Correction
23 Dec 2025: Quyen NK, Dang LV, Ngoc NP, Phuong Thao PT, Hung NN (2025) Correction: Determination of nutritional sufficiency ranges for pomelo (Citrus grandis Osbeck) grown on alluvial soils using DRIS. PLOS ONE 20(12): e0339695. https://doi.org/10.1371/journal.pone.0339695 View correction
Figures
Abstract
Pomelo is an important tropical fruit with a high nutrient content and economic value in the Vietnamese Mekong Delta (VMD). The Diagnosis and Recommendation Integrated System (DRIS) helps determine the leaf nutrient status of various plants worldwide. However, the DRIS-based nutritional balance in pomelo leaves remains to be established. Therefore, in this study, we aimed to (i) construct the DRIS norms and indices for nutrients, including macronutrients (N, P, K, Ca, and Mg) and trace elements (Cu, Fe, Zn, and Mn) in pomelo leaves, and (ii) establish nutrient sufficiency value ranges for sustainable pomelo cultivation in the VMD. We collected 270 leaf samples at three stages of pomelo growth, i.e., flowering, fruit development, and postharvest, and calculated DRIS indices for various nutrients. The DRIS indices established for various nutrients in pomelo leaves were accurate and reliable, as indicated by the high coefficient of determination (R2 = 0.43–0.93, p < 0.05) between nutrient concentrations and their DRIS indices. We observed that pomelo leaves were deficient in N (IN = −6.82), P (IP = −24.0), and Fe (IFe = −0.40) at the flowering stage and most deficient in P (IP = −15.6), K (IK = −11.7), Fe (IFe = −0.50), and Mn (IMn = −2.31) at the fruit development stage. However, only N (IN = −2.64) and P (IP = −13.4) shortages were observed at the postharvest stage. Thus, in this study, we evaluated nutrient value ranges (deficient, balanced, and excess) in pomelo leaves at their different growth stages and established DRIS indices for various nutrients. The results contribute to our understanding of the nutritional status of pomelo leaves, which can help growers improve plant health for sustainable pomelo production.
Citation: Quyen NK, Dang LV, Ngoc NP, Phuong Thao PT, Hung NN (2024) Determination of nutritional sufficiency ranges for pomelo (Citrus grandis Osbeck) grown on alluvial soils using DRIS. PLoS ONE 19(10): e0312231. https://doi.org/10.1371/journal.pone.0312231
Editor: Muhammad Raziq Rahimi Kooh, Universiti Brunei Darussalam, BRUNEI DARUSSALAM
Received: July 12, 2024; Accepted: October 2, 2024; Published: October 16, 2024
Copyright: © 2024 Quyen et al. This is an open access article distributed under the terms of the Creative Commons Attribution License, which permits unrestricted use, distribution, and reproduction in any medium, provided the original author and source are credited.
Data Availability: All relevant data are within the manuscript.
Funding: The research was funded by the People’s Committee of Hau Giang, grant number 14/HĐ-KHCN. The funders had no role in study design, data collection and analysis, decision to publish, or preparation of the manuscript.
Competing interests: The authors have declared that no competing interests exist.
Introduction
Pomelo (Citrus grandis Osbeck) is a citrus fruit cultivated in Southeast Asia where is tropical and subtropical climatic regions [1]. In Vietnam, various varieties of pomelo are grown from north to south. The ‘Nam Roi’ cultivar widely used in the VMD, and they are delicious, and contains few seeds and many essential nutrients [2]. The mean weight of these fruits’ ranges from 1.5–2.5 kg, and their skin transforms from green to yellow upon ripening. Pomelo is considered to be a poverty-reducing plant because of its high value in domestic and export markets [3]. Most pomelo cultivation areas in the VMD have alluvial soils with high fertility and nutrient abundance [4]. However, the production of pomelo has become unstable because of soil fertility reduction and poor nutrients management. Growers use large amounts of chemical fertilizers to obtain maximum yield. Past studies indicated that soil pH in pomelo orchards is significantly reduced because of the runoff/washing of exchangeable cations from surface soil under tropical conditions [4, 5], which may negatively affect the availability of soil nutrients such as P, Ca, and Mg, resulting in reduced nutrient uptake in plants.
