplasm facility, Jiangsu Academy of Agricultural Sciences as materials for sensory analysis, electronic nose analysis, and composition analysis via high-performance liquid chromatography (HPLC). In the sensory analysis, we divided 212 peach germplasms into three clusters based on hierarchical cluster analysis (d = 5). No.27, No.151, and No.46 emerged as the most representative of these clusters. The electronic nose was used to conduct an evaluation of the aroma profiles of the 212 peach germplasms, revealing that the primary distinguishing factors of peach aroma can be attributed to three sensors: W1S (methane), W1W (terpenes and organosulfur compounds), and W5S (hydrocarbons and aromatic compounds). The primary differences in the aromatic substances were characterized by sensors W2W (aromatic compounds, sulphur, and chlorine compounds) and W1C (aromatic benzene). The HPLC analysis indicated that the persistence of peach sensory characteristics was positively correlated with acids and sourness and negatively correlated with sweetness and the ratio of sugar to acids. The overall impression of the 212 peach germplasms revealed a negative correlation with acids, while a positive correlation was observed between the overall impression and the ratio of sugar to acids. Therefore, this study substantially contributes to the preliminary screening of the analysed specific characteristics of peach germplasms such as No.27, No.46, No.151, and No.211. These selections may provide valuable information for the potential creation of superior germplasm resources.

Keywords: Prunus perica (L.) Batsch, germplasm, palate, flavour, sugars, acids

1. Introduction

Peaches (Prunus persica (L.) Batsch) are the most important fruits in the world. Peaches are native to China and widely planted over 10,000 hectares (15.02 million tons, FAOSTAT, 2020), accounting for over 60% of the global total of peaches and nectarines. The evaluation of peach germplasm resources is important for their protection and utilization and the full exploitation of their potential economic, social, and ecological value in China [1]. The evaluation indexes used in this regard include morphological and biological characteristics, quality characteristics, stress resistances, and pest resistance. Recent studies have mainly focused on morphological and quality characteristics [2].

Peach fruit quality is composed of fruit appearance; internal, nutritional, and flavour quality; storage qualities; and stress tolerance [3]. Sensory evaluation, electronic nose analysis, electronic tongue analysis, and GC-MS are used to assess fruit flavour and palate as well as in comprehensive evaluation methods. Sensory evaluation involves the comprehensive and objective evaluation of the colour, aroma, taste, and appearance of food using human sensory organs (eyes, nose, mouth, teeth, hands, etc.), providing real data for mathematical and statistical analyses [4]. Previous research has been conducted on fruit wine and strawberry jam [5,6]. Sensory quality analysis plays a crucial role in the development of new food varieties, market prediction, setting product standards, and determining product shelf life [7]. Liu et al. [8] used fuzzy comprehensive judgment and the percentage total score method to objectively evaluate the colour, taste, and flavour of canned yellow peaches. However, there is limited research on the sensory analysis of fresh peach germplasm resources.

An electronic nose is a sensitive device used to detect a wide range of volatile compounds through the overall response of a specific sensor and a pattern recognition system [9]. Its advantages are its simplicity, rapidity, and facilitation of non-destructive sample analysis and automatic data collection. It is widely used in food testing, environmental monitoring, air-quality monitoring, and healthcare [10]. In the context of fruits, it can be used for variety identification, harvest and shelf-life judgement, disease identification, and the determination of freshness, ripeness, and decay [11]. An electronic nose not only enables the comparison and analysis of the odour information from different samples but also facilitates the establishment of a database by collecting the fingerprints of standard samples. This database can be used for the qualitative and quantitative analysis of the unknown components in samples [12].

This study combines sensory evaluation and electronic nose analysis with HPLC to explore the differences in aroma and palate among peach fruits with different flesh types and colours in 212 peach germplasms. The findings contribute to the selection, breeding, and utilization of excellent peach germplasms and improve the evaluation methods for peach germplasm resources, meeting the new demand pertaining to production and consumption.

2. Method and Materials

2.1. Plant Materials

The 212 varieties of peaches/nectarines (Appendix A) analysed were harvested at the National Peach Germplasm Repository (Nanjing, China, 32°20′ N, 118°52′ E, located 11 m above sea level) from May to July 2022, with each variety represented by two trees. The test varieties were 5-year-old mature trees with a Y shape and a row spacing of 3 to 5 m, and conventional cultivation measures were employed. Samples (50 peaches/nectarines) of each variety were randomly collected upon reaching maturity (defined as the disappearance of green coloration on the bottom of the fruit) from the two trees [13,14]. Samples were harvested before 11:00 a.m. A total of 30 fruits of each variety were immediately stored in a freezer (−80 °C) for E-nose and HPLC measurement. A total of 20 fruits of each variety were taken into the sensory room for evaluation the following afternoon.

2.2. Sensory Analysis

The quantitative descriptive analysis method was used to train the sensory panel and carry out the sensory analysis according to the Sensory Analysis–Methodology Paired comparison test (ISO, 5495:2005) [15]. Different samples of peaches and nectarines were used to allow the panel members to recognize their qualitive characteristics. Based on their availability, health, and general food habits, ten candidates (postgraduate students and researchers from JAAS, comprising five females and five males) were pre-screened. They volunteered for the project. All subjects gave their informed consent for inclusion before they participated in the study. In this study, materials were taken from the National Peach Germplasm Repository, Nanjing, China. These materials are safe for sensory research. All the experimental procedures involving volunteers were conducted in accordance with the Declaration of Helsinki. Also, the volunteers had the ability to discriminate between products according to basic taste thresholds and to describe their perceptions. Panel descriptions and definitions for peach and nectarine attributes (flavour, palate, persistence, and overall impression) were developed through brainstorming and round-table consensus.

The next step was to develop the score sheet for the different attributes for analysis. Flavour was evaluated according to being fruity, floral, earthy, woody, caramel, nutty and herbaceous, or vegetative. Palate (aroma, sweetness, sourness, and bitterness and astringency), persistence, and over impression were evaluated by assigning categorical scores from 0 to 10 (0, no sensation; 0.1–1.9, absence of sensation; 2.0–4.9, weak; 5.0–7.9, moderate; 8.0–10, intense) [16]. Each of them independently estimated 20 fruits of typical size and appearance and with similar ripeness per germplasm. Then, each panellist randomly chose two fruits from each variety for palate evaluation. The evaluated samples were not named until the end of the evaluation. The evaluations were judged at 10 a.m in individual booths under white light.

