Justice Amponsah, Patrick Kumah, Francis Appiah, Irene Akua Idun, Paul Kweku Tandoh
ABSTRACT. Mango is an important fruit with nutritional and economic benefits. However, the impact of varying paclobutrazol (PBZ) concentrations, soil types, and production seasons on its quality is less known in the literature. This study investigated the effects of varying PBZ concentrations, soil types, and production seasons on the quality of Keitt mangoes, aiming to optimise fruit attributes for both domestic and export markets. Conducted over three years in the Eastern Region of Ghana, this study had a 5×3×3 factorial design, with 5 PBZ concentrations (0, 10, 12.5, 20, and 25 mL), 3 soil types (Agawtaw, Akuse, and Baraku), and 3 production seasons (major, minor, and off-season). PBZ application had a concentration-dependent influence on the physical attributes of Keitt mango fruit, particularly fruit size, density, and firmness. Lower PBZ concentrations (0–12.5 mL) improved fruit size and total soluble solids (TSS) content, while higher concentrations (20–25 mL) reduced these parameters. Soil fertility played a key role, with fertile soils, such as Agawtaw, producing larger, heavier fruit with higher TSS and moisture contents. Seasonal variations also influenced the outcomes, with the major season favouring optimal fruit development due to favourable climatic conditions. Non-treated trees (0 mL PBZ) produced the largest and heaviest fruit, while the 25 mL PBZ treatment increased fruit firmness and extended the shelf life by reducing the total titratable acidity. The study emphasises the need to tailor PBZ applications to soil fertility and seasonal factors to achieve the desired fruit quality. These findings offer valuable insights for mango growers, promoting sustainable practices that enhance yield, quality, and economic viability in Keitt mango production to meet the growing global demand.
Keywords: Agawtaw soil series; Baraku soil series; Keitt mango; paclobutrazol.
Cite
ALSE and ACS Style
Amponsah, J.; Kumah, P.; Appiah, F.; Idun, I.A.; Tandoh, P.K. Influence of paclobutrazol concentrations, soil types and production seasons on physicochemical attributes of Keitt mangoes. Journal of Applied Life Sciences and Environment 2025, 58 (1), 85-120.
https://doi.org/10.46909/alse-581167
AMA Style
Amponsah J, Kumah P, Appiah F, Idun IA, Tandoh PK. Influence of paclobutrazol concentrations, soil types and production seasons on physicochemical attributes of Keitt mangoes. Journal of Applied Life Sciences and Environment. 2025; 58 (1): 85-120.
https://doi.org/10.46909/alse-581167
Chicago/Turabian Style
Amponsah, Justice, Patrick Kumah, Francis Appiah, Irene Akua Idun and Paul Kweku Tandoh. 2025. “Influence of paclobutrazol concentrations, soil types and production seasons on physicochemical attributes of Keitt mangoes.” Journal of Applied Life Sciences and Environment 58, no. 1: 85-120.
https://doi.org/10.46909/alse-581167
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Influence of paclobutrazol concentrations, soil types and production seasons on physicochemical attributes of Keitt mangoes
Justice AMPONSAH*, Patrick KUMAH, Francis APPIAH, Irene Akua IDUN and Paul Kweku TANDOH
Department of Horticulture, Kwame Nkrumah University of Science and Technology, Kumasi, Ghana
*Correspondence: justiceauspy@gmail.com
Received: Jan. 24, 2025. Revised: Mar. 26, 2025. Accepted: Apr. 02, 2025. Published online: May 05, 2025
ABSTRACT. Mango is an important fruit with nutritional and economic benefits. However, the impact of varying paclobutrazol (PBZ) concentrations, soil types, and production seasons on its quality is less known in the literature. This study investigated the effects of varying PBZ concentrations, soil types, and production seasons on the quality of Keitt mangoes, aiming to optimise fruit attributes for both domestic and export markets. Conducted over three years in the Eastern Region of Ghana, this study had a 5×3×3 factorial design, with 5 PBZ concentrations (0, 10, 12.5, 20, and 25 mL), 3 soil types (Agawtaw, Akuse, and Baraku), and 3 production seasons (major, minor, and off-season). PBZ application had a concentration-dependent influence on the physical attributes of Keitt mango fruit, particularly fruit size, density, and firmness. Lower PBZ concentrations (0–12.5 mL) improved fruit size and total soluble solids (TSS) content, while higher concentrations (20–25 mL) reduced these parameters. Soil fertility played a key role, with fertile soils, such as Agawtaw, producing larger, heavier fruit with higher TSS and moisture contents. Seasonal variations also influenced the outcomes, with the major season favouring optimal fruit development due to favourable climatic conditions. Non-treated trees (0 mL PBZ) produced the largest and heaviest fruit, while the 25 mL PBZ treatment increased fruit firmness and extended the shelf life by reducing the total titratable acidity. The study emphasises the need to tailor PBZ applications to soil fertility and seasonal factors to achieve the desired fruit quality. These findings offer valuable insights for mango growers, promoting sustainable practices that enhance yield, quality, and economic viability in Keitt mango production to meet the growing global demand.
Keywords: Agawtaw soil series; Baraku soil series; Keitt mango; paclobutrazol.
INTRODUCTION
Mango (Mangifera indica L.) is a highly valued tropical fruit known for its exceptional taste, nutritional benefits, and culinary versatility (Mwaurah et al., 2020). The Keitt variety stands out due to its large size, vibrant colour, and superior flavour, making it a top choice for both local and export markets (Bura et al., 2023). Producing high-quality mangoes necessitates optimised agronomic practices, including the use of growth regulators (Bisht et al., 2018), soil fertility management (Liu et al., 2022), and seasonal adjustments in production (Pérez et al., 2018). These strategies are crucial for ensuring consumer satisfaction and maintaining postharvest quality in competitive global markets (Alfarisi et al., 2024).
Paclobutrazol (PBZ), a widely used plant growth regulator, plays a vital role in managing vegetative growth and promoting reproductive development in fruit trees, including mango (Kishore et al., 2015). PBZ functions by inhibiting gibberellin biosynthesis and redirecting assimilates toward fruit production, which enhances yield and fruit quality (Malhotra et al., 2018).
However, its effectiveness is influenced by factors such as soil type and production season, requiring calibration to avoid negative effects, such as reduced fruit size, weight, and physicochemical properties (Zanamwe, 2014). This study examines how different PBZ concentrations interact with soil types and seasonal variations to affect Keitt mango quality, aiming to optimise these parameters for improved fruit production.
Keitt mangoes are highly valued for their sensory appeal, nutritional benefits, and economic importance (Datir and Regan, 2022). Rich in vitamins A and C, antioxidants, and dietary fibre, they play a crucial role in combating malnutrition and oxidative stress-related disorders (Lenucci et al., 2022; Yahia et al., 2011). Economically, mango cultivation supports smallholder farmers and serves as a key export commodity, driving rural development and income generation in tropical regions (Akrong, 2020; Mitra, 2016). Additionally, their versatility extends beyond fresh consumption to processed products, such as juices, jams, and dried slices, underscoring their significance in global food systems and value chains (Ambuko and Owino, 2023).
Despite the significant potential of Keitt mangoes in promoting food security, nutrition, and economic growth, several challenges impede their production and postharvest quality (Onyango et al., 2023). Variability in soil fertility (Kumar et al., 2012) and fluctuating seasonal conditions often compromise fruit development (Cavalcante, 2022). Moreover, inconsistent PBZ application has been linked to reductions in fruit size, weight, and sweetness (Babu et al., 2022). These challenges highlight the need for targeted research to optimise PBZ application while considering soil and climatic variability to ensure consistent production of high-quality Keitt mango. This study explores the interaction between PBZ concentrations, soil types, production seasons, and their combined effects on the physicochemical quality of Keitt mango. Given the growing global demand for premium-quality mangoes, refining production practices is essential FOR enhancing their competitiveness in export markets. Additionally, this research provides actionable insights for mango growers, promoting evidence-based practices to optimise yield, quality, and profitability.
The main objective of this research was to evaluate the effects of the PBZ concentration, soil type, and production season on the physicochemical quality attributes of Keitt mango. By examining the interactions among these factors, this study aimed to identify optimal conditions for maximising the quality and market value of Keitt mango, thereby contributing to the development of sustainable and economically viable mango production systems.
MATERIALS AND METHODS
This study was conducted in two distinct phases. The first phase involved a field experiment in which PBZ was applied to randomly selected Keitt mango trees cultivated on various soil types across different production seasons. The second phase comprised laboratory analyses aimed at evaluating how varying PBZ applications influenced the quality attributes of Keitt mango fruit grown under these differing soil and seasonal conditions.
Study Area
The study took place in Ghana’s Eastern Region (Figure 1), specifically within the Manya Krobo and Yilo Krobo municipalities. Yilo Krobo Municipality encompasses approximately 594 km2 and had a population of 122,705 in 2021. The municipal capital, Somanya, is located about 69 km from Accra and 50 km from Koforidua.
This region experiences a bimodal rainy season, with annual rainfall of 750–1600 mm, temperatures of 24.9–29.9°C, and relative humidity levels of 60–93%. The ecological landscape transitions between semi-deciduous rainforests and coastal savannah.
Laboratory analyses were conducted at the Kwame Nkrumah University of Science and Technology (KNUST) in Kumasi, utilising facilities from the Departments of Horticulture, Crops, and Soil Science, Pharmacology, and the Central Laboratory.
Location and extent of the mango farms
The following three mango farms in Ghana’s Eastern Region were selected for the study, each geo-referenced at specific soil profile pits: Farm 1 in Lower Manya, located at latitude 6°07’21.70”N and longitude 0°00’57.20”E and characterised by the Agawtaw soil series (Calcic Vertisol); Farm 2 in Lower Manya, situated at latitude 6°06’54.0”N and longitude 0°01’14.60”E and identified as the Akuse soil series (Calcic Vertisol); and Farm 3 in Somanya, positioned at latitude 6°02’51.70”N and longitude 0°00’52.50”W and characterised by the Beraku soil series (Gleyic Cambisol).
Experimental design
A 5×3×3 factorial design, with 5 PBZ concentrations (0, 10, 12.5, 20, and 25 mL), 3 soil types (Agawtaw, Akuse, and Baraku), and 3 production seasons (major, June–August; minor, January–February; and off-season, April–May). Each factor combination was replicated 3 times, resulting in 135 experimental units. The three dominant soils identified on the mango farms were Agawtaw series, Akuse series, and Beraku series, representing Farms 1, 2, and 3, respectively. A total of 540 mature mango fruits were used per year for this analysis, resulting in 1620 fruits overall.
Experiment planning, tree selection, and randomisation
This study involved the systematic selection and randomization of 135 ten-year-old Keitt mango trees across 3 farms representing the Agawtaw, Akuse, and Baraku soil series, with 45 trees from each farm. Trees were chosen based on their uniform size, canopy width, and vigour, with buffer zones established to prevent edge effects. Unique alphanumeric identifiers reflecting soil type, production season, and PBZ concentration (e.g., AGMJC0 for Agawtaw, major season, PBZ concentration 0) were assigned to each tree. Randomisation was achieved through the lottery method, in which identifiers were drawn from a container to allocate treatments impartially.
Treatment identifiers varied by soil series and season (major, minor, and off-season) and included PBZ concentrations ranging from 0 to 25 mL. Identifiers for trees in each soil series, such as AGMJC0 for Agawtaw, AKMJC0 for Akuse, and BKMJC0 for Baraku, ensured comprehensive categorisation. To maintain accuracy, trees were reviewed for duplicates and conformity to experimental criteria, with durable plastic tags attached for identification. A database and data collection sheet were created to record each tree’s details, facilitating organised data collection and ensuring reliable experimental tracking. The HPW manual for commercial mango farmers was followed for all three years of production.
PBZ characterisation and determination of heavy metal content using the sample digestion method
In this study, PBZ (trade name: Cultar) was characterised, and its heavy metal content was determined through a sample digestion method. A 5 mL sample of Cultar solution was accurately measured in a Kjeldahl digestion tube. A mixture of perchloric acid, nitric acid, and hydrochloric acid in a 1:2:3 volumetric ratio was added. The mixture was heated to 450°C until the solution turned whitish, indicating the completion of digestion, which typically occurred in 30–60 min. After cooling, the digest was diluted to 100 mL with deionised water. The clear supernatant was analysed for heavy metals, including zinc (Zn), copper (Cu), manganese (Mn), iron (Fe), cadmium (Cd), mercury (Hg), lead (Pb), arsenic (As), and nickel (Ni), using atomic absorption spectrophotometry (AAS). This method allowed the precise quantification of heavy metals, providing insights into the chemical profile and potential environmental implications of PBZ.
Database and field documentation
A spreadsheet was designed to log tree information, including soil type, season, PBZ concentration treatments, and unique identifiers. Data entry protocols were established to ensure accuracy and consistency. A detailed schematic was created to indicate the spatial distribution of the experimental trees within each farm. The map included tree ID, soil type, and PBZ concentration of treatment allocations.
Harvesting, cleaning, packaging, and transportation to laboratory for analysis and data collection
A total of 270 treated Keitt mango fruits were randomly harvested by hand at the hard green stage of maturity from three farms, ensuring each treated tree was represented. The fruit was carefully washed with chlorinated water (200 ppm sodium hypochlorite) to eliminate microorganisms and remove foreign matter, such as dust and dirt. Efforts were made to select fruits that were uniform in size, of good quality, and free of injury or disease. The orchard management practices were adapted from HPW’s guidelines for commercial mango farmers and were consistently applied in subsequent productions for the second and third years.
Evaluated parameters
Determination of the respiration rate of treated Keitt mango after harvest
The respiration rate was measured by determining the amount of carbon dioxide (CO2) released by the fruit over time. Mango fruit was placed in an airtight 1-L glass jar, sealed with a rubber septum, and incubated at 25 ± 2°C for 1–2 h. A 1-mL gas sample was extracted from the headspace using a gas-tight syringe and injected into a gas chromatograph (GC) equipped with a thermal conductivity detector (TCD) and a stainless-steel column packed with Porapak Q. The GC was operated with an injector temperature of 100°C, a column temperature of 60°C, and a detector temperature of 200°C, using helium or nitrogen as the carrier gas at a flow rate of 40 mL min−1. The CO2 concentration was quantified using a calibration curve generated from standard CO2 gas concentrations.
The respiration rate (mgCO2 kg−1 h−1) was calculated using Equation (1), as follows:
where C is the CO2 concentration in the headspace; V is the headspace volume; 44 is the molecular weight of CO2; M is the fruit mass; T is the incubation time.
Determination of ethylene production of treated Keitt mango after harvest
Ethylene production was measured in mango fruit using the closed-system GC method. An individual mango was placed in an airtight 1-L glass jar, sealed with a rubber septum, and incubated at room temperature (25 ± 2°C) for 1–2 h to allow ethylene accumulation. A 1-mL gas sample was then extracted from the headspace using a gas-tight syringe and injected into a gas chromatograph equipped with a flame ionisation detector and a stainless-steel column packed with Porapak Q.
