Results 161 to 170 of about 7,897 (203)
The effect of picloram on clover
Proceedings of the New Zealand Weed and Pest Control Conference, 1965 openaire +2 more sources
Characterisation and Expression Analysis of LdSERK1, a Somatic Embryogenesis Gene in Lilium davidii var. unicolor. [PDF]
Plants (Basel)Wang S +11 more
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Enhancing Sensitivity and Selectivity: Current Trends in Electrochemical Immunosensors for Organophosphate Analysis. [PDF]
Biosensors (Basel)Shen Y, Zhao S, Chen F, Lv Y, Fu L.
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Environmental Toxicology and Chemistry, 1984
Abstract The toxicity of technical picloram acid (93.8% active ingredient), picloram potassium salt (43.5% active ingredient) and picloram triisopropanolamine salt (65.2% active ingredient) to aquatic organisms was evaluated in static acute toxicity tests.
Monte A. Mayes, D. C. Dill
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Abstract The toxicity of technical picloram acid (93.8% active ingredient), picloram potassium salt (43.5% active ingredient) and picloram triisopropanolamine salt (65.2% active ingredient) to aquatic organisms was evaluated in static acute toxicity tests.
Monte A. Mayes, D. C. Dill
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Photochemical Degradation of Picloram
Pesticide Science, 1982AbstractThe rate of photochemical degradation of aqueous solutions of picloram under ultraviolet light was measured by five different methods of analysis. These were chosen to assay the loss of picloram, dechlorination, alteration or loss of the aromatic amino group, loss of aromaticity, and decarboxylation.
James R. Gear +2 more
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Journal of Agricultural and Food Chemistry, 1988
Mecanisme de l'elimination du piclorame dans les eaux souterraines par formation de complexes de nickel II et fer II insolubles dans l ...
Hope Heaster Michaud, Patrick E. Hoggard
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Mecanisme de l'elimination du piclorame dans les eaux souterraines par formation de complexes de nickel II et fer II insolubles dans l ...
Hope Heaster Michaud, Patrick E. Hoggard
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Soil Science Society of America Journal, 1974
Abstract Picloram (4‐amino‐3,5,6‐trichloropicolinic acid) adsorption‐desorption isotherms were derermined on six western USA soils. Adsorption isotherms were determined as a function of temperature, soil/solution ratio, and solution ionic strength.
W. J. Farmer, Y. Aochi
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Abstract Picloram (4‐amino‐3,5,6‐trichloropicolinic acid) adsorption‐desorption isotherms were derermined on six western USA soils. Adsorption isotherms were determined as a function of temperature, soil/solution ratio, and solution ionic strength.
W. J. Farmer, Y. Aochi
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Herbicide Analysis by Pulse Polarography-Picloram
International Journal of Environmental Analytical Chemistry, 1973Abstract The herbicide picloram, 4-amino-3,5,6-trichloro-picolinic acid, can be determined at 0.02 ppm, without concentration, by pulse polarography. The effects of pH, ionic strength, and buffer constituents on the catalytic hydrogen process have been studied to optimize conditions for highest sensitivity for picloram.
D D, Gilbert, J M, Mann
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Journal of Toxicology and Environmental Health, 1981
Two studies of the carcinogenicity of the herbicide picloram in animals were reviewed. Examination of histological sections showed that picloram is highly carcinogenic in rats and mice. Neoplasms at all sites, including malignant neoplasms, were increased in male and female rats given both low and high doses of picloram in the National Cancer Institute
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Two studies of the carcinogenicity of the herbicide picloram in animals were reviewed. Examination of histological sections showed that picloram is highly carcinogenic in rats and mice. Neoplasms at all sites, including malignant neoplasms, were increased in male and female rats given both low and high doses of picloram in the National Cancer Institute
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Subcellular Distribution of Picloram
Physiologia Plantarum, 1973AbstractGas chromatographic and radioisotopic analyses were made of cell wall, chloroplast, mitochondria and the remaining cytoplasm fractions of cowpea (Vigna sinensis Endl. cv. Southern Blackeye) trifoliates acropetal to primary leaves treated with the growth regulator 4‐amino‐3,5,6‐trichloro‐picolinic acid (picloram).
J. R. BAUR, J. J. BOWMAN
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