Introduction
The Single Seed Descent (SSD) method is a highly efficient breeding approach for advancing segregating populations, particularly in self-pollinated crops such as wheat, rice, soybean and barley. SSD emphasises rapid attainment of homozygosity while retaining broad genetic variability. Although the core idea is simple — advancing each plant by taking a single seed to the next generation — the method has profound practical implications in modern breeding programs.
Historical background
The SSD concept dates back to Goulden (1939) working in barley and was later championed for practical breeding by Brim (1966) in soybean. Since then, SSD has become a widely used strategy for developing inbred lines where neutral handling of segregating generations and speed are priorities. With the advent of speed-breeding facilities and molecular markers, SSD has become even more valuable.
Why SSD? Rationale and need
Early-generation selection (for example in F2 or F3) can be misleading because environmental influences often mask the true genetic potential of genotypes. Moreover, selecting too early may eliminate rare but valuable recombinants. SSD avoids these pitfalls by postponing selection until lines approach homozygosity (usually F5–F6), when genotype expression is stable and less confounded by environment.
Principle of SSD
Central principle: Each plant in a segregating generation contributes exactly one seed to the next generation, regardless of its phenotype. This ensures equal probability for all genotypes to be advanced and minimizes breeder-induced bias during the early segregation phase.
Detailed procedure (step-by-step)
1. Parental crosses and F1
The breeder chooses parents with contrasting or complementary traits and makes the cross. F1 seeds are harvested and grown to produce the segregating F2 generation.
2. Handling the F2 population
A large population of F2 plants is grown. From each F2 plant, one seed is collected and bulks of those single seeds are used to grow the F3 generation. No selection is applied at this stage, even though plants may vary widely in phenotype.
3. Successive single-seed generations (F3 → F4 → ... )
This one-seed-per-plant rule is repeated for successive generations. It can be done in field plots, greenhouse benches, off-season nurseries, or pots. Because the method does not require recording individual pedigrees or evaluating each plant, it is space- and labour-efficient. As selfing continues, heterozygosity declines rapidly and lines approach homozygosity.
4. Attaining homozygosity and beginning selection
By about F5–F6 most loci will be homozygous (theoretically >95–98% homozygosity). At this point, each line behaves like a stable pure line and breeders begin systematic phenotypic selection (yield, disease resistance, quality traits), followed by replicated trials and multi-location testing.
Year-wise timeline (practical schedule)
Year 1: Make parental crosses and obtain F1 seed.
Year 2: Grow F1, harvest F2 seeds.
Year 3: Grow large F2 population; harvest one seed/plant → produce F3 bulk.
Year 4: Grow F3 bulk; again harvest one seed/plant → F4.
Year 5: F4 → F5 by SSD; segregation reduced significantly.
Year 6: F5 to F6; most lines are near homozygosity; begin preliminary evaluation.
Year 7: Conduct replicated yield trials on promising lines.
Year 8–9: Multi-location testing and stability assessment.
Year 10+: Candidate lines proposed for release if consistent performance is recorded.
Year 2: Grow F1, harvest F2 seeds.
Year 3: Grow large F2 population; harvest one seed/plant → produce F3 bulk.
Year 4: Grow F3 bulk; again harvest one seed/plant → F4.
Year 5: F4 → F5 by SSD; segregation reduced significantly.
Year 6: F5 to F6; most lines are near homozygosity; begin preliminary evaluation.
Year 7: Conduct replicated yield trials on promising lines.
Year 8–9: Multi-location testing and stability assessment.
Year 10+: Candidate lines proposed for release if consistent performance is recorded.
Genetic basis (mathematical expectation)
Under repeated selfing, the proportion of heterozygous loci halves each generation. For example, after n generations of selfing starting from F1, expected heterozygosity = (1/2)n. By F6 (i.e., 5 generations of selfing from F2 to F6 or counting from F1), expected homozygosity is very high—typically above 95–98%—making selection reliable.
Advantages (detailed)
- Simplicity: Low record-keeping; one seed per plant makes logistics easier.
- Preservation of variability: Avoids early culling and preserves recombinants that may later prove valuable.
- Speed: Rapid attainment of homozygosity compared with pedigree selection.
