Literature DB >> 36092875

Genetic evaluation of Jatropha backcross hybrid clones (BC4F1) for yield and oil quality.

M V Jawahar Vishnu1, K T Parthiban1, M Umadevi2, R Jude Sudhagar1, C Cinthia Fernandaz1, Talha Javed3, Uttam Kumar4, Saqer S Alotaibi5.   

Abstract

Jatropha curcas is a tropical species that has been recognized as a promising biodiesel plant. During 2018-2021, researchers at Forest College and Research Institute, Mettupalayam, elicited information on Jatropha's biochemical characteristics, growth performance, variability, and association studies for biometric variables using five backcross (BC4F1) hybrid clones of Jatropha with a control variety TNMC 7. In terms of seed yield, two hybrid clones, CJH 13 (1,218.60 g) and CJH 12 (1,034.40 g), outperformed the other hybrid clones. The seed oil content was higher in CJH 5 (34.19%). The seed oil content had moderate PCV (16.49%) and GCV (16.39%) values, as well as high heritability (99%) and genetic advance (33.56%) as a percentage of the mean. The number of fruits per bunch (0.845 and 0.850) and the number of bunches per branch (0.771 and 0.788) had significant positive phenotypic and genotypic correlations with seed yield, respectively. The iodine numbers, cetane numbers, and saponification values of all hybrid clones were acceptable and satisfactory and were in good compliance with Indian and international biodiesel standards.
Copyright © 2022 Jawahar Vishnu, Parthiban, Umadevi, Sudhagar, Fernandaz, Javed, Kumar and Alotaibi.

Entities:  

Keywords:  Jatropha; biochemical analysis; correlation; genetic analysis; heritability

Year:  2022        PMID: 36092875      PMCID: PMC9449966          DOI: 10.3389/fgene.2022.953486

Source DB:  PubMed          Journal:  Front Genet        ISSN: 1664-8021            Impact factor:   4.772


Introduction

Automobile pollution, which causes climate change, has greatly accelerated environmental degradation. Numerous studies conducted in this area have focused on alternative fuels that can increase efficiency and reduce emissions (Seela et al., 2019). According to the British Petroleum statistical review report, nearly 80% of the world’s energy needs are met by fossil fuels. Between 2015 and 2019, fossil fuels accounted for an average of 85.16% of primary energy consumption; their consumption could reach 143 and 191 MT by 2025 and 2030, respectively, based on an increase of 6% per annum (Sayyed et al., 2022). India is a rapidly growing country with a population predicted to outgrow the rest of the world. India, as a country with limited fossil fuel sources, relies on imports of fossil fuels, the most common of which is crude oil. While rising fuel consumption has prompted a thorough assessment of alternate energy sources, fossil fuel reserves are being depleted (Witze, 2007). The government of India approved a National Policy on Biofuels in 2009, which established a non-mandatory target of 20% blending of biodiesel by 2017 (Bandyopadhay, 2015). India imports 40–50% of its edible oil for human use, making the utilization of edible oil resources for biofuel generation unfeasible. Under such circumstances, it is imperative to seek alternate, non-edible sources for biodiesel production. In India, more than 100 species of tree-borne oilseeds have been identified as sources of biodiesel. Among these, the tropical physic nut tree (Jatropha curcas), a non-edible oil-bearing tree, has gained the attention of several development agencies and the Planning Commission of India. The genus Jatropha belongs to the family Euphorbiaceae, which originated in Central and South America and is distributed across tropical and subtropical regions of Africa and America. J. curcas is widely considered as a potential source for biodiesel production because of its short gestational period, small canopy suitable for high-density planting, convenience of seed collection, high seed oil content, ease of propagation through seeds and cuttings, drought hardiness, long productive period (40 years), rapid growth, resistance to animal grazing, productivity in both good and degraded soils, and widespread adaptability (Basha and Sujatha, 2007). The seeds are high in protein and are a key source of oil. The protein content of J. curcas seed meal has been shown to compare favorably to soybean meal, with a decent balance of essential amino acids (excluding lysine) (Basha and Sujatha, 2007). J. curcas is valuable to consider because it does not compete with the food industry. The required amount of production is attainable, given that J. curcas has a productive life of roughly 50 years and reaches its peak productivity after only 4–5 years (Divakara et al., 2012). Additionally, this species has demonstrated the capacity to adapt to various agroclimatic situations, including infertile soils, making it appropriate for growing in damaged soils while guarding against erosion. These traits make the cultivation of J. curcas appropriate for conventional agriculture in marginal lands, where it could raise farmers’ socioeconomic standing and quality of life, especially in developing nations (Bekalu and Fekad, 2020). Jatropha breeding programs are limited in comparison to other oil seed species such as soybean, cotton, peanut, sunflower, and castor, and there is inadequate research that precisely and scientifically authenticates the effect of field activity on the seed yield of J. curcas (Che Hamzah et al., 2020). Interspecific hybridization, in combination with backcross breeding, is a powerful tool for transferring a desired gene into a cultivar and can be used with a variety of plants. Interspecific hybridization with sexually compatible species facilitates the introgression of desirable characters, such as high oil content, oil quality, resistance to insect pests and diseases, reduced toxicity, and improved growth in problematic sites (Sujatha, 2020). Hence, Forest College and Research Institute (FC&RI) initiated an interspecific hybridization program using J. curcas as the female recipient; other Jatropha species, including Jatropha integerrima, Jatropha podagrica, Jatropha villosa, Jatropha tanjorensis, Jatropha gossypifolia, Jatropha glandulifera, Jatropha multifeda, and Jatropha maheswari, were used as pollen donors, resulting in novel hybrids with high production potential, root rot resistance, and frost tolerance. Among the several crossings, J. curcas and J. integerrima generated successful hybrids with higher seed sets, whereas others failed to produce seeds due to crossability barriers in the pre-zygotic or post-zygotic states (Parthiban et al., 2011). The F1 progeny of successful hybrids exhibited robust growth but had small fruit resembling J. integerrima. The resulting successful hybrid was backcrossed with J. curcas to produce offspring with distinct fruit, yield, and oil characteristics (Parthiban et al., 2009). The most reliable and efficient method of evaluating genetic diversity is to study morphometric features in field trials. Because analyzed genetic differences are the best input for breeding and conservation efforts, field trial data are crucial (Eriksson et al., 1995). Since trees have high levels of variability, tree-improvement programs require comprehensive studies of variation. In Jatropha, such extensive research on backcross hybrids is lacking. Any crop-improvement program requires knowledge of existing genetic variability and of the relationships between various yield-related factors. In Jatropha, research on genetic variability and heritability in terms of growth and yield qualities is still in its early stages. Most traits of economic importance are complexly inherited, and the component characters show different types of associations with other traits. As a result, it is worthwhile to investigate the relationship between yield and yield related attributes, which indicated the yield contributing characters, for which systematic investigations in backcross Jatropha hybrids are insufficient. Jatropha seed is higher in protein, carbohydrate, and lipid content than other seeds, and it is well known for its high fuel value. It has a 40–50 percent oil content. The chemical properties of oil (viz., acid number, free fatty acid content, iodine number, saponification value, and cetane number) directly influence the quality of oil for biodiesel production. However, such reports are inadequate in backcross hybrid clones of Jatropha. Against this backdrop, the current study investigated aspects of backcross (BC4F1) hybrid clones of Jatropha. It aimed 1) to evaluate BC4F1 clones for growth and yield attributes through clonal tests, 2) to analyze the genetic parameters and study the associations among the growth and yield attributes, and 3) to determine the oil content and oil quality of the promising clones.

