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. 2026 Jan 5;16:491. doi: 10.1038/s41598-025-29338-y

Optimizing boron and zinc supplementation for cane growth and its residual effect on the ratoon crop

Vallabh Jerambhai Zinzala 1, Jagadish Vitthalbhai Patel 2, Sonal Tripathi 1, Kamlesh Ganeshbhai Patel 1, Jaimin Ranjitrai Naik 1, Narendra Singh 1, Nitin Varshney 3, Deepasree Ammamkuzhiyil 1,✉
PMCID: PMC12775421  PMID: 41491185

Abstract

Sugarcane (Saccharum officinarum L.), as a long-duration and nutrient-intensive crop, is particularly susceptible to micronutrient depletion, especially under intensive cultivation. Despite the essential roles of zinc (Zn) and boron (B) in plant growth and metabolism, their management is often neglected, and their residual effects on ratoon crops remain underexplored. The present study aims to optimize Zn and B supplementation to enhance yield and quality in plant cane while assessing their carry-over effects on ratoon productivity for improved and sustainable micronutrient management in tropical agroecosystems. Field experiments were conducted at three sites on the College Farm, NAU, Navsari during the winter seasons from 2017 to 18 to 2019–20 for plant cane and from 2018 to 19 to 2020–21 for ratoon cane, to evaluate the direct effects of B and Zn application on plant sugarcane and their residual effects on ratoon sugarcane. The treatments included four levels of boron (0, 1.0, 2.0, and 3.0 kg ha⁻¹) and four levels of zinc (0, 5.0, 7.5, and 10.0 kg ha⁻¹), applied along with the recommended dose of fertilizers. The experiment was laid out in a factorial randomized block design with three replications, and the data were subjected to pooled analysis of variance over the years. Significant individual effects of boron and zinc on sugarcane growth and yield was observed. Millable cane height, weight, and the yield of cane and green trash were significantly higher with a B application of 3 kg ha-1 and a Zn application of 10 kg ha-1. Nutrient application influenced the chemical composition of sugarcane, increasing brix (%), sucrose (%), and commercial cane yield (%), particularly at the same application rates. Nutrient content and uptake in sugarcane, specifically nitrogen (N), phosphorus (P₂O₅), potassium (K₂O), boron (B), and zinc (Zn) increased significantly with the application of boron at 3 kg ha-1 and zinc at 10 kg ha-1. No noticeable interaction effect was observed between B and Zn on the yield and quality parameters of both the sugarcane and its ratoon.

Supplementary Information

The online version contains supplementary material available at 10.1038/s41598-025-29338-y.

Keywords: Boron fertilization, Micronutrient management, Nutrient use efficiency, Ratoon crop, Residual effect, Soil fertility, Sugarcane productivity, Zinc application

Subject terms: Agroecology, Sustainability

Introduction

Sugarcane is a globally important cash crop, valued for its economic, industrial, and nutritional significance 1,2. It contributes approximately 21% of global crop production (2000–2022 average). In India, where it is the primary source of sugar, it supports the livelihoods of over 2.8 lakh farmers and more than 11 lakh individuals through direct and indirect employment 3,4. With an annual production of 439.93 million metric tons over 5.883 million hectares5, India is the world’s second-largest sugarcane producer and largest consumer. Despite its economic prominence, sugarcane productivity in India remains suboptimal, constrained by biotic and abiotic factors, among which soil fertility and micronutrient availability are critical limiting factors.

Micronutrient deficiencies, especially of zinc (Zn) and boron (B), are widespread in intensively cultivated regions, including the tropical and subtropical soils of India6,7. In South Gujarat’s black soil zones, factors such as high soil pH, calcareousness, and clay content further restrict Zn and B bioavailability8,9. Zinc deficiency is particularly prevalent due to its strong adsorption to clay colloids, while boron deficiency is exacerbated by leaching losses and a narrow threshold between deficiency and toxicity. Over 40% of sugarcane fields in Gujarat show micronutrient limitations, with Zn and B among the most critical.

Zinc is a structural and catalytic component of numerous enzymes involved in protein and carbohydrate metabolism, photosynthesis (e.g., pyruvic carboxylase), auxin biosynthesis (tryptophan synthetase), and carbon fixation (carbonic anhydrase)10–12. It enhances photosynthetic efficiency and sugar accumulation, particularly under Zn-deficient conditions in sugarcane13. Field studies have shown that Zn application improves yield, nutrient use efficiency, and physiological performance of sugarcane under tropical conditions14. Boron, on the other hand, plays vital roles in cell wall formation, sugar transport, carbohydrate metabolism, membrane stability, and cell division15–17. In sugarcane, boron deficiency impairs sugar translocation and weakens structural integrity, leading to impaired growth and reduced productivity 18. Recent studies emphasize the critical role of B in sustaining yield, improving nutrient uptake, and supporting soil fertility in intensively cultivated soils 8.

However, the use of micronutrients in sugarcane cultivation remains relatively limited in regions like South Gujarat. The introduction of high-yielding sugarcane varieties necessitates revised nutrient management strategies tailored to site-specific micronutrient needs. Studies by19–21 demonstrated that targeted Zn and B application significantly improved cane yield and sugar recovery. Additionally, balanced and site-specific micronutrient application not only improves plant growth and quality but may also provide residual benefits to the succeeding ratoon crop-a component often neglected in existing research.

Therefore, this study was undertaken to evaluate the direct effects of boron and zinc levels on the growth, yield, quality, and the content and uptake of major and micronutrients by plant crop sugarcane (CoN 5071), as well as their residual effects on the succeeding ratoon crop.

Materials and methods

Experimental site

A field experiment was conducted at the College Farm of Navsari Agricultural University (20o 37’ N latitude and 72o 54’ E longitude) during the winter season over multiple years: from 2017–18 to 2019–20 for the plant sugarcane crop and from 2018–19 to 2020–21 for the ratoon sugarcane crop. The study site falls under the ‘Am’ category (tropical monsoon climate) of the Köppen climate classification system, characterized by high humidity, heavy seasonal rainfall, and mean annual temperatures above 24 °C. The monsoon season is warm and humid with significant rainfall and starts during the third week of June with an average annual rainfall of 1633 mm. The total number of rainy days is around 59 (the average of the last ten years). In general, rainfall does not occur in the winter and summer seasons. The overall meteorological data, including monthly temperature, rainfall, and relative humidity (RH) recorded during the experimental period (2017–2022), are presented in the supplementary material (supplementary table S1). The data revealed that the weather conditions were normal and conducive for the adequate growth and development of sugarcane over the period of study. The soil of the experimental location is classified under the order “Inceptisols” according to the 7th Approximation, which includes members of the fine, montmorillonitic, isohyperthermic great soil group of Vertic Ustrochrepts and Jalapore series. According to the USDA soil taxonomy, the soil texture is classified as clay. Locally, these soils are referred to as “deep black soils.” Dry soil is a dark brown, clay-like substance. When the earth is dry, it develops extensive cracks and gets quite hard; when it’s moist, it gets plastic and sticky.