2.3. E-Nose Measurement for Fruit Aroma

In total, 15 fruits were randomly divided into 3 blocks for E-nose measurement and analysed in triplicate. Measurements were performed using a portable, commercially available E-nose (PEN3.5, Airsense Analytics GmbH, Schwerin, Germany). The sensor array of the PEN3.5 has ten metal oxide semiconductor-type chemical sensors (Table 1) capable of operating at high temperatures to permit the classification and identification of different volatile species. When the sensors were exposed to volatiles, the changes in the conductivity (G)-to-initial-conductivity (G0) ratio (G/G0, relative conductivity or response value) depended on G conductivity. The concentration of volatiles led to the deviation of G/G0 (greater than or less than 1). In this study, 10 g of flesh from each sample was placed into a 300 mL beaker covered with sealing film. The beaker was kept at 25 °C for 30 min for E-nose evaluation. The aroma measurement method used followed that reported by Yan et al. [17], with some modifications. We inserted the E-nose sampling needle into the sealing film and extracted the gas in the beaker for detection. The volatile gas was pumped over the sensors of the E-nose at a flow rate of 400 mL/min. The E-nose analyses were recorded over a range from 0 to 60 s. One to three stable signals (response values) were observed to be in the middle period of the data stabilization time [18]. After each analysis, the sampling chamber was washed with an air-dried flow for 60 s.

Table 1.

Electronic nose sensor array (PEN 3.5) using the portable E-nose (Air-sense Analytics GmbH, Germany).

Sensor Name Sensor Sensitives
W1C Sensitive to aromatic benzene
W3C Sensitive to ammonia and aromatic compounds
W5C Sensitive to nitrogen oxides
W1S Sensitive to short-chain alkanes such as methane
W2S Sensitive to alcohols, ethers, aldehydes, and ketones
W3S Sensitive to long-chain alkanes
W5S Sensitive to hydrocarbons and aromatic compounds
W6S Sensitive to hydrogen
W1W Sensitive to terpenes and organosulfur compounds
W2W Sensitive to aromatic compounds and sulphur and chlorine compounds

2.4. HPLC Measurement for Sugars and Acids

A total of 15 fruits were randomly divided into 3 groups for HPLC measurement and analysed in triplicate. The method of HPLC measurement for sugars and acids followed was modified by Shen et al. [19]. Using 5 mL of extracting solution (ethanol: 0.2% metaphoric acid v/v), 0.5 g of the flesh was ground and extracted using ultrasound waves for 1 h. The solution was centrifuged for 5 min at 10,000 rpm and 4 °C. The 0.8 mL supernatant was dried using a concentrator (Eppendorf, Concentrator plus, Sigma Aldrich, Saint Louis, MO, USA, 230 V/50–60 Hz) for 2 h. A total of 1.6 mL of ultrapure water was added to the concentrate to obtain sugar/organic acid solution. The samples were filtered through a 0.22 μm nylon syringe filter into an HPLC glass vial and capped tightly. Then, 0.5 μL portions of the samples were injected into an HPLC system with a 10 μm, 250 × 6 mm CARBOSep CHO-620 CA column (Transgenomic, Omaha, NE, USA) to detect soluble sugars at 80 °C using a differential refractive index detector. For the mobile phase, we used ultrapure water added at 0.5 mL min−1.

A total of 0.5 μL of the samples was injected into an HPLC system with a 5 μm, 250 × 4.6 mm ZORBAX Eclipse XDB-C18 column (Agilent, Santa Clara, CA, USA) to analyse organic acids at 2 °C using a VWD UV detector (λ = 214 nm). The mobile phase was 0.02 mol/L of KH2PO4 (pH 2.7) for 0.5 mL min−1. Data were analysed using the Chemstation (Agilent) chromatography data system. KH2PO4 was used as a standard for each batch of samples. A total of 0.02 mol/L of KH2PO4 (pH 2.7) (3.333, 1.667, 0.333, 0.167, and 0.033 g/L) was used to establish a standard curve for reporting organic acids. Soluble sugars and organic acids were identified by their retention times, and their concentrations were calculated in parallel to calibrate the internal ultrapure water and 0.02 mol/L of KH2PO4 (pH 2.7) standard curves.

2.5. Statistical Analysis

Sensory and HPLC data were tested in terms of their average characteristics at maturity using IBM SPSS Statistics 22 (IBM, Armonk, NY, USA). Pearson correlation test (p < 0.05) was conducted to analyse the relationship between sensory indexes and sugars and acids. Principal component analysis (PCA) and hierarchical cluster analysis were performed using OriginPro 2021 (OriginLab Corporation, Northampton, MA, USA). Data related to E-nose were processed using the WinMuster program in PEN3.5 (Airsense Analytics GmbH, Schwerin, Germany) and OriginPro 2021. The main sensors used for main peach smell detection were analysed via loading analysis (LOA) using WinMuster software (Version 1.6.2.15–2011, Airsense Analytics, Schwerin, Germany). Principal component analysis (PCA) and hierarchical cluster analysis were performed using OriginPro 2021 based on main and aromatic substance sensors.

3. Results

3.1. Sensory Analysis

The sensory evaluation results for the 212 peach germplasms are shown in Appendix A, including the scores for sweetness (0–9.2), sourness (0–7.5), astringency (0–6.3), and bitterness (0–3.1). In Figure 1A, sweetness has a larger area than sourness, astringency, and bitterness. Five germplasms exhibited intense sweetness (8–10 points); five germplasms elicited no sensation (0); and nine germplasms provoked a near absence of sensation (0.1–1.9). The most prominent sweetness was that of No.134. Regarding sourness, 79 resources elicited no sensation of sourness, 33 scored between 0 and 2.4, and 101 scored between 2.5 and 7.5. Only a small percentage of germplasms elicited astringent or bitter sensations. Astringency was weak in 17 germplasms and moderate in No.200. Three germplasms (No.2, No.11, and No.37) had weak bitterness.

Figure 1.

Figure 1

(A). Palate scores of 212 peach germplasm resources: blue area corresponds to sweetness scores; orange area corresponds to sourness; grey area corresponds to astringency; and yellow area corresponds to bitterness. (B). Persistence and overall impression scores of 212 peach germplasm resources: blue area corresponds to persistence, and orange area corresponds to overall impression.

Persistence was described as the duration of flavours and aromas for a peach, ranging from none to long. As indicated in Figure 1B, No.164 showed no persistence, 39 germplasms had a short finish (0.1–1.9), and 112 peach fruits exhibited short to medium persistence (2.0–4.9), constituting the largest group in the study. No.38, No.47, and No.119 had long finishes (8.0–10.0). Overall impression encompassed final thoughts with a rating (score out of 10) and freestyle impressions, aiding in distinguishing the participants’ favourite peaches. Germplasms were evaluated as excellent (8.0–10.0), good (5.0–7.9), medium (2.0–4.9), and poor (0.1–1.9), with 40 poor, 88 medium, 77 good, and 7 excellent germplasms. No.76 had a poor overall impression, while the highest scores for excellent impressions were those for No.209 and No.134.