Materials and methods

The genus Jatropha belongs to the family Euphorbiaceae and contains 176 species, of which J. curcas L.—variously denoted as physic nut, ratanjot, or Barbados nut—is assumed to be the original form, from which other Jatropha species have evolved with variations in vegetative and reproductive characters (Dehgan and Webster, 1978). The plant is native to South America and Africa but was later distributed to other countries around the world by the Portuguese colonizers (Gübitz et al., 1999). Today, it is found in almost all the tropical and subtropical regions of the world. The botanist Carl Von Linne first classified the plant in 1753, giving it the botanical name “Jatropha curcas” from the Greek word “Jatros” (meaning a “Doctor”) and “trophe” (meaning “nutrition”). The plant is considered to be a shrub or small tree, with a height generally up to 5 m. The lifespan of the plant is up to 50 years (Azam et al., 2005). The shrub produces fruits in winter, when it is leafless, and it may produce several crops during the year if the soil moisture is good and temperatures are acceptable. Flowering in J. curcas depends on its locality and agroclimatic conditions. In Tamilnadu, flowering and fruiting occur nearly all year, but in North India, flowering generally occurs from August to December. Fruits mature within 2 months of flowering (Paramathma, 2010). Jatropha seeds may be harvested after 5 months of age, and the productivity is steady after 1 year of age. Jatropha seeds contain viscous oil, having seed oil content of 30–48.5%, which is a promising source of biodiesel (Parthiban et al., 2009). The material for the present study consisted of five BC4F1 backcross hybrid clones of Jatropha: CJH 3, CJH 5, CJH 9, CJH 12, and CJH 13. The successful hybrid clones were developed through interspecific crosses between J. curcas and J. integerrima. The promising F1 plants (11.1% fruit setting with small fruit size) were then backcrossed with J. curcas (TNMC 7) to increase seed size (Parthiban et al., 2011). The resultant BC1F1 progenies were raised to the second generation and investigated for flowering and fruiting character. The superior hybrid clones of BC1F1 progenies (clones) were backcrossed with J. curcas, which resulted in BC2F1 hybrids. The superior hybrid clones of BC2F1 hybrids (clones) were further backcrossed with J. curcas, resulting in BC3F1 hybrids. The superior BC3F1 hybrid clones were backcrossed again with J. curcas, resulting in BC4F1 hybrids. From successive and continued back crossing (Figure 1), five BC4F1 backcross derivative clones were identified by their superior growth, seed, and oil yield. These were multiplied using apical shoot cuttings and are termed hybrid clones. The seeds were used to raise the first generation, and the first-generation apical shoot cuttings were used to develop clonal plantlets. The plantlets were deployed in field trials at FC&RI in Mettupalayam (11˚19′ N; 76˚56′ E; 300 m above MSL), along with the control variety (TNMC 7), in a randomized block design with four replications with 3 m × 3 m spacing. The hybrid clones were pruned once per year after fruiting season; the cumulative seed yield provided in the table represents 6–7 harvests per year.
FIGURE 1

Thematic representation of breeding program.

Thematic representation of breeding program. The following observations (viz., plant height, basal diameter, sturdiness quotient, number of primary branches, number of secondary branches, number of male flowers, number of female flowers, male-female flower ratio, number of fruits per bunch, number of bunches per branch, seed yield per plant, hundred-fruit weight, fruit length, fruit width, fruit aspect ratio, hundred-seed weight, shelling percent, seed length, seed width, seed aspect ratio, kernel oil content, and seed oil content) were recorded for 3 years. The seed oil was extracted via solvent extraction, using hexane (40–60°C) as a solvent (A.O.A.C., 1975).

Determination of the acid value and free fatty acid content

The acid number and free fatty acid content of oil were determined by the procedures of A.O.A.C. (1975): where V = volume of KOH used. N = normality of KOH. W = weight of the sample (g).

