This document provides information on the floral biology and seed production of greengram. It discusses the plant's taxonomic classification, origin in India, nutritional value, uses, and botanical description. Key aspects of greengram's floral biology covered include its inflorescence, floral parts, self-pollination during the bud stage, and techniques for artificial hybridization. Objectives of greengram breeding and important varieties are also summarized. The document concludes with details on seed production, including ideal agro-climatic conditions, isolation requirements, and steps involved from land preparation to seed treatment.
What is Rouging?
Rouging for quality seed production,
A major source of off-type plant,
Rouging in Certified Seed Production,
Rouging During rice seed production.
What is Rouging?
Rouging for quality seed production,
A major source of off-type plant,
Rouging in Certified Seed Production,
Rouging During rice seed production.
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There is a huge demand for Mango worldwide. Hence, exporting to other countries we earn foreign currency. And, especially in Bangladesh, the suitable climate and soil condition is a positive sign of Mango cultivation. With the help of cut-edged technology here is a possibility of increased production.
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This Presentation is about Lentil (Lens culinaris), also known as Massur, Masoor, Masura. This Presentation includes Introduction, Biological Classification, Morphology of Lentil Plant, Floral Biology, Origin, Cytology, Breeding Objectives, Breeding Procedures, Diseases and Insects damage the Lentil Crop,
There is a huge demand for Mango worldwide. Hence, exporting to other countries we earn foreign currency. And, especially in Bangladesh, the suitable climate and soil condition is a positive sign of Mango cultivation. With the help of cut-edged technology here is a possibility of increased production.
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It consists of a basic introduction related to hybrid seed production related to rice.
Carrot cultivation based on botany, plant characteristic, soil, climate, variety and varietal characteristic, problem in cultivation and their management practices and storage and post harvest handling.
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What is greenhouse gasses and how many gasses are there to affect the Earth.moosaasad1975
What are greenhouse gasses how they affect the earth and its environment what is the future of the environment and earth how the weather and the climate effects.
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The ambient solar wind that flls the heliosphere originates from multiple
sources in the solar corona and is highly structured. It is often described
as high-speed, relatively homogeneous, plasma streams from coronal
holes and slow-speed, highly variable, streams whose source regions are
under debate. A key goal of ESA/NASA’s Solar Orbiter mission is to identify
solar wind sources and understand what drives the complexity seen in the
heliosphere. By combining magnetic feld modelling and spectroscopic
techniques with high-resolution observations and measurements, we show
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A brief information about the SCOP protein database used in bioinformatics.
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Introduction:
RNA interference (RNAi) or Post-Transcriptional Gene Silencing (PTGS) is an important biological process for modulating eukaryotic gene expression.
It is highly conserved process of posttranscriptional gene silencing by which double stranded RNA (dsRNA) causes sequence-specific degradation of mRNA sequences.
dsRNA-induced gene silencing (RNAi) is reported in a wide range of eukaryotes ranging from worms, insects, mammals and plants.
This process mediates resistance to both endogenous parasitic and exogenous pathogenic nucleic acids, and regulates the expression of protein-coding genes.
What are small ncRNAs?
micro RNA (miRNA)
short interfering RNA (siRNA)
Properties of small non-coding RNA:
Involved in silencing mRNA transcripts.
Called “small” because they are usually only about 21-24 nucleotides long.
Synthesized by first cutting up longer precursor sequences (like the 61nt one that Lee discovered).
Silence an mRNA by base pairing with some sequence on the mRNA.
Discovery of siRNA?
The first small RNA:
In 1993 Rosalind Lee (Victor Ambros lab) was studying a non- coding gene in C. elegans, lin-4, that was involved in silencing of another gene, lin-14, at the appropriate time in the
development of the worm C. elegans.
Two small transcripts of lin-4 (22nt and 61nt) were found to be complementary to a sequence in the 3' UTR of lin-14.
Because lin-4 encoded no protein, she deduced that it must be these transcripts that are causing the silencing by RNA-RNA interactions.