Field experiment

The study aimed to evaluate the effects of micronutrient fertilization specifically B and Zn on the sugarcane variety CoN-5071. A two-factorial randomized block design (FRBD) with three replications was employed, comprising four levels of boron (0, 1.0, 2.0, and 3.0 kg ha⁻¹) and four levels of zinc (0, 5.0, 7.5, and 10.0 kg ha⁻¹), resulting in sixteen treatment combinations. The selection Zn and B application rates were guided by soil test-based recommendations and supported by previous regional research. Initial soil analysis indicated marginal to deficient levels of available Zn and B (Table 1). The chosen rates span a range from low to high doses that are agronomically safe and widely studied in tropical sugarcane systems19,20. This design enabled evaluation of both the immediate effects on plant crop performance and the residual impacts on ratoon productivity, while remaining within practical fertilization limits followed by farmers.

Table 1.

Details on planting time, irrigation frequency and intercultural operations.

Plant Sugarcane Ratoon Sugarcane
Year 2017-18 2018-19 2019-20 2018-19 2019-20 2020-21
Site F 4(B) B−5 F-11 F 4(B) B−5 F-11
Sowing date 24/01/18 27/12/18 07/01/20 16/01/19 02/03/20 02/01/21
Harvesting date 15/01/19 29/02/20 01/01/21 11/02/20 04/03/21 25/01/22
Number of irrigations (Year-wise) 11 12 11 9 9 10
Number of weeding 2 2 1 2 1 3
Number of inter culturing 2 2 2 2 2 2
Previous crop Rice Rice Rice Plant cane Plant cane Plant cane
Pest and diseases NIL NIL NIL NIL NIL NIL
Plantstand and seasonal conditions Normal Normal Normal Normal Normal Normal
Rainfall 1675 mm 48 Day 2170 mm 66 Day 2310 mm 63 Day 2170 mm 66 Day 2310 mm 63 Day 1709 mm 66 Day

Table 2.

Initial soil properties of three different sites.

Parameters 2017-18 [F 4(B)] 2018-19[B-5] 2019-20[F-11]
pH (1:2.5) 7.59 8.24 7.47
EC (1:2.5) (dS/m) 0.18 0.93 0.22
OC (%) 0.42 0.57 0.74
Av. N (kg ha− 1) 203 226 223
Av. P2O5 (kg ha− 1) 48.24 60.32 80.00
Av.K2O (kg ha− 1) 301 443 305
Av. S (mg kg− 1) 23 16 21
Boron (mg kg− 1) 0.16 0.34 0.21
Zinc (mg kg− 1) 0.42 0.40 0.48

*Site location was given in parenthesis.

Three budded setts of sugarcane which were procured from agronomy farm, Navsari Agricultural University, Navsari were planted at an inter row spacing of 90 cm. The fertilizer dose for the plant crop was 250:125:125 kg ha−1 of N: P₂O₅: K₂O. The same field was used for the ratoon crop and the recommended doses of NPK (325:62.5:125 kg ha−1 of N: P₂O₅: K₂O) were added. Fertilizers were applied using di-ammonium phosphate (DAP), urea, muriate of potash, borax, and zinc sulfate.

The entire phosphorus (P) and potash (K) doses were applied at the time of planting, whereas N was applied in four equivalent splits. At the time of planting, micronutrients were applied to the soil according to the treatments. Recommended agronomic practices such as earthing up, weedicide spray, hoeing and irrigation practices were regularly followed across all the treatments. Details on planting time, irrigation frequency and intercultural operations are summarized in Table 2. No incidence of pest and diseases was noted throughout the crop growth period.

Soil and plant analysis

Composite soil samples were collected from each plot at a depth of 0–15 cm using a screw auger, both before the initiation of the experiment and after the harvest of the crop. Each composite sample consisted of five subsamples collected diagonally across the plot, excluding border rows. Soil samples were dried, ground, and sieved (<2 mm) before being analyzed for their chemical properties. The following soil parameters were analyzed: pH was measured using 0.01 M CaCl₂ in a 1:2.5 soil-to-solution ratio and electrical conductivity (EC) was determined using 1 M KCl22. Organic carbon content was estimated by the dichromate oxidation method 23. Available nitrogen (N) was determined using the alkaline permanganate method24. Available phosphorus (P₂O₅) was extracted with 0.5 M NaHCO₃ (Olsen’s extractant) at pH 8.5 and estimated colorimetrically22. Available potassium (K₂O) was extracted using 1 N ammonium acetate (NH₄OAc) at neutral pH and measured with a flame photometer22. Available zinc (Zn) was extracted using 0.005 M DTPA buffered at pH 7.325, and available boron (B) was extracted with hot water and quantified colorimetrically using the azomethine-H method26.

Using random sample technique, several plant morphological characteristics were noted during the experiment. Numerous observations were made before (growth attributes), during (yield attributes and quality metrics) and after harvest (growth attributes) of the crop. Data on yield metrics such as total plant height (cm), millable cane height (cm), millable cane weight (kg cane−1), cane yield (t ha−1) and green top yield (t ha−1) were recorded at the time of harvest. For the estimation of quality parameters, such as brix value, sucrose content, and commercial cane sugar (CCS) yield, ten stalks from both the plant cane and ratoon crop in each plot were collected on the day of harvest. Brix value which is a measure of soluble solids, was measured using a refractometer (ATAGO, PAL-BX/RI) from the juice of the stalk27. Sucrose percentage in freshly extracted and filtered juice samples was estimated using an ATAGO AP-300 automatic polarimeter, after clarification with basic lead acetate. The sucrose content was determined using the standard Schmitz’s table, following the procedure described by28. Five randomly selected plants were harvested from the net plot area of 4.6 m x 3.6 m (gross plot area: 7.2 m x 6 m) in each treatment plot at peak maturity. The plants were separated into stalk and leaf components.

Fresh plant samples collected were cleaned, weighed, oven dried at 65 °C and ground for estimating nutrient contents. The concentration of N, P and K in plant was analyzed using standard procedure. Wet digestion with concentrated H₂SO₄ using the Kjeldahl apparatus was adopted for the determination of total N29. Wet digestion of samples with a 4:1 mixture of HNO₃ and HClO₄, followed by the adoption of the Vanado-molybdate method & flame emission photometry, and was used for the determination of phosphorus (P) and potassium (K), respectively22. Zinc content in plant samples was estimated following wet digestion of dried and finely ground material using a diacid mixture (HNO₃: HClO₄ in a 3:1 ratio), as per the method described by Lindsay25, using an ADS1000 FSX atomic absorption spectrophotometer (Motras Scientific, India). Boron content in plant samples was determined using the azomethine-H colorimetric method, as described by30, with readings taken at 420 nm using a 1600 V spectrophotometer (Motras Scientific, India). Total uptake of nutrients by sugarcane plant was calculated by multiplying the nutrient concentration (%) with cane yield (q ha−1).

Statistical analysis

The data collected from the experiment were subjected to pooled analysis of variance (ANOVA) using a factorial randomized block design to assess the main effects and interactions of Zn and B doses31. Prior to analysis, the assumptions of ANOVA were verified, including normality of residuals using the Shapiro-Wilk test (p > 0.05 indicates normal distribution) while homoscedasticity was evaluated with Levene’s test (p > 0.05 suggests equal variances). Since the treatments were based on quantitative doses, regression analysis was also performed to evaluate dose-response relationships on various parameters under study using the following model (Supplementary table S2).

graphic file with name d33e780.gif 1
  • Yijk: sugarcane yield for the ith level of Boron, jth level of Zinc, kth replication.

  • µ = overall mean.

  • Bi = effect of the ith Boron level.

  • Zj =effect of the jth Zinc level.

