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Squishy lipids: Temperature effects on the betaine and galactolipid profiles of a C 18 / C 18 peridinin‐containing dinoflagellate, S ymbiodinium microadriaticum ( D inophyceae), isolated from the mangrove jellyfish, C assiopea xamachana

https://doi.org/10.1111/pre.12093

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What this work says

Outgoing claims: the papers this work cites, builds on, or argues with.

inferredcites →https://doi.org/10.1002/rcm.1142openalex-snapshot

A new solution for an old problem: the regiochemical distribution of the acyl chains in galactolipids can be established by electrospray ionization tandem mass spectrometry

inferredcites →https://doi.org/10.1007/978-90-481-2863-1_10openalex-snapshot

Lipids in the Structure of Photosystem I, Photosystem II and the Cytochrome b 6 f Complex

inferredcites →https://doi.org/10.1007/s00203-009-0486-7openalex-snapshot

Involvement of digalactosyldiacylglycerol in cellular thermotolerance in Synechocystis sp. PCC 6803

inferredcites →https://doi.org/10.1007/s00227-006-0344-yopenalex-snapshot

Viable algae released by the seastar Dermasterias imbricata feeding on the symbiotic sea anemone Anthopleura elegantissima

inferredcites →https://doi.org/10.1007/s00227-008-1011-2openalex-snapshot

Phylogenetic analyses of potentially free-living Symbiodinium spp. isolated from coral reef sand in Okinawa, Japan

inferredcites →https://doi.org/10.1007/s00227-010-1401-0openalex-snapshot

The relative contribution of dinoflagellate photosynthesis and stored lipids to the survivorship of symbiotic larvae of the reef-building corals

inferredcites →https://doi.org/10.1007/s002270050035openalex-snapshot

Fecal discharge of zooxanthellae in the giant clam Tridacna derasa , with reference to their in situ growth rate

inferredcites →https://doi.org/10.1007/s10750-013-1790-4openalex-snapshot

The long and short of it: temperature-dependent modifications of fatty acid chain length and unsaturation in the galactolipid profiles of the diatoms Haslea ostrearia and Phaeodactylum tricornutum

inferredcites →https://doi.org/10.1007/s12562-009-0204-zopenalex-snapshot

Effects of lectin in the scleractinian coral Ctenactis echinata on symbiotic zooxanthellae

inferredcites →https://doi.org/10.1016/0010-406x(68)90959-6openalex-snapshot

Transfer of photosynthetic products from zooxanthellae to coelenterate hosts

inferredcites →https://doi.org/10.1016/0031-9422(96)00115-xopenalex-snapshot

Distribution of betaine lipids in marine algae

inferredcites →https://doi.org/10.1016/j.jembe.2008.06.034openalex-snapshot

Methods for sampling free-living Symbiodinium (zooxanthellae) and their distribution and abundance at Lizard Island (Great Barrier Reef)

inferredcites →https://doi.org/10.1016/j.phytochem.2006.01.010openalex-snapshot

The effect of phosphate starvation on the lipid and fatty acid composition of the fresh water eustigmatophyte Monodus subterraneus

inferredcites →https://doi.org/10.1016/j.plipres.2006.06.001openalex-snapshot

Lipids in photosynthetic reaction centres: Structural roles and functional holes

inferredcites →https://doi.org/10.1016/s0022-0981(97)00139-1openalex-snapshot

The role of temperature in survival of the polyp stage of the tropical rhizostome jellyfish Cassiopea xamachana

inferredcites →https://doi.org/10.1034/j.1399-3054.1997.1000106.xopenalex-snapshot

Lipid synthesis and metabolism in the plastid envelope

inferredcites →https://doi.org/10.1038/nsmb.1559openalex-snapshot

Cyanobacterial photosystem II at 2.9-Å resolution and the role of quinones, lipids, channels and chloride

inferredcites →https://doi.org/10.1046/j.1529-8817.2000.00018.xopenalex-snapshot

LIPID CLASS DISTRIBUTION OF HIGHLY UNSATURATED LONG CHAIN FATTY ACIDS IN MARINE DINOFLAGELLATES

inferredcites →https://doi.org/10.1080/09670260802419481openalex-snapshot

Mono- and digalactosyldiacylglycerol composition of dinoflagellates. I. Peridinin-containing taxa

inferredcites →https://doi.org/10.1080/09670260802524611openalex-snapshot

Mono- and digalactosyldiacylglycerol composition of dinoflagellates. II.Lepidodinium chlorophorum,Karenia brevis, andKryptoperidinium foliaceum, three dinoflagellates with aberrant plastids