Types of RNAi ( non coding RNA)
MiRNA
Length (23-25 nt)
Trans acting
Binds with target MRNA in mismatch
Translation inhibition
Si RNA
Length 21 nt.
Cis acting
Bind with target Mrna in perfect complementary sequence
Piwi-RNA
Length ; 25 to 36 nt.
Expressed in Germ Cells
Regulates trnasposomes activity
MECHANISM OF RNAI:
First the double-stranded RNA teams up with a protein complex named Dicer, which cuts the long RNA into short pieces.
Then another protein complex called RISC (RNA-induced silencing complex) discards one of the two RNA strands.
The RISC-docked, single-stranded RNA then pairs with the homologous mRNA and destroys it.
THE RISC COMPLEX:
RISC is large(>500kD) RNA multi- protein Binding complex which triggers MRNA degradation in response to MRNA
Unwinding of double stranded Si RNA by ATP independent Helicase
Active component of RISC is Ago proteins( ENDONUCLEASE) which cleave target MRNA.
DICER: endonuclease (RNase Family III)
Argonaute: Central Component of the RNA-Induced Silencing Complex (RISC)
One strand of the dsRNA produced by Dicer is retained in the RISC complex in association with Argonaute
ARGONAUTE PROTEIN :
1.PAZ(PIWI/Argonaute/ Zwille)- Recognition of target MRNA
2.PIWI (p-element induced wimpy Testis)- breaks Phosphodiester bond of mRNA.)RNAse H activity.
MiRNA:
The Double-stranded RNAs are naturally produced in eukaryotic cells during development, and they have a key role in regulating gene expression .
Slide 1: Title Slide
Extrachromosomal Inheritance
Slide 2: Introduction to Extrachromosomal Inheritance
Definition: Extrachromosomal inheritance refers to the transmission of genetic material that is not found within the nucleus.
Key Components: Involves genes located in mitochondria, chloroplasts, and plasmids.
Slide 3: Mitochondrial Inheritance
Mitochondria: Organelles responsible for energy production.
Mitochondrial DNA (mtDNA): Circular DNA molecule found in mitochondria.
Inheritance Pattern: Maternally inherited, meaning it is passed from mothers to all their offspring.
Diseases: Examples include Leber’s hereditary optic neuropathy (LHON) and mitochondrial myopathy.
Slide 4: Chloroplast Inheritance
Chloroplasts: Organelles responsible for photosynthesis in plants.
Chloroplast DNA (cpDNA): Circular DNA molecule found in chloroplasts.
Inheritance Pattern: Often maternally inherited in most plants, but can vary in some species.
Examples: Variegation in plants, where leaf color patterns are determined by chloroplast DNA.
Slide 5: Plasmid Inheritance
Plasmids: Small, circular DNA molecules found in bacteria and some eukaryotes.
Features: Can carry antibiotic resistance genes and can be transferred between cells through processes like conjugation.
Significance: Important in biotechnology for gene cloning and genetic engineering.
Slide 6: Mechanisms of Extrachromosomal Inheritance
Non-Mendelian Patterns: Do not follow Mendel’s laws of inheritance.
Cytoplasmic Segregation: During cell division, organelles like mitochondria and chloroplasts are randomly distributed to daughter cells.
Heteroplasmy: Presence of more than one type of organellar genome within a cell, leading to variation in expression.
Slide 7: Examples of Extrachromosomal Inheritance
Four O’clock Plant (Mirabilis jalapa): Shows variegated leaves due to different cpDNA in leaf cells.
Petite Mutants in Yeast: Result from mutations in mitochondrial DNA affecting respiration.
Slide 8: Importance of Extrachromosomal Inheritance
Evolution: Provides insight into the evolution of eukaryotic cells.
Medicine: Understanding mitochondrial inheritance helps in diagnosing and treating mitochondrial diseases.
Agriculture: Chloroplast inheritance can be used in plant breeding and genetic modification.
