The second revised and enlarged edition covers the contents of ICAR syllabus. New To This Edition
Chapter on hormones and seed dormancy
Chapter on seed production in forage legumes and grasses
Chapter on fruit seed production
Chapter on flower seed production
Chapter on seed production in plantation crops and organic seed
Chapter on traditional varieties and technologies
Chapter on establishment of seed processing plant
Chapter on establishment of seed testing laboratory
The revised and enlarged edition is highly useful for UG and PG students of Agriculture and allied fields.
Preface to the Second Edition
Preface to the First Edition
List of Figures
UNIT 1 : SEED BIOLOGY
1. Floral Biology
1. Inflorescence
1.1. Types of inflorescence
2. Flower
2.1. Parts of flower
2.2. Types of placentation
2.3. Types of perianth aestivation
2.4. Stamen position
2.5. Types of gynoecia
2.6. Ovary position
3. Flower Types
3.1. Sepals and petals
2. Flowering and Pollination
1. Flowering
1.1. Synchronisation in flowering
1.2. Non synchronization
2. Anthesis
2.1. Types
3. Pollination
3.1. Self pollination (Autogamy)
3.2. Cross pollination (Allogamy)
3.3. Often cross pollination
4. Sex Expression in Plants
5. Steps in Pollination
5.1. Prepollination
5.2. Emasculation
5.3. Crossing/Pollination
5.4. Selfing
5.5. Postpollination steps
3. Fruit and Its Structure
1. Fruits
1.1. Types
4. Seed and Its Structure
1. Seed
2. Importance of Seed in Crop Production
3. Characteristics of Good Seed
4. Differentiate Between Seed and Grain
5. Types of Seed
5.1 Monocot seeds / Monocotyledons
5.2. Dicot seeds / Dicotyledons
6. Components of Seed
7. Appendages of Seeds
8. Parts of Normal Seedling
9. Seed Structure of Various Crops
9.1. Importance
9.2. Cereals
9.3. Pulses
9.4. Oilseeds
9.5. Fibre crops
9.6. Vegetables
5. Vegetative Propagules
1. Vegetative Propagule
2. Differentiate Between Asexual Reproduction and Sexual Reproduction
3. Propagation By Vegetative Propagules
3.1. Bulbs
3.2. Corm
3.3. Sucker
3.4. Rhizome
3.5. Tuber
3.6. Runner
3.7. Stolon
3.8. Offset (Offshoot)
3.9. Crown
3.10. Bulbil
6. Seed Formation and Development
1. Ovule Development
1.1. Funicle, hilum, chalaza and raphe
1.2. Nucellus
1.3. Integuments
1.4. Integumentary outgrowths
1.5. Integumentary tapetum
1.6. Micropyle
1.7. Epistase
2. Development and Formation of Female Gametophyte
2.1. Megasporogenesis
2.2. Megagametogenesis
3. Microsporogenesis and Microgametogenesis
4. Fertilization
5. Seed Development
5.1. Embryogeny
5.2. Endosperm development
6. Comparison Between Monocot and Dicot Embryo Development ....
7. Summary
7. Apomixis, Parthenocarpy and Polyembryony
1. Apomixis
1.1. Non-recurrent apomixis
1.2. Recurrent apomixis
1.3. Adventive embryony or sporophytic budding
1.4. Change of flowers into vegetative reproductive bodies
1.5. Significance of apomixis
2. Parthenocarpy
2.1. Stimulative parthenocary
2.2. Vegetative parthenocarpy
2.3. Artificial parthenocarpy
2.4. Commercial importance
2.5. Misconceptions
3. Polyembryony
3.1. Origin of polyembryony
3.2. Cleavage polyembryony
3.3. Origin of embryos from cells of the embryo sac other than the egg cell
3.4. Embryos developing from additional embryo sacs in anovule
3.5. Induced polyembryony
8. Synthetic Seed
1. Definition
2. Concept
3. Procedure for Production of Synthetic Seed
4. Artificial Seed Production Methods
4.1. Desiccated system
4.2. Hydrated system
5. Methods for Artificial Seed Encapsulation
5.1. Dropping method
5.2. Molding method
6. Types of Gelling Agents Used For Encapsulation
7. Merits
9. Seed Maturity Indices
1. Seed Maturity
1.1. Physiological maturity
1.2. Harvestable maturity
1.3. Caution
2. Physiological and Harvestable Maturity Symptoms in Different Crops
10. Chemical Composition of Seeds
1. Carbohydrates
1.1. Starch
1.2. Cellulose
1.3. Hemicelluloses
1.4. Raffinose series oligosaccharides
1.5. Fructans
2. Proteins
2.1. Storage proteins
3. Lipids
4. Other Chemical Compounds Found in Seeds
4.1. Alkaloids
4.2. Tannins
4.3. Saponins
4.4. Phytin
4.5. Vitamins
5. Hormones
5.1. Abscisic acid
5.2. Gibberellins
5.3. Ethylene
5.4. Cytokinins
5.5. Auxins
5.6. Brassinosteroid
6. Factors Affecting Chemical Composition of Seeds
11. Seed Dormancy and Methods to Break the Dormancy
1. Introduction
2. Terms and Definitions
3. Why Dormancy is Needed?
4. Ecological Significance of Dormancy
5. Physiology of Seed Dormancy
5.1. Location of dormancy in fruit and seeds
6. Seed Dormancy Types
6.1. Primary dormancy
6.2. Secondary dormancy
7. Causes of Seed Dormancy
7.1. Exogenous dormancy
7.2. Endogenous dormancy
7.3. Secondary dormancy
8. Dormancy Breaking Treatments
8.1. Physical methods
8.2. Physiological methods
8.3. Chemical methods
9. Summary
12. Hormones and Seed Dormancy
1. Introduction
2. Hormones Synthesis and Functions
2.1. Auxins- IAA
2.2. Cytokinins (CKs) - Zeatin
2.3. Ethylene (ET) - Ethylene
2.4. Gibberellins (GAs)
2.5. Abscisic Acid (ABA)
2.6. Brassinosteroids (BAs) - Brassinolid
2.7. Jasmonates (JAs) - Jasmonic Acid
2.8. Salicylates (SAs) - Salicylic acid
3. Role of Hormones in Dormancy and Germination Control
3.1. ABA
3.2. GA
3.3. Brassinosteroids promote seed germination
3.4. Cytokinins and auxins
13. Seed Germination
1. Seed Germination
2. Types of Germination
3. Requirements for Seed Germination
4. Metabolic Events of Seed Germination
4.1. Imibition
4.2. Enzyme activation
4.3. Breakdown of storage tissues
4.4. Protrusion of radicle
4.5. Seedling establishment
5. Environmental Conditions Affecting Seed Germination
5.1. Moisture
5.2. Aeration
5.3. Light
5.4. Substrate
5.5. Germination stimulants
5.6. pH
5.7. Orientation
UNIT 2 : SEED PRODUCTION
14. Principles and Methods of Plant Breeding
1. Plant Domestication and Introduction
1.1. Changes in plant species under domestication
2. Plant Introduction
2.1. Types of introduction
2.2. Procedure
3. Selection in Self Pollinated Crops
3.1. Progeny test
3.2. Functions
4. Breeding Methods for Self Pollinated Crops
4.1. Pure line selection
4.2. Mass selection
4.3. Hybridization
4.4. Pedigree method
4.5. Bulk method
4.6. Modified bulk method
4.7. Single seed descent method
4.8. Back cross method
4.9. Multiline varieties
4.10. Population approach
4.11. Hybrid varieties
5. Breeding Methods for Cross Pollinated Crops
5.1. Synthetic varieties
5.2. Composite varieties
5.3. Heterosis and inbreeding depression
6. Breeding Methods for Asexually Reproduced Crops
6.1. Characteristics of asexually propagated crops
6.2. Clone
6.3. Characteristics
6.4. Methods of improvement of asexually propagated species ..
7. Resistance Breeding
7.1. Methods of breeding for disease resistance
7.2. Method of breeding for insect resistance
7.3. Breeding for abiotic stress resistance
7.4. Salt tolerance
7.5. Flood resistance
7.6. Cold tolerance
8. Mutation Breeding
8.1. Causes of mutation
8.2. Procedure
8.3. Merits
8.4. Demerits
9. Polyploidy Breeding
9.1. Procedure for aneuploidy production
9.2. Procedure for autoploidy production
15. Development and Release of Varieties and Hybrids
1. Variety
2. Composite Variety
2.1. Features of composite variety
2.2. Procedure or steps to develop composite variety
2.3. Examples of composite variety
3. Development of Hybrids
3.1. Heterosis
3.2. Constraints for hybrid technology
3.3. Types of hybrids
3.4. Benefits of hybrids
4 . Steps Involved in Release of A Variety
4.1. Variety release
5. DUS Test
16. Deterioration of Varieties
1. Developmental Variations
2. Mechanical Mixtures
3. Mutations
4. Natural Crossing
5. Minor Genetic Variations
6. Selective Influence of Diseases