Mineral nutrients play crucial roles in citrus growth and yield [6]. N regulates in many biochemical and physiological characteristics in citrus plants, including root activity and development, photosynthesis, and crop productivity [7]. It has been shown that P is required for many vital functions in plants [8]. Moreover, P is required for optimal citrus blossom, fruit setting and development [9]. K is an essential element in citrus juices and plays important roles in the regulation of water relations, and acid metabolism [10]. Ca plays a crucial role in forming pedicel attachment to the proximal fruit, thereby preventing fruit drop [11]. Astiari et al. [12] reported that Ca deficiency produces rough, thick, and poor-quality rind. Mg is vital for chlorophyll and sugar production. Cu helps decrease fruit drop rate and improves fruit quality [13]. Fe enhances the contents of Brix, total sugar, and juices in fruits [14]. Zn is considered the main factor that increases the ascorbic acid and anthocyanin content in the fruit [15]. Mn decreases the acidity of fruit juices [16]. Xu et al. [17] reported an interaction between the mineral nutrients within plants. For example, a reduction in Mg uptake occurs at high K concentrations in crops, whereas the absorption of Na and Ca increases with K deficiency [17]. Therefore, the determination and balancing of mineral nutrients in plants is important for maintaining crop health and sustainable agriculture.
Several studies [18, 19] have described methods for evaluating the nutritional status of plants through leaf analysis. The Critical Value Approach (CVA) evaluates leaf concentrations of nutrients at above 90% of maximum productivity [20]. This method would be effective if only a nutrient showed deficient results because the relationships between nutrients were not assessed [21]. The Sufficiency Range Approach (SRA) is used to evaluate the status of nutrients in leaves, including deficiency or excess [22]. However, it does not evaluate balance or interactions of nutrients [23]. Thus, the disadvantages of the CVA and SRA methods are that they cannot be used to evaluate the interactions between mineral nutrients or calculate the critical levels of each nutrient [24]. Occasionally, the results contain more errors when applied to different plant growth stages [25]. The Diagnostic and Recommendation Integrated System (DRIS) was developed by Beaufils [26] and has since been improved or modified by many crop scientists for easier and more accurate use [27, 28]. There are two main steps for establishing a DRIS: (1) determining DRIS norms based on nutrient ratio pairs and (2) calculating DRIS indices based on DRIS norms [29]. The DRIS indices indicate whether leaves are deficient (negative value), balanced (zero value), or have an excess (positive value) of mineral nutrients. The benefit of using the DRIS is the determination of specific nutrients based on the values of all nutrients in the DRIS norms. Therefore, these results are reliable and precise for determining the nutritional status of crops [30, 31]. Globally, the DRIS has been applied to determine the sufficiency ranges for mangoes [32], guavas [33], star apples [24], and pineapples [31]. DRIS is an interesting method for assessing the nutritional status of crops; however, DRIS norms need to be established for each crop. This is because the accuracy of DRIS is affected by environmental conditions (e.g., soil and climate) and plant species.
DRIS has been used to assess leaf nutritional status in star apples [24], durians [34], and pineapples [31]. However, information on the application of DRIS to pomelos is lacking. Therefore, to establish DRIS norms and indices for pomelos, we investigated 90 pomelo orchards in the VMD and examined soil properties and concentrations of leaf mineral nutrients (N−P−K−Ca−Mg−Cu−Fe−Zn−Mn). The objectives of the study were to (i) construct and create a DRIS for pomelo leaves at three stages (flowering, fruit development, and postharvest) and (ii) calculate and recommend optimal nutrient concentration ranges for pomelo leaves.
