Enhancement of Sweet Gourd Seedling Qualities Priming With H2o2
Enhancement of Sweet Gourd Seedling Qualities Priming With H2o2
9(10), 485-494
RESEARCH ARTICLE
ENHANCEMENT OF SWEET GOURD SEEDLING QUALITIES PRIMING WITH H2O2
Md. Rahim Badsha1, Fahadul Haque2, Farzana Sultana2, Abdullah Al Mahmud1 and Aklima Khatun3
1. MS Student, Dept. of Horticulture, Hajee Mohammad Danesh Science and Technology University (HSTU),
Dinajpur.
2. Assistant Director, Bangladesh Agricultural Development Corporation (BADC), Motijheel, Dhaka.
3. Department of Agricultural Extension, Khamarbari, Dhaka.
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Manuscript Info Abstract
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Manuscript History A study with three independent experiments for the seeds of three
Received: 24 August 2021 vegetable species was set at the roof top of Sunway Dormitory near the
Final Accepted: 27 September 2021 Bus Terminal, Dinajpur, Bangladesh, during March to May, 2019. The
Published: October 2021 aims were to evaluate the physiological fluctuations in the seeds of
sweet gourd cv. Monitaraprimed with the aqueous solutions of H 2O2
and to find the suitable concentration. Each experiment had eight
treatments: T1 (control/no priming), T2 (hydro-priming in plain H2O)
and other six aquatic solutions of H2O2: T3 (0.5), T4 (1.0), T5 (1.5), T6
(2.0), T7 (2.5) and T8 (3.0%). The seeds were soaked for six hours in
those seven media (T2 toT8). The seeds were dibbled in wooden seed
flats filled-in with coarse sand. The experiments were laid-out in the
Randomized Complete Block Design with three replications. Data
collected for the 13 traits viz. % germination, % abnormal seedlings,
shoot length, root length, seedling length, shoot dry matter, root dry
matter, seedling dry matter, number of secondary roots (>1cm) per
seedling, number of true leaves per seedling, relative growth rate,
seedling vigor index, and root : shoot ratio (dry weight basis). Except
the first two traits, the rest 11 were collected at three stagesviz.10, 20
and 30 days after dibbling (DAD). It was lucid that H2O2 was
significantly (P≤0.05%) effective to improve most of the traits noted.
Treatment T4 (1% concentration) was utmost helpful for sweet gourd
and >1.5%, others were toxic and hindered the maximum parameters
for all the three species. Nevertheless, further studies with different
varieties of those three vegetables species with variable doses of H 2O2,
priming time and temperature could be explored before drawing valid
conclusions.
cradle of protein and furthermore having the pharmacological properties such as antifungal, anti-diabetic and anti-
inflammation characteristics (Nkosiet al. 2006). The seed extracts have been used as an antidiabetic, antitumor,
antibacterial, anticancer and antioxidant (Cl et al.2006).
Seed germination is one of the vital stages in the life cycle of seeded plants. Germination is a very complex process
starting with the imbibition of H2O and involves events related with the transition of a dry quiescent and/or dormant
seed to the metabolically active state (Kranneret al., 2011, and Schopferet al., 2001). The emergence of the
embryonic axis through structures surrounding the embryo is the final stage of germination (Weitbrechtet al., 2011).
In this link, seed priming is used as a means to enhance seed performance, notably in terms to the rate and the
uniformity of germination (Taylor and Harman, 1998). Seed priming is known as the pre-sowing approach to govern
seed germination and seedling development by modulating pre-germination metabolic activities prior to emergence
of the radicle and usually enhances germination rate and plant growth (Bradford, 1986, and Taylor and Harman,
1998).Various physiological and bio-chemical changes happen in seeds during priming as a result of osmotic
conditioning. A wide range of pre-sowing hydration techniques is used to enhance seed germination responses.
These include equilibrium under conditions of high humidity (Finnertyet al., 1992), soaking in plain H2O (Coolbear
and McGill, 1990) or osmotic solutions (Knypl and Khan, 1981) and having equilibrium with a matric potential
controlling surface (Hardegree and Emmerich, 1992). Hydro-priming, osmo-priming (with mannitol or PEG 6000)
and halo-priming (with KCl, KNO3 or calcium salts) are effective for seedling establishment under harsh conditions
(Toselli and Casenav, 2003). The priming enhances rapid and uniform emergence, high vigor and better yield, which
has practical utilities, preferably under water stress conditions (Black et al., 2006).