  • (BZ)ij= interaction effect.

  • ϵ ijk = random error term assumed N (0, Inline graphic).

Treatment means were compared using the Critical Difference (CD) at 5% probability level, and standard error of the mean (SEm) was reported for each parameter.

Results and discussion

Given the consistent lack of significant interaction between zinc and boron levels in both plant cane and ratoon crops, their individual effects could be distinctly evaluated and are therefore presented separately (Supplementary table S3 and S4). The results represent a comprehensive pooled analysis of data collected over three years for both crop cycles.

Effect of B fertilization on growth, yield, quality and nutrient composition of sugarcane

The pooled analysis of the data from three years revealed that individual effect of B and Zn were significant on growth and yield attributes of sugarcane (Table 3). In both cane and ratoon crops, no appreciable variations in the overall plant height were imparted by boron treatments. The tallest plants, however, were observed with the application of B @ 2 kg ha⁻¹ (364 cm) in the plant cane, and its residual effect (320 cm) in the ratoon crop. The results of growth and yield attributes viz. millable cane height and millable cane weight in pooled analysis were affected significantly by different levels of boron except for millable cane height of ratoon cane. There were notable variations in the millable cane height of plant cane, with application of B @ 3 kg ha−1 having the maximum height (211 cm). In both cane and ratoon crops, the amount of boron applied had a considerable impact on the millable cane weight where B@ 2 kg ha−1 produced the maximum weight at 1.20 kg cane−1 for the ratoon crop, and B at 3 kg ha−1 produced the highest weight at 1.39 kg cane−1 for the plant cane. These effects may be credited to physiological role of the nutrient in promoting cell division and elongation, regulating hormone activity, and facilitating carbohydrate partitioning, all of which contribute to enhanced vegetative growth and overall sugarcane productivity32,33. Surprisingly, in contrast to our results34, found that boron had no apparent effect on the weight of cane, with performance analogous to that of the control and other micronutrients.

Table 3.

Effect of B and Zn on growth and yield attributes of sugarcane.

Treatments Total plant height (cm) Millable cane height (cm) Millable cane weight (kg cane− 1) Cane yield (t ha− 1) Green top yield (t ha− 1)
Cane Ratoon Cane Ratoon Cane Ratoon Cane Ratoon Cane Ratoon
Boron
B @ 0 kg ha⁻¹ 355a 311a 196b 185a 1.23c 1.09 b 83.19c 68.40a 16.93c 11.75a
B @ 1 kg ha⁻¹ 359a 316a 200b 187a 1.27bc 1.13 ab 86.02bc 70.90a 17.38bc 11.98a
B @ 2 kg ha⁻¹ 364a 320a 203ab 191a 1.34ab 1.20 a 89.01ab 71.84a 18.19ab 12.21a
B @ 3 kg ha⁻¹ 360a 319a 211a 192a 1.39a 1.18 a 91.53a 73.54a 18.84a 12.18a
S.Em. ± 4.75 4.13 3.25 2.72 0.03 0.02 1.179 1.351 0.316 0.178
Zinc
Zn @0 kg ha⁻¹ 351 b 306 b 193 c 182 b 1.19 c 1.07 c 81.14 d 66.91 b 16.67 c 11.49 c
Zn @5 kg ha⁻¹ 356 b 314 b 198 bc 188 ab 1.28 b 1.14 bc 85.17 c 71.01 a 17.49 bc 11.87 bc
Zn @7.5 kg ha⁻¹ 360 ab 317 ab 207 ab 190 a 1.32 b 1.17 ab 89.25 b 72.31 a 18.26 ab 12.08 b
Zn @10 kg ha⁻¹ 371 a 329 a 212 a 195 a 1.43 a 1.23 a 94.17 a 74.44 a 18.92 a 12.67 a
S.Em. ± 4.85 4.15 3.34 2.71 0.03 0.025 1.162 1.354 0.306 0.177
Interaction 0.81 (NS)

0.416

(NS)

0.567 (NS) 0.972 (NS) 0.204 (NS) 0.607 (NS) 0.949 (NS) 0.849 (NS) 0.685 (NS)

0.645

(NS)

CV% 8.03 8.04 9.91 8.84 13.80 13.01 8.14 11.69 10.46 9.01
Adj. R2 0.576 0.778 0.721 0.690 0.678 0.625 0.823 0.266 0.567 0.682

Pooled data over three years (2017–2020 for plant cane and 2018–2021 for ratoon cane) are presented. Means followed by the same letter within a column are not significantly different at p ≤ 0.05 according to Duncan’s Multiple Range Test (DMRT).

Boron application significantly enhanced plant cane yield, with B at 3 kg ha⁻¹ and 2 kg ha⁻¹ resulting in approximately 10 and 7% increases over the control, respectively; though, the difference between the two treatments was not statistically significant. Green top yield in plant cane also responded positively, showing an increase of nearly 11% with B at 3 kg ha⁻¹. Boron’s positive impact on sugarcane yield and growth is supported by various studies. The vital role of boron in promoting plant growth and reproduction was emphasized by20. Application of boron improves the growth traits in crops by transporting photo assimilates from leaves to roots35,36. All of these studies supports the idea that increased sugarcane productivity is positively correlated with boron treatment. However, in contrast with our findings, many previous studies reported little to no effect of boron application on sugarcane yield and productivity, particularly when doses exceed 2 kg ha−121,37. A previous study [20] reported that B application and its residual effect at rates of 1 and 2 kg ha⁻¹ led to reduced sugarcane yields, likely due to boric acid toxicity. However, the required dose of this nutrient largely depends on factors such as soil conditions, cultivar response, environmental conditions or the form of B applied, which can influence the necessity for either higher or lower boron supplementation. The residual effect of B application showed no significant impact on cane yield, despite a slight numerical increase of approximately 7.5% at the highest dose. Similarly, the ratoon crop exhibited only marginal (~ 4%) improvement with B at 2 kg ha⁻¹, with no significant variation observed among treatments. These findings are consistent with those of38, who reported toxicity at the highest B dose (8.8 kg ha⁻¹) and along with no residual effect in the first ratoon. Similarly21,39, also reported no residual impact of B application on stalk or aboveground biomass yields in subsequent ratoon crops. Although B application in our study significantly enhanced cane and green top yields in the plant cane, its residual effect was not evident in the ratoon crop, aligning with the observations reported in these earlier studies.

