1974
DOI: 10.2307/2442023
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Spore Wall Formation and Chloroplast Development During Sporogenesis in the Moss Fissidens limbatus

Abstract: The sequence of wall formation in spores of Fissidens limbatus Sullivant is as follows: The exine is formed around the protoplasts after the sporocyte has undergone meiosis. The fully enlarged spores then become coated by the perine; this is followed by intine formation. The source of the intine and exine appears to be from within the spore, but the perine is of an apparent exogenous origin. Ornamentation of the spore is due solely to deposition of the perine. Each spore originally has a single plastid. Plasti… Show more

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Cited by 14 publications
(14 citation statements)
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References 16 publications
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“…McClymont and Larson (1964) observed a separating layer in spore walls of each of the mosses they examined and they determined that this layer is not an artifact of the fixation process. A similar separating layer also has been identified recently in the spore wall of the moss Fissidens limbatus (Mueller, 1974). Whether or not this part of the wall represents the inner region of the exine as proposed by McClymont and Larson (1964) or the outer region of the intine as Mueller (1974) suggested is still unknown.…”
supporting
confidence: 59%
“…McClymont and Larson (1964) observed a separating layer in spore walls of each of the mosses they examined and they determined that this layer is not an artifact of the fixation process. A similar separating layer also has been identified recently in the spore wall of the moss Fissidens limbatus (Mueller, 1974). Whether or not this part of the wall represents the inner region of the exine as proposed by McClymont and Larson (1964) or the outer region of the intine as Mueller (1974) suggested is still unknown.…”
supporting
confidence: 59%
“…O esporoderma apresentou os três estratos mais freqüentes em musgos: perina, exina e intina e esta última camada foi perdida durante o processo de acetólise. Estes resultados comprovam as descrições de outros autores como Mueller (1974), Olensen & Mogensen (1978), Mogensen (1978Mogensen ( , 1981, Neidhart (1979), Brown & Lemmon (1984a, 1984b que analisaram a esporogênese de diferentes espécies de musgos e concluíram a presença dos três estratos acima citados na parede dos esporos.…”
Section: Discussionunclassified
“…Uehara & Kurita (1991), señalan que en Lycopodium los esporocitos se encuentran densamente empaquetados en el tejido esporógeno de la cavidad esporangial y se comunican entre sí por medio de la cubierta mencionada; a medida que maduran, la cubierta se disuelve permitiendo la liberación de los esporocitos premeióticos en el fluido de la cavidad esporangial. Esta condición también se observó en H. brevifolia y ha sido registrada para algunos briófitos (Mueller 1974). En Lycopodiella, en cambio, la cubierta original de los esporocitos persiste durante todo el proceso de esporogénesis, lo que podría sugerir que no es tan importante para el transporte de materiales precursores que formarán la pared de las esporas, y que existirían otros mecanismos de transporte entre el tapete y aquellas (Rincón Barón et al, en prep.).…”
Section: Discussionunclassified
“…En Lycopodiella, en cambio, la cubierta original de los esporocitos persiste durante todo el proceso de esporogénesis, lo que podría sugerir que no es tan importante para el transporte de materiales precursores que formarán la pared de las esporas, y que existirían otros mecanismos de transporte entre el tapete y aquellas (Rincón Barón et al, en prep.). Mueller (1974), observó que la degradación de la cubierta de los esporocitos en Fissidens limbatus Sullivant los prepara para la meiosis posterior y facilita el proceso de transporte entre el tapete y las esporas. Según Uehara & Kurita (1991) esto se cumple para L. clavatum.…”
Section: Discussionunclassified