- Space efficiency: Can be performed in limited space (pots, greenhouse benches, or offseason nurseries).
- Neutrality: Minimises environmental bias because selection is delayed until line stabilization.
- Compatibility with modern tools: Can be combined with marker-assisted selection, doubled-haploid (DH) techniques, or speed breeding.
Disadvantages and risks (detailed)
- Single-seed bottleneck: Taking only one seed per plant increases the risk that a valuable recombinant may be lost by accident (disease, seed damage, poor germination).
- No early culling: Inefficient use of resources in later generations because undesirable lines are carried forward until F5/F6.
- Fixation of deleterious alleles: Without early selection, harmful recessive alleles may get fixed.
- Population reduction: Natural losses during selfing (sterility, disease) reduce effective population size.
- Not ideal for certain traits: Traits expressed only in seedling stage or those needing early selection (e.g., seedling vigour) may not be suited to pure SSD.
Modifications and enhancements
Modified SSD (mSSD): Collecting more than one seed per plant (for example 2–3 seeds) to reduce the chance of losing rare recombinants and buffer against germination failure.
Accelerated SSD (aSSD): Use of off-season nurseries, growth chambers, controlled environment facilities and speed-breeding (extended photoperiods and supplemental lighting) to advance multiple generations per year.
Marker-assisted SSD: Use molecular markers to screen bulks or individual lines for presence of desired alleles even before final selection; speeds up recovery of target genes while still benefiting from SSD's neutral advancement.
SSD combined with Doubled Haploids (DH): DH can produce completely homozygous lines in 1–2 generations; combining DH and SSD can be efficient when DH is available for the crop.
Accelerated SSD (aSSD): Use of off-season nurseries, growth chambers, controlled environment facilities and speed-breeding (extended photoperiods and supplemental lighting) to advance multiple generations per year.
Marker-assisted SSD: Use molecular markers to screen bulks or individual lines for presence of desired alleles even before final selection; speeds up recovery of target genes while still benefiting from SSD's neutral advancement.
SSD combined with Doubled Haploids (DH): DH can produce completely homozygous lines in 1–2 generations; combining DH and SSD can be efficient when DH is available for the crop.
Practical applications
SSD is widely adopted in self-pollinated cereals and legumes: wheat, barley, rice, soybean, chickpea, lentil and common bean. It is particularly valuable where rapid generation turnover is possible (greenhouse or off-season nurseries) and where preserving maximum recombination is important. SSD is also frequently used in modern breeding programs that incorporate genotyping; breeders advance generations neutrally and later screen almost-homozygous lines using molecular tools and phenotyping.
Comparison with other breeding approaches
Criteria | Pedigree Selection | Bulk Method | Single Seed Descent (SSD) |
---|---|---|---|
Selection stage | Early generations | Natural selection in bulk | Postponed until F5/F6 |
Record keeping | High | Low | Minimal |
Speed to homozygosity | Slow | Moderate | Fast |
Retention of diversity | May lose diversity due to early selection | High (natural selection) | High, but single-seed rule introduces risk |
Land requirement | Large | Large | Small (pots/greenhouse possible) |
Best used when | Traits with high heritability and pedigree info useful | Harsh selection environments | Rapid neutral advancement, molecular breeding pipelines |
Recommendations and best practices
- Start with a large F2 population to capture broad recombination.
- If resources permit, collect 2 seeds per plant instead of 1 (modified SSD) to provide a safety margin against seed loss or poor germination.
- Combine SSD with marker-assisted selection to recover target alleles early while keeping the population advance neutral.
- Use controlled environments or off-season nurseries to accelerate generation turnover.
- Keep careful records of bulk identity (cross ID and year) even if individual pedigree tracking is not done.
Conclusion
Single Seed Descent is a robust, pragmatic method that balances rapid homozygosity with preservation of genetic variation. It is particularly useful for breeders working with self-pollinated crops and for programs that combine classical breeding with modern molecular tools. While the one-seed rule brings efficiency it also brings risk; many breeders therefore adopt minor modifications (multiple seeds, marker-assisted screens, or combining SSD with DH). Overall, SSD remains a preferred strategy where neutral advancement and time-efficiency are primary objectives.