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. 2018 Nov 29;38(2):195–209. doi: 10.1007/s00299-018-2362-x

Table 1.

Plant regeneration in isolated microspore cultures of DH lines of winter triticale as the effect of various tiller pre-treatments (experiment 1)

DH line Regeneration per spike LT LT + 3–8d GSH LT + GSH
DH18 Total 3.8 ± 1.0bcd 16.8 ± 5.9a 16.7a
Green plant 2.0 ± 0.5b 0.5 ± 0.3b 2.0b
DH19 Total 0.0
Green plant 0.0
DH28 Total 11.8 ± 8.2abc 13.8 ± 1.2ab 12.6 ± 1.8abc
Green plant 9.8 ± 6.2a 9.6 ± 1.1a 12.3 ± 4.2a
DH44 Total 0.6 ± 0.4d 9.3 ± 2.0abcd 3.5 ± 1.5cd
Green plant 0.4 ± 0.4b 1.7 ± 1.0b 1.0 ± 1.0b
DH47 Total 4.4 ± 0.9bcd 1.0 ± 0.3d 10.0 ± 3.1abcd
Green plant 0.9 ± 0.6b 0.0 3.0 ± 0.3b
DH101 Total 1.5 ± 0.6d 4.3 ± 2.0bcd
Green plant 0.5 ± 0.3b 1.0 ± 0.6b
DH119 Total 0.0
Green plant 0.0
Source of variation Mean squares/p
Total regeneration Green plant regeneration
DH line 176.128/*** 102.652/***
Treatment 63.148/* 1.936/ns
DH line × treatment 33.911/* 1.722/ns

The mean from at least three biological replications (isolations) ± SE. Data marked with the same letter do not differ according to the Duncan test (p ≤ 0.05). The sources of variance for regeneration potential were as follows: seven DH lines, three treatments, and interaction between DH line and treatment. *, ***Significant at p ≤ 0.05, 0.001, respectively;  ns not significant

LT low temperature pre-treatment of tillers (21 days at 4 °C); LT + 3–8d GSH low temperature pre-treatment of tillers (21 days at 4 °C) combined with short GSH pre-treatment (0.3 mM GSH applied 3–8 days before microspore isolation); LT + GSH low temperature pre-treatment of tillers (21 days at 4 °C) combined with long GSH pre-treatment (0.3 mM GSH applied 21 days before microspore isolation)

‘–’ embryo-like structure was not developed