The effect of boron treatments on sugarcane quality metrics such as brix (%), juice sucrose percentage, and CCS yield in both plant cane and ratoon crops is presented in Table 4. Both cane and ratoon crops’ brix percentage (soluble solids content of the sugarcane) was considerably impacted by B treatments. With 23.05% for the plant cane and 22.43% for the ratoon crop, B applied at 3 kg ha−1 had the highest brix values. Higher boron levels appear to promote sugar accumulation, as indicated by the gradual rise in brix percentage. The sucrose content in juice of plant cane varied significantly, with application of B at 3 kg ha−1 having the highest figure (19.97%), but was at par with treatment supplied B at 2 kg ha−1 (19.56%). Boron improves sugarcane production and quality by strengthening cell wall structure ( B is known to be involved in pectin cross-linking and maintaining membrane integrity) facilitating sucrose transport, and sugar metabolism. Concerning the ratoon crop, the residual effect of boron fertilization did not lead to any significant increase in sucrose yield, though B at 3 kg ha−1 continued to have a numerical advantage of 19.63%. Boron application significantly impacted CCS yield in both crops with plant cane production of 12.45 t ha−1 and a ratoon crop yield of 9.95 t ha−1, at the level of 3 kg ha−1 maximum. The significant rise in CCS yield with application of B emphasizes how the nutrient improves sugar yield and sugarcane quality. All three quality parameters studied showed higher value in plant cane compared to ratoon crop at all levels of boron application40. reported that applying B at a rate of 1.5 kg ha⁻¹, along with the recommended dose of NPK fertilizers, resulted in optimum cane yield and sugar recovery. B is primarily associated with sugar transport and sucrose metabolism, contributing to increased sucrose accumulation in sugarcane.35. In a two-year study conducted on sandy loam soils, the application of boron at a rate of 10 kg ha−1, followed by a 2% FeSO₄ spray, resulted in an increased sucrose percentage in cane juice at harvest33. A study by19 reported that a 0.1% foliar spray application of boron resulted in a higher brix percentage of 21.9%. Positive effects of boron fertilizers on sugarcane crop and its quality have been reported by other researchers also20,32. These studies highlight the importance of maintaining an optimal boron level for maximizing both yield and sucrose content in sugarcane.

Table 4.

Effect of Boron and zinc on quality parameters of sugarcane and Ratoon cane.

Treatments Brix (%) Sucrose (%) in juice CCS yield (t ha− 1)
Cane Ratoon Cane Ratoon Cane Ratoon
Boron
B @ 0 kg ha⁻¹ 22.19 c 21.79 b 19.12 b 18.95a 10.86 c 8.88 b
B @ 1 kg ha⁻¹ 22.51 bc 22.09 ab 19.34 b 19.30a 11.33 bc 9.40 ab
B @ 2 kg ha⁻¹ 22.79 ab 22.38 a 19.56 ab 19.30a 11.80 ab 9.46 ab
B @ 3 kg ha⁻¹ 23.05 a 22.43 a 19.97 a 19.63a 12.45 a 9.95 a
S.Em. ± 0.159 0.16 0.203 0.20 0.24 0.226
Zinc
Zn @0 kg ha⁻¹ 22.13 c 21.99 a 19.17a 19.07a 10.63 c 8.73 c
Zn @5 kg ha⁻¹ 22.44 bc 22.08 a 19.30a 19.15a 11.19 c 9.32 bc
Zn @7.5 kg ha⁻¹ 22.75 ab 22.19 a 19.62a 19.32a 11.91 b 9.57 ab
Zn @10 kg ha⁻¹ 23.22 a 22.43 a 19.89a 19.64a 12.70 a 10.09 a
S.Em. ± 0.160 0.16 0.203 0.20 0.23 0.226
Interaction 0.450 (NS) 0.713 (NS) 0.822 (NS) 0.909 (NS) 0.995 (NS) 0.823 (NS)
CV% 4.30 4.30 6.32 6.33 12.40 14.77
Adj. R2 0.368 0.143 0.155 0.137 0.589 0.194

Pooled data over three years (2017-2020 for plant cane and 2018-2021 for ratoon cane) are presented. Means followed by the same letter within a column are not significantly different at p ≤ 0.05 according to Duncan’s Multiple Range Test (DMRT).

Nutritional content and uptake (mg kg−1) of cane and green trash in sugarcane crops was affected by varying levels of B and Zn. The individual effect of different levels of B was found non-significant on primary nutrient contents of sugarcane in both plant cane (Fig. 1A) and ratoon cane (Fig. 1B) except for N content in plant cane. Though non-significant, B application at the rate of 3 kg ha−1 recorded higher nutrient concentrations in the crop and its ratoon (Fig. 2A). This may be attributed to interactions of boron with other nutrients, as evidenced by its ability to enhance nitrate reductase activity, stimulate ATPase activity41 and induce β-K⁺ channels in roots42, all of which reflect B–nutrient interactions. Similarly, B application up to 3 kg ha⁻¹, along with its residual effect, had no significant influence on zinc status (Fig. 1C and D). Overall, neither direct boron application nor its carryover effect substantially affected Zn accumulation. In contrast to its negligible effect on macro nutrients and Zn, different levels of boron and its residual impact significantly influenced boron accumulation in both cane and trash components. In plant cane, B content increased by 13.3% in cane and by 15.3% in trash at 3 kg ha⁻¹ compared to the control. This trend sustained in the ratoon crop, where its residual effect raised cane and trash B content by 6.7% and 10% , respectively. These differences were statistically significant across both crop cycles, underscoring the direct and residual roles of boron in enhancing its own uptake and accumulation within the plant system. This minimal response may be explained by the fact that B primarily influences structural and reproductive activities rather than directly improving macronutrient absorption. Additionally, its relationship with NPK uptake may not be apparent unless B levels are low or high, especially in soils that already contain adequate B.

Fig. 1.

Fig. 1

Effect of boron fertilization on N, P₂O₅, and K₂O content in (A) plant cane and (B) ratoon cane; Zn and B content in (C) plant cane and (D) ratoon cane in cane and green trash. Bars represent means ± SE for Zn @ 0, 1, 2, and 3 kg ha− 1. Different letters indicate significant differences (p < 0.05).

Fig. 2.

Fig. 2

Effect of zinc fertilization on N, P₂O₅, and K₂O content in (A) plant cane and (B) ratoon cane; Zn and B content in (C) plant cane and (D) ratoon cane in cane and green trash. Bars represent means ± SE for Zn @ 0, 5, 7.5, and 10 kg ha− 1. Different letters indicate significant differences (p < 0.05).

Table 5.

Effect of boron and zinc on nutrient uptake of sugarcane and ratoon cane.

Treatments N uptake (kg ha− 1) P2O5 uptake (kg ha− 1) K2O uptake (kg ha− 1) B uptake (g ha− 1) Zn uptake (g ha− 1)
Cane Ratoon Cane Ratoon Cane Ratoon Cane Ratoon Cane Ratoon
Boron
B @ 0 kg ha⁻¹ 149c 136 c 65.59a 60.47 c 207c 168 b 558d 418 c 609b 509a
B @ 1 kg ha⁻¹ 159b 144 b 71.04a 64.30 bc 218bc 179 ab 605c 455 b 657a 525a
B @ 2 kg ha⁻¹ 172a 147 ab 71.38a 66.21 ab 231ab 186 a 655b 470 ab 685a 525a
B @ 3 kg ha⁻¹ 179a 152 a 70.75a 68.64 a 241a 191 a 699a 481 a 686a 526a
S.Em. ± 3.32 2.42 1.920 1.431 4.55 4.43 10.09 8.94 14.69 10.92
Zinc
Zn @0 kg ha⁻¹ 148d 133 c 65.25c 63.23a 203d 162 c 579c 429 b 520d 458 c
Zn @5 kg ha⁻¹ 160c 143 b 67.90bc 65.35a 217c 177 b 607c 458 a 620c 509 b
Zn @7.5 kg ha⁻¹ 170b 149 ab 71.65ab 64.75a 231b 187 ab 650b 464 a 698b 539 b
Zn @10 kg ha⁻¹ 181a 154 a 73.94a 66.29a 246a 198 a 680a 473 a 799a 579 a
S.Em. ± 3.32 2.45 1.945 1.418 4.53 4.42 10.15 9.08 15.27 10.93
Interaction 0.884 (NS) 0.748 (NS) 0.353 (NS) 0.622 (NS) 0.372 (NS) 0.961 (NS) 0.981 (NS) 0.418 (NS) 0.785 (NS) 0.440 (NS)
CV% 12.07 10.10 16.81 13.49 12.38 14.92 9.83 11.91 13.59 12.81
Adj. R2 0.648 0.380 0.373 0.410 0.650 0.589 0.842 0.701 0.830 0.619

Pooled data over three years (2017–2020 for plant cane and 2018–2021 for ratoon cane) are presented. Means followed by the same letter within a column are not significantly different at p ≤ 0.05 according to Duncan’s Multiple Range Test (DMRT).