The GC operating conditions were as follows: injector temperature of 100–120°C, column temperature of 80°C, and detector temperature of 200°C, with nitrogen or helium as the carrier gas at a flow rate of 30 mL min⁻¹. Ethylene concentrations were quantified by comparing peak areas with standard calibration curves, and the ethylene production rate (µL kg⁻¹ h⁻¹) was calculated accordingly (Equation 2).
where C is the ethylene concentration in the headspace; V is the headspace volume; M is the fruit mass; and T is the incubation time.
Determination of fruit geometrical diameter (cm) of treated Keitt mango after harvest
The geometric diameter (Dg, cm) was derived using Equation (3), as given by Mohsenin (1986), using the length (L), width (W), and thickness (T):
Determination of fruit solid density of treated Keitt mango trees
A 100-mL beaker was filled with distilled water to the 50-mL mark. The mass of the mango fruit was weighed on a digital balance. The new volume was recorded after the fruit was suspended in the water in the beaker. The displaced volume was then determined. This was repeated three times. The solid density (ρs, g cm−3) was calculated using Equation (4) (Shittu et al., 2012):
where Mgs is the mass of the mango fruit; and Vdw is the volume of water displaced by the fruit.
Determination of eaten ripe fruit firmness (N) of treated Keitt mango tree
The firmness of ripe Keitt mango fruit was assessed non-destructively using a Shore C digital durometer. Each mango was placed on a horizontal laboratory bench, and measurements were collected at three points: the middle, stem end, and blossom end.
The durometer’s pressure needle was gently pressed against the fruit’s surface at each location, and the firmness readings were recorded in triplicate. The average of these readings was calculated and expressed in Newtons (N). This method allowed for consistent firmness evaluation without damaging the fruit.
Determination of the dry matter content (%) of ripened Keitt mango fruit pulp
The mango was weighed, placed in a moisture can or dish, and dried to constant weight at 70°C in a drying oven for 72 h. The sample was then placed in the desiccator and weighed again. Fruit dry matter was then calculated using Equation (5).
Determination of the moisture content (%) of ripened fruit pulp of treated Keitt mango
The moisture content (MC) was determined by weighing 2 g of the sample in a pre-weighed moisture can, drying it at 60°C for 24 h, cooling it in a desiccator, and reweighing. This process was repeated until a constant weight was achieved. The MC (%) was calculated using Equation (6):
where A is the crucible weight; B is the sample weight; C is the dry sample weight; and D is the moisture weight.
Determination of the total soluble solids content of ripened Keitt mango fruit pulp
To determine the total soluble solids (TSS) content (°Brix) of treated ripe Keitt mangoes, 30 g of peeled pulp was blended with 90 mL of distilled water. The mixture was filtered, and a few drops of the filtrate were placed onto the prism of a calibrated refractometer (HI 96801, Germany). After each measurement, the prism was cleaned with methanol and distilled water to ensure accuracy for subsequent readings.
Data analysis
The laboratory results were analysed with Statistix software version 9. When there were significant differences, treatment means were separated using the honestly significant difference (HSD) at the 1% probability level.
RESULTS AND DISCUSSION
Respiration rate of treated Keitt mango fruit after harvest
The respiration rate is a vital physiological parameter in climacteric fruit, such as mango, directly influencing the postharvest shelf life, metabolic activity, and ripening kinetics. as shown in Tables 1–3, a consistent trend of respiration rate suppression was observed in Keitt mango treated with increasing PBZ concentrations over 3 years. The findings confirm that PBZ application significantly reduced the respiration rate (p < 0.01), with notable interactions among the PBZ concentration, soil type, and season.
Across all 3 years, non-treated mango exhibited the highest respiration rate, while fruit treated with the highest PBZ concentration showed the lowest values. In the first year, the respiration rate decreased from 38.2 (0 mL PBZ) to 29.7 mgCO2 kg−1 h−1 (25 mL PBZ). A similar pattern was observed in the second (43.3 to 26.8 mgCO2 kg−1 h−1) and third years (39.7 to 27.6 mgCO2 kg−1 h−1). This concentration-dependent decline aligns with previous research showing that PBZ reduces respiration by inhibiting gibberellin biosynthesis, thereby limiting ethylene synthesis and delaying climacteric ripening (Gill et al., 2023).
PBZ primarily reduces respiration in mangoes by inhibiting gibberellin biosynthesis, which slows cell expansion and carbohydrate metabolism, thereby lowering the energy demand and CO2 evolution (Rossouw et al., 2024). By suppressing ethylene biosynthesis through the downregulation of 1-aminocyclopropane-1-carboxylic acid synthase (ACS) and 1-aminocyclopropane-1-carboxylic acid oxidase (ACO), PBZ prevents the climacteric respiration peak, further reducing the metabolic activity (Li et al., 2020; Sebastian et al., 2019). Additionally, PBZ alters mitochondrial function by inhibiting key respiratory enzymes, such as cytochrome oxidase and succinate dehydrogenase, leading to lower ATP production and oxygen consumption (Shan et al., 2023).
PBZ also affects carbohydrate metabolism by inhibiting starch degradation and amylase activity, restricting glycolysis and the TCA cycle function (Santos et al., 2021). Furthermore, it enhances the antioxidant activity, reducing reactive oxygen species (ROS) production and oxidative stress, which stabilises cellular metabolism and delays senescence (Kamran et al., 2020). Another key mechanism is the PBZ-induced accumulation of abscisic acid (ABA), which suppresses ethylene synthesis and decreases fruit transpiration, reducing the respiratory activity (Maheshwari et al., 2022). These combined mechanisms explain the observed reduction in respiration rates from 34.5 in non-treated mango to 29.7 mgCO2 kg−1 h−1 in fruit treated with 25 mL PBZ.
Soil type significantly influenced the respiration rate, with mangoes grown in Agawtaw soil consistently exhibiting higher respiration rates compared to Akuse and Baraku soils. This suggests that soil fertility, water-holding capacity, and organic matter content influence fruit’s metabolic activity (Kumar et al., 2021). Agawtaw soil, which is potentially richer in nutrients, may have promoted higher respiration, while the relatively compact or less fertile Baraku and Akuse soils may have imposed slight physiological constraints, leading to lower CO2 emissions in PBZ-treated mango (Medina and Aguiar, 2017).
Seasonal variability also played a crucial role, with off-season mangoes exhibiting the highest respiration rates across all three years. In the first year, off-season fruit had a mean respiration rate of 34.3 mgCO2 kg−1 h−1 compared to 34.0 mgCO₂ kg−1 h−1 in the major season and 33.4 mgCO2 kg−1 h−1 in the minor season.
A similar trend was observed in the second (34.6, 34.9, and 32.1 mgCO2 kg−1 h−1 for off-season, major, and minor seasons, respectively) and third years (34.5, 34.1, and 33.5 mgCO2 kg−1 h−1 for off-season, major, and minor seasons, respectively).
The elevated respiration rate in off-season mango is likely due to increased temperatures and humidity, which accelerate metabolic activity and ethylene production, thus expediting ripening (Wang et al., 2022). Additionally, environmental stressors, such as irregular water availability and fluctuating diurnal temperatures, may have contributed to increased respiration rates, as previously reported in mango postharvest physiology studies (Adak et al., 2016).
The PBZ-induced reduction in respiration rate offers significant benefits for postharvest management, as lower metabolic activity translates to delayed ripening, extended shelf life, and improved storage potential. This is particularly advantageous for mango exporters, as PBZ-treated fruit may be better suited for long-distance transportation and extended market availability (Singh and Singh, 2019).
However, excessive respiration suppression may lead to undesirable textural changes or altered sensory attributes, necessitating careful optimisation of PBZ application.
Ethylene production (30 µL kg−1 h−1) of treated Keitt mango fruit after harvest
Ethylene production, a critical determinant of fruit ripening, was significantly influenced by PBZ application, soil type, and seasonal fluctuations (p < 0.01). PBZ consistently reduced ethylene emissions in a concentration-dependent manner across all 3 years (Tables 4–6), with higher concentrations (20 and 25 mL) resulting in the most substantial suppression. This finding aligns with the established role of PBZ as a gibberellin biosynthesis inhibitor, which indirectly restricts ethylene synthesis by disrupting the mevalonate pathway (Bai et al., 2021; Rademacher, 2016). The suppression of ethylene by PBZ can also be attributed to its direct impact on the ethylene biosynthesis pathway. By downregulating ACS and ACO (Mohapatra and Sahu, 2022), PBZ reduces the conversion of S-adenosylmethionine (SAM) to aminocyclopropane-1-carboxylic acid (ACC), the immediate precursor of ethylene (Sutaoney et al., 2023).
Studies on mango and other fruit crops, including apple (Malus domestica), pear (Pyrus communis), and tomato (Solanum lycopersicum), have confirmed that PBZ-treated plants exhibit decreased ACS and ACO activity, leading to delayed ripening and prolonged shelf life (Babu et al., 2022).
Table 1
Respiration rate (mgCO₂ kg-1 h-1) of harvested treated Keitt mango fruits with varied PBZ concentrations applied on different soil types during different production seasons for year one
Soil Type |
Seasons |
Concentrations |
Means |
||||
0 |
10 |
12.5 |
20 |
25 |
|||
Major |
40.2a |
37.2abcdefg |
34.6bcdefghij |
30.7ijklm |
31.1hijklm |
34.7a |
|
Agawtaw |
Minor |
37.6abcdef |
37.8abcdef |
32.9efghijkl |
30.0jklm |
28.3lm |
33.3a |
Off-season |
38.5abc |
38.7abc |
35.9abcdefgh |
31.6hijklm |
30.2jklm |
35.0a |
|
Means |
38.8a |
37.9a |
34.5bc |
30.8d |
29.9d |
34.3a |
|
Major |
37.4abcdefg |
35.7abcdefghi |
33.6cdefghijk |
30.4jklm |
32.4ghijklm |
33.9a |
|
Akuse |
Minor |
40.0a |
35.7abcdefghi |
32.8fghijkl |
30.6ijklm |
28.4lm |
33.5a |
Off-season |
38.0abcde |
39.2ab |
34.6bcdefghij |
29.2klm |
29.5jklm |
34.1a |
|
Means |
38.5a |
36.9ab |
33.7c |
30.1d |
30.1d |
33.8a |
|
Major |
37.4abcdefg |
35.7abcdefghi |
33.6cdefghijk |
30.4jklm |
30.3jklm |
33.5a |
|
Baraku |
Minor |
37.1abcdefg |
38.4abcd |
33.3defghijkl |
30.6ijklm |
27.5m |
33.4a |
Off-season |
37.3abcdefg |
39.2ab |
34.6bcdefghij |
29.2klm |
29.5jklm |
34.0a |
|
Means |
37.3a |
37.8a |
33.8c |
30.1d |
29.1d |
33.6a |
|
Concentrations Grand means 38.2a |
37.5a |
34.0b |
30.3c |
29.7c |
|||
Seasons Mean |
Major |
38.3ab |
36.2bcd |
33.9de |
30.5fgh |
31.3fg |
34.0ab |
Minor |
38.2ab |
37.3abc |
33.0ef |
30.4fgh |
28.1h |
33.4b |
|
Off-season |
37.9ab |
39.0a |
35.0cde |
30.0gh |
29.7gh |
34.3a |
|
CV 4.07 |
|||||||
HSD (0.01); PBZ concentrations =1.2652; seasons=0.8734; soil types=0.8734; PBZ concentration*seasons=2.6219; season*soil= 1.8819; PBZ concentration*soil types=2.6219; PBZ concentrations*seasons*soil types=5.1597. |
*Mean followed by the same alphabets are not significantly different (p>0.01) from each other.
CV: Coefficient of Variation; HSD: Honet Significant Difference; PBZ: Paclobutrazol
Table 2
Respiration rate (mgCO₂ kg-1 h-1) of harvested treated Keitt mango fruits with varied PBZ concentrations applied on different soil types during different production seasons for year two
Soil Type |
Seasons |
Concentrations |
Means |
|||||
0 |
10 |
12.5 |
20 |
25 |
||||
Agawtaw |
Major |
44.3ab |
35.3bcdef |
41.6abc |
34.1bcdef |
27.4f |
36.5a |
|
Minor |
40.7abcd |
35.1bcdef |
31.7cdef |
28.2ef |
25.8f |
32.3ab |
||
Off-season |
41.2abc |
35.9bcdef |
36.1bcdef |
31.8cdef |
29.0def |
34.8ab |
||
Means |
42.1ab |
35.4cd |
36.5bc |
31.4cdef |
27.4ef |
34.6a |
||
Akuse |
Major |
44.3ab |
35.3bcdef |
31.8cdef |
33.3bcdef |
27.4f |
34.4ab |
|
Minor |
40.0bcde |
34.1bcdef |
30.0cdef |
27.8f |
25.8f |
31.5b |
||
Off-season |
52.2a |
33.3bcdef |
36.4bcdef |
30.5cdef |
26.4f |
35.8ab |
||
Means |
45.5a |
34.2cd |
32.7cde |
30.5cdef |
26.5f |
33.9a |
||
Baraku |
Major |
44.3ab |
35.3bcdef |
31.8cdef |
30.5cdef |
27.4f |
33.9ab |
|
Minor |
42.0abc |
35.6bcdef |
31.9cdef |
27.8f |
25.8f |
32.6ab |
||
Off-season |
40.3abcde |
33.3bcdef |
36.4bcdef |
30.5cdef |
26.4f |
33.4ab |
||
Means |
42.2ab |
34.7cd |
33.4cde |
29.6def |
26.5f |
33.3a |
||
Concentrations Grand means 43.3a |
34.8b |
34.2b |
30.5c |
26.8d |
||||
Seasons Mean |
Major |
44.3a |
35.3bc |
35.1bc |
32.6cd |
27.4de |
34.9a |
|
Minor |
40.9ab |
34.9bc |
31.2cde |
27.9de |
25.8e |
32.1b |
||
Off-season |
44.6a |
34.2c |
36.3bc |
30.9cde |
27.3de |
34.6a |
||
CV 9.57; HSD (0.01); PBZ concentrations =2.9709; Seasons=2.0510; Soil types=2.0510; PBZ concentration*seasons=6.1568; season*Soil= 4.4191; PBZ concentration*soil types=6.1568; PBZ concentrations*seasons*soil types=12.116. |
*Mean followed by the same alphabets are not significantly different (p>0.01) from each other.
