1. Variety and germplasm development.
Each year we will develop a minimum of 100 new populations involving elite and exotic parents to produce new MG3 through 5 progeny to meet program objectives. Parents will be selected based on achieving the goals of producing progeny with competitive seed yield, increased genetic diversity in the US soybean gene pool, optimal seed composition, multiple pest resistance, high oleic oil and/or drought tolerance. Progeny will be advanced using winter nursery facilities in Puerto Rico to speed development. Each season 6,000 to 10,000 new F4-derived lines will be evaluated in progeny rows followed by replicated testing in Kansas and throughout the US in the Uniform Soybean Tests, the Northern Regional Soybean Cyst Nematode Tests, and the Diversity Cooperative Tests. Lines will be evaluated under both dryland and irrigation conditions in replicated plots in KS and the US to characterize performance over a wide range of environments. Lines will be evaluated for resistance to several pathogens, including soybean cyst nematode, Phytophthora root rot, soybean sudden death syndrome (SDS), and stem canker, depending upon the population. Seed composition will be measured using near infrared reflectance in our KSU lab, and in the USDA-ARS, National Center for Agricultural Utilization Research at Peoria, IL. Release decisions will generally be based on information from 30 to 50 environments. Time to complete one cycle of selection (from the time the crosses are made until release) will be about 8 years. Throughout these breeding activities we will continue to try and engage provate breeders in collaborative activities to help them develop new materials for the farmer.
2. Implement and evaluate breeding technologies.
Through support from the North Central Soybean Research Program (NCRSP), a genomic selection model has been developed by the Univ. of Minnesota soybean breeder, Aaron Lorenz. We will use this model to implement selection of genotypes. This process will involve intermating a population of F1 genotypes to produce 100 to 130 new F1s per generation. Genomic selection will identify progeny to use in intermating. This process will be repeated 3 times per year (once in the summer, once in the fall greenhouse, and once in the spring greenhouse). Evaluation of this selection and intermating process will be accomplished by producing F4 derived lines from each generation for evaluation in replicated yield trials in 2022 and later. We will also continue our efforts to use remote sensing technology to improve the speed and accuracy of identifying superior breeding material. We will focus this project in using remote sensing during the progeny row stage when selection is generally based on visual evaluations. Selections based on thermal and spectral data will be compared in replicated tests with visual and random selections from progeny rows to determine if gain from selection has been improved using this technology.
3. Screen for Dectes stem borer resistance.
Initially screen 500 accessions for stem breakage on a 1-5 scale, presence of stem girdling and presence of stem borer larva in year one (2020) after plant maturity. Screening will be conducted at one location (Manhattan) in replicated (2 reps) short-row plots where incidence of plants infested with stem borer often exceeds 60%. About 25% of the lines evaluated in year one will be advanced for further evaluation in year two in a three replicate test. Antixenosis and antibiosis screening will be conducted at one location in replicated (4 reps) short-row plots. Characterizing antixenosis and antibiosis is labor intensive and time consuming, so we will limit screening to 20 accessions at a time for evaluation. Three to five plants per plot will be scored for oviposition punctures and the number of live larvae in the stem as described by Niide et al. (2012). In the second year a new set of 20 accessions will be screened using the same procedures.
4. Breed transgenic events into elite breeding lines.
Transgenic lines will be crossed into elite varieties with and without traditional sources of resistance. Currently we are incorporating the transgenes into KS4117Ns, and early MG4 variety with excellent yield potential and conventional resistance to SCN, and K12-2333, another MG4 line with excellent yield potential but susceptible to SCN. Based on screening results for 2019, additional parents will be selected to incorporate the transgene(s). Presence of the transgene(s) in progeny will be determined using molecular markers. Lines will be rescreened for SCN resistance in greenhouse and field bioassays.