Whole-fruit weight and external morphometric dimensions
Whole-fruit weight and shape index showed significant inter-cultivar variation (p<0.05), as presented in Table 4. Fruit weight ranged from 5.83±0.21 kg in Koozha (C2) to 11.33±2.30 kg in Chembarathi Varikka (C3), reflecting the wide genetic diversity in fruit size among the evaluated cultivars. Chembarathi Varikka (C3) was the heaviest cultivar (group a), while Koozha (C2) was the lightest (group c). Pullichira Jack (C1), Muttom Varikka (C4) and Honey Dew (C5) formed an intermediate group (group b), with weights of 8.49, 7.57 and 6.83 kg, respectively. These data are consistent with the broad size range reported for Indian jackfruit accessions, where fruit weight has been documented to vary from 2.5 to over 25 kg depending on genotype
(Jagadeesh et al., 2007; Natta et al., 2025).
In contrast, fruit length (range: 40.33-48.33 cm), breadth (range: 22.50-27.83 cm) and girth (range: 69.10-85.17 cm) did not differ significantly among cultivars (all NS, Table 4), indicating that while cultivars diverge substantially in total mass, their external linear and circumferential dimensions overlap considerably within the variability of a small replication set (n = 3). The high standard deviations observed for these parameters - particularly for Koozha (girth SD = 14.16 cm) - reflect the inherent morphological variability within individual cultivars and underscore the limitation of n = 3 in resolving linear dimension differences among cultivars that may be naturally variable in shape.
The shape index (SI) was significant (F = 52.56, p<0.01). Muttom Varikka (2.01±0.05) and Honey Dew (1.96 ±0.02) recorded the highest SI values (group a), indicating distinctly more elongated fruit morphology. Pullichira Jack (1.73±0.05) and Koozha (1.69±0.05) formed group b, while Chembarathi Varikka (1.64±0.01) was the most compact cultivar (group c). These values fall within the range of 1.5-2.3 reported for jackfruit accessions
(Jagadeesh et al., 2007; Natta et al., 2025), confirming that SI is a cultivar-discriminating morphometric trait of practical utility for grading, packing and transport efficiency assessments.
Correlation analysis among morphometric and fraction-weight traits
Pearson’s correlation analysis among fruit weight, morphometric dimensions and major fraction weights is presented in Table 5. Fruit weight exhibited strong positive correlations with fruit length (r = 0.86, p<0.01) and fruit breadth (r = 0.82, p<0.01), indicating that larger fruits are generally more elongated and broader. These relationships highlight the potential of non-destructive external dimensions as reliable predictors of fruit mass for grading and sorting, consistent with reports on Karnataka accessions
(Natta et al., 2025) and Ugandan germplasm
(Gwokyalya et al., 2024). Moderate positive correlations were recorded between fruit weight and bulb weight (r = 0.78, p<0.05) and seed weight (r = 0.74, p<0.05), suggesting that increases in fruit size are associated with higher edible biomass, though not in direct proportion, possibly due to the contribution of structural components. Rind, core-rachis and rag fractions showed comparatively weaker correlations with fruit weight (r = 0.65, 0.60 and 0.58, respectively), indicating a relatively consistent distribution of non-edible components across fruit sizes. Among inter-fraction relationships, bulb weight was positively correlated with seed weight (r = 0.76, p<0.05), suggesting coordinated development of edible tissues. Rind weight showed a significant association with core–rachis weight (r = 0.70, p<0.05), reflecting structural interdependence within the fruit.
Fraction-wise mass distribution - non-edible fractions
The fraction-wise gravimetric composition of the five cultivars is presented in Table 6. The total rind fraction was the dominant non-edible component across all cultivars, ranging from 21.88±1.23% (C1, Pullichira Jack) to 44.00±1.63% (C3, Chembarathi Varikka). The exceptionally high rind fraction of C3 - which substantially exceeds the 20-35% range commonly reported for jackfruit pericarp
(Hossain et al., 2022; Gayatri et al., 2020) - is likely an intrinsic characteristic of this homestead cultivar, possibly associated with a thicker and more protective pericarp structure that may have been selectively favoured for improved transport tolerance in traditionally unprocessed, whole-fruit marketing contexts. From a valorisation standpoint, this exceptionally high rind fraction positions Chembarathi Varikka as the most advantageous raw material source for rind-derived value-added products, including pectin and dietary fibre.
