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Keynote lecture at the Organic World Congress, Namyangju City, Gyeonggi Province, Republic of 
Korea, 26.09.-05.10.2011 
Organic Plant Breeding: Achievements, Opportunities, and 
Challenges 
Dr. Bernd Horneburg 
Georg-August-University Göttingen, Department of Crop Sciences, Von-Siebold-Str. 8, D-37075 
Göttingen, bhorneb@gwdg.de, Tel: +49 (0)551-394360, Fax: +49 (0)551-394601, http://www.uni-goettingen. 
1 
de/de/48392.html 
During the development of the organic agriculture movement it became obvious that 
crop plant varieties released from conventional breeding programs do not cover all 
requirements and demands of organic systems. A number of organizations were 
founded around 1980 to 1990 to i) safeguard genetic resources on farm and in 
garden, ii) produce and distribute organic seed, and iii) start organic breeding 
programs. Organizations include e. g. MASIPAG / Philippines, Seeds of Change / 
USA, De Bolster / Netherlands, Arche Noah / Austria, Pro Specie Rara / Switzerland, 
Kultursaat and Dreschflegel / Germany, and Garden Organic`s Heritage Seed Library 
/ England. Prior to this time little organic seed was available exclusively from a few 
pioneers. 
Aims that many of us agreed upon were 
· the adaptation of varieties to organic growing conditions, 
· to (re-)establish farmers and gardeners as breeders, 
· reduce external input (seed) into the farm organism, 
· appreciate the holistic nature of the plant and its integrity, 
· use the potential of open pollinated varieties, 
· create a cooperation between breeders, growers, and consumers, 
· increased varietal diversity, and 
· high food quality. 
In the meantime some organic breeding projects have yielded encouraging results 
and some academic working groups have investigated and improved organic 
breeding methods. The first academic textbook “Organic Plant Breeding” (Lammerts 
van Bueren and Myers) is to be published in 2012. The objective of this article is to 
highlight some successful approaches to organic plant breeding and to encourage 
the organic movement to engage in an increasing number of organic breeding and 
organic breeding research projects. 
The need for organic breeding programs 
In paired organic / conventional selection experiments with wheat (Murphy et al. 
2007, Reid et al. 2011) and maize (Burger et al. 2008) it has been demonstrated that 
the best genotypes for organic cropping are selected within the organic system. 
Murphy et al. (2007) have demonstrated that the top yielding soft white winter wheat 
breeding lines in organic management did not correlate to the top yielding ones in 
conventional management in four out of five paired trials (Fig. 1). Spearman’s rank 
correlation coefficient revealed no positive genotypic rank correlations among 
systems in locations 1-4. Direct selection in organic systems produced yields 15%, 
7%, 31% and 5% higher than the yields resulting from indirect selection for locations 
1–4, respectively. Differences observed at location 5 were not significant.
Keynote lecture at the Organic World Congress, Namyangju City, Gyeonggi Province, Republic of 
Korea, 26.09.-05.10.2011 
Fig. 1. Genotypes’ change in rank between organic and conventional wheat 
nurseries. The top five ranking genotypes for yield in both organic and conventional 
systems were compared at each location. Genotypes are ranked from 1 = highest 
yield to 35 = lowest yield (Murphy et al. 2007). 
Burger et al. (2008) tested experimental single-cross maize hybrids in two paired 
conventional and organic trials. The results shown in Fig. 2 clearly indicate that the 
top ranking hybrid varieties in organic management do coincide with those adapted 
to conventional management only to a very limited extent. 
In the words of Murphy et al. (2007) “With crop cultivars bred in and adapted to the 
unique conditions inherent in organic systems, organic agriculture will be better able 
to realize its full potential as a high-yielding alternative to conventional agriculture.” 
The superior performance of breeding lines selected within organic system is the 
result of a number of important traits some of which will be dealt with in the next sub-chapters. 
It is an advantage of breeding within organic systems to be able to select 
for individual traits like weed tolerance, nutrient use efficiency, and field resistance 
against pests and diseases as well as the interactions among these traits. 
2
Keynote lecture at the Organic World Congress, Namyangju City, Gyeonggi Province, Republic of 
Korea, 26.09.-05.10.2011 
3 
120 
110 
100 
90 
80 
70 
60 
Best organic 
varieties 
Both 
systems 
Best 
conven-tional 
varieties 
70 80 90 100 110 120 130 
Grain yield [dt/ha] in conventional management 
Grain yield [dt/ha] in organic management 
Fig. 2. Performance of maize hybrids in conventional and organic management 
(Burger et al. 2008, modified). 
Crucial traits 
for many crops in organic systems are weed tolerance, field resistance against 
pests and diseases, nutrient use efficiency, and adaptation to nutrient 
dynamics. These traits are of varying importance in conventional system depending 
on the input level of herbicides, fungicides, pesticides, and mineral fertilizer.They may 
be beneficial to reduce input and solve particular problems. Organic breeding has the 
potential to improve conventional agriculture, too. 
Weed tolerance 
is a very complex trait. Few experiments have investigated varietal differences. No 
results from breeding programs for weed tolerance were available for this article. The 
most important aspect is the morphological weed suppression ability that for instance 
in cereal grains includes height, early season growth, tillering capacity, and leaf area 
index (Mason and Spaner 2006). The identification of competitive crop idiotypes may 
assist organic breeders in the development of competitive varieties. The tolerance to 
mechanical weed control is important in many organic systems. It may be related to 
the strength of the roots, root distribution, and leaf-arrangement. Generally 
competition in the root sphere is little investigated. 
In breeding projects intercropping with suitable cultivated plants of selected species 
can be used to simulate weed competition, because natural weed pressure 
frequently is not evenly spread throughout the test plots. This approach, however, 
has a little drawback: it fails to investigate allelopathic effects between weeds and 
crop plants that may either be positive or negative for crop development. Wolfe et al. 
(2008) stated that little is known about allelopathic effects under field conditions.
Keynote lecture at the Organic World Congress, Namyangju City, Gyeonggi Province, Republic of 
Korea, 26.09.-05.10.2011 
Breeding for field resistance against diseases has been successful for e.g. barley 
and tomato. 
