Precision Phenotyping of Nectar-Related Traits Using X-ray Micro Computed Tomography.
Laurent BegotFilip SlavkovicMyriam OgerClement PichotHalima MorinAdnane BoualemAnne-Laure FavierAbdelhafid BendahmanePublished in: Cells (2022)
Flower morphologies shape the accessibility to nectar and pollen, two major traits that determine plant-pollinator interactions and reproductive success. Melon is an economically important crop whose reproduction is completely pollinator-dependent and, as such, is a valuable model for studying crop-ecological functions. High-resolution imaging techniques, such as micro-computed tomography (micro-CT), have recently become popular for phenotyping in plant science. Here, we implemented micro-CT to study floral morphology and honey bees in the context of nectar-related traits without a sample preparation to improve the phenotyping precision and quality. We generated high-quality 3D models of melon male and female flowers and compared the geometric measures. Micro-CT allowed for a relatively easy and rapid generation of 3D volumetric data on nectar, nectary, flower, and honey bee body sizes. A comparative analysis of male and female flowers showed a strong positive correlation between the nectar gland volume and the volume of the secreted nectar. We modeled the nectar level inside the flower and reconstructed a 3D model of the accessibility by honey bees. By combining data on flower morphology, the honey bee size and nectar volume, this protocol can be used to assess the flower accessibility to pollinators in a high resolution, and can readily carry out genotypes comparative analysis to identify nectar-pollination-related traits.
Keyphrases
- computed tomography
- high resolution
- dual energy
- image quality
- positron emission tomography
- contrast enhanced
- genome wide
- climate change
- magnetic resonance imaging
- high throughput
- magnetic resonance
- electronic health record
- dna methylation
- mass spectrometry
- machine learning
- deep learning
- tandem mass spectrometry
- high speed
- single cell
- drug induced
- cell wall
- molecularly imprinted
- photodynamic therapy