Updated December 11, 2024:
Updated June 5, 2025:
A- Relay Cropping Field trials:
• Year 1: Fall 2023: winter small grains (rye, barley) and oilseeds (canola, camelina) planting.
Spring 2024: soybean planting.
Location 1: Agricultural Engineering & Agronomy (AEA) Research Farm near Boone, IA.
In a randomized complete block design, winter cereals [Organic rye, Hazlet (90 lb/ac), and Organic MN-Equinox barley (96 lb/ac)] and winter oilseeds [camelina (Albert Lea, 6-8 lb/ac) and canola (Sitro, 3.5-5 lb/ac)] were drilled (in a 7.5-inch row spacing) separately in a 900 sq. ft. plot (30 ft. wide × 30 ft. long) per replication on October 10, 2023.
On May 17, 2024, soybean variety P14A12E was planted at 140k seeds/ac in a 30-inch row spacing using a 6-row John Deere 640 R planter in cereal rye and barley at the boot leaf stage. There was no emergence of canola in spring. The camelina emerged but did not survive the very low temperatures registered in March 2024. Earlier planting days, hardy winter seeds, and new locations in Iowa will be evaluated in our next field trials. Soybeans were planted in these plots to minimize weed infestations.
On April 11, 2024, cereal rye and barley plots were evaluated for emergence and growth stages and seedling diseases. Recorded growth stages, plant heights, and stand counts in soybean on May 28, 2024. On June 10, 2024, we assessed weed infestation (across 18 weed species) and types of weed infestation. In winter barley-soybean relay crop (SRC) and cereal rye-SRC, was significantly low (P<0.05) compared with no-till fallow/soybean monoculture plots. In the no-till soybean monoculture plots, 90-95% of weeds represented were downy brome, little barley, yellow foxtail, woolly cup grass, giant foxtail, and barnyard grass. Whereas in barley-SRC and cereal rye-SRC plots, yellow foxtail, giant foxtail, and waterhemp were observed with very low to low infestations (Navi et al, 2024). Cereal rye, barley, and soybean were monitored for seedling, foliar, stem, and panicle diseases at regular intervals starting June 17, 2024, and cereal rye and barley were harvested on July 19, 2024, using a portable Bushel Plus Mini-Combine, and soybean plots were combined on September 26, 2024.
• Year 1: Fall 2023: mix of winter small grain (rye) and oilseed (camelina) planting.
Spring 2024: soybean planting.
Location 2: Farmer-partner in Monticello, NE-IA.
Following a no-till 2023 corn field, a mixture of winter camelina (1-2 lb/ac) and cereal rye (35 lb/ac), both VNS seeds, was drilled. Interestingly, no soybeans were planted in the past 6 years. This field had a history of white mold, but after switching to winter cropping, no white mold was observed. Soybean variety (RR) P30A75E was planted on May 12, 2024, at 140K seed/ac in a 30-inch row spacing when cereal rye and winter camelina were in the vegetative growth stage. We flagged eight plots, 25 ft. wide and 375 ft. long, for our evaluations. Seedling, foliar, stem, and panicle diseases in cereal rye, camelina, and soybean were assessed. No major weed infestations were observed across eight replications. Cereal rye and camelina were harvested using R75, Gleaner on July 12, 2024, and soybeans on October 8, 2024.
Disease evaluation at farms in Boone and Monticello (Summer 2024):
Soybean: No major diseases of soybean were observed in soybean relay cropped with cereals (except soybean vein necrosis) compared with monocropping/solo soybean, wherein Phytophthora root rot, sudden death syndrome, and Cercospora leaf blight were observed at the Monticello location. Such diseases were not observed at the Boone location.
Winter rye and barley:
a) Seedling: Early in the season, symptomatic seedlings with root/basal stem rot sampled from barley and cereal rye plots revealed the occurrence of four species of Alternaria, including Ascochyta, Bipolaris, Epicoccum, and Pyrenophora, five species of Fusarium, and three species of Pythium at AEA farm (Navi et al, 2024). No seedling diseases were observed at the farm in Monticello.
b) Foliar: Cereal rye rust (Puccinia triticinia) was observed at both locations. The disease severity varied from 20 to 30%.
c) Panicles: Ergot (Claviceps purpurea) of cereal rye and smooth bromegrass, and Fusarium head blight in cereal rye were observed in both locations.
Inputs to income of the winter cereals–soybean relay cropping systems compared to the mono-cropped soybean systems, based on yields observed in Boone and Monticello, IA, in 2024, revealed some advantages.