Slide 9: Recent Research and Advances
Gene Editing: Techniques like CRISPR-Cas9 are being used to edit mitochondrial and chloroplast DNA.
Therapies: Development of mitochondrial replacement therapy (MRT) for preventing mitochondrial diseases.
Slide 10: Conclusion
Summary: Extrachromosomal inheritance involves the transmission of genetic material outside the nucleus and plays a crucial role in genetics, medicine, and biotechnology.
Future Directions: Continued research and technological advancements hold promise for new treatments and applications.
Slide 11: Questions and Discussion
Invite Audience: Open the floor for any questions or further discussion on the topic.
1. Sam Higginbottom University of Agriculture, Technology and Sciences.
Allahabad- 211007, UtTar pradesh, India
TOPIC:- FLORALBIOLOGYandseedproductionOFGREENGRAM
2. Contents...
Introduction
Taxonamic Classification
Origin and Distribution
Botanical Discription
Floral Biology
Anthesis and Pollination
Artificial Hybridization
Shivashankar method of crossing
Breeding Objectives
Varieties of Green Gram
Seed Production of Green gram
3. INTRODUCTION
It is also called as Mung Bean.
It is a Sort duration, Day Neutral crop, Self Pollinated and Leguminous Crop.
Mung bean is the Hardiest crop among all the Pulses.
It is the Third most important Pulse crop in India.
India ranks 1st Place in Area and Production.
India accounts about 50 to 55% of total world production.
It is grown as as Sole crop, Inter crop, Multiple cropping system.
The are under Green gram production has got doubled in past two decades at
a rate of 2.5% Annually.
4. TAXONOMICAL CLASSIFICATION OF GREEN GRAM
Botanical Name : Vigna radiata
Kingdom : Plantae
Division : Spermatophytes
Sub Division : Angiosperm
Class : Dicotyledoneae
Order : Leguminosae
Family : Fabaceae / Papilionoideae
Genus : Vigna
Species : radiata
Chromosome Number : 2n = 2x = 22
5. ORIGIN AND DISTRIBUTION
ORIGIN :-
Primary centre of Origin is “INDIA”.
DISTRIBUTION :-
Mung bean is cultivated in India, Thailand, China, Philippines, Srilanka,
Myanmar, Pakistan, Bangladesh, Indonesia etc.
In India it is Cultivated in Rajasthan, Maharsatra, Karnataka, Orissa, Bihar,
Andhra Pradesh, Uttar Pradesh and Madhya Pradesh.
Cultivated in All Three Seasons – Kharif, Rabi and Jaid.
Phaseolus aureus is the Wild form.
6. Nutritional status
Nutritional Components Range of Total Seed Percentage
Protein 20 to 28 %
Fats 3.3 %
Fiber 5.9 %
Carbohydrates 51.2 %
Sugars 4 to 10 %
K, Na, Mg, P, Ca Traces
Moisture 10.2 %
7. Uses :-
Mungbean is an excellent source of high quality protein, fiber and iron.
Ascorbic acid (Vitamin C) is synthesized in sprouted seeds of mungbean with
increment in riboflavin and thiamine are very beneficial for us.
Mungbean has the capacity to fix atmospheric nitrogen through symbiotic
nitrogen fixation. It is also used as green manure crop..
Being a short duration crop it also provides an excellent green fodder for
cattle.
It fits well in various multiple and intercropping systems. After picking of
pods, mungbean plants may be used as green fodder or can be incorporated as
green manure.
Pulses are less productive.....
A large conc. of proteins in seeds may require early mobilization of protein
of leaves, thus impairing their capacity for the prolonged photosynthesis.
The maintenance of symbiotic N fixation in root nodules requires prolonged
use photosynthate and thus may reduce energy available for the storage in
seeds.
8. Botanical description
Habit :-
Annual, Herbaceous, erect/semi erect.
Root :-
Tap root system, provided with nodules for Atmospheric Nitrogen fixation.