‘The Davis Wine Aroma Wheel’ is an ideal tool for identifying and visualising the various tastes, smells, and aromatic qualities in most wines, regardless of grape variety. According to this wheel, the 212 peach germplasms contain special flavours such as fruity (passion fruit, lemon, citrus, apple, green apple, honeydew, mango, apricot, juicy honey peach, and yellow peach), floral (gardenia, jasmine, rose, and violet), herbaceous or vegetative (herb, grass, celery, carrot, and lotus seed), caramel (candy, popcorn, molasses, and honey), woody (smoky and rubber), nutty (peanut, cereal, and red bean), animal (butter/milk), and pungent (metal) as well as faults like being spoiled and exuding off-odours.

Table 2 indicates that 137 germplasms possessed one or more special flavours, while 75 germplasms lacked any special flavour. Notably, No.15 and No.196 each had three distinct flavours (lemon, gardenia, and smoky for No.15; mango, violet, and butter/milk for No.196). A total of 29 germplasms had a violet aroma, and 31 germplasms had a butter/milk aroma. Certain aromas were unique to one germplasm, such as apricot (No.207), herb (No.173), celery (No.137), lotus seed (No.168), carrot (No.118), and rubber (No.111). Seven germplasms exhibited faults, including being spoiled (No.38, No.50, and No.76) and exuding an off-odour (No.11, No.123, No.160, and No.199).

Table 2.

Special flavours in 212 peach germplasm resources.

Aroma Type Flavour Peach Germplasm Number
Fruity Citrus 59, 181
Apple 29, 54, 62, 91, 117, 163, 200
Green Apple 18, 31, 208
Honeydew 56, 161
Mango 84, 99, 172, 182, 184, 196
Apricot 207
Juicy Honey Peach 188, 195, 205
Yellow-Flesh Peach 147, 159, 167, 179, 197
Passionfruit 8, 14, 19, 23, 100
Lemon 15, 20, 87, 147
Floral Gardenia 15, 30, 44, 45, 66, 185
Jasmine 64, 178
Rose 28, 63, 70, 99, 109, 144, 148, 183, 186
Violet 22, 24, 41, 65, 68, 69, 71, 80, 83, 97, 106, 107, 108, 110, 112, 118, 120, 121, 122, 125, 127, 129, 130, 131, 132, 133, 134, 135, 137, 139, 141, 146, 171, 177, 189, 196, 197, 199, 202, 204, 210
Herbaceous or Vegetative Herb 173
Grass 34, 53, 92, 174, 176, 203, 206
Celery 137
Lotus Seed 168
Carrot 118
Animal Butter/Milk 9, 21, 55, 56, 59, 60, 61, 68, 76, 80, 86, 89, 91, 101, 112, 115, 128, 133, 134, 141, 144, 146, 152, 162, 165, 172, 176, 179, 181, 188, 196
Caramel Candy 153, 189
Popcorn 3, 57, 82, 94, 149
Molasses 82, 201
Honey 58, 165
Nutty Peanut 32, 74, 78, 114, 143, 154
Cereal 37, 145
Red Bean 13
Woody Smoky 15, 139, 152
Rubber 111
Pungent Metal 50, 71, 190, 195
Faults Spoiled 38, 50, 76
Off-Odour 11, 123, 160, 199

Principal component analysis (PCA) revealed the influence of each sensory descriptor on the evaluation of peach germplasm resource (Figure 2A). The first principal component (PC1) accounted for 46.1% of the variance, with sweetness and overall impression contributing significantly. Sourness and persistence also had negative loadings for PC1. The variance contribution of the second principal component (PC2) was 19.2%, with astringency and bitterness serving as major contributors. Thus, PC1 reflected an enjoyable taste, while PC2 was associated with negative feedback. No.211 was characterized as sweet with a great impression, while No.101 was perceived as astringent and bitter with an unpleasant impression. No.119 had light sweetness, strong sourness, and a long finish, resulting in a harsh impression. Additionally, sweetness correlated closely with overall impression, as did sourness with persistence. Cluster analysis categorized the 212 germplasms into three groups (Figure 2B), with 127 in cluster 1, 13 in cluster 2, and 72 in cluster 3. No.27, No.151, and No.46 were the most representative of their respective clusters.

Figure 2.

Figure 2

(A). Principal component analysis (PCA) of sensory evaluations for 212 peach germplasm resources: red dots, 212 peach germplasms; blue arrow lines, loadings. (B). Hierarchical cluster analysis of sensory analysis for 212 peach germplasm resources: red, Class I germplasms; green, Class II germplasms; blue, Class III germplasms.

3.2. Instrumental Analysis

Response to Different Sensors Evaluated via E-Nose

Based on the response values of 10 sensors, 212 peach germplasm samples were divided into four categories (d = 15) (Figure 3): 186 were assigned to Class I, 23 were assigned to Class II, 2 were assigned to Class III, and 1 was assigned to Class IV. Consequently, No.82, No.91, and No.193 were deemed notable for their distinction from Class I and II.

Figure 3.

Figure 3

Hierarchical cluster analysis of E-nose performance for 212 peach germplasm resources: red, Class I germplasms; blue, Class II germplasms; green, Class III germplasms.

In Figure 4A, the W1W sensor had an influence on both the first and second principal components. The sensors W1S and W5S contributed to the first principal component. To validate the significance of sensors W1W, W1S and W5S in differentiating the peach fruit aromas, the three sensors were analysed in the current mode, as depicted in Figure 4B. They collectively accounted for 99.99% of the total contribution, signifying a substantial role in the discrimination of peach fruit aromas in the experiment.

Figure 4.

Figure 4

Aroma loading analysis conducted using E-nose in relation to 212 peach germplasm resources ((A): ten sensors; (B): three sensors).

Figure 5 exhibits the response values of No.193 to the various sensors of an electronic nose, with peak values around at 24s. A stable period for further analysis was determined to be from 35 s to 37 s. Among the ten sensors, W1S (short-chain alkanes) exhibited the greatest response, followed by W5S (hydrocarbons and aromatic compounds), W1W (terpenes and organosulfur compounds), W2S (alcohols, ethers, aldehydes, and ketones), W6S (hydrogen), W2W (aromatic components and sulphur and chlorine compounds), W5C (nitrogen oxides), W3C (ammonia and aromatic compounds), and W1C (aromatic benzene). The largest response value was observed for W1S (32.702 ± 0.015), followed by W5S (32.803 ± 0.067), W1W (24.373 ± 0.102), and W2S (8.789 ± 0.005). The other sensors had lower response values of around 1. The coefficients of variation for W5C, W2W, and W1W were 1.24%, 0.74%, 0.39%, and 0.42%, respectively. W1C and W3S displayed relatively minor coefficients of variation, amounting to 0.14% and 0.04%, respectively.

