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Direct estimation of functional PSII reaction center concentration and PSII electron flux on a volume basis: a new approach to the analysis of Fast Repetition Rate fluorometry (FRRf) data

Direct estimation of functional PSII reaction center concentration and PSII electron flux on a volume basis: a new approach to the analysis of Fast Repetition Rate fluorometry (FRRf) data
Direct estimation of functional PSII reaction center concentration and PSII electron flux on a volume basis: a new approach to the analysis of Fast Repetition Rate fluorometry (FRRf) data
Phytoplankton primary productivity is most commonly measured by 14C assimilation although less direct methods, such as O2 exchange, have also been employed. These methods are invasive, requiring bottle incubation for up to 24 h. As an alternative, Fast Repetition Rate fluorometry (FRRf) has been used, on wide temporal and spatial scales within aquatic systems, to estimate photosystem II (PSII) electron flux per unit volume (JVPSII), which generally correlates well with photosynthetic O2 evolution. A major limitation of using FRRf arises from the need to employ an independent method to determine the concentration of functional photosystem II reaction centers ([RCII]); a requirement that has prevented FRR fluorometers being used, as stand-alone instruments, for the estimation of electron transport. Within this study, we have taken a new approach to the analysis of FRRf data, based on a simple hypothesis; that under a given set of environmental conditions, the ratio of rate constants for RCII fluorescence emission and photochemistry falls within a narrow range, for all groups of phytoplankton. We present a simple equation, derived from the established FRRf algorithm, for determining [RCII] from dark FRRf data alone. We also describe an entirely new algorithm for estimating JVPSII, which does not require determination of [RCII] and is valid for a heterogeneous model of connectivity among RCIIs. Empirical supporting evidence is presented. These data are derived from FRR measurements across a diverse range of microalgae, in parallel with independent measurements of [RCII]. Possible sources of error, particularly under nutrient stress conditions, are discussed.
1541-5856
142-154
Oxborough, Kevin
16d1da54-ed48-400e-9acf-d03536a1401e
Moore, C. Mark
7ec80b7b-bedc-4dd5-8924-0f5d01927b12
Suggett, David J.
9100a791-1264-40e4-9403-8491190c3430
Lawson, Tracy
6b62f544-1615-4620-b2f2-a3ce846495b7
Chan, Hoi Ga
42238275-4452-49f8-bef4-9ba02eb368a5
Geider, Richard J.
f1432d5c-8c1d-48ab-ac52-e81ee5ce7f42
Oxborough, Kevin
16d1da54-ed48-400e-9acf-d03536a1401e
Moore, C. Mark
7ec80b7b-bedc-4dd5-8924-0f5d01927b12
Suggett, David J.
9100a791-1264-40e4-9403-8491190c3430
Lawson, Tracy
6b62f544-1615-4620-b2f2-a3ce846495b7
Chan, Hoi Ga
42238275-4452-49f8-bef4-9ba02eb368a5
Geider, Richard J.
f1432d5c-8c1d-48ab-ac52-e81ee5ce7f42

Oxborough, Kevin, Moore, C. Mark, Suggett, David J., Lawson, Tracy, Chan, Hoi Ga and Geider, Richard J. (2012) Direct estimation of functional PSII reaction center concentration and PSII electron flux on a volume basis: a new approach to the analysis of Fast Repetition Rate fluorometry (FRRf) data. Limnology and Oceanography: Methods, 10, 142-154. (doi:10.4319/lom.2012.10.142).

Record type: Article

Abstract

Phytoplankton primary productivity is most commonly measured by 14C assimilation although less direct methods, such as O2 exchange, have also been employed. These methods are invasive, requiring bottle incubation for up to 24 h. As an alternative, Fast Repetition Rate fluorometry (FRRf) has been used, on wide temporal and spatial scales within aquatic systems, to estimate photosystem II (PSII) electron flux per unit volume (JVPSII), which generally correlates well with photosynthetic O2 evolution. A major limitation of using FRRf arises from the need to employ an independent method to determine the concentration of functional photosystem II reaction centers ([RCII]); a requirement that has prevented FRR fluorometers being used, as stand-alone instruments, for the estimation of electron transport. Within this study, we have taken a new approach to the analysis of FRRf data, based on a simple hypothesis; that under a given set of environmental conditions, the ratio of rate constants for RCII fluorescence emission and photochemistry falls within a narrow range, for all groups of phytoplankton. We present a simple equation, derived from the established FRRf algorithm, for determining [RCII] from dark FRRf data alone. We also describe an entirely new algorithm for estimating JVPSII, which does not require determination of [RCII] and is valid for a heterogeneous model of connectivity among RCIIs. Empirical supporting evidence is presented. These data are derived from FRR measurements across a diverse range of microalgae, in parallel with independent measurements of [RCII]. Possible sources of error, particularly under nutrient stress conditions, are discussed.

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Published date: 2012
Organisations: Ocean Biochemistry & Ecosystems

Identifiers

Local EPrints ID: 344913
URI: http://eprints.soton.ac.uk/id/eprint/344913
ISSN: 1541-5856
PURE UUID: 62fdfa4b-5ff3-451e-b8c1-1d7d351c972e
ORCID for C. Mark Moore: ORCID iD orcid.org/0000-0002-9541-6046

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Date deposited: 06 Nov 2012 10:35
Last modified: 15 Mar 2024 03:03

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Contributors

Author: Kevin Oxborough
Author: C. Mark Moore ORCID iD
Author: David J. Suggett
Author: Tracy Lawson
Author: Hoi Ga Chan
Author: Richard J. Geider

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