H2O2 is a reactive molecule playing crucial roles in plants, especially under unfavorable germination conditions,
developmental processes and in resisting stresses in reactive oxygen species/ROS (El-Maarouf-Bouteau and Bailly,
2008). H2O2 acts as a signaling molecule in the beginning of seed germination involving specific changes at the
proteomic, transcriptomic and hormonal levels (Afghani and Taheri, 2012, and Demiret al., 2012). Priming of seeds
with H2O2 leads to break primary dormancy (Jann and Amen, 1997); secondary dormancy provoked by salinity
(Jiaet al., 2002) and germination inhibitors (Ogawa and Masaki, 2001). It acts as a stress signal in plants and hence
exogenous uses of H2O2 in the right dose ameliorates seed germination, reduces time to germinate and seedling
growth in many crops (Patadeet al., 2012). So, it has special roles, especially in invigorating seeds with low vigor
including long-term stored seeds in gene banks.So, instead of H2O, seed priming with aqueous solution of H2O2 with
the appropriate dose could be an applicable technology (Copeland and Mcdonald, 1985). The objective of the study
was to evaluate the physiological changes of the seedlings of sweet gourd primed with of H2O2and find the best
concentration.
Experimental treatments
This single factor experiment was designed with eight treatments viz. T 1 (control/no priming), T2 (hydro-priming in
plain H2O) and other six aquatic solutions of H2O2: T3 (0.5%), T4 (1.0%), T5 (1.5%), T6 (2.0%), T7 (2.5%) and T8
(3.0%). This single factor experiment was set in the Randomized Complete Block Design (RCBD) with three
replications.
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Priming process
At first, only H2O and those six solutions were taken in plastic glasses separately. The glasses were marked about
the treatments and replications with a permanent glass marker. Then the 200 seeds for each replication were taken in
plastic glasses to soak in the desired solutions for six hours in the Laboratory of Horticulture (Plate 2).
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Data collection
The data were collected for % germination and % abnormal seedlings at 10 days of dibbling and shoot length, root
length, seedling length, shoot dry matter, root dry matter, seedling dry matter, number of secondary roots (>1cm) per
seedling, number of true leaves per seedling, relative growth rate, seedling vigor index, and root shoot ratio (dry
weight basis) at 10, 20 and 30 DAD.
Germination (%) and normal seedling (%) were observed and counted as per the ISTA (2010) rules daily up to 10
DAD. For dry matter the normal seedlings were cut and divided into roots and shoots with a razor blade from each
treatment and replication wise. Then those were first sundried separately for two days. After that, those were dried at
80°C for 48 hours in an electric oven (Memmrert, ULP 400). Then the dry weights of shoots were recorded up to
four decimal places with an electric digital balance (Ohaus, pioneer pro PA214). Finally, the dry weights were
expressed in gram per 100-seedling basis. Those processes were repeated with the normal seedlings only obtained
from the 10, 20 and 30 DAD. Relative growth rate (RGR)was calculated as per Williams (1946) formula and
Seedling vigor index (SVI) was calculated as per Orchard (1977) and Baki and Anderson (1973) viz. SVI = Mean
seedling (root + shoot) length (MSL) in cm ×% germination (PG)
Statistical analyses
The analyses of variances (ANOVA) were done and the means were separated using Duncan’s Multiple Range Test
(DMRT). The MSTAT-C Statistical Package program was used for it.
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90.00 a
90
87.00 ab
85.67 ab
85.33 ab
88
Percentage Germination (%)
86
83.33 b
82.33 b
82.00 b
84
81.33 b
82
80
78
76
T₁ T₂ T₃ T₄ T₅ T₆ T₇ T₈
Treatment
Fig.1:- Effect of seed priming with H2O2 on the % germination of sweet gourd.
5.66 a
5.00 a
5.00 a
6
4.66 ab
Percentage Abnormality (%)
4.00 ab
5
3.00 bc
3.00 bc
4
2.00 c
0
T₁ T₂ T₃ T₄ T₅ T₆ T₇ T₈
Treatment
Fig. 2:- Effect of seed priming with H2O2 on the %abnormal seedlings of sweet gourd.
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Table 1:- Effect of priming seedwith H2O2 onshoot, root and seedling length in sweet gourd.
Treatme Shoot length (cm) Root length (cm) Seedling length (cm)
nts 10 DAD 20 DAD 30 DAD 10 DAD 20 DAD 30 DAD 10 DAD 20 DAD 30 DAD
T1 6.38ab 8.77ab 9.08bc 5.07ab 11.76c 17.87a 11.46ab 20.54a 26.96ab
T2 5.95bc 8.13cd 9.27ab 4.37cd 12.60b 19.52a 10.33c 20.73a 28.79a
T3 6.26ab 8.33bc 9.39ab 5.03ab 12.56b 19.05a 11.30ab 20.89a 28.44a
T4 6.68a 8.94a 9.73a 5.34a 13.46a 20.02a 12.03a 22.40a 28.75a
T5 6.08abc 8.00cd 8.97bc 4.79bc 11.62c 17.41a 10.74bc 19.63a 26.38bc
T6 5.86bc 7.67de 8.99bc 4.47c 12.65b 12.82b 10.34c 20.33a 25.15bc
T7 6.22ab 7.79de 9.06bc 4.56c 11.70c 16.74ab 10.79bc 19.50a 25.80bc
T8 5.53c 7.45e 8.62c 4.02d 11.46c 16.03ab 9.555d 15.25b 24.54c
LSD(0.05) 0.619 0.476 0.522 0.418 0.771 3.772 0.751 3.705 1.794
CV % 5.78 3.35 3.26 5.07 3.60 12.36 3.97 10.63 3.81
The figures with different letters differ among themselves at the 5% level of probability.
