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Hybrid Seed Production in Mustard

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0% found this document useful (0 votes)
77 views4 pages

Hybrid Seed Production in Mustard

Uploaded by

shirodog35
Copyright
© © All Rights Reserved
We take content rights seriously. If you suspect this is your content, claim it here.
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Lecture 18

Advances in Seed Production of Mustard (Brassica nigra)


Rai (B. juncea), Benarasi rai ([Link]) and pahadi rai ([Link] var rugosa) belong to mustard
and cultivated for edible oil seed.
Nucleus and breeder seed production of open pollinated varieties
The procedure of nucleus/breeder seed production varies from crop to crop according
to their breeding behavior. The field should be selected where no Brassica species had been
grown for last three years, unless the crop was raised for nucleus seed production of the same
variety. Field should be properly isolated from the other field of any Brassica species. An
isolation distance of 200 m is recommended for production of nucleus and breeder seed of
self-incompatible (cross pollinated) crops, including B. rapa var. toria; B. rapa var. brown
sarson and E. sativa (taramira) and self compatible (self pollinated) crops, including B.
juncea (Indian mustard), B. rapa var yellow sarson and B. carinata (Karan rai).
Approximately 500 true-to type plants are selected from the basic bulk or
multiplication plot for nucleus seed production of self pollinated crops while 2500 or more
plants are selected in cross pollinated crops to prevent the narrowing of genetic base of these
crops. Five border rows of the same variety (true to type) should be planted around the plot.
Selected plants are harvested and threshed separately. The seed lot from each selected plant
should be examined critically for seed characters like shape, colour etc. Off type seed lots (or
plants) are discarded and only the true to type lots (plants) are maintained separately for
raising nucleus seed plot. Sowing for nucleus seed plot is done from the selected individual
nucleus plants in plant to progeny rows. Each progeny row is examined critically at different
growth stages for diagnostic characteristics. If any progeny row shows any variation the
entire progeny row should be uprooted before flowering.
In case off-types are found after flowering, the surrounding rows should also be
uprooted to avoid contamination. Single plants (about 500 in self pollinated and about 2500
in cross pollinated crops) are harvested and their seed is kept separately for raising the next
cycle of nucleus progeny rows next year. Remaining seed of progenies should be bulked to be
used for production of breeder seed.
Roguing:
The removal of off type plants should be carried out at 3 stages. First, the off-type
plants distinguishable on the basis of morphological characteristics should be removed before
flowering. Second, the off-type plants, which are identified at flowering, should be removed
before pod-formation. Third, the off-type plants should be removed on the basis of siliqua
and seed characteristics and also on the basis of maturity duration. Disease infected plants
should also be removed. The field should be kept free from all kinds of weeds particularly
from Argemone mexicana (Satyanashi) which should be uprooted altogether before it flowers.