Stem :-
Erect /Sub erect, sometime twinning in upper branches, furrowed &
branches moderately/sparsely haired.
Leaves :-
Alternate, Trifoliate, entire ovate & rarely lobed with long Petiole.
9. Fruit :- ( Legume or Pod )
It is a Dry dehiscent Fruit.
Immature pods are usually green, mature
pods are iron gray/olive gray/snuff brown
color, round slander with short & moderate
pubescence.
Dehisces by both (dorsal & ventral) sutures
into two halves.
It contains 9-16 seeds per Pod.
Seeds :-
One to many seeds, Non endospermic and
has two cotyledons.
Seeds are Globular, green, surface has fine
wavy ridges.
Hilum (Point of attachment of seed to
follicle) is white, more or less flat.
Germination is epigeal.
11. FLORAL BIOLOGY
Inflorescence:-
Axillary Raceme carrying Ten to Twenty Flowers
on a long Peduncle.
Corolla :-
Papilionaceous corolla,Petals are Five and they
are Polypetalous,consists of three kinds of petals as
below
1. Standard :- Large posterior petal.
2. Wing :-Two lateral petals.
3. Keel :- Anterior Two fused petals.
Calyx :
Sepals are Five, Gamosepalous, Imbricate
aestivation.
14. ANDROECIUM :-
Male reprductive part Stamen has got
two parts as below :-
Anther
Filament
Stamens are 10 in Number, Diadelphous
(9)+1, Anther dithecous.
GYNOECIUM :-
The Female reproductive part Carpel/
Pistil has got three parts as below :-
Stigma
Style
Ovary
Monocarpellary, unilocular half superior ovary
with many ovules on marginal placentation
style is single long terminal. Stigma is simple.
16. ANTHESIS AND POLLINATION
In Mung Bean Pollination occurs a night prior to opening of the flowers.
Anthers start dehiscing from 9 am and completely dehisced by 3 pm.
Stigma are by then receptive and are thoroughly covered with pollen.
Flowers open between 6 am and 8 am amd remain open till 11 am later they
close between 2 pm and 4 pm.
Pollen sheeding takes place long before the petals open I.e,. During bud stage.
Cleistogamy occurs to an extent of 46%
So, The Pollination occur in the bud stage on the night previous to the opening of
the flowers.
17. ArtifiCIAL hybridization
Emasculation:-
The Removal of Male parts in
Bisexual Flowers to prevent
unwanted selfing is referred as
Emasculation.
Preferred time is during 4.00-6.00pm.
For emasculation the young bud is kept
between thumb and forefinger.
Point of dissecting needle is inserted just
under the standard in an oblique position
along the top of the bud.
The left side of standard & wing petal
are pushed outwards & held with thumb.
18. The left hand of keel is removed in pieces with
forceps.
Pistil and stamens are well exposed. Then
remove the Anthers with forceps .
Pollination:-
Pollination is done in morning (8-11am) collect
mature anthers from desired open flowers and
gently pressing the ripe anthers against stigma.
Flower may be bagged after pollination until
pods are matured.
19. SHIVASENKAR’S METHOD OF CROSSING
This Method of crossing technique is used in
all Pulses.
On the evening of Previous to the day of the
pollen shedding, transverse cut is made in
flower bud.
It Facilitates removal of upper portion of
the corolla like a cap without causing injury
to the gynoecium.
Anthers are clipped off automatically and
remains inside the corolla cap which is
removed.
The Stigma is then pollinated with desired
pollen on the next morning.
20. BREEDING OBJECTIVES
High Yield
Different Maturation durations.
Resistence to shattering.
Better Plant type.
Resistence to diseases like MYMV and CLS.
Resistence to pets like Pod borer, Aphids, Whitefly.
Betterquality ( Protein, Methionin content ).
Development of synchronous varieties.
21. VARIETIES
The First Variety released is T1 in 1948.
