Characterizing Photosymbiosis Between Fraginae Bivalves and Symbiodinium Using Phylogenetics and Stable Isotopes

Photosymbiotic associations between heterotrophic hosts and photosynthetic algae play crucial roles in maintaining the trophic and structural integrity of coral reef ecosystems. The marine bivalve subfamily Fraginae contains both non-symbiotic and photosymbiotic lineages, making it an ideal comparat...

Full description

Bibliographic Details
Main Authors: Jingchun Li, Megan Volsteadt, Lisa Kirkendale, Colleen M. Cavanaugh
Format: Article
Language:English
Published: Frontiers Media S.A. 2018-04-01
Series:Frontiers in Ecology and Evolution
Subjects:
Online Access:http://journal.frontiersin.org/article/10.3389/fevo.2018.00045/full
id doaj-009a1a37206249feb96e44229f6e32ce
record_format Article
spelling doaj-009a1a37206249feb96e44229f6e32ce2020-11-24T22:51:58ZengFrontiers Media S.A.Frontiers in Ecology and Evolution2296-701X2018-04-01610.3389/fevo.2018.00045341530Characterizing Photosymbiosis Between Fraginae Bivalves and Symbiodinium Using Phylogenetics and Stable IsotopesJingchun Li0Jingchun Li1Jingchun Li2Megan Volsteadt3Megan Volsteadt4Lisa Kirkendale5Colleen M. Cavanaugh6Department of Organismic and Evolutionary Biology, Harvard University, Cambridge, MA, United StatesMuseum of Natural History, University of Colorado Boulder, Boulder, CO, United StatesDepartment of Ecology and Evolutionary Biology, University of Colorado Boulder, Boulder, CO, United StatesDepartment of Organismic and Evolutionary Biology, Harvard University, Cambridge, MA, United StatesDepartment of Biology, University of Guam, Mangilao, GU, United StatesDepartment of Aquatic Zoology, Western Australian Museum, Perth, WA, AustraliaDepartment of Organismic and Evolutionary Biology, Harvard University, Cambridge, MA, United StatesPhotosymbiotic associations between heterotrophic hosts and photosynthetic algae play crucial roles in maintaining the trophic and structural integrity of coral reef ecosystems. The marine bivalve subfamily Fraginae contains both non-symbiotic and photosymbiotic lineages, making it an ideal comparative system to study the origin and evolutionary adaptations of photosymbiosis. The symbiotic species exhibit unique morphological adaptations to photosymbiosis. However, the basic biology of these photosymbiotic relationships, such as symbiont diversity and nutritional benefits, has not been thoroughly characterized. In this study, we examined the general morphology of four Fraginae species occupying different depths (0–10 m): Corculum cardissa, Fragum fragum, Fragum scruposum, and Fragum sueziense. Abundant symbionts were found in the mantle, gill, and part of the foot, contained in tubular networks within host tissues. We used molecular phylogenetics to investigate the algal symbiont community of these Fraginae species. Results showed that symbionts from all four species are dinoflagellates belonging to the Symbiodinium clade C and we did not detect any host-specific or geographic-specific genetic structures within the symbionts. We also used stable carbon isotope analyses to examine whether the cockles are directly utilizing photosynthetically derived carbon sources. All species show less depleted 13C compared to filter-feeding bivalves, suggesting at least part of their organic carbon is derived directly from the symbionts. However, 13C depletion of Fragum sueziense collected from deeper habitats are less distinguishable from filter-feeding bivalves. This indicates that species in deeper habitats may rely less on photosymbiosis due to the reduced light availability. Given that the symbiotic fragines exhibit varying morphologies, habitats, and utilization of symbiont photosynthesis, the subfamily represents an ideal model system to study differential adaptations to photosymbiosis.http://journal.frontiersin.org/article/10.3389/fevo.2018.00045/fullsymbiosissymbiodiniumdinoflagellatecardiidaefragumcorculum
collection DOAJ
language English
format Article
sources DOAJ
author Jingchun Li
Jingchun Li
Jingchun Li
Megan Volsteadt
Megan Volsteadt
Lisa Kirkendale
Colleen M. Cavanaugh
spellingShingle Jingchun Li
Jingchun Li
Jingchun Li
Megan Volsteadt
Megan Volsteadt
Lisa Kirkendale
Colleen M. Cavanaugh
