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"Optimum numbers of clones in seed orchards “ Raleigh Feb 7, 2003 "Optimum numbers of clones in seed orchards “ Raleigh Feb 7, 2003 Dag Lindgren Department.

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Presentation on theme: ""Optimum numbers of clones in seed orchards “ Raleigh Feb 7, 2003 "Optimum numbers of clones in seed orchards “ Raleigh Feb 7, 2003 Dag Lindgren Department."— Presentation transcript:

1 "Optimum numbers of clones in seed orchards “ Raleigh Feb 7, 2003 "Optimum numbers of clones in seed orchards “ Raleigh Feb 7, 2003 Dag Lindgren Department of Forest Genetics and Plant Physiology Swedish University of Agricultural Sciences S-901 83 Umeå, Sweden

2 Reservation At this moment I am not going to discuss the most relevant question; to what degree each clone should be represented (unequal proportion deployment. Clone number is easier to understand. And do not expect me to reveal the secret, why we need diversity. I do not have the answer, just some speculations. Neither time permits to go in depth, I will focus on the number of clones in seed orchards. This is a study which started <two months ago. Thus I am very interested in listeners input.

3 More provocative question: “Is not one clone enough?” One clone would be pollinated by lots of fathers outside the seed orchard. A one clone seed orchard would deploy more diversity than found in half of US current pine plantations!!!

4 How many clones…?  One of the first and most evident questions  One of the most important, “key” questions  It is easy for a manager to adapt to the answer, the difficulty is the answer  The number is used for control, certification and monitoring

5 Number of clones in seed orchards  Two previous studies has the agenda in the title: Lindgren-D 1974. Aspects of suitable number of clones in a seed orchard (proceedings); Hattemer-HH et al. 1982. Klonanzahl forstlicher Samenplantagen und genetische Vielfalt (in German).  Few citations (most self-citations), others have not tried to think much or deep.  I have not found a in depth discussions in a journal paper. Surprising, considering the importance of the subject!  So, I decided to make a new study during Xmas holidays. Even if the exact answers I try to give are not accepted, at least I go through the issue a bit more systematic.

6 Seed orchard size and clone number (Kang et al 2001)

7 Pines in south US (McKeand et al. 2003, in press)  Rough average  24 clones in lob SO  42 clones in slash SO  6 SO with only 5-10 clones

8 First seed orchards  For early seed orchards with untested clones, many clones may be right.  They differ little in expected breeding value  Its easier to get support for selecting plus trees and testing clones if they are in seed orchards. Thus many clones in seed orchards was a way to get tree breeding financed.  Material for grafting may sometimes be limiting. More plus trees means more material.  Seed orchards functioned as clonal archives  Thus, there have not been strong reasons to argue for low numbers until recently

9 A model which considers  Gain  Breeding value of available candidates  Gene diversity  Selfing  Fertility differences  Pollen contamination  Close neighbor pollination

10 Gain  G = genetic gain i = selection intensity r = correlation between measured “height at 6 years at some test environments” and goal “value for forestry over a future range of plantation sites”  A variation in desired goal character (CV additive) r and  A are constant, gain depends only on selection intensity

11 The fewer selected, the higher the gain!

12 Scenarios  Swedish Scots pine  American loblolly pine

13 Scale and chosen entries  G BV related to average of candidates in “value for forestry” i = i(n,300) n clones selected from 300 candidates r = 0.7 for Sweden r = 0.8 for America (“older” and more uniform field trials and the “value for forestry” refers to a closer future)  A = 0.125

14 Diversity In my previous seminar in this series (January 17), I suggested diversity to be quantified by status number (or equivalently group coancestry or gene diversity). Effective population size of an orchard is best described as foreseen status number of the seed orchard crop.

15 It should be diversity of some value for the seed orchard manager or forester  Evolutionary potential is not such a criterion, that is National or regional problem. Seed orchard designs are rather unimportant for this problematic.  Allele richness has a value only if it can save the stand, alleles in a frequency below 15% cannot save the stand, thus no argument for high clonal number.  Similarity with natural conditions could be an argument. From a fine-grained structure (half sib groups) point of view, seed orchards with more than 25 clones form a less natural population structure than a natural forest.  Non-overlapping flowering can be a problem if less than say 6 clones.

