1982
DOI: 10.1111/j.1469-8137.1982.tb03360.x
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ABSCISIC ACID EFFECTS ON SPORE GERMINATION AND PROTONEMAL GROWTH IN THE FERN, MOHRIA CAFFRORUM

Abstract: SUMMARYThe effects of abscisic acid (ABA) and its interaction with gibbereOic acid (GA), indoleacetic acid (IAA) and kinetin on the germination of spores and growth of protonemata of the fern, Mohria caffrorum Sw. -were studied. ABA did not affect the initial divisions of the spore protoplast leading to the formation of rhizoid and protonenna, but inhibited the subsequent elongation of the latter. The apparent reversal of ABA-induced inhibition of protonemal elongation by GA appears to be due to an overall gro… Show more

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Cited by 18 publications
(8 citation statements)
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“…ABA is present in the gametophytic tissues such as spores and filamentous gametophytes of Anemia phyllitidis (Bürcky, 1977;Cheng and Schraudolf, 1974). ABA inhibits the elongation of protonema in Mohria caffrorum, the formation of adventitious gametophytes from nonmeristematic explants of A. phyllitidis and antheridiogeninduced antheridia formation in Ceratopteris richardii (Chia and Raghavan, 1982;Hickok, 1983;Reynolds, 1981). ABA induces the land form of morphological characteristics in the plants of Marsilea quadrifolia (Lin, 1984).…”
Section: Phytohormones In Pteridophytes and Their Rolementioning
confidence: 99%
“…ABA is present in the gametophytic tissues such as spores and filamentous gametophytes of Anemia phyllitidis (Bürcky, 1977;Cheng and Schraudolf, 1974). ABA inhibits the elongation of protonema in Mohria caffrorum, the formation of adventitious gametophytes from nonmeristematic explants of A. phyllitidis and antheridiogeninduced antheridia formation in Ceratopteris richardii (Chia and Raghavan, 1982;Hickok, 1983;Reynolds, 1981). ABA induces the land form of morphological characteristics in the plants of Marsilea quadrifolia (Lin, 1984).…”
Section: Phytohormones In Pteridophytes and Their Rolementioning
confidence: 99%
“…Microarray analysis of spore germination in the fern Ceratopteris implicated involvement of GA signalling and downregulation of ABA signalling in this process, similarly to seeds (Yao et al, 2008). However, different fern species' spores have different sensitivities to GA and ABA application (Weinberg & Voeller, 1969;Chia & Raghavan, 1982;Singh et al, 1990;Kagawa & Michizo, 1991;Haas et al, 1992). The GA biosynthesis inhibitor AMO-1618, which blocks the first step(s) in the GA biosynthesis pathway (Rademacher, 2000), can inhibit some (but not all) light-induced fern spore germination (Weinberg & Voeller, 1969;Nester & Coolbaugh, 1986;Kagawa & Michizo, 1991).…”
Section: Introductionmentioning
confidence: 99%
“…It has been shown that ABA is present in various fern species (Weiler 1979;Cheng and Schraudolf 1974;Yamane et al 1980Yamane et al , 1988Pilate et al 1989) and in some lycophytes. In ferns, ABA plays roles in inhibition of growth (Swami and Raghavan 1980;Chia and Raghavan 1982;Hickok 1983), control of sex determination (Hickok 1983;Warne and Hickok 1991), and heterophyllous switch in aquatic fern plants (Liu 1984;Hsu et al 2001;Lin et al 2005). In addition, ABA is thought to play a role in desiccation tolerance in ferns and lycophytes (Reynolds and Bewley 1993a, b;Pence 2000;Liu et al 2008).…”
Section: Introductionmentioning
confidence: 99%