Determination of the saponification number

The saponification number was assessed per the method of A.O.A.C. (1975): where b = ml of 0.5 N HCL required by the blank. a = ml of 0.5 N HCL required by the sample.

Determination of the iodine number

The iodine number was determined by the Hanus iodine method (A.O.A.C., 1975): where B = ml of 0.1 N sodium thiosulfate required by blank. S = ml of 0.1 N sodium thiosulfate required by sample. N = normality of sodium thiosulfate solution.

Determination of the cetane number

The cetane number of the Jatropha methyl esters was predicted per Krisnangkura (1986) : where SN = saponification number. IV = iodine value.

Statistical analysis

The data for growth performance, variability, association analysis, and biochemical features of seed oil were analyzed using one-way analysis of variance (ANOVA), and Duncan’s multiple range test was employed to compare treatment means. The data was analyzed using the IBM-SPSS analytical software program, version 20.0 (IBM Corporation, USA). Correlation coefficients were utilized to assess the relationships between the various variables in the experiment (F-test) (Goulden, 1936). The genotypic correlation coefficients were divided into direct and indirect effects using path coefficient analysis (Dewey and Lu, 1959).

Results

Variation in growth and yield attributes

Duncan’s multiple comparison study for growth performance differed significantly (p = 0.05) across different hybrid clones over 3 years, as shown in Tables 1 and 2.
TABLE 1

Mean performance in growth parameters of Jatropha hybrid clones.

ClonesPlant height (cm)Basal diameter (cm)Sturdiness quotientNo. of primary branchesNo. of secondary branchesNo. of male flowersNo. of female flowersMale/female flower ratioFruits/bunchBunches/BranchCumulative seed yield (g)
First year (2018–2019)
CJH 3117.33 ± 5.51b 5.24 ± 0.06ab 22.39 ± 0.58bc 3.17 ± 0.03d 4.75 ± 0.02a 158.50 ± 8.23c 24.25 ± 0.15ab 6.54 ± 0.22c 15.20 ± 0.60b 4.25 ± 0.16ab 353.29 ± 17.75d
CJH 5112.44 ± 5.82b 5.07 ± 0.21ab 22.18 ± 0.56bc 3.11 ± 0.01d 4.52 ± 0.15a 172.25 ± 2.28c 26.85 ± 0.62a 6.42 ± 0.22c 16.50 ± 0.00ab 4.00 ± 0.09b 381.40 ± 18.90cd
CJH 9108.44 ± 0.50b 5.48 ± 0.17a 19.79 ± 0.23c 4.12 ± 0.15c 3.95 ± 0.19b 169.25 ± 2.60c 26.65 ± 0.95a 6.35 ± 0.30c 16.40 ± 0.62b 4.75 ± 0.24a 397.23 ± 3.00bc
CJH 12116.56 ± 3.42b 5.00 ± 0.12ab 23.31 ± 1.18b 4.70 ± 0.04a 4.35 ± 0.12ab 196.75 ± 9.06b 24.50 ± 1.23ab 8.03 ± 0.27b 18.35 ± 0.90a 4.75 ± 0.24a 426.90 ± 0.11b
CJH 13132.22 ± 1.92a 5.03 ± 0.22ab 26.29 ± 1.31a 4.33 ± 0.01b 4.61 ± 0.13a 192.25 ± 2.74b 22.25 ± 1.03b 8.64 ± 0.07b 18.35 ± 0.63a 4.25 ± 0.01ab 484.40 ± 13.05a
TNMC 7 (Control)106.11 ± 3.73b 4.72 ± 0.11b 22.48 ± 0.37b 2.55 ± 0.03e 3.20 ± 0.16c 225.50 ± 6.00a 18.25 ± 0.94c 12.35 ± 0.40a 12.90 ± 0.24c 4.00 ± 0.01b 297.40 ± 4.76e
p value0.007ns 0.85ns 0.003ns <0.0001 a <0.0001 a <0.0001 a <0.0001 a <0.0001 a <0.0001 a 0.14ns <0.0001 a
Second year (2019–2020)
 CJH 3121.24 ± 5.10ab 12.40 ± 0.09bc 9.78 ± 0.31b 7.17 ± 0.05b 6.75 ± 0.07a 233.25 ± 4.79 b 34.50 ± 0.22bc 6.80 ± 0.02bb 21.40 ± 0.91a 6.25 ± 0.30ab 827.65 ± 29.64b
 CJH 5120.63 ± 1.48ab 13.98 ± 0.54a 8.6 ± 0.35c 6.11 ± 0.32c 7.52 ± 0.26bcd 227.75 ± 6.09 b 36.95 ± 1.89c 6.20 ± 0.20cd 22.35 ± 0.98a 6.00 ± 0.10b 819.74 ± 26.33b
 CJH 9118.27 ± 0.20b 12.74 ± 0.19b 9.28 ± 0.06bc 9.12 ± 0.02a 9.95 ± 0.49a 217.75 ± 1.46 b 36.89 ± 1.88c 5.90 ± 0.16d 21.35 ± 0.90a 6.75 ± 0.02a 887.43 ± 11.47ab
 CJH 12116.70 ± 5.41b 12.40 ± 0.25bc 9.41 ± 0.44bc 7.70 ± 0.12b 8.35 ± 0.00b 213.25 ± 4.35 b 34.51 ± 1.07bc 6.20 ± 0.14cd 22.35 ± 0.05a 6.75 ± 0.25a 913.50 ± 46.60a
 CJH 13131.97 ± 1.18a 11.23 ± 0.47c 11.75 ± 0.22a 7.33 ± 0.21b 7.61 ± 0.15bc 216.75 ± 9.86b 32.51 ± 0.29b 6.70 ± 0.31bc 23.35 ± 1.14a 6.25 ± 0.19ab 934.58 ± 5.22a
 TNMC 7 (Control)109.70 ± 4.02b 11.49 ± 0.46c 9.55 ± 0.43bc 6.55 ± 0.16cc 7.20 ± 0.26cd 281.75 ± 8.59a 28.70 ± 0.65c 9.80 ± 0.03a 16.90 ± 0.85b 6.00 ± 0.04b 526.12 ± 9.02c
p value0.19ns 0.003ns <0.0001 a <0.0001 a <0.0001 a <0.0001 a 0.004ns <0.0001 a 0.003ns 0.37ns <0.0001 a
Third year (2020–2021)
 CJH 3125.15 ± 2.63abc 19.44 ± 0.96b 6.44 ± 0.08bc 7.15 ± 0.04c 9.50 ± 0.08a 245.75 ± 4.94b 35.50 ± 0.59ab 6.92 ± 0.12b 22.50 ± 0.39b 7.20 ± 0.17a 924.80 ± 17.72cd
 CJH 5128.83 ± 3.82ab 22.78 ± 0.48a 5.66 ± 0.10d 7.12 ± 0.05c 9.62 ± 0.06a 252.50 ± 10.56b 38.75 ± 1.78a 6.52 ± 0.10bc 22.25 ± 0.36b 6.50 ± 0.23b 859.70 ± 22.48d
 CJH 9128.10 ± 4.51ab 19.78 ± 0.22b 6.48 ± 0.20b 9.50 ± 0.16a 9.85 ± 0.45a 237.25 ± 10.69b 34.25 ± 0.66b 6.93 ± 0.02b 22.25 ± 0.49b 6.20 ± 0.17b 950.90 ± 33.68c
 CJH 12116.85 ± 5.34bc 19.89 ± 0.39b 5.87 ± 0.26d 8.42 ± 0.05b 9.25 ± 0.18a 226.75 ± 7.54b 36.50 ± 1.56ab 6.21 ± 0.19c 23.50 ± 1.20b 7.50 ± 0.11a 1,034.40 ± 33.47b
 CJH 13131.72 ± 6.09a 18.11 ± 0.26b 7.27 ± 0.15a 9.52 ± 0.31a 9.60 ± 0.22a 238.25 ± 8.98b 36.50 ± 1.49ab 6.53 ± 0.03bc 26.25 ± 0.84a 7.50 ± 0.21a 1,218.60 ± 21.91a
 TNMC 7 (Control)113.30 ± 0.67c 19.11 ± 0.91b 5.93 ± 0.15cd 7.50 ± 0.37c 8.25 ± 0.25b 316.50 ± 10.12a 29.50 ± 1.15c 10.73 ± 0.29a 17.50 ± 0.19c 6.00 ± 0.13b 653.66 ± 16.12e
p value0.57ns 0.004ns <0.0001 a <0.0001 a 0.007ns <0.0001 a 0.005ns <0.0001 a <0.0001 a <0.0001 a <0.0001 a

