Update:
Identifying Effective Cover Crops for Management of Soybean Cyst Nematode
PI: Guiping Yan, Ph.D.
Collaborators: Drs. Marisol Berti, Sam Markell, and Berlin Nelson
Objectives of the research
1. Evaluate the effects of ten cover crop species/cultivars on hatching of soybean cyst nematode juveniles.
2. Evaluate the effects of ten cover crops species/cultivars on penetration of soybean cyst nematode juveniles.
Completed work
Soil samples were collected from a field with SCN in Richland County, North Dakota based on our previous work. All the soil samples were pooled together and thoroughly mixed to distribute nematode evenly throughout the soil. After thorough mixing, sub-samples were taken to extract SCN cysts and then those cysts were crushed to release eggs which were quantified under a microscope to determine the initial population density of SCN. The well-mixed field soil was then used for the growth chamber experiment.
Ten entries of cover crops including Alfalfa (Bullseye), Daikon radish (Eco-till), Faba bean (Petite), Foxtail millet (Siberian), Oilseed radish (Concorde and Control), Red clover (Allington), Turnip (Purple top), White mustard (Master) and Winter rye (Dylan) were selected for the experiment using the SCN-infested field soil. The susceptible soybean (cv. Barnes), common rotational crop corn (DKC44-13), and a non-planted control were also included. All entries were replicated four times and were planted in plastic cone-containers each containing an average 163 g of soil in a growth chamber maintained at 27 °C (Figure 1). Those entries were planted on August 26 in two sets each containing all the entries, and were terminated 15 days after planting and 30 days after planting, respectively. After termination of the experiment, plant parts above soil surface were removed and all the soil samples along with plant roots were stored in a cold room (4°C) until nematodes were extracted and roots were stained.
Plant roots were gently separated from the soil before the cyst and juvenile extraction. Cysts were extracted from the soil from each cone-container using the sieving and decanting and sugar centrifugal floatation methods. In the meantime, hatched juveniles were also extracted from soil. Extracted cysts were crushed to release eggs which were then counted under a microscope. The separated roots were washed carefully and stained with red food coloring dye (Figure 2). Those stained roots are being observed under a microscope and second-stage juveniles and nematodes in other life stages inside the stained roots are being quantified.
Preliminary results
The initial SCN population density in the infested field soil collected from Richland County, ND was 2,300 per 200 g of soil (˜ 100 cc soil). The average SCN number in each cone-container was 1,877 eggs and juveniles since each cone-container holds approximately 163 g of soil on average.
Out of ten cover crops used in this experiment, nine entries including Alfalfa (Bullseye), Daikon radish (Eco-till), Faba bean (Petite), Foxtail millet (Siberian), Oilseed radish (Concorde and Control), Red clover (Allington), White mustard (Master) and Winter rye (Dylan) did not show any reproduction of SCN from the field. Also, the common rotational crop corn (DKC44-13) did not support any SCN reproduction. These results indicate that these crops are non-host of SCN, which supports the results obtained from our previous study. One cover crop Turnip (Purple top) showed limited reproduction of SCN with the numbers of white females from 2 to 8 suggesting poor host ability. The susceptible soybean cultivar Barnes showed high reproduction with white females from 216 to 262. Similarly, all the tested cover crops along with corn and non-planted control produced smaller numbers of SCN eggs and second-stage juveniles in the soil as compared to soybean (Barnes) at 30 days after planting.
The results of host range of cover crops to SCN from our previous work have been summarized and presented in a manuscript which was published in the journal, Crop Protection in 2020. The results of effects of cover crops on population reduction of SCN were also summarized and now are in press in the journal, Plant Disease, to disseminate the research findings.
Work to be completed
As the stained roots are being observed under a microscope, we will identify and quantify second stage SCN juveniles and other life stages inside the roots. The quantification of the numbers of SCN inside the roots along with the numbers of second-stage juveniles from soil and the numbers of SCN obtained from cyst crushing will help us accomplish the objectives of this project to identify effective cover crops. We will determine the hatching ability for each of the cover crops and their ability to allow juveniles to penetrate the roots. The data obtained will be analyzed using the software SAS 9.4. The ability of cover crops to enhance SCN egg hatching and penetration by juveniles will be summarized after data analysis. The performance of these cover crops will be ranked and made available to the soybean farmers at field days, extension meetings, or in extension publications.
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