CV: Coefficient of Variation; HSD: Honet Significant Difference; PBZ: Paclobutrazol
Table 3
Respiration rate (mgCO₂ kg-1 h-1) of harvested treated Keitt mango fruits with varied PBZ concentrations applied on different soil types during different production seasons for year three
Soil Type |
Seasons |
Concentrations |
Means |
||||
0 |
10 |
12.5 |
20 |
25 |
|||
Agawtaw |
Major |
38.7abc * |
37.5bc |
38.6abc |
29.5ef |
29.4ef |
34.7a |
Minor |
40.0abc |
37.0bcd |
37.2bcd |
28.4ef |
26.3f |
33.8ab |
|
Off-season |
40.47ab |
37.9abc |
37.3bcd |
30.2ef |
28.8ef |
34.9a |
|
Means |
39.7a |
37.5abc |
37.7abc |
29.4e |
28.2e |
34.5a |
|
Major |
38.7abc |
37.5bc |
35.3cd |
29.5ef |
27.5ef |
33.7ab |
|
Akuse |
Minor |
37.9abc |
37.5abc |
32.4de |
29.5ef |
26.2f |
32.7b |
Off-season |
42.5a |
36.8bcd |
36.2bcd |
28.9ef |
28.3ef |
34.5a |
|
Means |
39.7a |
37.3 abc |
34.6d |
29.3e |
27.3e |
33.6b |
|
Baraku |
Major |
38.7abc |
37.5bc |
35.6bcd |
29.5ef |
27.5ef |
33.8ab |
Minor |
40.6ab |
37.1bcd |
36.5bcd |
29.5ef |
26.2f |
34.0ab |
|
Off-season |
39.3abc |
36.8bcd |
36.2bcd |
28.9ef |
28.3ef |
33.9ab |
|
Means |
39.5ab |
37.1cd |
36.1cd |
29.3e |
27.3e |
33.9ab |
|
Concentrations Grand means 39.7a |
37.3b |
36.1b |
29.3c |
27.6d |
|||
Seasons Mean |
Major |
38.7abc |
37.5bcd |
36.5cd |
29.5e |
28.1ef |
34.1ab |
Minor |
39.5ab |
37.2bcd |
35.3d |
29.1e |
26.2f |
33.5b |
|
Off-season |
40.8a |
37.2bcd |
36.6cd |
29.3e |
28.5ef |
34.5a |
|
CV 3.92; HSD (0.01); PBZ concentrations =1.2189; seasons=0.8415; soil types=0.8415; PBZ concentration*seasons=2.5261; season*Soil= 1.8132; PBZ concentration*soil types=2.5261; PBZ concentrations*seasons*soil types=4.9712. |
*Mean followed by the same alphabets are not significantly different (p>0.01) from each other.
CV: Coefficient of Variation; HSD: Honet Significant Difference; PBZ: Paclobutrazol
In addition to ethylene biosynthesis inhibition, PBZ interacts with other plant hormones to further suppress ethylene production. One such interaction occurs with ABA, a key phytohormone known to counteract ethylene synthesis. PBZ treatment enhances ABA accumulation, which inhibits ACS and ACO activity and further reduces ethylene biosynthesis (Kumar et al., 2021). Additionally, PBZ mitigates oxidative stress, which is a known inducer of ethylene production. Reactive Oxygen Species (ROS), particularly hydrogen peroxide (H2O2), enhance ACS and ACO activity under stress conditions, accelerating fruit ripening (Khan et al., 2023). By reducing ROS accumulation and enhancing antioxidant enzyme activity, PBZ indirectly suppresses ethylene synthesis and prolongs fruit storage life (Patel et al., 2022). Furthermore, PBZ delays fruit softening by inhibiting ethylene-induced expression of cell wall-degrading enzymes, such as polygalacturonase, cellulase, and pectin methylesterase, thereby preserving fruit firmness and preventing postharvest deterioration (Elad, 1997). In addition to PBZ application type played a significant role in ethylene production (Khan et al., 2020), with mangoes grown on Agawtaw soil consistently exhibiting higher emissions than those grown on Akuse and Baraku soils. This suggests that soil properties, such as organic matter content, nutrient availability, and moisture retention, influence ethylene biosynthesis (Spokas et al., 2010). The likely higher organic matter and nutrient content in the Agawtaw soil may have promoted greater metabolic activity, leading to increased ethylene production. In contrast, Baraku and Akuse soils, which are potentially more compact or nutrient-deficient, may have imposed mild physiological constraints on ethylene biosynthesis, leading to lower ethylene emissions (Medina and Aguiar, 2017). Seasonal variability further impacts ethylene production (Li et al., 2022), with off-season mangoes exhibiting signify-scantly higher ethylene emissions com-pared to those harvested in the major and minor seasons. This trend was observed consistently over the 3-year study period and was attributed to climatic fluctuations, particularly changes in temperature and humidity, which are known to influence ethylene biosynthesis and accelerate fruit ripening (Biale et al., 2018). Additionally, environmental stressors, such as irregular water availability and fluctuating diurnal temperatures, likely triggered stress-induced ethylene production, a phenome-non commonly reported in studies on tropical fruit physiology (Riaz et al., 2024).
Physical attributes of treated Keitt mango trees
Geometrical diameter of treated Keitt mango fruit
This study revealed a significant (p ≤ 0.01) inverse relationship between PBZ concentration and mango fruit geometrical diameter, with non-treated trees producing the largest fruit, while those treated with the highest PBZ concentration (25 mL) yielded the smallest (Tables 1–3). This reduction in fruit size is primarily due to PBZ’s inhibition of gibberellin biosynthesis, which restricts cell elongation and carbohydrate allocation, thereby limiting fruit expansion (Reddy and Kurian, 2008; Sebastian et al., 2019; Yeshitela et al., 2004).
Table 4
Ethylene production (µL kg-1 h-1) of harvested treated Keitt mango fruits with varied PBZ concentrations applied on different soil types during different production seasons for year one
Soil Type |
Seasons |
Concentrations |
Means |
||||
0 |
10 |
12.5 |
20 |
25 |
|||
Major |
92.4abc |
91.6abc |
86.9c |
76.5d |
69.5d |
83.4a |
|
Agawtaw |
Minor |
99.7a |
97.1abc |
94.4abc |
70.0d |
68.3d |
85.9a |
Off-season |
98.8ab |
95.2abc |
90.0abc |
72.1d |
70.3d |
85.3a |
|
Means |
97.0a |
94.6ab |
90.4b |
72.9c |
69.4c |
84.8a |
|
Major |
92.4abc |
91.6abc |
88.9bc |
70.5d |
69.5d |
82.6a |
|
Akuse |
Minor |
93.8abc |
90.6abc |
95.2abc |
66.5d |
68.8d |
83.0a |
Off-season |
98.3ab |
94.3abc |
95.2abc |
72.3d |
69.8d |
86.0a |
|
Means |
94.8ab |
92.2ab |
93.1ab |
69.8c |
69.4c |
83.8a |
|
Major |
92.4abc |
91.6abc |
88.9bc |
70.5d |
69.5d |
82.6a |
|
Baraku |
Minor |
95.5abc |
92.3abc |
88.9bc |
66.5d |
68.8d |
82.4a |
Off-season |
96.5abc |
94.3abc |
95.2abc |
72.3d |
69.8d |
85.6a |
|
Means |
94.8ab |
92.7ab |
91.0b |
69.8c |
69.4c |
83.5a |
|
concentration Grand means 95.5a |
93.2ab |
91.5b |
70.8c |
69.4c |
|||
Seasons Mean |
Major |
92.4bc |
91.6bc |
88.2c |
72.5d |
69.5d |
82.8b |
Minor |
96.3ab |
93.3abc |
92.8abc |
67.7d |
68.6d |
83.8b |
|
Off-season |
97.9a |
94.6ab |
93.5ab |
72.2d |
70.0d |
85.6a |
|
CV= 3.27; HSD (0.01); PBZ concentrations =2.5153; soil types=1.7365; seasons= 1.7365; PBZ concentrations * seasons= 5.2127; PBZ concentrations * soil types=5.2127; seasons *soil types= 3.7415; PBZ concentrations *seasons *soil types= 10.258. |
*Mean followed by the same alphabets are not significantly different (p>0.01) from each other
CV: Coefficient of Variation; HSD: Honet Significant Difference; PBZ: Paclobutrazol
Table 5
Ethylene production (µL kg-1 h-1) of harvested treated Keitt mango fruits with varied PBZ concentrations applied on different soil types during different production seasons for year two
Soil Type |
Seasons |
Concentrations |
Means |
||||
0 |
10 |
12.5 |
20 |
25 |
|||
Major |
103.4ab |
97.9abcdef |
85.2hi |
68.8jk |
66.8jk |
84.4cde |
|
Agawtaw |
Minor |
102.2abc |
90.6defgh |
88.9efgh |
67.9jk |
63.1k |
82.6de |
Off-season |
107.5a |
90.8defgh |
91.0defgh |
76.17ij |
66.7jk |
86.4abc |
|
Means |
104.4a |
93.1bc |
88.4c |
71.0d |
65.5e |
84.5a |
|
Major |
105.4ab |
102.4abc |
85.2hi |
65.8k |
66.8jk |
85.1bcd |
|
Akuse |
Minor |
100.7abcd |
88.3fgh |
87.3gh |
64.9k |
62.8k |
80.8e |
Off-season |
99.2abcde |
95.7bcdefg |
92.2cdefgh |
88.5fgh |
66.3jk |
88.4ab |
|
Means |
101.8a |
95.5b |
88.2c |
73.1d |
65.3e |
84.8a |
|
Major |
105.4ab |
102.4abc |
85.2hi |
65.8k |
66.8jk |
85.1bcd |
|
Baraku |
Minor |
105.4ab |
91.4defgh |
87.3gh |
64.9k |
62.8k |
82.3de |
Off-season |
103.0ab |
95.7bcdefg |
92.2cdefgh |
88.5fgh |
66.3jk |
89.2a |
|
Means |
104.6a |
96.5b |
88.2c |
73.1d |
65.3e |
85.5a |
|
concentration Grand means 103.6a |
95.0b |
88.3c |
72.4d |
65.4e |
|||
Major |
104.7a |
100.9a |
85.2de |
66.8f |
66.8f |
84.9b |
|
Seasons Mean |
Minor |
102.8a |
90.1bcd |
87.8cde |
65.9f |
62.9f |
81.9c |
Off-season |
103.2a |
94.1b |
91.8bc |
84.4e |
66.4f |
88.0a |
|
CV= 3.27; HSD (0.01); PBZ concentrations =2.5396; soil types=1.7533; seasons= 1.7533; PBZ concentrations * seasons= 5.2630; PBZ concentrations * soil types=5.2630; seasons *soil types= 3.7777; PBZ concentrations *seasons *soil Types= 10.357. |
*Mean followed by the same alphabets are not significantly different (p>0.01) from each other
CV: Coefficient of Variation; HSD: Honet Significant Difference; PBZ: Paclobutrazol
Table 6
Ethylene production (µL kg-1 h-1) of harvested treated Keitt mango fruits with varied PBZ concentrations applied on different soil types during different production seasons for year three
Soil Type |
Seasons |
Concentrations |
Means |
||||
0 |
10 |
12.5 |
20 |
25 |
|||
Major |
103.3abc |
96.7abcde |
96.1abcde |
87.8abcdefghi |
69.3hijk |
90.6a |
|
Agawtaw |
Minor |
105.8ab |
96.3abcde |
85.7bcdefghijk |
69.3hijk |
65.4jk |
84.5a |
Off-season |
108.2a |
95.1abcdef |
87.1abcdefghij |
81.4cdefghijk |
67.0ijk |
87.8a |
|
Means |
105.8a |
96.0ab |
89.6bc |
79.5cd |
67.2e |
87.6a |
|
Major |
105.3ab |
98.2abcd |
88.9abcdefghi |
75.4efghijk |
64.3k |
86.4a |
|
Akuse |
Minor |
103.3abc |
98.4abcd |
88.0abcdefghi |
78.7defghijk |
73.7fghijk |
88.4a |
Off-season |
98.4abcd |
98.8abcd |
92.3abcdefg |
75.3efghijk |
64.4k |
85.8a |
|
Means |
102.3a |
98.8ab |
89.7bc |
76.5de |
67.5e |
86.9a |
|
Major |
103.9ab |
96.7abcde |
89.7abcdefgh |
68.8hijk |
67.3ijk |
85.3a |
|
Baraku |
Minor |
105.8ab |
92.0abcdefg |
85.3bcdefghijk |
70.4ghijk |
64.3k |
83.6a |
Off-season |
106.7ab |
97.4abcde |
88.5abcdefghi |
75.2efghijk |
68.5hijk |
87.3a |
|
Means |
105.5a |
95.4ab |
87.8bc |
71.5de |
66.7e |
85.4a |
|
concentration Grand means 104.5a |
96.6b |
89.1c |
75.8d |
67.1e |
|||
Seasons Mean |
Major |
104.2a |
97.2ab |
91.6b |
77.3cd |
67.0d |
87.4a |
Minor |
105.0a |
95.6ab |
86.3bc |
72.8d |
67.8d |
85.5a |
|
Off-season |
104.4a |
97.1ab |
89.3b |
77.3cd |
66.6d |
86.9a |
|
CV= 6.87; HSD (0.01); PBZ concentrations =5.4479; soil types=3.7611; seasons= 3.7611; PBZ concentrations * seasons= 11.290; PBZ concentrations * soil types=11.290; seasons *soil types= 8.1037; PBZ concentrations *seasons *soil types= 22.218. |
*Mean followed by the same alphabets are not significantly different (p>0.01) from each other
CV: Coefficient of Variation; HSD: Honet Significant Difference; PBZ: Paclobutrazol
Gibberellins play a crucial role in fruit growth by promoting cell division, elongation, and sugar mobilization from leaves to developing fruit. PBZ application disrupts this process, causing carbohydrate accumulation in vegetative tissues rather than in fruit, slowing fruit development (Bai et al., 2021). Furthermore, PBZ suppresses cell wall-loosening enzymes, such as expansions and pectinases, increasing rigidity and further restricting fruit expansion (Medina and Aguiar, 2017).
Additionally, PBZ enhances ABA accumulation, which counteracts gibberellin activity, reducing the fruit growth potential and photosynthetic efficiency and further contributing to a smaller fruit size (Maheshwari et al., 2022).
Soil type significantly influences the fruit diameter, with mangoes grown in Agawtaw soil being the largest, followed by those from Akuse and Baraku soils. The superior performance of Agawtaw soil may be attributed to its higher fertility and water-holding capacity, which supports fruit expansion, whereas Baraku soil, which has a lower fertility, amplified PBZ’s growth-suppressing effects, further reducing fruit size (Fosu and Tetteh, 2008; Yeshitela et al., 2004).
Seasonal variations also played a crucial role, with mangoes harvested in the major season, exhibiting larger fruit diameters due to optimal climatic conditions, including adequate rainfall and moderate temperatures, which enhanced photosynthesis and nutrient uptake. Conversely, minor and off-season fruit was smaller due to water stress and reduced nutrient availability (Litz, 2009; Taiz and Zeiger, 2018).
