Amélie Bauer · CV · Plant Biology
Growing the plant…
Amélie Bauer

Looking for a job

I am looking for a position in biology, imaging or image analysis in Melbourne and the surrounding region.

Open to projects with French companies in Melbourne

This website is the interactive CV of

Amélie Bauer

Researcher studying plant morphogenesis

ORCID 0000-0002-5630-5837
PhD
University of Melbourne & ENS de Lyon
Postdoc
Plant Biology Research Institute, Montréal, 2024–2026
Visa
Bridging visa, permanent residency (subclass 186) in progress

What controls plant morphogenesis?

Organ morphogenesis depends on mechanical interactions between cells and tissues. These interactions generate forces that are sensed by cells and affect key cellular processes. How mechanical forces, together with genetic and biochemical signals, shape complex organs remains largely unclear.

I address this question in Arabidopsis, using the seed and the fruit as model systems. Cell growth results from a balance between turgor pressure, which drives expansion, and the properties of the cell wall, which restrict it. At the organ scale, inner tissues grow under compression and place the epidermis under tension, so that the response of each cell layer to these forces shapes the organ.

In the seed, I showed that an initial phase of rapid anisotropic growth depends on the response of cortical microtubules to shape-driven stresses in the outermost layer of the seed coat, whereas later isotropic growth depends on an inner layer that stiffens its walls under tension. Together, this work supports a model in which spatiotemporally distinct mechanical responses control seed shape. My postdoctoral research, not yet published, focused on the control of fruit valve margin development.

Model organism

Arabidopsis thaliana

Reference model for plant molecular genetics

All my projects have focused on Arabidopsis thaliana, a member of the Brassicaceae, a family that includes crops of agronomic importance such as mustard and cabbage. My work centred on reproductive organs.

Cellular resolution

From cell to organ

I combine live confocal time-lapse imaging with cell-level quantification to relate the growth of individual cells to organ morphogenesis.

cell wallsnuclei

Molecular biology

Molecular tools

Design and cloning of constructs to generate fluorescent reporter lines, and molecular characterisation of the resulting lines.

Plant genetics

Genetic resources

Generation and maintenance of transgenic lines: crosses, floral-dip transformation, selection of transformants and genotyping.

I also established the in vitro culture of individual immature seeds for live imaging of seed development, a method I was the first to develop (Bauer et al., EMBO J 2024).

Plant mechanics

Mechanical perturbations

To assess the contribution of mechanical forces to organ shape, I apply controlled compression between two plates and image the resulting responses of cells and cortical microtubules.

Compression set-up based on Creff et al., 2015, used in Bauer et al., EMBO J 2024

Microscopy

Live imaging

I develop time-lapse protocols that sustain organ growth in vitro on the microscope stage, so that the same cells can be followed over several days.

  • StereomicroscopeDissection, whole organs, line screening
  • Brightfield & DICZeiss Axio Imager 2
  • ConfocalZeiss LSM 800, Leica TCS SP8, Nikon C2
  • Spinning diskZeiss Axio Observer
  • AiryscanZeiss LSM 980, microtubule imaging

Image analysis · code

Image analysis in Fiji

I write Fiji macros for the batch processing of complete experiments, and perform downstream statistical analysis and data visualisation in Python and R.


      

Example macro: batch projection and cell segmentation. A full automated pipeline is shown further down.

MorphoGraphX · 3D

3D cell growth analysis

Using MorphoGraphX, I perform 3D segmentation of individual cells and track their growth over time, layer by layer. Shown here: the two cell layers of the epidermis.

Time-lapse 0 hsegmentation → cell growth

cell volume increaseSchematic representation

3D segmentation in MorphoGraphX: video ↗

PhD · EMBO Journal 2024

Seed morphogenesis

Seed growth proceeds through an initial stage of rapid, anisotropic growth, followed by isotropic growth later in development.

Anisotropic growth depends on the response of cortical microtubules in the outermost cell layer of the seed coat to shape-derived mechanical forces.

Day 0.0Length / width 0.80anisotropic growth
03 days7 days after anthesis

growth rategrowth anisotropymicrotubules

Schematic representation, based on Bauer et al., EMBO J 2024

From anisotropic to isotropic

Transition to isotropic growth

The later, isotropic phase of growth depends on an inner layer of the seed coat, whose walls stiffen under tension, and on the reorganisation of its cortical microtubules.

The switch to isotropic growth is accompanied by reduced mechanosensitivity of cortical microtubules. Spatiotemporally distinct responses to mechanical forces thus shape the developing seed.

Day 0.0Length / width 0.80anisotropic growth
03 days7 days after anthesis

Schematic representation, based on Bauer et al., EMBO J 2024

Publications, talks and teaching

Beyond the bench

Six publications, including a first-author article in The EMBO Journal; talks in Paris and Melbourne; and training of students in confocal and Airyscan imaging.