An example for fungal pathogens restricted to organic agriculture are the smut fungi 
of cereals, e.g. loose smut (Ustilago nuda) and covered smut (Ustilago hordei) in 
barley. In conventional agriculture smuts can be controlled completely by seed 
treatment with fungicides. In organic management seed borne spores can be 
controlled e. g. by hot water treatment. This method, however, is not efficient enough 
to meet the threshold given by the authorities for the production of certified seed. 
Screening for resistance within organic systems was successfully carried out by 
Lorenz et al. (2006). 
The host – pathogen system Tomato – late blight (Phytophthora infestans) is rapidly 
evolving on the global scale favouring more aggressive Phytophthora strains (Foolad 
et al. 2008, Deahl et al. 2008). As a consequence the cheap and resource-efficient 
outdoor tomato production has almost ceased to exist in those regions of Europe with 
humid climate. Horneburg and Becker (2011) have developed successful selection 
methods for improved field resistance in organic management. Screening and 
breeding in organic management was carried out with participation of market and 
amateur gardeners, seed savers, advisors, seed traders, and scientists and led to the 
registration of new improved varieties for low input organic outdoor production 
(Horneburg 2010). Colleagues in conventional agriculture can profit from our work 
because the waiting time after a fungicide treatment in some cases does interfere 
with the tomato harvest. 
Nutrient use efficiency and adaptation to nutrient dynamics and abiotic stress 
have only been investigated to a limited extend in organic agriculture and research 
results are barely used in breeding. Presterl et al. (2002) have shown in conventional 
studies with varying nitrogen (N) supply that the potential for selection is high in 
maize. Experimental hybrids of European elite breeding lines selected at low N (L) 
out yielded those selected at high N level (H), when tested in low N field trials (Fig. 
3). 
4
Keynote lecture at the Organic World Congress, Namyangju City, Gyeonggi Province, Republic of 
Korea, 26.09.-05.10.2011 
Fig. 3. Relationship between grain yields at low and high soil nitrogen levels of 25 H x 
H and 24 L x L maize hybrids, respectively (Presterl et al. 2002). 
Ceccarelli (1996) evaluated extensive trials with barley in low input semi arid 
environments. The predominant abiotic stress factor was water deficit. Breeding 
lines selected in low and high yielding environments, respectively, were compared in 
trials covering a wide range of yield level (Fig. 4). Lines selected in low yielding 
environments performed better at a low yield level while they were out yielded by 
lines selected in high yielding environments at high yielding environments. Farmers’ 
fields corresponded to low yielding environments; breeding stations were managed at 
a high yield level. This study did not investigate a single nutrient in a factorial design, 
but the general nutrient level and the interactions with water supply and cultivation 
techniques. Organic agriculture needs varieties that perform well with a limited 
nutrient level and that are adapted to the nutrient dynamics that occur in times with 
little mineralization. 
5
Keynote lecture at the Organic World Congress, Namyangju City, Gyeonggi Province, Republic of 
Korea, 26.09.-05.10.2011 
6 
6,0 
5,0 
4,0 
3,0 
2,0 
1,0 
0,0 
Farmers’ field 
Experimental station 
0.6 1.5 2.3 3.5 4.3 
Site means (t ha-1) 
Line means (t ha-1) 
High yielding selection 
Low yielding selection 
Fig. 4. Cross-over genotype x environment interaction in barley: Yield of lines 
selected in high and low yielding environments, respectively and then tested in 21 
location-year combinations. The location-year combinations are combined in five 
groups according to the average grain yield of 64 barley lines (Ceccarelli 1996). 
Other areas of excellence of organic breeding 
Other important aspects like participation in the breeding process, organoleptic 
quality, and site-specific adaptation are not inherent to any of the production 
systems, but awareness is much higher in organic than in conventional agriculture. 
The priciples of organic agriculture – health, ecology, fairness, and care (IFOAM 
2011 a) – include responsibility for biodiversity, present and future genetic 
resources. 
Participatory rice breeding was developed in the Philippines by MASIPAG since 
1987 (Medina 2009, Vicente et al. 2009). The objective was the creation of a seed 
system as an alternative to high input varieties propagated by the Green Revolution. 
Targeted at resource poor farming without chemical input, farmers identify the 
breeding objectives, are involved in producing crosses, select in segregating 
generations, evaluate and maintain the best populations. MASIPAG runs a central 
backup station, regional backup stations, and regional test farms. Presently more 
than 35,000 farmers in 47 provinces use regionally adapted selections. 
An organoleptic quality assay was developed in a small organic breeding program 
with parsnip (Pastinaca sativa L.), a neglected root vegetable of temperate regions 
(Horneburg et al. 2009). In a first step individual plants were selected within two 
varieties for organoleptic quality by a technique developed in the project. The 
procedure allows harvesting seeds from the tested (and tasted!) plant. In a second 
step, progenies of positive- and negative-selected plants were compared with the 
original population. Organoleptic quality was scored and sugar content was analysed 
(Fig. 5). Organoleptic selection significantly improved sweetness, flavour, and sugar 
content. As a result the best quality variety was put on the market.
Keynote lecture at the Organic World Congress, Namyangju City, Gyeonggi Province, Republic of 
Korea, 26.09.-05.10.2011 
7 
9 
8 
7 
6 
5 
4 
3 
2 
1 
225 
210 
195 
180 
165 
150 
135 
120 
Positive selection 
Original population 
Negative selection 
Sweet-ness 
Flavour Sugar 
total 
Score 
Sugar total (μm/g) 
Aromata White King 
Sweet-ness 
Flavour 
LSD=1.59** 
LSD=2.44** 
LSD=1.72* 
LSD=1.04 
Each circle represents one progeny. 
Differences between progenies * significant at p<0.05, ** significant at p<0.01 
Sugar total = Glucose, fructose and sucrose 
Fig. 5. Quality improvement of parsnip by one generation of organoleptic selection 
(Horneburg et al. 2009, modified). 
Site-specific adaptation indicates that populations selected at a specific location are 
at this location superior in yield to populations selected at other locations. 
Almekinders et al. (2007) distributed early segregating generations of Phaseolus 
bean crosses to five farmer breeders in Nicaragua. All got the same 15 progenies 
and selected during five generations for disease resistance, plant architecture, yield, 
drought stress tolerance, and culinary quality. The resulting best selection from each 
farm was tested on all five farms. The results given in Table 1 indicate that in four out 
of five cases the selection originating from the test site outperformed the other four 
selections and the test variety. A similar result was demonstrated with lentil landraces 
by Horneburg and Becker (2008b).