7. Techniques of Plant Breeder
17. Maintenance Breeding
1. Basic Nucleus Seed
1.1. Maintenance of nucleus seed year after year
1.2 Production of nucleus seed in large quantity
2. Nucleus and Breeder Seed Production
2.1. Methods of maintenance of nucleus and breeder seed in self fertilised crops
18. Seed Generation System
1. Seed Classes
1.1. Nucleus seed
1.2. Breeder seed (Stage I and Stage II)
1.3. Foundation seed (Stage I and Stage II)
1.4. Registered seed
1.5. Certified seed (Stage I and Stage II)
1.6. Truthful labeled seed
2. Differences Between Certified Seed and Truthful Labeled Seed .
19. Seed Village
1. Definition
2. History of Seed Villages
3. Seed Village: Empowerment of Farm Women and Livelihood Security
4. Success Story of Seed Village
4.1. Advanta India Seed Village (Indian Tobacco Company)
4.2. Association of Indian Development (AID)– Seed Village....
4.3. MSSRF seed village
5. Kkv Seed Village, Konkan Krishi Vidhyapeeth, Dapoli
5.1. Objectives
5.2. Activities
6. Npdp (National Pulses Development Project) Seed Village Programme
6.1. Selection of village/farmers
6.2. Seed procurement, cleaning and storage
6.3. Financial assistance
7. Lakshmi Farm Seeds Seed Village
8. Advantages of Seed Village
9. Disadvantages of Seed Village
20. Seed Planning
1. Introduction
2. Demand Forecasting
3. Factors Influencing Seed Planning to Meet Seed Demand
3.1. Seed Multiplication Ratio (SMR)
3.2. Seed Renewal Period (SRP)
3.3. Seed Replacement Rate (SRR)
4. Planning for Seed Production
4.1. Varieties
4.2. Hybrids
4.3. Basic formulae used in planning
21. Seed Policy
1. Introduction
2. Seed Production Scenario
3. Structure of Seed Industry as Per Seed Act (1966)
4. Seed Policies Formulated For Governing Seed Quality Control System
5. Organizations Involved In Implementation of Seed Policy
5.1. Seed production
5.2. Seed quality control system
6. Seed Production and Research Programme of India and Its Function
6.1. ICAR - National Seed Project
7. Current Challenges Before Seed Industry
8. Suggestions for Further Strengthening of Seed Industry
22. Seed Quality
1. Seed
2. Characteristics of Good Quality Seed
2.1. Improved variety
2.2. Genetic quality
2.3. Physical quality
2.4. Seed germination and vigor (Physiological quality)
2.5. Planting value
2.6. Health quality
2.7. Seed moisture
2.8. It should be free from other crop seeds
2.9. It should be free from objectionable weed seeds
2.10. It should have good shape, size, colour, etc., according to specifications of variety
2.11. It should possess high longevity and shelf life
3. Advantages of Quality Seed
4. Concept of Seed Quality
5. Role of Seed in Agriculture
5.1. Seeds acts as a carrier of a new technology
5.2. Seed is a basic tool for secured food supply
5.3. Seed acts as a principal means to secure crop yield under less favourable production areas
5.4. Seed acts as a medium for rapid rehabilitation of agriculture in case of natural disaster
6. Goals of Seed Technology
6.1. Rapid multiplication
6.2. Timely supply
6.3. Assured high quality seeds
6.4. Reasonable price
23. Principles of Seed Production
1. Genetic Principles
1.1. Maintenance of genetic purity during seed production
1.2. Control of seed source
1.3. Preceeding crop requirements
1.4. Isolation
1.5. Roguing of seed fields
1.6. Seed certification
1.7. Grow-out tests
2. Agronomic Principles
2.1. Varietal seed production
2.2. Hybrid seed production
24. Heterosis and Hybrid Vigour
1. Heterosis
1.1. Definition
1.2. Inbreeding depression
1.3. Types
1.4. Measurement of heterosis
1.5. Genetic basis of hetrosis
2. Hybrids
2.1. Definition
2.2. Attributes of F1 hybrids
2.3. Steps in breeding
2.4. Types of hybrids
3. Composites
3.1. Features of composite variety
3.2. Steps to develop composite variety
3.3. Examples
4. Synthetics
4.1. Features of synthetic variety
4.2. Development or production of synthetic variety from established inbred lines
4.3. Development or production of synthetic variety from plants
4.4. Examples
25. Techniques of Hybrid Seed Production
1. Hand Emasculation and Pollination
2. Monoecious Nature of The Plant
3. Male Sterility
3.1. Cytoplasmic Male Sterility (CMS)
3.2. Genetic Male Sterility (GMS)
3.3. Cytoplasmic Genetic Male Sterility (CGMS)
3.4. Environment Sensitive Genic Male Sterility (EGMS) system
3.5. Gametocide
26. Seed Production in Field Crops
1. Land Requirements
2. Isolation Distance
3. Climate and Season
4. Seed Rate
5. Presowing Seed Treatment
5.1. Egg floatation technique for rice seed upgradation
5.2. Live seed separation in groundnut
5.3. Acid delinting in cotton
6. Field Preparation
7. Spacing
8. Fertilizers and Manures
9. Weeding
10. Roguing
11. Designated Diseases
12. Objectionable Weeds
13. Harvesting and Maturity
14. Seed Processing and Storage
15. Seed Standards (Certified Seed)
27. Seed Production in Vegetables
1. Land Requirements
2. Isolation Distance
3. Season and Climate
4. Seed Rate
5. Presowing Seed Treatment
6. Spacing
7. Manures and Fertilizers
8. Weeding
9. Roguing
10. Designated Diseases
11. Objectionable Weeds
12. Harvesting and Maturity
13. Seed Processing
14. Seed Standards
28. Hybrid Seed Production
1. Techniques of Hybrid Seed Production
1.1. Field crops
1.2. Vegetables
2. Land Requirements
3. Isolation Distance
3.1. Time isolation
3.2. Barrier isolation
4. Season and Climate
5. Seed Rate
6. Pre-Sowing Seed Treatment
7. Field Preparation
8. Spacing
9. Planting Ratio
10. Manures and Fertilizers
11. Weeding
12. Roguing
12.1. Field standards
13. Harvesting
14. Seed Standards
15. Synchronisation
15.1. Rice
15.2. Sorghum
16. Supplementary Pollination
16.1. Rice
16.2. Sunflower
29. Seed Production in Forage Legumes and Grasses
1. Forage Legumes
1.1. Isolation
1.2. Climate and season
1.3. Seed rate, spacing and fertilizers
1.4. Rogueing
1.5. Physiological maturity
1.6. Seed standards
2. Grasses
2.1. Isolation
2.2. Climate and season
2.3. Seed rate
2.4. Spacing
2.5. Fertilizers and manures
2.6. Roguing
2.7. Seed standards
30. Fruit Seed Production
1. Tropical Fruits
1.1. Common name, botanical name and family
1.2. Floral biology
1.3. Flowering and pollination
1.4. Method of propagation
1.5. Seed development, maturity, collection, extraction and drying
1.6. Seed dormancy and germination improvement
1.7. Storage behaviour
2. Minor Tropical and Subtropical Fruits
2.1. Common name, botanical name and family
2.2. Floral biology
2.3. Flowering, pollination and fruit set
2.4. Method of propagation
2.5. Seed development, maturity, collection, extraction and drying
2.6. Seed dormancy
2.7. Types of seed dormancy and germination improvement
2.8. Seed storage
3. Temperate Fruits and Nuts
3.1. Common name, botanical name and family
3.2. Floral biology
3.3. Flowering, pollination and fruit set
3.4. Method of propagation
3.5. Seed dormancy
3.6. Type of dormancy and germination improvement
3.7. Type of seed storage and initial moisture
3.8. Seed storage
4. Field Standards
31. Flower Seed Production
1. Cut Flowers
1.1. Common name, scientific name and family
1.2. Origin and distribution
1.3. Floral biology
1.4. Flowering and pollination
1.5. Method of propagation
1.6. Seed development, maturity, collection, extraction and drying
1.7. Seed dormancy
1.8. Seed dormancy and germination improvement
1.9. Type of seed storage and initial moisture
1.10. Seed storage
2. Loose and Ornamental Flowers
2.1. Common name, scientific name and family
2.2. Origin and distribution
2.3. Floral biology
2.4. Flowering and pollination
2.5. Method of propagation
2.7. Evidence of dormancy
2.8. Germination improvement
