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USDA-ARS, P.O. Box 748, Coastal Plain Exp. Stn., Tifton, GA 31793 USA
holbrook{at}tifton.cpes.peachnet.edu
| ABSTRACT |
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2.5. Thirty-six core accessions showed a reduction in root galling, egg-mass rating, egg count per root system, and egg count per gram of root in comparison to Florunner. Twenty-one accessions showed a 70% reduction in egg count per root system and per gram of root, and two accessions showed a 90% reduction of these variables in comparison with Florunner. The 56 resistant indicators from screening the core collection identified 39 clusters in the entire germplasm collection that should be examined more thoroughly. China and Japan appear to be valuable geographical sources for resistance to this nematode. | INTRODUCTION |
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Only moderate levels of resistance have been observed in naturally occurring germplasm of A. hypogaea. Holbrook and Noe (1992) evaluated 1321 peanut plant introductions for resistance to M. arenaria and identified 17 accessions that supported fewer egg masses and seven genotypes that supported less egg production per gram of fresh root weight compared with the cultivar Florunner. Holbrook et al. (1996) evaluated 1000 plant introductions and identified eight additional accessions that had significantly higher levels of resistance (lower egg mass rating) than Florunner. Although none of the eight had a significantly higher level of resistance than those reported by Holbrook and Noe (1992), two of the eight exhibited significantly higher yield than all others when grown in soil heavily infested with M. arenaria.
More desirable sources of resistance to M. arenaria may exist in A. hypogaea since less than one-third of the germplasm collection has been examined for resistance based on nematode reproduction. A core collection has been selected to represent the U.S. germplasm collection of peanut (Holbrook et al., 1993). Theoretically this core collection could be used to more efficiently identify desirable traits, such as nematode resistance, in the entire collection (Brown, 1989; Frankel, 1984). Data on resistance to late leaf spot [Phaeoisariopsis personata (Berk. & M.A. Curtis) Arx. syn. Cercosporidium personatum (Berk. & M.A. Curtis)] for the entire collection was used to empirically evaluate the peanut core collection (Holbrook and Anderson, 1995). The results demonstrated that the use of the peanut core collection would have improved the efficiency of identifying resistance to late leaf spot in the entire collection.
Very high levels of resistance to M. arenaria exist in related Arachis spp. (Nelson et al., 1989; Holbrook and Noe, 1990). The level of resistance thus far observed in A. hypogaea has not been as high as that observed in wild species or interspecific material derived from these species. Screening of the peanut core collection should indicate whether high levels of resistance to M. arenaria occur in A. hypogaea.
The objectives of this study were (i) to use the core collection to identify sources of resistance (ii) to estimate the level of resistance available in the germplasm collection of A. hypogaea, and (iii) to examine the geographical distribution for resistance in peanut germplasm to indicate areas within the collection for further study.
| Materials and methods |
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Approximately 90 d after inoculation, plants were uprooted and washed clean of soil. The roots were placed in 1000-mL beakers containing 300 mL of phloxine B solution for 3 to 5 min (Daykin and Hussey, 1985). Each plant was indexed for root galls and egg masses on the following scale: 0 = no galls or no egg masses, 1 = 1 to 2, 2 = 3 to 10, 3 = 11 to 30, 4 = 31 to 100, 5 = more than 100 galls or egg masses per root system (Taylor and Sasser, 1978).
Means for egg mass ratings were calculated and resistant selections were made based on a mean rating of less than or equal to three (
30 egg masses). These resistant selections were further evaluated in a greenhouse experiment that was planted on 20 Dec. 1996 in a randomized complete-block design with seven replications. Germinated seedlings were inoculated with 3500 eggs 10 d after planting. Egg-masses and root-gall ratings were measured on 25 and 26 March, as described above. Roots from four replications were blotted dry and weighed, and eggs were collected with NaOCl (Hussey and Barker, 1973) and counted.
Data were subjected to analysis of variance and genotypic means were compared by Fisher's protected least significant difference (LSD). Unless otherwise stated, all differences referred to in the text were significant at P
0.05.
For each country of origin represented by at least one nematode resistant core accession, the expected number of resistant accessions was calculated. Expected values were calculated by multiplying the number of accessions in the core collection from each country of origin by the percentage of resistant accessions in the core collection. Chi-square analysis was used to test for significant deviations from expected.
| Results and discussion |
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Extremely high levels of resistance to M. arenaria are available in related Arachis spp. (Baltensperger et al., 1986; Nelson et al., 1989; Holbrook and Noe, 1990). Starr et al. (1995) observed high levels of resistance (<97% reduction of eggs per gram of roots compared with the susceptible recurrent parent) in F2 individuals from the second, third, and fourth backcross generations derived from the resistant parent TxAG-7 (Simpson et al., 1993). None of the A. hypogaea accessions identified in our studies showed a level of resistance as high as the highest levels observed in wild species or interspecific material derived from these species. Twenty-one accessions from the core collection showed a 70% reduction in eggs per root system and in eggs per gram of root in comparison with Florunner (Table 1). Two of these accessions (PI 269064 and PI 295747) showed a 90% reduction in these variables compared with Florunner.
Theoretically, the reaction of a core accession should serve as an indicator for the cluster in the entire germplasm collection from which the accession was selected. The frequency of additional resistant accessions should be higher in clusters with resistant indicator values. Resistant indicators from screening the core collection identified 39 clusters in the entire germplasm collection that should be examined more thoroughly (Table 2) . Screening material from these clusters would require examining 871 accessions.
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The only striking geographical pattern observed were relatively large numbers of resistant accessions from China and Japan (Table 3) . Eleven of the resistant accessions identified were from China. This was 20% of the resistant accessions, whereas <4% of the germplasm collection originated from China. Seven percent of the resistant accessions were from Japan, although <2% of the germplasm collection originated from Japan.
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| ACKNOWLEDGMENTS |
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Received for publication July 29, 1999.
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