Highly significant difference at p < 0.001 level of probability, and ns - no significance. Values with different superscripts were significantly different at p < 0.05 level of probability.

TABLE 2

Mean performance in fruit and seed attributes of Jatropha hybrid clones.

Clones100 Fruit weight (g)Fruit length (cm)Fruit width (cm)Fruit aspect ratio100 seed weight (g)Seed length (cm)Seed width (cm)Seed aspect ratioShelling percentSeed oil content (%)Kernel oil content (%)
CJH 3112.57 ± 0.74a 2.00 ± 0.04b 1.57 ± 0.04c 1.28 ± 0.02ab 59.37 ± 0.52abc 1.73 ± 0.00a 0.79 ± 0.03a 2.19 ± 0.02ab 61.57 ± 2.13a 27.93 ± 0.00b 54.80 ± 0.80a
CJH 5110.68 ± 2.39a 2.10 ± 0.08b 1.69 ± 0.01abc 1.26 ± 0.00ab 57.48 ± 0.45bc 1.72 ± 0.06a 0.80 ± 0.00a 2.15 ± 0.05ab 61.96 ± 1.24a 34.19 ± 0.37a 53.60 ± 1.96a
CJH 9112.66 ± 0.13a 2.12 ± 0.07b 1.63 ± 0.05bc 1.33 ± 0.05a 59.46 ± 1.93abc 1.74 ± 0.00a 0.80 ± 0.02a 2.18 ± 0.03ab 60.43 ± 2.50a 23.74 ± 0.58d 43.50 ± 0.17b
CJH 12114.40 ± 2.32a 2.05 ± 0.09b 1.74 ± 0.01ab 1.18 ± 0.05b 61.20 ± 1.46ab 1.68 ± 0.07a 0.78 ± 0.00a 2.17 ± 0.09ab 62.22 ± 1.32a 25.76 ± 0.38c 45.40 ± 2.10b
CJH 13116.81 ± 4.36a 2.16 ± 0.02b 1.78 ± 0.07ab 1.22 ± 0.05ab 63.61 ± 1.70a 1.71 ± 0.02a 0.81 ± 0.03a 2.12 ± 0.07b 58.99 ± 0.45a 24.64 ± 0.54cd 53.20 ± 2.55a
TNMC 7 (Control)109.56 ± 2.29a 2.37 ± 0.02a 1.80 ± 0.05a 1.33 ± 0.00a 56.36 ± 1.06c 1.75 ± 0.06a 0.75 ± 0.00a 2.34 ± 0.06a 63.85 ± 0.58a 21.92 ± 0.62e 35.40 ± 0.26c
p value0.399ns 0.024ns 0.030ns 0.135ns 0.025ns 0.939ns 0.624ns 0.628ns 0.401ns <0.0001 a <0.0001 a

Highly significant difference at p < 0.001 level of probability, and ns - no significance. Values with different superscripts were significantly different at p < 0.05 level of probability.

