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. 2017 Feb 14;119(7):1115–1129. doi: 10.1093/aob/mcx001

Table 5.

Quantitative trait loci (QTLs) associated with seedling root traits in the ‘pouch and wick’ system in a growth chamber as well as yield, yield components and phenology in field trials for the recombinant inbred line mapping population of Forno × Oberkulmer

Trait/chromosome Year Position (cM) LOD R2* Additive effect Closest marker
Seedling root traits
Seminal root number
2A 2014 24·2 8·7 18·0 0·18 Xglk197-2AS
2014 93·7 11·1 22·3 0·20 Xpsr380-2A
2B 2014 38·2 2·9 6·3 –0·19 Xglk302a-2BS
3DL 2014 34·2 3·5 7·7 –0·11 AC29-3DL
4A 2014 41·1 6·6 14·0 0·17 Xpsr914-4A
2014 220·8 5·5 11·8 –0·15 Xpsr115-4A
5A 2014 43·3 3·1 6·8 –0·11 Xpsr945a-5A
2014 234·0 4·4 9·5 0·13 Xgwm6c-5AL
5B 2014 158·3 3·1 6·7 0·13 Xpsr580b-5B
7AL 2014 27·9 4·2 9·0 –0·14 pwir232a-7AL
7B 2014 217·4 8·1 16·8 –0·17 Xglk576-7BL
7D 2014 7·0 3·7 8·0 –0·13 Xpsr618-7D
Seminal root length (mm)
3A 2014 66·9 3·5 7·6 –4 Xprs570-3A
3B 2014 49·2 4·8 10·4 5 Xpsr919a-3B
Total root length (mm)
2A 2014 25·5 4·1 9·0 22 Xglk197-2AS
2014 95·9 8·5 17·6 31 Xpsr919b-2A
3A 2014 63·9 5·6 11·9 –30 Xprs570-3A
3B 2014 51·9 3·3 7·3 21 Xpsr1101b-3B
3DL 2014 34·2 3·0 6·6 –19 AC29-3DL
4A 2014 42·1 8·5 17·6 35 Xpsr914-4A
2014 220·8 6·4 13·6 –28 Xpsr115-4A
4DL 2014 3·0 3·3 7·2 23 Xglk348b-4DL
5A 2014 43·3 4·5 9·8 –23 Xpsr945a-5A
2014 232·8 4·7 10·2 25 Xpsr1201a-5A
5B 2014 160·3 5·2 11·1 29 Xpsr143-5B
7AL 2014 28·9 4·1 8·8 –24 Xpsr121-7AL
7B 2014 217·4 10·1 20·6 –34 Xglk576-7BL
Maximum width (mm)
2A 2014 97·9 3·3 7·3 5 Xglk293b-2AL
4A 2014 220·9 4·5 9·8 –5 Xpsr115-4A
5A 2014 0·1 3·6 7·9 –5 Xpsr549-5A
7B 2014 217·4 4·0 8·6 –5 Xglk576-7BL
7D 2014 0·1 3·1 6·9 –4 Xglk184a-7DS
Maximum depth (mm)
3A 2014 65·9 4·1 9·0 –6 Xprs570-3A
3B 2014 40·9 4·1 9·0 5 Xpsr902-3B
4A 2014 32·2 3·0 6·6 5 Xpsr59a-4A
5A 2014 28·1 3·5 7·6 –5 Xpsr644a-5A
5B 2014 134·6 3·2 6·9 5 Xpsr370-5B
Emergence angle of seminal root (°)
7D 2014 2·0 3·4 7·5 –0·9 Xglk184b-7DS
Yield traits
Machine-harvested yield (t ha–1)
1DS 2012 2·0 3·2 7·1 0·26 Xpsr168-1DS
2B 2012 198·6 3·4 20·1 –0·36 Xpsr956a-2B
3A 2012 67·9 3·5 20·6 –0·42 Xprs570-3A
2013 39·9 6·1 13·1 –0·74 Xpsr598-3A
3B 2012 42·1 2·8 6·3 0·23 Xpsr902-3B
4A 2013 210·2 3·8 8·4 –0·42 Xmwg710b-4A
5A 2013 218·5 9·3 19·2 0·68 Xpsr918b-5A
Grains m–2
3A 2012 37·9 4·1 9·0 –1202 Xpsr598-3A
2012 106·4 5·0 11·0 –847 Xglk118-3AL
2013 43·9 6·0 12·9 –1520 Xpsr598-3A
2013 107·4 3·5 7·7 –838 Xglk577-3AL
4A 2013 23·7 4·6 10·0 1018 Xpsr59a-4A
2013 212·2 2·8 6·3 –826 Xmwg710b-4A
4B 2012 61·8 3·2 7·1 1186 Xpsr921-4B
5A 2012 163·4 4·1 9·1 1562 Xpsr120a-5A
2013 165·4 4·6 10·1 1955 Xpsr145-5A
2013 222·5 6·2 13·3 1284 Xpsr1201a-5A
7B 2013 217·4 3·9 8·5 –811 Xglk576-7BL
Spikes m–2
3A 2013 50·9 3·2 12·7 –27 Xpsr598-3A
4A 2012 20·7 3·7 21·4 45 Xglk315-4AS
2012 60·2 3·6 21·0 42 Xglk331-4A
7B 2012 188·5 3·7 21·5 –58 Xglk750-7BL
Grains per spike
2B 2013 94·7 3·1 12·0 –2·2 Xglk687b-2BS
