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ACCESSIONPLANT NAMETAXONOMYORIGINGENEBANKIMAGEAVAILABILITYRECEIVEDSOURCE TYPESOURCE DATECOLLECTION SITECOORDINATESELEVATIONHABITATIMPROVEMENT LEVELNARRATIVE
0PI 561861OK91G109Triticum aestivum L. subsp. aestivum Oklahoma, United StatesNSGCKERNELS1992DEVELOPED1992Genetic materialPairs of near-isolines differing for the presence or absence of 1RS.1BL were developed by selfing heterozygous plants (1RS.1BL//1B) in the F2 to F4 generations. One pair of homozygous near-isolines was isolated in each of 27 F5 families descending from a different F2 plant. No selection was imposed except for chromosome type. Segregation has been observed for plant stature (mostly semi-dwarf, some dwarf), and reaction to soil-born mosaic virus and tan spot (Pyrenophora tritici-repentis). This variation is not linked to chromosome type 1B or 1RS.1BL. [See PI 561861-561914 for accessions from the same Crop Science registration.]1456833PI 561861
1PI 561862OK91G110Triticum aestivum L. subsp. aestivum Oklahoma, United StatesNSGCKERNELS1992DEVELOPED1992Genetic materialPairs of near-isolines differing for the presence or absence of 1RS.1BL were developed by selfing heterozygous plants (1RS.1BL//1B) in the F2 to F4 generations. One pair of homozygous near-isolines was isolated in each of 27 F5 families descending from a different F2 plant. No selection was imposed except for chromosome type. Segregation has been observed for plant stature (mostly semi-dwarf, some dwarf), and reaction to soil-born mosaic virus and tan spot (Pyrenophora tritici-repentis). This variation is not linked to chromosome type 1B or 1RS.1BL. [See PI 561861-561914 for accessions from the same Crop Science registration.]1456834PI 561862
2PI 561863OK91G111Triticum aestivum L. subsp. aestivum Oklahoma, United StatesNSGCKERNELS1992DEVELOPED1992Genetic materialPairs of near-isolines differing for the presence or absence of 1RS.1BL were developed by selfing heterozygous plants (1RS.1BL//1B) in the F2 to F4 generations. One pair of homozygous near-isolines was isolated in each of 27 F5 families descending from a different F2 plant. No selection was imposed except for chromosome type. Segregation has been observed for plant stature (mostly semi-dwarf, some dwarf), and reaction to soil-born mosaic virus and tan spot (Pyrenophora tritici-repentis). This variation is not linked to chromosome type 1B or 1RS.1BL. [See PI 561861-561914 for accessions from the same Crop Science registration.]1456835PI 561863
3PI 561864OK91G112Triticum aestivum L. subsp. aestivum Oklahoma, United StatesNSGCKERNELS1992DEVELOPED1992Genetic materialPairs of near-isolines differing for the presence or absence of 1RS.1BL were developed by selfing heterozygous plants (1RS.1BL//1B) in the F2 to F4 generations. One pair of homozygous near-isolines was isolated in each of 27 F5 families descending from a different F2 plant. No selection was imposed except for chromosome type. Segregation has been observed for plant stature (mostly semi-dwarf, some dwarf), and reaction to soil-born mosaic virus and tan spot (Pyrenophora tritici-repentis). This variation is not linked to chromosome type 1B or 1RS.1BL. [See PI 561861-561914 for accessions from the same Crop Science registration.]1456836PI 561864
4PI 561865OK91G113Triticum aestivum L. subsp. aestivum Oklahoma, United StatesNSGCKERNELS1992DEVELOPED1992Genetic materialPairs of near-isolines differing for the presence or absence of 1RS.1BL were developed by selfing heterozygous plants (1RS.1BL//1B) in the F2 to F4 generations. One pair of homozygous near-isolines was isolated in each of 27 F5 families descending from a different F2 plant. No selection was imposed except for chromosome type. Segregation has been observed for plant stature (mostly semi-dwarf, some dwarf), and reaction to soil-born mosaic virus and tan spot (Pyrenophora tritici-repentis). This variation is not linked to chromosome type 1B or 1RS.1BL. [See PI 561861-561914 for accessions from the same Crop Science registration.]1456837PI 561865
5PI 561866OK91G114Triticum aestivum L. subsp. aestivum Oklahoma, United StatesNSGCKERNELS1992DEVELOPED1992Genetic materialPairs of near-isolines differing for the presence or absence of 1RS.1BL were developed by selfing heterozygous plants (1RS.1BL//1B) in the F2 to F4 generations. One pair of homozygous near-isolines was isolated in each of 27 F5 families descending from a different F2 plant. No selection was imposed except for chromosome type. Segregation has been observed for plant stature (mostly semi-dwarf, some dwarf), and reaction to soil-born mosaic virus and tan spot (Pyrenophora tritici-repentis). This variation is not linked to chromosome type 1B or 1RS.1BL. [See PI 561861-561914 for accessions from the same Crop Science registration.]1456838PI 561866
6PI 561867OK91G115Triticum aestivum L. subsp. aestivum Oklahoma, United StatesNSGCKERNELS1992DEVELOPED1992Genetic materialPairs of near-isolines differing for the presence or absence of 1RS.1BL were developed by selfing heterozygous plants (1RS.1BL//1B) in the F2 to F4 generations. One pair of homozygous near-isolines was isolated in each of 27 F5 families descending from a different F2 plant. No selection was imposed except for chromosome type. Segregation has been observed for plant stature (mostly semi-dwarf, some dwarf), and reaction to soil-born mosaic virus and tan spot (Pyrenophora tritici-repentis). This variation is not linked to chromosome type 1B or 1RS.1BL. [See PI 561861-561914 for accessions from the same Crop Science registration.]1456839PI 561867