2.9. Seed storage behaviour
2.10. Seed storage methods and conditions
3. Field Standards
4. Seed Standards
32. Seed Production in Plantation Crops
1. Floral Biology
2. Climate and Season
3. Seed Rate and Spacing
4. Fertilizers
5. Harvesting
6. Dormancy and Germination Improvement
7. Seed Storage
33. Nursery Management
1. Selection of Site
2. Preparation of Seed Beds
3. Seed Sowing
4. Preparation of Cover Soil for the Nursery
5. Mulching and Irrigation for the Nursery
6. Selection of Seedlings for Transplanting
7. Seedling Hardening-Off Treatment
34. Micropropagation
1. Definition
2. Objectives
3. Methods
3.1. Meristem culture
3.2. Callus culture
3.3. Embryo culture
3.4. Protoplast culture
4. Stages of Micropropagation
4.1. Stage 0
4.2. Stage I
4.3. Stage II
4.4. Stage III
4.5. Stage IV
5. Micropropagation of Selected Plants
6. Advantages
7. Disadvantages
35. Organic Seed – Traditional Varieties and Technologies
1. Introduction
2. Traditional Varieties
2.1. Indian farmers rediscover advantages of traditional rice varieties
2.2. Notification of traditional varieties
2.3. Indigenous varieties
3. Technologies for Organic Seed Production
3.1. Choice of crop and varieties
3.2. Organic seed treatment
3.3. Organic nutrient management
3.4. Organic management of pests and diseases
4. Seed Storage
UNIT 3 : SEED PROCESSING
36. Harvesting and Threshing
1. Types of Harvests
2. Methods lf Harvest
2.1. Manual harvesting
2.2. Machine harvesting
3. Traditional Threshing Practices
3.1. Rubbing and squeezing
3.2. Beating
3.3. Stripping
3.4. Treading method
3.5. Flailing and pounding
3.6. Animal threshing
3.7. Tractor/power tiller threshing
4. Need and Function of Threshers
4.1. Functions of Thresher
5. Power Threshers
5.1. Pedal thresher
5.2. Drum thresher
5.3. Multi crop thresher
5.4. Paddy thresher
5.5. Maize thresher
5.6. Sunflower thresher
5.7. Axial flow groundnut thresher (Decorticator)
5.8. Vegetable seed extractor
5.9. Axial flow vegetable thresher
37. Seed Extraction
1. Seed Extraction
2. Methods of Seed Extraction
2.1. Dry extraction
2.2. Wet extraction
2.3. Mechanical method
2.4. Ash gourd seed extraction
38. Seed Drying
1. Seed Drying
2. Stage of Moisture Elimination
3. Equilibrium Moisture Content
4. Factors Affecting Drying
5. Methods of Drying
5.1. Physical drying / Natural drying / Sun drying
5.2. Mechanical drying or artificial drying
6. Tempering
39. Seed Processing
1. Seed Processing
1.1. Purpose
1.2. Physical characteristics that aid in grading and upgrading ..
2. Precleaning
2.1. Precleaning
3. Cleaning and Grading
3.1. Air-screen cleaner cum grader
4. Upgrading
4.1. Specific gravity separator
4.2. Indented cylinder separator
4.3. Magnetic separator
4.4. Colour separator
4.5. Friction cleaning
4.6. Spiral separator
5. Liquid/Water Floatation
40. Establishment of Seed Processing Plant
1. Introduction
2. Layout of Seed Processing Plant
2.1. Receiving-cum-drying platform
2.2. Processing area
2.3. Auxiliary building
3. Analysis of Operation
3.1. Processing sequence
3.2. Matching capacity
3.3. Conveying
4. Type of Layouts
4.1. Multistorey
4.2. Single level
4.3. Combined designs
5. Planning
6. Movement of Seed in a Processing Plant
7. Physical Characteristics Used to Separate Seeds
8. Types of Materials Removed During Processing
9. Usage of Processing Equipments
41. Seed Quality Enhancement
1. Seed Fortification
2. Seed Infusion
3. Seed Hardening
4. Seed Priming
4.1. Methods of priming
5. Irradiation
6. Magnetic Seed Treatment
7. Seed Pelleting
8. Polykote Film Coating
9. Seed Colouring
10. Fluid Drilling or Gel Seeding
UNIT 4 : SEED QUALITY CONTROL
42. Seed Act and Rules
1. Seed Act 1966
1.1. Sanctioning legislation
1.2. Regulatory legislation
1.3. Minimum limit and labeling of the notified kind / varieties of seed
1.4. Seed certification
1.5. Restriction of export and import of seeds - Seed Control Order, 1983
1.6. New Seed Policy
43. Seed Certification
1. Seed Certification
1.1. Phases of Seed Certification
1.2. Seed certification procedures
1.3. Verification of seed source
1.4. Concepts of seed certification
2. Purity Maintenance
2.1. Roguing
2.2. Special types of rogues in hybrid seed production
2.3. Objectionable weed plant
3. Field Inspection
3.1. Field inspection stages
3.2. Field counts
3.3. Field rejection
3.4. Inspection of seed processing
3.5. Sampling and sending to STL
3.6. Tagging and sealing
3.7. Control plot testing
3.8. Extension of the validity period
44. Field Inspection
1. Unit of Certification
2. Methods of Field Inspection
2.1. Counting procedure
3. Crop Stages for Field Inspection
3.1. Number of field inspection
4. Key Factors to be Observed
4.1. Cropping history of the field
4.2. Source of seed
4.3. Isolation distance
4.4. Presence of rogues and off-types
45. Objectionable Weeds
1. Presence of Objectionable Weeds
2. Identification of Objectionable Weeds
2.1. Objectionable weeds in field crops
2.2. Objectionable weeds in fodder crops
2.3. Objectionable weeds in vegetables
46. Seed Certification Standards
1. Minimum Seed Certification Standards
1.1. General seed certification standards
1.2. Specific crop standards
47. Seed Sampling
1. Seed Lot
2. Sampling
3. Types of Samples
3.1. Primary sample
3.2. Composite sample
3.3. Submitted sample
3.4. Working sample
3.5. Sample for moisture estimation
4. Sealed Sample
5. Sampling Intensity
6. Sampling Devices
6.1. Triers: Sleeve or Stick type trier
6.2. Bin sampler
6.3. Nobbe trier
7. Sampling Procedures
7.1. Bag sampling
7.2. Bulk sampling
7.3. Hand sampling
7.4. Automatic sampling
48 Mixing and Dividing of Seed
1. Mixing and Dividing
2. Types of Mechanical Dividers
2.1. Boerner divider
2.2. Soil divider
2.3. Centrifugal or Gamet divider
3. Method of Mixing And Dividing
3.1. Mechanical method
3.2. Random cup method
3.3. Modified halving method
3.4. Spoon method
3.5. Hand halving method
49. Purity Analysis
1. Seed Purity and Its Components
1.1. Pure seed
1.2. Other crop seed
1.3. Weed seed
1.4. Inert matter
2. Objectives of Purity Test
3. Purity Test Equipment
3.1. Purity work board
3.2. Optical aids
3.3. Balances
3.4. Sieves
3.5. Other equipments and tools
4. Procedure
4.1. Duplicate tests
4.2. Purity analysis in groundnut
4.3. Determination of huskless seeds
5. Sources of Error in Purity Analysis
5.1. Moisture
5.2. Computing error
50. Seed Moisture Determination
1. Seed Moisture
1.1. Principle
1.2. Precautions
2. Methods of Seed Moisture Estimation
2.1. Indirect method
2.2. Direct method
3. Reporting of Results
51. Germination Test
1. Germination Test Procedures
1.1. Top of Paper (TP)
1.2. Between Paper (BP)
1.3. Sand
1.4. Carry out the germination test
2. Seedling Evaluation
2.1. Normal seedlings
2.2. Abnormal seedlings
2.3. Hard seeds
2.4. Fresh ungerminated seeds
2.5. Dead seeds
3. Report the Results
52. Quick Viability Test
1. Principle
2. Method
2.1. Preparation of TZ solution
2.2. Preconditioning of seed
2.3. Preparation steps for staining
2.4. Staining in tetrazolium solution
2.5. Interpretation of TZ results
53. Grow-Out Test
1. Field of Applicability
2. Size of Sample
3. Procedure
3.1. Location of the Grow-Out Test
3.2. Standard sample
3.3. Method of raising the crop
3.4. Methods for taking observations
3.5. Calculation and Interpretation of the results
3.6. Reporting of results
54. Seed Vigour
1. Definition
2. Vigour Tests
2.1. Physical tests
2.2. Performance tests
2.3 Stress tests
2.4. Biochemical tests
55. Variety Identification
1. Introduction
2. Approaches to Varietal Identification
2.1. Morphological approaches / physical tests
2.2. Physiological tests
