The DOI matches its Crossref record; 2 of the 2 references it cites were found in a registry or an index.
pH-Regulated Leaf Cell Expansion in Droughted Plants Is Abscisic Acid Dependent
Open accessAbstract
Elongation rates of barley (Hordeum vulgare L. cv Hanna) leaves decreased with decreasing soil water content, whereas the pH of xylem sap increased from 5.9 to 6.9 over 6 d as the soil dried. The reduction in leaf-elongation rate (LER) was correlated with the increase in sap pH. Artificial sap buffered to different pH values was fed via the subcrown internode to derooted seedlings. Although leaves elongated at in planta rates when fed artificial sap at a well-watered pH of 6.0, LER declined with increasing sap pH. This effect persisted in the light and in the dark. pH had no effect on the relative water content or the bulk abscisic acid (ABA) concentration of the growing zone of these leaves. LERs of the ABA-deficient mutant Az34 were uniformly high over the pH range tested, whereas those of its isogenic wild-type cultivar Steptoe were reduced as the artificial sap pH was increased from 6.0 to 7.0. However, supplying a well-watered concentration of ABA (3 × 10−8 m) in the artificial xylem sap restored the pH response of the Az34 mutant. The results suggest that increased xylem sap pH acts as a drought signal to reduce LER via an ABA-dependent mechanism.
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Citations
Cites
Plant productivity and environment
Boyer, J. S. (1982) · Science · doi:10.1126/science.218.4571.443 · Cited by 3,959
Climate and the efficiency of crop production in Britain
Monteith, J. L. (1977) · Philosophical Transactions of the Royal Society of London. B, Biological Sciences · doi:10.1098/rstb.1977.0140 · Cited by 3,484 · cited 1×
“The direct relationship between crop yield and the rate of leaf production and expansion (Monteith, 1977), coupled with the high sensitivity of the leaf growth process to drought (Hsiao, 1973), provide both academic and economic motives to further our understanding of the mechanism by which leaf…”
Background
Cited by
Understanding plant responses to drought—from genes to the whole plant.
Chaves, M. M., Maroco, J. P., & Pereira, J. S. (2003) · Functional Plant Biology · doi:10.1071/fp02076 · Cited by 3,845
Role of ABA in integrating plant responses to drought and salt stresses
Zhang, J., Jia, W., Yang, J., & Ismail, A. M. (2006) · Field Crops Research · doi:10.1016/j.fcr.2005.08.018 · Cited by 1,018
ABA, ethylene and the control of shoot and root growth under water stress
Sharp, R. E., & LeNoble, M. E. (2002) · Journal of Experimental Botany · doi:10.1093/jexbot/53.366.33 · Cited by 499
Sharp, R. E. (2002) · Plant, Cell & Environment · doi:10.1046/j.1365-3040.2002.00798.x · Cited by 478
Sauter, A., Davies, W. J., & Hartung, W. (2001) · Journal of Experimental Botany · doi:10.1093/jexbot/52.363.1991 · Cited by 316
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Metadata
- Authors
- Bacon, M. A., Wilkinson, S., & Davies, W. J.
- Venue
- Plant Physiology
- Publisher
- Oxford University Press (OUP)
- Published
- 1998-12-01
- Volume
- 118
- Issue
- 4
- Pages
- 1507-1515
- ISSN
- 0032-0889 (ISSN-L)
- 1532-2548
- OpenAlex
- W2007004704
- Cited by
- 200
- References
- 2
- FWCI
- 8.17
- Type
- journal article
- Language
- en
- Open access
- green
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Contains information from the Semantic Scholar Academic Graph Datasets, made available under the ODC Attribution License (ODC-BY 1.0).
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