Nutrient uptake responded positively to boron application, with a marked increase observed under higher doses (Table 5). Among the treatments, boron applied at 3 kg ha⁻¹ resulted in the highest uptake of N and K2O in both plant cane and ratoon crops. Although the effect of boron fertilization on phosphorus (P₂O₅) uptake in plant cane was not statistically significant; however, its residual effect was evident, with the highest uptake (68.64 kg ha⁻¹) recorded at the highest dose. This trend was consistent for micronutrient accumulation as well, with B at 3 kg ha⁻¹ leading to the highest uptake of boron (699 g ha⁻¹ in cane and 481 g ha⁻¹ in ratoon) and zinc (686 g ha⁻¹ in cane and 526 g ha⁻¹ in ratoon). Compared with the different levels of B supplementation, control treatment (0 kg ha−1 B) showed the lowest nutrient uptake ability in both the plant and ratoon crops highlighting the positive influence of B on nutrient accumulation. Similar results were reported by21, who observed consistently higher B uptake at an application rate of 2 kg ha⁻¹, though they noted phytotoxicity symptoms at higher doses (4 kg ha⁻¹). However, no phytotoxic effects were witnessed in our study, where the maximum B dose was restricted to 3 kg ha⁻¹. The enhanced nutrient uptake in response to B fertilization can be attributed to boron’s critical role in modulating enzymatic reactions that govern nutrient absorption and transport. This is further supported by20, who emphasized boron’s contribution to improved nutrient assimilation through its stimulation of root growth and function. Furthermore18, highlighted the role of boron in maximizing plant nutrient use efficiency. Its role in auxin synthesis and enzymatic activity could be the reason for the increase in nutrient uptake. According to the available data, boron is essential for improving nutrient concentration and uptake, which in turn promotes better sugarcane growth and harvest.

Effect of zinc fertilization

The application of zinc at 10 kg ha⁻¹ markedly enhanced growth and yield attributes in plant cane resulting in greater total plant height (371 cm), millable cane height (212 cm), and millable cane weight (1.43 kg) (Table 3). A similar trend was evident in the ratoon crop, where the residual effect of zinc application continued to enhance growth parameters, though the magnitude of improvement was relatively lower compared to the plant cane. These findings are in close agreement with43, who observed that zinc application at 12.5 kg ha⁻¹ significantly increased plant height and number of millable canes, highlighting zinc’s strong influence on crop performance. The increased cane height could be attributed to more vegetative development due to the availability of balanced Zn nutrition21 and its critical role in the enhancement of plant growth33, revealed that the application of micronutrients, particularly Zn, significantly enhances sugarcane weight, thereby contributing to increased cane yield. The improvement in stripped cane height44 succeeding the application of micronutrients, particularly those containing Zn, might be attributed to involvement of the nutrient in the biosynthesis of tryptophan, a critical precursor in protein metabolism processes.

The application of ZnSO₄ has been shown to significantly enhance cane yield and green top yield in sugarcane cultivation. The dosage of Zn at 10 kg ha⁻¹ produced significantly higher cane and green top yields in both plant (94.17 t ha⁻¹ and 18.92 t ha⁻¹, respectively) and ratoon crops (74.44 t ha⁻¹ and 12.67 t ha⁻¹, respectively). A consistent and progressive increase in both cane and green top yields was evident with increasing Zn levels from 0 to 10 kg ha⁻¹. Higher number of millable canes and greatest cane yield (98.1 t ha−1) were recorded with application of 50 kg ZnSO4 ha−1 in combination with N and P fertilization by4519. also reported a remarkable cane yield of 111.9 tons per hectare, accompanied by the highest millable cane production, achieved through the application of zinc at a rate of 15 kg ha−1 to the soil. He further reported no significant interaction between B and Zn, which corroborates and reinforces the validity of our findings. In agreement with our findings that Zn fertilisation led to higher cane and green top yields21, reported enhanced aboveground biomass (green matter) and stalk yield after Zn treatment during the plant cane cycle. In both studies, the yield obtained from the residual effect of Zn in the ratoon crop was significantly lower than that of the plant cane, although the difference was statistically insignificant. The fundamental function of zinc in plant processes such as photosynthesis, protein synthesis46, plant metabolism, enzyme activity and chlorophyll production could be the likely cause of the increased growth attributes (millable cane height, cane weight, cane yield, and green top yield) noticed when it is applied. Zn deficiency reduces hormone production, which results in shortened internodes and restricted leaf growth47. Adequate Zn nutrition, on the other hand, promotes overall sugarcane growth by supporting increase in internode elongation, cane diameter, and cane weight43,48. As these internodes are the primary sites for sucrose accumulation, the optimal application of micronutrients, especially Zn, is essential for enhancing yield-contributing traits such as cane height, girth, and weight, thereby promoting vigorous growth and overall development of sugarcane49,50. Additional evidence supporting the beneficial effect of zinc fertilization on the growth potential and quality traits of sugarcane is provided by20, who reported that a Zn application rate of 3.9 kg ha⁻¹ resulted in higher ratoon crop yield, highlighting its sustained influence on crop performance. Positive effects of zinc (Zn) application on sugarcane growth and yield have also been reported by48,50–56. Conversely, several studies from the literature have indicated minimal or no response of sugarcane to Zn fertilization, even under conditions of low soil Zn levels, findings that differ from our results, which established an evident progress in crop growth and yield with Zn application57,58.

Data depicted that the application of Zn significantly improved the brix percentage in the plant cane and the CCS yield in both cane and ratoon crops (Table 4). Overall, in Zn dose at 10 kg ha−1, 19 and 15% higher CCS yield was noted in plant and ratoon crop, respectively, than unamended control. Higher stalk and sugar yields in sugarcane were reported by59 in a study investigating the residual effects of micronutrient application (B, Zn, Cu, Mn, Fe, and Mo), with or without the use of filter cake. Application of Zn at the rate of 15 kg ha−1 resulted in higher brix percentage of 23.1%19. Although a similar increasing trend was observed in brix percentage of the ratoon crop and sucrose percentage of both plant and ratoon crops with higher Zn doses, the differences were statistically non-significant. Remarkably, the control treatment (without Zn application) consistently recorded the lowest values across all parameters. Higher brix percentage in canes supplied with zinc may be attributed to its role in photosynthesis and carbohydrate metabolism. Multiple investigations have indicated an elevation in sucrose content across different levels of Zn, likely attributable to augmented sucrose synthase activity6061,62. reported higher sucrose percentage in cane juice with the application of Zn in combination with N, P, K fertilization. However, these findings contrast with our results. In agreement with our observations63, reported a non-significant effect of Zn fertilization on sucrose percentage in cane juice. However, unlike their findings, we observed a noticeable influence of Zn application on overall sugar yield. Similarly higher sugar yield was reported by34 with the application of micronutrients, especially Zn over control. Results supporting the effect of Zn on sugarcane quality parameters have been recorded previously52,64.