Keynote lecture at the Organic World Congress, Namyangju City, Gyeonggi Province, Republic of 
Korea, 26.09.-05.10.2011 
Table 1. Yield (kg/ha) of five farmer selected bean populations at all five selection 
sites (Almekinders et al. 2007, modified). 
One line represents one test site. The highest yielding selection is indicated in bold. 
Test site Selection site Mean 
8 
Altitude Santa 
Rosa 
Paso 
Hondo 
La 
Lima 
El 
Rosario 
Rio 
Abajo 
Test 
variety 
Santa Rosa 850 m 2005 1551 2717 2069 2127 1875 2057 
Paso Hondo 630 m 969 2522 2134 2134 2263 1616 1940 
La Lima 1000 m 969 839 1948 1098 1164 1551 1262 
El Rosario 650 m 1035 1016 1180 1722 1275 1057 1214 
Rio Abajo 600 m 2328 1616 1357 1482 2522 2269 1929 
Mean 1461 1509 1867 1701 1870 1674 
Intrinsic value of plants 
The organic movement values the plant as an integral being. Its integrity exists aside 
from the economic value of the species. Organic plant breeding respects the integrity 
of plants by respecting their natural reproductive ability and barriers, and their 
relationship with the living soil (Lammerts van Bueren et al. 2003). 
Present and future sources for organic breeding 
In the Central European Organic Outdoor Tomato Project the importance of genetic 
resources from organic seed savers became obvious (Horneburg and Becker 
2008a). The main screening and breeding locations were three organic market 
gardens. Additionally a smaller number of genotypes were tested at up to 34 
locations per year in amateur-, market-, and botanical gardens as well as in research 
institutions. After three years of evaluation, 88% of the best performing 33 varieties 
had originally been provided by non-commercial sources, i.e. genebanks, NGO and 
private seed savers. More than 60% were originally maintained / selected and 
recommended by seed savers and NGO within organic horticulture (Fig. 6). These 
findings also highlight ex situ conservation and dynamic conservation on farm as 
complementary systems.
Keynote lecture at the Organic World Congress, Namyangju City, Gyeonggi Province, Republic of 
Korea, 26.09.-05.10.2011 
33 top ranking varieties 2005 
Seed trade 
(conventional) 
Genebanks 
(conventional) 
NGO and seed 
savers (organic) 
60,6 % 
12,1 % 
27,3 % 
Fig. 6. Origin of the best performing organic outdoor tomato genotypes based on 
3,500 accessions after 3 years of screening at 3 locations in Central 
Europe (data from Horneburg and Becker 2008a). 
Organic breeders should make use of all genotypes available, as long as their use is 
in accordance with the regulations for organic agriculture. The breeders of Sativa / 
Switzerland had to rely on recent hybrid varieties to develop an open pollinated 
supersweet sweetcorn variety (personal communication F. Ebner). The supersweet 
genetics, reducing sugar transformation during shelf life, had so far exclusively been 
used in hybrid breeding. To “dehybridize the hybrids (Deppe 2000)” they used about 
30 commercial hybrid varieties in multiple crosses and subsequent pedigree and 
mass selection. An additional variety had to be deleted due to contamination with 
GMO. Already after four cycles of selection 95% of the yield level of the hybrid 
varieties was attained (Fig. 7). 
9 
120 
100 
80 
60 
40 
20 
0 
F1 1 2 3 4 
Selection cycle 
Yield in % of F1 
Fig. 7. Yield development during the selection for an open pollinated sweetcorn 
variety compared to the performance of hybrid varieties (F1) (personal 
communication Sativa).
Keynote lecture at the Organic World Congress, Namyangju City, Gyeonggi Province, Republic of 
Korea, 26.09.-05.10.2011 
Open pollinated varieties create an open access source for further development. 
Hybrid varieties contribute very little to future genetic resources, because they are 
only in exceptional cases stored in genebanks or taken into dynamic development on 
farm, due to the segregation in the F2-generation (Horneburg 2010). Patenting, non 
restored cytoplasmatic male sterility, gene technology incl. terminator technology, 
etc. further reduce the availability of future genetic resources. 
Outlook 
It is an open question whether breeding for organics (varieties bred in conventional 
agriculture tested in organics) or breeding within organics will be the main 
approach of the future. Especially the biodynamic movement has taken steps to 
foster organic breeding within organics and make the breeding process transparent 
to the public. Accordingly to my knowledge the first and only certification system for 
organic varieties was established by Demeter Germany (abdp 2011). IFOAM had to 
“Complete work on the draft plant breeding standards as soon as possible with the 
view of adopting them as IFOAM (certification) standards (Motion 26.2, IFOAM 
2008)”. The topic was brought in to the IFOAM Standard for Organic Production and 
Processing (IFOAM 2011 b). 
A controversial issue is the use of hybrid varieties and special techniques involved 
in hybrid breeding. The IFOAM General Assembly 2008 at Vignola / Italy carried 
motion 15.3 “to encourage the use of seeds within organic systems that are bred and 
maintained using open pollination and natural pollination techniques” and motion 
26.1 “that cell fusion, including protoplast and/or cytoplast fusion breeding 
techniques, do not comply with the principles of Organic Agriculture. Therefore we 
urge the IFOAM World Board to develop clear guidelines on how to deal with 
varieties derived from cell fusion [...] (IFOAM 2008)”. 
The “IFOAM Position on the Use of Organic Seed and Plant Propagation Material in 
Organic Agriculture” was approved by the World Board recently (IFOAM 2011 c). 
Aims like more independence from the market dominating companies, improving the 
legal situation, and advocacy for breeder exemptions and farmers’ privilege need a 
lot of coordinated input to improve the present situation. 
How do we choose the optimal selection environment? In most organic breeding 
projects the selection is carried out within practical organic agriculture. Thus, the 
breeding approaches are well aimed at the target environment. Conventional formal 
and company breeding projects still frequently work at higher input levels. To be able 
to chose or create the optimal organic selection environment we need to gain a much 
better understanding of the interactions within the entire agricultural biocoenosis 
including the actions and interactions of biotic and abiotic stress conditions, soil biota 
– plant interactions, crop rotation, livestock, and cultivation practices. We need to 
investigate observations that selection in a sub-optimal environment may lead to 
improved performance in more favourable environments (Horneburg and Becker 
2008a). 