Mean performance in growth parameters of Jatropha hybrid clones. Highly significant difference at p < 0.001 level of probability, and ns - no significance. Values with different superscripts were significantly different at p < 0.05 level of probability. Mean performance in fruit and seed attributes of Jatropha hybrid clones. Highly significant difference at p < 0.001 level of probability, and ns - no significance. Values with different superscripts were significantly different at p < 0.05 level of probability. The mean performance of 5 Jatropha hybrid clones, along with the control variety, in their growth and yield attributes is presented in Table 1. The hybrid clone CJH 13 exhibited superiority in characteristics including plant height (131.72 ± 6.09 cm) and the number of fruits per bunch (26.25 ± 0.84). The number of fruit bunches per branch was higher in CJH 12 and CJH 13. The seed yield from the hybrid clones collected for the third year (7 harvests) varied significantly and ranged from 1,218.60 ± 21.91 g (CJH 13) to 653.66 ± 16.12 g (TNMC 7).

Variability in fruit and seed characters

CJH 13 exhibited superiority in terms of hundred-fruit weight (116.81 ± 4.36 g) and hundred-seed weight (63.61 ± 1.70 g), whereas TNMC 7 showed an advantage in terms of fruit length, fruit width, and shelling percent. Seed oil content varied between 34.19 ± 0.37 percent (CJH 5) and 21.92 ± 0.62 percent (TNMC 7). The kernel oil content ranged between 54.80 ± 0.80 percent (CJH 3) and 35.40 ± 0.26 percent (TNMC 7).

Genetic estimates of growth, yield, and yield-contributing characters

The male–female flower ratio demonstrated moderate PCV (21.22%) and GCV (21.10%), followed by seed yield, number of primary branches, number of secondary branches, number of male flowers, and number of fruits per bunch (Table 3). All the traits recorded high heritability (>60%). The genetic advance as percent over the mean was moderate for the male–female flower ratio (43.22%) and seed yield (32.85%). Among the fruit’s physical attributes, fruit yield exhibited moderate PCV (19.14%) and GCV (19.11%) values. All traits recorded high heritability (>60%), except for fruit aspect ratio (31%) and fruit width (54%). Fruit yield (39.32%) alone recorded high genetic advance as a percentage of mean compared to other parameters. Among the seed parameters, seed oil content registered moderate PCV (16.49%) and GCV (16.39%) values. All parameters recorded high heritability (>60%), except for seed length (43%) and seed width (46%). Seed oil content (33.56) alone recorded high genetic advance as a percentage of mean (Table 3).
TABLE 3

Genetic estimates of hybrid clones for biometrical, fruit, and seed characters.

TraitsPCV %GCV %Heritability (%)GA (%) of mean
Plant height6.085.8392.0011.50
Basal diameter5.244.9689.009.67
Sturdiness quotient5.184.6480.008.56
No. of primary branches14.7114.6595.0030.03
No. of secondary branches14.4514.4195.0029.59
No. of male flowers11.1411.0394.0022.49
No. of female flowers9.139.0995.0018.64
F:M ratio21.2221.1095.0043.22
No. of fruits/bunch10.7810.7395.0022.01
No. of bunches/branch5.605.4893.0011.05
Seed yield16.0516.0095.0032.85
Hundred-fruit weight2.502.2380.004.11
Fruit length6.415.9686.0011.41
Fruit width6.544.8054.007.27
Fruit aspect ratio6.863.8031.004.33
Fruit yield19.1419.1195.0039.32
Hundred-seed weight4.724.2280.007.77
Seed length1.881.2343.001.67
Seed width3.802.5746.003.60
Seed aspect ratio3.843.4480.006.35
Shelling percent3.062.5570.004.38
Seed oil content16.4916.3995.0033.56
Genetic estimates of hybrid clones for biometrical, fruit, and seed characters.

Association between yield and yield-contributing characters

Highly significant and positive phenotypic and genotypic correlations were recorded between the number of fruits per bunch (0.845 and 0.850) and the number of bunches per branch (0.771 and 0.788) on seed yield, followed by the number of female flowers (0.555 and 0.557), respectively (Table 4). Significant and negative phenotypic and genotypic correlations were recorded between the number of male flowers (–0.843 and –0.852) and male–female flower ratio (–0.760 and –0.765) on seed yield, respectively. The number of female flowers was positively correlated with the number of fruits per bunch (0.739 and 0.745) (Table 4).
TABLE 4

Phenotypic and genotypic correlation coefficients among biometrical traits on seed yield.

TraitsPlant heightBasal diameterSturdiness quotientNumber of primary branchesNumber of secondary branchesNumber of male flowersNumber of female flowersMale female flower ratioNumber of fruits/bunchNumber of bunches/branchSeed yield
Plant heightP1.0000.5810.5990.1830.181–0.5980.585–0.6390.536–0.0500.149
G1.0000.6340.5950.2070.182–0.6470.611–0.6780.558–0.0270.161
Basal diameterP1.000–0.3040.6890.557–0.6110.759 a –0.7130.4590.5350.322
G1.000–0.2440.7290.594–0.6540.815 a –0.764 a 0.4830.5660.341
Sturdiness quotientP1.000–0.456–0.325–0.095–0.065–0.0410.171–0.581-0.144
G1.000–0.492–0.378–0.129–0.084–0.0520.191–0.621-0.154
No. of primary branchesP1.0000.840 a –0.5170.373–0.4680.2770.864 a 0.502
G1.0000.847 a 0.5230.381–0.4750.2780.883 a 0.504
No. of secondary branchesP1.000–0.4330.467–0.4410.2270.7260.494
G1.000–0.4410.470–0.4460.2240.747 a 0.497
No. of male flowersP1.000–0.761 a 0.959 a –0.947 a –0.598–0.843 a
G1.000–0.768 a 0.960 a –0.960 a –0.631–0.852 a
No. of female flowersP1.000–0.911 a 0.739 a 0.4190.555
G1.000–0.914 a 0.745 a 0.4360.557
Male-female flower ratioP1.000–0.922 a –0.541–0.760 a
G1.000–0.932 a –0.569–0.765 a
No. of fruits/bunchP1.0000.4760.845 a
G1.0000.4870.850 a
No. of bunches/branchP1.0000.771 a
G1.0000.788 a
Seed yieldP1.000
G1.000

Significant at 5% level (F test).