There was no significant effect of Zn fertilization or its residual impact on the N, P, and K content of either the plant cane (Fig. 2A) or ratoon crop (Fig. 2B). Though non-significant, increase in N and K2O content has been noticed in both cane and green trash, with N content in cane rising from 0.35 (Zn@0 kg ha−1) to 0.37% (Zn@10 kg ha−1) and potassium content increasing from 0.55 to 0.58% over the same treatments. Unlike the gradual increase in N and K2O content with the progressive application of Zn, no consistent trend was observed in P₂O₅ content across the zinc levels. However, the ratoon cane consistently exhibited higher P₂O₅ accumulation than the plant cane at all nutrient doses, highlighting the residual effect of zinc fertilization. The decrease in P content with increasing Zn levels suggests the existence of an antagonistic relationship between Zn and P, which may be attributed to the influence of Zn on root physiology, phosphorus mobilization, or its availability in the soil65. Analysis of Zn content in cane and green trash exposed a clear linear upsurge in accumulation with increasing zinc application levels (0 to 10 kg ha⁻¹), signifying a marked effect in the plant cane (Fig. 2C) and a remarkable residual impact in the ratoon crop (Fig. 2D). The importance of an adequate zinc source for nutrient uptake and plant growth is emphasized by21, who also found that applying a higher dose of Zn (6 kg ha⁻¹) to the soil directed to superior micronutrient buildup over time compared to lower Zn levels. The trend indicates how fertilization with zinc improves its accumulation in sugarcane. Due to its vital role in several enzymes that drive numerous metabolic events in all crops, zinc fertilization and its residual effect may be the cause of the improved nutritional content in both cane and its ratoon. Interestingly20, reported no increase in Zn content in leaves with Zn fertilization, which might be attributed to a dilution effect caused by greater sugarcane growth in response to higher Zn doses. The boron concentration in plant cane and ratoon crop did not significantly change across zinc treatments, suggesting that zinc has little effect on boron uptake. With only minor fluctuations among Zn levels, the amount of boron in green trash also stayed fairly constant and non-significant. Zn@10 kg ha−1 recorded the highest N, P2O5, K2O, B and Zn uptake in plant cane (181 kg ha−1, 73.94 kg ha−1, 246 kg ha−1, 680 g ha−1, 799 g ha−1 respectively) and ratoon crop (154 kg ha−1, 66.29 kg ha−1, 198 kg ha−1, 473 g ha−1and 579 g ha−1respectively) (Table 5), compared to the lowest value of control. Soil application of Zn at the rate of 15 kg ha−1 resulted in increased uptake of nutrients in sugarcane and thus higher N (2.4%), K2O (0.7%), B (31.7 ug g−1) and Zn (68.5 ug g−1) content in crop19. Similar studies have been conducted by51,53,55 reporting the positive effects of Zn on sugarcane nutrition. The supplementation of Zn and other micronutrients within an optimal range positively impacts the nutrient uptake of sugarcane34,46,64, however, excessive supplementation beyond this range does not provide additional benefits and may sometimes cause adverse toxic effects66.

Conclusions

This study was undertaken to evaluate the individual and residual effects of graded levels of boron (B) and zinc (Zn) on the growth, yield, quality, and nutrient dynamics of sugarcane (CoN 5071) and its succeeding ratoon crop under the black soil conditions of South Gujarat. The experimental soils were marginal to deficient in Zn and B, which likely contributed to the significant crop responses observed. No significant interaction between Zn and B was found, but their individual application significantly enhanced growth attributes, cane and green top yields, and Commercial Cane Sugar (CCS) yield in plant cane. Zinc at 10 kg ha⁻¹ and boron at 3 kg ha⁻¹ proved most effective. Although the residual effects in the ratoon crop were less pronounced, Zn continued to show a statistically significant influence on yield and nutrient uptake. Nutrient composition and uptake were also positively affected, particularly for N, K, and the applied micronutrient. Boron’s role in sugar metabolism and Zn’s contribution to enzymatic and photosynthetic activity were reflected in improved quality and productivity traits. These results affirm that targeted application of Zn and B in marginally deficient soils can significantly boost sugarcane productivity and nutrient use efficiency.

Hence, for soils marginal to deficient in Zn and B, site-specific application of boron at 3 kg ha⁻¹ and zinc at 10 kg ha⁻¹ is recommended to optimize sugarcane performance and partially sustain ratoon productivity under similar agroecological conditions.

Supplementary Information

Below is the link to the electronic supplementary material.

Supplementary Material 1 (15.7KB, docx)
Supplementary Material 2 (22.2KB, docx)
Supplementary Material 3 (50.3KB, docx)

Acknowledgements

Authors would like to thank the Central Instrumentation Laboratory and Department of Soil Science, Navsari Agricultural University for the structural support to conduct this study.

Author contributions

All authors contributed equally to the research design, development, and the writing of the manuscript. All authors have read and agreed to the published version of the manuscript.

Funding

The research was funded by the Department of Soil Science, N. M. College of Agriculture, Navsari Agricultural University, Navsari 396450.

Data availability

The data supporting this study are available from the corresponding author upon reasonable request.

Declarations

Conflict of interest

The authors declare no conflicts of interest. The funders had no role in the design of the study; in the collection, analyses, or interpretation of data; in the writing of the manuscript; or in the decision to publish the results.