In some crops closing the gap in performance between recent hybrids and 
traditional varieties is a demanding task. 
10
Keynote lecture at the Organic World Congress, Namyangju City, Gyeonggi Province, Republic of 
Korea, 26.09.-05.10.2011 
For the next three years and to the OWC 2014 I want to propose 
· sessions for the exchange between organic plant breeders, and the 
· creation of new cooperative projects in organic breeding and breeding 
11 
research. 
The encouraging results given in the preceding sub-chapters support the need for a 
much greater number of state of the art organic breeding projects. We have to bear in 
mind, though, that not every practical breeding approach and every breeding 
research project will give such positive or apprehensive output as in the examples 
shown above. Not using the opportunities offered by organic breeding, however, 
would be careless in a world with one billion starving and a growing demand for food 
and feed. Organic breeding has a great potential to create spin-off effects for other 
forms of agriculture! 
References 
abdp (2011) http://www.abdp.org/index.php?id=117 verified 20.9.2011. 
Almekinders C, Aguilar E, Herrera R (2007) New bean seeds and the struggle for 
their dissemination. LEISA Magazine 23.2:14-16. 
Burger H, Schloen M, Schmidt W, Geiger HH (2008) Quantitative genetic studies on 
breeding maize for adaptation to organic farming. Euphytica 163:501-510. 
Ceccarelli, S 1996: Adaptation to low/high input cultivation. Euphytica 92: 203-214. 
Deahl KL, Jones RW, Black LL, Wang TC, Cooke LR (2008) First Report of the A2 
Mating Type of Phytophthora infestans on Tomato Crops in Taiwan, Republic of 
China. Plant Disease 92:978. 
Deppe C (2000) Breed your own vegetable varieties. The gardener's and farmer's 
guide to plant breeding and saving. Chelsea Green Publishing, Totnes, England. 
Foolad, M.R.; Merk, H.L.; Ashrafi, H. 2008: Genetics, Genomics and Breeding of Late 
Blight and Early Blight Resistance in Tomato. Critical Reviews in Plant Sciences, 
27: 75–107. 
Horneburg B (2010) Participation, utilization and development of genetic resources in 
the Organic Outdoor Tomato Project. In: Goldringer I, Dawson J, Rey F, Vettoretti 
A (eds.) Breeding for resilience: a strategy for organic and low-input farming 
systems? EUCARPIA 2nd Conference of the "Organic and Low-Input Agriculture" 
Section. P. 139-142. 
http://orgprints.org/18171/1/Breeding_for_resilience%2DBook_of_abstracts.pdf 
Horneburg B, Bauer D, Bufler G (2009) Züchterische Verbesserung der sensorischen 
Qualität der Pastinake (Pastinaca sativa L.) im Praxisbetrieb. In: Mayer J, Alföldi 
T, Leiber F et al. (Ed.): Werte – Wege – Wirkungen. Beiträge zur 10. 
Wissenschaftstagung Ökologischer Landbau, Zürich, 11.-13.2.2009; Vol. 1. 
Köster, Berlin:232-235. 
Horneburg B, Becker HC (2011) Selection for Phytophthora field resistance in the F2 
generation of organic outdoor tomatoes. Euphytica: 180:357-367.
Keynote lecture at the Organic World Congress, Namyangju City, Gyeonggi Province, Republic of 
Korea, 26.09.-05.10.2011 
Horneburg B, Becker HC (2008a) Does regional organic screening and breeding 
make sense? Experimental evidence from organic outdoor tomato breeding. In: 
Neuhoff D., Halberg N., Alföldi T. et al. (Ed.): Cultivating the Future Based on 
Science. Vol. 1 - Organic Crop Production. Proceedings of the Second Scientific 
Conference of the International Society of Organic Agriculture Research 
(ISOFAR) 18 – 20 June 2008 in Modena, Italy. ISOFAR, Bonn:670-673. 
Horneburg B, Becker HC (2008b) Crop adaptation in on-farm management by natural 
and conscious selection. A case study with lentil. Crop Sci 48:203-212. 
IFOAM (2011 a) http://www.ifoam.org/about_ifoam/principles/index.html verified 
12 
20.9.2011. 
IFOAM (2011 b) 
http://www.ifoam.org/about_ifoam/standards/norms/IS_V0.1.withcommentsandres 
ponses_final20110819.pdf verified 20.9.2011. 
IFOAM (2011 c) 
ftp://ifoam.org/WB%20Korea%20Docs/1.3%20a%20Seed_Position_Paper.pdf 
verified 20.9.2011. 
IFOAM (2008) In Action No 99. http://bioforum.be/v2/cms/documenten/IA-99_en.pdf 
verified 20.9.2011. 
Lammerts van Bueren E, Myers JR (eds.) Organic Plant Breeding. Wiley-Blackwell 
(accepted). 
Lammerts van Bueren ET, Struik PC, Tiemens-Hulscher M, Jacobsen E (2003) 
Concepts of intrinsic value and integrity of plants in organic plant breeding and 
propagation. Crop Sci 43:1922-1929. 
Lorenz N, Klause S, Müller K-J, Spieß H (2006) Screening of winter barley varieties 
(Hordeum vulgare) for resistance against loose smut (Ustilago nuda) and covered 
smut (Ustilago hordei) in Germany. XV. Biennial Workshop on the Smut Fungi, 
Czech Republic, Prague, June 11-14, 2006. In: Czech Journal of Genetics and 
Plant Breeding, Research Institute of Crop Production, CZ-Prague, Vol. 42. 
Mason HE, Spaner D (2006) Competitive ability of wheat in conventional and organic 
management systems: A review of the literature. Canadian Journal of Plant 
Science 86:333-343. 
Medina CP (2009) Participatory and Farmer-Led Rice Breeding for Organic 
Production. Proceedings of the 1st IFOAM international conference on organic 
animal and plant breeding, Breeding Diversity. August 25-28, 2009 Santa Fe, 
New Mexico / USA: 365-372. 
Murphy KM, Campbell KG, Lyon SR, Jones SS (2007) Evidence of varietal 
adaptation to organic farming systems. Field Crops Research 102:172–177. 
Presterl T, Groh S, Landbeck M, Seitz G, Schmidt W, Geiger HH (2002) Nitrogen 
uptake and utilization efficiency of European maize hybrids developed under 
conditions of low and high nitrogen input. Plant Breeding 121:480—486. 