2.3. Chemical tests
2.4. Plant morphological traits
2.5. Molecular markers for varietal identification
56. International Seed Testing Association (ISTA)
1. Vision and Mission
2. Achievements
3. Technical Committees
4 ISTA Certificates
5. Publications
57. Establishment of a Seed Testing Laboratory
1. Seed Testing
2. Seed Testing Laboratory
3. Layout Plan and Furnishing of the Seed Testing Laboratory ..
3.1. General principles
3.2. Space requirements of a seed laboratory
3.3. Building
3.4. Furnishing of the building
4. Equipments
4.1. Sampling, mixing and dividing
4.2. Purity Analysis equipments
4.3. Moisture determination
4.4. Germination test
4.5. Viability test
4.6. Seed health testing
4.7. Miscellaneous equipments
4.8. Furniture for sample reception
4.9. Furniture for office and reception
5. Staffing
5.1. Requirement of staff
6. Reporting of Results
7. Maintenance of Records
UNIT 5 : SEED STORAGE
58. Seed Storage
1. Seed Storage
1.1. Importance of seed storage
1.2. Principles of storage
1.3. Stages of seed storage
1.4. Classification of seed storage
2. Factors Affecting Seed Storage
2.1. Internal factors (Seed factors)
2.2. External factors
3. Seed Packaging
3.1. Packaging materials or containers
4. Storage Godowns and Their Maintenance
5. Seed Store Sanitation or Godown Sanitation
59. Seed Deterioration
1. Definition
2. Changes Associated with Seed Deterioration
2.1. Morphological changes
2.2. Ultrastructural changes
2.3. Biochemical changes
2.4. Genetic changes
2.5. Physiological changes
2.6. New consensus – common cause of deterioration
60. Seed Treatment
1. Seed Treatment
2. Seed Treaters
2.1. Methods of seed dressing
2.2. Equipment used for seed treatment
2.3. Fumigation chamber
3. Types of Prestorage Treatments
3.1. Halogenation
3.2. Antioxidant treatment
3.3. Seed protectants
4. Mid Storage Treatments
4.1. Hydration – Dehydration (H-D)
4.2. Types of H-D treatments
61. Germplasm Conservation and Cryopreservation
1. Germplasm
1.1. Conservation methods
2. Cryopreservation
2.1. Methods of cryopreservation
2.2. Advantages
UNIT 6 : SEED HEALTH
62. Seed Pathology
1. Seed Pathology
2. Types of Pathogen
3. Nature of Pathogen Infection
3.1. Soil borne disease
3.2. Seed borne diseases
4. Mechanism of Pathogen Infection
4.1. Systemic infection of the seed
4.2. Seed contamination or infestation
5. Seed Transmission
5.1. Systemic transmission
5.2. Non systemic transmission
6. Designated Diseases
7. Symptoms and Management of Few Seed Borne Diseases
7.1. Rice
7.2. Wheat
7.3. Sorghum
7.4. Pearl millet
7.5. Triticale
7.6. Sunflower
7.7. Sesamum
7.8. Cotton
7.9. Cowpea
7.10. Tomato
7.11. Brinjal
7.12. Chilli
7.13. Potato
7.14. Tapioca
7.15. Sweet potato (Fusarium spp.)
7.16. Celery
7.17. Parsley
7.18. Cole crops
7.19. Lettuce
63 Seed Health Testing
1. Introduction
2. Field Fungi
3. Storage Fungi
4. Objectives of Seed Health Testing
5. Methods in Seed Health Testing
5.1. Detection method for seed borne fungi
5.2. Detection method for seed borne bacteria
5.3. Detection of seed- borne viruses
64. Seed Storage Insects
1. Storage Losses Due to Insects
2. Identification of Storage Pests
2.1. Rice weevils - Sitophilus oryzae
2.2. Angoumois grain moth - Sitotroga cerealella
2.3. Lesser grain borer - Rhizopertha dominica
2.4. Larger grain borer - Prostephanus truncates
2.5. Bruchids - Callosobruchus maculatus
2.6. Indian meal moth: Plodia interpunctella
2.7. Rice moth: Corcyra cephalonica
2.8. Red flour beetle- Tribolium castaneum
2.9. Khapra beetle - Trogoderma granaria
2.10. Saw-tooth grain beetles: Oryzaephilus surinamensis
2.11. Flat grain beetle – Lagmophilocus minutus
2.12. Granary weevil: Sitophilus granarius
2.13. Confused flour beetle- (Tribolium surinamensis)
2.14. Long headed flour beetle - (Leatheticus oryzae)
3. Management of Storage Pests
3.1. Sanitation
3.2. Seed store sanitation
3.3. Fumigation
4. Methods to Assess the Damage
4.1. Visual inspection
4.2. X- ray radiography
4.3. Transparency test
65. Seed Borne Nematodes
1. Nematodes
1.1. Nematodes
2. Important Seed Borne Nematodes
3. Detection of Seed Borne Nematode
UNIT 7 : SEED INDUSTRY AND MARKETING
66. Seed Industry
1. Seed Industry Before Independence
2. Seed Industry After Independence
2.1. First Five Year Plan (1951-56)
2.2. Second Five Year Plan (1956-61)
2.3. Third Five Year Plan (1961-66)
2.4. Annual Plans (1966 to 1969)
2.5. Fourth Five Year Plan (1969-74)
2.6. Fifth Five Year Plan (1974-79)
2.7. Sixth Five Year Plan (1980-85)
2.8. Seventh Five Year Plan (1985-90)
2.9. Eighth Five Year Plan (1992-97)
3. Important Events of Seed Industry
67. Seed Marketing
1. Definition
2. Seed Marketing Comprises the Following
2.1. Demand forecast (Assessment of Effective Demand)
2.2. Marketing structure
2.3. Arrangements for storage of seeds
2.4. Sales promotional activities
2.5. Post sales service
2.6. Economics of seed production and seed prices
3. Marketing Activities
4. Purpose of Seed Marketing
5. Approaches to Seed Marketing
6. Types of Seed Production and Distribution Organizations
6.1. Government departments
6.2. State-owned corporations
6.3. Private enterprise
7. Channels of Marketing of Seeds
8. Export and Import of Seeds
UNIT 8 : PPV & FR
68. Protection of Plant Varieties and Farmers Rights Act (PPV & FR Act)
1. PPV & FR Act
1.1. Notable features of act
1.2. Registration of plant varieties
1.3. Objectives
2. Salient Features of the Act
2.1. Farmers rights (sec 39)
2.2. Breeders Rights (sec 27 & 28)
2.3. Essentially Derived Variety (EDV)
2.4. Researchers Right
2.5. National Gene Fund (Section 45 of the Act). .
2.6. Benefit sharing and registration of varieties
2.7. Compulsory licensing (sec 47)
2.8. Plant Variety Journal of India (PVJ of India)
2.9. Plant Variety Registry
69. DUS test
1. Dus Test
1.1. Requirements
1.2. Distinctness
1.3. Uniformity
1.4. Stability
2. Distinguishing Characters of Different Crops
Preface Seeds are of immense biological and economic importance. It is the most vital and crucial input for crop production and one of the ways to increase crop productivity. Importance of quality seeds has been recognized from the time immemorial. The old script, Manu Smriti says “Subeejam Shukshetre Jaayate Sampradayte” means “Good seed in good soil yields abundantly”. Although the importance of seed was recognized in ancient agriculture, the need for organised seed production was known only at the beginning of twentieth century when Royal Commission of Agriculture (1925) recommended spread of improved varieties and seed distribution. The National Commission on Agriculture (1970-76) emphasized the need for teaching seed production technology in Agricultural Universities/Colleges. The discipline Seed Science and Technology involves seed biology, seed production technology of agricultural and horticultural crops including principles and maintenance breeding, post harvest handling and management of seed, seed quality enhancement, seed legislation and enforcement, seed health, seed storage, seed industry and marketing, and plant variety protection and farmers right. The second edition of an illustrated text book on Seed Science and Technology is revised and enlarged without changing the contents of ICAR UG syllabus. New chapters included are hormones and seed dormancy (Unit 1); seed production in forage legumes and grasses, fruit seed production, flower seed production, seed production in plantation crops and organic seed: traditional varieties and technologies (Unit 2); establishment of seed processing plant (Unit 3); and establishment of seed testing laboratory (Unit 4).
