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pg. 50 North American Academic Research , Volume 2, Issue 3 – March ; 2019, 2(3) : 50-57 ©TWASP,
USA
North American Academic Research
Contents lists available at : www.twasp.info
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Research
Evaluation of Seed Quality and Health of Some Aus Rice Genotypes
Md. Sadiqur Rahman1*, Taslima Jahan2, Monjur Morshed3, Md. Riyadh Arefin4, Dr. M.
Moynul Haque 5 1Scientific Officer, Regional Agricultural Research Station, Bangladesh Agricultural
Research Institute, Moulvibazar, Bangladesh 2Scientific Officer, Plant Genetic Resources Centre, Bangladesh Agricultural Research
Institute, Bangladesh 3Department of Soil Science, Bangabandhu Sheikh Mujibur Rahman Agricultural University,
Gazipur–1706, Bangladesh 4Scientific Officer, Bangladesh Tea Research Institute, Bangladesh 5Professor, Seed Technology Division, Bangabandhu Sheikh Mujibur Rahman Agricultural
University, Gazipur–1706, Bangladesh
*Corresponding Author :
Md. S. Rahman
Email: [email protected]
Mobile: 01714492070
Published online : 05 March, 2019
Abstract: An experiment was conducted at Seed Technology and Plant Pathology laboratory of
Bangabandhu Sheikh Mujibur Rahman Agricultural University to evaluate the seed quality and
health of some Aus rice genotypes viz. Chehrang Sub1, Shengyon 11-25, Shengyon 11-26, NERICA
10, Pariza, BU dhan1, and BRRI dhan48 were used in this experiment. Significant variation in
respect of germination (%), germination rate, leachate conductivity, normal seedling (%), un-
germinated fresh seed (%) and pathogenic infection was observed in different genotypes. Among
the genotypes, BRRI dhan48 had a higher percentage of germination and normal seedling with
higher germination rate having lower leachate conductivity. In the case
of pathogen, Fusarium moniliforme was dominant, and its prevalence was highest in Chehrang Sub1
genotype and in the case of Alternaria padwickii the highest prevalence was observed in Pariza
genotype. The percent of abnormal seedlings and the pure live seed of all genotypes were
statistically similar. Among the treatments, germination % was lowest in BU dhan1. The highest
lethal seed infection was caused by Fusarium moniliforme;
Alternaria padwickii and Curvularia lunata also caused lethal seed infection, might have an effect on
germination rate and leachate conductivity.
Keywords: Germination rate,leachate conductivity, prevalence of seed borne fungi
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Introduction:
Seed health refers primarily to the presence or absence of disease-causing organisms such as
fungi, nematodes, bacteria, viruses, and insects associated with seed. Physiological conditions
such as trace element deficiency may also affect seed health (ISTA 1985). Farmers often use
seeds that have impurities and contaminants and are infected with pathogens (Fujisaka,
Guino, Lubigan, and Moody1993,149-157). The importance of seed quality in realizing the
full potential of a variety is well known. The three major aspects of seed quality are a) genetic
and physical purity, b) high germination percentage and vigor, and c) free from seed-borne
diseases and insects (Seshu and Dadlani 1989). Seed vigor is recognized as an important seed
quality parameter distinct from germinability (Seshu, Krishnasamy and Siddique 1988, 315-
329). According to Thomson (1979), high-quality seed is a critical input on which all other inputs
will depend on for their full effectiveness. If the seed is not standard quality, the use of other inputs
is less useful. Production is affected due to inferior seed quality and incurred economic loss due to
misuse of other inputs. Inferior seeds may decrease production. Quality means suitability for its
sowing to achieve a satisfactory yield. In general, this is determined by the quality components of
seed. The components are seed size, purity, moisture content, germination percentage, seed
health, viability, and seed vigor, etc.
Healthy seeds play a vital role in improving the yield of any crop. They carry the genetic
characteristics for successful crop production. It is important that healthy seeds must be used
as planting materials in order to increase crop productivity. Contaminated seeds can often
result in poor germination, poor seedling vigor, and unhealthy crop. The deterioration of the
seed vigor in crops accounted for 20 percent of the yield losses (Shenoy, Paris and Duff
1988). The present investigation was carried out to establish whether seed-borne fungi are
responsible for seedling abnormalities, the possibility of combining germination tests and
seed health tests to determine the effect of seed treatments and seed processing procedures on
germination and seedling vigor.
Materials and Methods:
The experiment was conducted at Seed Technology and Plant Pathology laboratory of
Bangabandhu Sheikh Mujibur Rahman Agricultural University. A total of seven seed samples
were collected from the harvested rice seeds viz. Chehrang Sub1, Shengyon 11-25, Shengyon
11-26, NERICA 10, Pariza, BU dhan1, and BRRI dhan48, and kept in the Seed Technology
Laboratory of Bangabandhu Sheikh Mujibur Rahman Agricultural University (BSMRAU),
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Gazipur. Quality and health attributes of the harvested seeds were determined according to
ISTA rules.