inferredcites →https://doi.org/10.1080/09670260902787977openalex-snapshot

Mono- and digalactosyldiacylglycerol composition of dinoflagellates. III. Four cold-adapted, peridinin-containing taxa and the presence of trigalactosyldiacylglycerol as an additional glycolipid

inferredcites →https://doi.org/10.1080/09670260903171650openalex-snapshot

Mono- and digalactosyldiacylglycerol composition of dinoflagellates. IV. Temperature-induced modulation of fatty acid regiochemistry as observed by electrospray ionization/mass spectrometry

inferredcites →https://doi.org/10.1080/09670262.2013.809610openalex-snapshot

Mono- and digalactosyldiacylglycerol composition of dinoflagellates. VI. Biochemical and genomic comparison of galactolipid biosynthesis betweenChromera velia(Chromerida), a photosynthetic alveolate with red algal plastid ancestry, and the dinoflagellate,Lingulodinium polyedrum

inferredcites →https://doi.org/10.1098/rspb.1969.0077openalex-snapshot

Maltose excretion by the symbiotic algae of Hydra viridis

inferredcites →https://doi.org/10.1098/rspb.2004.2757openalex-snapshot

Different algal symbionts explain the vertical distribution of dominant reef corals in the eastern Pacific

inferredcites →https://doi.org/10.1104/pp.105.2.635openalex-snapshot

Cloning of a Higher-Plant Plastid [omega]-6 Fatty Acid Desaturase cDNA and Its Expression in a Cyanobacterium

inferredcites →https://doi.org/10.1104/pp.107.106781openalex-snapshot

Digalactosyldiacylglycerol Is Required for Stabilization of the Oxygen-Evolving Complex in Photosystem II

inferredcites →https://doi.org/10.1111/fwb.12321openalex-snapshot

Temperature‐induced changes in lipid biomarkers and mycosporine‐like amino acids in the psychrophilic dinoflagellate P eridinium aciculiferum

inferredcites →https://doi.org/10.1111/j.0022-3646.1997.00975.xopenalex-snapshot

THE EFFECT OF GROWTH TEMPERATURE AND CULTURE DENSITY ON THE MOLECULAR SPECIES COMPOSITION OF THE GALACTOLIPIDS IN THE RED MICROALGA PORPHYHDIUM CRUENTUM (RHODOPHYTA)1

inferredcites →https://doi.org/10.1111/j.1365-294x.2007.03612.xopenalex-snapshot

Variation in symbiont distribution between closely related coral species over large depth ranges

inferredcites →https://doi.org/10.1111/j.1365-3040.2006.01527.xopenalex-snapshot

Characterization of the Arabidopsis thermosensitive mutant atts02 reveals an important role for galactolipids in thermotolerance

inferredcites →https://doi.org/10.1111/j.1365-3040.2008.01802.xopenalex-snapshot

Metabolic interactions between algal symbionts and invertebrate hosts

inferredcites →https://doi.org/10.1111/j.1440-1835.2010.00590.xopenalex-snapshot

Betaine lipids in chlorarachniophytes

inferredcites →https://doi.org/10.1111/j.1529-8817.2008.00567.xopenalex-snapshot

CORRESPONDENCE BETWEEN COLD TOLERANCE AND TEMPERATE BIOGEOGRAPHY IN A WESTERN ATLANTIC SYMBIODINIUM (DINOPHYTA) LINEAGE1

inferredcites →https://doi.org/10.1111/j.1529-8817.2008.00621.xopenalex-snapshot

SYMBIODINIUM NATANS SP. NOV.: A “FREE‐LIVING” DINOFLAGELLATE FROM TENERIFE (NORTHEAST‐ATLANTIC OCEAN) 1

inferredcites →https://doi.org/10.1111/j.1529-8817.2009.00797.xopenalex-snapshot

COMPARISON OF ENDOSYMBIOTIC AND FREE-LIVING SYMBIODINIUM (DINOPHYCEAE) DIVERSITY IN A HAWAIIAN REEF ENVIRONMENT1

inferredcites →https://doi.org/10.1111/j.1574-6968.1985.tb01143.xopenalex-snapshot

Phospholipid, ester-linked fatty acid profiles as reproducible assays for changes in prokaryotic community structure of estuarine sediments

inferredcites →https://doi.org/10.1111/j.1755-0998.2009.02549.xopenalex-snapshot

Isolation and characterization of microsatellite loci in Symbiodinium B1/B184, the dinoflagellate symbiont of the Caribbean sea fan coral, Gorgonia ventalina

inferredcites →https://doi.org/10.1128/ec.1.4.653-656.2002openalex-snapshot

Synthesis of Chloroplast Galactolipids in Apicomplexan Parasites

inferredcites →https://doi.org/10.1146/annurev.arplant.42.1.467openalex-snapshot

Glycerolipid Synthesis: Biochemistry And Regulation

inferredcites →https://doi.org/10.1146/annurev.ecolsys.34.011802.132417openalex-snapshot