Materials and methods
Study area and environmental conditions
‘Nam Roi’ pomelo is cultivated in the Hau Giang and Vinh Long provinces, VMD [35]. The Chau Thanh district of Hau Giang province is considered the largest area of pomelo production [3]. Therefore, we investigated the leaf mineral nutrients and soil characteristics of 90 pomelo gardens in this region. The People’s Committee of Hau Giang approved and supported field surveys, contract number 14/HĐ-KHCN. The meteorological characteristics of this area have been described in our previous study [5]; the average monthly rainfall and air temperatures between January and December 2018 were 160 mm and 27.2°C, respectively.
In this study, most pomelo trees were grown on raised bed soil with a distance of 4.0 m × 4.0 m [36]. Our previous study [37] showed that the average amounts of N−P−K fertilizers applied for pomelo were 652–164–149 g tree−1 year−1, respectively. They were separated into six different application times [5]: (1) the application of 20%N–30%P after a month of fruit harvesting; (2) 15%N–40%P–30%K 2 months before pomelo blossoming; (3) 20%N–10%P–15%K after a month of fruit setting; (4) 25%N− 10%P–15%K after 2.5 months of fruit setting; (5) 20%N–10%P–20%K after 4 months of fruit setting; and (6) 20%K 2 months before fruit harvesting. Complex fertilization schedules, such as N–P–K + trace elements (TEs) (e.g., 16–16–16+TEs or 20–20–15+TEs) and diammonium phosphate (DAP, 18%N–46%P) were used by farmers. However, the amounts of TEs in fertilizers remain unknown. Therefore, we considered and recorded pomelo orchards wherein TEs (Cu, Fe, Zn, and Mn) were applied.
Sampling, collection, and analysis
Plants.
In this study, 90 pomelo orchards were surveyed through 2018. The ages of the pomelo trees in this study ranged from 4.0 to 4.5 years, and they have been cultivated since 2014. We collected leaves at three different pomelo growth stages: flowering (30–50% of flowers opened, May 2018), fruit development (2 months after fruit set, August 2018), and postharvest (1 month after fruit harvest, December 2018). At each stage, we collected the third and fourth pomelo leaves from the 3-month-old branches of four plants per orchard, and there were 16 leaves from each orchard. The leaves did not exhibit any symptoms of disease or pest damage. A total of 270 leaf samples were taken (90 samples in three stages). After taking, the leaves were washed at least three times with distilled water. Finally, they were put in an oven at 70 °C for 80 h, then ground to a powder, and stored in a plastic bag to analyze their mineral nutrient contents.
The leaf mineral nutrient contents were measured as described by Houba et al. [38]. First, the leaf samples were digested to transform them from their organic state to an inorganic state using a solution containing 36 mL water, 12 g salicylic acid, and 200 mL 96% H2SO4. During the digestion stage, we added 3–5 drops of 30% H2O2 solution. After leaf sample digestion, N concentration was measured using the Kjeldahl method. Samples were distilled with 20 mL NaOH (40%) and titrated with 0.01 N H2SO4 solution. Total P was extracted using a solution containing H2SO4 (96%) and HClO4 and colorimetric ascorbic acid solution and measured using an ultraviolet (UV) spectrophotometer (UV-1800, Shimadzu), and K, Ca, Mg, Cu, Fe, Zn, and Mn were determined using atomic absorption spectrophotometry (AAS, iCE 3500, Thermo Scientific) at the wavelengths of 766.5, 422.7, 285.2, 342.8, 248.3, 213.9, and 279.5 nm, respectively.
Soils.