T1 = Control/no priming, T2 =Hydro-priming in plain H2O), T3 = 0.5% aquatic solutions of H2O2, T4 = 1.0% aquatic
solutions of H2O2, T5 = 1.5% aquatic solutions of H2O2, T6 = 2.0% aquatic solutions of H2O2, T7 = 2.5% aquatic
solutions of H2O2 and T8 = 3.0% aquatic solutions of H2O2
Table 2:- Effect of priming seedwith H2O2 onshoot, root and seedling dry matter of sweet gourd.
Treatments Shoot dry matter Root dry matter Seedling dry matter
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Table 3:- Effect of priming seedwith H2O2 on number of secondary root and true leaves of sweet gourd.
Treatments Number of secondary roots Number of true leaves
10 DAD 20 DAD 30 DAD 10 DAD 20 DAD 30 DAD
T1 6.85def 12.36cd 21.08ab 0.860b 3.13a 4.61b
T2 7.25cde 13.30b 18.50cd 0.833bc 2.56a 4.50b
T3 9.33b 10.81e 20.94ab 0.883ab 2.55a 4.55b
T4 11.05a 14.35a 21.53a 0.933a 3.14a 5.03a
T5 8.31bc 10.25ef 18.40cd 0.850bc 2.59a 4.66ab
T6 7.75cd 13.20bc 18.50cd 0.850bc 2.85a 4.61b
T7 6.21ef 11.85d 19.75bc 0.866b 2.85a 4.63b
T8 6.00f 9.67f 18.01d 0.800c 2.50a 4.36b
LSD (0.05) 1.124 0.889 1.479 0.055 0.638 0.375
CV % 8.18 4.25 4.31 4.11 13.16 4.63
The figures with different letters differ among themselves at the 5% level of probability.
T1 = Control/no priming, T2 =Hydro-priming in plain H2O), T3 = 0.5% aquatic solutions of H2O2, T4 = 1.0% aquatic
solutions of H2O2, T5 = 1.5% aquatic solutions of H2O2, T6 = 2.0% aquatic solutions of H2O2, T7 = 2.5% aquatic
solutions of H2O2 and T8 = 3.0% aquatic solutions of H2O2
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Table 4:- Effect of seed priming with H2O2 on Seedling vigor index,relative growth rate and root shoot ratio of
sweet gourd.
Treatments Seedling vigor index Relative growth rate Root shoot ratio
10 DAD 20 DAD 30 DAD 10-20 20-30 10 DAD 20 DAD 30 DAD
DAD DAD
T1 997.0b 1787b 2346b 0.050a 0.083a 0.156a 0.280b 0.286a
T2 884.9c 1776b 2466ab 0.046a 0.090a 0.163a 0.250b 0.266a
T3 941.6bc 1763b 2370b 0.046a 0.096a 0.200a 0.250b 0.260a
T4 1083.0a 2016a 2588a 0.046a 0.090a 0.176a 0.336a 0.286a
T5 881.0c 1609c 2163c 0.046a 0.086a 0.170a 0.230b 0.243a
T6 882.3c 1735b 2146cd 0.053a 0.083a 0.166a 0.350a 0.253a
T7 888.1c 1605c 2124cd 0.036a 0.086a 0.143a 0.240b 0.300a
T8 777.0d 1511d 1996d 0.050a 0.090a 0.153a 0.226b 0.263a
LSD (0.05) 62.50 53.88 153.2 0.055 0.055 0.055 0.055 0.055
CV % 3.89 1.78 3.85 10.87 5.45 10.04 12.07 7.21
The figures with different letters differ among themselves at the 5% level of probability.
T1 = Control/no priming, T2 =Hydro-priming in plain H2O), T3 = 0.5% aquatic solutions of H2O2, T4 = 1.0% aquatic
solutions of H2O2, T5 = 1.5% aquatic solutions of H2O2, T6 = 2.0% aquatic solutions of H2O2, T7 = 2.5% aquatic
solutions of H2O2 and T8 = 3.0% aquatic solutions of H2O2
Conclusions:-
It canbe concluded thatH2O2had optimistic effects on the seedling qualities. Again, among the six concentrations of
the H2O2, 1%was the most effective one for sweet gourd and sweet gourd while 1.5% was suitable for radish seeds.
Above those concentrations, others were somewhat toxic as those hindered a lot of the parameters evaluated.
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