16  Public Relations, green certification etc. has an evident market value, and staff is also more happy if operations are sustainable and in reasonable harmony with environment. From this point of view it is a large advantage if the situation appears as monitored and controlled. Status number (=gene diversity) considerations contributes to filling that function.

17 Diversity in a plantation Genetic diversity in is likely to favour biological production: One genotype demands the same things at the same time, several use the site resources better! In a mix another genotype may take over the ecological space left by a failed one. A disease spreads faster in a uniform crop. This expectation has generally been confirmed by a number of experiments with different agricultural crops

18 Too much diversity in plantations?! Most crop- and many forest managers do not like diversity,  Uniform trees = better economy, more valuable crop, simpler management;  Genetic superiority of the best clones is much larger than the loss in biomass production by uniformity;  The current demand for diversity in intensively managed forests is – in my opinion - unreasonable expensive in lost future gain;  Most of the benefits with diversity is obtained by five genotypes instead of an infinite number.

19 Gives the probability for interaction between related tree, e.g.  competition for resources  complementing shortcomings  mating (inbreeding in plantations)  disease or pest “jump” to the same substrate Thus the “best” quantification Group coancestry (Status number)

20 Quantification of low diversity loss A high group coancestry can be assumed to cause production losses, calamities and more severe epidemics, but how much? The loss is proportional to group coancestry, but what is the coefficient? I call it DivCoeff. The loss (on the same scale as gain) is Loss=DivCoeff* 

21 Value of DivCoeff?  This Monday Steve McKeand (et al 2003) said 59% of all loblolly is deployed as half sib family blocks and no problems reported! 5% loss by  =0.14 (Kang et al 2002) would be observed, thus DivCoeff<0.35!  Many experiments and some forestry with full sib families. 10% loss by  =0.25 would be observed, thus DivCoeff<0.4!  Many experiments with monoclone plots and some clonal forestry. 10% loss by  =0.5 would be observed, thus DivCoeff<0.2!  Mixes of agricultural lines (  =0.5) probably 2.5% superior to pure lines (  =1), thus DivCoeff=0.05!

22 DivCoeff  Swedish scenario DivCoeff = 0.4  American scenario DivCoeff = 0.2  Difference as south US get more experience with low diversity forestry, less worries, less restrictions, shorter rotation times, less “Nature” (industry forestry replaced cotton, not old growth)

23 Gain and gene diversity are generally in conflict and must be compromised

24 Sibling coefficient  Trees give rise to different amounts of seed and pollen.  Can be expressed by sibling coefficient, , (probability that seedlings share a parent, Kang 2001)  Consequences of a high  :  Less gene diversity (more relatedness)  More selfing  Value:  =2 (Kang et al. in press)

25 Related clones  No related clones in the model;  A few related clones will cause negligable inbreeding depression, but reduce gene diversity rather considerable;  I suggest: it may sometimes be worth considering to have fewer clones rather than related.

26 Selfing  Pollen from the ramet itself (10% pollen)  Pollen from other ramets of the same clone (40% pollen)*(sibling coeff)/(clone number)  Not the same clone in the close neighborhood (10% pollen)  Compared to outcrossing, selfing pollen is less efficient (dead zygotes because of genetic load).  Reduction in seed yield and yield of plantable seedlings to 0.3 for Swedish, 0.1 for America  Selfed seedlings reduce “forest value” 50%.

27 Pollen contamination  Decreases gain  Increases gene diversity  Estimate: 40% pollen (that’s almost 50% of seeds)  Estimate of breeding value of aliens: 0.94 for Swedish; 0.85 for America (America more advanced, but even contamination “improved) (average candidate =1)

28 “Goodness” of seed orchard Goodness, B (“benefit”)=

29 Just to put into a worksheet! Results Parameters Seedorchardmanager at www.genfys.slu.se/staff/dagl

30 Result  Swedish scenario: optimal number 16  American scenario: optimal number 8  Main cause for difference: less problems with selfing and gene diversity in American scenario

31 Sensitivity analyses  Pollination pattern not critical. Breeding value of contaminates unimportant. Large contamination favors few clones.  Selfing important. Self-fertility favors many clones.  High potential to get gain favors few clones  Many candidates moderately favors many clones  The value assigned to gene diversity is a very important factor, a high value favors many clones.

32 Optimum seems smooth!


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