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

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

You might also read

Related Articles

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

Sort by
Same author

[Scapular belt for the treatment of comminuted fractures of scapula].

Zhongguo gu shang = China journal of orthopaedics and traumatology·2010
Same author

Manipulation of ordered nanostructures of protonated polyoxometalate through covalently bonded modification.

Chemistry (Weinheim an der Bergstrasse, Germany)·2010
Same author

Developments in nonsteroidal antiandrogens targeting the androgen receptor.

ChemMedChem·2010
Same author

Dynamic presentation of immobilized ligands regulated through biomolecular recognition.

Journal of the American Chemical Society·2010
Same author

[Research on crop-weed discrimination using a field imaging spectrometer].

Guang pu xue yu guang pu fen xi = Guang pu·2010
Same author

A palladium/copper bimetallic catalytic system: dramatic improvement for Suzuki-Miyaura-type direct C-H arylation of azoles with arylboronic acids.

Chemistry (Weinheim an der Bergstrasse, Germany)·2010

Related Experiment Video

Updated: Aug 26, 2025

Time Multiplexing Super Resolving Technique for Imaging from a Moving Platform
06:25

Time Multiplexing Super Resolving Technique for Imaging from a Moving Platform

Published on: February 12, 2014

8.5K

Single photon imaging with multi-scale time resolution.

Zhen Chen, Bo Liu, Guangmeng Guo

    Optics Express
    |October 12, 2022
    PubMed
    Summary
    This summary is machine-generated.

    This study introduces a novel single photon imaging method with multi-scale time resolution. It effectively separates echo photons from noise, improving depth accuracy and reducing computational load in challenging environments.

    More Related Videos

    Author Spotlight: Comparative Imaging of Neural Activity in Awake and Freely Moving States
    06:25

    Author Spotlight: Comparative Imaging of Neural Activity in Awake and Freely Moving States

    Published on: January 19, 2024

    1.1K
    Multi-photon Intracellular Sodium Imaging Combined with UV-mediated Focal Uncaging of Glutamate in CA1 Pyramidal Neurons
    10:29

    Multi-photon Intracellular Sodium Imaging Combined with UV-mediated Focal Uncaging of Glutamate in CA1 Pyramidal Neurons

    Published on: October 8, 2014

    14.1K

    Related Experiment Videos

    Last Updated: Aug 26, 2025

    Time Multiplexing Super Resolving Technique for Imaging from a Moving Platform
    06:25

    Time Multiplexing Super Resolving Technique for Imaging from a Moving Platform

    Published on: February 12, 2014

    8.5K
    Author Spotlight: Comparative Imaging of Neural Activity in Awake and Freely Moving States
    06:25

    Author Spotlight: Comparative Imaging of Neural Activity in Awake and Freely Moving States

    Published on: January 19, 2024

    1.1K
    Multi-photon Intracellular Sodium Imaging Combined with UV-mediated Focal Uncaging of Glutamate in CA1 Pyramidal Neurons
    10:29

    Multi-photon Intracellular Sodium Imaging Combined with UV-mediated Focal Uncaging of Glutamate in CA1 Pyramidal Neurons

    Published on: October 8, 2014

    14.1K

    Area of Science:

    • Photonics and optical sensing
    • Signal processing for imaging

    Background:

    • Single photon imaging is susceptible to noise in challenging terrains.
    • Accurate depth measurement is crucial for various applications.

    Purpose of the Study:

    • To develop a single photon imaging mechanism with multi-scale time resolution.
    • To improve echo photon separation from noise.
    • To reduce computational overheads in depth estimation.

    Main Methods:

    • Utilizing a multi-scale time resolution imaging mechanism.
    • Employing an adaptively thresholding technique to create multiple histograms.
    • Clustering echo photons into time bins for noise separation.

    Main Results:

    • Reduced positional uncertainty from kilometers to 300 meters using microsecond-scale resolution.
    • Achieved depth accuracy of less than 0.15 m under specific conditions (8 echo photons, 1 Mcps background).
    • Successfully distinguished echoes from noise across a background count rate range of 200 kcps to 1 Mcps.

    Conclusions:

    • The proposed method enhances depth accuracy and noise separation in single photon imaging.
    • It offers significant computational savings by focusing on relevant depth ranges.
    • The technique is suitable for digital signal processor (DSP) implementation due to low data volumes and computational demands.