Footnotes

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References

  • 1.Ranganathan, K. et al. Spatio-temporal distribution of sugarcane shoot borer, Chilo infuscatellus (Lepidoptera: Crambidae) and its associated natural enemy Sturmiopsis inferens (Diptera: Tachinidae) in India. Int. J. Trop. Insect Sci.43, 277–287 (2023). [Google Scholar]
  • 2.Varma, P. K., Kumar, K. V. K., Suresh, M., Raja Kumar, N. R. & Sekhar, V. C. Potentiality of native Pseudomonas spp. In promoting sugarcane seedling growth and red rot (Colletotrichum falcatum Went) management. Int. J. Curr. Microbiol. Appl. Sci.7, 2855–2863. 10.20546/ijcmas.2018.702.348 (2018). [Google Scholar]
  • 3.FAO. FAOSTAT Statistical Database. Food and Agriculture Organization of the United Nations, Rome, Italy. Available online: (2023). https://www.fao.org/faostat/
  • 4.Kumar, A. & Tiwari, O. K. Socio-economic symptoms of sugarcane growers in meerut district of Western U.P., India. Bull. Environ. Pharmacol. Life Sci.10, 218–221 (2021). [Google Scholar]
  • 5.Directorate of Economics and Statistics, Ministry of Agriculture and Farmers Welfare. Agricultural Statistics Report. Government of India. (2024).
  • 6.Chakrabarti, S., Dutta, A. & Singh, A. K. Micronutrient status of Indian soils: current challenges and management strategies. J. Soil. Sci. Plant. Nutr.24, 280–294. 10.1007/s42729-024-01350-5 (2024). [Google Scholar]
  • 7.Rana, L. et al. Unlocking potential: the role of zinc fortification combating hidden hunger and enhancing nutritional security. J. Exp. Agric. Int.46, 625–642. 10.1016/j.eja.2025.127801 (2024). [Google Scholar]
  • 8.Rashid, A., Zia, M. & Ahmad, W. Micronutrient Fertilizer Use in Pakistan: Historical Perspective and 4R Nutrient Stewardship (CRC, 2022).
  • 9.Shukla, A. K., Behera, S. K. & Singh, G. Micronutrient fertilizers in Indian agriculture – product profile, availability, forecast and agronomic effectiveness. Indian J. Fert. 17, 348–360 (2021). [Google Scholar]
  • 10.Mousavi, S. M., Sedaghat, A. & Esmaeili, M. Zinc in plants: Biochemical functions and dependent signaling. In Metals and Metalloids in Plant Signaling; Aftab, T. (Ed.), Springer Nature, Cham, Switzerland, pp. 241–263 (2024). 10.1007/978-3-031-59024-5_12
  • 11.Nandal, V. & Solanki, M. The Zn as a vital micronutrient in plants. J. Microbiol. Biotechnol. Food Sci.11, e4026 (2021). [Google Scholar]
  • 12.Cabot, C. et al. A role for Zn in plant defense against pathogens and herbivores. Front. Plant. Sci.10, 1171. 10.3389/fpls.2019.01171 (2019). [DOI] [PMC free article] [PubMed] [Google Scholar]
  • 13.Zhou, J., Wang, Y., Li, R. & Zhang, J. Foliar application of zinc improves physiological responses and sugar accumulation in sugarcane under Zn-deficient soils. Field Crops Res.299, 108965. 10.1016/j.fcr.2023.108965 (2023). [Google Scholar]
  • 14.Madaan, I. et al. Zinc and plant hormones: an updated review. In Zinc in Plants 193–223 (Elsevier, 2025). 10.1016/B978-0-323-91314-0.00016-8. [Google Scholar]
  • 15.Mehdi, F. et al. Factors affecting the production of sugarcane yield and sucrose accumulation: suggested potential biological solutions. Front. Plant. Sci.15, 1374228. 10.3389/fpls.2024.1374228 (2024). [DOI] [PMC free article] [PubMed] [Google Scholar]
  • 16.Tanaka, M. & Fujiwara, T. Physiological roles and transport mechanism of boron: perspective from plants. Eur. J. Physiol.456, 671–677 (2008). [DOI] [PubMed] [Google Scholar]
  • 17.Tariq, M. & Mott, C. J. B. The significance of Boron in plant nutrition and environment—A review. J. Agron.6, 1–10 (2007). [Google Scholar]
  • 18.Wang, X., Liu, Y. & Wu, X. Boron deficiency affects sugar transport and cell wall integrity in sugarcane. Plant. Physiol. Biochem.182, 38–45. 10.1016/j.plaphy.2022.04.007 (2022). [Google Scholar]
  • 19.Mangrio, N., Kandhro, M. N., Soomro, A. A., Mari, N. & Shah, Z. H. Growth, yield and sucrose percent response of sugarcane to zinc and Boron application. Sarhad J. Agric.36, 459–469. 10.17582/journal.sja/2020/36.2.459.469 (2020). [Google Scholar]
  • 20.Marangoni, F. F. et al. Soluble sources of zinc and Boron on sugarcane yield in Southeast Brazil. Sugar Tech.21, 917–924. 10.1007/s12355-019-00716-x (2019). [Google Scholar]
  • 21.Franco, H. C. J. et al. Sugarcane response to Boron and zinc in southeastern Brazil. Sugar Tech.13, 86–95. 10.1007/s12355-010-0057-x (2011). [Google Scholar]
  • 22.Jackson, M. L. Soil Chemical Analysis (Prentice Hall of India Pvt. Ltd., 1979).
  • 23.Walkley, A. & Black, I. A. An examination of the Degtjareff method for determining soil organic matter, and a proposed modification of the chromic acid Titration method. Soil. Sci.37, 29–38. 10.1097/00010694-193401000-00003 (1934). [Google Scholar]
  • 24.Subbiah, B. V. & Asija, G. L. A rapid procedure for the Estimation of available nitrogen in soils. Curr. Sci.25, 259–260 (1956). [Google Scholar]
  • 25.Lindsay, W. L. & Norvell, W. A. Development of a DTPA soil test for zinc, iron, manganese and copper. Soil. Sci. Soc. Am. J.42, 421–428. 10.2136/sssaj1978.03615995004200030009x (1978). [Google Scholar]
  • 26.Gupta, U. C. Boron nutrition of crops. Adv. Agron.31, 273–307. 10.1016/S0065-2113(08)60142-X (1980). [Google Scholar]
  • 27.Rao, C. Selection Procedure in Sugarcane Varietal Testing pp. 11–14 (Sugarcane Breeding Institute, 1986).
  • 28.George, P. Cane Sugar Handbook, 17th ed.; John Wiley & Sons: New York, London, Sydney, Toronto, pp. 124–129 (1963).
  • 29.Bremner, J. M. Total nitrogen. In Methods of Soil Analysis. Part 2: Chemical and Microbial Properties (ed. Black, C. A.) 1049–1178 (American Society of Agronomy, 1965). [Google Scholar]
  • 30.Bingham, F. T. & Boron in In Methods of Soil Analysis, Part 2. 431–448 (eds Page, A. L.) (American Society of Agronomy, 1982).
  • 31.Panse, V. G. & Sukhatme, P. V. Statistical Methods for Agricultural Workers (Indian Council of Agricultural Research, 1978).
  • 32.Mishra, A. K. et al. Evaluation of critical limit of Boron in calcareous soil under sugarcane cultivation. Agrica6, 104–107. 10.5958/2394-448X.2017.00024.4 (2017). [Google Scholar]
  • 33.Madhuri, K. V. N., Sarala, N. V., Hemanth Kumar, M., Subba Rao, M. & Giridhar, V. Influence of micronutrients on yield and quality of sugarcane. Sugar Tech.15, 187–191. 10.1007/s12355-013-0230-7 (2013). [Google Scholar]
  • 34.Majeed, A. et al. Balanced use of Zn, Cu, Fe, and B improves the yield and sucrose contents of sugarcane juice cultivated in sandy clay loam soil. Agronomy12, 696. 10.3390/agronomy12030696 (2022). [Google Scholar]
  • 35.Bithy, S. et al. Foliar application of Boron boosts the performance of tropical sugar beet. J. Bangladesh Agril Univ.18, 537–544. 10.5455/JBAU.121026 (2020). [Google Scholar]
