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  • 1
    Electronic Resource
    Electronic Resource
    s.l. : American Chemical Society
    Analytical chemistry 50 (1978), S. 1474-1479 
    ISSN: 1520-6882
    Source: ACS Legacy Archives
    Topics: Chemistry and Pharmacology
    Type of Medium: Electronic Resource
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  • 2
    Electronic Resource
    Electronic Resource
    s.l. : American Chemical Society
    Industrial & engineering chemistry 18 (1926), S. 433-433 
    ISSN: 1520-5045
    Source: ACS Legacy Archives
    Topics: Chemistry and Pharmacology , Process Engineering, Biotechnology, Nutrition Technology
    Type of Medium: Electronic Resource
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  • 3
    Electronic Resource
    Electronic Resource
    Oxford, UK : Blackwell Publishing Ltd
    Weed research 15 (1975), S. 0 
    ISSN: 1365-3180
    Source: Blackwell Publishing Journal Backfiles 1879-2005
    Topics: Agriculture, Forestry, Horticulture, Fishery, Domestic Science, Nutrition
    Notes: Glyphosate was applied to Cyperus rotundus L. in combination with a range of other herbicides and certain non-herbicidal additives. Most herbicides tended to have an antagonistic effect with glyphosate, especially those which inhibit photosynthesis. On the other hand 2,4-D amine and aminotriazole showed at least additive and sometimes synergistic effects. Striking activation was obtained with ammonium sulphate added at rates between 1·25 and 10 kg/ha. Other compounds causing almost equal activation were several ammonium phosphates, ammonium butyl-phosphate and urea. The activity of glyphosate on C. rotundus was considerably greater when applied 3 weeks after planting than at 9 weeks. The activation was also greater at 3 weeks but was still apparent at 9 weeks.Lutte contre le Cyperus rotundus avec el glyphosate: influence du sulfate d’ammonium et d'autres adjuvantsLe glyphosate a été appliqué au Cyperus rotundus L. en association avec une série d'autres herbicides et certains adjuvants non-herbicides. La plupart des herbicides manifestèrent un effet antagoniste avec le glyphosate, particulièrement ceux qui inhibent la photosynthèse. D'autre part, le 2,4-D sel d'amine et l'aminotriazole montrérent des effets au moins additifs et quelquefois synergiques. Une activation frappante fut obtenue avec le sulfate d'ammonium ajoutéà des doses comprises entre 1,25 et 10 kg/ha. D'autres produits ont provoqué une activation à peu près équivalente: plusieurs phosphates d'ammonium, le butylphosphate d'ammonium et l'urée. L'efficacité du glyphosate sur C. rotundus a été considérablement plus élevée lorsqu'il a été appliqué 3 semaines après plantation, au lieu de 9 semaines. L'activation fut aussi plus grande à 3 semaines, mais était encore apparente à 9 semaines.Bekämpfung von Cyperus rotundus mit Glyphosate: Der Einfluss von Ammoniumsulfat und anderen Zusätzen Cyperus rotundus L. wurde mit Glyphosate in Kombination mit einer Reihe anderer Herbizide und bestimmter nicht-herbizider Zusätze behandelt. Die meisten Herbizide zeigten mit Glyphosate die Tendenz einer antagonistischen Wirkung, insbesondere solche, die die Photosynthese hemmen. Andererseits wirkten 2,4-D-Amin und Aminotriazol zumindest additiv und manchmal auch synergistisch. Eine beeindruckende Aktivierung wurde mit Ammoniumsulfat bei Aufwandmengen zwischen 1·25 und 10 kg/ha erreicht. Andere Verbindungen, die eine fast gleichwertige Aktivierung bewirkten, waren verschiedene Ammoniumphosphate, Ammoniumbutylphosphat und Harnstoff. Die Aktivität von Glyphosate war beträchtlich höher, wenn es 3 Wochen, statt 9 Wochen nach dem Pflanzen angewendet wurde. Die Steigerung war zwar nach 3 Wochen grösser, war aber auch noch nach 9 Wochen festzustellen.
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  • 4
    Electronic Resource
    Electronic Resource
    Oxford, UK : Blackwell Publishing Ltd
    Weed research 13 (1973), S. 0 
    ISSN: 1365-3180
    Source: Blackwell Publishing Journal Backfiles 1879-2005
    Topics: Agriculture, Forestry, Horticulture, Fishery, Domestic Science, Nutrition
    Type of Medium: Electronic Resource
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  • 5
    Electronic Resource
    Electronic Resource
    Oxford, UK : Blackwell Publishing Ltd
    Weed research 16 (1976), S. 0 
    ISSN: 1365-3180
    Source: Blackwell Publishing Journal Backfiles 1879-2005
    Topics: Agriculture, Forestry, Horticulture, Fishery, Domestic Science, Nutrition
    Notes: A series of synthetic germination stimulants for the plant parasites Striga and Orobanche has been prepared. These compounds, analogues of the natural Striga germination stimulant, strigol (I), (Cook et al., 1966, 1972) cause signiticant germination of Striga hermonthica (Del.) Benth. seed at concentrations as low as 10−9 M, and an even greater activity against species of Orobanche has been demonstrated. Initial outdoor box trials of the compounds against Striga asiatica (L.) O. Ktze. in Hyderabad, India, have shown a reduction of up to 65% of the seed after a single treatment of the soil 6 weeks before the planting of the sorghum host.