7PI 561868OK91G116Triticum aestivum L. subsp. aestivum Oklahoma, United StatesNSGCKERNELS1992DEVELOPED1992Genetic materialPairs of near-isolines differing for the presence or absence of 1RS.1BL were developed by selfing heterozygous plants (1RS.1BL//1B) in the F2 to F4 generations. One pair of homozygous near-isolines was isolated in each of 27 F5 families descending from a different F2 plant. No selection was imposed except for chromosome type. Segregation has been observed for plant stature (mostly semi-dwarf, some dwarf), and reaction to soil-born mosaic virus and tan spot (Pyrenophora tritici-repentis). This variation is not linked to chromosome type 1B or 1RS.1BL. [See PI 561861-561914 for accessions from the same Crop Science registration.]1456840PI 561868
8PI 561869OK91G117Triticum aestivum L. subsp. aestivum Oklahoma, United StatesNSGCKERNELS1992DEVELOPED1992Genetic materialPairs of near-isolines differing for the presence or absence of 1RS.1BL were developed by selfing heterozygous plants (1RS.1BL//1B) in the F2 to F4 generations. One pair of homozygous near-isolines was isolated in each of 27 F5 families descending from a different F2 plant. No selection was imposed except for chromosome type. Segregation has been observed for plant stature (mostly semi-dwarf, some dwarf), and reaction to soil-born mosaic virus and tan spot (Pyrenophora tritici-repentis). This variation is not linked to chromosome type 1B or 1RS.1BL. [See PI 561861-561914 for accessions from the same Crop Science registration.]1456841PI 561869
9PI 561870OK91G118Triticum aestivum L. subsp. aestivum Oklahoma, United StatesNSGCKERNELS1992DEVELOPED1992Genetic materialPairs of near-isolines differing for the presence or absence of 1RS.1BL were developed by selfing heterozygous plants (1RS.1BL//1B) in the F2 to F4 generations. One pair of homozygous near-isolines was isolated in each of 27 F5 families descending from a different F2 plant. No selection was imposed except for chromosome type. Segregation has been observed for plant stature (mostly semi-dwarf, some dwarf), and reaction to soil-born mosaic virus and tan spot (Pyrenophora tritici-repentis). This variation is not linked to chromosome type 1B or 1RS.1BL. [See PI 561861-561914 for accessions from the same Crop Science registration.]1456842PI 561870
10PI 561871OK91G119Triticum aestivum L. subsp. aestivum Oklahoma, United StatesNSGCKERNELS1992DEVELOPED1992Genetic materialPairs of near-isolines differing for the presence or absence of 1RS.1BL were developed by selfing heterozygous plants (1RS.1BL//1B) in the F2 to F4 generations. One pair of homozygous near-isolines was isolated in each of 27 F5 families descending from a different F2 plant. No selection was imposed except for chromosome type. Segregation has been observed for plant stature (mostly semi-dwarf, some dwarf), and reaction to soil-born mosaic virus and tan spot (Pyrenophora tritici-repentis). This variation is not linked to chromosome type 1B or 1RS.1BL. [See PI 561861-561914 for accessions from the same Crop Science registration.]1456843PI 561871
11PI 561872OK91G120Triticum aestivum L. subsp. aestivum Oklahoma, United StatesNSGCKERNELS1992DEVELOPED1992Genetic materialPairs of near-isolines differing for the presence or absence of 1RS.1BL were developed by selfing heterozygous plants (1RS.1BL//1B) in the F2 to F4 generations. One pair of homozygous near-isolines was isolated in each of 27 F5 families descending from a different F2 plant. No selection was imposed except for chromosome type. Segregation has been observed for plant stature (mostly semi-dwarf, some dwarf), and reaction to soil-born mosaic virus and tan spot (Pyrenophora tritici-repentis). This variation is not linked to chromosome type 1B or 1RS.1BL. [See PI 561861-561914 for accessions from the same Crop Science registration.]1456844PI 561872
12PI 561873OK91G121Triticum aestivum L. subsp. aestivum Oklahoma, United StatesNSGCKERNELS1992DEVELOPED1992Genetic materialPairs of near-isolines differing for the presence or absence of 1RS.1BL were developed by selfing heterozygous plants (1RS.1BL//1B) in the F2 to F4 generations. One pair of homozygous near-isolines was isolated in each of 27 F5 families descending from a different F2 plant. No selection was imposed except for chromosome type. Segregation has been observed for plant stature (mostly semi-dwarf, some dwarf), and reaction to soil-born mosaic virus and tan spot (Pyrenophora tritici-repentis). This variation is not linked to chromosome type 1B or 1RS.1BL. [See PI 561861-561914 for accessions from the same Crop Science registration.]1456845PI 561873