Characterizing Photosymbiosis Between Fraginae Bivalves and Symbiodinium Using Phylogenetics and Stable Isotopes
Frontiers in Ecology and Evolution
symbiosis
symbiodinium
dinoflagellate
cardiidae
fragum
corculum
author_facet Jingchun Li
Jingchun Li
Jingchun Li
Megan Volsteadt
Megan Volsteadt
Lisa Kirkendale
Colleen M. Cavanaugh
author_sort Jingchun Li
title Characterizing Photosymbiosis Between Fraginae Bivalves and Symbiodinium Using Phylogenetics and Stable Isotopes
title_short Characterizing Photosymbiosis Between Fraginae Bivalves and Symbiodinium Using Phylogenetics and Stable Isotopes
title_full Characterizing Photosymbiosis Between Fraginae Bivalves and Symbiodinium Using Phylogenetics and Stable Isotopes
title_fullStr Characterizing Photosymbiosis Between Fraginae Bivalves and Symbiodinium Using Phylogenetics and Stable Isotopes
title_full_unstemmed Characterizing Photosymbiosis Between Fraginae Bivalves and Symbiodinium Using Phylogenetics and Stable Isotopes
title_sort characterizing photosymbiosis between fraginae bivalves and symbiodinium using phylogenetics and stable isotopes
publisher Frontiers Media S.A.
series Frontiers in Ecology and Evolution
issn 2296-701X
publishDate 2018-04-01
description Photosymbiotic associations between heterotrophic hosts and photosynthetic algae play crucial roles in maintaining the trophic and structural integrity of coral reef ecosystems. The marine bivalve subfamily Fraginae contains both non-symbiotic and photosymbiotic lineages, making it an ideal comparative system to study the origin and evolutionary adaptations of photosymbiosis. The symbiotic species exhibit unique morphological adaptations to photosymbiosis. However, the basic biology of these photosymbiotic relationships, such as symbiont diversity and nutritional benefits, has not been thoroughly characterized. In this study, we examined the general morphology of four Fraginae species occupying different depths (0–10 m): Corculum cardissa, Fragum fragum, Fragum scruposum, and Fragum sueziense. Abundant symbionts were found in the mantle, gill, and part of the foot, contained in tubular networks within host tissues. We used molecular phylogenetics to investigate the algal symbiont community of these Fraginae species. Results showed that symbionts from all four species are dinoflagellates belonging to the Symbiodinium clade C and we did not detect any host-specific or geographic-specific genetic structures within the symbionts. We also used stable carbon isotope analyses to examine whether the cockles are directly utilizing photosynthetically derived carbon sources. All species show less depleted 13C compared to filter-feeding bivalves, suggesting at least part of their organic carbon is derived directly from the symbionts. However, 13C depletion of Fragum sueziense collected from deeper habitats are less distinguishable from filter-feeding bivalves. This indicates that species in deeper habitats may rely less on photosymbiosis due to the reduced light availability. Given that the symbiotic fragines exhibit varying morphologies, habitats, and utilization of symbiont photosynthesis, the subfamily represents an ideal model system to study differential adaptations to photosymbiosis.
topic symbiosis
symbiodinium
dinoflagellate
cardiidae
fragum
corculum
url http://journal.frontiersin.org/article/10.3389/fevo.2018.00045/full
work_keys_str_mv AT jingchunli characterizingphotosymbiosisbetweenfraginaebivalvesandsymbiodiniumusingphylogeneticsandstableisotopes
AT jingchunli characterizingphotosymbiosisbetweenfraginaebivalvesandsymbiodiniumusingphylogeneticsandstableisotopes
AT jingchunli characterizingphotosymbiosisbetweenfraginaebivalvesandsymbiodiniumusingphylogeneticsandstableisotopes
AT meganvolsteadt characterizingphotosymbiosisbetweenfraginaebivalvesandsymbiodiniumusingphylogeneticsandstableisotopes
AT meganvolsteadt characterizingphotosymbiosisbetweenfraginaebivalvesandsymbiodiniumusingphylogeneticsandstableisotopes
AT lisakirkendale characterizingphotosymbiosisbetweenfraginaebivalvesandsymbiodiniumusingphylogeneticsandstableisotopes
AT colleenmcavanaugh characterizingphotosymbiosisbetweenfraginaebivalvesandsymbiodiniumusingphylogeneticsandstableisotopes
_version_ 1725667886793490432