1. INFLORESCENCE An inflorescence is a group or cluster of flowers arranged on a stem that is composed of a main branch or a complicated arrangement of branches. 1.1. Types of inflorescence Inflorescences can be simple or compound. 1.1.1. Simple inflorescence Inflorescence of sessile disc florets forming the capitulum 1.1.1.1. Indeterminate Indeterminate simple inflorescences are generally called racemose. The main kind of racemose inflorescence is the raceme. The other kind of racemose inflorescences can all be derived from this one by dilation, compression, swelling or reduction of the different axes. Some passage forms between the obvious ones are commonly admitted.
1. FLOWERING The flowering goes through a phase of vegetative growth producing more stems and leaves and a flowering phase where they produce the organs for sexual reproduction. 1.1. Synchronisation in flowering Synchronous flowering refers to the phenomenon of coincident, simultaneous flowering of all population of a given species in a large region.
1. FRUITS Fruit is a part of a flowering plant that derives from specific tissues of the flower, mainly one or more ovaries. 1.1. Types 1.1.1. Fleshy 1.1.1.1. Simple fleshy fruits Develop from a flower with a single pistil.
1. SEED A seed is defined as a ‘mature ovule’ or a reproductive unit formed from fertilized ovule, consisting of an embryo, reserve food and a protective cover. Seed is the basic input in agriculture upon which other inputs are applied. A good vigorous seed utilities all the resources and realized as a reasonable output to the grower. It is wealth to the farmer, it is the yesterday’s harvest and tomorrow’s hope. Good seed in good soil realize good yield. Seeds exhibit a great range of variation in shape, size, colour and behaviour. The most essential factor for the success of plantation is the ready availability of quality seeds. The quality of seed is totally responsible for the future return / performance of each and every seedling.
1. VEGETATIVE PROPAGULE Vegetative propagation or asexual propagation is the method of propagating plants with the use of organs other than the seed and spore. In contrast to sexual propagation, the union of the male and female sexual gametes (fertilization) is not a requisite to the production of new plants. Hence the word “asexual”, which means “without sex” or “not sexual”.
1. OVULE DEVELOPMENT The development of ovule occurs within the ovary, which provides a location for nurture and development of the female gametophyte, its sexual fusion with in the male gametophyte, and embryo development, survival, and eventual regrowth (Fig. 1). Ovule growth begins as a small outgrowth within the nucellus. As megasporogenesis and megagametogenesis continue, the region of the nucellus that is to become the ovule enlarges and differentiates into definite morphological characteristics. Secondary outgrowths, or collars (integuments), soon appear around the periphery of the nucellar outgrowths and envelop it. These usually consist of the inner and outer integuments and ultimately become the testa (seed coat) of the mature ovule.
1. APOMIXIS Development of seed without fertilization. When the seed formation occurs without sexual fusion, the process is known as apomixis. This occurs by several mechanism, however all apomitic seed have genetic material only from the female plant Apomixis may or may not require pollination and pollen tube germination to initiate seed formation, however sexual union.
1. DEFINITION Artificial seed technology involves the production of tissue culture derived somatic embryos encased in a protective coating. Artificial seeds have also been often referred to as synthetic seeds. However, the term ‘synthetic seed’ should not be confused with commercial seeds of a synthetic cultivar which is defined as an advanced generation of an open pollinated population composed of a group of selected inbred clones or hybrids. The concept of artificial or synthetic seed is shown in Figure 1.
1. SEED MATURITY Harvesting should be done after the attainment of physiological maturity, when the seeds reached complete maturity to avoid harvesting of immature and ill-filled seeds. 1.1. Physiological maturity It is the stage of accumulation of maximum drymatter within the seeds. It is expressed by maximum seed weight, germination and vigour potential. The moisture content of the seed at this stage is around 25-30% depending up on the species. 1.2. Harvestable maturity The physiological maturity is represented to a seed and this maturity will not be the same for all the seeds of a single plant / population, due to continuous differential flowering habit. Hence, the stage of attainment of physiological maturity by 80% of the population is considered as the harvestable maturity stage. The moisture content of the seed will be lesser than the physiological maturity stage (18-20%).
The chemical composition of seeds is basically determined by genetic factors and varies among different species and seed parts (Table 1). However, it is influenced by environmental and cultural practices.
1. INTRODUCTION In general, seed dormancy refers to lack of growth due to any external or internal cause. It also refers to a state in which viable seeds fail to germinate even when given favourable environmental condition i.e. adequate moisture, appropriate temperature regime, a normal atmosphere and in some cases light. There are various degrees of dormancy varying from very slight to very strong (deep). Sometimes the development or degree of dormancy changes during the lifetime of the seed, usually as a response to external conditions. Hence, dormancy may be innate, develop, be broken and redevelop in seed. Several types of dormancy exist, and sometimes more than one type of dormancy occurs in the same seed. In nature, dormancy is broken gradually or by a particular environmental event. The type of event that may break dormancy depends on dormancy type. Dormancy caused by a hard seed coat may be overcome by a gradual or an instant abrasion, and darkness induced dormancy by exposure to light. In seed handling, the natural dormancy breaking mechanism is applied or simulated during the process of pretreatment. “Pretreatment” is a term used for conditions or processes applied to break dormancy prior to germination, while “treatment” is used for application of pesticides for control of pests and diseases.
1. INTRODUCTION In plants, seed dormancy is controlled by temperature, light and hormones. Unlike animals, which secrete hormones from special glands, hormones are always present in plant cells. Each plant hormone plays multiple roles, depending on the site of action, the life stage of the plant and the hormone’s concentration. A plant hormone is any chemical that is produced in one part of the plant that has a targeted function elsewhere. Certain hormones induce and keep seeds in a dormant state, while others cause seeds to break dormancy and initiate germination They are stored in regions where stimulus are and then released for transport through either phloem or mesophyll when the appropriate stimulus occurs. These are chemical messengers influencing many patterns of plant development The first theory is that the five classic plant hormones, auxin, cytokinins (CKs), gibberellins (GAs), ethylene, and abscisic acid (ABA), plus the new plant hormones, brassinosteroids (BAs), and salicylates or salicylic acids (SAs) can be gathered into three groups. These are growth hormones, stress hormones and shock hormones. Auxin and CKs are growth hormones. Ethylene, GAs, and brassinosteroids are stress hormones. ABAs and SAs are shock hormones. All three types of hormones are similar in that they fall within the classic definition of an intercellular hormone. They are made by a cell and are meant to affect the behavior of other cells, either in nearby tissue or at the opposite end of the plant. ABA, also known as abscisic acid plays a direct role in dormancy release and germination. Ethylene and the gibberellins group of hormones are indirectly involved.
1. SEED GERMINATION The process whereby seeds sprout and begin to grow is known as germination. Germination is the onset growth of a seed, often following a period of dormancy, in response to suitable environmental conditions. During germination (the growth and development process) of a seed, the water is absorbed through micropyle, and the formerly dormant embryo resumes growth and emerges from the seed.
1. PLANT DOMESTICATION AND INTRODUCTION Domestication is the process of bringing wild species under human management. Under domestciation, the crop species have changed considerably as compared to the wild species from which they originated.
1. VARIETY Variety is a seed/crop which suit the prevailing agroclimatic conditions, high yielding and possessing desirable attributes such as disease resistance, earliness and grain quality. Similarly, the seed should be pure, appropriate classes, and obtained from an authorised official agency.