Nucleus and breeder seed production of parental lines


Hybrids developed in rapeseed-mustard are based upon Cytoplasmic Genetic Male
Sterility system. Parental lines are multiplied in different plots. The seed parent (A line) is
maintained by growing the rows of A and B lines in a specific ratio. Normally, 3:1 ratio of
seed parent (A line) and maintainer (B line) are followed. The maintainer rows (B line) are
harvested first. Later on, the remaining rows of seed (A line) parent are harvested and bulked.
Strict roguing is advised during flowering to rogue out the fertile plants from seed parent. The
seed production of B and R line is similar to any other varietal seed production. The
commercial F1 hybrid seed is produced by growing seed parent (A line) and restorer (R line)
in 3: 1 ratio as followed in case of maintenance of seed parent. The rows of restorer parent (R
lines) are harvested first and bulked followed by harvesting of seed parent. The seed from the
seed parent is processed and packed as hybrid seed. Honeybees play an important role in
enhancing the transfer of pollen, hence 3-4-honeybee boxes/ha may be kept to ensure proper
pollination and good seed set.
Harvesting and threshing:
Border row plants of 1 m area from all sides of the plot should first be harvested
separately. The seed plots should be harvested at the stage when 70-80% plants turn yellow.
The harvested crop is staked and dried before threshing. Staking of crop is important to
obtain good lusture of seed. Threshing may be done either manually or by thresher. Essential
precautions should be taken to avoid mechanical mixture during threshing.
Seed processing and packaging:
After threshing, the seed should be dried either in sunshine or in mechanical seed
drier to bring the seed moisture down to 8%. The temperature of air in seed drier should not
exceed 40 °C. A random sample from the dried seed is taken and analysed for quality
characters and oil content before the grading.
Seed testing:
After processing, a sample of seed is taken to seed testing laboratory for the
examination in respect of seed standards. The seed purity, germination percentage and
moisture content in seed is thoroughly checked in seed testing laboratory. Breeder seed is
considered of high quality because it is used for further seed multiplication chain.
Storage:
Seed should be dried to bring the moisture content upto 8% before storage. Seed
should be stored preferably at less than 20 °C and at less than 30% Relative Humidity (RH).
The godown should be properly fumigated to avoid storage pests.
Foundation and Certified Seed Production of Varieties:
Land Requirements
The land selected should not be cultivated with Rape seed and mustard in the previous
season. In addition the field should be well drained and should be free of volunteer plants.
Isolation requirements:
Rape seed and mustard is partially self and cross pollinated crop. The extent of natural
cross pollination varies from 30 % to 35 % according to insect activity. For foundation seed
400 m and for certified seed 200 m is recommended from fields of other varieties of same
species and fields of the same variety not confirming to varietal purity.
Brief cultural practices:
Obtain nucleus/breeder’s/foundation seed from a source approved by a seed
certification agency. First fortnight of October to mid November is the most appropiate time
for sowing . Seed rate is 5 to 8 kg/ ha. Spacing adopted is 45 cm row to row and plant to plant
is 10-15 cm.
Roguing:
All the off type plants , easily distinguishable plant characteristics , and other species
plants must be removed before flowering to ensure pure seed production. Remaining offtypes
, if any , distinguishable on the basis of siliqua characteristics should be removed before
maturity. Argemone mexicana is the most objectionable weed in Rape and mustard seed
production. The weed should be removed altogether as required.
Field inspection
A minimum of three inspections will be done, one at the stage of 6-7 pairs of leaves
on plants, second at flowering and third at maturity stage prior to harvesting by the Seed
Certification Officer.
Field standards
Foundation seed Certified seed
Isolation distance 400 200 m
Off-types 0.10% 0.20%
Harvesting:
It is important to harvest the crop after plants start turning light yellow. At this stage
most of the siliqua turns light yellow and the seed inside the siliqua will be light brown.
Before storage, dry the seeds to reduce moisture content to eight percent.
Seed yield
The average seed yield varies from 15 to 20 quintals per hectare.

Common questions

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In seed testing, key quality parameters such as seed purity, germination percentage, and moisture content are examined. Seed testing is critical for breeder seed as it ensures high-quality seed that will serve as the basis for further multiplication in the seed production chain, thereby affecting future crop yields and quality. By verifying these parameters, seed testing helps to maintain seed standards, contributing to better agricultural outcomes and ensuring that the seeds meet specific industry and regulatory standards .

The maintenance of parental lines in hybrid seed production of mustard differs from typical varietal seed production due to the use of the Cytoplasmic Genetic Male Sterility system. In this system, parental lines, especially the male sterile A line and the fertility restorer R line, are multiplied in specific ratios to ensure male sterility and hybrid vigor. This process requires the maintenance of A and B lines in a 3:1 ratio to preserve male sterility in the parent line, which is not a requirement in typical varietal seed production where self-pollination suffices. Roguing of fertile plants from the A line is also conducted rigorously. Such specialized maintenance ensures successful hybrid seed production with desired characteristics that cannot be achieved through regular varietal methods .