Soil samples were collected from 90 pomelo orchards during the first stage of leaf collection (flowering) in May 2018. All soil samples (0–20 cm) were air-dried for 15 d and then ground to pass through 0.5- and 2-mm sieves. Soil properties, such as pH, electrical conductivity (EC), soil organic carbon (SOC), total N (Ntot), available P (Pavail), and the concentrations of mineral nutrients (Cu, Fe, Zn, and Mn) and exchangeable cations (K+, Ca2+, and Mg2+), were measured. The soil analysis was conducted as described by Houba et al. [38]. Briefly, soil pH and EC were determined at a 1:5 soil: water ratio (10 g soil: 50 mL distilled water) and measured using a digital pH/EC meter. The soil organic matter content was measured using the Walkley–Black method, and soil was extracted using a solution containing 10 mL K2Cr2O7 + 20 mL H2SO4 (96%) and titrated with a 0.5 M FeSO4 solution. Ntot was determined using the Kjeldahl method, i.e., soil was extracted using a solution containing H2SO4 (96%)−CuSO4−Se at a ratio of 100–10–1 and distilled with 10 mL NaOH (40%) and then titrated with 0.01 N H2SO4 solution. Pavail was analyzed using the Bray II method, i.e., soil was extracted using a solution containing 0.1 N HCl + 0.03 N NH4F at a ratio of 1:7, and the P content in the extract was measured using a UV spectrophotometer (UV-1800; Shimadzu). Exchangeable cations (K+, Ca2+, and Mg2+) were extracted using 0.1 M BaCl2. Fe present in the soil was extracted using oxalate/ oxalic acid. Cu, Mn, and Zn were extracted using nitric/ perchloric acid. Finally, the concentrations of K+, Ca2+, Mg2+, Fe, Mn, Cu, and Zn were measured using an AAS, as described above.
DRIS norms
To establish the DRIS norms for pomelos, the data were first divided into two (low and high) yield groups. According to Aliyu et al. [39], the yield groups were calculated based on the average of all pomelo fruit yield populations + (0.5 × standard deviation). We recorded pomelo fruit yields from the 90 orchards in November 2018. We successfully separated two yield groups, including the high-fruit yield (≥14.7 t ha−1) and low-fruit yield (<14.7 t ha−1) groups (Table 1). Finally, DRIS norms were established as follows: (i) the construction of nutrient ratio pairs (A/B, B/A, B/C, C/B, … Y/Z, Z/Y) and (ii) the determination of mean values, coefficient of variation (CV), and variance (σ2) of the high- and low-yield groups.
Calculation of DRIS indices
The DRIS indices were calculated after establishing the DRIS norms. According to Khuong et al. [25] and Aliyu et al. [39], the DRIS indices need to be determined using the following equations:
(1)
(2)
where IA and IB are the DRIS indices for nutrients A and B, respectively. f(A/B) is the function calculated for the A and B nutrient ratio; f(A/B) = [((A/B)/(a/b)) − 1] × (1000/CV) if (A/B) ≥ (a/b), and f(A/B) = [1 − ((a/b)/(A/B))] × (1000/CV) if (A/B) < (a/b). A/B is the nutrient ratio for diagnosis, and a/b is the value of the nutrient ratio determined from the DRIS norms. CV is the coefficient of variation, and X is the number of functions used for calculating the total nutrients.
Establishment of optimum nutrient ranges in pomelo leaves
The ranges of optimum nutrients (ON) in leaves were determined using the mean (M) and SD of mineral nutrient concentrations in the high-yielding population [29]. Leaf nutrient ranges of pomelo leaves were computed as described by Morales et al. [29], as excessive [ON > (4/3 × SD + M)], high [(2/3 × SD + M) < ON < (M + SD × 4/3)], optimum [(– 2/3 × SD + M) < ON < (M + SD × 2/3)], low [(−4/3 × SD + M) < ON < (M + SD × −2/3)], and deficient (< −4/3 × SD + M). We established five classes of foliar pomelo diagnoses.
Statistical analysis
Data was summarized using Microsoft Excel (ver. 16), and IBM SPSS Statistics (ver. 20) was used for data analysis. We used the Student’s t-test to compare the averages of soil properties between the low- and high-yield groups. Relationships between the soil parameters were assessed using Pearson’s correlation analysis.