The interaction among PBZ concentration, soil type, and season further highlights the complexity of fruit development. The largest mangoes were observed in non-treated trees on Agawtaw soil during the major season, while the smallest were recorded in mango treated with 25 mL PBZ on Agawtaw soil in the off-season. This suggests that PBZ effectiveness is highly dependent on environmental conditions (Malhotra et al., 2018), emphasising the need for site-specific PBZ application strategies. Adjusting PBZ concentrations based on soil fertility and seasonal conditions is essential for balancing vegetative growth regulation and optimal fruit development.
At higher concentrations, PBZ suppresses fruit cell division by downregulating cyclin-dependent kinases (CDKs) and mitotic regulators, leading to fewer total cells and permanently smaller fruit (Patel et al., 2022). It also disrupts the gibberellin–auxin balance, causing abnormal fruit morphology compared to non-treated mango, which exhibit normal hormone interactions that support optimal fruit growth (Singh and Singh, 2019).
These findings suggest that although PBZ is effective in managing vegetative growth, its excessive use may negatively impact fruit size, necessitating careful concentration optimisation to prevent undesirable reductions in mango fruit quality.
Table 7
Fruit geometrical diameter (cm) of treated Keitt mango tree with varied PBZ concentrations applied on different soil types during different production seasons for year one
Soil type |
Seasons |
Concentrations |
Means |
||||
0 |
10 |
12.5 |
20 |
25 |
|||
Major |
21.7a* |
19.9abc |
18.6abcde |
17.4abcdef |
16.0cdef |
18.7a |
|
Agawtaw |
Minor |
19.8abc |
18.5abcdef |
17.8abcdef |
15.5cdef |
15.1cdef |
17.3abc |
Off-season |
19.4abc |
18.6abcde |
17.7abcdef |
15.6cdef |
13.7f |
17.0abc |
|
Means |
20.3a |
19.0ab |
18.1abc |
16.2cde |
14.9e |
17.7a |
|
Major |
21.4ab |
19.0abcde |
18.1abcdef |
17.3abcdef |
16.4cdef |
18.4ab |
|
Akuse |
Minor |
19.3abcd |
18.8abcde |
17.0abcdef |
16.3cdef |
15.0cdef |
17.3abc |
Off-season |
19.5abc |
16.8bcdef |
16.2cdef |
16.0cdef |
14.1ef |
16.5c |
|
Means |
20.0a |
18.2abc |
17.1bcde |
16.5bcde |
15.2de |
17.4a |
|
Major |
18.8abcde |
16.7bcdef |
16.6bcdef |
15.3cdef |
14.4def |
16.4c |
|
Baraku |
Minor |
17.4abcdef |
18.2abcdef |
15.8cdef |
15.3cdef |
15.0cdef |
16.3c |
Off-season |
18.6abcde |
17.4abcdef |
16.5bcdef |
16.0cdef |
15.4cdef |
16.8bc |
|
Means |
18.3abc |
17.4bcd |
16.3cde |
15.5de |
14.9e |
16.5b |
|
concentration Grand means 19.5a |
18.2b |
17.2bc |
16.1cd |
15.0d |
|||
Seasons Mean |
Major |
20.6a |
18.5abc |
17.8bcd |
16.7cdef |
15.6def |
17.8a |
Minor |
18.8abc |
18.5abc |
16.9bcde |
15.7def |
15.0ef |
17.0b |
|
Off-season |
19.2ab |
17.6bcd |
16.8bcdef |
15.9def |
14.4f |
16.8b |
|
CV= 7.64 |
|||||||
HSD (0.01); PBZ concentrations =1.2030; soil types=0.8306; seasons= 0.8306; PBZ concentrations * seasons= 2.4932; PBZ concentrations * soil types=2.4932; seasons *soil types= 1.7895; PBZ concentrations *seasons *soil types= 4.9064. |
*Mean followed by the same alphabets are not significantly different (p>0.01) from each other
CV: Coefficient of Variation; HSD: Honet Significant Difference; PBZ: Paclobutrazol
Table 8
Fruit geometrical diameter (cm) of treated Keitt mango tree with varied PBZ concentrations applied on different soil types during different production seasons for year two
Soil type |
Seasons |
Concentrations |
Means |
||||
0 |
10 |
12.5 |
20 |
25 |
|||
Major |
21.1a* |
18.9abc |
17.1abcdefgh |
17.4abcdefg |
14.9cdefgh |
17.9a |
|
Agawtaw |
Minor |
18.4abcd |
16.8bcdefgh |
17.7abcdef |
14.9cdefgh |
14.0efgh |
16.3abc |
Off-season |
17.8abcdef |
16.9bcdefgh |
16.6bcdefgh |
15.8bcdefgh |
13.7efgh |
16.2bc |
|
Means |
19.1a |
17.5ab |
17.2abc |
16.0bcde |
14.2de |
16.8a |
|
Major |
20.0ab |
17.4abcdefg |
16.7bcdefgh |
15.5cdefgh |
14.1efgh |
16.8ab |
|
Akuse |
Minor |
18.6abcd |
17.5abcdefg |
15.8bcdefgh |
15.4cdefgh |
14.5defgh |
16.4abc |
Off-season |
17.7abcdef |
17.0abcdefgh |
14.7cdefgh |
14.6defgh |
13.2gh |
15.4bc |
|
Means |
18.8a |
17.3abc |
15.7bcde |
15.2cde |
14.0e |
16.2a |
|
Major |
16.9abcdefgh |
15.5cdefgh |
15.9bcdefgh |
14.4defgh |
13.1h |
15.2c |
|
Baraku |
Minor |
17.6abcdef |
16.7bcdefgh |
15.2cdefgh |
13.6fgh |
13.3gh |
15.3bc |
Off-season |
17.9abcde |
16.6bcdefgh |
15.1cdefgh |
14.5defgh |
15.3cdefgh |
15.9bc |
|
Means |
17.5ab |
16.3bcd |
15.4bcde |
14.2de |
13.9e |
15.4b |
|
concentration Grand means 18.4a |
17.0b |
16.1bc |
15.1c |
14.0d |
|||
Seasons Mean |
Major |
19.4a |
17.3abcd |
16.6bcdef |
15.8cdefgh |
14.0h |
16.6a |
Minor |
18.2ab |
17.0bcde |
16.2bcdefg |
14.6fgh |
13.9h |
16.0ab |
|
Off-season |
17.8abc |
16.8bcde |
15.5defgh |
14.9efgh |
14.1gh |
15.8b |
|
CV= 7.08; HSD (0.01); PBZ concentrations =1.0453; soil types=0.7216; seasons=0.7216; PBZ concentrations * seasons= 2.1662; PBZ concentrations * soil types=2.1662; seasons *soil types= 1.5548; PBZ concentrations *seasons *soil types= 4.2629. |
*Mean followed by the same alphabets are not significantly different (p>0.01) from each other
CV: Coefficient of Variation; HSD: Honet Significant Difference; PBZ: Paclobutrazol
Table 9
Fruit geometrical diameter (cm) of treated Keitt mango tree with varied PBZ concentrations applied on different soil types during different production seasons for year three
Soil Type |
Seasons |
Concentrations |
Means |
||||
0 |
10 |
12.5 |
20 |
25 |
|||
Major |
21.4a* |
19.2abcde |
17.0bcdefghijkl |
15.8defghijklm |
15.1efghijklm |
17.7a |
|
Agawtaw |
Minor |
20.8abc |
17.6abcdefghijk |
15.3efghijklm |
14.5hijklm |
13.0lm |
16.2abc |
Off-season |
17.6abcdefghijk |
14.5hijklm |
15.0efghijklm |
14.1jklm |
12.7 m |
14.8c |
|
Means |
19.9a |
17.1bcde |
15.8defgh |
14.8fghi |
13.6i |
16.2a |
|
Major |
21.0ab |
19.1abcde |
17.1bcdefghijkl |
15.8defghijklm |
13.4klm |
17.3a |
|
Akuse |
Minor |
19.1abcde |
17.9abcdefghij |
15.9defghijklm |
14.6ghijklm |
13.4klm |
16.2abc |
Off-season |
18.8abcdefg |
17.6abcdefghijk |
15.9defghijklm |
15.2efghijklm |
14.2jklm |
16.4ab |
|
Means |
19.6a |
18.2abc |
16.3cdef |
15.2efghi |
13.7hi |
16.6a |
|
Major |
18.7abcdefgh |
18.2abcdefghij |
16.6cdefghijklm |
14.7fghijklm |
13.9jklm |
16.4ab |
|
Baraku |
Minor |
18.9abcdef |
16.9bcdefghijklm |
15.6defghijklm |
13.1lm |
13.4klm |
15.6bc |
Off-season |
18.5abcdefghi |
18.5abcdefghi |
16.1defghijklm |
14.3ijklm |
13.5klm |
16.5ab |
|
Means |
19.2ab |
17.9abcd |
16.1cdefg |
14.1ghi |
13.5i |
16.2a |
|
concentration Grand means 19.6a |
17.7b |
16.1c |
14.7d |
13.6e |
|||
Seasons Mean |
Major |
20.4a |
18.8abc |
16.9cd |
15.4def |
14.1efg |
17.1a |
Minor |
19.6ab |
17.5bcd |
15.6def |
14.1efg |
13.2g |
16.0b |
|
Off-season |
18.7abc |
16.9cd |
15.7de |
14.5efg |
13.5fg |
15.9b |
|
CV= 7.03; HSD (0.01); PBZ concentrations =1.0506; soil types=0.7253; seasons=0.7253; PBZ concentrations * seasons= 2.1773; PBZ concentrations * soil types=2.1773; seasons *soil types= 1.5628; PBZ concentrations *seasons *soil types= 4.2847. |
*Mean followed by the same alphabets are not significantly different (p>0.01) from each other
CV: Coefficient of Variation; HSD: Honet Significant Difference; PBZ: Paclobutrazol
Density of treated Keitt mango fruit
PBZ application significantly reduced mango fruit density, with non-treated trees consistently producing denser fruit than PBZ-treated trees. Over 3 years, mean densities of 1.71, 1.53, and 1.55 gcm–³ were recorded in non-treated trees, whereas those treated with the highest PBZ concentration (25 mL) had the lowest densities (1.25–1.33 gcm–³). This inverse relationship between PBZ concentration and fruit density is linked to its effects on gibberellin inhibition, carbohydrate metabolism, cell wall modification, and water retention (Singh and Singh, 2019). PBZ suppresses gibberellin biosynthesis by inhibiting ent-kaurene oxidase, limiting cell division and expansion and leading to smaller, denser cells. However, at higher PBZ concentrations, excessive gibberellin suppression restricts intercellular expansion, increasing air spaces, and reducing the overall fruit density (Rademacher, 2016). Additionally, PBZ alters carbohydrate partitioning by diverting sugars to vegetative tissues instead of fruit development, thus reducing dry matter accumulation and fruit density (Bai et al., 2021). Research has shown that PBZ-treated mango trees exhibit increased leaf carbohydrate retention at the expense of fruit growth, contributing to decreased pulp firmness (Lalel et al., 2020). Soil type significantly influenced fruit density, with Agawtaw soil producing the densest fruit across all 3 years (1.54, 1.33, and 1.49 gcm–³), while Baraku soil yielded the lowest, especially in PBZ-treated trees. Agawtaw soil’s high organic matter and superior water retention supported optimal root function and fruit development, enhancing carbo-hydrate accumulation and improving fruit density (Brady and Weil, 2017). However, Baraku soil, with low fertility and poor nutrient retention, exacerbated PBZ’s negative effects by further restricting sugar accumulation in fruit tissues (Scholtz, 2020). Akuse soil, which exhibited intermediate density values, likely had moderate nutrient availability, limiting its capacity to support fruit growth under PBZ application (Lal and Stewart, 2015). Seasonal variations also played a crucial role, with fruit from the major season consistently exhibiting higher densities (1.56, 1.40 and 1.42 g cm–³ across 3 years) compared to that from the minor season and off-season. The higher densities in the major season were due to favourable climatic conditions, including adequate rainfall, moderate temperatures, and high solar radiation, which enhanced sugar accumulation and strengthened cell walls (Litz, 2009). Conversely, minor and off-season fruit had lower densities due to irregular rainfall and temperature fluctu-ations, which restricted carbohydrate translocation. However, in the third year, off-season fruit (1.46 g cm–³) was slightly denser than minor-season fruit (1.38 g cm–³), suggesting improved environmen-tal conditions or adaptive physiological responses (Yadav et al., 2013). PBZ also impacts fruit density by influencing cell wall composition and water retention. Gibberellins regulate enzymes, such as expansions and pectinases, which facilitate cell wall loosening. PBZ downregulates these enzymes, increasing cell rigidity but also creating more air pockets and reducing fruit density (Medina and Aguiar, 2017). Additionally, PBZ-induced ABA accumulation reduces stomatal conductance, limiting water uptake and further decreasing fruit density (Maheshwari et al., 2022). At the cellular level, PBZ suppresses mitotic activity by inhibiting CDKs, leading to fewer, loosely packed cells, increasing fruit porosity, and reducing density (Patel et al., 2022).