2D 2013 44·9 4·7 17·8 –6·0 Xpsr933b-2D
3B 2013 8·1 3·7 14·4 –2·7 Lrk10c-3BS
4A 2012 38·1 3·5 20·5 2·5 Xpsr914-4A
2013 151·3 3·6 14·0 5·5 Xglk354-4A
5A 2013 64·4 4·5 17·3 2·9 Xglk424-5A
2013 213·4 5·1 19·2 –2·9 Xpsr918b-5A
7B 2012 137·8 3·2 18·7 –3·6 Xpsr129c-7B
2013 127·8 3·1 12·2 –3·4 Xpsr593c-7B
Thousand grain weight (g)
2A 2012 94·9 3·5 20·6 –1·74 Xpsr919b-2A
2013 133·7 3·5 13·8 –2·00 Xglk699b-2AL
3B 2012 80·5 4·2 23·9 1·95 Xpsr1054-3B
2013 2·9 3·4 13·4 1·61 C970a-3B
2013 80·5 5·1 19·3 1·91 Xpsr1054-3B
4A 2012 20·7 6·6 35·1 –2·65 Xglk315-4AS
2013 31·2 4·8 18·1 –2·09 Xpsr59a-4A
5B 2012 154·3 3·0 17·7 –1·80 Xpsr580b-5B
7B 2012 190·5 5·2 28·9 3·04 Xmwg710a-7B
2013 187·5 3·2 12·7 2·24 Xglk750-7BL
Phenology
GS39 (full flag leaf emergence, °Cd)
5A 2012 222·4 2·9 17·5 –10·3 Xpsr1201a-5A
2013 209·9 4·0 15·2 –10·3 Xpsr918b-5A
GS61 (anthesis, °Cd)
2D 2013 45·9 3·7 14·3 –24·3 Xpsr933b-2D
4DL 2012 107·0 3·1 18·4 15·1 Xpsr1101a-4DL
5A 2013 58·3 3·8 14·8 13·3 Xglk424-5A
2013 209·9 3·9 15·1 –12·0 Xpsr918b-5A
7B 2012 77·6 5·0 27·9 –15·8 Xglk478-7BL
2013 77·6 4·5 17·1 –12·9 Xglk478-7BL
GS92 (maturity, °Cd)
2A 2012 94·9 5·1 28·6 39·9 Xpsr919b-2A
2013 94·9 4·2 16·1 32·8 Xpsr919b-2A
2B 2012 91·7 3·8 22·0 –38·0 Xpsr961-2B
2013 81·7 4·3 16·4 –40·5 Xpsr961-2B
2D 2013 56·9 4·4 17·0 –81·1 Xpsr335-2D
4DL 2012 97·0 4·4 25·2 50·5 Xglk302b-4DL
5A 2013 210·9 3·8 14·8 –36·2 Xpsr918b-5A
5B 2012 162·2 3·7 21·7 41·9 Xpsr143-5B
7AL 2012 0·1 4·1 23·7 –39·1 Xpsr129b-7AL
7B 2012 72·7 5·2 29·1 –42·3 Xpsr927-7B
2012 185·5 3·8 22·2 –51·2 Xglk750-7BL
2013 73·3 5·3 19·7 –38·6 Xpsr927-7B
2013 173·5 3·7 14·3 –35·9 Xglk750-7BL
GS31 (onset of stem elongation)−GS39 (°Cd)
5A 2013 5·4 3·4 13·2 8·6 Xglk163a-5A
GS39−GS61 (°Cd)
2D 2013 33·9 3·1 12·2 –10·1 Xpsr933b-2D
3B 2013 0·1 3·3 12·9 –5·4 Xglk683-3BS
2013 35·7 3·8 14·6 –6·1 Xglk538-3BS
4B 2013 59·8 5·4 20·3 –12·0 Xpsr921-4B
4DL 2013 45·2 3·3 13·0 –10·0 Xpsr59b-4DL
7B 2012 18·6 5·3 29·6 –13·7 Xpsr952-7B
2012 61·7 4·7 26·4 –11·6 Xglk598-7BL
2013 11·0 4·6 17·6 –7·6 Xpsr952-7B
2013 99·7 3·5 13·6 –6·4 pwir232b-7B
GS31−GS61 (°Cd)
1DS 2013 0·1 3·2 12·5 –8·8 Xpsr168-1DS
4DL 2012 108·0 3·7 21·4 18·9 Xpsr1101a-4DL
5A 2013 3·0 3·3 12·9 9·2 Xpsr549-5A
GS61−GS92 (°Cd)
2A 2012 94·9 5·2 28·8 34·6 Xpsr919b-2A
2013 94·9 5·6 20·7 28·0 Xpsr919b-2A
2B 2012 92·7 4·1 23·6 –34·1 Xglk687b-2BS
2013 81·7 4·2 16·2 –30·3 Xpsr961-2B
2D 2013 61·9 4·0 15·4 –54·8 Xpsr335-2D
4A 2012 47·1 3·4 19·9 33·4 CD16·2-4A
4DL 2012 92·0 3·3 19·3 33·7 Xglk302b-4DL
5A 2013 211·9 3·0 11·9 –24·0 Xpsr918b-5A
5B 2012 161·2 3·3 19·4 34·7 Xpsr143-5B
2013 157·2 2·9 11·6 24·8 Xpsr580b-5B
7AL 2012 0·1 4·4 25·3 –34·9 Xpsr129b-7AL
2013 0·1 3·4 13·2 –23·3 Xpsr129b-7AL
7B 2012 185·5 4·5 25·5 –47·4 Xglk750-7BL
2013 73·3 4·7 17·9 –27·7 Xpsr927-7B
2013 174·5 4·9 18·5 –31·7 Xglk750-7BL
*

R2, the proportion of phenotypic variation explained by individual QTLs.

Positive and negative additive effects indicate that the alleles from Forno and Oberkulmer increase the values of the traits, respectively.