Phenotypic and genotypic correlation coefficients among biometrical traits on seed yield. Significant at 5% level (F test). At both the phenotypic and genotypic levels, correlation studies found that hundred-fruit weight (0.540 and 0.605) had a positive relationship with fruit output. Except for fruit length (–0.720) and fruit aspect ratio (–0.838), which had significant negative correlations with fruit yield at the genotypic level, all other fruit parameters were negative and non-significant (Table 5). At both the phenotypic and genotypic levels, seed width (0.325 and 0.464) had a positive connection with seed oil content. The link between seed oil content and all other seed parameters was negative and non-significant (Table 6).
TABLE 5

Phenotypic and genotypic correlation coefficients among fruit attributes on fruit yield.

TraitsHundred-fruit weightFruit lengthFruit widthFruit aspect ratioFruit yield
Hundred -fruit weightP1.000−0.4080.157−0.5400.540
G1.000−0.4280.048−0.773 a 0.605
Fruit lengthP1.0000.5480.342−0.672
G1.0000.800 a 0.563−0.720 a
Fruit widthP1.000−0.454−0.144
G1.000−0.159−0.205
Fruit aspect ratioP1.000−0.459
G1.000−0.838 a
Fruit yieldP1.000
G1.000

Significant at 5% level (F test).

TABLE 6

Phenotypic and genotypic correlation coefficients among seed attributes on seed oil content.

TraitsHundred- seed weightSeed lengthSeed widthSeed aspect ratioShelling percentSeed oil content
Hundred- seed weightP1.000−0.5320.549−0.721 a −0.651−0.155
G1.000−0.5990.679−0.760 a −0.878 a −0.188
Seed lengthP1.000−0.2250.4340.200−0.224
G1.000−0.2800.732 a 0.135−0.341
Seed widthP1.000−0.780 a −0.6460.325
G1.000−0.985 a −0.895 a 0.464
Seed aspect ratioP1.0000.649−0.444
G1.0000.865 a −0.471
Shelling percentP1.000−0.002
G1.000−0.002
Seed oil contentP1.000
G1.000

Significant at 5% level (F test).

Phenotypic and genotypic correlation coefficients among fruit attributes on fruit yield. Significant at 5% level (F test). Phenotypic and genotypic correlation coefficients among seed attributes on seed oil content. Significant at 5% level (F test).

Biochemical properties of Jatropha hybrid clones

The acid value ranged between 7.05 ± 0.20 (CJH 12) and 5.18 ± 0.00 (TNMC 7). Free fatty acid content differed significantly among the different hybrid clones, ranging from 3.54 ± 0.16 percent (CJH 12) to 2.60 ± 0.05 percent (TNMC 7). Saponification values ranged between 203.36 ± 5.35 (CJH 12) and 201.12 ± 1.85 (TNMC 7). Iodine value extended from 116.64 ± 1.93 (CJH 13) to 107.56 ± 3.39 (CJH 3). The hybrid clones varied from 49.20 ± 0.69 (CJH 3 and TNMC 7) to 47.12 ± 0.18 (CJH 13) in terms of the cetane number (Table 7).
TABLE 7

Biochemical Properties of Jatropha hybrid clones.

ClonesAcid valueFree fatty acid content (%)Saponification valueIodine valueCetane number
CJH 35.27 ± 0.05d 2.65 ± 0.05d 201.40 ± 1.47a 107.56 ± 0.03a 49.20 ± 0.69a
CJH 55.60 ± 0.06cd 2.81 ± 0.20cd 201.96 ±6.97a 110.59 ± 5.52a 48.44 ± 1.27a
CJH 96.25 ± 0.15b 3.14 ± 0.00b 202.24 ± 9.68a 114.26 ± 1.72a 47.58 ± 0.70a
CJH 127.05 ± 0.20a 3.54 ± 0.16a 203.36 ± 5.35a 114.80 ± 3.91a 47.31 ± 2.28a
CJH 135.78 ± 0.19c 2.90 ± 0.02c 201.68 ± 3.27a 116.64 ± 1.93a 47.12 ± 0.18a
TNMC 7 (control)5.18 ± 0.00d 2.60 ± 0.05d 201.12 ± 1.85a 107.74 ± 3.39a 49.20 ± 1.21a
p value<0.0001 a <0.0001 a 1.000ns 0.296ns 0.728ns

Highly significant difference at p < 0.001 level of probability, and ns—no significance. Values with different superscripts were significantly different at p < 0.05 level of probability.

Biochemical Properties of Jatropha hybrid clones. Highly significant difference at p < 0.001 level of probability, and ns—no significance. Values with different superscripts were significantly different at p < 0.05 level of probability.