A notable finding from the present study is the substantially elevated rag (perigones) fraction in Pullichira Jack (11.73±0.98%, group b) and particularly in Koozha (16.05±0.49%, group a), compared to the remaining three cultivars, which recorded approximately 5% rag (group c). This pattern suggests that koozha-type jackfruit - characterised by softer, less defined arils - may possess a more extensively developed fibrous perianth architecture. The practical consequence of this high rag fraction in Koozha is a substantially greater fibrous by-product stream per unit of edible output. This aspect warrants attention in the design of cultivar-specific processing lines.
Core-rachis fraction ranged from 6.00±0.00% (C4, Muttom Varikka) to 8.80±0.31% (C2, Koozha), consistent with previously reported ranges for this fruit component. The seed-coat/perianth membrane fraction increased progressively from C1 (4.40%) and C2 (5.26%) through C3 (8.98%) and C4 (10.57%) to C5 (14.67%), with Honey Dew recording the highest value (group a). This gradient likely reflects differences in the number and size of seeds across cultivars, as larger and more numerous seeds would correspondingly bear a greater total membranous envelope. The NFI ranged from 46.46±2.36% (C1, Pullichira Jack) to 65.47±0.05% (C3, Chembarathi Varikka), confirming that non-edible fractions constitute a substantial proportion of total fresh fruit weight across all evaluated cultivars, underscoring the critical need for integrated valorisation pipelines targeting rind, seed-coat membrane, core-rachis and rag recovery
(Nair et al., 2021; Yang et al., 2023).
Edible fraction, yield indices and quality attributes
The edible fraction composition and associated quality parameters are presented in Table 7. Bulb percentage (fleshy perianth, seedless) ranged from 28.70±1.97% (C2, Koozha, group b) to 40.33±0.58% (C4, Muttom Varikka, group a). The Edible Recovery Index (ERI), which encompasses both bulb and seed fractions, ranged from 34.53±0.05% (C3, Chembarathi Varikka) to 53.54±2.36% (C1, Pullichira Jack). Pullichira Jack (C1) and Muttom Varikka (C4) were statistically equivalent in ERI (both groups: 53.54% and 51.13%, respectively), recording the highest total edible biomass utilisation among the five cultivars. This equivalence is noteworthy because C1 achieves its high ERI primarily through an exceptionally large seed fraction (16.88±4.20%, group a - the highest among all cultivars), whereas C4 derives its high ERI from superior bulb development (40.33% bulb fraction). These contrasting mechanisms of edible fraction accumulation - seed-driven in C1 versus bulb-driven in C4 - have distinct practical implications: C4 (Muttom Varikka) is superior for fresh bulb yield and processing efficiency, while C1 (Pullichira Jack) presents a seed-rich profile warranting separate valorisation as a starch and protein source (
Mukprasirt and Sajjaanantakul, 2004).
The seed fraction of Koozha (C2) was 12.80±0.38%, substantially higher than commonly reported values for koozha-type jackfruit, which are generally characterised by smaller, fewer seeds. Chembarathi Varikka (C3) recorded the lowest seed fraction (4.53±0.05%, group c), suggesting that despite its firm varikka-type flesh, this cultivar invests relatively little biomass in seed development - a characteristic that may be of value for cultivars targeted at fresh processing where large seeds are considered a disadvantage. The large SD observed for C1 seed fraction (±4.20%) reflects substantial variation in seed allocation across its three replications and is partly attributable to the high natural variability in seed number and size in this locally selected, non-standardised genotype.
TSS values ranged from 23.20
oBrix (C3) to 29.13
oBrix (C5) and pH values ranged from 5.03 to 5.30 across cultivars. Although Honey Dew and Muttom Varikka recorded numerically higher TSS values, consistent with their reputation as premium dessert-type cultivars, the inter-cultivar differences in TSS were not statistically significant (F = 3.198, NS). This non-significance is attributable to the high within-cultivar variability in TSS (SD ±2.10-2.55 oBrix) relative to the between-cultivar differences, in the context of the small replication number (n = 3). Similarly, pH did not differ significantly among cultivars (F = 0.886, NS). These findings are consistent with the reported range of 20-30
oBrix and pH 4.9–5.6 for ripe jackfruit pulp
(Ranasinghe et al., 2019; Hossain et al., 2022; Ramachandra et al., 2022) and indicate that while trends in sweetness are apparent, confirmation of cultivar-level TSS differences would require a larger replication set to achieve adequate statistical power.