  • 36.Abbas, M. S., Dewdar, M. D. H., Gaber, E. I. & El-Aleem, H. A. A. Impact of boron foliar application on quantity and quality traits of sugar beet (Beta vulgaris L.) in Egypt.. Res. J. Pharm. Biol. Chem. Sci5, 143–151 (2014).
  • 37.Mellis, E. V. et al. Micronutrientes em cana-de-açúcar: novidade lucrativa. In Congresso Brasileiro de Ciência do Solo (2009).
  • 38.Espironelo, A., Brasil Sobrinho, M. O. C. & Moraes, R. S. Efeitos do Boro Em cana-de-açúcar cultivada Em Vasos Contendo solo. Bragantia35, 259–272 (1976). [Google Scholar]
  • 39.Andrade, L. A. B., Casagrande, A. A., Vitti, G. C. & Perecin, D. Efeitos Das aplicações de Fritas e de fontes solúveis de boro, Cobre e zinco, via solo, Na cultura de cana-de-açúcar (Saccharum spp.), variedade SP70–1143. STAB. - Açúcar Álcool E Subprodutos. 13, 21–27 (1995). [Google Scholar]
  • 40.Mazhar, S. Impact of zinc and Boron application on growth, cane yield and recovery in sugarcane. Int. J. Life Sci.10, 30–37 (2016). [Google Scholar]
  • 41.Shireen, F. et al. Functions and approaches to enhance its availability in plants for sustainable agriculture. Int. J. Mol. Sci.19, 1856. 10.3390/ijms19061856 (2018). [DOI] [PMC free article] [PubMed] [Google Scholar]
  • 42.Li, W. & Johnson, C. E. Relationships among pH, aluminum solubility and aluminum complexation with organic matter in acid forest soils of the Northeastern united States. Geoderma271, 234–242. 10.1016/j.geoderma.2016.03.020 (2016). [Google Scholar]
  • 43.Kumar, N., Rana, L., Kumar, V., Sow, S. & Nanda, G. Zinc fertilization and bud chip transplanting: effects on zinc fractions, uptake and sugarcane productivity in calcareous soils. Eur. J. Agron.171, 127801. 10.1016/j.eja.2025.127801 (2025). [Google Scholar]
  • 44.Wu, W., Fu, W., Alatalo, J. M., Ma, Z. & Bai, Y. Effects of coupling water and fertilizer on agronomic traits, sugar content and yield of sugarcane in Guangxi, China. Agronomy10.3390/agronomy12020321 (2022). [Google Scholar]
  • 45.Chitkala Devi, T. C., Bharathalakshmi, M., Kumari, M. B. G. S. & Naidu, N. V. Effect of sources and levels of phosphorus with zinc on yield and quality of sugarcane. Sugar Tech.14, 195–198. 10.1007/s12355-012-0144-2 (2012). [Google Scholar]
  • 46.Naeem, A. et al. Biofortification of diverse basmati rice cultivars with iodine, selenium, and zinc by individual and cocktail spray of micronutrients. Agronomy12, 49. 10.3390/agronomy12010049 (2021). [Google Scholar]
  • 47.Broadley, M. R., White, P. J., Hammond, J. P., Zelko, I. & Lux, A. Zinc in plants. New. Phytol. 173, 677–702. 10.1111/j.1469-8137.2007.01996.x (2007). [DOI] [PubMed] [Google Scholar]
  • 48.Ghaffar, A. et al. Effect of trench spacing and micronutrients on growth and yield of sugarcane (Saccharum officinarum L). Aust J. Crop Sci.6, 1–9 (2012). [Google Scholar]
  • 49.Nadia, M., Kandhro, M. N., Soomro, A. A., Mari, N. & Shah, Z. U. H. Growth, yield and sucrose percent response of sugarcane to zinc and Boron application. Sarhad J. Agric.36, 459–469 (2020). [Google Scholar]
  • 50.Deshmukh, D. P., Navale, A. M. & Deokar, C. D. Influence of zinc solubilising consortiums on yield parameters of Suru sugarcane. Int. J. Agric. Innov. Res.8, 83–87 (2019). [Google Scholar]
  • 51.Filho, M. C. M. T. et al. Rates and sources of zinc applied in sugarcane grown on sandy soil in Brazil. Afr. J. Agric. Res.10, 477–484 (2015). [Google Scholar]
  • 52.Muhammad, I. et al. Response of sugarcane to different doses of Zn at various growth stages. Pure Appl. Biol.5, 311–316. 10.19045/bspab.2016.50040 (2016). [Google Scholar]
  • 53.Jha, C. K. & Thakur, S. K. Integrated effect of sugarcane trash mulch, Pressmud and Zn nutrition on soil fertility and productivity of sugarcane in calcareous soil. J. Agric. Search.6, 4–7 (2019). [Google Scholar]
  • 54.Cunha, F. N. et al. Productive potential of nitrogen and zinc fertigated sugarcane. Agronomy10, 1096. 10.3390/agronomy10081096 (2020). [Google Scholar]
  • 55.Dhaliwal, S. S. et al. Assessment of optimum mineral zinc fertilizer rate for quantitative and qualitative production of sugarcane in North-Western India. J. Trace Elem. Min.2, 100021. 10.1016/j.jtemin.2022.100021 (2022). [Google Scholar]
  • 56.Silva, M. A. et al. P. Sugarcane productivity as a function of zinc dose and application method. Agriculture12, 1843. 10.3390/agriculture12111843 (2022). [Google Scholar]
  • 57.Alvarez, R., Wutke, C. P. A., Arruda, H. V. & Godoy Júnior, G. Adubação Da cana-de-açúcar. XV. Experimentos com micronutrientes Nas regiões Canavieiras do Estado de São Paulo. Bragantia31, 19–25 (1979). [Google Scholar]
  • 58.Marinho, M. F. & Albuquerque, G. A. C. Efeitos do Cobre e do Zinco Na produção de cana-de-açúcar Em solos de tabuleiros de Alagoas. Brasil Açucareiro. 98, 41–50 (1981). [Google Scholar]
  • 59.Crusciol, C. A. C. et al. Filter cake as a long-standing source of micronutrients for sugarcane. J. Soil. Sci. Plant. Nutr.21, 813–823. 10.1007/s42729-020-00403-x (2021). [Google Scholar]
  • 60.Pawar, M. W., Joshi, S. S. & Amodkar, V. T. Effect of foliar application of phosphorus and micronutrients on enzyme activities and juice quality in sugarcane. Sugar Tech.5, 161–165. 10.1007/BF02943628 (2003). [Google Scholar]
  • 61.Thangavelu, S. Zinc and sugarcane production. Indian Sugar. 57, 39–46 (2007). [Google Scholar]
  • 62.Dhanasekaran, K. & Bhuvaneswari, R. Effect of zinc and iron humate application on the yield and quality of sugarcane. Indian Sugar. 53, 907–912 (2004). [Google Scholar]
  • 63.Abd El-Mageed, T. A., Rady, M. O. A., Semida, W. M., Shaaban, A. & Mekdad, A. A. A. Exogenous micronutrients modulate morphophysiological attributes, yield, and sugar quality in two salt-stressed sugar beet cultivars. J. Soil. Sci. Plant. Nutr.21, 1421–1436. 10.1007/s42729-021-00450-y (2021). [Google Scholar]
  • 64.Ghaffar, A., Ehsanullah, N. A. & Khan, S. H. Influence of zinc and iron on yield and quality of sugarcane planted under various trench spacings. Pak J. Agric. Sci.48, 25–33 (2011). [Google Scholar]
  • 65.Xian, X. et al. Effects of combined application of phosphorus and zinc on growth and physiological characteristics of Apple rootstock M9-T337 seedlings (Malus domestica Borkh). BMC Plant. Biol.24, 998. 10.1186/s12870-024-05724-y (2024). [DOI] [PMC free article] [PubMed] [Google Scholar]
  • 66.Nayyer, V. K., Singh, S. P. & Takkar, P. N. Response of sugarcane to zinc and iron sources. J. Res. Punjab Agric. Univ.21, 134–136 (1989). [Google Scholar]

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Supplementary Materials

Supplementary Material 1 (15.7KB, docx)
Supplementary Material 2 (22.2KB, docx)
Supplementary Material 3 (50.3KB, docx)

Data Availability Statement

The data supporting this study are available from the corresponding author upon reasonable request.


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