Discussion

Through selection and further deployment in evaluation programs, any tree-improvement program utilizes existing genetic variability (Chaturvedi and Pandey, 2001). In this study, the plant height, basal diameter, sturdiness quotient, number of primary branches, number of secondary branches, number of male flowers, number of female flowers, male–female flower ratio, number of fruits per bunch, and number of bunches per branch all changed considerably under field settings. For various growth characteristics, the hybrid clones CJH 13 and CJH 5 recorded much higher values. Paramathma (2010); Maurya ; Subashini ; and Gawali found comparable and considerable variance in growth indices in J. curcas. J. curcas is a monoecious tree with a minimal number of female flowers relative to its numerous male flowers, which is the key reason for its low yield. Increasing the number of female flowers in the inflorescence may result in increased fruit set and, in turn, increased seed yield. In the present study, CJH 5 demonstrated superiority in terms of the number of female flowers (38.75) and registered a lower male–female flower ratio (6.52) compared to the other hybrid clones. Similar noteworthy studies on the floral characters of J. curcas were previously conducted by Paramathma (2010); Maurya and Subashini and lend support to the current investigation. The seed yield of a tree is influenced by biometric traits (viz., number of branches, crown diameter, and age). In the present investigation, two hybrid clones, CJH 13 (1,218.60 g) and CJH 12 (1,034.40 g), showed significant performance for seed yield per plant at early stages of growth and development. These two hybrid clones are prominent, and the consistency and fidelity expressed by these hybrid clones could be useful for future improvement programs. Parthiban observed that the fruit yield of Jatropha hybrid clones ranges from 131.78 to 857.51 g per plant. Divakara , in the case of Pongamia pinnata, also reported that not only plant growth characters but also environmental factors have vital roles in seed yield. Biabani evaluated different Jatropha populations and reported that the seed yield per plant was highest in Indonesia, which recorded 46, 399, and 222 (g) for the first, second, and average years’ harvests, respectively. Indonesia was closely followed by the Philippines, with values of 35 (g) for the first year, and Malaysia, with values of 262 and 146 (g) for the second and average years’ harvests, respectively. Nature offers plants with enormous energy potential. Jatropha is one of the most significant species that can be utilized in the form of biodiesel. The basic aim for any tree-breeding program is to exploit the available natural variability within a species, ultimately resulting in higher production in terms of yield. In the present investigation, significant differences were observed in the fruit’s physical traits (viz., fruit length, fruit width, fruit aspect ratio, and hundred-fruit weight). The hybrid clone CJH 13 recorded the highest significant values for hundred-fruit weight (116.81 g), whereas TNMC 7 exhibited superiority in terms of fruit length (2.37 cm), fruit width (1.80 cm), and fruit aspect ratio (1.33). Similar variability in the physical fruit parameters of J. curcas was previously recorded (Gawali et al., 2013), affirming the findings of the current study. The study of seed parameters, along with oil content, is often considered to be a suitable step in the study of genetic variability in case of tree-borne oil seeds. Thus, seeds from trees with higher seed weights and oil content may be used for further improvement programs (Kaushik et al., 2007). The hybrid clone CJH 13 recorded the highest significant values for seed width (0.81 cm) and hundred-seed weight (63.61 g), CJH 5 registered the highest significant value for seed oil content (34.19%), and CJH 3 recorded high kernel oil content (54.80%). Comparable findings in J. curcas were previously reported by Tripathi and Singh , which supports the results of present study. Variation describes noticeable changes across individuals for a specific trait. These differences are partially due to genetic control and partially due to the influence of the environment. All the growth attributes under study exhibited higher heritability values (0.80–0.99), suggesting that these traits are under strong genetic control. Lower heritability for vegetative characters and moderate-to-high heritability for reproductive characters have been reported in backcross populations of Jatropha (Subashini et al., 2014). There were high significant variations among the populations with regard to the yield and yield components, and results of ANOVA on these traits indicated highly significant variation among populations for first, second, and average years of harvesting (Biabani et al., 2012). Ghosh and Singh (2011) identified similar phenotypic variations in seed length, seed width, hundred-seed weight, oil content, seed yield, oil content percentage, and seed oil yield among J. curcas populations. Traits such as the number of branches, number of female flowers, number of fruits per bunch, and seed yield exhibited higher heritability (0.99) with moderate genetic advance; hence, these traits are under strong genetic control. The current findings corroborate earlier studies in Jatropha (Reeja, 2018), suggesting that the traits involved in high heritability with moderate genetic gain may be due to the presence of additive genes. Phenotypic correlation is a product of the interaction between genotype and environment, whereas genotypic correlation is an assessed value. The complexity of seed yield is mostly influenced by the quantity of characteristics, which in turn affects the production of oil. In order to create a valuable and feasible breeding program for increasing seed yield, knowledge of the associations between these traits would be very supportive. Fruit yield recorded high PCV (19.14) and GCV (19.11), and high heritability (0.99) and maximum genetic advance (39.32), followed by fruit length and hundred-fruit weight. Hence, this parameter could be used as a reliable trait for selection. The hundred-fruit weight, fruit length, fruit width, and fruit aspect ratio recorded low PCV and GCV, which agrees with the result of Gawali et al. (2013) in J. curcas. The seed oil content demonstrated higher phenotypic (16.49) and genotypic (16.39) coefficients of variation. The seed aspect ratio, seed length, seed width, shelling percent, and hundred-seed weight documented low PCV and GCV. Similar results have been observed in J. curcas (Gawali et al., 2013) and in backcross populations of Jatropha (Subashini et al., 2014), which corroborates the current findings. In the present investigation, seed oil content expressed high heritability (0.99), which indicated additive gene action and moderate heritability for seed length and seed width, showing that they are governed partly by additive gene actions. The distinctly higher heritability can be regarded as a key feature for Jatropha improvement because of its strong genetic control. Correlation studies are important in determining the suitability of numerous traits for selection since selection of particular traits may bring desirable or undesirable changes in the related traits. For all the traits investigated, the genotypic correlation coefficient was higher than the corresponding phenotypic correlation coefficient, indicating that in the majority of cases, the environment has not