CIE L*, a*, b* colorimetric characterisation of jackfruit bulbs
CIE colorimetric analysis revealed striking and statistically significant inter-cultivar differences in all three colour parameters (L*, a* and b*), as presented in Table 8. Pullichira Jack (C1) exhibited a uniquely distinctive creamy white/off-white bulb colour characterised by a very high L* value (82.27±1.61, group a), indicating the highest lightness among all cultivars. Its near-zero a* (1.17±0.25, group d) and exceptionally low b* (10.63±1.05, group e) are consistent with a predominantly achromatic, low-carotenoid colour profile. This colouration, which is uncommon among varikka-type jackfruit cultivars - which are typically associated with yellow-to-golden bulb pigmentation - suggests that C1 possesses either a markedly reduced capacity for carotenoid biosynthesis or enhanced carotenoid catabolism in ripening arils. The fact that C1 is classified as a varikka-type (firm-flesh) cultivar yet displays markedly lower b* values than all other varikka-type entries (C3: 52.50, C4: 55.43, C5: 58.23) conclusively demonstrates that flesh texture type and carotenoid-driven yellow pigmentation are independently inherited phenotypic traits and do not co-segregate within the varikka classification.
Honey Dew (C5) exhibited the brightest golden-yellow colour, recording the highest b* value (58.23±1.26, group a) and the highest L* among the yellow-pigmented cultivars (71.47±1.37, group b), indicating a luminous, saturated yellow hue. The 5.5-fold difference in b* values between C1 (10.63) and C5 (58.23) represents the most pronounced inter-cultivar colorimetric contrast observed and identifies b* as the primary discriminating colorimetric parameter among these cultivars, consistent with
Natta et al., (2025). A progressive and statistically significant increase in b* was observed from C2 (47.27) through C3 (52.50) and C4 (55.43) to C5 (58.23), with each cultivar occupying a distinct DMRT group (d, c, b and a, respectively), reflecting a continuous gradient of carotenoid accumulation independent of flesh-type classification.
For the a* (red-green axis), Chembarathi Varikka (C3) recorded the highest value (11.37± 0.45, group a), indicating the greatest redness component, while Muttom Varikka (C4) and Honey Dew (C5) formed a common group b (10.20 and 9.57, respectively). Koozha (C2) was intermediate (8.50, group c) and Pullichira Jack (C1) was distinctly the lowest (1.17, group d), consistent with its near-achromatic colour profile. The Munsell notations recorded (Table 8) provide supplementary qualitative validation of the instrumental CIE values and are presented as descriptive reference data.
Implications for post-harvest valorisation
The present dataset has direct and quantifiable implications for jackfruit processing system design and by-product valorisation. With non-edible fractions constituting 46.46-65.47% of fresh fruit weight, even modest processing volumes generate substantial biomass streams. A hypothetical unit processing one tonne of jackfruit per day would yield approximately 219-440 kg of rind, 60-88 kg of core-rachis, 50-161 kg of rag and 44-147 kg of seed-coat membrane - totalling 465-655 kg of non-edible biomass per tonne processed. The rind stream alone justifies a dedicated pectin or dietary fibre extraction operation at this scale, given its documented pectin content (
Leong, 2016), while the residual biomass including rind, core and undeveloped perigones also holds demonstrated potential for fermented value-added product development (
Bensi and Divakar, 2026) and the considerable inter-cultivar variation in rind-related traits observed here aligns with previous reports on indigenous jackfruit variability
(Hazarika et al., 2025).
The seed fraction, classified as part of the edible biomass (ERI) in the present study, ranged from 4.53% (C3) to 16.88% (C1) of fruit weight. Seeds are a well-documented source of starch (~22-26% dry weight) and protein (~6-10%), both commercially valorisable (
Mukprasirt and Sajjaanantakul, 2004;
Nair et al., 2021). Cultivars with high seed fractions - notably Pullichira Jack (C1) - may be strategically processed to direct seeds towards starch or flour extraction, simultaneously maximising edible recovery and industrial value. The wide cultivar-dependent variation in fraction yields underscores that mass-balance inputs for biorefinery cascade modelling
(Yang et al., 2023) must be parameterised at the cultivar level rather than derived from generic species-wide estimates.