Table 10
Fruit density (g cm–³) of treated Keitt mango tree with varied PBZ concentrations applied on different soil types during different production seasons for year one
Soil Type |
Seasons |
Concentrations |
Means |
||||
0 |
10 |
12.5 |
20 |
25 |
|||
Major |
2.07a* |
1.75ab |
1.51ab |
1.39ab |
1.36ab |
1.61a |
|
Agawtaw |
Minor |
1.85ab |
1.83ab |
1.82ab |
1.30b |
1.32b |
1.62a |
Off-season |
1.50ab |
1.55ab |
1.39ab |
1.27b |
1.19b |
1.38ab |
|
Means |
1.81a |
1.71ab |
1.57abcde |
1.32cde |
1.29de |
1.54a |
|
Major |
1.79ab |
1.72ab |
1.67ab |
1.27b |
1.21b |
1.53a |
|
Akuse |
Minor |
1.60ab |
1.64ab |
1.48ab |
1.25b |
1.31b |
1.46ab |
Off-season |
1.60ab |
1.55ab |
1.34b |
1.21b |
1.17b |
1.38ab |
|
Means |
1.67abc |
1.64abcd |
1.49abcde |
1.25e |
1.23e |
1.45ab |
|
Major |
1.84ab |
1.51ab |
1.56ab |
1.45ab |
1.35b |
1.54a |
|
Baraku |
Minor |
1.45ab |
1.24b |
1.17b |
1.21b |
1.14b |
1.24b |
Off-season |
1.65ab |
1.48ab |
1.52ab |
1.37ab |
1.23b |
1.45ab |
|
Means |
1.65abcd |
1.41bcde |
1.42bcde |
1.34bcde |
1.24e |
1.41b |
|
concentration Grand means 1.71a |
1.59ab |
1.49b |
1.30c |
1.25c |
|||
Major |
1.90a |
1.66ab |
1.58abcd |
1.37bcde |
1.31bcde |
1.56a |
|
Seasons Mean |
Minor |
1.63abc |
1.57abcd |
1.49bcde |
1.26de |
1.26de |
1.44ab |
Off-season |
1.58abcd |
1.53bcde |
1.41bcde |
1.29cde |
1.20e |
1.40b |
|
CV= 13.17; HSD (0.01); PBZ concentrations =0.1771; soil types=0.1223; seasons= 0.1223; PBZ concentrations * seasons= 0.3670; PBZ concentrations * soil types=0.3670; seasons *soil types= 0.2634; PBZ concentrations *seasons *soil types= 0.7223. |
*Mean followed by the same alphabets are not significantly different (p>0.01) from each other
CV: Coefficient of Variation; HSD: Honet Significant Difference; PBZ: Paclobutrazol
Table 11
Fruit density (g cm–³) of treated Keitt mango tree with varied PBZ concentrations applied on different soil types during different production seasons for year two
Soil Type |
Seasons |
Concentrations |
Means |
||||
0 |
10 |
12.5 |
20 |
25 |
|||
Major |
1.91a* |
1.62ab |
1.17b |
1.10b |
1.30ab |
1.42a |
|
Agawtaw |
Minor |
1.45ab |
1.30ab |
1.13b |
1.24ab |
1.22ab |
1.27a |
Off-season |
1.49ab |
1.25ab |
1.17b |
1.36ab |
1.24ab |
1.30a |
|
Means |
1.62a |
1.39abc |
1.16c |
1.23bc |
1.25bc |
1.33a |
|
Major |
1.62ab |
1.39ab |
1.30ab |
1.10b |
1.26ab |
1.33a |
|
Akuse |
Minor |
1.34ab |
1.32ab |
1.23ab |
1.34ab |
1.12b |
1.27a |
Off-season |
1.40ab |
1.22ab |
1.24ab |
1.17b |
1.12b |
1.23a |
|
Means |
1.45abc |
1.31abc |
1.26bc |
1.20bc |
1.17bc |
1.28a |
|
Major |
1.77ab |
1.59ab |
1.35ab |
1.34ab |
1.22ab |
1.46a |
|
Baraku |
Minor |
1.40ab |
1.49ab |
1.37ab |
1.24ab |
1.22ab |
1.34a |
Off-season |
1.39ab |
1.41ab |
1.34ab |
1.24ab |
1.17b |
1.31a |
|
Means |
1.52ab |
1.49abc |
1.35abc |
1.27abc |
1.20bc |
1.37a |
|
concentration Grand means 1.53a |
1.40ab |
1.26bc |
1.24bc |
1.21c |
|||
Seasons Mean |
Major |
1.77a |
1.53ab |
1.27b |
1.18b |
1.26b |
1.40a |
Minor |
1.40b |
1.37b |
1.24b |
1.27b |
1.19b |
1.29ab |
|
Off-season |
1.43ab |
1.29b |
1.25b |
1.26b |
1.18b |
1.28b |
|
CV= 14.30; HSD (0.01); PBZ concentrations =0.1734; soil types=0.1197; seasons= 0.1197; PBZ concentrations * seasons= 0.3594; PBZ concentrations * soil types=0.3594; seasons *soil types= 0.2580; PBZ concentrations *seasons *soil types= 0.7073. |
*Mean followed by the same alphabets are not significantly different (p>0.01) from each other
CV: Coefficient of Variation; HSD: Honet Significant Difference; PBZ: Paclobutrazol
Table 12
Fruit density (g cm–³) of treated Keitt mango tree with varied PBZ concentrations applied on different soil types during different production seasons for year three
Soil Type |
Seasons |
Concentrations |
Means |
||||
0 |
10 |
12.5 |
20 |
25 |
|||
Major |
1.71a* |
1.45a |
1.37a |
1.41a |
1.56a |
1.47a |
|
Agawtaw |
Minor |
1.91a |
1.45a |
1.30a |
1.27a |
1.41a |
1.47a |
Off-season |
1.56a |
1.30a |
1.51a |
1.63a |
1.60a |
1.52a |
|
Means |
1.73a |
1.40ab |
1.34ab |
1.44ab |
1.52ab |
1.49a |
|
Major |
1.73a |
1.37a |
1.22a |
1.26a |
1.44a |
1.43a |
|
Akuse |
Minor |
1.32a |
1.29a |
1.19a |
1.46a |
1.57a |
1.36a |
Off-season |
1.45a |
1.26a |
1.27a |
1.27a |
1.49a |
1.35a |
|
Means |
1.50ab |
1.31b |
1.28b |
1.33b |
1.50ab |
1.38a |
|
Major |
1.54a |
1.35a |
1.29a |
1.30a |
1.29a |
1.35a |
|
Baraku |
Minor |
1.38a |
1.24a |
1.32a |
1.21a |
1.31a |
1.29a |
Off-season |
1.33a |
1.53a |
1.54a |
1.66a |
1.54a |
1.52a |
|
Means |
1.42ab |
1.37ab |
1.38ab |
1.39ab |
1.38ab |
1.39a |
|
concentration Grand means 1.55a |
1.36ab |
1.33b |
1.39ab |
1.47ab |
|||
Seasons Mean |
Major |
1.66a |
1.39a |
1.29a |
1.32a |
1.43a |
1.42a |
Minor |
1.54a |
1.33a |
1.27a |
1.31a |
1.43a |
1.38a |
|
Off-season |
1.45a |
1.36a |
1.44a |
1.52a |
1.54 a |
1.46a |
|
CV= 14.80; HSD (0.01); PBZ concentrations =0.1924; soil types=0.1328; seasons= 0.1328; PBZ concentrations * seasons= 0.3987; PBZ concentrations * soil types=0.3987; seasons *soil types= 0.2862; PBZ concentrations *seasons *soil types= 0.7846. |
*Mean followed by the same alphabets are not significantly different (p>0.01) from each other
CV: Coefficient of Variation; HSD: Honet Significant Difference; PBZ: Paclobutrazol
These findings highlight the complex interactions between PBZ, soil properties, and seasonal conditions in regulating mango fruit density. Although PBZ effectively controls vegetative growth, excessive concentrations may compromise fruit quality by reducing the density. Optimising the PBZ concentration based on soil fertility and seasonal conditions can help mitigate these negative effects and sustain fruit quality.
Ripe fruit firmness of treated Keitt mango
PBZ application significantly enhanced fruit firmness across all 3 years, with higher concentrations (25 mL) consistently producing firmer fruit (46.0–46.3 N). In contrast, non-treated trees produced the least firm fruit, with values ranging from 39.9 to 41.0 N. The increase in firmness with PBZ application can be attributed to several physiological mechanisms. PBZ inhibits gibberellin biosynthesis, leading to reduced cell expansion and enhanced lignification, which strengthens the fruit structure (Kumar, 2023). Furthermore, PBZ increases calcium and pectin deposition, fortifying cell walls and delaying enzymatic degradation during ripening (Reddy and Kurian, 2008). PBZ-treated mangoes have also been reported to exhibit reduced polygalacturonase and pectin methylesterase activities, which are responsible for breaking down cell wall components during ripening (Lobo and Sidhu, 2017). The findings of this study align with those of previous research showing that PBZ improves firmness in fruit crops by promoting cell wall reinforcement and delaying ethylene-mediated softening (Srivastava and Dwivedi, 2000). However, while PBZ enhances fruit firmness, excessive concentrations may lead to stress-induced metabolic imbalances, necessitating precise concentration optimisation for maintaining fruit quality without compromising plant physiology. The soil type significantly influenced firmness outcomes, with variations observed across the years. In the first year, Akuse soil yielded the firmest fruit (42.8 N), while Baraku soil produced the firmest fruit in the second and third years, with values of 43.0 N and 43.9 N, respectively. Agawtaw soil produced consistently high firmness values across all years, indicating its ability to support optimal fruit development under PBZ treatments.
The role of soil fertility in modulating fruit firmness is well established. Well-structured soils rich in organic matter, such as Agawtaw, facilitate efficient calcium uptake, which is essential for stabilising pectin within the fruit’s middle lamella, thereby enhancing firmness (Brady and Weil, 2017). Calcium plays a crucial role in cross-linking pectin molecules, strengthening cell walls, and reducing enzymatic degradation during ripening (White and Broadley, 2003). Baraku soil, despite its lower fertility compared to Agawtaw soil, exhibited improved firmness levels under higher PBZ concentrations. This suggests that in nutrient-limited soils, PBZ may enhance firmness by improving resource allocation efficiency and compensating for deficiencies in organic matter and micronutrients (Scholtz, 2020). However, Akuse soil, which initially produced firmer fruit, was outperformed by Baraku soil in later years. This could be attributed to Akuse soil’s moderate cation exchange capacity (CEC), which may have limited the long-term availability of calcium and potassium, both of which are essential for maintaining fruit firmness (Sebastian et al., 2019). These findings highlight the importance of tailoring PBZ application to specific soil conditions to optimise fruit firmness outcomes. Nutrient management strategies, including calcium supplementation, may be necessary to sustain long-term firmness improvements, particularly in soils with lower fertility. Seasonal variations significantly influenced fruit firmness, with the off-season producing the firmest fruit in the first and second years (42.8 and 43.6 N, respectively). However, in the third year, the major season yielded the highest mean firmness (43.9 N). The minor season consistently exhibited intermediate firmness values, reflecting a transitional effect between the favourable conditions of the major season and the environmental stressors of the off-season.
The increased firmness observed during the minor season and off-season can be attributed to slower vegetative growth, which allows for extended cell wall thickening and structural reinforcement. Cooler temperatures and reduced growth rates during these seasons promote the accumulation of structural carbohydrates, such as cellulose and hemicellulose, leading to firmer fruit (Patanè and Cosentino, 2010). In contrast, fruit harvested during the major season, characterised by rapid growth and higher temperatures, exhibited slightly reduced firmness due to accelerated ripening and increased enzymatic softening (Litz, 2009).
Table 13
Ripe fruit firmness (N) of treated Keitt mango tree with varied PBZ concentrations applied on different soil types during different production seasons for year one
Soil Type |
Seasons |
Concentrations |
Means |
||||
0 |
10 |
12.5 |
20 |
25 |
|||
Major |
39.9cde* |
43.6abcde |
42.3abcde |
41.4abcde |
44.7abcde |
42.4a |
|
Agawtaw |
Minor |
39.6cde |
41.2abcde |
41.8abcde |
40.9bcde |
47.9a |
42.3a |
Off-season |
40.2cde |
41.6abcde |
45.2abcde |
44.0abcde |
45.2abcde |
43.2a |
|
Means |
39.9bc |
42.1bc |
43.1ab |
42.1bc |
45.9a |
42.6a |
|
Major |
41.7abcde |
43.9abcde |
42.0abcde |
42.1abcde |
46.0abcd |
43.1a |
|
Akuse |
Minor |
40.2cde |
41.4abcde |
41.3abcde |
43.2abcde |
46.2abcd |
42.5a |
Off-season |
39.4de |
40.8bcde |
43.4abcde |
43.4abcde |
46.4abc |
42.7a |
|
Means |
40.4bc |
42.1bc |
42.3bc |
42.9ab |
46.2a |
42.8a |
|
Major |
39.8cde |
40.6cde |
40.1cde |
41.1abcde |
44.1abcde |
41.2a |
|
Baraku |
Minor |
38.9e |
42.8abcde |
43.6abcde |
43.6abcde |
47.1ab |
43.2a |
Off-season |
39.5de |
42.6abcde |
42.6abcde |
42.0abcde |
46.2abcd |
42.6a |
|
Means |
39.4c |
42.0bc |
42.1bc |
42.3bc |
45.8a |
42.3a |
|
concentration Grand means 39.9c |
42.1b |
42.5b |
42.4b |
46.0a |
|||
Seasons Mean |
Major |
40.5def |
42.7bcdef |
41.5cdef |
41.5cdef |
44.9abc |
42.2a |
Minor |
39.7f |
41.8cdef |
42.3cdef |
42.6bcdef |
47.1a |
42.7a |
|
Off-season |
39.7ef |
41.7cdef |
43.7abcd |
43.1bcde |
45.9ab |
42.8a |
|
CV= 4.32; HSD (0.01); PBZ concentrations =1.6836; soil types=1.1623; seasons= 1.1623; PBZ concentrations * seasons= 3.4891; PBZ concentrations * soil types=3.4891; seasons *soil types= 2.5044; PBZ concentrations *seasons *soil types= 6.8663. |
*Mean followed by the same alphabets are not significantly different (p>0.01) from each other
CV: Coefficient of Variation; HSD: Honet Significant Difference; PBZ: Paclobutrazol
Table 14
Ripe fruit firmness (N) of treated Keitt mango tree with varied PBZ concentrations applied on different soil types during different production seasons for year two
Soil Type |
Seasons |
Concentrations |
Means |
||||
0 |
10 |
12.5 |
20 |
25 |
|||
Major |
41.9ab* |
42.3ab |
46.0ab |
42.4ab |
44.3ab |
43.4a |
|
Agawtaw |
Minor |
39.2b |
41.3ab |
42.3ab |
42.5ab |
46.4ab |
42.3a |
Off-season |
40.2ab |
45.6ab |
41.4ab |
42.6ab |
47.5a |
43.5a |
|
Means |
40.4c |
43.0abc |
43.2abc |
42.5bc |
46.1ab |
43.1a |
|
Major |
21.4ab |
41.7ab |
42.7ab |
42.3ab |
46.3ab |
42.8a |
|
Akuse |
Minor |
41.0ab |
43.8ab |
42.9ab |
41.8ab |
46.4ab |
43.2a |
Off-season |
40.4ab |
43.4ab |
45.6ab |
44.7ab |
47.1ab |
44.2a |
|
Means |
40.9c |
43.0abc |
43.8abc |
42.9abc |
46.6a |
43.4a |
|
Major |
39.5b |
43.2ab |
41.4ab |
142.3ab |
43.8ab |
42.0a |
|
Baraku |
Minor |
40.2ab |
43.7ab |
42.6ab |
44.4ab |
47.9a |
43.8a |
Off-season |
40.8ab |
42.0ab |
42.5ab |
43.8ab |
46.2ab |
43.1a |
|
Means |
40.2c |
43.0abc |
42.2bc |
43.5abc |
46.0ab |
43.0a |
|
concentration Grand means 40.5c |
43.0b |
43.1b |
43.0b |
46.2a |
|||
Major |
40.9bc |
42.4bc |
43.4abc |
42.3bc |
44.8ab |
42.6a |
|
Seasons Mean |
Minor |
40.1c |
42.9abc |
42.6bc |
42.9abc |
46.9a |
43.1a |
Off-season |
40.5c |
43.7abc |
43.2abc |
43.7abc |
46.9a |
43.6a |
|
CV= 4.95; HSD (0.01); PBZ concentrations =1.9561; soil types=1.3505; seasons= 1.3505; PBZ concentrations * seasons= 4.0539; PBZ concentrations * soil types=4.0539; seasons *soil types= 2.9098; PBZ concentrations *seasons *soil types= 7.9778. |
*Mean followed by the same alphabets are not significantly different (p>0.01) from each other
CV: Coefficient of Variation; HSD: Honet Significant Difference; PBZ: Paclobutrazol
Table 15
Ripe fruit firmness (N) of treated Keitt mango tree with varied PBZ concentrations applied on different soil types during different production seasons for year three
Soil Type |
Seasons |
Concentrations |
Means |
||||
0 |
10 |
12.5 |
20 |
25 |
|||
Major |
43.5ab* |
43.7ab |
43.8ab |
44.1ab |
46.1ab |
44.2a |
|
Agawtaw |
Minor |
40.8ab |
43.6ab |
41.7ab |
44.5ab |
46.1ab |
43.3a |
Off-season |
39.9b |
41.9ab |
43.4ab |
41.5ab |
47.1ab |
42.8a |
|
Means |
41.4de |
143.1bcde |
43.0bcde |
43.4abcde |
46.4ab |
43.4a |
|
Major |
42.0ab |
43.3ab |
43.7ab |
44.3ab |
45.8ab |
43.8a |
|
Akuse |
Minor |
40.5ab |
41.8ab |
42.3ab |
42.0ab |
45.0ab |
42.3a |
Off-season |
42.0ab |
41.8ab |
41.0ab |
42.7ab |
44.7ab |
42.4a |
|
Means |
41.5de |
42.3cde |
42.3cde |
43.0bcde |
45.2abcd |
42.9a |
|
Major |
39.9b |
43.3ab |
46.4ab |
42.2ab |
46.9ab |
43.7a |
|
Baraku |
Minor |
40.4ab |
43.5ab |
46.0ab |
43.1ab |
47.8a |
44.2a |
Off-season |
39.7b |
43.2ab |
46.2ab |
43.1ab |
46.9ab |
43.8a |
|
Means |
40.0e |
43.3bcde |
46.2abc |
42.8bcde |
47.2a |
43.9a |
|
concentration Grand means 41.0c |
42.9b |
43.8b |
43.1b |
46.3a |
|||
Major |
41.8cd |
43.4abcd |
44.6abc |
43.5abcd |
46.3ab |
43.9a |
|
Seasons Mean |
Minor |
40.6d |
43.9abcd |
43.3abcd |
43.2abcd |
46.3a |
43.3a |
Off-season |
40.5d |
42.3cd |
43.5abcd |
42.4bcd |
46.2ab |
43.0a |
|
CV= 4.70; HSD (0.01); PBZ concentrations =1.8671; soil types=1.2890; seasons= 1.2890; PBZ concentrations * seasons= 3.8694; PBZ concentrations * soil types=3.8694; seasons *soil types= 2.7774; PBZ concentrations *seasons *soil types= 7.6147. |
*Mean followed by the same alphabets are not significantly different (p>0.01) from each other
CV: Coefficient of Variation; HSD: Honet Significant Difference; PBZ: Paclobutrazol
The observed seasonal variations in firmness also suggest an interaction between PBZ application and climatic conditions. Studies indicate that PBZ is more effective in enhancing fruit firmness under moderate climatic conditions, in which slower fruit growth rates allow for the prolonged accumulation of cell wall-strengthening compounds (Kishore et al., 2015). In contrast, high temperatures and rapid fruit expansion during the major season may dilute the effects of PBZ by accelerating metabolic processes that contribute to softening (Yadav et al., 2013).