Reid TA, Yang R-C, Salmon DF, Navabi A, Spaner D (2011) Realized gains from 
selection for spring wheat grain yield are different in conventional and organically 
managed systems. Euphytica 177:253–266.
Keynote lecture at the Organic World Congress, Namyangju City, Gyeonggi Province, Republic of 
Korea, 26.09.-05.10.2011 
Vicente PR, Medina CP, Buena RA (2009) Modified bulk selection method of 
breeding rice for broader genetic diversity. Proceedings of the 1st IFOAM 
international conference on organic animal and plant breeding, Breeding 
Diversity. August 25-28, 2009 Santa Fe, New Mexico / USA:153-160. 
Wolfe MS, Baresel JP, Desclaux D, Goldringer I, Hoad S, Kovacs G, Löschenberger 
F, Miedaner T. Østergaard H, Lammerts van Bueren ET (2008) Developments in 
breeding cereals for organic agriculture. Euphytica 163:323–346. 
13

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  • 1. Keynote lecture at the Organic World Congress, Namyangju City, Gyeonggi Province, Republic of Korea, 26.09.-05.10.2011 Organic Plant Breeding: Achievements, Opportunities, and Challenges Dr. Bernd Horneburg Georg-August-University Göttingen, Department of Crop Sciences, Von-Siebold-Str. 8, D-37075 Göttingen, bhorneb@gwdg.de, Tel: +49 (0)551-394360, Fax: +49 (0)551-394601, http://www.uni-goettingen. 1 de/de/48392.html During the development of the organic agriculture movement it became obvious that crop plant varieties released from conventional breeding programs do not cover all requirements and demands of organic systems. A number of organizations were founded around 1980 to 1990 to i) safeguard genetic resources on farm and in garden, ii) produce and distribute organic seed, and iii) start organic breeding programs. Organizations include e. g. MASIPAG / Philippines, Seeds of Change / USA, De Bolster / Netherlands, Arche Noah / Austria, Pro Specie Rara / Switzerland, Kultursaat and Dreschflegel / Germany, and Garden Organic`s Heritage Seed Library / England. Prior to this time little organic seed was available exclusively from a few pioneers. Aims that many of us agreed upon were · the adaptation of varieties to organic growing conditions, · to (re-)establish farmers and gardeners as breeders, · reduce external input (seed) into the farm organism, · appreciate the holistic nature of the plant and its integrity, · use the potential of open pollinated varieties, · create a cooperation between breeders, growers, and consumers, · increased varietal diversity, and · high food quality. In the meantime some organic breeding projects have yielded encouraging results and some academic working groups have investigated and improved organic breeding methods. The first academic textbook “Organic Plant Breeding” (Lammerts van Bueren and Myers) is to be published in 2012. The objective of this article is to highlight some successful approaches to organic plant breeding and to encourage the organic movement to engage in an increasing number of organic breeding and organic breeding research projects. The need for organic breeding programs In paired organic / conventional selection experiments with wheat (Murphy et al. 2007, Reid et al. 2011) and maize (Burger et al. 2008) it has been demonstrated that the best genotypes for organic cropping are selected within the organic system. Murphy et al. (2007) have demonstrated that the top yielding soft white winter wheat breeding lines in organic management did not correlate to the top yielding ones in conventional management in four out of five paired trials (Fig. 1). Spearman’s rank correlation coefficient revealed no positive genotypic rank correlations among systems in locations 1-4. Direct selection in organic systems produced yields 15%, 7%, 31% and 5% higher than the yields resulting from indirect selection for locations 1–4, respectively. Differences observed at location 5 were not significant.
  • 2. Keynote lecture at the Organic World Congress, Namyangju City, Gyeonggi Province, Republic of Korea, 26.09.-05.10.2011 Fig. 1. Genotypes’ change in rank between organic and conventional wheat nurseries. The top five ranking genotypes for yield in both organic and conventional systems were compared at each location. Genotypes are ranked from 1 = highest yield to 35 = lowest yield (Murphy et al. 2007). Burger et al. (2008) tested experimental single-cross maize hybrids in two paired conventional and organic trials. The results shown in Fig. 2 clearly indicate that the top ranking hybrid varieties in organic management do coincide with those adapted to conventional management only to a very limited extent. In the words of Murphy et al. (2007) “With crop cultivars bred in and adapted to the unique conditions inherent in organic systems, organic agriculture will be better able to realize its full potential as a high-yielding alternative to conventional agriculture.” The superior performance of breeding lines selected within organic system is the result of a number of important traits some of which will be dealt with in the next sub-chapters. It is an advantage of breeding within organic systems to be able to select for individual traits like weed tolerance, nutrient use efficiency, and field resistance against pests and diseases as well as the interactions among these traits. 2
  • 3. Keynote lecture at the Organic World Congress, Namyangju City, Gyeonggi Province, Republic of Korea, 26.09.-05.10.2011 3 120 110 100 90 80 70 60 Best organic varieties Both systems Best conven-tional varieties 70 80 90 100 110 120 130 Grain yield [dt/ha] in conventional management Grain yield [dt/ha] in organic management Fig. 2. Performance of maize hybrids in conventional and organic management (Burger et al. 2008, modified). Crucial traits for many crops in organic systems are weed tolerance, field resistance against pests and diseases, nutrient use efficiency, and adaptation to nutrient dynamics. These traits are of varying importance in conventional system depending on the input level of herbicides, fungicides, pesticides, and mineral fertilizer.They may be beneficial to reduce input and solve particular problems. Organic breeding has the potential to improve conventional agriculture, too. Weed tolerance is a very complex trait. Few experiments have investigated varietal differences. No results from breeding programs for weed tolerance were available for this article. The most important aspect is the morphological weed suppression ability that for instance in cereal grains includes height, early season growth, tillering capacity, and leaf area index (Mason and Spaner 2006). The identification of competitive crop idiotypes may assist organic breeders in the development of competitive varieties. The tolerance to mechanical weed control is important in many organic systems. It may be related to the strength of the roots, root distribution, and leaf-arrangement. Generally competition in the root sphere is little investigated. In breeding projects intercropping with suitable cultivated plants of selected species can be used to simulate weed competition, because natural weed pressure frequently is not evenly spread throughout the test plots. This approach, however, has a little drawback: it fails to investigate allelopathic effects between weeds and crop plants that may either be positive or negative for crop development. Wolfe et al. (2008) stated that little is known about allelopathic effects under field conditions.
