1. Introduction
Huanglongbing (HLB), caused by (
Candidatus Liberibacter asiaticus) is the most devastating disease threatening citrus production due to its complex nature and resistance to management [
1,
2,
3]. It severely impairs root function and nutrient uptake, leading to poor tree health, reduced yields, and unmarketable fruit characterized by small size, misshapen form, bitter taste, thick rinds, and dry pithy interiors [
4,
5,
6,
7,
8,
9,
10]. HLB disrupts nutrient transport by damaging phloem tissues, causing widespread deficiencies in essential nutrients [
11]. Nutrient deficiencies exacerbate physiological disorders, impairing nutrient translocation and further stressing nutrient-deprived trees [
12,
13]. Additionally, the sandy soils in Florida present notable challenges for citrus production due to their well-drained nature, low organic matter and nutrient content, poor nutrient-holding capacity, and high permeability [
14,
15]. These characteristics often result in nutrient leaching, limiting the efficiency of soil-applied fertilizers, a common practice among citrus growers [
16,
17]. Consequently, the combined impact of HLB and the inherent challenges of sandy soils threatens the sustainability of Florida’s citrus production. Researchers and citrus growers are still looking for strategies to mitigate HLB, but there is no cure to date.
Unfortunately, there are no commercial cultivars, varieties, or scion rootstock combinations with resistance to HLB
CLas infection [
18,
19]. However, in recent years, Sugar Belle
® ‘LB8-9’ mandarin hybrid (SB; “Clementine” mandarin × “Minneola” tangelo) has been popular due to apparent HLB tolerance under Florida natural HLB-endemic conditions [
20,
21]. Sugar Belle
® is typically known for its vigor, heavy fruit load, and good juice quality, even under HLB conditions. Nevertheless, recent reports have highlighted a decline in fruit quality, with issues such as low juice total soluble solids (TSS), small fruit size, peel creasing, and increased fruit softness [
22]. Florida citrus growers have also faced challenges regarding fruit splitting, damage during harvest and transportation, and problems with fruit peels being ripped off during processing, all of which impact the quality of fresh and processed citrus products. In addition, early-season mandarin fruits are often subjected to poor peel color development due to insufficient low temperatures that are needed to induce chlorophyll degradation and carotenoid accumulation [
23,
24].
Besides cultivar and climatic issues, imbalanced nutrition in citrus production has been reported to have significant impacts on thin peel size, fruit splitting, poor juice quality, small fruit size, and poor fruit texture [
25,
26,
27]. Potassium (K) is an essential macronutrient for fruit trees, playing key roles in various biological and physiological processes [
28]. It contributes to energy conversion, carbon fixation, and the transport of photosynthetic products, highlighting its importance in regulating fruit quality [
29]. Several studies have suggested that potassium fertilization significantly improves fruit quality by enhancing fruit size and peel thickness and reducing the incidence of peel disorders [
30,
31,
32]. However, excessive K could result in undesirable outcomes, such as thick, rough peel, reduced juice quantity, increased juice acidity, and a decreased brix/acid ratio [
33]. Therefore, proper management of K fertilization could enhance the fruit’s external and internal properties, while soil fertilization is an easy method of nutrient application, nutrient uptake can be hindered by poor root systems, particularly in HLB-affected trees and in poor sandy soils with additional stress factors like salinity or drought [
34].
Foliar application of minerals has been shown to be more effective in correcting nutrient deficiencies, minimizing soil toxicity, and preventing the fixation of micronutrients in the soil [
35,
36]. Studies have shown that foliar K application positively influences peel thickness and juice quality [
37,
38]. It has been found that foliar application of K after flowering increased the fruit size of Valencia oranges and the fruit yield of
Citrus sinensis cv. Jaffa [
39]. This indicates that the timing of K application is crucial, as it affects nutrient uptake, fruit size, and overall fruit quality. Research by Calvert [
40] demonstrated that two foliar sprays of potassium nitrate (KNO
3) resulted in higher leaf potassium content compared to more frequent sprays, while late-season applications were less effective in improving fruit size [
41]. Boman [
42] found positive effects of (KNO
3) applied at key growth stages in Sunburst tangerine. Likewise, a previous study observed that spraying 8% KNO
3 three times produced the highest percentage of large-sized fruits (57–63 mm) in
Clementine var.
Cadoux [
37]. Sangwan et al. [
38] reported that a 2% KNO
3 foliar treatment resulted in the greatest number of large fruits in Kinnow.