Chemical parameters of treated Keitt mango trees
Moisture content (%) of treated Keitt mango fruit
PBZ application consistently reduced the MC across all 3 years, with non-treated trees producing the highest MC values (80.9–81.5%) and trees treated with 25 mL exhibiting the lowest MC (76.7–77.6%). The suppressive effect of PBZ on MC was most pronounced in fruit grown on Baraku soil during the minor season, in which the lowest MC values were recorded (74.6% in the first year and 73.1% in the third year) (Tables 16–18). The observed reduction in MC aligns with PBZ’s physiological effects on plant water relations. By inhibiting gibberellin biosynthesis, PBZ limits vegetative growth and reduces transpiration, decreasing water uptake and movement to fruit tissues (Kumar, 2023). PBZ has also been reported to suppress xylem differentiation, further restricting water transport to reproductive structures (Reddy and Kurian, 2008). Similar trends have been observed in other fruit crops, in which PBZ-induced reductions in hydraulic conductivity lead to lower fruit hydration levels (Srivastava and Dwivedi, 2000). Despite PBZ’s overall suppressive effect on MC, moderate application rates (10–15 mL) maintained relatively higher hydration levels while still controlling vegetative growth. Lobo and Sidhu (2017) reported that moderate PBZ concentrations balanced water conservation and fruit firmness, thereby improving postharvest quality. These findings suggest that optimising PBZ concentrations is essential for sustaining fruit moisture and achieving growth regulation benefits. Soil fertility and water retention significantly influenced MC across all PBZ treatments and seasons. Akuse and Agawtaw soils consistently supported the highest mean MC values (79.3–79.7%), while Baraku soil yielded the lowest values (77.0–77.8%). The higher MC levels observed in fruit grown on Akuse and Agawtaw soils could be attributed to their superior organic matter content and water-holding capacity, which facilitate sustained water availability for fruit development (Brady and Weil, 2017). These results align with those of White and Broadley (2003), who emphasised that well-structured soils enhance root hydraulic conductivity, improving water absorption and translocation within plants. In contrast, Baraku soil, characterised by a lower water retention and reduced CEC, amplified PBZ’s restrictive effects on fruit hydration. Lal and Stewart (2015) and Sebastian et al. (2019) showed that nutrient-poor soils exacerbated water stress conditions, limiting fruit moisture retention. The lowest MC values (73.1%) were recorded in fruit grown on Baraku soil under 25 mL PBZ, underscoring the compounded effects of soil infertility and growth regulator-induced water limitations on fruit hydration. Seasonal variations significantly influenced MC, with the major season generally producing the highest values, while the off-season consistently yielded the lowest values. In the first and second years, the major season recorded the highest MC (79.3 and 78.7%, respectively), while in the third year, the minor season marginally surpassed the major season (79.2 and 79.0%). The off-season consistently recorded the lowest MC (78.2–78.4%). The higher MC values observed in the major and minor seasons were attributed to favourable climatic conditions, including optimal rainfall and humidity, which enhance water absorption and retention in fruit pulp (Litz, 2009). Increased soil moisture during these periods facilitated sustained xylem flow, leading to higher fruit hydration levels. Conversely, off-season fruit exhibited lower MC values due to cooler temperatures, lower light intensity, and reduced soil moisture availability, all of which limit water uptake and translocation (Patanè and Cosentino, 2010). The persistent impact of PBZ on fruit MC was particularly evident in Baraku soil, in which fruit treated with 25 mL exhibited consistently lower hydration levels across all seasons. These results align with those of Srivastava and Dwivedi (2000), who reported that high PBZ concentrations induced prolonged water stress by modifying the xylem vessel structure and reducing the transpiration efficiency. However, the gradual convergence of MC values over time suggests that these residual effects may diminish with improved soil fertility management.
Table 16
Moisture content (%) of ripened fruit pulp of Keitt mango trees treated with varied PBZ concentrations on different soil types during different production seasons for year one
Soil Type |
Seasons |
Concentrations |
Means |
|||||
0 |
10 |
12.5 |
20 |
25 |
||||
Major |
82.7a* |
79.9abcdefgh |
78.5cdefghi |
79.2abcdefghi |
78.1cdefghij |
79.7ab |
||
Agawtaw |
Minor |
82.7ab |
80.3abcdefg |
78.6cdefghi |
78.9bcdefghi |
77.5efghij |
79.6ab |
|
Off-season |
81.8abc |
79.5abcdefghi |
77.5efghij |
76.6ghij |
78.4cdefghij |
78.8bcd |
||
Means |
82.4a |
79.9bc |
78.2bcd |
78.2bcd |
78.0cdef |
79.3a |
||
Major |
82.5ab |
81.2abcde |
79.2abcdefghi |
79.6abcdefgh |
79.3abcdefghi |
80.4a |
||
Akuse |
Minor |
82.6ab |
80.0abcdefgh |
78.6cdefghi |
77.7efghij |
78.6cdefghi |
79.5ab |
|
Off-season |
81.6abcd |
78.9abcdefghi |
76.9fghij |
81.3abcde |
77.9defghij |
79.3abc |
||
Means |
82.2a |
80.0b |
78.3bcd |
79.5bcd |
78.6bcd |
79.7a |
||
Major |
80.2abcdefg |
78.2cdefghij |
78.5cdefghi |
75.7ij |
77.1fghij |
77.9cde |
||
Baraku |
Minor |
80.6abcdef |
78.5cdefghi |
77.3fghij |
76.5ghij |
74.6j |
77.5de |
|
Off-season |
78.5cdefghi |
77.5efghij |
77.2fghij |
76.1hij |
76.9fghij |
77.3e |
||
Means |
79.8bc |
78.1cde |
77.7def |
76.1f |
76.2ef |
77.6b |
||
Concentrations Grand means 81.5a |
79.3b |
78.0c |
77.9c |
77.6c |
||||
Seasons Mean |
Major |
81.8a |
79.7bc |
78.7bcde |
78.1cde |
78.1cde |
79.3a |
|
Minor |
82.0a |
79.6bcd |
78.2cde |
77.7de |
76.9e |
78.9ab |
||
Off-season |
80.6ab |
78.6cde |
77.2e |
78.0cde |
77.7de |
78.4b |
||
CV=1.30HSD (0.01); PBZ concentrations =0.9370; seasons=0.6469; soil types=0.6469; PBZ concentration*seasons=1.9419; season*soil= 1.3939; PBZ concentration*soil types=1.9419; PBZ concentrations*seasons*soil types=3.8216. |
*Mean followed by the same alphabets are not significantly different (p>0.01) from each other.
CV: Coefficient of Variation; HSD: Honet Significant Difference; PBZ: Paclobutrazol
Table 17
Moisture content (%) of ripened fruit pulp of Keitt mango trees treated with varied PBZ concentrations on different soil types during different production seasons for year two
Soil Type |
Seasons |
Concentrations |
Means |
||||
0 |
10 |
12.5 |
20 |
25 |
|||
Major |
81.1abcd* |
79.2bcdefghijk |
77.2ghijklmnop |
79.0bcdefghijkl |
78.6cdefghijklm |
79.0ab |
|
Agawtaw |
Minor |
81.4abc |
78.1defghijklmno |
77.4fghijklmnop |
77.6fghijklmno |
76.4klmnop |
78.2bc |
Off-season |
81.0abcde |
78.2defghijklmn |
76.9ijklmnop |
78.1defghijklmno |
76.6jklmnop |
78.2bc |
|
Means |
81.2ab |
78.5de |
77.2efg |
78.2de |
77.2efg |
78.5b |
|
Major |
82.6a |
80.3abcdef |
79.2bcdefghijk |
78.1efghijklmno |
77.3ghijklmnop |
79.5a |
|
Akuse |
Minor |
81.9ab |
80.1abcdefgh |
78.6cdefghijklm |
76.3klmnop |
77.0hijklmnop |
78.8ab |
Off-season |
81.7ab |
80.2abcdefg |
77.7fghijklmno |
79.7abcdefghi |
79.6abcdefghij |
79.8a |
|
Means |
82.1a |
80.2bc |
78.5de |
78.0de |
78.0def |
79.4a |
|
Major |
79.8abcdefghi |
78.8bcdefghijklm |
77.2ghijklmnop |
76.8ijklmnop |
75.2op |
77.6cd |
|
Baraku |
Minor |
79.2bcdefghijk |
77.5fghijklmno |
76.2klmnop |
76.1lmnop |
74.4p |
76.7d |
Off-season |
79.1bcdefghijkl |
76.7jklmnop |
75.8mnop |
76.2klmnop |
75.4nop |
76.6d |
|
Means |
79.4cd |
77.7efg |
76.4gh |
76.4gh |
75.0h |
77.0c |
|
Concentrations Grand means 80.9a |
78.8b |
77.4cd |
77.5c |
76.7d |
|||
Seasons Mean |
Major |
81.2a |
79.5bc |
77.9def |
78.0cdef |
77.0defg |
78.7a |
Minor |
80.8ab |
78.6cd |
77.4defg |
76.6fg |
75.9g |
77.9b |
|
Off-season |
80.6ab |
78.3cde |
76.8efg |
78.0cdef |
77.2defg |
78.2ab |
|
CV=1.05; HSD (0.01); PBZ concentrations =0.2231; seasons=0.5179; soil types=0.5179; PBZ concentration*seasons=1.5547; season*soil= 1.1159; PBZ concentration*soil types=1.5547; PBZ concentrations*seasons*soil types=3.0596. |
*Mean followed by the same alphabets are not significantly different (p>0.01) from each other.
CV: Coefficient of Variation; HSD: Honet Significant Difference; PBZ: Paclobutrazol
Table 18
Moisture content (%) of ripened fruit pulp of Keitt mango trees treated with varied PBZ concentrations on different soil types during different production seasons for year three
Soil Type |
Seasons |
Concentrations |
Means |
|||||||||
0 |
10 |
12.5 |
20 |
25 |
||||||||
Major |
82.9a * |
78.7abcdefg |
78.1abcdefgh |
78.5abcdefg |
77.5cdefgh |
79.1abc |
||||||
Agawtaw |
Minor |
82.7ab |
80.3abcdefg |
78.8abcdefg |
79.9abcdefg |
78.8abcdefg |
80.1a |
|||||
Off-season |
81.9abcd |
79.6abcdefg |
77.5bcdefgh |
75.9gh |
78.5abcdefg |
78.7abc |
||||||
Means |
82.5a |
79.5bc |
78.2cde |
78.1cde |
78.3cd |
79.3a |
||||||
Major |
82.5abc |
81.3abcdef |
78.8abcdefg |
78.6abcdefg |
78.5abcdefg |
79.9a |
||||||
Akuse |
Minor |
82.3abc |
79.9abcdefg |
78.3abcdefg |
78.4abcdefg |
78.7abcdefg |
79.5ab |
|||||
Off-season |
81.6abcde |
78.2abcdefgh |
78.9abcdefg |
79.6abcdefg |
77.9abcdefgh |
79.3abc |
||||||
Means |
82.1ab |
79.8bc |
78.7cd |
78.9c |
78.4cd |
79.6a |
||||||
Major |
80.2abcdefg |
78.6abcdefg |
78.8abcdefg |
75.7gh r |
76.9defgh |
78.0bc |
||||||
Baraku |
Minor |
80.5abcdefg |
81.8abcde |
77.4cdefgh |
76.7efgh |
73.1h |
77.9bc |
|||||
Off-season |
78.7abcdefg |
77.8abcdefgh |
77.4cdefgh |
76.3fgh |
76.8defgh |
77.4c |
||||||
Means |
79.8bc |
79.4c |
77.9cde |
76.2de |
75.6e |
77.8b |
||||||
Concentrations Grand means 81.5a |
79.6b |
78.2c |
77.7c |
77.4c |
||||||||
Seasons Mean |
Major |
81.8a |
79.5abc |
78.6bcd |
77.6cd |
77.6cd |
79.0a |
|||||
Minor |
81.8a |
80.7ab |
78.2bcd |
78.3bcd |
76.9d |
79.2a |
||||||
Off-season |
80.8ab |
78.6bcd |
77.9cd |
77.2cd |
77.8cd |
78.4a |
||||||
CV=1.75; HSD (0.01); PBZ concentrations =1.2632; seasons=0.8721; soil types=0.8721; PBZ concentrations* seasons = 2.6178; seasons*soil types=1.8790; PBZ concentrations*soil types= 2.6178; PBZ concentration*season*soil type=5.1516. |
*Mean followed by the same alphabets are not significantly different (p>0.01) from each other.