The removal of off-type plants is critical in mustard seed production to maintain genetic purity and ensure that the seed batch remains true to type. Off-types should be rogued at three stages: before flowering, where morphological differences can be detected; before pod formation, where flowering differences are visible; and based on siliqua and seed characteristics before maturity. This systematic removal prevents contamination and ensures the integrity of the seed production process, crucial for maintaining consistent crop traits and quality .

Honeybees play a crucial role in the pollination process of mustard crops by enhancing pollen transfer. To ensure adequate pollination and good seed set, it is recommended to maintain 3-4 honeybee boxes per hectare. This practice is significant because it improves the seed yield and quality by facilitating cross-pollination and gene flow, which is especially beneficial in cross-pollinated mustard varieties. Enhanced pollination also leads to better fruit set and overall plant health .

The appearance of mustard siliquas is significant during harvesting because it indicates the optimal stage for harvesting. When plants start turning light yellow, it is important to harvest because most siliquas turn light yellow and the seeds inside become light brown, signaling maturity. Visual inspection of seed color is crucial as it helps in determining the right time to harvest, ensuring that seeds are mature and have reached desired quality standards. This practice prevents premature harvesting, which could result in low yield and inferior seed quality due to immature seeds .

The Cytoplasmic Genetic Male Sterility (CGMS) system is pivotal in hybrid seed production of mustard. It involves growing parental lines (A line and B line) in a specific 3:1 ratio for multiplication. The male sterile seed parent (A line) is maintained alongside a maintainer (B line) that restores fertility. During flowering, rigorous roguing is conducted to eliminate any fertile plants from the A line. For commercial F1 hybrid seed production, the seed parent (A line) and the restorer (R line) are sown in a similar 3:1 ratio, facilitating the efficient production of hybrid seeds. The CGMS system ensures that hybrids benefit from heterosis while maintaining male sterility, which is crucial for hybrid vigor and seed yield .

Precise seed moisture content and temperature control are crucial during the storage of mustard seeds to prevent deterioration and ensure seed viability. The seed moisture content should be reduced to 8% to minimize fungal growth and prevent deterioration. Temperature, ideally below 20 °C, and relative humidity less than 30%, help in avoiding the proliferation of storage pests and microbial contamination. Proper storage conditions prolong the shelf-life of seeds and maintain seed quality, which is essential for successful germination and high yield in subsequent planting seasons .

Field isolation requirements have significant implications on mustard seed production, primarily concerning the maintenance of genetic purity. For foundation seed, a 400 m isolation distance is mandated, while for certified seed, 200 m is recommended. These distances prevent unwanted cross-pollination between different varieties or species, which could lead to genetic contamination and the dilution of desirable traits. Effective isolation forms a critical part of the strategy to ensure that the seed remains true to type, maintaining varietal characteristics that are essential for consumer acceptance and agronomic performance .

Nucleus seed production procedures for mustard crops, such as Brassica juncea and Brassica nigra, involve several critical steps to maintain genetic integrity. The field must be isolated from other Brassica species, with a minimum distance of 200 meters recommended to prevent contamination from cross-pollination. Approximately 500 true-to-type plants are selected in self-pollinated crops and 2500 in cross-pollinated crops to ensure a diverse genetic base. Off-type plants are rigorously removed at three stages: before flowering, before pod formation, and based on siliqua characteristics. Seeds from selected plants are individually harvested and analyzed for key traits. These procedures are necessary to maintain varietal purity and prevent genetic narrowing, which ensures the consistent quality and characteristics of future seed generations .

Key cultural practices for successful foundation and certified seed production in rape and mustard include selecting land not previously cultivated with these crops in the prior season, ensuring the field is well-drained and free of volunteer plants, and applying a specific isolation distance (400 m for foundation seed and 200 m for certified seed) to maintain varietal purity. The timing for sowing is crucial, typically from the first fortnight of October to mid-November, using a seeding rate of 5-8 kg/ha and maintaining 45 cm row spacing and 10-15 cm plant spacing. Frequent inspections and removal of off-type plants during critical growth stages ensure the production of pure seed .

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