Genetic purity (trueness to type) of a variety can deteriorate due to several factors during production cycles. The best means to insure genetic purity therefore, would be to overcome to the greatest possible extent the various factors responsible for genetic deterioration. The important factors of apparent and real deterioration of varieties as listed by Kadam (1942) are as follows: Developmental variations Mechanical mixtures Mutations Natural crossing Minor genetic variations Selective influence of diseases The technique of the plant breeder
1. BASIC NUCLEUS SEED The seed of the notified variety collected from the evolving institute with all the passport information is considered as basic nucleus seed. This seed is sown in prepared healthy field with more row to row and plant to plant distance than the normal recommendation at required isolation distance. Prescribed dose of fertilizer, irrigation and required plant protection measures are provided. Off types and diseases plants are rogued out at seedling, before flowering, flowering and at physiological maturity stages. Plants are marked with contrast color thread and observed regularly. Marked plants are harvested separately and its produce is used as source seed for production of nucleus seed for next year. Produce of unmarked plants are used as nucleus seed for production of breeders seed. Harvesting threshing and drying are done without reducing physical and genetic purity. The discolored and diseased seeds are removed. The pure seed obtained is the nucleus seed for seed multiplication chain
1. SEED CLASSES Generation system of seed multiplication is nothing but the production of a particular class of seed from specific class of seed up to certified seed stage. The choice of a proper seed multiplication model is the key to further success of a seed programme, which basically depends upon
1. DEFINITION Seed village definition is to see that the aim right from the start is to make a holistic transformation in the village. Seed village concept is a “Win-Win model”, says Deepak Mullick, one of India’s foremost professionals in agribusiness. It is also known as “Compact area approach”. Seed village area should be suitable for crop or varieties. Seed in compact area, whole village should be involved. The whole farmers in the village cultivate same crop, same variety and follow same cultivation practices.
1. INTRODUCTION Indian population is estimated to increase to about 1400 million by 2025. Consequently, India’s requirements for food grains and other food products to feed the increasing population will continue to rise. The food grain requirements are estimated at 350 to 370 million tonnes by 2025. The demand pattern for agricultural commodities for the domestic market will also shift as a result of increasing incomes and faster urbanization. Compared to 26% increase in 1991, the urban population is projected to increase by 42% in 2020. For competing in the global market, the product pattern will shift to high value commodities like fruits, vegetables, floriculture, dairy products, meat and marine products. In such a future scenario, it is necessary to increase agricultural production through improved cropping system, judicious use of agro-inputs and wide use of modern agricultural technology. It is also important to augment and streamline the existing marketing system including handling, transportation, storage, processing and distribution.
1. INTRODUCTION Seed is the most important determinant of agricultural production potential, on which the efficacy of other agriculture inputs is dependent. Seeds of appropriate characteristics are required to meet the demand of diverse agro-climatic conditions and intensive cropping systems. Sustained increase in agriculture production and productivity is dependent, to a large extent, on development of new and improved varieties of crops and an efficient system for timely supply of quality seeds to farmers..
1. SEED It is a matured ovule usually developed after fertilization. Seed can also be defined as the embryonic plant in resting stage, usually supplied with food reserves in the cotyledons or endosperm or in perisperm with the protective structure called seed coat. In a nutshell, it is a dry dispersal unit of a plant. It develops into an individual similar to the one that produced it
1. GENETIC PRINCIPLES 1.1. Maintenance of genetic purity during seed production The methods suggested by Home (1953) and Hartmann and Kester (1968) may be used wholly or in part to maintain high levels of genetic purity during seed production. The various steps suggested by Home (1953) to maintain varietal purity are as follows:
1. HETEROSIS 1.1. Definition Heterosis or hybrid vigor or outbreeding enhancement, is the increased function of any biological quality in a hybrid offspring. It is the occurrence of a genetically superior offspring from mixing the genes of its parents. 1.2. Inbreeding depression Inbreeding depression is the reduced fitness in a given population as a result of breeding of related individuals. In general, the higher the genetic variation within a breeding population, the less likely it is to suffer from inbreeding depression.
1. HAND EMASCULATION AND POLLINATION The male part of seed parent is removed by hand before anthesis to check the self pollination from the crop plants with bisexual flower having fertile male and female part. This process is known as emasculation. These emasculated flowers are then pollinated by the pollens collected from pollinator parent to produce hybrid seed (Fig. 1). Eg. Cotton, tomato, brinjal.
1. LAND REQUIREMENTS Land should be fertile with selected irrigation and good drainage facilities. It should be free from volunteer plants. The field should not have been grown with the same crop in the previous season. If grown, it should be the production of same class of seed for the same variety.
1. TECHNIQUES OF HYBRID SEED PRODUCTION 1.1. Field crops Table 1: Techniques of hybrid seed production in field crops
1. FORAGE LEGUMES 1.1. Isolation
1. TROPICAL FRUITS 1.1. Common name, botanical name and family
1. CUT FLOWERS 1.1. Common name, scientific name and family
1. SELECTION OF SITE Select a location where one could ensure semi-shady conditions. Well drained medium-loam soil; rich in organic matter and neutral soil pH. An irrigation source in the vicinity with natural pH water is highly desirable.
1. DEFINITION Micropropagation is the growing of plants from meristematic tissue or somatic cells of superior plants on nutrient suitable media under controlled aseptic physical conditions.
1. INTRODUCTION Green Revolution Technologies (GRT) such as greater use of synthetic agrochemicals like fertilizers and pesticides, adoption of nutrient responsive high yielding varieties, greater exploitation of irrigation potentials etc. have boosted the production output in most cases. However, continuous use of these high energy inputs indiscriminately now leads to decline in production and productivity of various crops as well as deterioration of soil health and environment. The most unfortunate impacts of GRT on Indian Agriculture are imbalance in production, dependency on synthetic chemical fertilizers, increase in secondary and micronutrient deficiencies, increase in pesticide use, unscientific water management and distribution, reduction in productivity, reduction in quality of the produce, extinction of gene pool, environmental pollution and imbalance in social and economic status. Moreover, today the rural economy is now facing a challenge of over dependence on outside inputs and day-by-day increase in price of these inputs. Further, Indian Agriculture will face the market competition due to globalization of trade as per World Trade Organization (WTO). Thus, apart from quantity, quality will be the important factor. Such varieties of concern and problems of modern Indian Agriculture gave birth to various new concepts of farming such as organic farming, natural farming, biodynamic agriculture, do-nothing agriculture, eco-farming, etc. Therefore, for sustaining the productivity of the crop, maintaining the soil health and healthy ecosystem, there is a need for adoption of an alternative farming system, may be the organic farming. Organic farming is not new to Indian farming community. Several forms of organic farming are being successfully practiced in diverse climate, particularly in rainfed, tribal, mountain hills and resource poor areas of the country. It safeguards/improves quality of resources and environment. It is labour intensive and provides an opportunity to increase rural employment. For a product to be called and labelled “organic”, it should have been produced from start (seed) to end (the produces, the consumer is buying) in an organic way. International Federation of Organic Movement (IFOAM) has clearly laid down the condition that in order to get organic certification to the produces, the seed used for sowing should also have been produced organically. To enter into organic agriculture, timely research has been warranted to study the strategies and efficacies of organic seed production to fulfill the global organic seed demand. Organic seed production system involves use of organic seed quality enhancement treatments, integrated organic nutrient management practices viz., organic manures, green manures and biofertilizers etc., and integrated organic plant protection viz., agronomic practices, crop rotation, growing border/trap crops and use of botanicals, biopesticides and biocontrol agents apart from encouraging natural parasites, predators and parasitoids etc.
2. METHODS OF HARVEST The seed can be harvested either manually or mechanically. In mechanical harvesting, single harvest is possible, but care should be taken to avoid mechanical injury. In manual harvesting, crops can be harvested either as single harvest or as periodical harvest. The crops having continuous flowering habit are to be harvested in different harvests/ pickings. 2.1. Manual harvesting Harvesting any crop can be done manually. Manual harvesting is done by the hand of harvest worker. Multipicking in pulses and vegetables is done by manual methods.
1. SEED EXTRACTION The processing of seeds starts from the extraction of seed material from the plant parts. The seed removal in dry fruits is known as threshing, while that of wet fruits is known as extraction. 2. METHODS OF SEED EXTRACTION 2.1. Dry extraction Dry extraction is done either manually or mechanically. Manual extraction is by beating with pliable bamboo stick or by beating against a hard surface. Threshers are used for mechanical extraction. In this, care should be taken to avoid mechanical injury. Eg. All agricultural crops.
