Jove
Visualize
Contact Us
JoVE
x logofacebook logolinkedin logoyoutube logo
ABOUT JoVE
OverviewLeadershipBlogJoVE Help Center
AUTHORS
Publishing ProcessEditorial BoardScope & PoliciesPeer ReviewFAQSubmit
LIBRARIANS
TestimonialsSubscriptionsAccessResourcesLibrary Advisory BoardFAQ
RESEARCH
JoVE JournalMethods CollectionsJoVE Encyclopedia of ExperimentsArchive
EDUCATION
JoVE CoreJoVE BusinessJoVE Science EducationJoVE Lab ManualFaculty Resource CenterFaculty Site
Terms & Conditions of Use
Privacy Policy
Policies

Related Concept Videos

Phase Contrast and Differential Interference Contrast Microscopy01:26

Phase Contrast and Differential Interference Contrast Microscopy

8.3K
Phase-Contrast Microscopes
In-phase-contrast microscopes, interference between light directly passing through a cell and light refracted by cellular components is used to create high-contrast, high-resolution images without staining. It is the oldest and simplest type of microscope that creates an image by altering the wavelengths of light rays passing through the specimen. Altered wavelength paths are created using an annular stop in the condenser. The annular stop produces a hollow cone of...
8.3K
Confocal Fluorescence Microscopy01:16

Confocal Fluorescence Microscopy

13.5K
Confocal microscopy is an advanced microscopic technique. The prime advantage of the confocal microscope over other microscopy techniques is its ability to block the out-of-focus light from the illuminated samples using pinholes. It is widely used with fluorescence optics to obtain high-resolution, sharp contrast images. Unlike optical microscopes, confocal microscopes use a focused beam of light laser to scan the entire sample surface at different z-planes. These microscopes are, therefore,...
13.5K
Overview of Microscopy Techniques01:22

Overview of Microscopy Techniques

10.6K
The early pioneers of microscopy opened a window into the invisible world of microorganisms. In 1830, Joseph Jackson Lister created an essentially modern light microscope. The 20th century saw the development of microscopes that leveraged nonvisible light, such as fluorescence microscopy that uses an ultraviolet light source and electron microscopy that uses short-wavelength electron beams. These advances significantly improved magnification, image resolution, and contrast. By comparison, the...
10.6K
Super-resolution Fluorescence Microscopy01:37

Super-resolution Fluorescence Microscopy

7.1K
Super-resolution fluorescence microscopy (SRFM) provides a better resolution than conventional fluorescence microscopy by reducing the point spread function (PSF). PSF is the light intensity distribution from a point that causes it to appear blurred. Due to PSF, each fluorescing point appears bigger than its actual size, and it is the PSF interference of nearby fluorophores that causes the blurred image. Various approaches to achieving higher resolution through SRFM have recently been...
7.1K
Two-Dimensional Microscopy in Microbiology01:29

Two-Dimensional Microscopy in Microbiology

135
Two-dimensional (2D) microscopy encompasses a range of optical techniques that capture images within a single focal plane, offering detailed representations of microscopic structures. These techniques are essential in biological and medical research, enabling the visualization of cellular and subcellular structures with different levels of contrast and specificity.There are several major types of 2D microscopy, each with strengths and applications.Bright-Field MicroscopyBright-field microscopy...
135
Imaging Biological Samples with Optical Microscopy01:18

Imaging Biological Samples with Optical Microscopy

4.9K
Optical microscopy uses optic principles to provide detailed images of samples. Antonie van Leeuwenhoek designed the first compound optical microscope in the 17th century to visualize blood cells, bacteria, and yeast cells. In 1830, Joseph Jackson Lister created an essentially modern light microscope. The 20th century saw the development of microscopes with enhanced magnification and resolution.
In optical microscopy, the specimen to be viewed is placed on a glass slide and clipped on the stage...
4.9K

You might also read

Related Articles

Articles linked to this work by shared authors, journal, and citation graph.

Sort by
Same author

Influence of diffractive surface geometry on optical quality and halo formation in sinusoidal trifocal intraocular lenses.

Scientific reports·2026
Same author

Hybrid spectral-spatial domain registration for nanometric tracking in digital in-line holographic microscopy.