  • 4. Keynote lecture at the Organic World Congress, Namyangju City, Gyeonggi Province, Republic of Korea, 26.09.-05.10.2011 Breeding for field resistance against diseases has been successful for e.g. barley and tomato. An example for fungal pathogens restricted to organic agriculture are the smut fungi of cereals, e.g. loose smut (Ustilago nuda) and covered smut (Ustilago hordei) in barley. In conventional agriculture smuts can be controlled completely by seed treatment with fungicides. In organic management seed borne spores can be controlled e. g. by hot water treatment. This method, however, is not efficient enough to meet the threshold given by the authorities for the production of certified seed. Screening for resistance within organic systems was successfully carried out by Lorenz et al. (2006). The host – pathogen system Tomato – late blight (Phytophthora infestans) is rapidly evolving on the global scale favouring more aggressive Phytophthora strains (Foolad et al. 2008, Deahl et al. 2008). As a consequence the cheap and resource-efficient outdoor tomato production has almost ceased to exist in those regions of Europe with humid climate. Horneburg and Becker (2011) have developed successful selection methods for improved field resistance in organic management. Screening and breeding in organic management was carried out with participation of market and amateur gardeners, seed savers, advisors, seed traders, and scientists and led to the registration of new improved varieties for low input organic outdoor production (Horneburg 2010). Colleagues in conventional agriculture can profit from our work because the waiting time after a fungicide treatment in some cases does interfere with the tomato harvest. Nutrient use efficiency and adaptation to nutrient dynamics and abiotic stress have only been investigated to a limited extend in organic agriculture and research results are barely used in breeding. Presterl et al. (2002) have shown in conventional studies with varying nitrogen (N) supply that the potential for selection is high in maize. Experimental hybrids of European elite breeding lines selected at low N (L) out yielded those selected at high N level (H), when tested in low N field trials (Fig. 3). 4
  • 5. Keynote lecture at the Organic World Congress, Namyangju City, Gyeonggi Province, Republic of Korea, 26.09.-05.10.2011 Fig. 3. Relationship between grain yields at low and high soil nitrogen levels of 25 H x H and 24 L x L maize hybrids, respectively (Presterl et al. 2002). Ceccarelli (1996) evaluated extensive trials with barley in low input semi arid environments. The predominant abiotic stress factor was water deficit. Breeding lines selected in low and high yielding environments, respectively, were compared in trials covering a wide range of yield level (Fig. 4). Lines selected in low yielding environments performed better at a low yield level while they were out yielded by lines selected in high yielding environments at high yielding environments. Farmers’ fields corresponded to low yielding environments; breeding stations were managed at a high yield level. This study did not investigate a single nutrient in a factorial design, but the general nutrient level and the interactions with water supply and cultivation techniques. Organic agriculture needs varieties that perform well with a limited nutrient level and that are adapted to the nutrient dynamics that occur in times with little mineralization. 5
  • 6. Keynote lecture at the Organic World Congress, Namyangju City, Gyeonggi Province, Republic of Korea, 26.09.-05.10.2011 6 6,0 5,0 4,0 3,0 2,0 1,0 0,0 Farmers’ field Experimental station 0.6 1.5 2.3 3.5 4.3 Site means (t ha-1) Line means (t ha-1) High yielding selection Low yielding selection Fig. 4. Cross-over genotype x environment interaction in barley: Yield of lines selected in high and low yielding environments, respectively and then tested in 21 location-year combinations. The location-year combinations are combined in five groups according to the average grain yield of 64 barley lines (Ceccarelli 1996). Other areas of excellence of organic breeding Other important aspects like participation in the breeding process, organoleptic quality, and site-specific adaptation are not inherent to any of the production systems, but awareness is much higher in organic than in conventional agriculture. The priciples of organic agriculture – health, ecology, fairness, and care (IFOAM 2011 a) – include responsibility for biodiversity, present and future genetic resources. Participatory rice breeding was developed in the Philippines by MASIPAG since 1987 (Medina 2009, Vicente et al. 2009). The objective was the creation of a seed system as an alternative to high input varieties propagated by the Green Revolution. Targeted at resource poor farming without chemical input, farmers identify the breeding objectives, are involved in producing crosses, select in segregating generations, evaluate and maintain the best populations. MASIPAG runs a central backup station, regional backup stations, and regional test farms. Presently more than 35,000 farmers in 47 provinces use regionally adapted selections. An organoleptic quality assay was developed in a small organic breeding program with parsnip (Pastinaca sativa L.), a neglected root vegetable of temperate regions (Horneburg et al. 2009). In a first step individual plants were selected within two varieties for organoleptic quality by a technique developed in the project. The procedure allows harvesting seeds from the tested (and tasted!) plant. In a second step, progenies of positive- and negative-selected plants were compared with the original population. Organoleptic quality was scored and sugar content was analysed (Fig. 5). Organoleptic selection significantly improved sweetness, flavour, and sugar content. As a result the best quality variety was put on the market.
  • 7. Keynote lecture at the Organic World Congress, Namyangju City, Gyeonggi Province, Republic of Korea, 26.09.-05.10.2011 7 9 8 7 6 5 4 3 2 1 225 210 195 180 165 150 135 120 Positive selection Original population Negative selection Sweet-ness Flavour Sugar total Score Sugar total (μm/g) Aromata White King Sweet-ness Flavour LSD=1.59** LSD=2.44** LSD=1.72* LSD=1.04 Each circle represents one progeny. Differences between progenies * significant at p<0.05, ** significant at p<0.01 Sugar total = Glucose, fructose and sucrose Fig. 5. Quality improvement of parsnip by one generation of organoleptic selection (Horneburg et al. 2009, modified). Site-specific adaptation indicates that populations selected at a specific location are at this location superior in yield to populations selected at other locations. Almekinders et al. (2007) distributed early segregating generations of Phaseolus bean crosses to five farmer breeders in Nicaragua. All got the same 15 progenies and selected during five generations for disease resistance, plant architecture, yield, drought stress tolerance, and culinary quality. The resulting best selection from each farm was tested on all five farms. The results given in Table 1 indicate that in four out of five cases the selection originating from the test site outperformed the other four selections and the test variety. A similar result was demonstrated with lentil landraces by Horneburg and Becker (2008b).