13PI 561874OK91G122Triticum aestivum L. subsp. aestivum Oklahoma, United StatesNSGCKERNELS1992DEVELOPED1992Genetic materialPairs of near-isolines differing for the presence or absence of 1RS.1BL were developed by selfing heterozygous plants (1RS.1BL//1B) in the F2 to F4 generations. One pair of homozygous near-isolines was isolated in each of 27 F5 families descending from a different F2 plant. No selection was imposed except for chromosome type. Segregation has been observed for plant stature (mostly semi-dwarf, some dwarf), and reaction to soil-born mosaic virus and tan spot (Pyrenophora tritici-repentis). This variation is not linked to chromosome type 1B or 1RS.1BL. [See PI 561861-561914 for accessions from the same Crop Science registration.]1456846PI 561874
14PI 561875OK91G123Triticum aestivum L. subsp. aestivum Oklahoma, United StatesNSGCKERNELS1992DEVELOPED1992Genetic materialPairs of near-isolines differing for the presence or absence of 1RS.1BL were developed by selfing heterozygous plants (1RS.1BL//1B) in the F2 to F4 generations. One pair of homozygous near-isolines was isolated in each of 27 F5 families descending from a different F2 plant. No selection was imposed except for chromosome type. Segregation has been observed for plant stature (mostly semi-dwarf, some dwarf), and reaction to soil-born mosaic virus and tan spot (Pyrenophora tritici-repentis). This variation is not linked to chromosome type 1B or 1RS.1BL. [See PI 561861-561914 for accessions from the same Crop Science registration.]1456847PI 561875
15PI 561876OK91G124Triticum aestivum L. subsp. aestivum Oklahoma, United StatesNSGCKERNELS1992DEVELOPED1992Genetic materialPairs of near-isolines differing for the presence or absence of 1RS.1BL were developed by selfing heterozygous plants (1RS.1BL//1B) in the F2 to F4 generations. One pair of homozygous near-isolines was isolated in each of 27 F5 families descending from a different F2 plant. No selection was imposed except for chromosome type. Segregation has been observed for plant stature (mostly semi-dwarf, some dwarf), and reaction to soil-born mosaic virus and tan spot (Pyrenophora tritici-repentis). This variation is not linked to chromosome type 1B or 1RS.1BL. [See PI 561861-561914 for accessions from the same Crop Science registration.]1456848PI 561876
16PI 561877OK91G125Triticum aestivum L. subsp. aestivum Oklahoma, United StatesNSGCKERNELS1992DEVELOPED1992Genetic materialPairs of near-isolines differing for the presence or absence of 1RS.1BL were developed by selfing heterozygous plants (1RS.1BL//1B) in the F2 to F4 generations. One pair of homozygous near-isolines was isolated in each of 27 F5 families descending from a different F2 plant. No selection was imposed except for chromosome type. Segregation has been observed for plant stature (mostly semi-dwarf, some dwarf), and reaction to soil-born mosaic virus and tan spot (Pyrenophora tritici-repentis). This variation is not linked to chromosome type 1B or 1RS.1BL. [See PI 561861-561914 for accessions from the same Crop Science registration.]1456849PI 561877
17PI 561878OK91G126Triticum aestivum L. subsp. aestivum Oklahoma, United StatesNSGCKERNELS1992DEVELOPED1992Genetic materialPairs of near-isolines differing for the presence or absence of 1RS.1BL were developed by selfing heterozygous plants (1RS.1BL//1B) in the F2 to F4 generations. One pair of homozygous near-isolines was isolated in each of 27 F5 families descending from a different F2 plant. No selection was imposed except for chromosome type. Segregation has been observed for plant stature (mostly semi-dwarf, some dwarf), and reaction to soil-born mosaic virus and tan spot (Pyrenophora tritici-repentis). This variation is not linked to chromosome type 1B or 1RS.1BL. [See PI 561861-561914 for accessions from the same Crop Science registration.]1456850PI 561878
18PI 561879OK91G127Triticum aestivum L. subsp. aestivum Oklahoma, United StatesNSGCKERNELS1992DEVELOPED1992Genetic materialPairs of near-isolines differing for the presence or absence of 1RS.1BL were developed by selfing heterozygous plants (1RS.1BL//1B) in the F2 to F4 generations. One pair of homozygous near-isolines was isolated in each of 27 F5 families descending from a different F2 plant. No selection was imposed except for chromosome type. Segregation has been observed for plant stature (mostly semi-dwarf, some dwarf), and reaction to soil-born mosaic virus and tan spot (Pyrenophora tritici-repentis). This variation is not linked to chromosome type 1B or 1RS.1BL. [See PI 561861-561914 for accessions from the same Crop Science registration.]1456851PI 561879
19PI 561880OK91G128Triticum aestivum L. subsp. aestivum Oklahoma, United StatesNSGCKERNELS1992DEVELOPED1992Genetic materialPairs of near-isolines differing for the presence or absence of 1RS.1BL were developed by selfing heterozygous plants (1RS.1BL//1B) in the F2 to F4 generations. One pair of homozygous near-isolines was isolated in each of 27 F5 families descending from a different F2 plant. No selection was imposed except for chromosome type. Segregation has been observed for plant stature (mostly semi-dwarf, some dwarf), and reaction to soil-born mosaic virus and tan spot (Pyrenophora tritici-repentis). This variation is not linked to chromosome type 1B or 1RS.1BL. [See PI 561861-561914 for accessions from the same Crop Science registration.]1456852PI 561880