Moreover, Alva et al. [
34] reported that different sources of K are equally effective for correcting K deficiency; however, they failed to report the possible consequence on fruit quality and peel thickness due to other additional nutrients (like P in mono/di-potassium phosphate). Citrus responses to P fertilization result in higher yield, higher juice content, soluble solid–acid ratio, and decreased rind thickness [
43,
44]. Although well-balanced P fertilization is necessary for crop and fruit improvement, foliar application of P along with K sources could increase P uptake, which negatively impacts peel thickness, peel coloration, fruit firmness, fruit quality parameters, and also the internal leaf nutrient concentrations [
45,
46,
47]. Additionally, foliar application of B could contribute to the qualitative characteristics of fruit firmness, size, and yield [
48,
49], while there are several publications about the benefits of K spraying on tree and fruit growth, the optimal spraying time and efficacy of K sources are still not well studied with respect to fruit peel thickness, peel color, and fruit quality improvement in HLB-tolerant Sugar Belle
® mandarin grown in Florida sandy soil. Given the significant role of potassium (K) in fruit quality and the challenges posed by HLB and Florida’s sandy soils, we hypothesized that foliar application of K during the cell division stage significantly improves fruit juice quality, peel thickness, fruit size, and firmness in HLB-tolerant mandarin. Therefore, this study aimed to explore the effect of K foliar application timing and fertilizer sources on the external and internal fruit quality of Sugar Belle
® mandarin grown in Florida’s sandy soils.
4. Discussion
The results of this study demonstrated that foliar application of potassium (K) significantly influenced fruit diameter and peel thickness of Sugar Belle mandarin grown in Florida’s sandy soil (
Table 2). These findings align with previous research showing that K application enhances fruit size and peel thickness in citrus [
32,
60,
61,
62]. Foliar K application is significantly more effective and facilitates faster nutrient uptake, enhancing fruit growth benefits compared to soil-applied fertilizers [
36,
40]. The larger fruit size of mandarin is generally desirable for yielding and bringing higher prices. Our study revealed that an increase in fruit diameter, especially in treatments where Potassium Nitrate (PN) was applied once in July (PN
J) or twice in May and July with B (PNB
MJ), suggested that the time, frequency, and source of K application influenced fruit growth. Foliar supplementation of K and B plays a crucial role in fruit growth with synchronizing K and B uptake. Nasir et al. [
63] and Zekri and Obreza [
33] reported that the supply of K promotes the synthesis of carbohydrates, regulates several enzymatic functions, and maintains cell extensibility that significantly affects fruit growth and development. Previous studies supported greater mobility of assimilated K to the developing fruit, which acts as a potent metabolic sink [
64,
65]. The study on grapefruits with foliar K supply during fall was less effective in average fruit size [
41] but increased fruit size when K was applied before fall [
61]. Additionally, nutrient B application supports fruit setting, carbohydrate transportation, and nutrient uptake efficiencies, increasing fruit size [
66,
67,
68]. Our results were supported by Saleh and El-Monem [
69], who stated that foliar K and B produce higher fruit sets and larger fruit sizes in mango and ‘Kinnow’ mandarin, respectively. On the other hand, repeated applications of PN and DKP would increase the concentration of N and P, respectively, along with K supply, which could negatively impact fruit growth and partition the nutrients toward vegetative growth instead of fruit development. Although several studies supported the fruit size increment with K fertilization, higher N and P negatively impacted fruit growth and development due to higher fruit set and canopy volume growth [
44,
70,
71].
Regarding the peel thickness of Sugar Belle mandarin grown in Florida sandy soil, the study revealed that the foliar application of K improved the peel thickness; however, application time, source, and micronutrient integration impacted peel growth. The result is consistent with earlier studies that reported improved peel quality with K supply [
25,
37,
60,
61,
71,
72]. The increased peel thickness in treatments with a one-time PN application in May or July (PN
M and PN
J) highlights the efficient K uptake when applied at the right time that enhances fruit peel expansion and protection, possibly due to its role in strengthening cell walls [
41,
73]. High K application could increase leaf nutrient concentration and negatively impact the peel thickness (
Table A2). This effect was especially evident at the stylar end of the fruit; however, no significant differences were noted in the equatorial section, suggesting that the impact of K on peel thickness may be location-specific within the fruit. In contrast, frequent foliar K applied either from PN, DKP, or additional B did not enhance the peel thickness of Sugar Belle
®, suggesting that not all K sources and multiple applications were effective. In contrast, excessive or poorly timed K foliar application may be detrimental. Frequent K supply through PN and DKP also resulted in more N and P uptake that perhaps counteract peel expansion [
43,
71].
Shahzad et al. [
32] reported that the puncture resistance force was significantly higher when potassium (K) was applied with boron (B) compared to the control, suggesting that this application may improve fruit resistance to handling stresses—an important factor for postharvest handling and storage. Correlation results illustrated the positive response with leaf K and B concentration (
Table A2). A similar trend was observed in our study, where fruit puncture force was higher with GA and K+B application. However, the results were not statistically significant, possibly due to the small fraction of the nutrient supply.