Optics letters·2026
Same author

Optometrist-guided versus self-driven subjective refraction using tunable optics: quantifying the professional's impact.

Journal of optometry·2026
Same author

Spatial-shifting cepstrum: holography without a known reference beam.

Optics express·2025
Same author

Speckle suppression in digital in-line holographic microscopy through liquid crystal dynamic scattering.

Optics letters·2025
Same author

Exploring the do-it-yourself approach in subjective refraction.

PloS one·2025

Related Experiment Video

Updated: Aug 6, 2025

Optical Scatter Microscopy Based on Two-Dimensional Gabor Filters
14:58

Optical Scatter Microscopy Based on Two-Dimensional Gabor Filters

Published on: June 2, 2010

9.6K

Single-shot wavelength-multiplexed phase microscopy under Gabor regime in a regular microscope embodiment.

Vicente Micó1, Mikołaj Rogalski2, José Ángel Picazo-Bueno3

  • 1Departamento de Óptica y Optometría y Ciencias de la Visión, Universidad de Valencia, C/Doctor Moliner 50, 46100, Burjassot, Spain. vicente.mico@uv.es.

Scientific Reports
|March 15, 2023
PubMed
Summary

This study introduces a single-shot wavelength multiplexing technique to improve phase imaging microscopy. It effectively reduces coherent noise and twin image disturbances for clearer quantitative phase information.

More Related Videos

Author Spotlight: Unveiling the Potential of VSFG Microscopy in Studying Mesoscopically Heterogeneous Self-Assembled Structures
08:49

Author Spotlight: Unveiling the Potential of VSFG Microscopy in Studying Mesoscopically Heterogeneous Self-Assembled Structures

Published on: December 1, 2023

1.5K
Transmission of Multiple Signals through an Optical Fiber Using Wavefront Shaping
09:43

Transmission of Multiple Signals through an Optical Fiber Using Wavefront Shaping

Published on: March 20, 2017

10.0K

Related Experiment Videos

Last Updated: Aug 6, 2025

Optical Scatter Microscopy Based on Two-Dimensional Gabor Filters
14:58

Optical Scatter Microscopy Based on Two-Dimensional Gabor Filters

Published on: June 2, 2010

9.6K
Author Spotlight: Unveiling the Potential of VSFG Microscopy in Studying Mesoscopically Heterogeneous Self-Assembled Structures
08:49

Author Spotlight: Unveiling the Potential of VSFG Microscopy in Studying Mesoscopically Heterogeneous Self-Assembled Structures

Published on: December 1, 2023

1.5K
Transmission of Multiple Signals through an Optical Fiber Using Wavefront Shaping
09:43

Transmission of Multiple Signals through an Optical Fiber Using Wavefront Shaping

Published on: March 20, 2017

10.0K

Area of Science:

  • Optics and Photonics
  • Microscopy
  • Biomedical Imaging

Background:

  • Phase imaging microscopy offers coherent sensing capabilities for standard bright-field microscopes.
  • Gabor holography provides quantitative phase information but suffers from coherent noise and twin images.
  • Existing methods for Gabor holography require complex setups or multiple exposures.

Purpose of the Study:

  • To present a single-shot wavelength multiplexing technique to mitigate coherent noise and twin image disturbances in Gabor phase imaging microscopy.
  • To develop a novel algorithm for enhanced quantitative phase retrieval.
  • To validate the technique experimentally on static and dynamic phase samples.

Main Methods:

  • Utilizing a multi-illumination laser source (3 diode lasers) for sample illumination.
  • Employing a color digital sensor (RGB camera) to capture wavelength-multiplexed Gabor holograms in a single exposure.
  • Implementing a novel algorithm based on a modified Gerchberg-Saxton kernel for image reconstruction.

Main Results:

  • Successfully mitigated coherent noise and twin image disturbances in retrieved phase distributions.
  • Achieved enhanced quantitative phase images with improved clarity and reduced artifacts.
  • Demonstrated experimental validation using resolution test targets and living spermatozoa.

Conclusions:

  • The single-shot wavelength multiplexing technique offers a robust solution for overcoming limitations in Gabor phase imaging microscopy.
  • This method enhances the quality of quantitative phase information, enabling clearer visualization of microscopic samples.
  • The technique is compatible with standard microscope setups and applicable to both static and dynamic biological samples.