1974
DOI: 10.1093/oxfordjournals.pcp.a075049
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Spectral quality influence of light during development of Arabidopsis thaliana plants in regulating seed germination

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Cited by 71 publications
(44 citation statements)
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“…In addition to the light environment, germination is known to depend on multiple variables including temperature, length of seed dormancy, cold treatment during tlormancy, and light conditions during seed maturation (Hayes and Klein, 1974;Derkx and Karssen, 1993). Therefore, we confirmed these germination results by studying germination in populations segregating for the phyA or phyB mutations (see "Material:; and Methods").…”
Section: Phenotypes Caused By Loss Of Phyamentioning
confidence: 56%
See 1 more Smart Citation
“…In addition to the light environment, germination is known to depend on multiple variables including temperature, length of seed dormancy, cold treatment during tlormancy, and light conditions during seed maturation (Hayes and Klein, 1974;Derkx and Karssen, 1993). Therefore, we confirmed these germination results by studying germination in populations segregating for the phyA or phyB mutations (see "Material:; and Methods").…”
Section: Phenotypes Caused By Loss Of Phyamentioning
confidence: 56%
“…Far-red light pushes the phytochrome photoequilibrium toward the redlight-absorbing form, and therefore (for stable phytochromes) far-red light should mimic the effect of a loss-of-function phytochrome mutation. Earlier data on reversibility (inhibition) of germination by far-red light were interpreted as indicating inactivation of phytochrome by conversion to Pr (Shropshire et al, 1961;McCullough and Shropshire, 1970;Hayes and Klein, 1974;Cone and Kendrick, 1985). However, we have found that for germination of a p h y A mutant, and to a lesser extent the wild type, the phyB nu11 mutation actually compensates for the apparent inhibitory effect of far-red light on germination.…”
Section: Dlscusslonmentioning
confidence: 99%
“…To eliminate the effect of phytochrome to study temperature regulation of GA biosynthesis, wild-type seeds were imbibed in the dark, irradiated with an FR light pulse, and then incubated in the dark for 48 h at 22 or 48C (Figure 2A). The FR pulse treatment is necessary to inactivate phytochrome that is stored in dry seeds in the active form (Hayes and Klein, 1974). Under the light condition given in Figure 2A, wild-type seeds do not germinate at both temperatures (up to 96 h).…”
Section: Some Ga Biosynthesis Genes Are Responsive To Low Temperaturementioning
confidence: 99%
“…The ability of plants to sense the environment also provides them with some ability to respond to that environment in ways that can alter their exposure to it (Donohue 2003). Plastic environmental cueing of germination can be a precise mechanism of habitat selection in plants that can determine both biotic and abiotic conditions that germinants experience (McCullough and Shropshire 1970;Hayes and Klein 1974;Evans and Cabin 1995;Gutterman 2000; reviewed in Baskin and Baskin 1998).Germination responses to cues that predict season, in particular, have the potential to influence the environment experienced by young germinants and also by adult plants. For example, in winter annuals germination responses to warm after-ripening followed by a brief cold period would indicate autumn conditions in a temperate climate (Baskin and Baskin 1972Baskin et al 1992;Galloway 2001Galloway , 2002.…”
mentioning
confidence: 99%
“…The ability of plants to sense the environment also provides them with some ability to respond to that environment in ways that can alter their exposure to it (Donohue 2003). Plastic environmental cueing of germination can be a precise mechanism of habitat selection in plants that can determine both biotic and abiotic conditions that germinants experience (McCullough and Shropshire 1970;Hayes and Klein 1974;Evans and Cabin 1995;Gutterman 2000; reviewed in Baskin and Baskin 1998).…”
mentioning
confidence: 99%