20PI 561881OK91G129Triticum aestivum L. subsp. aestivum Oklahoma, United StatesNSGCKERNELS1992DEVELOPED1992Genetic materialPairs of near-isolines differing for the presence or absence of 1RS.1BL were developed by selfing heterozygous plants (1RS.1BL//1B) in the F2 to F4 generations. One pair of homozygous near-isolines was isolated in each of 27 F5 families descending from a different F2 plant. No selection was imposed except for chromosome type. Segregation has been observed for plant stature (mostly semi-dwarf, some dwarf), and reaction to soil-born mosaic virus and tan spot (Pyrenophora tritici-repentis). This variation is not linked to chromosome type 1B or 1RS.1BL. [See PI 561861-561914 for accessions from the same Crop Science registration.]1456853PI 561881
21PI 561882OK91G130Triticum aestivum L. subsp. aestivum Oklahoma, United StatesNSGCKERNELS1992DEVELOPED1992Genetic materialPairs of near-isolines differing for the presence or absence of 1RS.1BL were developed by selfing heterozygous plants (1RS.1BL//1B) in the F2 to F4 generations. One pair of homozygous near-isolines was isolated in each of 27 F5 families descending from a different F2 plant. No selection was imposed except for chromosome type. Segregation has been observed for plant stature (mostly semi-dwarf, some dwarf), and reaction to soil-born mosaic virus and tan spot (Pyrenophora tritici-repentis). This variation is not linked to chromosome type 1B or 1RS.1BL. [See PI 561861-561914 for accessions from the same Crop Science registration.]1456854PI 561882
22PI 561883OK91G131Triticum aestivum L. subsp. aestivum Oklahoma, United StatesNSGCKERNELS1992DEVELOPED1992Genetic materialPairs of near-isolines differing for the presence or absence of 1RS.1BL were developed by selfing heterozygous plants (1RS.1BL//1B) in the F2 to F4 generations. One pair of homozygous near-isolines was isolated in each of 27 F5 families descending from a different F2 plant. No selection was imposed except for chromosome type. Segregation has been observed for plant stature (mostly semi-dwarf, some dwarf), and reaction to soil-born mosaic virus and tan spot (Pyrenophora tritici-repentis). This variation is not linked to chromosome type 1B or 1RS.1BL. [See PI 561861-561914 for accessions from the same Crop Science registration.]1456855PI 561883
23PI 561884OK91G132Triticum aestivum L. subsp. aestivum Oklahoma, United StatesNSGCKERNELS1992DEVELOPED1992Genetic materialPairs of near-isolines differing for the presence or absence of 1RS.1BL were developed by selfing heterozygous plants (1RS.1BL//1B) in the F2 to F4 generations. One pair of homozygous near-isolines was isolated in each of 27 F5 families descending from a different F2 plant. No selection was imposed except for chromosome type. Segregation has been observed for plant stature (mostly semi-dwarf, some dwarf), and reaction to soil-born mosaic virus and tan spot (Pyrenophora tritici-repentis). This variation is not linked to chromosome type 1B or 1RS.1BL. [See PI 561861-561914 for accessions from the same Crop Science registration.]1456856PI 561884
24PI 561885OK91G133Triticum aestivum L. subsp. aestivum Oklahoma, United StatesNSGCKERNELS1992DEVELOPED1992Genetic materialPairs of near-isolines differing for the presence or absence of 1RS.1BL were developed by selfing heterozygous plants (1RS.1BL//1B) in the F2 to F4 generations. One pair of homozygous near-isolines was isolated in each of 27 F5 families descending from a different F2 plant. No selection was imposed except for chromosome type. Segregation has been observed for plant stature (mostly semi-dwarf, some dwarf), and reaction to soil-born mosaic virus and tan spot (Pyrenophora tritici-repentis). This variation is not linked to chromosome type 1B or 1RS.1BL. [See PI 561861-561914 for accessions from the same Crop Science registration.]1456857PI 561885
25PI 561886OK91G134Triticum aestivum L. subsp. aestivum Oklahoma, United StatesNSGCKERNELS1992DEVELOPED1992Genetic materialPairs of near-isolines differing for the presence or absence of 1RS.1BL were developed by selfing heterozygous plants (1RS.1BL//1B) in the F2 to F4 generations. One pair of homozygous near-isolines was isolated in each of 27 F5 families descending from a different F2 plant. No selection was imposed except for chromosome type. Segregation has been observed for plant stature (mostly semi-dwarf, some dwarf), and reaction to soil-born mosaic virus and tan spot (Pyrenophora tritici-repentis). This variation is not linked to chromosome type 1B or 1RS.1BL. [See PI 561861-561914 for accessions from the same Crop Science registration.]1456858PI 561886
26PI 561887OK91G135Triticum aestivum L. subsp. aestivum Oklahoma, United StatesNSGCKERNELS1992DEVELOPED1992Genetic materialPairs of near-isolines differing for the presence or absence of 1RS.1BL were developed by selfing heterozygous plants (1RS.1BL//1B) in the F2 to F4 generations. One pair of homozygous near-isolines was isolated in each of 27 F5 families descending from a different F2 plant. No selection was imposed except for chromosome type. Segregation has been observed for plant stature (mostly semi-dwarf, some dwarf), and reaction to soil-born mosaic virus and tan spot (Pyrenophora tritici-repentis). This variation is not linked to chromosome type 1B or 1RS.1BL. [See PI 561861-561914 for accessions from the same Crop Science registration.]1456859PI 561887