Flexibility and Specificity in Coral-Algal Symbiosis: Diversity, Ecology, and Biogeography of Symbiodinium

inferredcites →https://doi.org/10.2216/i0031-8884-32-3-234.1openalex-snapshot

Stichochrysis immobilis is a diatom, not a chrysophyte

inferredcites →https://doi.org/10.2307/1297526openalex-snapshot

Reef Corals: Mutualistic Symbioses Adapted to Nutrient-Poor Environments

inferredcites →https://doi.org/10.2307/1543184openalex-snapshot

Preferential expulsion of dividing algal cells as a mechanism for regulating algal-cnidarian symbiosis

inferredcites →https://doi.org/10.3354/meps09203openalex-snapshot

Revisiting the winners and the losers a decade after coral bleaching

inferredcites →https://doi.org/10.3354/meps284147openalex-snapshot

Closely related Symbiodinium spp. differ in relative dominance in coral reef host communities across environmental, latitudinal and biogeographic gradients

inferredcites →https://doi.org/10.3390/md8102546openalex-snapshot

Symbiodinium—Invertebrate Symbioses and the Role of Metabolomics

inferredcites →https://doi.org/10.3755/jcrs.9.1openalex-snapshot

A quantitative real-time PCR method for monitoring Symbiodinium in the water column

What points at this work

Incoming claims: where this work appears in other papers’ reference lists and arguments.

inferred← citeshttps://doi.org/10.1016/j.phytochem.2020.112579zenodo-depositor-declared

Lipidomes of phylogenetically different symbiotic dinoflagellates of corals

inferred← citeshttps://doi.org/10.1007/s00248-016-0893-7openalex-snapshot

Polar Lipids Analysis of Cultured Phytoplankton Reveals Significant Inter-taxa Changes, Low Influence of Growth Stage, and Usefulness in Chemotaxonomy

inferred← citeshttps://doi.org/10.1007/s00338-019-01865-xopenalex-snapshot

Lipidome analysis of Symbiodiniaceae reveals possible mechanisms of heat stress tolerance in reef coral symbionts

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Seasonal variation in the lipidome of two species of Millepora hydrocorals from Vietnam coastal waters (the South China Sea)

inferred← citeshttps://doi.org/10.1007/s00338-022-02222-1openalex-snapshot

Lipids of Indo-Pacific gorgonian corals are modified under the influence of microbial associations

inferred← citeshttps://doi.org/10.1007/s00338-025-02802-xopenalex-snapshot

Role of lipids in coral bleaching: lipidomic adaptations and responses under heat stress

inferred← citeshttps://doi.org/10.1007/s10600-020-02940-4openalex-snapshot

Investigation of the Total Lipidoma from a Zoantharia palythoa sp.

inferred← citeshttps://doi.org/10.1007/s10600-026-04929-xopenalex-snapshot

Molecular Profile of Membrane Lipids from a Mollusk Tridacna sp. from the South China Sea

inferred← citeshttps://doi.org/10.1016/b978-0-323-98819-3.00002-xopenalex-snapshot

Algal lipids: structural diversity, analysis and applications

inferred← citeshttps://doi.org/10.1016/bs.amb.2022.07.001openalex-snapshot

The diversity and ecology of Symbiodiniaceae: A traits-based review

inferred← citeshttps://doi.org/10.1016/j.algal.2015.12.005openalex-snapshot

Lipidomic analysis of the extremophilic red alga Galdieria sulphuraria in response to changes in pH

inferred← citeshttps://doi.org/10.1016/j.algal.2022.102850openalex-snapshot

How do algae endosymbionts mediate for their coral host fitness under heat stress? A comprehensive mechanistic overview

inferred← citeshttps://doi.org/10.1016/j.algal.2026.104649openalex-snapshot

Influence of a low atmospheric pressure on the growth and lipid composition of Chlorella vulgaris

inferred← citeshttps://doi.org/10.1016/j.bse.2021.104276openalex-snapshot

Lipidome of the reef-building coral Acropora cerealis: Changes under thermal stress