Results
Soil characteristics of the study sites
Table 2 describes the soil properties of the two pomelo fruit yield groups. The soil pH in the low-yield group (LYG) was lower by 0.52 units than that in the high-yield group (HYG). The SOC content in the HYG was higher by 3.2 g C kg−1 than that in the LYG. Similarly, Pavail concentrations in the HYG were higher by 5.8 mg P kg−1 than in the LYG. Further, the results of the exchangeable Ca2+ content analysis were similar; Ca2+ occurred at 4.98 and 5.36 cmol kg−1 concentrations in the LYG and HYG, respectively. However, there were no significant differences in EC, Ntot, K+, Mg2+, Cu, Fe, Zn, or Mn between the LYG and HYG. The value of EC ranged between 0.44 and 0.46 mS cm−1 in both yield groups. Similarly, the mean values of Ntot and K+ and Mg2+ ion concentrations were 1.40 g kg−1, 0.31 cmol kg−1, and 2.68 cmol kg−1, respectively, whereas the mean values of Cu, Fe, Zn, and Mn contents were 26.3, 11.1, 61.6, and 27.1 mg kg−1, respectively, in the entire population.
The relationships between the soil parameters in LYG and HYG are shown in Figs 1 & 2. SOC in the LYG was positively correlated with pH (r = −0.48**) and Zn (r = −0.48**) (Fig 1). A positive correlation exists between pH and Pavail (r = 0.72***) and between pH and Ca2+ (r = 0.72***). Similarly, Pavail was positively correlated with pH (r = 0.73***) and Ca2+ (r = 0.98***) but was negatively correlated with Fe (r = −0.53***). Negative correlations were observed between Fe and pH (r = −0.84***) and between Fe and Ca2+ (r = −0.55***). A correlation was observed among the soil properties in the HYG (Fig 2). pH was positively correlated with Pavail (r = 0.83***) and Ca2+ (r = 0.68***). Similarly, a negative correlation was recorded between Fe and Pavail (r = −0.81***), Fe and pH (r = −0.88***), and Fe and Ca2+ (r = −0.68***) in the HYG soil.
*, **, and *** indicates p < 0.05, p < 0.01, and p < 0.001, respectively.
*, **, and *** indicates p < 0.05, p < 0.01, and p < 0.001, respectively.
DRIS norms
Table 3 shows the values of the leaf nutritional components and nutrient pair ratios in the LYG and HYG. The means of macronutrients (N, P, K, Ca, and Mg) in the LYG were 24.9, 1.23, 19.9, 24.8, and 19.5 g kg−1, respectively. These values in the HYG were 27.8, 1.63, 20.8, 24.6, and 19.6 g kg−1. The concentrations of micronutrients (Cu, Fe, Zn, and Mn) in pomelo leaves of LYG were 27.3, 128, 31.1, and 39.5 mg kg−1, respectively. While they were 25.4, 142, 34.0, and 43.1 mg kg−1 in HYG, respectively. After establishing the nutrient ratios, we selected 36 that were used to calculate the DRIS indices. These included N/10P, N/K, N/10Ca, N/Mg, 10N/Cu, 100N/Fe, 10N/Zn, 10N/Mn, P/K, P/Ca, P/Mg, 10P/Cu, 100P/Fe, 10P/Zn, 100P/Mn, K/10Ca, K/Mg, K/Cu, 100K/Fe, 10K/Zn, 10K/Mn, Ca/Mg, 10Ca/Cu, 1000Ca/Fe, 100Ca/Zn, 100Ca/Mn, Mg/Cu, 100Mg/Fe, 10Mg/Zn, 100Mg/Mn, 100Cu/Fe, 10Cu/Zn, 10Cu/Mn, Fe/10Zn, Fe/10Mn, and Zn/Mn. The CV values for all nutrient ratios were approximately 30% lower in both the high- and low-fruit-yield group. Thus, DRIS norms were established to be highly reliable and accurate as the basis for DRIS indices.
