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 Experiment Videos

A method for continuous measurement of export from a leaf.

D R Geiger1, B R Fondy

  • 1Department of Biology, University of Dayton, Dayton, Ohio 45469.

Plant Physiology
|September 1, 1979
PubMed
Summary
This summary is machine-generated.

Related Concept Videos

You might also read

Related Articles

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

Sort by
Same author

Effect of environmental factors on whole plant assimilate partitioning and associated gene expression.

Journal of experimental botany·2011
Same author

Identification, purification, and molecular cloning of a putative plastidic glucose translocator.

The Plant cell·2000
Same author

Evidence for circadian regulation of starch and sucrose synthesis in sugar beet leaves.

Plant physiology·1992
Same author

Characterization and subcellular localization of debranching enzyme and endoamylase from leaves of sugar beet.

Plant physiology·1992
Same author

Carbon Assimilation and Leaf Water Status in Sugar Beet Leaves during a Simulated Natural Light Regimen.

Plant physiology·1991
Same author

Effect of N-(Phosphonomethyl)glycine on Carbon Assimilation and Metabolism during a Simulated Natural Day.

Plant physiology·1991
Same journal

Autoinhibition of Plasma Membrane H+-ATPase1 Regulates Systemic Herbivore Defense in Arabidopsis.

Plant physiology·2026
Same journal

A deep learning model captures position-specific preferences of plant regulatory sequences and suggests genes under complex regulation.

Plant physiology·2026
Same journal

Nissolia brasiliensis as a non-nodulating model legume.

Plant physiology·2026
Same journal

Auxin response factor OsARF22 controls rice seed vigor by suppressing ABA signaling.

Plant physiology·2026
Same journal

The primary nitrate response TGA1 and TGA4 transcription factors are negative regulators of sulfate uptake and metabolism.

Plant physiology·2026
Same journal

TaSPL14-D diverged from its ortholog to regulate tiller angle in rice: a caveat for orthology-based functional inference.

Plant physiology·2026
See all related articles

This study introduces a new method to measure the export of photosynthetically fixed carbon from plant leaves. The technique allows for continuous, non-destructive monitoring of carbon export rates in intact plants.

Area of Science:

  • Plant Physiology
  • Photosynthesis Research
  • Carbon Metabolism

Background:

  • Understanding carbon allocation is crucial for plant productivity.
  • Previous methods for measuring carbon export were often destructive or lacked continuous monitoring capabilities.
  • Accurate quantification of carbon export from source leaves is essential for plant science.

Purpose of the Study:

  • To develop and validate a non-destructive method for continuously measuring the rate of carbon export from a single leaf.
  • To correlate carbon export rates with leaf physiological status.
  • To enable real-time monitoring of photosynthate movement in plants.

Main Methods:

  • Utilized continuous photosynthesis in (14)CO(2) to label photosynthates.
  • Employed a Geiger-Müller detector placed adjacent to the leaf to monitor labeled material export.

Related Experiment Videos

  • Calculated export rates based on the difference between carbon retention and net photosynthesis.
  • Used a leaf thickness transducer to correct for counting efficiency changes due to water status variations.
  • Main Results:

    • The developed method provides continuous, non-destructive measurements of carbon export from source leaves.
    • Export data correlated well with direct measurements of (14)C arrival in sink tissues.
    • Isolated leaves showed near-zero export values, validating the method's sensitivity.
    • The technique can detect changes in carbon export with a resolution of 10-20 minutes.

    Conclusions:

    • This novel technique offers a significant advancement for studying carbon transport dynamics in plants.
    • The method allows for precise, real-time assessment of photosynthate export without harming the plant.
    • It provides a valuable tool for research in plant physiology, crop science, and understanding plant responses to environmental changes.