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Studies on foliar abscissionSullivan, William James, 1926- January 1954 (has links)
No description available.
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Use of ethephon in abscissionMayhenmahr, S. Wakeel January 2010 (has links)
Typescript (photocopy). / Digitized by Kansas Correctional Industries
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Abscission of flowers and fruits in the S̲o̲l̲a̲n̲a̲c̲e̲a̲e̲, with special reference to N̲i̲c̲o̲t̲i̲a̲n̲a̲Kendall, John Norman, January 1900 (has links)
Thesis (Ph. D.)--University of California, 1917. / Cover title. University of California publications in botany, v. 5, no. 12, March 6, 1918, with a special thesis t.p. dated May, 1917, attached to the cover-title. "Literature cited": p. 418-419.
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BOLL ABSCISSION AND FIBER PROPERTIES IN UPLAND COTTON AS INFLUENCED BY NITROGEN, MOISTURE, AND GIBBERELLIC ACID TREATMENTSMillhollon, Rex, 1931- January 1961 (has links)
No description available.
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Regulation of plant development in ArabidopsisLarue, Clayton T., January 2008 (has links)
Thesis (Ph. D.)--University of Missouri-Columbia, 2008. / The entire dissertation/thesis text is included in the research.pdf file; the official abstract appears in the short.pdf file (which also appears in the research.pdf); a non-technical general description, or public abstract, appears in the public.pdf file. Title from title screen of research.pdf file (viewed on June 19, 2009) Includes bibliographical references.
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The role of ethylene in fruit and petal abscission in the red raspberry (Rubus idaeus L. cv. Glen Clova)Burdon, Jeremy N. January 1987 (has links)
Weakening of fruit and petal abscission zones in Rubus idaeus L. cv. Glen Clova was accompanied by increased rates of ethylene production. Both processes were accelerated by a supply of exogenous ethylene. In the ripe fruit natural ethylene levels were saturating. The rise in ethylene production clearly preceded petal abscission but in fruit the increase virtually coincided with the start of weakening. Raspberry fruit of other varieties and blackberries clearly showed the abscission zone weakening could precede any increase in ethylene production. The internal ethylene concentrations of Glen Clova fruit at the mottled stage reached those levels which had to be added to stimulate abscission (ie 0.25 to 0.5 ppm). This is the very stage at which abscission zone weakening was first noticeable. Both fruit and petal abscission was retarded by the application of inhibitors of ethylene production ( AVG, Co 2+) or action (Ag+ ). Likewise a reduction in the internal ethylene under hypobaric pressure also retarded fruit abscission. None of these treatments were totally capable of preventing abscission. In fruit abscission the receptacle appears to have an important role. The increase in receptacle ethylene production precedes that of the drupelets. The enlargement and swelling of the receptacle tissues are important in both abscission zone weakening and ethylene production. This receptacle development may in turn be controlled by the development of fertilised drupelets. The ethylene production in both fruit and petal abscission is limited initially by the supply of ACC. In both cases endogenous ACC levels increase in step with ethylene production. Ethylene's role as a coordinating/accelerating agent in fruit and petal abscission is discussed.
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Photocontrol of leaf abscission.Decoteau, Dennis Roger 01 January 1982 (has links) (PDF)
No description available.
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Photocontrol of the abscission process in apple fruit.Brooks, Carolyn Anne 01 January 1980 (has links) (PDF)
No description available.
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Leaf senescence and water stress in wheat seedlings /French, Robert John. January 1985 (has links) (PDF)
Thesis (Ph. D.)--University of Adelaide, Dept. of Plant Physiology, 1985. / Includes bibliographical references (leaves 245-271).
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Apple fruit nonstructural carbohydrates and abscission as influenced by shade and terbacilPolomski, Robert January 1986 (has links)
The theory that fruit abscission may be the result of a reduction in metabolites available to the young fruit was addressed by this study. Shade cloth or terbacil, a photosynthetic inhibitor, were applied to limbs and whole trees to examine the influence of treatment and time of application on fruit nonstructural carbohydrates and abscission.
'Stayman' apple limbs shaded with 92% shade material from 5-15, 10-20, 15-25, 20-30, and 25-35 days after full bloom (April 22) had lower fruit retention than unshaded controls on 11 June. On 18 June, fruit diameter was greater on limbs shaded between 5-25 days after full bloom (DAFB) than on unshaded limbs. At 15, 20, 25, and 30 DAFB, fruit from limbs shaded for 10 days had lower total nonstructural carbohydrates (TNC), total sugars, and reducing sugars (% dry wt) than fruit from limbs shaded for 0 or 5 days.
Terbacil (3-tert-butyl-5-chloro-6-methyluracil) was applied at 0, 50, 100, and 200 ppm to whole nine-year-old 'Redchief Delicious' apple trees at 15 DAFB. Terbacil markedly inhibited Pn; recovery occurred by 9 and 26 DAA for the 50 and 100 ppm rates, respectively. Phytotoxicity prevented the determination of Pn in the 200 ppm treated trees. Fruit dry weight, TNC, total sugars, and reducing sugars (% dry wt and mg/fruit) declined with increasing rates of terbacil. Total fruit abscission was observed 12 DAA for the 100 and 200 ppm treatments, while the 0 and 50 ppm applications retained 4.6 and 1.4 fruit per cm² limb cross sectional area (LCSA) at 35 DAA, respectively. Compared to the control, 50 ppm terbacil decreased fruit number and weight at harvest, but increased fruit weight.
Terbacil at 75 ppm and 92% shade material were applied to whole, 3-year-old 'Redchief Delicious' trees at 18, 23, and 28 DAFB. Generally, fruit dry weight, total sugars, and reducing sugars were lowered by both shade and terbacil treatments. In most cases, fruit from shaded trees were lower in dry weight and measured nonstructural carbohydrates than fruit from terbacil-treated trees after 5 or 10 days of treatment. Shading for 5 or 10 days resulted in total fruit drop. Terbacil at 75 ppm resulted in 0.8 as opposed to 2.9 fruit per cm² LCSA on the controls at 54 DAFB. / M.S.
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