Purity analysis
The purity analysis of seed sample was performed to determine the pure seed, contamination
with inert materials, weed seeds and seeds of other crops. A working sample of 70 g was
drawn from each sample and spread on the purity analysis board provided with a light source
and a magnifying lens. From the working sample, inert materials, weed seeds, seeds of other
crops, insects damaged seeds, spotted seeds were separated manually. The weight of the
individual component was measured using digital electric balance having a capacity of 0.001-
400 g. The results were expressed in percentage based on the gross weight of the working
sample using the following formula:
The weight of the individual component/gross seed weight x 100
Germination test
Seeds were tested for germination capacity. From each sample, four replicates of one hundred
seeds were counted at random from well-mixed pure seed fraction. Seeds were placed
uniformly and adequately apart on three layers of moist filter paper substrate in 21 cm x 15.5
cm germination trays. Germination trays were kept in germinator maintained at 20ͦ C for 16
hours in dark and 30ͦ C for 8 hours with light for a total period of 14 days. Each and every
seedling was evaluated according to general principals laid down in ISTA rules in 2006. The
classification was made as a normal seedling, abnormal seedling, diseased seeds, and non-
germinated fresh seeds. Germination percentage was calculated as:
Number of seeds germinated
Germination (%) = ---------------------------------------- x 100
Number of seeds tested
Seed vigor (Leachate conductivity)
For electrical conductivity test, 50 gm seeds of each sample were taken in a conical flask
containing 50 ml de-ionized water and incubated at 20ͦ C for 20 hours; water of the beaker
containing seeds was decanted in order to separate the seeds. The electrical conductivity was
measured by the EC meter. Four replications of measurements were made for each sample of
seed and expressed in μs/cm.
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Seed viability
Seed viability was tested by tetrazolium salt test. A hundred seeds were soaked in 1%
colorless tetrazolium salt for 24 hours. The experiment was repeated three times, where the
colored embryo indicates viable seeds.
Germination rate
Germination rate (GR) was calculated from a daily count of germinated seeds until it reached
a constant value and calculated as:
GR= +……… +
Pure live seed
To calculate pure live seed (PLS), the percentage of pure seed is multiplied by the percent
germination (percent normal seedling) and the product is divided by 100.
% pure seed x % normal seedling
PLS (%) = --------------------------------------------------
100
Seed dormancy
The percentage of dormancy was calculated by deducting the germination percentage from
viable seed percentage.
Seed health testing
Seed health of rice i.e. fungi associated with the seed samples was tested by Standard blotter
method (Marcinkowska 2002). Three layers of sterilized wet filter paper (Whatman filter
paper no.1) were placed in the bottom of 9 cm Petri dishes. In this test, 400 seeds per sample
were used and 25 rice seeds were placed on filter paper of each Petri dish. The Petri dishes
containing seeds were incubated at 25±2ͦ C in an incubator for 7 days. The incubated seeds
were examined under a stereomicroscope and different fungi grew from seeds were
identified. For proper identification of fungi, temporary slides were prepared from the fungal
colony and observed under a compound microscope. The prevalence was expressed in
percentage based on the total number of seeds planted.
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Statistical analysis
All data were subjected to statistical analysis by analysis of variance (ANOVA). Microsoft
EXCEL and R stat program software. Means were separated using Duncan’s Multiple Range
Test (DMRT) at a significance level of 0.001, 0.01 and 0.05 (Gomez, Gomezand
Gomez1984).
Results and discussion:
Seed quality:
Germination percentage differed significantly among the different genotypes (Table 1). BRRI
dhan48 had the highest germination percentage (95.25%) which was statistically similar to
those of Chehrang Sub1, Shengyon 11-25 and Pariza. The lowest germination percentage was
recorded in BU dhan1 (89.67%) which was followed by Shengyon 11-26 and NERICA 10
(Table 1).
The level of seed dormancy did not vary significantly among the genotypes. It varied
from 3.83 to 7.83% depending upon the genotypes. Basically, indica rice show either non-
dormant, moderate or strong dormancy according to their growing seasons. But when rice is
sown in the Aus season, it shows non-dormant to moderate dormancy. In the present study,
seeds of different genotypes showed moderate dormancy which might be due to genetic
make-up and prevailing in seed formation and development of the variety.
The germination rate of seeds obtained from different genotypes differed when compared to
the germination percentage. BRRI dhan48 had the highest germination rate and the lowest
leachate conductivity. It also produced the highest pure live seeds while the maximum
percent of purity was observed in BU dhan1.
Purity is an important indicator of seed quality, while the pure live seed is a more important
indicator of seed quality because it expresses both purity and germination. In the present
study, all genotypes gave more than 85.53% pure live seed which indicates good quality seed.
