1935
DOI: 10.2307/2435957
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The Inter-Relations of Catalase, Respiration, After-Ripening, and Germination in Some Dormant Seeds of the Polygonaceae

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Cited by 11 publications
(8 citation statements)
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“…Within the dormancy release range determined in this work, the relationship between the dormancy release rate and temperature was logistic, with only a slight decrease in the rate of dormancy release between 2 and 10°C, and an abrupt reduction in this rate between 10 and 20°C. This result again agrees with observations made by Ransom (1935) who determined that optimum dormancy release temperature for seeds of various Polygonum spp. were between 3 to 6°C, and with temperature‐dependent dormancy release rates determined by Vleeshouwers and Bouwmeester (2001) for Polygonum persicaria , in which dormancy release was maximum at 1.8°C and minimum at 15.5°C.…”
Section: Discussionsupporting
confidence: 93%
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“…Within the dormancy release range determined in this work, the relationship between the dormancy release rate and temperature was logistic, with only a slight decrease in the rate of dormancy release between 2 and 10°C, and an abrupt reduction in this rate between 10 and 20°C. This result again agrees with observations made by Ransom (1935) who determined that optimum dormancy release temperature for seeds of various Polygonum spp. were between 3 to 6°C, and with temperature‐dependent dormancy release rates determined by Vleeshouwers and Bouwmeester (2001) for Polygonum persicaria , in which dormancy release was maximum at 1.8°C and minimum at 15.5°C.…”
Section: Discussionsupporting
confidence: 93%
“…Dormancy induction of Polygonum spp. seeds at temperatures between 20 and 25°C have been previously reported by other authors (Ransom, 1935; Courtney, 1968; Kruk & Benech‐Arnold, 1998; Batlla et al. , 2003; Batlla & Benech‐Arnold, 2004).…”
Section: Discussionsupporting
confidence: 75%
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“…These mechanisms do not reside in the embryo which develops at constant temperatures. The stimulatory effects of alternating temperatures on seed germination in some species have been attributed to increased permeability of the seed coat to water and gases, or to sufficient weakening of the integuments to permit the embryo to enlarge and rupture the coats (Crocker, 1906;Morinaga, 1926;Ransom, 1935;Thornton, 1945;Porter, 1949;Toole et al, 1956;Griesbach and Voth, 1957). These mechanisms do not appear to be involved in seeds of M. balbisiana, inasmuch as maximum imbibition by intact seeds occurs in approximately 3 days, and seeds mechanically scarified imbibe the same amount of water after approximately 2 days (unpublished data).…”
mentioning
confidence: 99%
“…High temperatures are usually responsible for the destruction of inhibitors in plants (Evenari, 1949), although in some seeds their accumulation is retarded by low temperatures (Thornton, 1945;Ransom, 1935;Went, 1953). The synthesis and activity of some plant enzymes, e.g., the mobilization of carbohydrates and proteins in the seed of Heracleum sphondylium L. (Stokes, 1953), and starch hydrolysis and phosphorylase activity in potato tubers (Arreguin-Lozana and Bonner, 1949), are usually greater [AVol.…”
mentioning
confidence: 99%