1973
DOI: 10.1111/j.1399-3054.1973.tb01187.x
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Studies on the Flowering Mechanism in Lemna

Abstract: A nitrogen source was needed for the flowering of Lemna gibba L., a long‐day plant, and L. perpusilla Torr., a shortday plant. The level of endogenous amino acids analyzed by an Amino Acid Analyzer, rose during the first few inductive cycles, but was reduced during later stages of the flowering process. Serine and threonine levels increased during the light period and decreased during the dark period in L. perpusilla. Exogenous serine and threonine added to the culture medium at 10−6M increased the rate of flo… Show more

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Cited by 53 publications
(26 citation statements)
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“…The only exception, terbuthylazine (log K ow : 3.2)25 showed EC 50 values comparable with those obtained on the basis of measured terbuthylazine concentrations 26. The L. minor plants were collected in Copenhagen in 1999, surface sterilised with hypochlorite and the resulting sterile clone was kept in Ehrlenmeyer flasks in ‘K’‐medium,27 pH 5, at 24 °C and a continuous photon flux density of 85–120 µmol m −2 s −1 photosynthetic active radiation (PAR). The flasks and medium were sealed with cotton wool and autoclaved before the weekly transfer of plants to new media.…”
Section: Methodssupporting
confidence: 59%
“…The only exception, terbuthylazine (log K ow : 3.2)25 showed EC 50 values comparable with those obtained on the basis of measured terbuthylazine concentrations 26. The L. minor plants were collected in Copenhagen in 1999, surface sterilised with hypochlorite and the resulting sterile clone was kept in Ehrlenmeyer flasks in ‘K’‐medium,27 pH 5, at 24 °C and a continuous photon flux density of 85–120 µmol m −2 s −1 photosynthetic active radiation (PAR). The flasks and medium were sealed with cotton wool and autoclaved before the weekly transfer of plants to new media.…”
Section: Methodssupporting
confidence: 59%
“…Concentrations were the same as those used for the algae test and were chosen on the basis of preliminary tests. Artemisinin was dissolved in acetone, and 250 μl of this solution were added to 0.5 L of growth medium prepared according to the method described by Maeng and Khudairi [33]. The solution was magnetically stirred and acetone allowed to evaporate for 3 h. The L. minor plants (type UTCC 490) were purchased from Judy Acreman, University of Toronto Culture Collection of Algae and Cyanobacteria (Toronto, ON, Canada), and were kept aseptically in Erlenmeyer flasks in growth medium at 24°C, pH 5, and a continuous photon flux density of 85 to 120 μmol/m 2 /s of PAR.…”
Section: Methodsmentioning
confidence: 99%
“…Lemna minor was collected from a local pond in Copenhagen, Denmark in 1999. The plants were surface sterilized according to Landolt and Kandeler16 and the clone has since then been kept in Ehrlenmeyer flasks in ‘K’‐medium,17 pH 5, at 24 °C and a continuous photon flux density of 85–120 µmol m −2 s −1 (photosynthetically active range; PAR). The flasks and medium are sealed with cotton wool and autoclaved before the weekly transfer of plants to new media.…”
Section: Methodsmentioning
confidence: 99%