inferred← citeshttps://doi.org/10.1016/j.isci.2023.107250openalex-snapshot

Smart utilization of betaine lipids in the giant clam Tridacna crocea

inferred← citeshttps://doi.org/10.1016/j.jare.2024.10.007openalex-snapshot

Metabolic responses of sea anemone and jellyfish to temperature and UV bleaching: Insights into stress adaptation using LCMS-based metabolomics, molecular networking and chemometrics

inferred← citeshttps://doi.org/10.1016/j.jembe.2019.151295openalex-snapshot

Effect of experimental thermal stress on lipidomes of the soft coral Sinularia sp. and its symbiotic dinoflagellates

inferred← citeshttps://doi.org/10.1016/j.phytochem.2017.04.012openalex-snapshot

Lipidomic profile in three species of dinoflagellates ( Amphidinium carterae , Cystodinium sp., and Peridinium aciculiferum ) containing very long chain polyunsaturated fatty acids

inferred← citeshttps://doi.org/10.1021/acs.est.5c13276openalex-snapshot

Nitrate Aggravates While Ammonium Mitigates Thermal Bleaching in Corals through Divergent Lipid-Mediated Pathways and Stress Response

inferred← citeshttps://doi.org/10.1038/s41598-025-90484-4openalex-snapshot

Lipidomic and physiological changes in the coral Acropora aspera during bleaching and recovery

inferred← citeshttps://doi.org/10.1080/09670262.2018.1469049openalex-snapshot

Red (hot) algae: modulation of mono- and digalactosyldiacylglycerol-associated fatty acids of Polysiphonia sp. and Porphyridium sp. in response to growth temperature

inferred← citeshttps://doi.org/10.1080/09670262.2018.1519602openalex-snapshot

Mono- and digalactosyldiacylglycerol composition of dinoflagellates. VIII. Temperature effects and a perspective on the curious case ofKarenia mikimotoias a producer of the unusual, ‘green algal’ fatty acid hexadecatetraenoic acid [16:4(n-3)]

inferred← citeshttps://doi.org/10.1080/09670262.2022.2092215openalex-snapshot

Galactolipids of the genus Amphidinium (Dinophyceae): an hypothesis that they are basal to those of other peridinin-containing dinoflagellates

inferred← citeshttps://doi.org/10.1101/2023.01.16.524159openalex-snapshot

Smart utilization of betaine lipids in giant clam Tridacna crocea

inferred← citeshttps://doi.org/10.1111/pre.12528openalex-snapshot

Betaine lipids of Symbiodiniaceae hosted by Indo‐Pacific corals

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Composition of galactolipids, betaine lipids and triglyceride‐associated fatty acids of the symbiotic dinoflagellate Zooxanthella (Brandtodinium) nutricula: A glimpse into polyunsaturated fatty acids available to its polycystine radiolarian host

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Sterols of the aberrant plastid, K areniacean dinoflagellate Asterodinium gracile : Chemotaxonomic overlap with amphisterol‐producing Amphidinium carterae

inferred← citeshttps://doi.org/10.1128/msystems.00856-24openalex-snapshot

Metabolomic profiles of stony coral species from the Dry Tortugas National Park display inter- and intraspecies variation

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Trophic Biomarkers in Some Mesopelagic Fish Species from the Irminger Sea

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A Lipidomic Approach to the Study of Biodiversity of Symbiotic Dinoflagellates in Millepora Hydrocorals from Vietnam Coral Reefs

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Coral Lipidomes and Their Changes during Coral Bleaching

inferred← citeshttps://doi.org/10.3389/fmars.2021.714778openalex-snapshot

Metabolomics of Healthy and Stony Coral Tissue Loss Disease Affected Montastraea cavernosa Corals

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Living Inside a Jellyfish: The Symbiosis Case Study of Host-Specialized Dinoflagellates, “Zooxanthellae”, and the Scyphozoan Cotylorhiza tuberculata

inferred← citeshttps://doi.org/10.3389/fmars.2023.1321271openalex-snapshot

Stony coral tissue loss disease: a review of emergence, impacts, etiology, diagnostics, and intervention

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Comparative Analysis of Membrane Lipids in Psychrophilic and Mesophilic Freshwater Dinoflagellates

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Influence of Habitat Alteration on the Molecular Profile of Membrane Lipids of the Coral Junceella fragilis

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Algal Adaptation to Environmental Stresses: Lipidomics Research

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Coral Holobionts Possess Distinct Lipid Profiles That May Be Shaped by Symbiodiniaceae Taxonomy

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Coral Lipidome: Molecular Species of Phospholipids, Glycolipids, Betaine Lipids, and Sphingophosphonolipids

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Wild or Reared? Cassiopea andromeda Jellyfish as a Potential Biofactory

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