.. title: Research
.. slug: research
.. date: 2016-07-02 18:57:49 UTC+02:00
.. tags: morphogenesis, modeling, tree, meristem, wood, phyllotaxis, auxin, PIN
.. category: 
.. link: 
.. description: 
.. type: text

My research activities encompass several aspects of plant development.

Models of wood formation
------------------------

Collaborators: Cyrille Rathgeber, Meriem Fournier, Bruno Moulia

.. image:: /images/rondelle_Douglas.png
   :width: 900px
   :height: 928px
   :scale: 40 %
   :alt: cross-section of a Douglas fir stem, with visible concentric growth rings

Above: cross-section of a Douglas fir stem.

In trees, wood fulfils many functions: mechanical support, posture control,
hydraulic conduction, and storage. These crucial functions demand permanent
adjustments in response to changing environmental constraints. Therefore, wood
formation is tightly regulated in order to react appropriately to internal and
external stimuli.

Each year, a new layer of wood forms during the growing season. This appears as
a succession of clearly visible rings on the cross-section of a stem. The
ability of trees to continuously produces new wood relies on a reservoir of
undifferentiated cells called the *vascular cambium*. The vascular cambium
generates not only wood, but also the phloem, a living tissue conducting
descending sap.

.. image:: /images/ecorche_bois_Meriem_en.jpg
   :width: 687px
   :height: 652px
   :scale: 60 %
   :alt: internal structure of a tree stem, with wood, cambium, phloem, and bark

Above: internal structure of a tree stem (by Meriem Fournier, under CC-BY-SA).

Cells exiting the cambium from its internal face progressively differentiate
into wood cells. Number and dimensions of wood cells produced depend on climatic
conditions and available resources. Internal regulatory mechanisms are also at
work in wood formation, although they are still poorly understood. With laboratories `LERFoB
<http://www6.nancy.inra.fr/foret-bois-lerfob>`_ and `PIAF
<https://www6.ara.inra.fr/piaf/>`_, I investigate the role of plant hormones and
other biochemical signals in these regulatory mechanisms.

References:

* `Article <http://dx.doi.org/10.1007/s13595-016-0613-y>`_ published in the *Annals of Forest Science* (`author version </files/Hartmann_et_al_2017_Annals_of_Forest_science.pdf>`_).

* `Ph.D. dissertation </files/these_Hartmann.pdf>`_ (in French).


3D modeling of phyllotaxis
--------------------------

Collaborators: Pierre Barbier de Reuille, Cris Kuhlemeier

`Phyllotaxis <https://en.wikipedia.org/wiki/Phyllotaxis>`_ refers to the regular
arrangement of leaves around a shoot. This geometrical pattern has aroused the
attention of natural scientists for a long time.

New leaves are generated at the tip of shoots by a stem cell niche called the
*shoot apical meristem*. The formation of a leaf starts with the apparition of a
bulge at the surface of the meristem. The bulge progressively develops into a
fully-grown leaf. A series of works has highlighted the prodominent role played
by the plant hormone *auxin* in the early stages of the process. Each bulging
event is preceded by a localized accumulation of auxin. As the young leaf
develops, auxin get canalized towards inner tissue. A new vein forms to connect
the new leaf to the vascular system of the plant, following the auxin canal.

These observations support the view that auxin determines the positioning of
leaves (i.e., phyllotaxis) and guides their connection to the main vasculature
of the plant. Several models have been proposed for explaining how auxin
converges on some spots, or how it get canalized from the new leaf to an
pre-existing vessel. With researchers from the `IPS
<http://www.ips.unibe.ch/research/deve/index_eng.html>`_ in Bern, I am working
on a 3D computational model integrating for the first time both aspects
(convergence and canalization).