27PI 561888OK91G136Triticum aestivum L. subsp. aestivum Oklahoma, United StatesNSGCKERNELS1992DEVELOPED1992Genetic materialPairs of near-isolines differing for the presence or absence of 1RS.1BL were developed by selfing heterozygous plants (1RS.1BL//1B) in the F2 to F4 generations. One pair of homozygous near-isolines was isolated in each of 27 F5 families descending from a different F2 plant. No selection was imposed except for chromosome type. Segregation has been observed for plant stature (mostly semi-dwarf, some dwarf), and reaction to soil-born mosaic virus and tan spot (Pyrenophora tritici-repentis). This variation is not linked to chromosome type 1B or 1RS.1BL. [See PI 561861-561914 for accessions from the same Crop Science registration.]1456860PI 561888
28PI 561889OK91G137Triticum aestivum L. subsp. aestivum Oklahoma, United StatesNSGCKERNELS1992DEVELOPED1992Genetic materialPairs of near-isolines differing for the presence or absence of 1RS.1BL were developed by selfing heterozygous plants (1RS.1BL//1B) in the F2 to F4 generations. One pair of homozygous near-isolines was isolated in each of 27 F5 families descending from a different F2 plant. No selection was imposed except for chromosome type. Segregation has been observed for plant stature (mostly semi-dwarf, some dwarf), and reaction to soil-born mosaic virus and tan spot (Pyrenophora tritici-repentis). This variation is not linked to chromosome type 1B or 1RS.1BL. [See PI 561861-561914 for accessions from the same Crop Science registration.]1456861PI 561889
29PI 561890OK91G138Triticum aestivum L. subsp. aestivum Oklahoma, United StatesNSGCKERNELS1992DEVELOPED1992Genetic materialPairs of near-isolines differing for the presence or absence of 1RS.1BL were developed by selfing heterozygous plants (1RS.1BL//1B) in the F2 to F4 generations. One pair of homozygous near-isolines was isolated in each of 27 F5 families descending from a different F2 plant. No selection was imposed except for chromosome type. Segregation has been observed for plant stature (mostly semi-dwarf, some dwarf), and reaction to soil-born mosaic virus and tan spot (Pyrenophora tritici-repentis). This variation is not linked to chromosome type 1B or 1RS.1BL. [See PI 561861-561914 for accessions from the same Crop Science registration.]1456862PI 561890
30PI 561891OK91G139Triticum aestivum L. subsp. aestivum Oklahoma, United StatesNSGCKERNELS1992DEVELOPED1992Genetic materialPairs of near-isolines differing for the presence or absence of 1RS.1BL were developed by selfing heterozygous plants (1RS.1BL//1B) in the F2 to F4 generations. One pair of homozygous near-isolines was isolated in each of 27 F5 families descending from a different F2 plant. No selection was imposed except for chromosome type. Segregation has been observed for plant stature (mostly semi-dwarf, some dwarf), and reaction to soil-born mosaic virus and tan spot (Pyrenophora tritici-repentis). This variation is not linked to chromosome type 1B or 1RS.1BL. [See PI 561861-561914 for accessions from the same Crop Science registration.]1456863PI 561891
31PI 561892OK91G140Triticum aestivum L. subsp. aestivum Oklahoma, United StatesNSGCKERNELS1992DEVELOPED1992Genetic materialPairs of near-isolines differing for the presence or absence of 1RS.1BL were developed by selfing heterozygous plants (1RS.1BL//1B) in the F2 to F4 generations. One pair of homozygous near-isolines was isolated in each of 27 F5 families descending from a different F2 plant. No selection was imposed except for chromosome type. Segregation has been observed for plant stature (mostly semi-dwarf, some dwarf), and reaction to soil-born mosaic virus and tan spot (Pyrenophora tritici-repentis). This variation is not linked to chromosome type 1B or 1RS.1BL. [See PI 561861-561914 for accessions from the same Crop Science registration.]1456864PI 561892
32PI 561893OK91G141Triticum aestivum L. subsp. aestivum Oklahoma, United StatesNSGCKERNELS1992DEVELOPED1992Genetic materialPairs of near-isolines differing for the presence or absence of 1RS.1BL were developed by selfing heterozygous plants (1RS.1BL//1B) in the F2 to F4 generations. One pair of homozygous near-isolines was isolated in each of 27 F5 families descending from a different F2 plant. No selection was imposed except for chromosome type. Segregation has been observed for plant stature (mostly semi-dwarf, some dwarf), and reaction to soil-born mosaic virus and tan spot (Pyrenophora tritici-repentis). This variation is not linked to chromosome type 1B or 1RS.1BL. [See PI 561861-561914 for accessions from the same Crop Science registration.]1456865PI 561893
33PI 561894OK91G142Triticum aestivum L. subsp. aestivum Oklahoma, United StatesNSGCKERNELS1992DEVELOPED1992Genetic materialPairs of near-isolines differing for the presence or absence of 1RS.1BL were developed by selfing heterozygous plants (1RS.1BL//1B) in the F2 to F4 generations. One pair of homozygous near-isolines was isolated in each of 27 F5 families descending from a different F2 plant. No selection was imposed except for chromosome type. Segregation has been observed for plant stature (mostly semi-dwarf, some dwarf), and reaction to soil-born mosaic virus and tan spot (Pyrenophora tritici-repentis). This variation is not linked to chromosome type 1B or 1RS.1BL. [See PI 561861-561914 for accessions from the same Crop Science registration.]1456866PI 561894
