‘Bailey’ (Reg. No. CV‐111, PI 659502) is a large‐seeded virginia‐type peanut (Arachis hypogaea L. subsp. hypogaea var. hypogaea) with partial resistance to five diseases that occur commonly in the Virginia‐Carolina production area: early leaf spot (caused by Cercospora arachidicola Hori), late leaf spot [caused by Cercosporidium personatum (Berk. & M.A. Curtis) Deighton], Cylindrocladium black rot [caused by Cylindrocladium parasiticum Crous, M.J. Wingf. & Alfenas], Sclerotinia blight (caused by Sclerotinia minor Jagger), and tomato spotted wilt (caused by Tomato spotted wilt tospovirus). It also has partial resistance to southern stem rot (caused by Sclerotium rolfsii Sacc.). Bailey was developed as part of a program of selection for multiple‐disease resistance funded by growers, seedsmen, shellers, and processors. Bailey was tested under the experimental designation N03081T and was released by the North Carolina Agricultural Research Service (NCARS) in 2008. Bailey was tested by the NCARS, the Virginia Agricultural Experimental Station, and five other state agricultural experiment stations and the USDA‐ARS units participating in the Uniform Peanut Performance Tests. Bailey has an alternate branching pattern, an intermediate runner growth habit, medium green foliage, and high contents of fancy pods and medium virginia‐type seeds. It has approximately 34% jumbo and 46% fancy pods, seeds with tan testas and an average weight of 823 mg seed−1, and an extra large kernel content of approximately 42%. Bailey is named in honor of the late Dr. Jack E. Bailey, formerly the peanut breeding project's collaborating plant pathologist.
Two tetraploid (2n = 4x = 40) peanut (Arachis hypogaea L. subsp. hypogaea var. hypogaea) germplasm lines, GP‐NC WS 16 (SPT 06‐06) (Reg. No. GP‐235, PI 669445) and GP‐NC WS 17 (SPT 06‐07) (Reg. No. GP‐236, PI 669446), derived from interspecific hybridization, were developed in the peanut genetics program at North Carolina State University (NCSU), Raleigh, NC. These two lines were tested extensively by the North Carolina Agricultural Research Service from 2006 through 2012 in disease evaluation tests. They have unique alleles introgressed from the diploid (2n = 2x = 20) wild species, A. cardenasii Krapov. & W.C. Gregory. The germplasm lines are also unique in that they exhibited multiple disease resistances superior to the germplasm lines derived from A. cardenasii that were released previously by NCSU. Resistance to multiple diseases included early leaf spot (ELS), Cylindrocladium black rot (CBR), Sclerotinia blight (SB), and tomato spotted wilt (TSW). One of the lines, GP‐NC WS 17, also exhibited drought tolerance in field and greenhouse studies. Thus, it can be concluded that these two peanut germplasm lines derived from diploid wild species have multiple biotic stress resistances, specifically for ELS, CBR, SB, and TSWV, as well as abiotic stress resistance in the case of GP‐NC WS 17. These two lines should provide unique, improved germplasm for breeders interested in multiple disease resistance and in expanding the germplasm pool of A. hypogaea.
Cylindrocladium black rot (CBR) caused by Cylindrocladium parasiticum and Sclerotinia blight caused by Sclerotinia minor are two economically important diseases of peanut (Arachis hypogaea) in the Virginia-Carolina production area. Developing cultivars with resistance to both diseases requires screening of new peanut breeding lines for resistance. Because field evaluations of resistance to these diseases often fail to produce usable results, greenhouse protocols were used to screen breeding lines and cultivars for resistance. For CBR, two seeds of a genotype were planted in a ''cone-tainer'' filled with a planting medium artificially infested with 25 microsclerotia of C. parasiticum per g of medium. After approximately 8 wk, the roots were washed and rated for degree of decay on a 0-5 proportional scale (0 5 no decay to 5 5 completely decayed). For Sclerotinia blight, plants were inoculated at 6 wk after planting by pushing a plug of potato dextrose agar (PDA) colonized by S. minor and protected from desiccation in a BEEM embedding capsule onto a freshly cut petiole on the main stem of the plant. Inoculated plants were placed in a mist chamber to maintain the high humidity necessary for infection. Lesion lengths were measured 4, 5, 6, and 7 days after inoculation, and areas under the disease progress curves (AUDPC) were calculated. All tests were conducted as incomplete block designs with six replications for CBR tests and four replications for Sclerotinia blight tests. Adjusted entry means were computed from each year's tests and used in summary analyses. Of the 125 breeding lines and checks tested at least once from 2003 through 2006, 51 were tested in at least two years, 34 in at least three years, and 15 lines were tested in all four years. Of the 15 lines tested in all four years, registered germplasm line N96076L had the lowest AUDPC for Sclerotinia blight (58 mm days), but had the greatest CBR root decay score (4.1 decay rating units). Several closely related breeding lines descended from a cross of N96076L and NC 12C were not significantly different from the most resistant line for either disease with scores ranging from 2.2-3.0 decay rating units for CBR and 63-99 mm days for Sclerotinia blight. Correlations of multiple-year greenhouse assay means with field disease incidence means were 0.83 for CBR and 0.35 for Sclerotinia blight. The greenhouse assay for CBR was a reasonably good predictor of field performance, but the assay for Sclerotinia blight was less reliable as a predictor.
Six Virginia-type peanut (Arachis hypogaea L.) cultivars and their paired backcross-derived high-oleate lines were grown during 2003 and 2004 in North Carolina to compare standard germination (SG), cool germination (CG), and electrical conductivity (EC) of seed. Oleic acid level had no influence on SG but did alter CG and EC compared to the corresponding normal oleate cultivars. Averaged across background genotypes, high-oleate lines had lower seed vigor than their paired lines with normal oleic content. The high-oleate lines of three of the six pairs had lower CG and higher EC. Planting and harvest date affected all the seed quality traits measured. Standard germination of both normal and high-oleate lines was reduced in 2004 when harvest was delayed, but was not affected in 2003. In 2003, CG of the high-oleate lines was lower than that of normal lines in three of the four production environments; EC was higher in the high-oleate lines in all planting date and harvest date combinations. In 2004, there was no difference between the CG of normal and high-oleate lines, but EC was higher in the high-oleate lines for three of the four environments. In the greenhouse, the Virginia-type cultivars NC-V 11 and Gregory, along with their paired backcross-derived high-oleate lines were compared at 22/18 C, 26/22 C and 30/26 C day/night temperature regimes. Seed oleic to linoleic acid (O/L) ratio of normal peanut grown in 30/26 C, 26/22 C, and 22/18 C, measured 1.9, 1.5, and 1.3, respectively. The O/L ratio for their high-oleate pairs decreased from 24.7 when grown in 30/26 C to 15.9 in 26/22 C and to 13.7 in 22/18 C. Temperature did not affect the fatty acid composition of axis total lipid or phospholipid fractions. The high-oleate trait was expressed in the axis lipids. The average O/L ratio of axes from normal peanut was 1.1 while that of high-oleate lines was 4.6. Likewise, axis phospholipids for normal and high-oleate lines were 1.0 and 5.9. A lower production environment temperature decreased the O/L ratio of seed oil of high-oleic peanut lines, and the high-oleate trait expressed in peanut seed storage lipids is also expressed in axis membrane lipids to a lesser degree.
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