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Conductivity of the phloem in Mangifera indica L.
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ABSTRACT
Mangifera indica
is the fifth most consumed fruit worldwide, and the most important in tropical regions, but its anatomy is quite unexplored. Previous studies examined the effect of chemicals on the xylem structure in the stems of mango, but the anatomy of the phloem has remained elusive, leaving the long distance transport of photo assimilates understudied.
In this work, we used a combination of fluorescence and electron microscopy to evaluate in detail the structure of the sieve tube elements composing the phloem tissue in the tapering branches of mango trees. We then used this information to better understand the hydraulic conductivity of the sieve tubes following current models of fluid transport in trees.
Our results revealed that the anatomy of the phloem in the stems changes from current year branches, where it was protected by pericyclic fibers, to older ones, where the lack of fibers was concomitant with laticiferous canals embedded in the phloem tissue. Callose was present in the sieve plates, but also in the walls of the phloem conduits, making them discernible from other phloem cells in fresh sections. A scaling geometry of the sieve tube elements, including the number of sieve areas and the pore size across tapering branches resulted in an exponential conductivity from current year branches to the base of the tree.
Our measurements of the phloem in mango fit with measurements of the phloem architecture in the stems of forest woody species, and imply that, despite agronomic pruning practices, the sieve conduits of the phloem scale with the tapering branches. As a result, the pipe model theory applied to the continuous tubing system of the phloem appears as a good approach to understand the “long distance” hydraulic transport of photoassimilates in fruit trees.
Title: Conductivity of the phloem in
Mangifera indica
L.
Description:
ABSTRACT
Mangifera indica
is the fifth most consumed fruit worldwide, and the most important in tropical regions, but its anatomy is quite unexplored.
Previous studies examined the effect of chemicals on the xylem structure in the stems of mango, but the anatomy of the phloem has remained elusive, leaving the long distance transport of photo assimilates understudied.
In this work, we used a combination of fluorescence and electron microscopy to evaluate in detail the structure of the sieve tube elements composing the phloem tissue in the tapering branches of mango trees.
We then used this information to better understand the hydraulic conductivity of the sieve tubes following current models of fluid transport in trees.
Our results revealed that the anatomy of the phloem in the stems changes from current year branches, where it was protected by pericyclic fibers, to older ones, where the lack of fibers was concomitant with laticiferous canals embedded in the phloem tissue.
Callose was present in the sieve plates, but also in the walls of the phloem conduits, making them discernible from other phloem cells in fresh sections.
A scaling geometry of the sieve tube elements, including the number of sieve areas and the pore size across tapering branches resulted in an exponential conductivity from current year branches to the base of the tree.
Our measurements of the phloem in mango fit with measurements of the phloem architecture in the stems of forest woody species, and imply that, despite agronomic pruning practices, the sieve conduits of the phloem scale with the tapering branches.
As a result, the pipe model theory applied to the continuous tubing system of the phloem appears as a good approach to understand the “long distance” hydraulic transport of photoassimilates in fruit trees.
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