1. SEED DRYING The process of elimination of moisture from the seed is called drying. 2. STAGE OF MOISTURE ELIMINATION The moisture from the seed is eliminated in 2 stages Surface moisture of the seed that initially removed by the drying air. The removal of the moisture in the surface cause an imbalance in the moisture potential in the surface of the seed and the inner portion of the seed which leads to the migration of moisture from the inner organ to the surface. The migration of moisture to the surface is slower than the evaporation and a moisture gradient is developed in the kernel. Elimination of moisture from the seed depends upon the relative humidity and temperature of the environment surrounding the seed.
1. SEED PROCESSING 1.1. Purpose Seed processing is necessary in order to dry the seeds to safe moisture level, remove or reduce to the extent possible the various undesirable materials, weed seeds, other crop seeds, deteriorated or damaged seeds, uniform size grading and seed treatment to upgrade the overall seed quality. 1.2. Physical characteristics that aid in grading and upgrading The threshed produce are pre-cleaned either manually or mechanically and are graded using different, but optimum sieves of specified sizes. This grading bring homogeneity in the lot which aids in obtaining uniformity among the population in the subsequent sowing. Different kinds of seeds can be separated when they differ in one or more physical characteristics. Physical characteristics normally used to separate seeds are size shape, length, weight, colour, surface texture, affinity to liquids, electrical conductivity, etc.
1. INTRODUCTION Field run seeds obtained from the seed production field posses high moisture and physical contaminants like trash and other inert materials (sand, stones, soil etc.,), diseased and pest damaged seeds, other crop seeds, weed seeds, deteriorated and damaged seeds, off-size and ill filled seeds, plant remnants etc. Seed processing is must to dry the seeds to safe moisture level, remove unwanted and inert materials as detailed above. Seed qualities such as vigour and viability are improved by certain physical characteristics of the seed i.e., shape, size, large, denser and sound seed, etc. So, if grading is done to obtain a particular range of size, shape, length and density of the seeds, the quality of the lot is upgraded. Seed processing refers to all the steps necessary for preparation of harvested seed for marketing namely handling, drying, shelling, preconditioning, cleaning, size grading, treating and packaging.
1. SEED FORTIFICATION It is process of enriching the seeds with bioactive chemicals for improving the germination and seedling vigour. To the known volume of seeds, one third volume of the nutrient solution is added and allowed to imbibe for short duration. The imbibed seeds should be dried under shade. The fortification treatments recommended for different crops are depicted
Any new variety produced by the Scientist has to be multiplied to many times to meet the needs of the farmers. In order to ensure the availability of quality seeds, Government of India have enacted Seed Act 1966 and Seed Rules, 1968. The Seed (Control) order 1983 was promulgated under essential commodities act, 1955 in order to ensure the production, marketing and distribution of the seeds. 1. SEED ACT 1966 The objective of Seed Act is for regulating the quality of certain notified kind / varieties of seeds for sale and for matters connected therewith. The Seed Act passed by the Indian Parliament in 1966 was designed to create a ‘climate’ in which the seeds man could operate effectively and to make good quality seed available to cultivators. Seed Rules under the Act were notified in September 1968 and the act was implemented in October 1969. This act extent to the whole of India and it has 25 sections.
1. SEED CERTIFICATION Seed Certification is a legally sanctioned system for quality control on seed multiplication and production. It involves field inspection, pre and post control tests and seed quality tests. 1.1. Phases of Seed Certification Certification shall be completed in six broad phases listed under
1. UNIT OF CERTIFICATION The entire area planted under seed production programme by an individual constitutes an unit, provided; All the seed production programme is to produce seed of one category and one variety. Area does not exceed 10 hectares and scattered fields constituting one unit (10 ha) should not be separated by more than 50 metres distance (Table 1). The crop of the entire area is more or less of the same growth stage. The seed crop is grown as sole crop and it is not heavily and uniformly lodged.
1. PRESENCE OF OBJECTIONABLE WEEDS Objectionable weeds present in the seed crop of the respective species should be removed and destroyed before flowering. They should be verified during field inspection (Table 1). The maximum permitted limit of objectionable weed in seed crop is presented in table 2.
1. MINIMUM SEED CERTIFICATION STANDARDS In a seed quality control programme through seed certification, the minimum seed certification standards, in fact, are the minimum standard conditions which must be met. The minimum seed certification standards, thus are the standards required for the certification of seeds by the certification agencies. The minimum seed certification standards can be broadly grouped into two groups.
1. SEED LOT A specified quantity of seed which is physically identifiable to the types of which certificates may be issued. 2. SAMPLING A sample is obtained from the seed lot by taking small portions at random from different position of the lot and combining them. It is a representative sample of a seed lot. The objective of sampling is to obtain a representative sample of a size suitable for test. When the sample originates from seed lot, it is expected that the results reflect the average quality of the seed lot.
1. MIXING AND DIVIDING The main objective of mixing and dividing of seeds is to obtain the representative homogenous seed sample for analysis by reducing the submitted sample to the desired size of working sample. 2. TYPES OF MECHANICAL DIVIDERS 2.1. Boerner divider The principle involved in mixing and dividing in gravitational force. It consists of a hopper, a cone and series of baffles directing the seeds into 2 spouts. The baffles are of equal size and equally spaced and every alternate one leading to one spout. They are arranged in circle and are directed inward. A valve at the base of the hopper retains the seeds in the hopper. When the valve is opened, the seeds fall by gravity over the cone where it is equally distributed and approximately equal quantity of seeds will be collected in each spout. A disadvantage of this divider is that it is difficult to check for cleanliness (Fig. 1).
1. SEED PURITY AND ITS COMPONENTS Seed purity analysis from the working sample taken from submitted sample is made in accordance to ISTA rules. The uncertified seed sample is generally a mixture of pure seeds, inert matter and biological impurities including genetically impure seeds of the variety. A buyer expects to have good seed and not a mixture of pure seed with a high percentage of chaff, straw, sand, weed seeds and other crop seeds and also genetically impure or mixed seeds. Purity analysis is a test to estimate the extent of biotic and abiotic impurities present in the seed lot of a variety.
1. SEED MOISTURE Seed moisture is one of the most important deciding factors of seed viability and quality during storage. Hence, determination of seed moisture content and drying to the safe moisture content is utmost important before transit and storage. According to ISTA (1985), moisture content of the sample is defined as that loss of weight when it is dried in accordance with the rules or the amount of water collected when it is distilled. It is expressed as percentage of the original weight of sample (wet basis). 1.1. Principle Moisture present in the seed is removed completely as much as possible without oxidation or decomposition or loss in other volatile substances by applying heat. The weight loss due to drying is estimated and the moisture content is calculated.
1. GERMINATION TEST PROCEDURES Although several methods are available for germination testing it is suggested that use one of the two major methods described here because these are adaptable to most environments and in general give uniform results Select 400 seeds randomly and used for germination in 4 replications. 1.1. Top of Paper (TP) Seeds are placed on one or more layers of moist filter paper or blotter paper in petriplates These petriplates are covered with lid and placed inside the gemination cabinet This is suitable for those seeds which required light Cut the paper to the size and shape of the dishes (Fig. 1). Place a layer of paper in each dish If the paper is too thin use a double layer Label the top and bottom of each dish with the accession number number of the replicates and date of the test Moisten the paper with water (Fig. 2)
The relative long periods of time required for completion of germination tests delays the seed marketing. This necessiated the development of rapid methods for estimating the germination capacity of seeds. This test was developed by Lakon (1942) in Germany. 1. PRINCIPLE It is a biochemical test, in which living cells are made visible by reduction of an indicator dye. The indicator used is 2,3,5 triphenyl tetrazolium chloride. Within the seed tissues, it interferes with the reduction processes of living cells and accepts hydrogen from the hydrogenases. By hydrogenation of the 2,3,5-triphenyl tetrazolium chloride, a red stable and non diffusible substance, triphenyl formazan is produced in living cells (Fig. 1).
1. FIELD OF APPLICABILITY Grow-out test is the official measure for controlling the genetic purity of the seed lot. It serves as ‘pre-control’ as well as a ‘post control’ test for avoiding genetic contaminations. According to the official regulations in India, it is prerequisite for seed certification of hybrids of certain species such as cotton, castor, musk melon and brinjal. The test is conducted for checking the sellers label with respect to genetic purity status of the seed lot under the provisions of the Seeds Act 1966. In addition, grow-out test can also be used as a measure to judge the efficacy of the certification agency or the inspector.