Figure 5.

Figure 5

No.193 response values to different sensors of an electronic nose.

Figure 6 and Figure 7 show the stable signals for Classes I and II in the response values of the three primary sensors and the three aromatic sensors. The response values of the three main sensors differed significantly between Class I and Class II. Compared with the response values of the three aroma sensors, germplasms in Class I responded notably to the sensor W1C, while germplasms in Class II responded significantly to sensor W2W. This result was consistent with the previous results for the coefficient of variation. It indicates that the differences in peach aromas predominantly arose from non-aromatic substances such as methane, nitrogen oxides, and hydrogen sulphide, with variations in aromatic substances primarily reflected in the response values of W2W and W1C.

Figure 6.

Figure 6

Figure 6

Main and aromatic sensors’ response values for Class I germplasms: (A), W5S sensitive to hydrocarbons, aromatic compounds; (B), W1S sensitive to short-chain alkanes such as methane; (C), W1W sensitive to terpenes and organosulfur compounds; (D), W2W sensitive to aromatic, sulfur and chlorine compounds; (E), W3S sensitive to long-chain alkanes; (F), W1C sensitive to aromatic benzene.

Figure 7.

Figure 7

Main and aromatic sensors’ response values for Class II germplasms: (A), W5S sensitive to hydrocarbons, aromatic compounds; (B), W1S sensitive to short-chain alkanes such as methane; (C), W1W sensitive to terpenes and organosulfur compounds; (D), W2W sensitive to aromatic, sulfur and chlorine compounds; (E), W3S sensitive to long-chain alkanes; (F), W1C sensitive to aromatic benzene.

3.3. Sugars and Acids Identified via HPLC

Figure 8A presents the sucrose, glucose, fructose, and sorbitol content of 212 germplasms determined via HPLC, with sucrose ranging from constituting 11.9% to 83.3% (from 4.61 mg/g to 118.28 mg/g) of the total sugar content, while sorbitol corresponded to the lowest content, ranging from 0.01 to 26.80 mg/g (from 0% to 18.6%), in the 212 germplasms. The glucose and fructose percentages were similar, spanning from 3.8% to 47.7%. No.158 had the lowest total sugar content at 25.86 mg/g, whereas the highest content was 172.61 mg/g, corresponding to No.73. In Figure 8B, the total acid content varies from 2.07 mg/g in No.150 to 33.61 mg/g in No.76. The quinic acid content ranges from 0.32 to 10.72 mg/g, accounting for 5.6% to 76.3% of the total acid content. The malic acid content also showed similar ranges (0.40 to 19.26 mg/g) and percentages (from 12.9% to 79.6%) across the germplasms. No citric acid was detected in No.36, No.157, and No.203, while the highest citric acid content was found in No.64.

Figure 8.

Figure 8

(A). Sucrose, glucose, fructose, and sorbitol content in 212 peach germplasms: blue area corresponds to sucrose scores; orange area corresponds to glucose; grey area corresponds to fructose; and yellow area corresponds to sorbitol. (B). Quinic, malic and citric acids content in 212 peach germplasms: blue area corresponds to quinic acid; orange area corresponds to malic acid; and grey area corresponds to citric acid.

PCA was performed to assess the impact of sugars and acids on the evaluation of peach germplasms (Figure 9). The first principal component (PC1) accounted for 49.5% of the variance, with sugars and acids providing the largest contributions. The second principal component (PC2) contributed 25.9% to the variance, with the ratio of sugars to acids and sucrose contributing significantly. Quinic, malic, and citric acids had negative loadings for PC2. Thus, PC2 reflects a taste profile emphasizing sweetness. No.107 was characterized by sweetness with light sourness, but No.155 was sour with a hint of sweetness. No.49 had negative loadings for both PC1 and PC2. Additionally, a close relationship was found between sweetness and total sugars, similar to the relationship between malic acids and total acids.

Figure 9.

Figure 9

PCA of sugars and acids in 212 peach germplasm resources: red dot, 212 peach germplasms; blue arrow lines, loadings.

3.4. Comparison of Instrumental and Sensory Results

A negative correlation existed between sweetness and quinic, malic, and citric acids (r > −0.7), while a positive correlation was observed between sweetness and the ratio of sugar to acids (r < 0.6) (Figure 10). Sourness negatively correlated with sweetness and the ratio of sugar to acids but positively correlated with acids. Persistence showed a positive correlation with acids and sourness and a negative correlation with sweetness and the sugar-to-acid ratio. Overall impression correlated negatively with acids and sourness while correlating positively with sweetness and the sugar-to-acid ratio.

Figure 10.

Figure 10

Correlation matrix heat map. Heat map of spearman correlation between sensory and HPLC analysis between each biomarker for the overall population analysed. * Indicated significant differences between instrumental and sensory parameters according to Pearson correlation coefficient (p < 0.05).

4. Discussion

Fruit quality evaluation is an important component of peach fruit quality research. Sensory evaluation is commonly used to assess fruit quality. Based on the evaluation criteria, different samples are scored, allowing for the calculation of the mean values [20,21]. This study included the sensory determination of 212 peach germplasm resources, focusing on aroma, palate (sweetness, sourness, astringency, and bitterness), persistence, and overall impression. In 212 peach germplasm resources, the predominant taste profiles, ranked from highest to lowest, were sweetness, sourness, astringency, and bitterness (Figure 1A). No.134 exhibited the most pronounced sweetness, with an excellent impression, resulting from its high total sugar content and low total acids content. The long-finish germplasms (No.38 and No.47) presented high total acid content (over 15 mg/g) and a small ratio of sugar to acid (below 5). The PCA revealed the influence of each sensory descriptor on the evaluation of peach germplasm resources. PC1 reflected an enjoyable taste, while PC2 corresponded with negative feedback. The sensory evaluation highlighted that No.211 was sweet with a great impression, but No.101 was astringent and bitter, resulting in an unpleasant impression. The profile of No.119 included light sweetness, strong sourness, and a long finish, leading to a harsh impression. These findings reveal the importance of a strong characteristic aroma in shaping consumer preferences. However, some germplasms can present a faulty flavour because of an excessively strong aroma. An overly strong passion fruit flavour had the potential to present bromhidrosis in one sensory evaluation [22]. Thus, it was crucial to screen for peach germplasms with intense sweetness and an appropriate characteristic aroma to enhance peach quality.