appreciably influenced the associated traits. The number of fruits per bunch and the number of bunches per branch showed positive and significant correlations with seed yield, whereas the number of male flowers and male–female flower ratio showed negative and significant correlations with seed yield. Such positive and highly significant correlations in Jatropha can be used for further breeding programs. Comparable positive and significant correlations have been observed by Subashini and Parthiban et al. (2011) in J. curcas and by Chauhan in neem, which supports the results of current study. In addition, the basal diameter, sturdiness quotient, number of primary branches, number of secondary branches, number of male flowers, number of female flowers, male–female flower ratio, number of fruits per bunch, and number of bunches per branch showed strong correlation among themselves, signifying that some genes governing these characters may be closely associated with each other. The number of male flowers, male–female flower ratio, number of fruits per bunch, and number of bunches per branch could serve as good predictors of seed yield in Jatropha. The traits of fruit length and fruit aspect ratio showed negative and significant correlations with fruit yield at the genotypic level only. Comparable results have been documented in J. curcas (Gawali et al., 2013; Singh et al., 2013). Seed width registered positive but non-significant correlation with seed oil content, which indicated that this parameter has contributed significantly to seed oil content and hence could act as a reliable index in Jatropha improvement programs. In contrast, all other seed parameters registered negative and non-significant correlations with seed oil content, which specified that these characters showed independent genetic control. Chemical properties are the vital properties that determine the present condition of oil (Nzikou et al., 2009). Several chemical properties of biodiesel permit it to burn cleanly and improve the combustion of diesel in blends. Some of the primary chemical properties which determine the suitability of oils for the utilization of biodiesel are acid value, iodine value, cetane number, free fatty acid content, and saponification value. Standards for these properties have been established worldwide and in India; the Bureau of Indian Standards has specified standards (IS:15,607, 2006). In this study, significant variations were documented for acid value of the seed oil of Jatropha hybrid clones. All the five hybrid clones recorded significantly higher acid values compared to the control variety, which was still higher than the standard value (0.5). The properties of triglycerides and biofuels depend upon the degree of fatty acids (unsaturated and saturated) present in the molecules. Free fatty acid percentage differed significantly among the different hybrid clones deployed in the current investigation. The free fatty acid percentage ranged from 3.54% (CJH 12) to 2.60% (TNMC 7), and the increase in free fatty acid content could be due to oil storage. High free fatty acid content (>1%) results in soap formation and hence difficulty in the splitting of products, leading to low recovery of biodiesel (Crabbe et al., 2001). The free fatty acid and moisture content influence the transesterification of glycerides with alcohol using a catalyst. High free fatty acid percentage (2.23%) has been recorded earlier in Jatropha oil seeds (Goodrum, 2002). Saponification value is an indicator of the extent of fatty acids present and rests on the molecular weight and percentage concentration of fatty acid components in the oil. Apart from biodiesel purposes, a high saponification value indicates that oils can be used in the production of liquid soap and shampoo. Only one hybrid clone (viz., CJH 12 (203.36)) recorded significantly higher saponification values compared to the control variety TNMC 7 (201.12). Similar studies on the saponification value of J. curcas hybrids have been reported by Ntaganda (2014). The iodine value reflects the degree of the unsaturation of fats and oils. Higher iodine values indicate higher unsaturation of fats and oils (Knothe, 2002). The iodine value ranged from 116.64 (CJH 13) to 107.56 (CJH 3). These values indicate that the oils of hybrid clones are well below the limit of 115 set by the European standards (EN:14,214, 2008). Hence, all the hybrid clones deployed in the current investigation are qualified to produce biodiesel with respect to iodine value. The iodine values of Jatropha lie in the semi-drying oil group. Jatropha’s higher iodine value is due to the presence of high amounts of unsaturated fatty acids, such as oleic acid and linoleic acid. The ignition quality of a fuel can be inferred through its cetane number (Azam et al., 2005). A fuel with high ignition quality also has a high cetane number, in which the ignition delay period between the start of fuel injection and the onset of auto ignition is short. These fuel properties are significant in deciding diesel engine operating features such as fuel conversion efficiency, smoothness of operation, misfire, smoke emissions, noise, and ease of starting. The cetane value was found to be significantly higher for CJH 3 and TNMC 7 (49.20), which is near the acceptable minimum standard value of 51, per the IS:15,607 (2006) biodiesel specification of the Bureau of Indian Standards. The minimum acceptable cetane number, per the American standards for biodiesel, is 47, and most of the hybrid clones recorded significantly higher cetane numbers compared to the American standard (ASTM D6751, 2002). All the hybrid clones deployed in the current investigation recorded cetane numbers in the range of 47–49, indicating their usability as biodiesel and substantiating the study of Sivaramakrishnan and Ravikumar (2012).

Conclusion

Through a holistic analysis, the current study identified the superiority of two hybrid clones (viz., CJH 13 and CJH 12) for productivity of seeds and one hybrid clone (viz., CJH 5) for higher seed oil content. The study also found that all the hybrid clones were amenable for biodiesel production due to their acceptable and satisfactory biofuel quality. Hence the hybrid clones with higher seed yield and superiority in chemical properties could be selected for further commercial exploitation to produce biofuel. The research has an excellent application value both in the biofuel sector and in the farming sector. A Jatropha-based multifunctional agroforestry system can act as an alternate and sustainable land-use system, while helping to generate significant income for farmers. It has an excellent application value for creating new start-ups and business enterprises in the form of seed processing, establishment of oil processing plants, and creation of decentralized transesterification plants at the rural level. These establishments will create self-reliance in the green energy sector, thereby extending their significant application value. However, the current research still needs further investigation into the performance of hybrid clones under different agroclimatic zones, coupled with associated physical, chemical, and other biodiesel properties, in order to successfully deploy Jatropha hybrid clones for biodiesel production on a commercial scale.
  1 in total

1.  Energy: that's oil, folks...

Authors:  Alexandra Witze
Journal:  Nature       Date:  2007-01-04       Impact factor: 49.962

  1 in total

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