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Calcium modulates leaf cell-specific phosphorus allocation in Proteaceae from south-western Australia
Over 650 Proteaceae occur in south-western Australia, contributing to the region’s exceptionally high biodiversity. Most Proteaceae occur exclusively on severely nutrient-impoverished, acidic soils (calcifuge), whilst only few also occur on young, calcareous soils (soil-indifferent), higher in calci...
Autores principales: | , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
Oxford University Press
2019
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6685658/ https://www.ncbi.nlm.nih.gov/pubmed/31049573 http://dx.doi.org/10.1093/jxb/erz156 |
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author | Hayes, Patrick E Clode, Peta L Guilherme Pereira, Caio Lambers, Hans |
author_facet | Hayes, Patrick E Clode, Peta L Guilherme Pereira, Caio Lambers, Hans |
author_sort | Hayes, Patrick E |
collection | PubMed |
description | Over 650 Proteaceae occur in south-western Australia, contributing to the region’s exceptionally high biodiversity. Most Proteaceae occur exclusively on severely nutrient-impoverished, acidic soils (calcifuge), whilst only few also occur on young, calcareous soils (soil-indifferent), higher in calcium (Ca) and phosphorus (P). The calcifuge habit of Proteaceae is explained by Ca-enhanced P toxicity, putatively linked to the leaf cell-specific allocation of Ca and P. Separation of these elements is essential to avoid the deleterious precipitation of Ca-phosphate. We used quantitative X-ray microanalysis to determine leaf cell-specific nutrient concentrations of two calcifuge and two soil-indifferent Proteaceae grown in hydroponics at a range of Ca and P concentrations. Calcium enhanced the preferential allocation of P to palisade mesophyll (PM) cells under high P conditions, without a significant change in whole leaf [P]. Calcifuges showed a greater PM [P] compared with soil-indifferent species, corresponding to their greater sensitivity. This study advances our mechanistic understanding of Ca-enhanced P toxicity, supporting the proposed model, and demonstrating its role in the calcifuge distribution of Proteaceae. This furthers our understanding of nutrient interactions at the cellular level and highlights its importance to plant functioning. |
format | Online Article Text |
id | pubmed-6685658 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2019 |
publisher | Oxford University Press |
record_format | MEDLINE/PubMed |
spelling | pubmed-66856582019-08-12 Calcium modulates leaf cell-specific phosphorus allocation in Proteaceae from south-western Australia Hayes, Patrick E Clode, Peta L Guilherme Pereira, Caio Lambers, Hans J Exp Bot Research Papers Over 650 Proteaceae occur in south-western Australia, contributing to the region’s exceptionally high biodiversity. Most Proteaceae occur exclusively on severely nutrient-impoverished, acidic soils (calcifuge), whilst only few also occur on young, calcareous soils (soil-indifferent), higher in calcium (Ca) and phosphorus (P). The calcifuge habit of Proteaceae is explained by Ca-enhanced P toxicity, putatively linked to the leaf cell-specific allocation of Ca and P. Separation of these elements is essential to avoid the deleterious precipitation of Ca-phosphate. We used quantitative X-ray microanalysis to determine leaf cell-specific nutrient concentrations of two calcifuge and two soil-indifferent Proteaceae grown in hydroponics at a range of Ca and P concentrations. Calcium enhanced the preferential allocation of P to palisade mesophyll (PM) cells under high P conditions, without a significant change in whole leaf [P]. Calcifuges showed a greater PM [P] compared with soil-indifferent species, corresponding to their greater sensitivity. This study advances our mechanistic understanding of Ca-enhanced P toxicity, supporting the proposed model, and demonstrating its role in the calcifuge distribution of Proteaceae. This furthers our understanding of nutrient interactions at the cellular level and highlights its importance to plant functioning. Oxford University Press 2019-08-01 2019-04-09 /pmc/articles/PMC6685658/ /pubmed/31049573 http://dx.doi.org/10.1093/jxb/erz156 Text en © The Author(s) 2019. Published by Oxford University Press on behalf of the Society for Experimental Biology. http://creativecommons.org/licenses/by-nc/4.0/ This is an Open Access article distributed under the terms of the Creative Commons Attribution Non-Commercial License (http://creativecommons.org/licenses/by-nc/4.0/), which permits non-commercial re-use, distribution, and reproduction in any medium, provided the original work is properly cited. For commercial re-use, please contact journals.permissions@oup.com |
spellingShingle | Research Papers Hayes, Patrick E Clode, Peta L Guilherme Pereira, Caio Lambers, Hans Calcium modulates leaf cell-specific phosphorus allocation in Proteaceae from south-western Australia |
title | Calcium modulates leaf cell-specific phosphorus allocation in Proteaceae from south-western Australia |
title_full | Calcium modulates leaf cell-specific phosphorus allocation in Proteaceae from south-western Australia |
title_fullStr | Calcium modulates leaf cell-specific phosphorus allocation in Proteaceae from south-western Australia |
title_full_unstemmed | Calcium modulates leaf cell-specific phosphorus allocation in Proteaceae from south-western Australia |
title_short | Calcium modulates leaf cell-specific phosphorus allocation in Proteaceae from south-western Australia |
title_sort | calcium modulates leaf cell-specific phosphorus allocation in proteaceae from south-western australia |
topic | Research Papers |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6685658/ https://www.ncbi.nlm.nih.gov/pubmed/31049573 http://dx.doi.org/10.1093/jxb/erz156 |
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