Fluorescence ratios normalized to PSI over time during high light (A, B, C), high light in the presence of DCMU (A’, B’, C’) and during dark, anaerobic conditions (A”, B”, C”). (A, A’, A”) show ratios for C. reinhardtii, (B, B’, B”) show ratios for N. oceanica and (C, C’, C”) show ratios for P. tricornutum. Fluorescence spectra for the fluorescent components located in each organism, which led to the selection of the wavelengths representing PSII, PSI and light harvesting complexes, are shown in Fig 4.</p
AbstractPSII antenna size heterogeneity has been intensively studied in the past. Based on DCMU fluo...
We have investigated the energy landscape of the bacterial photosynthetic peripheral light-harvestin...
In response to changes in the reduction state of the plastoquinone pool in its thylakoid membrane, t...
Calculated fluorescence spectra for photosynthetic components comprising fluorescence emission spect...
77 K fluorescence spectra from C. reinhardtii (A), N. oceanica (B) and P. tricornutum (C) recorded a...
In this work we present and discuss the single-molecule fluorescence spectra of a variety of species...
AbstractIn this work we present and discuss the single-molecule fluorescence spectra of a variety of...
In this work we present and discuss the single-molecule fluorescence spectra of a variety of species...
ABSTRACT In this work we present and discuss the single-molecule fluorescence spectra of a variety o...
<p>Graph series A shows the high light experiment performed without DBMIB (A’–fluorescence signal of...
ABSTRACT: We have investigated the energy landscape of the bacterial photosynthetic peripheral light...
<p><i>In vivo</i> fluorescence excitation spectra of <i>P. tricornutum</i> cultures after A) 0.5 h, ...
Variable fluorescence for (A) C. reinhardtii, (B) N. oceanica and (C) P. tricornutum. Black lines sh...
The intensity of the “steady-state” fluorescence of “aerobic”Anacystis nidulans is variable under pr...
This work presents a comparative study of the frequencies of spectral jumping of individual light-ha...
AbstractPSII antenna size heterogeneity has been intensively studied in the past. Based on DCMU fluo...
We have investigated the energy landscape of the bacterial photosynthetic peripheral light-harvestin...
In response to changes in the reduction state of the plastoquinone pool in its thylakoid membrane, t...
Calculated fluorescence spectra for photosynthetic components comprising fluorescence emission spect...
77 K fluorescence spectra from C. reinhardtii (A), N. oceanica (B) and P. tricornutum (C) recorded a...
In this work we present and discuss the single-molecule fluorescence spectra of a variety of species...
AbstractIn this work we present and discuss the single-molecule fluorescence spectra of a variety of...
In this work we present and discuss the single-molecule fluorescence spectra of a variety of species...
ABSTRACT In this work we present and discuss the single-molecule fluorescence spectra of a variety o...
<p>Graph series A shows the high light experiment performed without DBMIB (A’–fluorescence signal of...
ABSTRACT: We have investigated the energy landscape of the bacterial photosynthetic peripheral light...
<p><i>In vivo</i> fluorescence excitation spectra of <i>P. tricornutum</i> cultures after A) 0.5 h, ...
Variable fluorescence for (A) C. reinhardtii, (B) N. oceanica and (C) P. tricornutum. Black lines sh...
The intensity of the “steady-state” fluorescence of “aerobic”Anacystis nidulans is variable under pr...
This work presents a comparative study of the frequencies of spectral jumping of individual light-ha...
AbstractPSII antenna size heterogeneity has been intensively studied in the past. Based on DCMU fluo...
We have investigated the energy landscape of the bacterial photosynthetic peripheral light-harvestin...
In response to changes in the reduction state of the plastoquinone pool in its thylakoid membrane, t...