  • 8. Keynote lecture at the Organic World Congress, Namyangju City, Gyeonggi Province, Republic of Korea, 26.09.-05.10.2011 Table 1. Yield (kg/ha) of five farmer selected bean populations at all five selection sites (Almekinders et al. 2007, modified). One line represents one test site. The highest yielding selection is indicated in bold. Test site Selection site Mean 8 Altitude Santa Rosa Paso Hondo La Lima El Rosario Rio Abajo Test variety Santa Rosa 850 m 2005 1551 2717 2069 2127 1875 2057 Paso Hondo 630 m 969 2522 2134 2134 2263 1616 1940 La Lima 1000 m 969 839 1948 1098 1164 1551 1262 El Rosario 650 m 1035 1016 1180 1722 1275 1057 1214 Rio Abajo 600 m 2328 1616 1357 1482 2522 2269 1929 Mean 1461 1509 1867 1701 1870 1674 Intrinsic value of plants The organic movement values the plant as an integral being. Its integrity exists aside from the economic value of the species. Organic plant breeding respects the integrity of plants by respecting their natural reproductive ability and barriers, and their relationship with the living soil (Lammerts van Bueren et al. 2003). Present and future sources for organic breeding In the Central European Organic Outdoor Tomato Project the importance of genetic resources from organic seed savers became obvious (Horneburg and Becker 2008a). The main screening and breeding locations were three organic market gardens. Additionally a smaller number of genotypes were tested at up to 34 locations per year in amateur-, market-, and botanical gardens as well as in research institutions. After three years of evaluation, 88% of the best performing 33 varieties had originally been provided by non-commercial sources, i.e. genebanks, NGO and private seed savers. More than 60% were originally maintained / selected and recommended by seed savers and NGO within organic horticulture (Fig. 6). These findings also highlight ex situ conservation and dynamic conservation on farm as complementary systems.
  • 9. Keynote lecture at the Organic World Congress, Namyangju City, Gyeonggi Province, Republic of Korea, 26.09.-05.10.2011 33 top ranking varieties 2005 Seed trade (conventional) Genebanks (conventional) NGO and seed savers (organic) 60,6 % 12,1 % 27,3 % Fig. 6. Origin of the best performing organic outdoor tomato genotypes based on 3,500 accessions after 3 years of screening at 3 locations in Central Europe (data from Horneburg and Becker 2008a). Organic breeders should make use of all genotypes available, as long as their use is in accordance with the regulations for organic agriculture. The breeders of Sativa / Switzerland had to rely on recent hybrid varieties to develop an open pollinated supersweet sweetcorn variety (personal communication F. Ebner). The supersweet genetics, reducing sugar transformation during shelf life, had so far exclusively been used in hybrid breeding. To “dehybridize the hybrids (Deppe 2000)” they used about 30 commercial hybrid varieties in multiple crosses and subsequent pedigree and mass selection. An additional variety had to be deleted due to contamination with GMO. Already after four cycles of selection 95% of the yield level of the hybrid varieties was attained (Fig. 7). 9 120 100 80 60 40 20 0 F1 1 2 3 4 Selection cycle Yield in % of F1 Fig. 7. Yield development during the selection for an open pollinated sweetcorn variety compared to the performance of hybrid varieties (F1) (personal communication Sativa).
  • 10. Keynote lecture at the Organic World Congress, Namyangju City, Gyeonggi Province, Republic of Korea, 26.09.-05.10.2011 Open pollinated varieties create an open access source for further development. Hybrid varieties contribute very little to future genetic resources, because they are only in exceptional cases stored in genebanks or taken into dynamic development on farm, due to the segregation in the F2-generation (Horneburg 2010). Patenting, non restored cytoplasmatic male sterility, gene technology incl. terminator technology, etc. further reduce the availability of future genetic resources. Outlook It is an open question whether breeding for organics (varieties bred in conventional agriculture tested in organics) or breeding within organics will be the main approach of the future. Especially the biodynamic movement has taken steps to foster organic breeding within organics and make the breeding process transparent to the public. Accordingly to my knowledge the first and only certification system for organic varieties was established by Demeter Germany (abdp 2011). IFOAM had to “Complete work on the draft plant breeding standards as soon as possible with the view of adopting them as IFOAM (certification) standards (Motion 26.2, IFOAM 2008)”. The topic was brought in to the IFOAM Standard for Organic Production and Processing (IFOAM 2011 b). A controversial issue is the use of hybrid varieties and special techniques involved in hybrid breeding. The IFOAM General Assembly 2008 at Vignola / Italy carried motion 15.3 “to encourage the use of seeds within organic systems that are bred and maintained using open pollination and natural pollination techniques” and motion 26.1 “that cell fusion, including protoplast and/or cytoplast fusion breeding techniques, do not comply with the principles of Organic Agriculture. Therefore we urge the IFOAM World Board to develop clear guidelines on how to deal with varieties derived from cell fusion [...] (IFOAM 2008)”. The “IFOAM Position on the Use of Organic Seed and Plant Propagation Material in Organic Agriculture” was approved by the World Board recently (IFOAM 2011 c). Aims like more independence from the market dominating companies, improving the legal situation, and advocacy for breeder exemptions and farmers’ privilege need a lot of coordinated input to improve the present situation. How do we choose the optimal selection environment? In most organic breeding projects the selection is carried out within practical organic agriculture. Thus, the breeding approaches are well aimed at the target environment. Conventional formal and company breeding projects still frequently work at higher input levels. To be able to chose or create the optimal organic selection environment we need to gain a much better understanding of the interactions within the entire agricultural biocoenosis including the actions and interactions of biotic and abiotic stress conditions, soil biota – plant interactions, crop rotation, livestock, and cultivation practices. We need to investigate observations that selection in a sub-optimal environment may lead to improved performance in more favourable environments (Horneburg and Becker 2008a). In some crops closing the gap in performance between recent hybrids and traditional varieties is a demanding task. 10
