Accuracy of genomic prediction for seed oil concentration in high oleic soybean populations using a low‐density marker panel

Crop Science ◽  
2021 ◽  
Author(s):  
Joel Hemingway ◽  
Steve R. Schnebly ◽  
Istvan Rajcan
Author(s):  
Chunkao Wang ◽  
David Habier ◽  
Anna Wolc ◽  
Dorian J. Garrick ◽  
Rohan L. Fernando ◽  
...  

2011 ◽  
Vol 94 (7) ◽  
pp. 3642-3650 ◽  
Author(s):  
Z. Zhang ◽  
X. Ding ◽  
J. Liu ◽  
Q. Zhang ◽  
D.-J. de Koning

2015 ◽  
Vol 87 (9) ◽  
pp. 1106-1113 ◽  
Author(s):  
Shinichiro Ogawa ◽  
Hirokazu Matsuda ◽  
Yukio Taniguchi ◽  
Toshio Watanabe ◽  
Yoshikazu Sugimoto ◽  
...  

Crop Science ◽  
2003 ◽  
Vol 43 (1) ◽  
pp. 135 ◽  
Author(s):  
A. J. Leon ◽  
F. H. Andrade ◽  
M. Lee

1995 ◽  
Vol 24 (4) ◽  
pp. 213-218 ◽  
Author(s):  
Samuel L. Mackenzie

Developments in plant cell and tissue culture, and in gene manipulation techniques, have provided new tools for generating novel plant phenotypes not attainable solely by traditional selection breeding. Driven by the industrial potential, advances in fundamental plant biotechnology are now being directed to the development of new crops with seed oil compositions targeted towards specific applications. The targets encompass both the edible oil and chemical industries, the latter emphasizing those oils which contain unusual fatty acids with functionalities applicable to specific industrial uses. Traditional concepts of the compositions of plant seed oils must be set aside to embrace a new reality in which a high oleic acid oil can be produced in several current oilseed crops.


1996 ◽  
Vol 36 (1) ◽  
pp. 79 ◽  
Author(s):  
PJ Hocking ◽  
A Pinkerton ◽  
A Good

Sulfate-sulfur was applied to sulfur (S)-deficient canola at several growth stages in a field experiment at Cargo near Orange, New South Wales. Applications of 0, 10 or 40 kg S/ha (S0, S10 and S40) as mixtures of potassium sulfate and potassium chloride were made at sowing, the 5-6 leaf rosette stage, flower buds visible, stem elongation and first flowering. The plots received either 80 or 160 kg nitrogen (N)/ha at sowing. Plants from the S0 plots showed symptoms of severe S deficiency during rapid stem elongation, and had a 52% reduction in seed yield and a 21% reduction in seed oil concentration compared with the S40 plants. Application of S10 at sowing, or topdressing S-deficient plants with this rate of S, was inadequate because, although seed oil concentrations were normal (39-42%), seed yields were 25% lower than those from plots that received S40. Topdressing S-deficient plants with S40 at either the 5-6 leaf rosette stage, flower buds visible or stem elongation resulted in the same seed yields and seed oil concentrations as obtained when S40 was applied at sowing. However, there was a 15% reduction in seed yield but no reduction in seed oil concentration when the S40 topdressing was delayed until flowering. Although S10 was inadequate to correct the S deficiency, there was no reduction in either seed yield or seed oil concentration when S10 was topdressed as late as flowering, when compared with this rate of S applied at sowing. Seed meal protein levels were increased by the S40 topdressings. Concentrations of S in seed from the S0 and S10 plants were below the critical value of 0.36% for canola. Seed N:S concentration ratios of S-deficient plants were greater than 10, but 7.5 for plants which received adequate S. Total glucosinolates in seed were increased by the application of S, but the levels were still well below the limit set for the canola standard.


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