1. DEFINITION Sum of those properties of seed, which determine the potential level of activity and performance of the seed or seed lot during germination and seedling emergence. i.e., rapid and uniform production of healthy seedling and stand establishment under a wide range of field conditions is considered as seed vigour. In a vigour test, the seed is introduced to a stressful environment unfavorable to seedling development. This environment can be cool, cold or warm, or a combination of either high humidity and high temperatures, or heavy moisture at low temperatures. A vigor test cannot replace a germination test, but rather supplements it with more information about seed quality.
1. INTRODUCTION For maintenance of genetic purity in the field with the seed crop and to test verify the standards in certification programme, the studies on varietal characterization and identification have attracted the attention of breeders, breeder’s right protection institutions, farmers, the seed industry, certification agencies, and seed testing laboratories with a view to assure the quality of seed marketed to the consumers.
Founded in 1924, with the aim to develop and publish standard procedures in the field of seed testing, with member laboratories in over 70 countries world wide. ISTA membership is truly a global network. ISTA secretariat is located at Zurich, Switzerland. 1. VISION AND MISSION ISTA members work together to achieve their vision of ‘Uniformity in seed quality evaluation worldwide’. The association produces Internationally agreed rules for seed sampling and testing, accredits laboratories, promotes research, provides International seed analysis certificates and training and disseminates knowledge in Seed Science and Technology. This facilitates seed trading Nationally and Internationally and also contributes to food security.
1. SEED TESTING The science of evaluating the planting value of seed has been developed to achieve the following objectives for minimizing the risks of planting low quality seeds. To determine the seed quality and its suitability for planting To identify seed quality problems and their probable cause. To determine the need for drying and processing, if any. To determine if seed meets established quality standards for labeling. To establish quality and provide a basis for price and consumer discrimination among lots in the market.
1. SEED STORAGE Is the maintenance of high seed germination and vigour from harvest until planting. 1.1. Importance of seed storage Seed storage is important to get adequate plant stands in addition to healthy and vigorous plants.
1. DEFINITION Seed deterioration is defined as deteriorative changes occurring with time that increase the seed’s vulnerability to external challenges and decrease the ability of the seed to survive
1. SEED TREATMENT It refers to the application of pesticides (fungicides, insecticides or a combination of both) to seeds before sowing and/or storage in order to protect the seeds and young seedlings from soil borne pathogens and/or storage pathogens and insects. Seeds are thoroughly mixed with required quantities of chemicals namely bavistin (carbendezim) @ 2-4 g/kg of seeds.
1. GERMPLASM A germplasm is a collection of genetic resources for an organism. For plants, the germplasm may be stored as a seed collection or for trees, in a nursery. 1.1. Conservation methods 1.1.1. In situ conservation The conservation of species in their natural habitats, is considered the most appropriate way of conserving biodiversity. Conserving the areas where populations of species exist naturally is an underlying condition for the conservation of biodiversity. That’s why protected areas form a central element of any national strategy to conserve biodiversity.
1. SEED PATHOLOGY The area of science that studies the relationship between pathogens and seeds is seed pathology. 2. TYPES OF PATHOGEN Diseases of plants are caused primarily by three types of pathogens: bacteria, fungi, and viruses. Despite that fungi comprise the largest group of pathogens, the bulk of seed-specific diseases are caused by bacteria or viruses. This is due to the fact that bacteria and viruses are more adopt at entering and then travelling through the veins of the plant, a phenomenon known as ‘systemic infection,’ and from the vascular system may make their way into the developing embryos of seeds. Fungi, in contrast, tend to be restricted to the outer layers of the plant, where they initiate infection by means of air-borne spores and then proceed to spread by attacking nearby cells of the outer layers. Fungi are much less likely to enter the vascular system of the plant, and thus infect seed mostly when they either ‘crawl’ all the way to seed on the outside of the plant, or else send out spores that land on the seed. In either case, the fungal spores are on the outside of the seed, in the layers of the seed coat, spores on the seed coat are more prone to either dry up and die, or else to get sloughed off with the seed coat during seed germination, thereby failing to cause disease on the next generation of plants.
1. INTRODUCTION Seed health refers to the health status of a seed. Sowing healthy seeds of high quality is our concern to improve crop yields, thus increasing food production. It has a great concern to farmers and seed producing agencies where the disease is high and average yields are low and where more food is needed to feed the ever-increasing population. So, it is important to test the seeds for disease organism before they are sown in the field and to avoid harmful organisms traveling from infected to non-infected areas within a country or across international boundaries.
Weight loss: For grains or grain legumes in the tropics, a weight loss in the range of 10-30 per cent might be expected over a full storage season. Loss in quality/market value: Infested seed is contaminated with insect debris and has increased dust content. Seeds are holed and often discoloured, which fetch low price. Promotion of mould development: In humid conditions, without adequate ventilation, mould development and caking can spread rapidly, causing severe losses. Reduced germination in seed material: Damage to the embryo of the seed will usually prevent germination. Some storage pests prefer to attack the embryo.
1. NEMATODES Nematodes, also called eel-worms, are wormlike in appearance, but quite distinct taxonomically from true worms. They live freely in fresh or salt water or in soil. They are saprozoic and also parasitize animals (including man) and plants. Many species of nemotdes parasitize higher plants and cause disease symptoms. Plant parasitic nematodes are small (invisible to the naked eye), long, tubular, round in the cross section, unsegmented and smooth invertebrates. They inhibit different parts of plants, namely, roots, stem, flower buds and seeds. Depending on the host-parasite relationship, plant parasitic nematodes may be sedentary or migratory and ectoparasitic and/or endoparasitic in their feeding habits. 1.1. Nematodes Seed-borne nematodes may be internal or may occur as seed infestation. Several saprozoic soil nematodes occur in beds of soil mixed with seed. Seed infestation by nematodes does not produce any specific symptoms on seed, but in those that occur as endoparasites, the floral structure may be modified into a seed gall (Anguina spp.) may produce symptoms such as discoloration of testa in groundnut (Ditylenchus destructor) or may be symptomless as in paddy kernels infected by Aphelenchoides besseyi. Neergaard (1979) listed five genera - Anguina, Aphelenchoides, Ditylenchus, Heterodora and Rhadinaphelenchus - that are seed-transmitted. Heterodora and Rhadinaphelenchus occur as endoparasites in roots, stems, and leaves. The latter also affects the growing apex, inflorescence and husks of dropped nuts.
1. SEED INDUSTRY BEFORE INDEPENDENCE The Royal Commission on Agriculture (RCA) constituted in 1925 suggested the following for seed improvement There should be a separate organization within agriculture departments to deal with seed distribution and seed testing. The seed distribution enterprise should be self-sustaining. Seed distribution should be organized through co-operatives, other associations, seed merchants (whenever they are available), through seed agents, as well as through agricultural department staff and any other agency which could be considered suitable. Seed merchants of proven enterprise should be given every encouragement.
1. DEFINITION Seed marketing is the one of the most vital components of seed technology. On it depends the size and scope of the seed industry. Broadly it includes such activities as production, processing, storage, quality control and marketing of seeds. Seed marketing refers to the actual acquisition and selling of packed seeds, intermediate storage, delivery and sales promotional activities.
1. PPV & FR ACT With the signing of TRIPs agreement of the World Trade Organization (WTO), India has agreed to provide protection to plant varieties. The Government of India, therefore, enacted “ The Protection of Plant Varieties and Farmers Rights Act (PPV&FR Act)” in 2001 and the Regulations for implementing the Act were formulated in 2003. The Ministry of Agriculture, Government of India, has been identified as the nodal agency for implementing the PPV& FR Act through an Authority known as “The Protection of Plant Varieties and Farmer Rights Authority”. The Authority came into force in November, 2005. PPV & FR act has 11 chapters, 4 schedules and 97 sections.
1. DUS TEST A variety shall express distinct character(s) for verification, uniformity within population and stability for expression of such characters over the year and at different locations, then only its genetic purity is confirmed. 1.1. Requirements Authentic seeds of existing varieties, pure seeds of variety under tests, list of characters to be examined and their expression. This test is conducted in the most optimum conditions of soil and climate and the crop is exposed to the best agronomic management conditions to ensure full expression of the characters. 1.2. Distinctness The variety under test is compared with the existing varieties (having similar plant height, growth habit, days to flowering, days to maturity and reaction to diseases) for qualitative morphological characters at seed, seedling and plant levels. Biochemical differences may also be considered. To establish the distinctness, the test is performed for 2 years for self pollinated crops.
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