Paper
12 February 2007 Multiphoton and magnetic resonance imaging of Barley embryos: comparing micro-imaging techniques across scale and parameter barriers
Martin Stark, Bertram Manz, Iris Riemann, Frank Volke, Winfriede Weschke, Karsten König
Author Affiliations +
Abstract
Multiphoton stimulated autofluorescence microscopy and Magnetic resonance imaging (MRI) address different molecular properties of the sample and reach to a different length scale. MRI maps density or mobility of nuclei (here: hydrogen), and targets at whole objects from the scale of sub-millimetres to meters. Multiphoton imaging profits from the nonlinear absorption of light in the focus of a femtosecond laser source stimulating the autofluorescence of biomolecules. As this effect relies on a high light intensity the accessible field of view is limited, but the resolution is very high. Studying a plant embryo (barley) we compare the two techniques. At 770 nm excitation the cell walls of the embryo exhibited significant autofluorescence, allowing for a subcellular resolution. While details where imaged with an objective of N.A. 1.3, an overview was generated with a N.A. as low as 0.25. The overview image as well as merged images and tomographical data were used to link the high-resolution optical data with the three-dimensional highresolution MR images. There, images of the proton density were acquired using a standard 3D spin-echo imaging pulse sequence. While the optical high-resolution data provides a field of view restricted to only a small part of the embryo, the MR image contains the whole grain. Bridging the scales it might be possible to trace transport of e.g. nutrients from large structure of the plant to the cellular level.
© (2007) COPYRIGHT Society of Photo-Optical Instrumentation Engineers (SPIE). Downloading of the abstract is permitted for personal use only.
Martin Stark, Bertram Manz, Iris Riemann, Frank Volke, Winfriede Weschke, and Karsten König "Multiphoton and magnetic resonance imaging of Barley embryos: comparing micro-imaging techniques across scale and parameter barriers", Proc. SPIE 6442, Multiphoton Microscopy in the Biomedical Sciences VII, 644227 (12 February 2007); https://doi.org/10.1117/12.702364
Lens.org Logo
CITATIONS
Cited by 1 scholarly publication.
Advertisement
Advertisement
RIGHTS & PERMISSIONS
Get copyright permission  Get copyright permission on Copyright Marketplace
KEYWORDS
Magnetic resonance imaging

Luminescence

Multiphoton microscopy

Image segmentation

Magnetism

Objectives

3D image processing

Back to Top