The uniform and appealing color of mandarin is among the driving preferences for consumer purchase decisions [
74,
75]. The findings highlighted that foliar K application treatments did not influence change in fruit peel color attributes of mandarin, specifically the parameters of CIELAB a*, b*, and CCI, regardless of different K sources and application time. However, past studies reported that higher leaf nutrient concentration accumulation during ripening stages delays or inhibits peel chlorophyll degradation [
76,
77]. Despite the strong correlation between fruit color parameters and leaf nutrient concentrations (N, P, and K), surprisingly, the foliar application of PN and DKP had an insignificant effect regardless of application time and source (
Table A3). These results are aligned with previous research demonstrating that fruit nutrients such as N, P, and K could be partitioned into growing parts during maturation and perhaps peel color break with favorable weather conditions and ethylene phytohormone production [
78,
79]. Comparatively, foliar K treatments, particularly those with the combination of boron (PNB
MJ), were associated with more vibrant fruit color indexes, which could indicate enhanced physiological processes linked to fruit ripening and maturation. The synergistic effect of K and B could be linked to their role in enzyme activation and photosynthesis regulation, as these nutrients are essential for maintaining healthy fruit development and improving coloration throughout the maturation stages [
32]. Nevertheless, the significant reduction in green-to-red (a*) and blue-to-yellow (b*) gradient values observed with the GA treatment suggested that Gibberellic acid (GA) application may inhibit the color break process. The suppression of color break in citrus fruit by GA has been documented in other studies, where GA was shown to delay the color transition during fruit maturation, possibly due to its effects on ethylene biosynthesis [
80,
81]. The present study exhibited that GA application negatively affected the peel color attributes, which are crucial for marketability, especially for fresh fruit sales. The reductions in chroma and CCI values reported in the GA treatment further emphasize the detrimental effect of GA on fruit coloration. These indices, which measure color intensity and saturation, are essential in determining the visual appeal of citrus fruits. Overall, GA treatment significantly compromised peel coloration, but foliar K application did not impact color breaks. The results of this study suggested that foliar K application, particularly when combined with boron, can positively influence fruit peel color attributes.
This study demonstrated the significant influence of foliar application treatments on the fruit juice composition of mandarin, with particular emphasis on total soluble solids (TSS) and maturity index (MI). The findings aligned with previous studies that have emphasized the importance of potassium (K) in fruit quality by enhancing TSS content [
60,
63,
82]. The application of K, whether from Potassium Nitrate (PN) or Dipotassium Phosphate (DKP), resulted in a significant increase in TSS, where the PN
M treatment yielded the highest TSS content. This result was supported by prior research indicating that macronutrients (N, P, K) are a key nutrient in regulating the sugar accumulation in fruits, particularly when applied at the right time and amount [
31,
44]. The results of our correlation analysis showed that leaf N and fruit TSS (r = 0.48) were significant, possibly with higher N uptake with PN (
Table A3). Interestingly, the relationship between leaf nutrient content and P and K was negative, which might be possible nutrient distribution towards fruits and growing parts [
44]. Additionally, the additional B application also increased the TSS content of Mandarin when combined with PN [
44]. Interestingly, titratable acidity (TA) and MI did not show significant change with foliar K treatments. On the other hand, the application of Gibberellic acid (GA) had a detrimental effect on TSS, reducing its content by more than 10%. The reduced TSS and MI with GA application could be attributed to the hormonal imbalance induced by GA, which might have altered the natural accumulation of sugars during fruit maturation [
83,
84]. Over two years, the consistent improvement in TSS and MI with K application, regardless of the source (PN or DKP), underscored the reliability of K as a key determinant of fruit juice quality.
Adequate mineral nutrient is a prerequisite for ensuring high yield, fruit quality, and tree health [
85]. Foliar spray is regarded as a credible method to acquire a rapid response of nutrient supply, especially when soil and stress conditions limit the uptake of elements by roots during the growth periods [
36,
86]. However, the results of this study showed that foliar nutrient application did not significantly affect the leaf mineral content of HLB-tolerant mandarin grown in sandy soils except for micronutrient B. These findings are consistent with previous studies indicating that foliar applications of macronutrients, although beneficial in some contexts, may not always be retained in the leaves, especially in nutrient-deficient or stress-prone systems such as those affected by HLB [
39]. Uptake of nutrients could probably be distributed toward the growing roots, canopy, new flush, and fruit growth for being vigorous growing and highly productive characteristics of Sugar Belle mandarin [
20]. However, contrasting results were reported that K application via PN and DKP significantly increased the leaf P and K content [
39,
41,
87]. Leaf nutrient analysis of B concentration was significantly higher after B-applied with PN treatment (PNB
MJ) compared to the rest of the treatments. The results align with those described by Ullah et al. [
68], where leaf boron is known as phloem immobile within plant systems, which causes it to accumulate in the leaf tissue where it is applied rather than being translocated to other parts of the plant. This result also suggests that foliar B applications effectively boost leaf B levels, but their impact may be localized and not significantly alter broader nutrient dynamics within the plant. In terms of macronutrient concentrations, the foliar treatments did not elevate nitrogen (N), phosphorus (P), or potassium (K) levels beyond the lower end of the critical nutrient concentration range for Florida citrus (CNCFC), even with multiple applications. This reflects no potential impact on fruit quality and attributes due to foliar micronutrient supplementation, where leaf macronutrient concentration is often negatively correlated with fruit TSS, color indexes, fruit size, etc. Notably, despite a slight increase in leaf N and K concentrations in specific treatments, these changes did not impact overall nutrient balance or fruit quality.