CV: Coefficient of Variation; HSD: Honet Significant Difference; PBZ: Paclobutrazol
Total ash content (%) of treated Keitt mango fruit
PBZ significantly influenced the total ash content in Keitt mango pulp over 3 years (Tables 19–21), with higher PBZ concentrations (20–25 mL) consistently enhancing mineral accumulation. The highest ash content was observed in fruit treated with 25 mL PBZ, recording 8.40% in the first year and 8.44% in the second year, while non-treated fruit exhibited the lowest values, decreasing from 7.02 to 6.62%. By the third year, the effect of PBZ stabilised, with the highest mean ash content (6.57%) recorded under 10 mL PBZ treatment and the lowest (6.42%) under 12.5 mL PBZ, suggesting a diminishing residual effect over time.
The observed increase in ash content with PBZ application aligns with its role in modifying the hormone balance, which enhances root activity and nutrient uptake efficiency (Rademacher, 2016; Scholtz, 2020). By inhibiting gibberellin biosynthesis, PBZ limits vegetative growth, directing more nutrients to fruit tissues, particularly in the first two years, during which time mineral translocation is most pronounced. However, by the third year, metabolic adjustments likely normalised nutrient partitioning, reducing the impact of PBZ on mineral accumulation (Patel et al., 2020). Additionally, the genetic buffering capacity of the Keitt mango cultivar may have contributed to maintaining nutrient homeostasis despite continued PBZ application (Yahia et al., 2011). Soil type played a crucial role in determining the ash content, with Akuse and Agawtaw soils consistently yielding fruit with a higher mineral composition. Akuse soil recorded the highest mean ash content across the study period, ranging from 6.77% in the third year to 8.73% in the first year, followed closely by Agawtaw soil (6.59–8.49%). Conversely, Baraku soil consistently produced the lowest ash content (5.11–6.35%), likely due to its lower organic matter content and reduced CEC, which restricts nutrient absorption (Brady and Weil, 2017). These findings reinforce previous research on soil fertility’s impact on fruit mineral composition, emphasising that well-fertilised soils improve nutrient uptake of the roots and mineral deposition, while less fertile soils limit nutrient availability, reducing the total ash content (Lal and Stewart, 2015; Sebastian et al., 2019). Seasonal variations also influenced the ash content, with the off-season and minor season producing fruit with higher mineral accumulation. In the first year, the off-season recorded the highest mean ash content (8.43%), followed by the minor season (8.29%), while the major season had slightly lower values (7.76%). Similar trends were observed in the second year, with the minor season yielding the highest ash content (8.38%). By the third year, seasonal differences narrowed, with the off-season producing the highest ash content (6.66%), followed by the minor (6.54%) and major seasons (6.51%). The higher ash content during the off-season and minor seasons may be attributed to reduced metabolic competition for nutrients due to slower vegetative growth, allowing greater mineral allocation to fruit tissues. In contrast, the major season, characterised by rapid growth, higher temperatures, and increased transpiration, may have prioritised vegetative development over reproductive allocation, thereby limiting nutrient retention in fruit pulp (Litz, 2009).
PBZ-induced increases in ash content can be directly linked to its effects on nutrient absorption and accumulation. Ash content represents the total mineral matter present in fruit, including essential macro- and micronutrients, such as K, Ca, Mg, P, Fe, Zn, and Mn (Yadav et al., 2018). PBZ application enhances root biomass and modifies root architecture, improving the root-to-shoot ratio, which increases the nutrient uptake efficiency (Basak, 2021). As a result, minerals crucial for fruit firmness, structural integrity, and enzymatic functions become more concentrated. PBZ-treated trees exhibit higher Ca and Mg levels due to enhanced root uptake and reduced shoot growth, minimising competition for mineral resources (Babu et al., 2022). Additionally, PBZ facilitates K translocation into fruit, improving sugar transport and enzyme activity, indirectly enhancing the ash content (Shinde et al., 2020). PBZ reduces the transpiration rate, limiting overall water loss and having a concentration effect in fruit tissues. With reduced fruit expansion and water content, minerals and organic matter become more concentrated, contributing to the observed increase in ash content (Monti et al., 2008).
PBZ application also triggers several metabolic changes that further support increased mineral deposition in fruit. Elevated antioxidant enzyme activity, including that of peroxidase, catalase, and superoxide dismutase, in PBZ-treated mangoes enhances secondary metabolism, influencing membrane permeability and ion transport, which promotes mineral accumulation (Verma et al., 2021). Moreover, PBZ enhances carbohydrate accumulation in mango pulp by improving source–sink dynamics, which is closely linked to increased mineral retention, as K and Mg play crucial roles in sugar transport and enzymatic regulation (Singh et al., 2023).
Table 19
Total ash (%) of ripened fruit pulp of Keitt mango trees treated with varied PBZ concentrations on different soil types during different production seasons for year one
Soil Type |
Seasons |
Concentrations |
Means |
||||
0 |
10 |
12.5 |
20 |
25 |
|||
Major |
6.32de* |
7.60abcde |
8.05abcd |
7.92abcd |
8.46abc |
7.67ab |
|
Agawtaw |
Minor |
7.16abcde |
7.65abcde |
8.01abcd |
8.14abcd |
8.35abcd |
7.86ab |
Off-season |
7.74abcde |
7.87abcde |
8.14abcd |
8.32abcd |
8.50abc |
8.12ab |
|
Means |
7.07cd |
7.71abc |
8.07abc |
8.13ab |
8.44ab |
7.88ab |
|
Major |
7.69abcde |
7.78abcde |
7.92abcd |
8.55abc |
9.09a |
8.21a |
|
Akuse |
Minor |
7.69abcde |
7.78abcde |
7.92abcd |
7.96abcd |
8.46abc |
7.96ab |
Off-season |
7.51abcde |
7.69abcde |
7.74abcde |
8.23abcd |
8.64ab |
7.96ab |
|
Means |
7.63bc |
7.75abc |
7.86abc |
8.25ab |
8.73a |
8.04a |
|
Major |
6.55cde |
7.54abcde |
7.52abcde |
7.38abcde |
7.96abcd |
7.39b |
|
Baraku |
Minor |
6.68bcde |
7.98abcd |
7.93abcd |
8.11abcd |
8.05abcd |
7.75ab |
Off-season |
5.82e |
7.65abcde |
7.83abcde |
7.96abcd |
8.14abcd |
7.48ab |
|
Means |
6.35d |
7.72abc |
7.76abc |
7.82abc |
8.05abc |
7.54b |
|
Concentrations Grand means 7.02c |
7.73b |
7.89b |
8.06ab |
8.40a |
|||
Seasons Mean |
Major |
6.86d |
7.64abcd |
7.83abcd |
7.95abc |
8.50a |
7.76a |
Minor |
7.18bcd |
7.80abcd |
7.95abc |
8.07ab |
8.29a |
7.86a |
|
Off-season |
7.02cd |
7.74abcd |
7.90abc |
8.17ab |
8.43a |
7.85a |
|
CV 7.06; HSD (0.01); PBZ concentrations =0.5056; seasons=0.3491; soil types=0.3491; PBZ concentration*seasons=1.0479; season*soil= 0.7521; PBZ concentration*soil types=1.0479; PBZ concentrations*seasons*soil types=2.0621. |
*Mean followed by the same alphabets are not significantly different (p>0.01) from each other.
CV: Coefficient of Variation; HSD: Honet Significant Difference; PBZ: Paclobutrazol
Table 20
Total ash (%) of ripened fruit pulp of Keitt mango trees treated with varied PBZ concentrations on different soil types during different production seasons for year two
Soil Type |
Seasons |
Concentrations |
Means |
||||
0 |
10 |
12.5 |
20 |
25 |
|||
Major |
6.74cd* |
7.92abc |
7.96abc |
8.29abc |
8.24abc |
7.83ab |
|
Agawtaw |
Minor |
7.19abcd |
7.78abcd |
7.69abcd |
8.52ab |
8.73a |
7.98ab |
Off-season |
6.93bcd |
7.48abcd |
7.91abc |
8.01abc |
8.51ab |
7.77abc |
|
Means |
6.96d |
7.72bcd |
7.85abc |
8.27abc |
8.49ab |
7.86b |
|
Major |
7.91abc |
7.83abcd |
8.05abc |
8.42ab |
8.86a |
8.23a |
|
Akuse |
Minor |
7.87abcd |
8.05abc |
8.24abc |
8.38abc |
8.47ab |
8.20a |
Off-season |
7.61abcd |
8.01abc |
8.10abc |
8.19abc |
8.69a |
8.12a |
|
Means |
7.80bcd |
7.96abc |
8.13abc |
8.33abc |
8.67a |
8.18a |
|
Major |
6.21de |
7.49abcd |
7.72abcd |
7.68abcd |
8.26abc |
7.47bcd |
|
Baraku |
Minor |
4.70ef |
7.69abcd |
7.78abcd |
7.46abcd |
7.94abc |
7.11d |
Off-season |
4.43f |
7.51abcd |
7.69abcd |
8.10abc |
8.28abc |
7.20cd |
|
Means |
5.11e |
7.56cd |
7.73bcd |
7.74bcd |
8.16abc |
7.26c |
|
Concentrations Grand means 6.62c |
7.75b |
7.90b |
8.12ab |
8.44a |
|||
Seasons Mean |
Major |
6.95bc |
7.75ab |
7.91a |
8.13a |
8.45a |
7.84a |
Minor |
6.59c |
7.84a |
7.90a |
8.12a |
8.38a |
7.76a |
|
Off-season |
6.32c |
7.67ab |
7.90a |
8.10a |
8.50a |
7.70a |
|
CV 5.79; HSD (0.01); PBZ concentrations =0.4117; seasons=0.2842; soil types=0.2842; PBZ concentration*seasons=10.8532; season*soil= 0.6124; PBZ concentration*soil types=0.8532; PBZ concentrations*seasons*soil types=1.6791. |
*Mean followed by the same alphabets are not significantly different (p>0.01) from each other.
CV: Coefficient of Variation; HSD: Honet Significant Difference; PBZ: Paclobutrazol
Table 21
Total ash (%) of ripened fruit pulp of Keitt mango trees treated with varied PBZ concentrations on different soil types during different production seasons for year three
Soil Type |
Seasons |
Concentrations |
Means |
||||
0 |
10 |
12.5 |
20 |
25 |
|||
Agawtaw |
Major |
6.56a* |
6.56a |
6.41a |
6.57a |
6.74a |
6.57ab |
Minor |
6.50a |
6.58a |
6.47a |
6.55a |
6.50a |
6.52ab |
|
Off-season |
6.85a |
6.55a |
6.69a |
6.75a |
6.50a |
6.67ab |
|
Means |
6.64ab |
6.56abc |
6.52abc |
6.62ab |
6.58abc |
6.59a |
|
Akuse |
Major |
6.44a |
6.78a |
7.12a |
6.83a |
6.58a |
6.75ab |
Minor |
6.78a |
6.77a |
6.73a |
6.94a |
6.80a |
6.80a |
|
Off-season |
6.87a |
6.81a |
6.88a |
6.84a |
6.45a |
6.77a |
|
Means |
6.70ab |
6.79ab |
6.91a |
6.87ab |
6.61abc |
6.77a |
|
Baraku |
Major |
6.30a |
6.45a |
5.86a |
6.13a |
6.33a |
6.21bc |
Minor |
6.02a |
6.73a |
5.92a |
6.34a |
6.52a |
6.31abc |
|
Off-season |
6.26a |
5.88a |
5.72a |
5.86a |
5.77a |
5.90c |
|
Means |
6.19abc |
6.35abc |
5.83c |
6.11bc |
6.20abc |
6.14b |
|
Concentrations Grand means 6.51a |
6.57a |
6.42a |
6.53a |
6.46a |
|||
Seasons Mean |
Major |
6.43a |
6.59a |
6.46a |
6.51a |
6.55a |
6.51a |
Minor |
6.43a |
6.69a |
6.38a |
6.61a |
6.61a |
6.54a |
|
Off-season |
6.66a |
6.41a |
6.43a |
6.48a |
6.24a |
6.45a |
|
CV 6.31; HSD (0.01); PBZ concentrations =0.3755; seasons=0.2592; soil types=0.2592; PBZ concentration*seasons=0.7781; season*Soil= 0.5585; PBZ concentration*soil types=0.7781; PBZ concentrations*seasons*soil types=1.5312. |
*Mean followed by the same alphabets are not significantly different (p>0.01) from each other.
CV: Coefficient of Variation; HSD: Honet Significant Difference; PBZ: Paclobutrazol
Additionally, PBZ-treated fruit often exhibits higher phenolic compounds and organic acid content, particularly citric and malic acids, which act as chelators, improving mineral solubility and facilitating nutrient accumulation in fruit tissues (Sarker and Rahim, 2019).
The increased ash content in PBZ-treated mangoes has important implications for fruit quality. Higher mineral availability improves fruit firmness, extending postharvest life and making fruit more resistant to mechanical damage (Sarkar et al., 2021).
Additionally, elevated mineral concentrations, particularly K and Mg, enhance sugar metabolism and acid balance, improving flavour and sweetness perception in Keitt mangoes (Verghese et al., 2023).