Establishment of DRIS indices for pomelo
Table 4 shows the nutrient indices determined for pomelo at the three different growth stages. N, P, and Fe contents were below normal limits in pomelo leaves at the flowering stage, with indices below zero. The N and P indices with values of −6.82 and −24.0, respectively, indicated an extreme deficiency of these nutrients in pomelo leaves, whereas these leaves were slightly deficient in Fe, with a Fe index of −0.40. In contrast, the contents of K, Ca, Mg, Cu, Zn, and Mn in pomelo leaves were high because the indices were above zero. The nutrients P, K, Fe, and Mn are considered limiting factors at the fruit developmental stage. Of the nine nutrients investigated postharvest, only the indices of N and P were less than zero.
Fig 3 provides the relationship between leaf nutrient (N, P, K, Ca, Mg, Cu, Fe, Zn, and Mn) content and the DRIS indices, which were determined by regression analysis. The results showed a strong positive relationship between nutrient concentration and the DRIS index in all cases. Therefore, highly reliable DRIS indices were established for the nutrient diagnoses of pomelo trees. In this study, the DRIS indices of microelements (Cu, Fe, Zn, and Mn) aligned relatively more to their contents in leaves compared with that for the DRIS indices of macronutrients (N, P, K, Ca, and Mg), as the values of R2 between the concentrations and DRIS indices of micronutrients exceeded 0.80.
(IN: N index… IMn: Mn index); p < 0.05 (*) and p < 0.01 (**).
Concentrations of mineral nutrients in pomelo leaves at different growth stages
Table 5 shows the effects of the growth stages of pomelo on leaf nutrient concentrations. Mineral nutrient content was higher at the postharvest stage than at the flowering and fruit development stages, except for Cu content. The concentrations of N, P, Fe, and Zn during the post-harvest stage at 3.3 g N kg−1, 0.26 g P kg−1, 11.0 mg Fe kg−1, and 1.7 mg Zn kg−1 were higher than those during the flowering stage. Moreover, the contents of K, Mg, Zn, and Mn during the postharvest stage at 1.3 g K kg−1, 1.0 g Mg kg−1, 3.1 mg Zn kg−1, and 5.5 mg Mn kg−1 were higher than those during the fruit development stage. Therefore, nutrients were most abundant in pomelo leaves at the postharvest stage.
Optimal nutrient ranges for pomelo leaves during the different growth stages
We determined the optimal nutrient ranges for pomelo leaves during the different developmental stages based on the nutrient concentrations in the HYG (Table 6). In this study, we divided pomelo plants into five classes for leaf nutrient diagnosis: deficient, low content, optimum content, high content, and in excess for each nutrient during the flowering, fruit development, and postharvest stages.
In the flowering stage, the concentration of nutrients (N, P, K, Ca, Mg, Cu, Fe, Zn, and Mn) was considered as a deficient if they were less than 24.8 g kg−1, 1.29 g kg−1, 16.4 g kg−1, 18.3 g kg−1, 15.5 g kg−1, 22.0 mg kg−1, 98.0 mg kg−1, 31.2 mg kg−1, and 31.9 mg kg−1, respectively; the optimal ranges were 26.0–28.2 g N kg−1, 1.42–1.67 g P kg−1, 18.8–23.1 g K kg−1, 21.0–26.2 g Ca kg−1, 17.6–21.7 g Mg kg−1, 23.8–27.3 mg Cu kg−1, 120–163 mg Fe kg−1, 33.7–38.5 mg Zn kg−1, and 35.5–42.5 mg Mn kg−1, respectively; and these nutrients were considered excessive when they were higher than 29.3 g N kg−1, 1.79 g P kg−1, 25.4 g K kg−1, 28.8 g Ca kg−1, 23.7 g Mg kg−1, 29.1 mg Cu kg−1, 185 mg Fe kg−1, 40.9 mg Zn kg−1, and 46.0 mg Mn kg−1, respectively.
