1994
DOI: 10.2307/2445453
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Carbon Integration in Plantago aristata (Plantaginaceae): The Reproductive Effects of Defoliation

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Cited by 5 publications
(7 citation statements)
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References 34 publications
(56 reference statements)
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“…Support for the hypothesis that tolerance to defoliation in annuals increases from the vegetative rosette stage to the reproductive stage has previously been obtained in greenhouse experiments with A. thaliana [33] but see [28], Plantago aristata [17], Raphanus sativus [16], Sesbania macrocarpa and S. vesicaria [15], and in a field study of Ipomoea purpurea [13]. In contrast, no evidence of an ontogenetic increase in tolerance to defoliation was observed in a greenhouse experiment with Senecio vulgaris [34], or in a field study of Cucurbita pepo [35].…”
Section: Discussionmentioning
confidence: 69%
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“…Support for the hypothesis that tolerance to defoliation in annuals increases from the vegetative rosette stage to the reproductive stage has previously been obtained in greenhouse experiments with A. thaliana [33] but see [28], Plantago aristata [17], Raphanus sativus [16], Sesbania macrocarpa and S. vesicaria [15], and in a field study of Ipomoea purpurea [13]. In contrast, no evidence of an ontogenetic increase in tolerance to defoliation was observed in a greenhouse experiment with Senecio vulgaris [34], or in a field study of Cucurbita pepo [35].…”
Section: Discussionmentioning
confidence: 69%
“…There is some support for the predictions that leaf damage early in the season is more detrimental than damage late in the season, e.g. [13], [15], [16], and that the components of fitness most affected by herbivory shift along ontogeny in annual plants [17]. However, because responses to herbivory may often be context-dependent [7], [9], [11] and most studies of seasonal changes in tolerance to leaf herbivory have been conducted in the greenhouse rather than in the field, e.g.…”
Section: Introductionmentioning
confidence: 89%
“…Leaf removal moderately aected the number of seeds produced by early¯owers, but again these decreases in both fruit and seed set could not be ascribed to changes in pollination levels. In general, seed output in A. aurea seems to be well buered against damage to leaves close to the in¯orescence (Aizen and Raaele 1996), which contrasts with ®ndings for other species in which the removal of even small portions of leaves subtending in¯orescences may lead to strong eects on reproduction (Marquis 1988(Marquis , 1992Horton and Lacey 1994; but see Obeso and Grubb 1993). It might well be that rhizomes, specialized starch-storing roots, or even associated vegetative shoots (Bayer 1987) are important sources of carbohydrates and nutrients for reproduction in A. aurea in addition to the resources provided locally by the¯owering shoots themselves.…”
Section: Discussionmentioning
confidence: 85%
“…In one (Plantago virginica), the reproductive metamers are integrated by ~4C-assimilate transport, whereas in the other (P. aristata), the reproductive metamers appear to be quite independent with respect to carbon assimilated by neighbouring metamers, and so can be regarded as IPUs (Lacey & Marshall 1992). The latter conclusion is further supported by the response of individual metamers of P. aristata to defoliation, following which their reproductive performance is significantly reduced, thereby indicating the inability of the spike to be supplied with a significant amount of assimilate from adjacent metamers to buffer the local shortfall (Horton & Lacey 1994). It would therefore appear that adjacent reproductive metamers of this species are not connected by functional phloem, but this needs to be verified by anatomical investigation.…”
Section: Shoots and Branchesmentioning
confidence: 90%