Plant Physiol.
HOME HELP FEEDBACK SUBSCRIPTIONS ARCHIVE SEARCH TABLE OF CONTENTS
 QUICK SEARCH:   [advanced]


     


Plant Physiology 96:172-177 (1991)
© 1991 American Society of Plant Biologists

This Article
Right arrow Full Text (PDF)
Right arrow Alert me when this article is cited
Right arrow Alert me if a correction is posted
Services
Right arrow Email this article to a friend
Right arrow Similar articles in this journal
Right arrow Similar articles in PubMed
Right arrow Alert me to new issues of the journal
Right arrow Download to citation manager
Right arrow reprints & permissions
Citing Articles
Right arrow Citing Articles via CrossRef
Right arrow Citing Articles via Google Scholar
Google Scholar
Right arrow Articles by Peterson, R. B.
Right arrow Search for Related Content
PubMed
Right arrow PubMed Citation
Right arrow Articles by Peterson, R. B.
Agricola
Right arrow Articles by Peterson, R. B.
Membranes and Bioenergetics

Analysis of Changes in Minimal and Maximal Fluorescence Yields with Irradiance and O2 Level in Tobacco Leaf Tissue

Richard B. Peterson

Department of Biochemistry and Genetics, The Connecticut Agricultural Experiment Station, New Haven, Connecticut 06504

The responses of minimal and maximal fluorescence yields of chlorophyll a to irradiance of actinic white light were determined by pulse modulated fluorimetry in leaf discs from tobacco, Nicotiana tabacum, at 1.6, 20.5, and 42.0% (v/v) O2. Steady-state maximal fluorescence yield (Fm', measured during a saturating light pulse) declined with increasing irradiance at all O2 levels. In contrast, the steady-state minimal fluorescence yield (Fo', measured during a brief dark interval) increased with irradiance relative to that recorded for the fully dark-adapted leaf (Fo) or that observed after 5 minutes of darkness (Fo*). The relative magnitude of this increase was somewhat greater and extended to higher irradiances at the elevated O2 levels compared with 1.6% O2. Suppression of Fo' was only observed consistently at saturating irradiance. The results are interpreted in terms of the occurrence of photosystem II units possessing exceedingly slow turnover times (i.e. "inactive" units). Inactive units play an important role, along with thermal deactivation of excited chlorophyll, in determining the response of in vivo fluorescence yield to changes in irradiance. Also, a significant interactive effect of O2 concentration and the presence or absence of far red light on oxidation of photosystem II acceptors in the dark was noted.








HOME HELP FEEDBACK SUBSCRIPTIONS ARCHIVE SEARCH TABLE OF CONTENTS
ASPB Publications PLANT PHYSIOLOGY THE PLANT CELL
Copyright © 1991 by the American Society of Plant Biologists