For the fruit development stage, the contents of leaf nutrients (N, P, K, Ca, Mg, Cu, Fe, Zn, and Mn) ranged from 27.6–28.7 g N kg−1, 1.50–1.75 g P kg−1, 18.5–23.4 g K kg−1, 25.0–27.1 g Ca kg−1, 16.4–21.2 g Mg kg−1, 22.1–27.0 mg Cu kg−1, 127.1–176 mg Fe kg−1, 30.0–34.6 mg Zn kg−1, and 42.7–59.0 mg Mn kg−1, respectively, and were estimated as optimal for pomelo.
Finally, the optimal nutrient ranges (N, P, K, Ca, Mg, Cu, Fe, Zn, and Mn) for pomelo leaf postharvest were 28.0–29.0 g N kg−1, 1.70–1.82 g P kg−1, 18.9–22.1 g K kg−1, 21.1–27.5 g Ca kg−1, 18.5–22.3 g Mg kg−1, 24.4–28.3 mg Cu kg−1, 117.1–149 mg Fe kg−1, 29.8–36.9 mg Zn kg−1, and 36.3–42.9 mg Mn kg−1, respectively.
Discussion
We realized that the soil pH in the LYG orchards was lower than that in the HYG, resulting in reduced soil Pavail and exchangeable Ca concentrations (Table 2). Many studies have reported that low soil pH is considered the main causing affecting soil available P [40, 41]. After being fixed by Fe and Al, becomes transforms into an insoluble P compound, which reduces P-use efficiency and P uptake in plants [42]. The results from the DRIS indices also indicated that P was most deficient in the leaves at all pomelo growth stages (Table 4). The P index in the flowering (−24.0), fruit development (−15.6), and postharvest (−14.3) stages showed a negative value. In this study, we did not examine the Fe and Al content in the soils of pomelo orchards. However, our previous study [43] indicated that Al and Fe concentrations in the surface soil (0–20 cm) were 5.36 meq Al3+ 100g−1 and 5.20 g Fe2+ kg−1, respectively. Therefore, decreasing the concentration of these elements is necessary to improve soil available P in pomelo orchards. Considering the results of our previous studies in fruit orchards [4, 5], we recommend that gardeners use lime and soil amendment (compost or biochar) applications for their orchards. This is because they would increase soil pH and exchangeable Ca and decrease the contents of Al and Fe, thus improving the contents of soil available P and exchangeable cations. Previous studies [44, 45] have reported that a decrease in exchangeable Fe and Al cation concentrations increases soil Ptot and Pavail concentrations and inorganic and organic P fractions.
We successfully established the DRIS norms and indices for pomelos (Tables 3 and 4). The nutrient index was determined using the DRIS norms with high reliability, as they explained the relationship between the DRIS index and its concentration in leaves by a regression equation (Fig 3). These results were consistent with those of Teixeira et al. [46], Aliyu et al. [35], and Morales et al. [29]. They indicated that the DRIS method was more accurate and reliable for diagnosing the nutritional status of plants when there was a strong positive correlation between DRIS indices and their concentrations in leaves. We observed that N, P, and Fe were limited to the leaves at the flowering stage (Table 4). Meanwhile, the nutrients P, K, Fe, and Mn were limited at the fruit development stage, and N and P were deficient at the stage postharvest. Therefore, macronutrients such as N, P, and K were the most deficient in the leaves during the pomelo growth stages. As explained above, high soil acidity (pH < 5) is a reason for the decreased P concentration in pomelo leaves. According to Li et al. [47] low soil pH negatively affected P concentration in pummelo leaves. Therefore, improving soil pH is the most optimal solution for decreasing P deficiency in pomelo leaves.