Pusa Phalguni – IARI
Pusa Dofasali – IARI
F.S 68- Hissar
Some of the hybrid varieties of green gram are: RUM-1,HUM-12,BM-4,
PDM-54, JM-72, K-851, and PDM-11.
22. Some other Varieties of Mung bean
STATE OR UNION
TERITORY
Notified
Year
Names of Varieties
Central
government
2020 Azad Moong 1 (KM 2342), IPM 512-1, MH-
1142, Pant Mung 9 PM 09-11
Uttar Pradesh 2020 KPM 409-4
Central
government
2019 GM-7 (NMK-15-08), VBN 4 VGG 10-008
Uttar Pradesh 2019 ARUN(KM 2328)
Central
government
2018 GM-6, IPM 2K14-9, IPM 302-2, TRC MUNG 131-1
Tripura Moong-1
Uttar Pradesh 2018 Kanika (IPM 302-2), Pusa 1431, Varsha (IPM 2K-
14-9)
Gujarat 2018 Gujarat Anand Mung Bean-5 (GAM-5
Madhya Pradesh 2016 IPM 205-7(Virat), IPM 410-3 (Shikha)
Central
government
2014 BGS-9 (Somanathi), DGGV - 2 , MH 421
23. State/UT Notified
Year
Variety Name
Uttar Pradesh 2012 KM 2195 (SWATI)
Cental Government 2008 Pant Mung-6, PAU911, MH-2-15
Andhra Pradesh 2010 Madhira Pesara 347
Uttar Pradesh 2001 HUM-6 (Malvika Janpriya), PDM-139
Central Government 1995 Gujarat Mung-3, LAM-407, Pusa-9072,
Warangal-2, Pushkara
Uttar Pradesh 1983 Pant Moong-1
Madhya Pradesh 1974 JAWAHAR-45
Central Government 1978 ML-1, ML-5, Sunaina, TYPE-44
Central Government 1976 Kopargaon, Varsha
Central Government 1974 Pusha Baisakhi
Central Government 1973 Moong-305, Moong-54, Shining Moong
No 1
Central Government 1950 TYPE-1
24. SEED PRODUCTION OF GREEN GRAM
Agro-Climatic conditions :-
Best Climatic condition required for Green gram cultivation is warm humid.
Optimum temperature required is from 25°C – 35°C, with moderate rain fall
of 60 to 80 cms.It can tolerate drought to a great extent.
Best Season :- It can be grown is all three seasons.
For Kharif :- June to August ( Best season for cultivation of Green gram )
For Rabi season :- September to November
For Summer season :- February to March
Soil :-
The Mung bean require Well-drained sandy to loamy soils.
pH ranging from 6 to 7 is required for green seed production.
Stages of Seed production:-
Breeder Seed – Foundation Seed – Certified Seed
25. Isolation requirements :-
Since the Green gram is highly self pollinated crop with cross
pollination to an extent of 5 to 10% the crop should be raised in
isolation for the maintainence of varietal purity. The Isolation
required for green gram seed production is as below :-
1. Isolation for Foundation seed is 10 meters.
2. Isolation for certified seeds is 5 meters.
Land Preparation :-
The land should be prepared well by one to two
harrowings, followed by levelling.
The Field should be made free from volunteer
plants.
To supplement the soil with proper nutrients,
apply lime at the rate of 2 tones/ha along with
Farm Yard Manure @ 12.5 tones/hac.
26. Source of seed :-
Obtain the appropriate class seeds from a source approved by certification
agency.
Seed Treatment :-
Treat the seeds with Thiram or Carbendazim at 2 grams/kg of seed 1 day
before sowing the seeds
Treatment with Pseudomonas fluorescens @ 10 grams/kg seeds.
Treatment with Rhizobium @ 4 grams per kg seeds.
Method of sowing:-
The seed should be planted in rows (Dibbling).It would be helpful for making
Field inspections.
Seed Rate:-
Kharif and Rabi season crop 15 to 20 kg per hac.