An electronic nose (E-nose) is a simple, efficient, non-destructive, and stable device that imitates the human olfactory system. It has been used for assessing fruit quality and ripeness and in other applications [23,24]. In our research, W5S, W1S, and W1W could explain up to 99.99% of the total contributions, indicating that these non-aromatic substance classes (nitrogen oxides, methane, and hydrogen sulphide) distinguished the peach fruit aromas in our research. The distinction in aromatic substance classes corresponded mainly to the response values of two sensors (W2W and W1C); these values aligned with studies on pear and blueberry quality and aroma evaluation [25,26]. Upon comparing the results of the sensory evaluation and E-nose, the germplasms in Class I responded significantly to sensor W1C, which correlated with sensory perceptions of milk and caramel flavours. Germplasms in Class II showed a significant response to sensor W2W, associated with floral and herbaceous sensations. Notably, No.82, No.91, and No.193 were the most representative samples, with distinctive aromas of apple, butter/milk, and violet, respectively. These could serve as valuable indicators for fruit quality assessment and determining consumer preferences [27,28]. Thus, they could be used in developing new peach germplasm with excellent aroma profiles.

Sucrose and malic acid were identified as the predominant components in peach germplasms, corroborating the results of previous studies [29]. The correlation between the sensory and HPLC results indicated that the fruits’ sweetness was primarily determined by their sugar content. The relative sweetness perceptions of fructose, sucrose, and glucose has been rated as 1.75, 1, and 0.75, respectively [16]. Despite high levels of sugars, peach sweetness was not necessarily pronounced because of sucrose. Sucrose made up the largest share of total sugars and did not contribute as strongly to sweetness. Additionally, the types of sugars and their ratio with respect to acids also affected perceived sweetness. Malic acid, which imparted a soft, refreshing, slightly irritating, and long-lasting sour–bitter taste, was the primary acid in peaches, while citric acid provided a pleasant, quickly dissipating sour taste. Three germplasms (No.36, No.157, and No.203) lacked citric acid, resulting in less sourness detected in their sensory evaluations. Furthermore, for the 212 peach germplasms studied, it was observed that a sugar-to-acid ratio exceeding 20 corresponded to sweetness scores above 5. This finding supports the results of the research by Colaric et al. [14], who suggested that a sugar-to-acid ratio ranging from 20 to 60 is typically associated with a moderate level of perceived sweetness. This ratio is important because it provides a balance of flavours, contributing to the overall sensory pleasure elicited by and the acceptability of peach fruit by consumers. By analysing the sugar-to-acid ratio, breeders and researchers can better understand and predict the sweetness profiles of peaches, constituting a crucial factor in consumer satisfaction and the marketability of the fruit.

5. Conclusions

In this study, we employed sensory evaluation, an electronic nose (E-nose), and high-performance liquid chromatography (HPLC) to assess fruit quality attributes such as aroma, sugars, and acids across 212 peach germplasm resources. These methods significantly contributed to the preliminary screening of peach germplasms with specific desirable characteristics. This study provides essential information that could facilitate the creation of superior germplasm resources. Therefore, evaluating and analysing the aroma and taste profiles of peach germplasms hold significant theoretical and practical value for the discovery, development, and utilization of high-quality peach resources. For future research, the integration of the electronic nose technique with headspace solid-phase microextraction (HS-SPME) and gas chromatography–mass spectrometry (GC-MS) could enhance the discrimination of peach fruit aroma components and aid in identifying the key aroma compounds within peach germplasm resources. This multidisciplinary approach may lead to a deeper understanding of the complex interactions between volatile compounds and contribute to the advancement of peach breeding programs targeting improved fruit aromas and flavour.

