Plant shoots exhibit synchronized oscillatory motions

In animals, the ability to move has evolved as an important means of protection from predators and for enhancing nutrient uptake. In the animal kingdom, an individual's movements may become coordinated with those of other individuals that belong to the same group, which leads, for example, to t...

Full description

Bibliographic Details
Main Authors: Marzena Ciszak, Elisa Masi, František Baluška, Stefano Mancuso
Format: Article
Language:English
Published: Taylor & Francis Group 2016-09-01
Series:Communicative & Integrative Biology
Subjects:
Online Access:http://dx.doi.org/10.1080/19420889.2016.1238117
id doaj-2b316b7dc3984d77b19b2fd740021248
record_format Article
spelling doaj-2b316b7dc3984d77b19b2fd7400212482021-03-02T10:03:26ZengTaylor & Francis GroupCommunicative & Integrative Biology1942-08892016-09-019510.1080/19420889.2016.12381171238117Plant shoots exhibit synchronized oscillatory motionsMarzena Ciszak0Elisa Masi1František Baluška2Stefano Mancuso3Gonzaga University in FlorenceUniversity of FlorenceUniversity of BonnUniversity of FlorenceIn animals, the ability to move has evolved as an important means of protection from predators and for enhancing nutrient uptake. In the animal kingdom, an individual's movements may become coordinated with those of other individuals that belong to the same group, which leads, for example, to the beautiful collective patterns that are observed in flocks of birds and schools of fish or in animal migration. Land plants, however, are fixed to the ground, which limits their movement and, apparently, their interactions and collective behaviors. We show that emergent maize plants grown in a group exhibit synchronized oscillatory motions that may be in-phase or anti-phase. These oscillations occur in short bursts and appear when the leaves rupture from the coleoptile tip. The appearance of these oscillations indicates an abrupt increase in the plant growth rate, which may be associated with a sudden change in the energy uptake for photosynthesis. Our results suggest that plant shoots behave as a complex network of biological oscillators, interacting through biophysical links, e.g. chemical substances or electric signals.http://dx.doi.org/10.1080/19420889.2016.1238117anti-phase synchronizationcomplex networkin-phase synchronizationoscillatory motionplant shoots
collection DOAJ
language English
format Article
sources DOAJ
author Marzena Ciszak
Elisa Masi
František Baluška
Stefano Mancuso
spellingShingle Marzena Ciszak
Elisa Masi
František Baluška
Stefano Mancuso
Plant shoots exhibit synchronized oscillatory motions
Communicative & Integrative Biology
anti-phase synchronization
complex network
in-phase synchronization
oscillatory motion
plant shoots
author_facet Marzena Ciszak
Elisa Masi
František Baluška
Stefano Mancuso
author_sort Marzena Ciszak
title Plant shoots exhibit synchronized oscillatory motions
title_short Plant shoots exhibit synchronized oscillatory motions
title_full Plant shoots exhibit synchronized oscillatory motions
title_fullStr Plant shoots exhibit synchronized oscillatory motions
title_full_unstemmed Plant shoots exhibit synchronized oscillatory motions
title_sort plant shoots exhibit synchronized oscillatory motions
publisher Taylor & Francis Group
series Communicative & Integrative Biology
issn 1942-0889
publishDate 2016-09-01
description In animals, the ability to move has evolved as an important means of protection from predators and for enhancing nutrient uptake. In the animal kingdom, an individual's movements may become coordinated with those of other individuals that belong to the same group, which leads, for example, to the beautiful collective patterns that are observed in flocks of birds and schools of fish or in animal migration. Land plants, however, are fixed to the ground, which limits their movement and, apparently, their interactions and collective behaviors. We show that emergent maize plants grown in a group exhibit synchronized oscillatory motions that may be in-phase or anti-phase. These oscillations occur in short bursts and appear when the leaves rupture from the coleoptile tip. The appearance of these oscillations indicates an abrupt increase in the plant growth rate, which may be associated with a sudden change in the energy uptake for photosynthesis. Our results suggest that plant shoots behave as a complex network of biological oscillators, interacting through biophysical links, e.g. chemical substances or electric signals.
topic anti-phase synchronization
complex network
in-phase synchronization
oscillatory motion
plant shoots
url http://dx.doi.org/10.1080/19420889.2016.1238117
work_keys_str_mv AT marzenaciszak plantshootsexhibitsynchronizedoscillatorymotions
AT elisamasi plantshootsexhibitsynchronizedoscillatorymotions
AT frantisekbaluska plantshootsexhibitsynchronizedoscillatorymotions
AT stefanomancuso plantshootsexhibitsynchronizedoscillatorymotions
_version_ 1724237834756292608