Summer crop 25 to 30 kg per hac
27. Spacing:-
For Kharif and Rabi crop:-
Row to row spacing is 30 to 45 cm
Plant to plant spacing is 7 to 10 cm.
For Summer Crop :-
Row to row spacing is 20 to 25 cm
Summer crop - Plant to plant spacing is 7 to 10 cm.
1. Depth of Sowing is 1 to 1.5 cms.
Fertilisation :-
A Basal application of 25kg nitrogen, 50kg phosphorous and 25kg
potassium per hectare is recommended.
Spray 2% DAP at the time of first appearance of flowers and a second
spray 15 days after first spray for enhanced seed set.
Spray NAA 40 ppm at first flowering and a second spray after a fortnight
to reduce the flower drop.
28. Irrigation:-
Frequently irrigation for the summer crop is especially necessary. The kharif
crop normally does not require irrigation. One to two irrigation may be
required if there is prolonged dry period.
Interculture Operations:-
It is essential to keep the weeds under suppression. Hence,one or two
weddings and hoeings may be done.
Spraying of one kilogramme treflan(active compound) in 1000lt of water per
hectare on the soil, at the time of the final land preparation, has also been
found quite effective for controlling weeds.
Crop Duration :-
Green gram require 80 to 90 days for complete maturity.
29. Various Stages of Gream Gram Production
Earlier Stage
Flowering stage
Pod Formation Stage
Harvesting Stage
30. Field standards
Field Standards Foundation seed Certified seed
Isolation distance 10 mts 5mts
Off types (%) 0.10% 0.20%
Seed borne diseased
seeds
0.10% 0.20%
31. Field Inspections:-
A Minimum two field inspections are standardized for certification of
different seed production programmes in Pulse Crops.
For Green gram a minimum of two field inspections are required.
First one is before flowering stage.
Second inspection is during Pod formation stage to determine isolation,
volunteer plants, off types and diseased plants etc.
Roughing :-
The Off-type plant, pest infected, severaly disease plants should be
roughed out from time to time as required.
32. Pests of greengram:-
White fly (vector for 25 different diseases)
Hairy catterpillar
Semilooper
Pulse beetle
Diseases of Greengram:-
Mungbean Yellow Mosaic Virus (MYMV)
Powdery mildew (Erysiphe polygoni)
Anthracnose (Colletotrichum capsici)
Bacterial leaf blight (Xanthomonas phaseoli)
Rust (Uromyces ciceris arietini)
33. Harvesting :-
The Harvesting may be started when 90% of
pods turn brown or seeds attain
physiological maturity I.e., 30 days after
50% Flowering.
The Plants may be uprooted, stacked in
small heaps and allowed to dry in the field
for a week or so.
During Harvesting and Threshing operations
care should be taken to avoid mechanical
admixtures and contact of the seed with
moist soil.
34. Threshing and Processing :-
Threshing is done by a stationary thresher or by beating the pods
with a sticks.
After Threshing The seeds should be dried (nine percent of moisture
should be maintained) before storage.
The seeds are graded using BSS 7*7 wire mesh sieve and stored in
labelled bags based on duration of storage.
1. Short term – (8 to 12 months) - Gunny or cloth bags .
2. Medium term – (12 to 15 months) - Polylined gunny bags.
3. Long term – (Morethan 15 months) - 700 gauge polythene bags.
35. Seed standards
Seed Standards
Foundation
Seeds
Certified
seeds
Pure seed (Min) 98 98
Inert matter (Max) 2 2
Weed seeds (Max) 5 per kg 10 per kg
Other Distinguishable Varieties
seeds(Max)
10 per kg 20 per kg
Germination percentage 75 % 75 %
Moisture % for storage 8 - 9 8 - 9
36. REFERENCES
Seed technology second edition by Rattan lal Agrwal.
Chhabra AK. 2006. Practical Manual of Floral Biology of Crop Plants.
https://agritech.tnau.ac.in/seed_certification/seed_pul_greengram.
htm
https://seednet.gov.in/Index.aspx