Evidence map›Paper›PMID 28973910›Full record

ArticleProceedings of the National Academy of Sciences of the United States of America2017

Universal poroelastic mechanism for hydraulic signals in biomimetic and natural branches.

J-F Louf, G Guéna, E Badel, Y Forterre

Erratum issuedAbstract read
In one paragraph

Article in Proceedings of the National Academy of Sciences of the United States of America, 2017. The graph could read no effect estimate from its abstract, so it casts no vote on the map. An erratum has been issued. Cited by 8 papers.

0numbers the graph read from it
0cells of the map it votes in
8citing papers in PubMed
–field-weighted citation impact
1 · What the graph read from it

What it found

Each row is one number read from the abstract, on the scale the paper reported it, with its interval. Left of the dashed line favours the treatment, right favours the comparator. Under each row is the sentence it came from. New to these charts? A ten-minute tutorial.

The abstract states no effect estimate the extractor could read, or names no intervention and outcome on the map, so this paper lights no cell and moves no belief. It is still indexed, cited and linked below.

2 · The registry

The trial behind it

Trials whose registry record cites this paper, or whose number appears in the abstract. A trial that started after this paper was published is citing it as background, not reporting it.

Neither the registry nor the abstract names a trial number. If this is a trial report, that itself is worth knowing.

3 · Its place in the literature

Who cites it

8 citing papers in PubMed.

  1. A unified framework for hydromechanical signaling can explain transmission of local and long-distance signals in plants.Proceedings of the National Academy of Sciences of the United States of America · 2025
    Article
  2. Mechanics of pressurized cellular sheets.Journal of the Royal Society, Interface · 2025
    Article
  3. Review
  4. Review
  5. Article
  6. Article
  7. Drying of channels by evaporation through a permeable medium.Journal of the Royal Society, Interface · 2019
    Article
  8. Article
4 · The record

Corrections and comments

5 · Who and what money

Authors and funding

4 authors.

J-F LoufAix-Marseille Univ, CNRS, IUSTI (Institut Universitaire des Systèmes Thermiques Industriels), 13013 Marseille, France.
G GuénaAix-Marseille Univ, CNRS, IUSTI (Institut Universitaire des Systèmes Thermiques Industriels), 13013 Marseille, France.
E BadelUniversité Clermont Auvergne, INRA, PIAF, F-63000 Clermont-Ferrand, France.
Y ForterreAix-Marseille Univ, CNRS, IUSTI (Institut Universitaire des Systèmes Thermiques Industriels), 13013 Marseille, France; yoel.forterre@univ-amu.fr.

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

Plants constantly undergo external mechanical loads such as wind or touch and respond to these stimuli by acclimating their growth processes. A fascinating feature of this mechanical-induced growth response is that it can occur rapidly and at long distance from the initial site of stimulation, suggesting the existence of a fast signal that propagates across the whole plant. The nature and origin of the signal is still not understood, but it has been recently suggested that it could be purely mechanical and originate from the coupling between the local deformation of the tissues (bending) and the water pressure in the plant vascular system. Here, we address the physical origin of this hydromechanical coupling using a biomimetic strategy. We designed soft artificial branches perforated with longitudinal liquid-filled channels that mimic the basic features of natural stems and branches. In response to bending, a strong overpressure is generated in the channels that varies quadratically with the bending curvature. A model based on a mechanism analogous to the ovalization of hollow tubes enables us to predict quantitatively this nonlinear poroelastic response and identify the key physical parameters that control the generation of the pressure pulse. Further experiments conducted on natural tree branches reveal the same phenomenology. Once rescaled by the model prediction, both the biomimetic and natural branches fall on the same master curve, enlightening the universality of our poroelastic mechanism for the generation of hydraulic signals in plants.

Indexed as

Mechanotransduction, CellularModels, BiologicalTropismPinus sylvestrisQuercusTreesWaterWaterbiomimetismlong-distance signalingnonlinear beamsplant biomechanicsporoelasticity

Identifiers

PMID28973910
PMCPMC5651757

What OpenQuestion holds

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Registered trials

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Read under generation 80e0d062 · epoch 390. Bibliography from PubMed, PubMed Central and OpenAlex; grants from NIH RePORTER; trial links from ClinicalTrials.gov; estimates, votes and beliefs from the OpenQuestion graph.