34PI 561895OK91G143Triticum aestivum L. subsp. aestivum Oklahoma, United StatesNSGCKERNELS1992DEVELOPED1992Genetic materialPairs of near-isolines differing for the presence or absence of 1RS.1BL were developed by selfing heterozygous plants (1RS.1BL//1B) in the F2 to F4 generations. One pair of homozygous near-isolines was isolated in each of 27 F5 families descending from a different F2 plant. No selection was imposed except for chromosome type. Segregation has been observed for plant stature (mostly semi-dwarf, some dwarf), and reaction to soil-born mosaic virus and tan spot (Pyrenophora tritici-repentis). This variation is not linked to chromosome type 1B or 1RS.1BL. [See PI 561861-561914 for accessions from the same Crop Science registration.]1456867PI 561895
35PI 561896OK91G144Triticum aestivum L. subsp. aestivum Oklahoma, United StatesNSGCKERNELS1992DEVELOPED1992Genetic materialPairs of near-isolines differing for the presence or absence of 1RS.1BL were developed by selfing heterozygous plants (1RS.1BL//1B) in the F2 to F4 generations. One pair of homozygous near-isolines was isolated in each of 27 F5 families descending from a different F2 plant. No selection was imposed except for chromosome type. Segregation has been observed for plant stature (mostly semi-dwarf, some dwarf), and reaction to soil-born mosaic virus and tan spot (Pyrenophora tritici-repentis). This variation is not linked to chromosome type 1B or 1RS.1BL. [See PI 561861-561914 for accessions from the same Crop Science registration.]1456868PI 561896
36PI 561897OK91G145Triticum aestivum L. subsp. aestivum Oklahoma, United StatesNSGCKERNELS1992DEVELOPED1992Genetic materialPairs of near-isolines differing for the presence or absence of 1RS.1BL were developed by selfing heterozygous plants (1RS.1BL//1B) in the F2 to F4 generations. One pair of homozygous near-isolines was isolated in each of 27 F5 families descending from a different F2 plant. No selection was imposed except for chromosome type. Segregation has been observed for plant stature (mostly semi-dwarf, some dwarf), and reaction to soil-born mosaic virus and tan spot (Pyrenophora tritici-repentis). This variation is not linked to chromosome type 1B or 1RS.1BL. [See PI 561861-561914 for accessions from the same Crop Science registration.]1456869PI 561897
37PI 561898OK91G146Triticum aestivum L. subsp. aestivum Oklahoma, United StatesNSGCKERNELS1992DEVELOPED1992Genetic materialPairs of near-isolines differing for the presence or absence of 1RS.1BL were developed by selfing heterozygous plants (1RS.1BL//1B) in the F2 to F4 generations. One pair of homozygous near-isolines was isolated in each of 27 F5 families descending from a different F2 plant. No selection was imposed except for chromosome type. Segregation has been observed for plant stature (mostly semi-dwarf, some dwarf), and reaction to soil-born mosaic virus and tan spot (Pyrenophora tritici-repentis). This variation is not linked to chromosome type 1B or 1RS.1BL. [See PI 561861-561914 for accessions from the same Crop Science registration.]1456870PI 561898
38PI 561899OK91G147Triticum aestivum L. subsp. aestivum Oklahoma, United StatesNSGCKERNELS1992DEVELOPED1992Genetic materialPairs of near-isolines differing for the presence or absence of 1RS.1BL were developed by selfing heterozygous plants (1RS.1BL//1B) in the F2 to F4 generations. One pair of homozygous near-isolines was isolated in each of 27 F5 families descending from a different F2 plant. No selection was imposed except for chromosome type. Segregation has been observed for plant stature (mostly semi-dwarf, some dwarf), and reaction to soil-born mosaic virus and tan spot (Pyrenophora tritici-repentis). This variation is not linked to chromosome type 1B or 1RS.1BL. [See PI 561861-561914 for accessions from the same Crop Science registration.]1456871PI 561899
39PI 561900OK91G148Triticum aestivum L. subsp. aestivum Oklahoma, United StatesNSGCKERNELS1992DEVELOPED1992Genetic materialPairs of near-isolines differing for the presence or absence of 1RS.1BL were developed by selfing heterozygous plants (1RS.1BL//1B) in the F2 to F4 generations. One pair of homozygous near-isolines was isolated in each of 27 F5 families descending from a different F2 plant. No selection was imposed except for chromosome type. Segregation has been observed for plant stature (mostly semi-dwarf, some dwarf), and reaction to soil-born mosaic virus and tan spot (Pyrenophora tritici-repentis). This variation is not linked to chromosome type 1B or 1RS.1BL. [See PI 561861-561914 for accessions from the same Crop Science registration.]1456872PI 561900
