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Nakad, M.

Publications and source records attributed to Nakad, M..

3 recordsLinked to original sources

Impact of sucrose sinks on phloem transport

The movement of photosynthates within plants is a focus in plant physiology, ecohydrology, and earth systems modeling. The phloem, one of the plants hydraulic systems, facilitates this transport. It is believed to be optimized for efficient photosynthates transport, notably sucrose. This has implications ranging from local impacts on plant survival during drought to ecosystem-scale effects on carbon and water cycling. Most models for phloem transport rely on the pressure-flow hypothesis, where sucrose is loaded in leaves, drawing water from the xylem through osmosis, generating pressure gradients for transport. Experimental challenges in measuring sugar fluxes have led to reliance on theoretical models, though discrepancies exist, especially for long-distance transport. Criticism of the pressure-flow hypothesis notes low hydraulic conductance in sieve tubes, possibly hindering sucrose transport in taller plants. This research explores osmotically driven flows through the development of a new one-dimensional numerical model that includes sources from photosynthesis and sinks towards the stem and roots. The model also incorporates a concentration-dependent viscosity and the xylem water potential. It shows that different allocation schemes of sucrose sinks towards the stem of the plant influence the speed at which sucrose is transported. These findings provide insight into how carbon allocation along the phloem may have evolved to enhance the efficiency of transporting soluble compounds in the phloem. HighlightsO_LISucrose sinks along the phloem influence mass flux beyond simple reaction-like consumption dynamics C_LIO_LIMass flux is modulated by the sucrose allocation profile along the tree stem C_LIO_LIObservations of xylem-phloem water exchange can provide insights into the physical sucrose sink profile C_LI

ecology↗

Experiments on osmotically driven flow in idealized elastic membranes

The phloem provides a pathway for products of photosynthesis to be transported to different parts of the plant for consumption or storage. The Munch pressure flow hypothesis (PFH) is considered the leading framework to mathematically represent this transport. It assumes that osmosis provides the necessary pressure differences to drive the fluid flow and sucrose within the phloem. Mathematical models utilizing the PFH approximate the phloem by a relatively rigid semi-permeable tube. However, the phloem consists of living cells that contract and expand in response to pressure fluctuations. The effect of membrane elasticity on osmotically driven sucrose front speed has rarely been considered and frames the scope here. Laboratory experiments were conducted to elucidate the elastic-to-plastic pressure-deformation relation in membranes and their effect on sucrose front speeds. It is demonstrated that membrane elasticity acts to retard the sucrose front speed. The retardation emerges because some of the osmotic pressure performs mechanical work to expand the membrane instead of pressurizing water. These results offer a novel perspective about the much discussed presence of sieve plates through-out the phloem acting as structural dampers.

plant biology↗

Radial-axial transport coordination enhances sugar translocation in the phloem vasculature of plants

Mass transport of photosynthates in the phloem of plants is necessary for describing plant carbon allocation, productivity, and responses to water and thermal stress. Several hypotheses about optimization of phloem structure and function and limitations of phloem transport under drought have been proposed, and tested with models and anatomical data. However, the true impact of radial water exchange of phloem conduits with their surroundings on mass transport of photosynthates has not been addressed. Here, the physics of the Munch mechanism of sugar transport is re-evaluated to include local variations in viscosity resulting from the radial water exchange in two dimensions (axial and radial). Model results show that radial water exchange pushes sucrose away from conduit walls thereby reducing wall frictional stress due to a decrease in sap viscosity and an increase in sugar concentration in the central region of the conduit. These two co-occurring effects lead to increased sugar front speed and axial mass transport across a wide range of phloem conduit lengths. Thus, sugar transport operates more efficiently than predicted by previous models that ignore these two effects. A faster front speed leads to higher phloem resiliency under drought because more sugar can be transported with a smaller pressure gradient. SummaryThe overall speed of sap increased by including a concentrationdependent viscosity in axial and radial directions.

biophysics↗