Appendix A. Germplasm Resource Information of 212 Peaches

Number Germplasm Name Country of Origin Aroma Palate and Taste Persistence Overall Rating The Ratio of Sugars to Acids
Sweetness Sourness Astringency Bitterness
1 Li Xia Hong CHN 3.5 5 2 0 0 4 5 20.3
2 Chun Lei CHN 4 3.9 0 0 2.4 3.2 4 21.3
3 Zao Shuo Mi CHN 4.4 5.8 2.3 0 0 4.7 5.3 18.8
4 Zao Mei CHN 3.8 4.6 1.8 1.3 0 4.5 5.1 22.8
5 Chun Hua CHN 3.6 3.8 2.4 0 0 3.6 4.2 15.5
6 Hu 021 CHN 4 4.1 2.5 0 0 2 2.8 17.8
7 Zao Xia Lu CHN 3 4.4 3 0 0 4 4.6 17.2
8 04-13-40 CHN 5.5 5.2 2.6 0 0 4 5.2 14.8
9 Yun Long Shui Mi CHN 7.5 8 0 0 0 5 6.3 5.8
10 Zao Lu Pan Tao CHN 5.1 6 0 2.1 0 5.3 5 20.5
11 Jing Chun CHN 7.5 4.8 3 2.5 2 4.8 2 16.0
12 Chun Yan CHN 6 5 0 2 1.8 4.9 4 12.6
13 82-18-73 CHN 6.2 7.8 0 0 0 5 6 32.6
14 Mayfire USA 7 3 6 0 0 6 2.3 8.3
15 SpringCrest USA 4.8 5 4 0 0 6.1 5 7.6
16 Jin Shan Zao Hong CHN 7 6.8 0 0 0 4 4.8 14.3
17 Takeiwasehakuho JPN 6.2 5.2 0 0 0 4.3 4.5 14.4
18 Zao Hong Zhu CHN 6.3 6.4 2 0 0 3.8 4 17.9
19 Hua Guang CHN 2 3 1.8 0 1.8 4 2 13.2
20 Shu Guang CHN 3 6.2 3 0 0 5 4.8 10.6
21 Saotome JPN 6 7.5 0 0 0 3 5.4 27.7
22 Springtime USA 3 5 7 0 0 6 2.8 4.6
23 Bai Xiang Lu CHN 6.5 6.5 0 0 0 3 3.4 15.3
24 Jin Shan Zao Lu CHN 7 7.4 0 0 0 3 3.8 8.0
25 Armking USA 2.5 4 5.8 0 0 4.8 5 3.6
26 Xia Hui 3 CHN 7.4 7.4 0 1.8 0 3.2 4.1 15.9
27 Sha Ji 2 CHN 4.2 6.2 0 0 0 2.8 6 26.0
28 Zao Hong Bao Shi CHN 3.8 7.6 0 0 0 3 6.3 12.3
29 Tsukuba 86 JPN 2.4 4.8 1.2 1 0 3.1 5.2 13.6
30 Flordacrest USA 6.4 4.9 6.2 0 1.3 5.8 4.4 5.5
31 Sunsplash USA 0 3.2 6 0 0 5.8 4.1 6.1
32 NJN72 USA 6.8 6.8 3.3 0 0 4.9 4.1 6.4
33 Robin USA 7.1 7.6 0 0 0 3 6.1 21.5
34 Favolate 3 ITA 7.4 5 3.2 0 0 4.1 4.2 10.0
35 Hui Yu Lu CHN 7.5 7.1 0 0 0 3 6.5 19.7
36 Yang Zhou Zao Tian Tao CHN 3.2 4.1 1.8 0 0 2.1 3.8 15.1
37 Kun Ming Hong Rou Tao CHN 0 2.8 0 0 3.1 3 2.1 16.9
38 Mang Zhong Lu CHN 0 1.9 7.2 0 0 8 1.1 5.0
39 Xia Hui 1 CHN 3.2 6.3 1.8 1.1 0 2.6 4.8 17.9
40 Spring Snow USA 4.1 4.5 2.6 0 0 4.5 3.3 13.7
41 Tropic Prince USA 6.1 3.8 6 0 0 6 5.2 8.3
42 Flordaking USA 7.2 7.1 4.9 0 0 4.8 4.5 5.5
43 Crimsonbaby USA 4.8 3.4 6.9 0 0 5.1 2.5 7.2
44 TX2B7N USA 5 7.2 7.1 0 0 6.2 3.2 5.4
45 Zi Jin Hong 1 CHN 7.1 5.9 2.6 0 1.1 2.1 4.8 10.5
46 Babiole FRA 6.9 4.2 6.3 0 0 5.8 2.3 8.8
47 Hong Tao CHN 0 1.8 7.2 0 0 8.2 1 4.4
48 85-13-24 CHN 9.5 7.5 1.9 0 0 2.1 3.4 8.4
49 63-15-75 CHN 1.2 6.8 0 1.2 0 1.8 4.2 12.8
50 Hong Rou Tao 1 CHN 0 0 6.1 0 0 5.8 0.9 13.0
51 Li Jiang Tao CHN 0 6.8 0 1.8 0 1.6 4.5 13.7
52 TX4C199 USA 0 7.4 0 0 0 2.1 6.8 26.4
53 Yu Hua 3 CHN 4.6 8 0 0 0 1.1 5.4 13.0
54 Jing Ling Huang Lu CHN 4.8 6.4 3 0 0 3 5.2 17.9
55 An Nong Shui Mi CHN 6.2 7.4 0 1.2 0 1.4 5.8 25.5
56 Jiang Jin IV2-9 CHN 6.5 6.9 0 1.1 0 1.2 5.6 17.5
57 Hikawa Hakuhou JPN 7.1 7.7 0 0 0 4.8 6.6 19.3
58 Early Chinese Cling CHN 3.8 5 6.1 3 0 2.8 2 11.8
59 Hatsukami JPN 6.6 3.9 6.2 3.6 0 5.8 1.2 7.5
60 Ying Hua Lu CHN 6.8 7.2 0.5 1.2 0 2.1 5.6 19.9
61 Early White Giant USA 5.8 4.8 6.3 1 0 3 2.3 12.9
62 TX4C189LN USA 0 6.4 3.1 0 0 3 6.5 28.8
63 Mei Gui Hong CHN 2.5 6.8 2 0 0 2.1 6 10.8
64 NJN70 USA 2 2 5.2 0 0 5 1.2 4.5
65 Hu You 018 CHN 4.8 6.9 0 0 0 1.8 5 19.9
66 Red June USA 6 4.9 6.2 0 0 5.3 1.4 4.1
67 Hu You 003 CHN 3.4 7.4 2.1 0 0 2.1 6.1 18.7
68 Rui Guang 22 CHN 6.9 5.2 3.2 0 0 1.8 3.8 9.0
69 Quetta IND 3.8 1.8 7.3 0 0 6.6 1.2 5.9
70 TX4C188LWN USA 6.6 6.9 1.1 0 0.6 1.4 6.3 8.4
71 TX2C104N USA 5 2.1 7 0 0 7.1 0.6 5.6
72 Sunraycer USA 4.2 4.2 5.8 0 0 4.5 1.1 6.4
73 Xian Yang Hong Rou Tao CHN 2.1 4.8 3.9 0 0 2.1 1.8 12.0
74 Xiao Hong Pao CHN 1.2 5.4 0 0 0 0.8 3.1 21.7
75 Shen Nong Hong Rou CHN 0 3 2.1 0 1 2.8 1.6 18.4
76 Bei Jing Yi Xian Hong CHN 1.6 0 6 0 0 5.8 0.1 3.9
77 Ye Ji Hong CHN 3.8 4.4 0 0 0 2.1 2.1 10.4
78 Tang Shan Tao CHN 0 4.8 0 0 1.2 1.1 3.4 9.2
79 Jie Tao CHN 0 6.3 0 0 0 0.8 5.1 6.5
80 Jin Xiang CHN 4.6 7 0 0 0 3 6.8 15.6
81 Chiyohime JPN 2.1 4.8 0 0 0 1.2 5.9 21.3
82 Nunomewase JPN 3 5 0 0 0 0.8 4.4 18.9
83 Zao Jin Lu CHN 2 4.9 0 0 0 5.1 3.8 15.8
84 Jin Hua Lu CHN 1.8 6.8 0 0 0 6.2 7.1 24.7
85 Jiu Yan CHN 0 7.2 0 3.2 0 1.4 6.4 7.5
86 Jing Hong CHN 4.2 7.1 0 1.3 0 3 6.8 11.6
87 Bao Pi Yang Tao JPN 6.8 1.8 7.2 0 0 5.6 0.2 6.5
88 Bei Nong 2 CHN 7.2 4.8 7.2 0 0 3.2 1.2 18.05
89 Natsuki JPN 3.8 4.8 1 0 0 2.8 1.4 23.25
90 Fertini Morettini ITA 3.2 4.9 7.2 1.2 0 6 2.1 10.5
91 Zhe Jin 2 CHN 7 4.5 7.2 0 0 6 1.1 7.2
92 Spring Gold USA 5 4.9 6 0 0 5.8 3.2 5.1
93 85-13-19 CHN 4.4 7.1 3 0 0 3.2 5.8 6.3
94 Jin Xu CHN 4.4 4.9 5 4.2 0 3.3 2.2 11.6
95 Nagin 1 JPN 0 5 4.8 0 0 4.9 3.4 23.2
96 Yu Hua Lu CHN 2.1 4.8 0 0 0 3 2.1 8.9
97 Yuan Dong Bai Tao CHN 1.4 7.4 0 0 0 3 7.6 14.4
98 Tou Xin Hong CHN 0 7.4 5 0 0 3 4.3 13.9
99 Sunking USA 6 5.2 7.1 0 0 5.2 1.1 5.9
100 NJN76 USA 7.4 5 6.3 0 0 5.2 3.8 9.4
101 Liu Yang Si Jin Tao CHN 1.8 6.3 2.2 3.2 0.9 3.1 3.2 10.5
102 Pegaso ITA 4.8 4.2 7.4 0 0 6 2.8 5.1
103 Sunblaze USA 2.1 0 7.2 0 0 3.5 0.2 5.1
104 Flordaglo USA 7 4.8 7.4 0 0 6.8 4.3 2.8
105 Maravilha USA 6.9 5 6.8 0 0 5.4 0.3 5.1
106 Hu You 004 CHN 0 7.1 2 0 0 4.2 6.8 19.6
107 Hu You 007 CHN 3.2 5.1 0 0 0 2.3 5.9 28.3