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Table 1. Seed and Seedling quality attribute of different Aus rice genotypes
Rice
genotypes
Germination% Dormancy
(%)
Viability% Germination
rate
Leachate
conductivity
(µs cm-1)
Purity
(%)
PLS
(%)
Chehrang
Sub1 92.67 ab 3.83 96.7 23.09 b 49.57 ab 95.78 88.43
Shengyon
11-25 92.67 ab 4.67 97.3 23.85 b 45.67 ab 95.02 88.02
Shengyon
11-26 90.83 b 5.83 96.7 24.33 ab 25.23 c 94.16 85.53
NERICA
10 91.83 b 5.5 97.3 23.81 b 44.23 ab 95.78 87.96
Pariza 92.75 ab 4.58 97.3 24.18 ab 49.91 ab 93.61 86.84
BU dhan1 89.67 b 7.83 97.7 23.28 b 51.33 a 96.16 86.41
BRRI
dhan48 95.25 a 4.08 99.3 25.46 a 18.10 c 96 91.45
CV (%) 1.77 33.35 1.27 3.09 26.93 1.94 2.88
Sig. Level * ns ns * ** ns ns
Means followed by same letter(s) in a column are not significantly different by DMRT.
Seedling quality
Parameters related to germination capacity of rice seeds, in terms of normal seedlings,
abnormal seedlings, diseased seeds and non-germinated fresh seeds in samples of seven
categories are presented in Table 2.
The percentage of normal seedlings varied significantly among the genotypes. The highest
percentage of normal seedlings was recorded in BRRI dhan48 (93.58%) which was
statistically identical to Chehrang Sub1 (91.25%) and Pariza (91.42%). The percentage of
normal seedlings was recorded in BU dhan1 (87.83%) which was statistically identical to
Shengyon 11-25 (89.98%), Shengyon 11-26 (89.25%) and NERICA 10 (89.58%).
Where the percentage of abnormal seedlings and diseased seedlings did not vary significantly
among the rice genotypes.
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Table 2. Seedling quality attributes of different Aus rice genotypes
Rice genotypes Normal seedling% Abnormal
seedling%
Un-germinated
Fresh seed%
Diseased
seedlings%
Chehrang sub1 91.25 ab 1.58 3.92 cd 3.25
Shengyon 11-25 89.98 bc 2.75 5.50 bc 1.83
Shengyon 11-26 89.25 bc 1.58 7.08 ab 2.08
Nerica 10 89.58 bc 2.35 6.58 ab 1.58
Pariza 91.42 ab 1.33 3.50 d 3.75
BU dhan1 87.83 c 2 8.33 a 1.75
BRRI dhan48 93.58 a 1.67 2.917 d 1.83
CV (%) 1.53 38.43 18.02 49.41
Sig. Level ** ns *** ns
Means followed by same letter(s) in a column are not significantly different by DMRT.
Health status of harvested seed samples of different Aus rice genotypes
A total of five species of fungi was detected in different seed samples of different genotypes.
In order of prevalence, they were Fusarium moniliforme,
Alternaria padwickii, Curvularia lunata, Aspergillus spp, Bipolaris oryzae (Table3). The
prevalence of all other fungi except Fusarium moniliforme was recorded low, where the
prevalence of Bipolaris oryzae was recorded very low and absent in Chehrang Sub1, BU
dhan1, and BRRI dhan48.
Table 3. Prevalence of major seed borne fungi associated with seeds of different Aus
rice genotypes
Rice Genotype
% Seed borne fungi
Fusariummo
niliforme
Alternariap
adwickii
Curvularial
unata
Aspergillus
spp.
Bipolaris
Oryzae
Chehrang Sub1 17.58 4.67 2.42 1.55 0.00
Shengyon 11-25 9.50 2.17 2.61 1.00 0.52
Shengyon11-26 7.66 3.34 1.53 0.90 1.04
NERICA 10 11.83 2.17 2.16 1.67 0.40
Pariza 6.17 4.61 1.67 2.61 2.66
BU dhan1 9.67 4.33 3.16 2.16 0.00
BRRI dhan48 4.67 2.27 1.63 1.05 0.00
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Conclusion
Prevalence of Fusarium moniliforme and Alternaria padwickii might have an effect on
germination rate because the maximum prevalence of these two fungi was recorded in
Chehrang Sub1 which might have an effect on the lowest germination rate (23.09) of
Chehrang Sub1. Germination rate (23.28%) of BU dhan1 was also lower than that of the
other five genotypes having a sound percentage of prevalence of these two fungi.
There is also a possibility of having more electrophorage leakage on seed surface which
permits releasing more ions as more affected by Curvularia lunata because leachate
conductivity was recorded highest of 51.33 µscm-1 in BU dhan1 and also the highest (3.16%)
prevalence of Curvularia lunata. It was also observed in Chehrang Sub1 having 49.57 µscm-1
leachate conductivity and 2.42% prevalence of Curvularia lunata. Whereas the lowest (18.10
µs cm-1) leachate conductivity was observed in BRRI dhan48 with a lower percentage
(1.63%) of the prevalence of Curvularia lunata.
Reference:
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management practices and resulting weed seed contamination in the
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