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Coupling of excitation energy to photochemistry in natural marine phytoplankton communities under iron stress

Coupling of excitation energy to photochemistry in natural marine phytoplankton communities under iron stress
Coupling of excitation energy to photochemistry in natural marine phytoplankton communities under iron stress
Oxygenic photosynthesis requires excitation energy transfer from light-harvesting complexes (LHCs) to reaction centers (RCs) to drive photochemical redox chemistry. The effective absorption cross section of RCs dynamically responds to the light environment on time scales of seconds to days, allowing rapid acclimations to changes in spectral irradiance and photoprotection under high light, thereby optimizing light absorption for photochemistry. Although energy coupling between LHC-RCs has been studied for decades in laboratory cultures, it remains poorly understood in real world conditions, where it is potentially influenced by nutrients. In the oceans, one of the most critical micronutrients for photosynthesis is iron (Fe). To investigate the effects of Fe stress on the energetic coupling between LHC-RCs in natural phytoplankton assemblages in the Southern Atlantic Ocean, we assessed photo-physiological responses using a pair of custom-built fluorometers measuring chlorophyll-a variable fluorescence and picosecond fluorescence lifetimes. Detailed analysis based on the functional absorption cross-section of the oxygen evolving complex, quantum yield of photochemistry, energetic connectivity of RCs, and the average lifetime of in vivo chlorophyll fluorescence suggested that between 10 and 25% of LHCs remain uncoupled from RCs and do not effectively contribute to photochemical charge separation. Addition of Fe to samples under trace metal-clean on-board incubations indicates relatively rapid recoupling (< 24 h) of antennae to photochemistry, followed by biophysical stabilization of recoupled complexes. Our findings highlight the crucial role of micronutrients in controlling the excitation energy transfer from LHCs to RCs in marine phytoplankton and the overall primary productivity in the real-world oceans.
0027-8424
Pupulewatte, Heshani
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Gorbunov, Maxim Y.
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Moore, C. Mark
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Selden, Corday
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Ryan-Keogh, Thomas J.
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Furby, Joseph
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Hawley, Ruth
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Lohan, Maeve C.
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Bibby, Thomas S.
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Falkowski, Paul G.
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Pupulewatte, Heshani
1d8fa035-6de5-4e95-a72e-d714cc402f8a
Gorbunov, Maxim Y.
c7db3a18-269a-4cde-bcc2-c6e097d6a49a
Moore, C. Mark
7ec80b7b-bedc-4dd5-8924-0f5d01927b12
Selden, Corday
295b95f6-cf34-4a61-8c11-d35106d9be2f
Ryan-Keogh, Thomas J.
df796601-6ed6-47c0-b8a0-fb926b444c35
Furby, Joseph
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Hawley, Ruth
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Lohan, Maeve C.
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Bibby, Thomas S.
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Falkowski, Paul G.
efa45553-13c5-4bfb-b1ed-17aaeb81288a

Pupulewatte, Heshani, Gorbunov, Maxim Y., Moore, C. Mark, Selden, Corday, Ryan-Keogh, Thomas J., Furby, Joseph, Hawley, Ruth, Lohan, Maeve C., Bibby, Thomas S. and Falkowski, Paul G. (2025) Coupling of excitation energy to photochemistry in natural marine phytoplankton communities under iron stress. Proceedings of the National Academy of Sciences of the United States of America, 122 (31), [e2511916122].

Record type: Article

Abstract

Oxygenic photosynthesis requires excitation energy transfer from light-harvesting complexes (LHCs) to reaction centers (RCs) to drive photochemical redox chemistry. The effective absorption cross section of RCs dynamically responds to the light environment on time scales of seconds to days, allowing rapid acclimations to changes in spectral irradiance and photoprotection under high light, thereby optimizing light absorption for photochemistry. Although energy coupling between LHC-RCs has been studied for decades in laboratory cultures, it remains poorly understood in real world conditions, where it is potentially influenced by nutrients. In the oceans, one of the most critical micronutrients for photosynthesis is iron (Fe). To investigate the effects of Fe stress on the energetic coupling between LHC-RCs in natural phytoplankton assemblages in the Southern Atlantic Ocean, we assessed photo-physiological responses using a pair of custom-built fluorometers measuring chlorophyll-a variable fluorescence and picosecond fluorescence lifetimes. Detailed analysis based on the functional absorption cross-section of the oxygen evolving complex, quantum yield of photochemistry, energetic connectivity of RCs, and the average lifetime of in vivo chlorophyll fluorescence suggested that between 10 and 25% of LHCs remain uncoupled from RCs and do not effectively contribute to photochemical charge separation. Addition of Fe to samples under trace metal-clean on-board incubations indicates relatively rapid recoupling (< 24 h) of antennae to photochemistry, followed by biophysical stabilization of recoupled complexes. Our findings highlight the crucial role of micronutrients in controlling the excitation energy transfer from LHCs to RCs in marine phytoplankton and the overall primary productivity in the real-world oceans.

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Accepted/In Press date: 30 June 2025
Published date: 29 July 2025

Identifiers

Local EPrints ID: 504677
URI: http://eprints.soton.ac.uk/id/eprint/504677
ISSN: 0027-8424
PURE UUID: 6baaef17-8b86-4055-8280-d2f1796fa96d
ORCID for C. Mark Moore: ORCID iD orcid.org/0000-0002-9541-6046
ORCID for Ruth Hawley: ORCID iD orcid.org/0009-0006-6013-0140
ORCID for Maeve C. Lohan: ORCID iD orcid.org/0000-0002-5340-3108
ORCID for Thomas S. Bibby: ORCID iD orcid.org/0000-0003-1743-473X

Catalogue record

Date deposited: 17 Sep 2025 16:52
Last modified: 18 Sep 2025 02:10

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Contributors

Author: Heshani Pupulewatte
Author: Maxim Y. Gorbunov
Author: C. Mark Moore ORCID iD
Author: Corday Selden
Author: Thomas J. Ryan-Keogh
Author: Joseph Furby
Author: Ruth Hawley ORCID iD
Author: Maeve C. Lohan ORCID iD
Author: Thomas S. Bibby ORCID iD
Author: Paul G. Falkowski

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