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Cellular traits regulate fluorescence-based light-response phenotypes of coral photosymbionts living in-hospite
Diversity across algal family Symbiodiniaceae contributes to the environmental resilience of certain coral species. Chlorophyll-a fluorescence measurements are frequently used to determine symbiont health and resilience, but more work is needed to refine these tools and establish how they relate to...
Autores principales: | , , , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
Frontiers Media S.A.
2023
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC10598705/ https://www.ncbi.nlm.nih.gov/pubmed/37885802 http://dx.doi.org/10.3389/fphys.2023.1244060 |
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author | McQuagge, Audrey Pahl, K. Blue Wong, Sophie Melman, Todd Linn, Laura Lowry, Sean Hoadley, Kenneth D. |
author_facet | McQuagge, Audrey Pahl, K. Blue Wong, Sophie Melman, Todd Linn, Laura Lowry, Sean Hoadley, Kenneth D. |
author_sort | McQuagge, Audrey |
collection | PubMed |
description | Diversity across algal family Symbiodiniaceae contributes to the environmental resilience of certain coral species. Chlorophyll-a fluorescence measurements are frequently used to determine symbiont health and resilience, but more work is needed to refine these tools and establish how they relate to underlying cellular traits. We examined trait diversity in symbionts from the generas Cladocopium and Durusdinium, collected from 12 aquacultured coral species. Photophysiological metrics (Φ(PSII), σ(PSII), ρ, τ(1), τ(2), antenna bed quenching, non-photochemical quenching, and qP) were assessed using a prototype multi-spectral fluorometer over a variable light protocol which yielded a total of 1,360 individual metrics. Photophysiological metrics were then used to establish four unique light-response phenotypic variants. Corals harboring C15 were predominantly found within a single light-response phenotype which clustered separately from all other coral fragments. The majority of Durusdinium dominated colonies also formed a separate light-response phenotype which it shared with a few C1 dominated corals. C15 and D1 symbionts appear to differ in which mechanisms they use to dissipate excess light energy. Spectrally dependent variability is also observed across light-response phenotypes that may relate to differences in photopigment utilization. Symbiont cell biochemical and structural traits (atomic C:N:P, cell size, chlorophyll-a, neutral lipid content) was also assessed within each sample and differ across light-response phenotypes, linking photophysiological metrics with underlying primary cellular traits. Strong correlations between first- and second-order traits, such as Quantum Yield and cellular N:P content, or light dissipation pathways (qP and NPQ) and C:P underline differences across symbiont types and may also provide a means for using fluorescence-based metrics as biomarkers for certain primary-cellular traits. |
format | Online Article Text |
id | pubmed-10598705 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2023 |
publisher | Frontiers Media S.A. |
record_format | MEDLINE/PubMed |
spelling | pubmed-105987052023-10-26 Cellular traits regulate fluorescence-based light-response phenotypes of coral photosymbionts living in-hospite McQuagge, Audrey Pahl, K. Blue Wong, Sophie Melman, Todd Linn, Laura Lowry, Sean Hoadley, Kenneth D. Front Physiol Physiology Diversity across algal family Symbiodiniaceae contributes to the environmental resilience of certain coral species. Chlorophyll-a fluorescence measurements are frequently used to determine symbiont health and resilience, but more work is needed to refine these tools and establish how they relate to underlying cellular traits. We examined trait diversity in symbionts from the generas Cladocopium and Durusdinium, collected from 12 aquacultured coral species. Photophysiological metrics (Φ(PSII), σ(PSII), ρ, τ(1), τ(2), antenna bed quenching, non-photochemical quenching, and qP) were assessed using a prototype multi-spectral fluorometer over a variable light protocol which yielded a total of 1,360 individual metrics. Photophysiological metrics were then used to establish four unique light-response phenotypic variants. Corals harboring C15 were predominantly found within a single light-response phenotype which clustered separately from all other coral fragments. The majority of Durusdinium dominated colonies also formed a separate light-response phenotype which it shared with a few C1 dominated corals. C15 and D1 symbionts appear to differ in which mechanisms they use to dissipate excess light energy. Spectrally dependent variability is also observed across light-response phenotypes that may relate to differences in photopigment utilization. Symbiont cell biochemical and structural traits (atomic C:N:P, cell size, chlorophyll-a, neutral lipid content) was also assessed within each sample and differ across light-response phenotypes, linking photophysiological metrics with underlying primary cellular traits. Strong correlations between first- and second-order traits, such as Quantum Yield and cellular N:P content, or light dissipation pathways (qP and NPQ) and C:P underline differences across symbiont types and may also provide a means for using fluorescence-based metrics as biomarkers for certain primary-cellular traits. Frontiers Media S.A. 2023-10-11 /pmc/articles/PMC10598705/ /pubmed/37885802 http://dx.doi.org/10.3389/fphys.2023.1244060 Text en Copyright © 2023 McQuagge, Pahl, Wong, Melman, Linn, Lowry and Hoadley. https://creativecommons.org/licenses/by/4.0/This is an open-access article distributed under the terms of the Creative Commons Attribution License (CC BY). The use, distribution or reproduction in other forums is permitted, provided the original author(s) and the copyright owner(s) are credited and that the original publication in this journal is cited, in accordance with accepted academic practice. No use, distribution or reproduction is permitted which does not comply with these terms. |
spellingShingle | Physiology McQuagge, Audrey Pahl, K. Blue Wong, Sophie Melman, Todd Linn, Laura Lowry, Sean Hoadley, Kenneth D. Cellular traits regulate fluorescence-based light-response phenotypes of coral photosymbionts living in-hospite |
title | Cellular traits regulate fluorescence-based light-response phenotypes of coral photosymbionts living in-hospite
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title_full | Cellular traits regulate fluorescence-based light-response phenotypes of coral photosymbionts living in-hospite
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title_fullStr | Cellular traits regulate fluorescence-based light-response phenotypes of coral photosymbionts living in-hospite
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title_full_unstemmed | Cellular traits regulate fluorescence-based light-response phenotypes of coral photosymbionts living in-hospite
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title_short | Cellular traits regulate fluorescence-based light-response phenotypes of coral photosymbionts living in-hospite
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title_sort | cellular traits regulate fluorescence-based light-response phenotypes of coral photosymbionts living in-hospite |
topic | Physiology |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC10598705/ https://www.ncbi.nlm.nih.gov/pubmed/37885802 http://dx.doi.org/10.3389/fphys.2023.1244060 |
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