108 Zi Jing Hong 2 CHN 1.8 6.8 2.1 0 0 5.4 6.1 27.2
109 Early Red 2 USA 6.8 6.7 5.8 0 0 5.8 4.8 7.3
110 Sheng Guang CHN 2.4 6.4 1.8 2.1 0 2 6.6 10.3
111 801 CHN 7.2 7.4 2.6 0 0 4.3 7.1 16.8
112 Rui Pan 1 CHN 6.8 7.4 0 0 0 3 6.8 18.5
113 Zao Feng Wang CHN 0 6.8 0 0 0 2.8 6.1 21.5
114 Kana Iwa JPN 0 7.4 0 0 0 2.4 6.9 16.0
115 Da Zhao Huang Tao CHN 5.8 7.4 0 0 0 2.3 8.3 21.6
116 Mei Ting CHN 2.1 4.8 0 0 0.9 2.8 4.5 17.4
117 Qu Jing Tian Tao CHN 1.8 4.6 3.1 0 0 2.8 2.2 6.1
118 63-15-59 CHN 1.3 7.3 0 0 0 5.4 8.1 13.0
119 Yi Xian Bai CHN 0 0 7.4 0 0 8.9 0.2 4.8
120 Rui Guang 7 CHN 1.2 4.2 5.4 0 0 3.1 2.1 11.9
121 Ao19 AUS 4.3 5 6.1 0 0 5.4 1.9 7.3
122 Rui Guang 19 CHN 6.9 7.2 3.1 0 0 3 6 18.0
123 Rui Guang 2 CHN 4.3 6.1 0 0 0 2.1 7.6 13.0
124 Feng Huang CHN 7 6.5 0 0 0 6.2 7.8 7.6
125 Redhaven USA 6.8 5 6.8 0 0 5.1 4.2 11.9
126 Vesuvio USA 4.2 4.8 4.5 1.1 0 3.2 3.2 10.6
127 Sunfre USA 0 1.8 6.2 0 0 5.4 0.8 5.5
128 Silver Load USA 4.1 4.3 3.8 0 1.2 3.4 2.8 8.2
129 Galaxy USA 4.2 6.5 0.8 0 0 3 7.7 13.2
130 TX4D170 USA 1.8 1.8 7 0 0 6 0.8 6.7
131 Ban Han CHN 7 2 0 0 0 1.1 1.3 12.2
132 Xia Hui 5 CHN 5.8 6.8 0 0 0 1.4 8.2 22.9
133 Mei Guo Hong Pan Tao USA 6.1 7.4 0 0.8 0 2.3 6.8 14.7
134 UFO4 ITA 9.2 9.2 0 0 0 6.3 9.4 18.2
135 Saturn USA 1.3 6.8 0 0 0 2.1 6.7 11.3
136 Jin Jiu Hong CHN 4.3 6.1 3 4.2 0 3.2 3.2 17.9
137 Nectaross USA 0 3.1 0 0 1.8 0.3 1.1 7.5
138 Hong Gan Lu CHN 3.2 6.9 0 0 0 1.2 6.1 23.2
139 You Dao CHN 6.8 6.5 3 0 0 2.5 6.3 21.5
140 Rui Guang 2 CHN 4.3 4.8 2.3 0 0 2 5.8 6.1
141 Yue 172 CHN 4.3 7.2 0 0 0 1.1 7.3 6.3
142 Qing Pi Qiu Tao CHN 4.4 5.3 0 0 0 1.2 4.8 23.3
143 Qing Guang CHN 3.1 7.4 3 0 0 3 6.9 13.8
144 Crimson Gold USA 0 4.3 6.2 0 0 5.8 2.3 5.2
145 Rui Guang Mei Yu CHN 1.2 4.1 1.8 0 0 3.4 3.1 10.4
146 Fuzalode FRA 6.9 3.2 7.2 0 0.9 5.6 0.6 3.9
147 TX4F244C USA 3.2 4.8 7.2 0 0 6 2.1 7.6
148 Rose Princess USA 1.3 5 5.3 0 0 5.1 1.2 5.0
149 Da Hong Pao CHN 7.3 6.9 0 1.3 0 5.3 6.1 5.3
150 Da Tian Tao CHN 0 5 1.8 0 0 3 3.1 19.2
151 Yi Xian Hong CHN 1.1 4.3 0 0 1 2.1 2.4 12.4
152 Lu Shui Tao 6 CHN 1.2 4.3 1.3 0 0 3.2 4.2 4.8
153 Xai Cui CHN 0 6.9 0 0 0 5 5.8 24.3
154 Tian Jin Shui Mi CHN 0 0 5.1 0 0 2.8 1.2 5.6
155 Flavor Gold USA 4.8 4.9 6.2 0 0 4.8 0.8 3.7
156 Xiang Jin Pan CHN 2.1 4.8 5.5 0 0 5.8 3.3 16.6
157 Xia Hui 6 CHN 1.8 5.5 0.8 0 0 1.5 6.2 21.2
158 Lu Lin CHN 0 4.8 0 0 0 1.1 4.2 6.9
159 Huang Nian He CHN 4.1 5.5 1.8 0 1.8 2.4 3.1 11.4
160 Miyako Hakuhou JPN 3.8 5.2 0 0 0 2.1 4.3 19.5
161 Tsukuba 89 JPN 1..2 5 1.2 1.8 0 2.1 2.6 19.1
162 Asama Hakuto JPN 4.6 7.1 0 0 0 1.4 7.6 10.1
163 Xiao Hong Hua CHN 1.3 6.5 1.1 0 0 2.1 6.8 21.9
164 Matsumori JPN 1.5 3.4 1.4 0 0 0 3.1 8.9
165 Ta Qiao CHN 5.8 8.6 2.5 0 0 3.5 5.8 18.6
166 Cullinan USA 0 2.1 5 2.2 1.2 5.8 2.2 10.7
167 Harken CAN 7.1 5.6 4.8 1.8 0 5.6 1.9 12.2
168 Frederica USA 5.2 3.8 6.2 0 0 6.3 0.8 12.8
169 Vista Rich ESP 0 2.4 6.9 0 0 6.2 2.2 5.9
170 Redtop USA 0 4.6 7.5 0 0 6.8 1.8 9.4
171 Lisbeth HUN 1.8 1.8 7.4 0 0 6.5 1.4 9.1
172 Catherina ESP 7.2 6.2 1.5 0 0 4.2 5.4 9.4
173 Zao Shu Huang Gan Tao CHN 6.5 1.8 4.8 0 1.1 3.8 1.8 8.3
174 Blaze Prince USA 0 5.4 4.8 0 0 4.1 2.1 6.0
175 Rumiana BGR 5.1 6.1 4.8 0 0 3.2 1.1 4.9
176 Rui Pan 5 CHN 3.8 7.6 0 2.1 0 2.1 7.4 19.6
177 Rui Pan 3 CHN 2.1 6.8 0 0 0 1.8 6.5 14.6
178 Yu Xia Pan Tao CHN 1.8 5.2 0 0 0 1.2 5.5 15.3
179 Jin Xia Pan Tao CHN 7.2 7.4 0 0 0 1.5 6.8 16.5
180 63-13-35 CHN 0 4.5 0 1.2 0 1.8 5.2 15.9
181 Babygold 5 USA 6.8 5.2 4.3 0 0 3 3.2 6.5
182 Babygold 6 USA 7.2 7.2 5 0 0 3.8 3.1 11.7
183 Stark Delicious USA 3.2 3.2 6.3 0 0 4.3 2.2 9.3
184 NJC3 USA 6.1 6.1 7.2 0 0 3.5 4.5 6.3
185 Fa Guo You Tao FRA 4.8 1.8 6.4 0 0 4.3 1.2 8.5
186 Stark Sunglo HUN 5.1 2.1 6.5 0 0 3.8 1.8 5.1
187 Yoshihime JPN 1.8 4.9 3.8 2.1 0 3.4 4.1 19.0
188 Xia Hui 7 CHN 6.4 5.8 0 0 0 1.1 6.2 17.3
189 Yang Shan 2 CHN 5 7.5 0 0.9 0 1.3 7.6 22.3
190 Jing Feng CHN 7.2 6.8 2.5 1.4 0 3 5.4 10.8
191 Gan Xuan 4 CHN 0 2 0 0 0 1.4 1.8 15.8
192 Kanto 5 JPN 6.9 6.8 0 0 0 1.2 6.2 13.2
193 Xi Zhuang 1 CHN 7.2 5 4.2 0 0 3.5 4.6 11.1
194 Yellow St.John USA 5.1 5 7.5 0 0 6.8 2.1 8.0
195 Yu Hua 2 CHN 7 7.6 0 3.2 0 2.4 6.8 11.0
196 Shasta USA 8.2 6.2 7.3 0 0 6.2 1.8 5.3
197 McNeely USA 6.8 5.2 6.9 0 0 3.5 1.6 5.8
198 Harbrite CAN 5 4.8 6.8 0 0 5.8 2.1 6.6
199 Da Jie Tao CHN 8.9 6.4 0 0.9 0 1.4 5.8 13.9
200 Hei You Tao CHN 0 5.8 6.1 4.3 0 5.4 3.2 6.9
201 Dixon USA 4.8 6.8 1.2 3.3 0 3 4.8 10.5
202 Veteran CAN 6.3 6.9 0 0 0 1.1 6.8 5.8
203 Nan Shan Tian Tao CHN 1.8 6.8 1.2 0 0 1.6 4.8 15.0
204 Huang Rou Pan Tao CHN 4.3 7.2 0 2.2 0 1.1 5.8 16.5
205 Xi Shan Pan Tao CHN 3.5 6.7 0 1.2 0 0.8 6.5 18.8
206 Qiu Kui CHN 0 4.2 6.2 1 0 4.5 3.2 6.4
207 Compact Roman USA 2.2 3.8 5.4 0 0 3.8 2.8 11.9
208 Xia Hui 8 CHN 0 6.4 0 0 0 1.2 8.8 36.4
209 Jin Xiu CHN 2.5 7.4 0 0 0 2.4 9.2 13.3
210 Shen Zhou Hong Mi CHN 3.1 4.8 6.4 0 0 3 3.8 8.6
211 A Chu Tao JPN 0 8.6 0 0 0 1.8 8.8 8.2
212 Mika JPN 0 7.3 0 1.4 0 1.2 6.8 11.8
Note: CHN, China; USA, the United States of America; JPN, Japan; CAN, Canada; FRA, France; ESP, Spain; ITA, Italy; BGR, Bulgaria; IND, India; AUS, Australia; HUN, Hungary.