40PI 561901OK91G149Triticum aestivum L. subsp. aestivum Oklahoma, United StatesNSGCKERNELS1992DEVELOPED1992Genetic materialPairs of near-isolines differing for the presence or absence of 1RS.1BL were developed by selfing heterozygous plants (1RS.1BL//1B) in the F2 to F4 generations. One pair of homozygous near-isolines was isolated in each of 27 F5 families descending from a different F2 plant. No selection was imposed except for chromosome type. Segregation has been observed for plant stature (mostly semi-dwarf, some dwarf), and reaction to soil-born mosaic virus and tan spot (Pyrenophora tritici-repentis). This variation is not linked to chromosome type 1B or 1RS.1BL. [See PI 561861-561914 for accessions from the same Crop Science registration.]1456873PI 561901
41PI 561902OK91G150Triticum aestivum L. subsp. aestivum Oklahoma, United StatesNSGCKERNELS1992DEVELOPED1992Genetic materialPairs of near-isolines differing for the presence or absence of 1RS.1BL were developed by selfing heterozygous plants (1RS.1BL//1B) in the F2 to F4 generations. One pair of homozygous near-isolines was isolated in each of 27 F5 families descending from a different F2 plant. No selection was imposed except for chromosome type. Segregation has been observed for plant stature (mostly semi-dwarf, some dwarf), and reaction to soil-born mosaic virus and tan spot (Pyrenophora tritici-repentis). This variation is not linked to chromosome type 1B or 1RS.1BL. [See PI 561861-561914 for accessions from the same Crop Science registration.]1456874PI 561902
42PI 561903OK91G151Triticum aestivum L. subsp. aestivum Oklahoma, United StatesNSGCKERNELS1992DEVELOPED1992Genetic materialPairs of near-isolines differing for the presence or absence of 1RS.1BL were developed by selfing heterozygous plants (1RS.1BL//1B) in the F2 to F4 generations. One pair of homozygous near-isolines was isolated in each of 27 F5 families descending from a different F2 plant. No selection was imposed except for chromosome type. Segregation has been observed for plant stature (mostly semi-dwarf, some dwarf), and reaction to soil-born mosaic virus and tan spot (Pyrenophora tritici-repentis). This variation is not linked to chromosome type 1B or 1RS.1BL. [See PI 561861-561914 for accessions from the same Crop Science registration.]1456875PI 561903
43PI 561904OK91G152Triticum aestivum L. subsp. aestivum Oklahoma, United StatesNSGCKERNELS1992DEVELOPED1992Genetic materialPairs of near-isolines differing for the presence or absence of 1RS.1BL were developed by selfing heterozygous plants (1RS.1BL//1B) in the F2 to F4 generations. One pair of homozygous near-isolines was isolated in each of 27 F5 families descending from a different F2 plant. No selection was imposed except for chromosome type. Segregation has been observed for plant stature (mostly semi-dwarf, some dwarf), and reaction to soil-born mosaic virus and tan spot (Pyrenophora tritici-repentis). This variation is not linked to chromosome type 1B or 1RS.1BL. [See PI 561861-561914 for accessions from the same Crop Science registration.]1456876PI 561904
44PI 561905OK91G153Triticum aestivum L. subsp. aestivum Oklahoma, United StatesNSGCKERNELS1992DEVELOPED1992Genetic materialPairs of near-isolines differing for the presence or absence of 1RS.1BL were developed by selfing heterozygous plants (1RS.1BL//1B) in the F2 to F4 generations. One pair of homozygous near-isolines was isolated in each of 27 F5 families descending from a different F2 plant. No selection was imposed except for chromosome type. Segregation has been observed for plant stature (mostly semi-dwarf, some dwarf), and reaction to soil-born mosaic virus and tan spot (Pyrenophora tritici-repentis). This variation is not linked to chromosome type 1B or 1RS.1BL. [See PI 561861-561914 for accessions from the same Crop Science registration.]1456877PI 561905
45PI 561906OK91G154Triticum aestivum L. subsp. aestivum Oklahoma, United StatesNSGCKERNELS1992DEVELOPED1992Genetic materialPairs of near-isolines differing for the presence or absence of 1RS.1BL were developed by selfing heterozygous plants (1RS.1BL//1B) in the F2 to F4 generations. One pair of homozygous near-isolines was isolated in each of 27 F5 families descending from a different F2 plant. No selection was imposed except for chromosome type. Segregation has been observed for plant stature (mostly semi-dwarf, some dwarf), and reaction to soil-born mosaic virus and tan spot (Pyrenophora tritici-repentis). This variation is not linked to chromosome type 1B or 1RS.1BL. [See PI 561861-561914 for accessions from the same Crop Science registration.]1456878PI 561906
46PI 561907OK91G155Triticum aestivum L. subsp. aestivum Oklahoma, United StatesNSGCKERNELS1992DEVELOPED1992Genetic materialPairs of near-isolines differing for the presence or absence of 1RS.1BL were developed by selfing heterozygous plants (1RS.1BL//1B) in the F2 to F4 generations. One pair of homozygous near-isolines was isolated in each of 27 F5 families descending from a different F2 plant. No selection was imposed except for chromosome type. Segregation has been observed for plant stature (mostly semi-dwarf, some dwarf), and reaction to soil-born mosaic virus and tan spot (Pyrenophora tritici-repentis). This variation is not linked to chromosome type 1B or 1RS.1BL. [See PI 561861-561914 for accessions from the same Crop Science registration.]1456879PI 561907