Automated image analysis

From raw images to a publication figure, in one script

  1. 1
    Raw confocal imagesA complete time-lapse experiment, every sample and time point.
  2. 2
    3D segmentation in MorphoGraphXEvery cell is segmented in 3D on the curved surface of the organ.
  3. 3
    Cell tracking manualCells are matched between time points to follow each lineage; this step is checked by hand.
  4. 4
    Tidy CSV exportOne row per cell: sample, genotype, time point, cell layer, growth rate and thickness.
  5. 5
    Python analysis and statisticsData are pooled, summarised and tested in a single reproducible script.
  6. 6
    Publication-ready figuresPlots are generated automatically in the journal format.
✎ MorphoGraphX · interactive segmentation and tracking
Step 1 of 6

Illustrative data. Segmentation and tracking are curated in MorphoGraphX; everything from the CSV export to the final figures is automated by one script, reused from one experiment to the next.

Publications

Each title opens the paper.

Two further manuscripts in preparation, including a first-author paper from my postdoc.

Talks & posters

Presenting at international meetings since 2021.

Talks

  • 2023
    CNRS / University of Melbourne SymposiumParis, France
  • 2022
    ComBio ConferenceFlash talk · Melbourne, Australia
  • 2021
    French Seed ConferenceFlash talk · online
  • 2021
    CNRS / University of Melbourne SymposiumOnline

Posters

  • 2025
    Global Image AnalysisKobe, Japan
  • 2023
    European Plant Cytoskeletal ClubHalle, Germany
  • 2022
    Plant BiomechanicsLyon, France
  • 2021
    French Seed ConferenceLyon, France
2021
Best poster and flash talk award
French Seed Conference

Experience

Eight years of research on Arabidopsis development, across three countries.

  1. 2024 – 2026

    Postdoctoral researcher

    Kierzkowski laboratory, Plant Biology Research Institute (IRBV), Montréal

    Investigated the genetic and mechanical control of valve margin development in the Arabidopsis fruit, combining confocal time-lapse imaging, 3D growth analysis in MorphoGraphX, reporter lines, cytoskeleton imaging and mechanical perturbations. Supervised two master's students and contributed to international collaborations. These results are not yet published; a first-author manuscript is in preparation.

  2. 2024

    Associate lecturer

    University of Montréal

    Taught the Plant Cell Signalling module to undergraduate students, covering phytohormones, mechanical forces in plant growth and microscopy methods. Designed interactive lectures, exercises and examinations.

  3. 2020 – 2024

    PhD in plant development

    Joint program, University of Melbourne & ENS de Lyon

    Investigated how mechanical forces shape the Arabidopsis seed. Developed an in vitro time-lapse imaging protocol for developing seeds, generated lines to dissect the contribution of individual cell layers, and validated the role of mechanics using external mechanical perturbations.

  4. 2019 – 2020

    Master's research internships

    ENS de Lyon

    Investigated the role of PI(4,5)P₂ phosphorylation in plant cell division using an inducible dephosphorylation tool.

Teaching & outreach

Sharing methods with students, peers and the public.

  • 2026
    Instructor, PCA Imaging Workshop webinar series“3D Segmentation in MorphoGraphX”, international, online
  • 2025
    Airyscan microtubule imaging trainingPhD, master's and undergraduate students, IRBV Montréal
  • 2024
    Peer reviewerAmerican Journal of Botany
  • 2024
    DéclicsResearch presented to high-school students through activities, Lyon
  • 2021
    One-week lab project for a high-school studentLyon
  • 2021
    Thesis project presented to master's studentsUniversité Claude Bernard Lyon 1

Education

  • 2024
    PhD, Plant Development and ReproductionUniversity of Melbourne & École normale supérieure de Lyon
  • 2020
    Master's in Molecular and Cellular Biology, bio-imaging specialisationUniversité Claude Bernard Lyon 1
  • 2018
    Bachelor's in Genetics and Cell BiologyUniversité Claude Bernard Lyon 1 · training in both animal and plant biology
  • 2017
    School of photographySEPR, Lyon

Let's talk

Based in Melbourne and seeking an opportunity in biology, imaging or image analysis in Melbourne and the surrounding region. Bridging visa, permanent residency (subclass 186) in progress. I am also open to scientific projects with French companies based in Melbourne.

Email
amelie.bauer28@gmail.com
Reporter line design
GreenGate cloning
Golden Gate cloning
PCR
Genotyping
Gel electrophoresis
Crosses
Plant transformation
In vitro culture: seedlings & immature seeds
Nuclear gene expression quantification
2D cell segmentation
Outer epidermal layer
Inner epidermal layer
Compression