Author Contributions

Conceptualization, M.S.; Methodology, J.Y.; Investigation, J.M.; Resources, Z.C.; Data curation, J.Y.; Writing—original draft, M.S.; Writing—review & editing, R.M.; Supervision, Y.X.; Project administration, M.Y.; Funding acquisition, Z.S. All authors have read and agreed to the published version of the manuscript.

Institutional Review Board Statement

All participants volunteered to take part in this project. All subjects gave their informed consent for inclusion before they participated in the study. In this study, materials were taken from the National Peach Germplasm Repository, Nanjing, China. These materials were safe for sensory research. All the experimental procedures involving volunteers were conducted in accordance with the Declaration of Helsinki.

Informed Consent Statement

Informed consent was obtained from all subjects involved in the study.

Data Availability Statement

Data are contained within the article.

Conflicts of Interest

The authors declare no conflict of interest.

Funding Statement

This work was supported by the China Agriculture Research System (CARS-30); the Species Conservation Project of the Ministry of Agriculture and Rural Affairs (19210895); National Crop Germplasm Resources Infrastructure in China (NHGRC2020-NH16); Accurate Identification of Peach and Strawberry Germplasm Resources in Southern China (19230697); and the Species Conservation Project of Crop Germplasm Resources (Peach and Strawberry) in Jiangsu Province (2023-SJ-011).

Footnotes

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Data Availability Statement

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