    Type of Medium: Electronic Resource
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  • 6
    Electronic Resource
    Electronic Resource
    Oxford, UK : Blackwell Publishing Ltd
    Annals of the New York Academy of Sciences 200 (1972), S. 0 
    ISSN: 1749-6632
    Source: Blackwell Publishing Journal Backfiles 1879-2005
    Topics: Natural Sciences in General
    Type of Medium: Electronic Resource
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  • 7
    Electronic Resource
    Electronic Resource
    Oxford, UK : Blackwell Publishing Ltd
    Physiologia plantarum 27 (1972), S. 0 
    ISSN: 1399-3054
    Source: Blackwell Publishing Journal Backfiles 1879-2005
    Topics: Biology
    Notes: Certain 6-acylaminopurines have been shown to exhibit activity in several cytokinin bioassays. The active compunds included 6-N,2′-O-dibutyryladenosine 3’:5′-cyclic monophosphate, but adenosine 3′:5′-cyclic monophosphate was inactive. The metabolites formed from [2,8-3H] 6-benzoylaminopurine by radish seedlings and excised radish cotyledons were investigated. When compared with zeatin, this amide showed considerable stability in vivo. Conversion to 6-benzylaminopurine and its riboside was not detected but slight degradation to adenine was indicated. The principal metabolite was an unidentified compund.
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  • 8
    Electronic Resource
    Electronic Resource
    Springer
    Planta 146 (1979), S. 71-74 
    ISSN: 1432-2048
    Keywords: Cytokinin metabolism ; Phaseolus
    Source: Springer Online Journal Archives 1860-2000
    Topics: Biology
    Notes: Abstract 6-[3H]Benzylaminopurine was supplied through the transpiration stream to de-rooted Phaseolus vulgaris L. seedlings. The principal metabolite formed was identified as β-(6-benzylaminopurin-9-yl)alanine by comparison with the synthetic compound.
    Type of Medium: Electronic Resource
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  • 9
    ISSN: 1432-2048
    Keywords: Cytokinin metabolism ; O-glucosylzeatin ; Lupinic acid ; Lupinus
    Source: Springer Online Journal Archives 1860-2000
    Topics: Biology
    Notes: Abstract [3H]zeatin was supplied through the transpiration stream to de-rooted lupin (Lupinus angustifolius L.) seedlings. The following previously known metabolites were identified chromatographically: 5′-phosphates of zeatin riboside and dihydrozeatin riboside, adenosine-5′-phosphate, zeatin riboside, zeatin-7-glucopyranoside, zeatin-9-glucopyranoside, adenine, adenosine and dihydrozeatin. Five new metabolites were purified; four of these contain an intact zeatin moiety. Two were identified unequivocally, one as l-β-[6-(4-hydroxy-3-methylbut-trans-2-enylamino)-purin-9-yl]alanine, a metabolite now termed lupinic acid, and the second as O-β-d-glucopyranosylzeatin. These two compounds were the major metabolites formed when zeatin solution (100 μM) was supplied to the de-rooted seedlings. The radioactivity in the xylem sap of intact seedlings, supplied with [3H]zeatin via the roots, was largely due to zeatin, dihydrozeatin and zeatin riboside. When [3H]zeatin (5 μM) was supplied via the transpiration stream to de-rooted Lupinus luteus L. seedlings, the principal metabolite in the lamina was adenosine, while in the stem nucleotides of zeatin and adenine were the dominant metabolites. O-Glucosylzeatin and lupinic acid were also detected as metabolites. The level of the latter varied greatly in the tissues of the shoot, and was greatest in the lower region of the stem and in the expanding lamina. Minor metabolites also detected chromatographically were: (a) dihydrolupinic acid, (b) a partially characterized metabolite which appears to be a 9-substituted adenine (also formed in L. angustifolius), (c) glucosides of zeatin riboside and/or dihydrozeatin riboside, and (d) O-glucosyldihydrozeatin. While lupinic acid supplied exogenously to L. luteus leaves underwent little metabolism, chromatographic studies indicated that O-glucosylzeatin was converted to its riboside, the principal metabolite formed, and also to adenosine, zeatin and dihydrozeatin. A thinlayer chromatography procedure for separating zeatin, dihydrozeatin, zeatin riboside and dihydrozeatin riboside is described.
    Type of Medium: Electronic Resource
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  • 10
    Electronic Resource
    Electronic Resource
    Springer
    Planta 114 (1973), S. 199-218 
    ISSN: 1432-2048
    Source: Springer Online Journal Archives 1860-2000
    Topics: Biology
    Notes: Summary [3H]Zeatin was supplied through the transpiration stream to radish (Raphanus sativus L.) seedlings with roots excised. Formation of dihydrozeatin was not detected but numerous other metabolites were formed, including adenine, adenosine, AMP, zeatin riboside and zeatin riboside-5′-monophosphate. However, in labelled seedlings which had been left in water for 15 h, an unknown compound (raphanatin) was the dominant metabolite and accounted for about 25% of the total radioactivity extracted. A procedure for the isolation of this metabolite was devised and yielded 70 μg from 1600 seedlings. Raphanatin was characterized by mass and ultraviolet spectra and has been identified as 7-glucosylzeatin. It is an active and very stable metabolite which was located mainly in the cotyledon laminae and may be a storage form of the hormone. In contrast, labelled nucleotides, the other major metabolites of zeatin, were largely confined to the hypocotyls and petioles. Zeatin riboside-5′-monophosphate was the dominant metabolite in hypocotyls of de-rooted seedlings supplied with zeatin for 0.5–2 h. The majority of the radioactivity in the xylem sap was due to zeatin, but about 10% was present as zeatin riboside; nucleotides accounted for less than 10% of the radioactivity and labelled raphanatin was not detected.
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