Maize Genetics Cooperation Newsletter vol 84 2010
Please Note: Notes submitted to the Maize Genetics
Cooperation Newsletter may be cited only with consent of authors.
Texas AgriLife Research, Texas A&M University, College Station, TX; Texas AgriLife Research, Lubbock, TX
Identifying maize germplasm with extremely late flowering and
photoperiod sensitivity in Texas
Murray, SC; Xu, W; Mayfield, KL
Maize cultivars that are extremely late to flower or fail to flower in the temperate/ sub-tropical summer are of interest: 1) to develop tall dedicated cellulosic feedstocks (non-grain), 2) to better understand genetic mechanisms of flowering, 3) to create genetic mapping populations for flowering time and other traits of interest, and 4) to identify genetic diversity in linkage with extreme flowering time genes that may otherwise be inadvertently selected against. We are also very interested in these tropical lines as an untapped source of aflatoxin resistance but flowering time confounds this analysis. We planted 55 accessions obtained from GRIN (USDA-ARS) and up to three checks (B73, Mo17, CML254), in three Texas locations, Weslaco (planted 2/18/2009), College Station (planted 3/20/2009), and Lubbock (planted 5/8/2009) if enough seed was available. Accessions of interest were identified based on previous MGNL notes, data found in GRIN and suggestions found on blogs. Plants were managed with normal agronomic practices for a breeding nursery but stress was still evident from a record breaking hot and dry summer across Texas. Flowering dates (Anthesis) were taken every few days in College Station and Lubbock, but estimated in Weslaco on May 15th by KLM and SCM. Because many of these accessions were heterogenous landraces, some within accession segregation was observed. For nearly all accessions, segregation was often no more than a week and plants appeared otherwise uniform. To increase seed and develop homozygous lines for future experiments, individuals were self or sibling pollinated in College Station. Many of the accessions that flowered very late failed to produce seed or had excessive ear rot due to late season stress. Asynchronous flowering was observed (always with silking after anthesis) within some accessions but attempts to sib pollinate were occasionally successful. The wild species Z. dipploperennis and Z. huehuetenangensis were the latest to flower while among domesticated accessions the latest were from Ecuador and Columbia.
Late flowering accessions were then also planted in a winter nursery in Weslaco, TX on August 10, 2009 to produce more seed for evaluation. Under winter nursery conditions (going into shorter days, moderate day temperatures, cool nights) most of the accessions flowered around the same time or slightly later than normal breeding material. This suggests that the delayed flowering in Summer was caused primarily by photoperiod response rather than by high temperatures. This confirms that the challenge of producing and evaluating genotypes that do not flower in the Summer can be overcome by making crosses and producing seed in a winter nursery under a short-day length.
Ultimately, we wish to develop extremely late flowering inbred lines out of landrace material that can be used for a variety of experiments, tests, and breeding objectives. It is clear that given the heat of Texas Summers and inbreeding of landrace material this is likely to be quite challenging and some crossing to elite adapted material may be necessary. We hope that crosses to elite material can also be utilized, in coordination with the Germplasm Enhancement of Maize (GEM) program, as sources of genetic diversity for continued maize improvement in areas such as aflatoxin resistance.
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Days After
Planting to Anthesis |
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GRIN # |
Origin |
CS |
WE |
LB |
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Ames
17675 |
Ecuador |
111 |
>103 |
na |
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Ames
1768 |
Ecuador |
77 |
87 |
70 |
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Ames 19945 |
Nayarit, Mexico |
95 |
na |
100 |
|
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Ames 19994 |
Oaxaca, Mexico |
91 |
na |
99 |
|
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Ames
26959 |
Wisconsin |
57 |
67 |
42 |
|
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Ames
2758 |
New York |
62 |
75 |
55 |
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NSL
2833 |
Mexico |
80 |
80 |
81 |
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NSL
5618 |
Virginia |
65 |
73 |
54 |
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NSL
95717 |
Puerto Rico |
81 |
83 |
na |
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PI
245133 |
Russia |
70 |
76 |
68 |
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PI
318728 |
Brazil |
82 |
92 |
79 |
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PI
331444 |
Ethiopia |
95 |
>103 |
103 |
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PI
357106 |
Ethiopia |
90 |
103 |
82 |
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PI
357127 |
Ethiopia |
90 |
92 |
91 |
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PI
369342 |
Benin |
79 |
84 |
81 |
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PI
377746 |
Thailand |
71 |
83 |
68 |
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PI
377746 |
Thailand |
71 |
na |
na |
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PI
390552 |
Equador |
75 |
82 |
59 |
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PI
390553 |
Equador |
111 |
97 |
>114 |
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PI
390553 |
Equador |
111 |
na |
na |
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PI
390554 |
Equador |
95 |
96 |
113 |
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PI
390554 |
Equador |
95 |
na |
na |
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PI
390573 |
Equador |
90 |
92 |
104 |
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PI
414181 |
Iowa |
81 |
83 |
71 |
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PI
414181 |
Iowa |
81 |
na |
na |
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PI
420250 |
Arizona |
70 |
80 |
58 |
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PI
420251 |
Arizona |
57 |
73 |
54 |
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PI
441932 |
Z. dipploperennis |
>111 |
na |
>114 |
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PI
441934 |
Z. huehuetenangensis |
>111 |
na |
216 |
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PI 443785 |
Montana, Columbia |
83 |
na |
100 |
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PI 443788 |
Montana, Columbia |
111 |
na |
>114 |
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PI 443793 |
Montana, Columbia |
111 |
na |
103 |
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PI
445082 |
Columbia |
111 |
>103 |
>114 |
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PI 445144 |
Montana, Columbia |
111 |
na |
94 |
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PI
451693 |
Iowa |
67 |
80 |
54 |
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PI
483809 |
Cuba |
80 |
87 |
82 |
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PI
484600 |
Puebla 94 |
105 |
>103 |
114 |
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PI
488664 |
Peru |
82 |
95 |
92 |
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PI
498533 |
Cuba |
83 |
88 |
90 |
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PI
498703 |
Trinidad |
88 |
94 |
96 |
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PI
511650 |
Mexico |
90 |
87 |
94 |
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PI
515534 |
Mexico |
75 |
95 |
82 |
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PI
576019 |
CIMMT population |
80 |
86 |
94 |
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PI
612343 |
Florida |
69 |
78 |
na |
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PI
612343 |
Florida |
69 |
na |
na |
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PI
614830 |
Florida |
71 |
78 |
na |
|
||||
PI
614830 |
Florida |
71 |
na |
na |
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PI 628463 |
Nayarit, Mexico |
88 |
na |
99 |
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PI
644099 |
Florida |
72 |
80 |
na |
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PI
644099 |
Florida |
72 |
na |
na |
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PI
644100 |
Florida |
74 |
na |
na |
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PI 645923 |
Nayarit, Mexico |
90 |
na |
100 |
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B73 |
check |
78 |
na |
69 |
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Mo17 |
check |
79 |
na |
68 |
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CML 254 |
check |
95 |
na |
na |
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CS - College Station, TX
WE -Weslaco, TX
LB – Lubbock, TX