  • 11. Keynote lecture at the Organic World Congress, Namyangju City, Gyeonggi Province, Republic of Korea, 26.09.-05.10.2011 For the next three years and to the OWC 2014 I want to propose · sessions for the exchange between organic plant breeders, and the · creation of new cooperative projects in organic breeding and breeding 11 research. The encouraging results given in the preceding sub-chapters support the need for a much greater number of state of the art organic breeding projects. We have to bear in mind, though, that not every practical breeding approach and every breeding research project will give such positive or apprehensive output as in the examples shown above. Not using the opportunities offered by organic breeding, however, would be careless in a world with one billion starving and a growing demand for food and feed. Organic breeding has a great potential to create spin-off effects for other forms of agriculture! References abdp (2011) http://www.abdp.org/index.php?id=117 verified 20.9.2011. Almekinders C, Aguilar E, Herrera R (2007) New bean seeds and the struggle for their dissemination. LEISA Magazine 23.2:14-16. Burger H, Schloen M, Schmidt W, Geiger HH (2008) Quantitative genetic studies on breeding maize for adaptation to organic farming. Euphytica 163:501-510. Ceccarelli, S 1996: Adaptation to low/high input cultivation. Euphytica 92: 203-214. Deahl KL, Jones RW, Black LL, Wang TC, Cooke LR (2008) First Report of the A2 Mating Type of Phytophthora infestans on Tomato Crops in Taiwan, Republic of China. Plant Disease 92:978. Deppe C (2000) Breed your own vegetable varieties. The gardener's and farmer's guide to plant breeding and saving. Chelsea Green Publishing, Totnes, England. Foolad, M.R.; Merk, H.L.; Ashrafi, H. 2008: Genetics, Genomics and Breeding of Late Blight and Early Blight Resistance in Tomato. Critical Reviews in Plant Sciences, 27: 75–107. Horneburg B (2010) Participation, utilization and development of genetic resources in the Organic Outdoor Tomato Project. In: Goldringer I, Dawson J, Rey F, Vettoretti A (eds.) Breeding for resilience: a strategy for organic and low-input farming systems? EUCARPIA 2nd Conference of the "Organic and Low-Input Agriculture" Section. P. 139-142. http://orgprints.org/18171/1/Breeding_for_resilience%2DBook_of_abstracts.pdf Horneburg B, Bauer D, Bufler G (2009) Züchterische Verbesserung der sensorischen Qualität der Pastinake (Pastinaca sativa L.) im Praxisbetrieb. In: Mayer J, Alföldi T, Leiber F et al. (Ed.): Werte – Wege – Wirkungen. Beiträge zur 10. Wissenschaftstagung Ökologischer Landbau, Zürich, 11.-13.2.2009; Vol. 1. Köster, Berlin:232-235. Horneburg B, Becker HC (2011) Selection for Phytophthora field resistance in the F2 generation of organic outdoor tomatoes. Euphytica: 180:357-367.
  • 12. Keynote lecture at the Organic World Congress, Namyangju City, Gyeonggi Province, Republic of Korea, 26.09.-05.10.2011 Horneburg B, Becker HC (2008a) Does regional organic screening and breeding make sense? Experimental evidence from organic outdoor tomato breeding. In: Neuhoff D., Halberg N., Alföldi T. et al. (Ed.): Cultivating the Future Based on Science. Vol. 1 - Organic Crop Production. Proceedings of the Second Scientific Conference of the International Society of Organic Agriculture Research (ISOFAR) 18 – 20 June 2008 in Modena, Italy. ISOFAR, Bonn:670-673. Horneburg B, Becker HC (2008b) Crop adaptation in on-farm management by natural and conscious selection. A case study with lentil. Crop Sci 48:203-212. IFOAM (2011 a) http://www.ifoam.org/about_ifoam/principles/index.html verified 12 20.9.2011. IFOAM (2011 b) http://www.ifoam.org/about_ifoam/standards/norms/IS_V0.1.withcommentsandres ponses_final20110819.pdf verified 20.9.2011. IFOAM (2011 c) ftp://ifoam.org/WB%20Korea%20Docs/1.3%20a%20Seed_Position_Paper.pdf verified 20.9.2011. IFOAM (2008) In Action No 99. http://bioforum.be/v2/cms/documenten/IA-99_en.pdf verified 20.9.2011. Lammerts van Bueren E, Myers JR (eds.) Organic Plant Breeding. Wiley-Blackwell (accepted). Lammerts van Bueren ET, Struik PC, Tiemens-Hulscher M, Jacobsen E (2003) Concepts of intrinsic value and integrity of plants in organic plant breeding and propagation. Crop Sci 43:1922-1929. Lorenz N, Klause S, Müller K-J, Spieß H (2006) Screening of winter barley varieties (Hordeum vulgare) for resistance against loose smut (Ustilago nuda) and covered smut (Ustilago hordei) in Germany. XV. Biennial Workshop on the Smut Fungi, Czech Republic, Prague, June 11-14, 2006. In: Czech Journal of Genetics and Plant Breeding, Research Institute of Crop Production, CZ-Prague, Vol. 42. Mason HE, Spaner D (2006) Competitive ability of wheat in conventional and organic management systems: A review of the literature. Canadian Journal of Plant Science 86:333-343. Medina CP (2009) Participatory and Farmer-Led Rice Breeding for Organic Production. Proceedings of the 1st IFOAM international conference on organic animal and plant breeding, Breeding Diversity. August 25-28, 2009 Santa Fe, New Mexico / USA: 365-372. Murphy KM, Campbell KG, Lyon SR, Jones SS (2007) Evidence of varietal adaptation to organic farming systems. Field Crops Research 102:172–177. Presterl T, Groh S, Landbeck M, Seitz G, Schmidt W, Geiger HH (2002) Nitrogen uptake and utilization efficiency of European maize hybrids developed under conditions of low and high nitrogen input. Plant Breeding 121:480—486. Reid TA, Yang R-C, Salmon DF, Navabi A, Spaner D (2011) Realized gains from selection for spring wheat grain yield are different in conventional and organically managed systems. Euphytica 177:253–266.
  • 13. Keynote lecture at the Organic World Congress, Namyangju City, Gyeonggi Province, Republic of Korea, 26.09.-05.10.2011 Vicente PR, Medina CP, Buena RA (2009) Modified bulk selection method of breeding rice for broader genetic diversity. Proceedings of the 1st IFOAM international conference on organic animal and plant breeding, Breeding Diversity. August 25-28, 2009 Santa Fe, New Mexico / USA:153-160. Wolfe MS, Baresel JP, Desclaux D, Goldringer I, Hoad S, Kovacs G, Löschenberger F, Miedaner T. Østergaard H, Lammerts van Bueren ET (2008) Developments in breeding cereals for organic agriculture. Euphytica 163:323–346. 13