Total soluble solids content (°Brix) of treated Keitt mango fruit
PBZ application significantly influenced TSS content across all 3 years, with higher concentrations (20–25 mL) consistently enhancing fruit sweetness. The 25 mL PBZ treatment yielded the highest TSS values, peaking at 19.78°Brix in the first year and 20.30°Brix in the second year. In contrast, non-treated trees consistently produced fruit with the lowest TSS content, ranging from 17.48 to 17.65°Brix. These results suggest that PBZ enhances sugar accumulation by altering source–sink dynamics and redirecting photosynthates from vegetative tissues to fruit development (Sebastian et al., 2019).
The physiological basis of this response lies in PBZ’s inhibition of gibberellin biosynthesis, which reduces shoot elongation and increases assimilate availability for reproductive growth (Reddy and Kurian, 2008). Additionally, PBZ has been shown to increase starch accumulation in developing mango fruit, which are later hydrolysed into soluble sugars during ripening, thereby elevating the TSS content (Patel et al., 2020). The effect of PBZ on TSS was particularly pronounced in the first two years, while in the third year, interactions among PBZ, soil type, and season became statistically non-significant.
This reduction in variability indicates a diminishing residual impact of PBZ on sugar metabolism, as observed by Patel et al. (2020). The stabilisation of the TSS content suggests that sustained PBZ application may have a cumulative effect in the early years, gradually normalising as metabolic adjustments occur within the plant system.
Soil fertility emerged as a key factor influencing the TSS content. Akuse and Agawtaw soils consistently supported the highest mean TSS content in the first and second years, with values exceeding 19.30°Brix. By the third year, the TSS content in these soils remained comparable (18.34 and 18.24°Brix), indicating their capacity to sustain high sugar biosynthesis under varying PBZ treatments. In contrast, Baraku soil consistently produced the lowest TSS values, ranging from 17.37 to 18.01°Brix across the study period.
The superior performance of Akuse and Agawtaw soils can be attributed to their higher organic matter content, improved CEC, and efficient nutrient cycling, which collectively enhances carbohydrate metabolism and photosynthate allocation to fruit tissues (Brady and Weil, 2017). In contrast, Baraku soil’s lower fertility and poor water retention likely constrained sugar accumulation, reducing TSS levels (Lal and Stewart, 2015).
These findings align with those of Falchi et al. (2020), who reported that soil nutrient availability plays a pivotal role in fruit sugar synthesis by modulating key enzymatic pathways involved in starch hydrolysis and sucrose metabolism.
Therefore, optimising soil fertility through targeted amendments can complement PBZ treatments and enhance fruit sweetness. Seasonal variations had a moderate but consistent influence on TSS accumulation. In the first and second years, the minor and major seasons generally recorded higher TSS contents compared to the off-season. In the first year, the minor season produced the highest mean TSS content (18.68°Brix), while in the second year, the major season exhibited the highest TSS content (18.74°Brix). By the third year, seasonal differences diminished, with the TSS content stabilising across all treatments.
The observed seasonal patterns align with the established physiological mechanisms governing sugar biosynthesis.
Optimal temperatures and adequate rainfall during the major and minor seasons enhance photosynthetic efficiency, promoting carbohydrate synthesis and translocation to fruit (Prasad et al., 2015).
In contrast, the off-season, characterised by cooler temperatures and reduced light intensity, exhibited slightly lower TSS levels due to slower enzymatic activity and reduced starch-to-sugar conversion (Litz, 2009).
Table 22
Total soluble solids (°Brix) of ripened fruit pulp of Keitt mango trees treated with varied PBZ concentrations on different soil types during different production seasons for year one
Soil Type |
Seasons |
Concentrations |
Means |
||||
0 |
10 |
12.5 |
20 |
25 |
|||
Major |
17.57abcde* |
17.83abcde |
17.90abcde |
19.93abcde |
19.70abcde |
18.59abc |
|
Agawtaw |
Minor |
17.23bcde |
17.60abcde |
18.57abcde |
20.93a |
20.53abcd |
18.97ab |
Off-season |
17.40abcde |
19.50abcde |
19.07abcde |
20.70abc |
20.13abcd |
19.36ab |
|
Means |
17.40de |
18.31bcde |
18.51bcde |
20.52a |
20.12ab |
18.97a |
|
Major |
18.10bcde |
19.23abcde |
19.27abcde |
19.93abcde |
20.77ab |
19.46ab |
|
Akuse |
Minor |
18.50abcde |
19.27abcde |
19.33abcde |
20.10abcde |
20.80ab |
19.60a |
Off-season |
18.03abcde |
18.77abcde |
18.57abcde |
19.07abcde |
19.73abcde |
18.83ab |
|
Means |
18.21cde |
19.09abcd |
19.06abcd |
19.70abc |
20.43a |
19.30a |
|
Major |
17.07cde |
18.13abcde |
18.87abcde |
18.77abcde |
19.20abcde |
18.41abc |
|
Baraku |
Minor |
16.43e |
17.00de |
17.40abcde |
17.87abcde |
18.57abcde |
17.45c |
Off-season |
16.97de |
17.9abcde |
18.87abcde |
18.87abcde |
18.53abcde |
18.18bc |
|
Means |
16.82e |
17.69de |
18.38bcde |
18.39bcde |
18.79abcd |
18.01b |
|
Concentrations Grand means 17.48d |
18.36cd |
18.65bc |
19.54ab |
19.78a |
|||
Seasons Mean |
Major |
17.58cd |
18.40abcd |
18.68abcd |
19.54ab |
19.89a |
18.82a |
Minor |
17.39d |
17.96bcd |
18.43abcd |
19.63ab |
19.97a |
18.68a |
|
Off-season |
17.47d |
18.73abcd |
18.83abcd |
19.43abc |
19.49ab |
18.79a |
|
CV 5.27; HSD (0.01); PBZ concentrations =0.9046; seasons=0.6245; soil types=0.6245; PBZ concentration*seasons=1.8746; season*soil= 1.3456; PBZ concentration*soil types=1.8746; PBZ concentrations*seasons*soil types=3.6891. |
*Mean followed by the same alphabets are not significantly different (p>0.01) from each other.
CV: Coefficient of Variation; HSD: Honet Significant Difference; PBZ: Paclobutrazol
Table 23
Total soluble solids (°Brix) of ripened fruit pulp of Keitt mango trees treated with varied PBZ concentrations on different soil types during different production seasons for year two
Soil Type |
Seasons |
Concentrations |
Means |
||||
0 |
10 |
12.5 |
20 |
25 |
|||
Major |
16.97ab* |
18.13ab |
18.07ab |
19.13ab |
19.47ab |
18.35ab |
|
Agawtaw |
Minor |
17.47ab |
17.40ab |
18.17ab |
19.43ab |
19.97ab |
18.49ab |
Off-season |
16.73ab |
17.53ab |
18.67ab |
19.37ab |
19.67ab |
18.39ab |
|
Means |
17.06de |
17.69cde |
18.30abcde |
19.31abc |
19.70ab |
18.41b |
|
Major |
19.33ab |
19.60ab |
19.40ab |
19.93ab |
19.73ab |
19.60a |
|
Akuse |
Minor |
18.60ab |
18.77ab |
19.20ab |
19.53ab |
20.10a |
19.24a |
Off-season |
18.63ab |
18.90ab |
19.13ab |
19.93ab |
20.30a |
19.38a |
|
Means |
18.86abcd |
19.09abc |
19.24abc |
19.80ab |
20.04a |
19.41a |
|
Major |
16.83ab |
18.93ab |
18.23ab |
18.97ab |
18.40ab |
18.27ab |
|
Baraku |
Minor |
16.70ab |
17.10ab |
16.73ab |
18.63ab |
19.00ab |
17.63b |
Off-season |
16.20b |
17.80ab |
17.73ab |
18.03ab |
18.40ab |
17.63b |
|
Means |
16.58e |
17.94bcde |
17.57cde |
18.54abcde |
18.60abcd |
17.85b |
|
Concentrations Grand means 17.50c |
18.24c |
18.37bc |
19.22ab |
19.45a |
|||
Seasons Mean |
Major |
17.71bc |
18.89abc |
18.57abc |
19.34ab |
19.20ab |
18.74a |
Minor |
17.59bc |
17.76abc |
18.03abc |
19.20ab |
19.69a |
18.45a |
|
Off-season |
17.19c |
18.08abc |
18.51abc |
19.11abc |
19.46ab |
18.47a |
|
CV 5.62; HSD (0.01); PBZ concentrations =0.9538; seasons=0.6585; soil types=0.6585; PBZ concentration*seasons=1.9765; season*soil= 1.4187; PBZ concentration*soil types=1.9765; PBZ concentrations*seasons*soil types=3.8897. |
*Mean followed by the same alphabets are not significantly different (p>0.01) from each other.
CV: Coefficient of Variation; HSD: Honet Significant Difference; PBZ: Paclobutrazol
Table 24
Total soluble solids (°Brix) of ripened fruit pulp of Keitt mango trees treated with varied PBZ concentrations on different soil types during different production seasons for year three
Soil Type |
Seasons |
Concentrations |
Means |
||||
0 |
10 |
12.5 |
20 |
25 |
|||
Major |
18.03a* |
18.50a |
16.93a |
18.93a |
18.93a |
18.27a |
|
Agawtaw |
Minor |
17.60a |
18.30a |
18.73a |
17.93a |
18.83a |
18.28a |
Off-season |
18.13a |
18.60a |
17.90a |
17.47a |
18.73a |
18.17a |
|
Means |
17.92a |
18.47a |
17.86a |
18.11a |
18.83a |
18.24a |
|
Major |
18.30a |
19.00a |
17.77a |
18.17a |
18.97a |
18.44a |
|
Akuse |
Minor |
17.97a |
18.00a |
18.43a |
18.57a |
18.53a |
18.30a |
Off-season |
18.23a |
19.23a |
17.70a |
17.57a |
18.73a |
18.29a |
|
Means |
18.17a |
18.74a |
17.97a |
18.10a |
18.74a |
18.34a |
|
Major |
17.63a |
16.97a |
16.63a |
17.50a |
17.60a |
17.27a |
|
Baraku |
Minor |
16.60a |
17.60a |
17.20a |
18.00a |
17.73a |
17.43a |
Off-season |
17.40a |
17.40a |
17.53a |
17.77a |
16.97a |
17.41a |
|
Means |
17.21a |
17.32a |
17.12a |
17.76a |
17.43a |
17.37b |
|
Concentrations Grand means 17.77a |
18.18a |
17.65a |
17.99a |
18.34a |
|||
Major |
17.99a |
18.16a |
17.11a |
18.20a |
18.50a |
17.99a |
|
Seasons Mean |
Minor |
17.39a |
17.97a |
18.12a |
18.17a |
18.37a |
18.00a |
Off-season |
17.92a |
18.41a |
17.71a |
17.60a |
18.14a |
17.95a |
|
CV 6.44; HSD (0.01); PBZ concentrations =1.0606; seasons=0.7322; soil types=0.7322; PBZ concentration*seasons=2.1979; season*soil= 1.5776; PBZ concentration*soil types=2.1979; PBZ concentrations*seasons*soil types=4.3253. |
*Mean followed by the same alphabets are not significantly different (p>0.01) from each other.
CV: Coefficient of Variation; HSD: Honet Significant Difference; PBZ: Paclobutrazol
The gradual convergence of TSS values by the third year suggests that PBZ’s residual effects on sugar metabolism decrease over successive growing seasons. This aligns with the results of Patel et al. (2020), who observed that PBZ-induced metabolic shifts in mango trees tended to stabilise over time, necessitating periodic adjustments in application rates to maintain optimal fruit quality.
CONCLUSIONS
This study demonstrated that PBZ application significantly affected the physical and chemical attributes of Keitt mangoes, with outcomes influenced by the application rate, soil fertility, and seasonal conditions. Higher PBZ concentrations (20–25 mL) reduced the fruit size and density by inhibiting gibberellin biosynthesis, which restricts cell elongation and carbohydrate translocation. This effect was more pronounced in less fertile soils, such as Baraku, in which nutrient limitations amplified PBZ’s growth-suppressing effects.
Conversely, fruit grown in fertile soils, such as Agawtaw, exhibited superior size and density due to better nutrient availability. Major-season mangoes were larger and had higher densities due to favourable rainfall and temperatures, while off-season fruit was smaller and less dense. Despite size reductions, PBZ enhanced fruit firmness by promoting lignification and calcium deposition, particularly in the minor season and off-season, when slower vegetative growth enabled greater structural reinforcement.
Higher PBZ concentrations reduced the MC by limiting transpiration and water uptake, with the effect being most pronounced in Baraku soil due to its poor water retention capacity. Fruit from Akuse and Agawtaw soils exhibited a higher MC and ash content, reflecting better soil fertility and water-holding capacity. Seasonally, major-season fruit retained more moisture due to increased rainfall, while off-season fruit had lower hydration levels. PBZ application increased the TSS content and enhanced fruit sweetness. Higher PBZ concentrations redirected photosynthates from vegetative growth to fruit development, increasing sugar biosynthesis. This effect was particularly pronounced in the minor season, when reduced vegetative competition allowed greater carbohydrate allocation to fruit. Soil fertility further influenced the TSS content, with mangoes from Akuse and Agawtaw soils exhibiting higher values due to superior nutrient cycling.
PBZ significantly suppressed the respiration rate and ethylene production, delaying ripening and extending the shelf life. Higher PBZ concentrations reduced CO₂ evolution and ethylene biosynthesis by inhibiting gibberellin pathways and ethylene-related enzymes and slowing metabolic activity and postharvest deterioration.
Seasonal and soil variations also contributed, with off-season mangoes and those from nutrient-rich soils exhibiting higher respiration and ethylene emissions. In conclusion, when carefully managed considering soil fertility and seasonal factors, PBZ application can effectively enhance Keitt mango quality and postharvest longevity, offering significant benefits for producers and exporters.
RECOMMENDATION
It is recommended that PBZ application be carefully managed to balance its growth-regulating effects with potential negative impacts on fruit size, weight, and MC, especially on less fertile soils. Lower concentrations (0–12.5 mL) are recommended for fertile soils to promote larger fruit, while marginal soils may require additional soil fertility management, such as organic matter or fertiliser supplementation.
Additionally, excessive PBZ concentrations (above 20 mL) should be avoided in nutrient-deficient soils. Seasonal variations should guide PBZ application, with moderate concentrations during the major production season to enhance fruit quality, and higher concentrations during the off-season to improve firmness and the shelf life. Improving soil fertility through sustainable practices, such as organic fertilisers and soil conservation measures, will amplify PBZ’s positive effects and improve fruit quality across seasons.
Author contributions: Conceptualization, methodology, data curation: AAA; Writing: AA; Review: AA; Supervision: ASA. All authors declare that they have read and approved the publication of the manuscript in its present form.
Funding: This study did not receive any external funding.
Acknowledgements: The authors extend their sincere gratitude to all field staff of the Institute of Agricultural Research and Training for their invaluable support during the field trial.
Conflicts of Interest: The authors affirm that no conflicts of interest are associated with this publication.
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