1990
DOI: 10.17660/actahortic.1990.272.11
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Control of Plant Morphogenesis and Flowering by Light Quality and Temperature

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Cited by 100 publications
(53 citation statements)
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“…Alternatively this reduction in stem length may be the result of the different greenhouse environmental conditions that the crop was grown under following each of the storage durations. Internode and stem length increase with increasing daily air temperature differential (Moe & Heins 1990). The temperature differential decreased from the first to the third planting and increased slightly between the third and fourth planting in a similar pattern to stem length.…”
Section: Discussionmentioning
confidence: 66%
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“…Alternatively this reduction in stem length may be the result of the different greenhouse environmental conditions that the crop was grown under following each of the storage durations. Internode and stem length increase with increasing daily air temperature differential (Moe & Heins 1990). The temperature differential decreased from the first to the third planting and increased slightly between the third and fourth planting in a similar pattern to stem length.…”
Section: Discussionmentioning
confidence: 66%
“…The reduction in time from sprouting to shoot emergence and from shoot emergence to stem harvest may have been because of warmer soil and air temperatures in the later plantings. Mean temperature has only a small effect on stem length but influences the growth rate (Moe & Heins 1990).…”
Section: Discussionmentioning
confidence: 99%
“…Two main light qualities were detected by pigment systems in plants, phytochrome and blueabsorbing pigments (BAPs). Phytochrome was most sensitive to red light and far-red light, while BAPs are influenced by B and ultraviolet-A (UV-A) light spectrum (Moe and Heins, 1990). Both light quantity of photon flux and wavelength were very important for plant growth and development (Moshe and Dalia, 2007).…”
Section: Introductionmentioning
confidence: 99%
“…The flowers apparently became a progressively larger sink for dry matter during development (Cockshull and Hughes 1968) and newly produced dry matter as well as reallocation from other plant parts (Fig. 3) (Erwin et al 1989;Moe and Heins 1990) including C. monfolium Karlsson and Heins 1986 Although plant dry matter at flowering varied from 3.6 to l'l .2 g and the number of SD to flower from 60 to 120 (Table 1), dry matter accumulation in roots, stems and leaves on a relative scale was similar.…”
mentioning
confidence: 99%