An imbalanced chemical fertilizer supply affects leaf nutrient concentrations [48, 49]. Our previous study indicated that growers in the region applied less than the recommended amounts of N−P−K [37]. The means of N−P−K fertilizers applied by the farmers were 652−164−149 g tree−1 year−1, respectively, while the Southern Horticultural Research Institute (SOFRI)-Vietnam recommended 900 N, 600 P, and 850 K (g tree−1 year−1), respectively. This may lead to insufficient nutrients for pomelo growth and development, decreasing their concentrations in leaves. Various studies have reported that plants received lower than the required nutrient amounts, leading to decreased nutrient concentrations in leaves, which negatively affected the growth and productivity of crops [49–51]. Therefore, we suggest that farmers should apply N−P−K fertilizers based on the SOFRI recommendation. The results showed that most pomelo orchards were not deficient in Ca, Mg, Cu, Zn, or Mn at any of the three growth stages (Table 4). As mentioned in the methods, farmers only applied N−P−K compound fertilizers, but these contained trace elements. However, we could not determine the exact dose of trace elements applied to pomelo orchards. However, this may have led to improved concentrations of these elements in the soil. Therefore, pomelo trees can use/uptake nutrients during their growth and developmental stages. In cases of Ca and Mg, gardeners did not apply any fertilizers that contained Ca or Mg via the roots. Nevertheless, these were supplied through foliar fertilization during the fruit development stage to prevent fruit cracking, resulting in increased concentrations of Ca and Mg in pomelo leaves. The foliar application of nutrients is a strategy to supplement nutrients for crops because it is not affected by soil pH or root health [36, 52]. Hence, we did not observe shortages in Ca and Mg contents in pomelo leaves.
In this study, we observed that the concentrations of mineral nutrients in pomelo leaves were highest in the post-harvest stage (Table 5). This may be because the pomelo trees do not produce flowers or fruits at this stage. Therefore, most of the nutrients are concentrated in the leaves. Nutrients in leaves are used to synthesize soluble compounds that play an important role in the formation of flowers and improve the fruit-set ratio during the flowering stage. Similarly, nutrients in leaves improve fruit size and quality during fruit development. These results agree with the findings of Raese et al. [53] and Lin et al. [54]. We proposed optimal nutrient ranges for pomelos at different growth stages (Table 6). These standard concentrations agree with the results of Nguyen et al. [55], who reported that the optimal nutrient (N, K, Ca, and Zn) concentrations in pomelo leaves in Thailand were 26.2–28.5 g kg−1, 17.9–22.1 g kg−1, 25.4–42.0 g kg−1, and 33.1–35.0 mg kg−1, respectively. Another study in China showed that the mean nutrient concentrations in pomelo leaves were 25.1 g N kg−1, 1.42 g P kg−1, 15.4 g K kg−1, 31.1 g Ca kg−1, 44.9 g Cu kg−1, 35.0 g Zn kg−1, and 78.0 g Mn kg−1 [47]. Therefore, we recommend that growers use this standard concentration for pomelo cultivation and production. These results will help determine pomelo health and nutrient demands at different growth stages. Therefore, farmers could apply suitable amounts of fertilizer to their orchards, resulting in improved incomes and benefits.
Conclusions
The pH of the soil in pomelo orchards in the VMD was low, leading to a decrease in soil available P. The DRIS indices showed that the concentrations of macronutrients (N, P, and K) in pomelo leaves were the most deficient compared with those of micronutrients during the different growth stages. The micronutrient (Cu, Fe, Zn, and Mn) indices explained the leaf nutrient content more clearly than the macronutrient indices. Therefore, improving soil acidity is considered the best method for enhancing leaf nutrient concentrations. Moreover, farmers need to apply enough amounts of N−P−K for pomelo based on the recommendation of fruit research institutes to improve their contents in leaves.
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