Soybean yields in the inter-cropped plots were generally slightly higher than those of mono-cropped soybeans. At Boone farm, the yield of soybean relayed with winter barley was 37.36 bu/ac, soybean relayed with winter cereal rye yielded 36.49 bu/ac, compared with monocropped soybean with 34.27 bu/ac for 1.4 maturity group of soybeans. This indicated a yield advantage of 3.09 bu/ac and 2.22 bu/ac, respectively. At Monticello farm, soybean yields of 70 bu/ac was recorded in soybean relay cropped with cereal rye compared with 67 bu/ac in monocropping soybeans for the 3.0 maturity group of soybeans.
In addition to the soybeans, the advantage is the economic return of cover crops (winter barley or rye relay with soybeans). Yields of winter barley were 20.50 bu/ac, yields of winter cereal rye were 30.47 bu/ac at Boone farm and 40 bu/ac at Monticello farm.
The gross advantages (USD/Ac) of relay cropping soybeans with winter cereals at the two locations will be calculated.
Summary: Inputs to income of relay cropping soybeans with winter cereal crops in Iowa of the first-year trial showed:
a. A significant (P<0.05) reduction in weeds and types of weed infestation in soybean relay cropped with cereals compared with monocropping soybean or sole soybean plots.
b. No major diseases of soybean were observed in soybean relay cropped with cereals (except soybean vein necrosis) compared with monocropping soybean.
c. Yields and economic advantages of relay cropping soybeans with cereals were observed at both locations (Boone and Monticello farms).
Remarks: These results are based on our results of the first-year trials. We may have comparable results in the next couple of years of studies at multiple locations.
UAV imagery collected at multiple growth stages of soybean relay cropping with cereals at the Boone location is being processed shortly.
• Year 2: Fall 2024: winter small grains (rye, barley) and oilseeds (canola, camelina) planting.
Spring 2025: soybean planting.
Location 1: Sorensen Research Farm, near Boone, IA.
After the first-year experience and several discussions with CO-PIs, farmers, and field crew, we conducted trials in strip-trials (15 ft. wide ×270 ft. long × 2) per crop. Each strip has four replications. This was mainly to adjust the relay cropping specific management practice better than in the RCBD in 2023-24. Winter small crops and oilseeds were planted on October 4, 2024, in a 6-inch row spacing, each with 20 rows. Seed rates for cereals were 90lb/ac, oilseeds 8 lb/ac. Soybeans were planted on May 14, 2025.
• Year 2: Fall 2024: winter small grain (rye) planting.
Spring 2025: soybean planting.
Location 2: Farmer-partner in Monticello, IA.
• Year 2: Fall 2024: mix of winter small grain (rye) and oilseed (canola) planting.
Spring 2025: soybean or corn planting, depending on crop rotation pattern at the farm.
Location 3: Farmer-partner in Sidney, IA.
B-Greenhouse Trials:
Experiment 1:
Fusarium graminearum (Fg) is a common pathogen on soybeans as well as cereal such as barley, wheat, and rye. We have conducted greenhouse experiments to assess (i) the susceptibility of cereals and oilseeds and soybeans to Fg and (ii) characterize the virulence of Fg in the varieties of soybean, winter cereal crops, and oilseeds that we are using in the field trials and to test whether rye, barley, canola, and/or cameline help to control Fusarium disease in soybean.
A total of 30 pots were filled with a potting mixture (2.83 L/pot), and Fg-inoculum (67 cc/pot) increased on white milo, while 30 other pots were filled with only potting mixture as uninoculated controls. Both the inoculated and uninoculated pots were planted with seeds of winter cereal rye, winter barley, winter camelina, winter canola, and soybeans. Also, 18 pots with cereal rye and 18 pots with barley were planted as borders around the experiment, laid out on greenhouse benches. Pots were irrigated twice daily and incubated on greenhouse benches with 12-h light from December 7, 2024, to May 6, 2025. Depending on the maturity dates of the cereals, oilseeds, and soybeans planted, the plants were harvested starting from March 28 to April 16, 2025, and assessed for stand counts (healthy and infected), fresh and dry weights of roots and shoots, number of pods and panicles, and nodules. After the harvests, pots were refilled with the potting mixture that was used at the planting, irrigated once daily until all the pots were planted with only soybeans on May 6, 2025. All these pots were evaluated for Fg-infections (if any), stand counts, and plant heights.
The results from this study will be presented at the APS-Plant Health Conference 2025 in Hawaii.
Experiment 2: A second experiment has been conducted since 4/22/2025 in order to characterize particularly the effect of F. graminearum (Fg) on root systems of soybeans and winter and spring variety of small crops and oilseeds using Rhizotrons.
Root health and biomass but also shoot health and biomass is been evaluated. As of now, the results are clearly distinguishable in the inoculated vs uninoculated on agronomic features (stand counts, plant height, root and shoot biomass) and disease incidence (%) of the crops studied so far.
The detailed methodology and results from this study will be presented at the APS-Plant Health Conference 2025 in Hawaii.