47PI 561908OK91G156Triticum aestivum L. subsp. aestivum Oklahoma, United StatesNSGCKERNELS1992DEVELOPED1992Genetic materialPairs of near-isolines differing for the presence or absence of 1RS.1BL were developed by selfing heterozygous plants (1RS.1BL//1B) in the F2 to F4 generations. One pair of homozygous near-isolines was isolated in each of 27 F5 families descending from a different F2 plant. No selection was imposed except for chromosome type. Segregation has been observed for plant stature (mostly semi-dwarf, some dwarf), and reaction to soil-born mosaic virus and tan spot (Pyrenophora tritici-repentis). This variation is not linked to chromosome type 1B or 1RS.1BL. [See PI 561861-561914 for accessions from the same Crop Science registration.]1456880PI 561908
48PI 561909OK91G157Triticum aestivum L. subsp. aestivum Oklahoma, United StatesNSGCKERNELS1992DEVELOPED1992Genetic materialPairs of near-isolines differing for the presence or absence of 1RS.1BL were developed by selfing heterozygous plants (1RS.1BL//1B) in the F2 to F4 generations. One pair of homozygous near-isolines was isolated in each of 27 F5 families descending from a different F2 plant. No selection was imposed except for chromosome type. Segregation has been observed for plant stature (mostly semi-dwarf, some dwarf), and reaction to soil-born mosaic virus and tan spot (Pyrenophora tritici-repentis). This variation is not linked to chromosome type 1B or 1RS.1BL. [See PI 561861-561914 for accessions from the same Crop Science registration.]1456881PI 561909
49PI 561910OK91G158Triticum aestivum L. subsp. aestivum Oklahoma, United StatesNSGCKERNELS1992DEVELOPED1992Genetic materialPairs of near-isolines differing for the presence or absence of 1RS.1BL were developed by selfing heterozygous plants (1RS.1BL//1B) in the F2 to F4 generations. One pair of homozygous near-isolines was isolated in each of 27 F5 families descending from a different F2 plant. No selection was imposed except for chromosome type. Segregation has been observed for plant stature (mostly semi-dwarf, some dwarf), and reaction to soil-born mosaic virus and tan spot (Pyrenophora tritici-repentis). This variation is not linked to chromosome type 1B or 1RS.1BL. [See PI 561861-561914 for accessions from the same Crop Science registration.]1456882PI 561910
50PI 561911OK91G159Triticum aestivum L. subsp. aestivum Oklahoma, United StatesNSGCKERNELS1992DEVELOPED1992Genetic materialPairs of near-isolines differing for the presence or absence of 1RS.1BL were developed by selfing heterozygous plants (1RS.1BL//1B) in the F2 to F4 generations. One pair of homozygous near-isolines was isolated in each of 27 F5 families descending from a different F2 plant. No selection was imposed except for chromosome type. Segregation has been observed for plant stature (mostly semi-dwarf, some dwarf), and reaction to soil-born mosaic virus and tan spot (Pyrenophora tritici-repentis). This variation is not linked to chromosome type 1B or 1RS.1BL. [See PI 561861-561914 for accessions from the same Crop Science registration.]1456883PI 561911
51PI 561912OK91G160Triticum aestivum L. subsp. aestivum Oklahoma, United StatesNSGCKERNELS1992DEVELOPED1992Genetic materialPairs of near-isolines differing for the presence or absence of 1RS.1BL were developed by selfing heterozygous plants (1RS.1BL//1B) in the F2 to F4 generations. One pair of homozygous near-isolines was isolated in each of 27 F5 families descending from a different F2 plant. No selection was imposed except for chromosome type. Segregation has been observed for plant stature (mostly semi-dwarf, some dwarf), and reaction to soil-born mosaic virus and tan spot (Pyrenophora tritici-repentis). This variation is not linked to chromosome type 1B or 1RS.1BL. [See PI 561861-561914 for accessions from the same Crop Science registration.]1456884PI 561912
52PI 561913OK91G161Triticum aestivum L. subsp. aestivum Oklahoma, United StatesNSGCKERNELS1992DEVELOPED1992Genetic materialPairs of near-isolines differing for the presence or absence of 1RS.1BL were developed by selfing heterozygous plants (1RS.1BL//1B) in the F2 to F4 generations. One pair of homozygous near-isolines was isolated in each of 27 F5 families descending from a different F2 plant. No selection was imposed except for chromosome type. Segregation has been observed for plant stature (mostly semi-dwarf, some dwarf), and reaction to soil-born mosaic virus and tan spot (Pyrenophora tritici-repentis). This variation is not linked to chromosome type 1B or 1RS.1BL. [See PI 561861-561914 for accessions from the same Crop Science registration.]1456885PI 561913
53PI 561914OK91G162Triticum aestivum L. subsp. aestivum Oklahoma, United StatesNSGCKERNELS1992DEVELOPED1992Genetic materialPairs of near-isolines differing for the presence or absence of 1RS.1BL were developed by selfing heterozygous plants (1RS.1BL//1B) in the F2 to F4 generations. One pair of homozygous near-isolines was isolated in each of 27 F5 families descending from a different F2 plant. No selection was imposed except for chromosome type. Segregation has been observed for plant stature (mostly semi-dwarf, some dwarf), and reaction to soil-born mosaic virus and tan spot (Pyrenophora tritici-repentis). This variation is not linked to chromosome type 1B or 1RS.1BL. [See PI 561861-561914 for accessions from the same Crop Science registration.]1456886PI 561914