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The physiological mechanisms behind endosymbiont expulsion remain under research but are speculated to involve various means of detachment of zooxanthellae or gastrodermal cells from host corals.<ref name="ladriere2008" /> During a bleaching event, entire gastrodermal cells containing zooxanthellae may leave the host. In other cases, gastrodermal cells will remain in the host tissues, but zooxanthellae contained in vacuoles may separately undergo damage or may physically leave the cells and enter the surrounding environment.<ref name="ladriere2008" />
The physiological mechanisms behind endosymbiont expulsion remain under research but are speculated to involve various means of detachment of zooxanthellae or gastrodermal cells from host corals.<ref name="ladriere2008" /> During a bleaching event, entire gastrodermal cells containing zooxanthellae may leave the host. In other cases, gastrodermal cells will remain in the host tissues, but zooxanthellae contained in vacuoles may separately undergo damage or may physically leave the cells and enter the surrounding environment.<ref name="ladriere2008" />

=== '''Clams and Zooxanthella''' ===
Coral is not the only aquatic organism to be affected by bleaching and the expulsion of zooxanthella; clams have also been found to undergo a similar process when temperatures become too high<ref name=":0">{{Citation |last=Moore |first=David |title=Farming Giant Clams in 2021: A Great Future for the ‘Blue Economy’ of Tropical Islands |date=2022 |url=https://doi.org/10.1007/978-3-030-94846-7_5 |work=Aquaculture: Ocean Blue Carbon Meets UN-SDGS |pages=131–153 |editor-last=Moore |editor-first=David |place=Cham |publisher=Springer International Publishing |language=en |doi=10.1007/978-3-030-94846-7_5.pdf |isbn=978-3-030-94846-7 |access-date=2022-04-25 |editor2-last=Heilweck |editor2-first=Matthias |editor3-last=Petros |editor3-first=Peter}}</ref>.  However, clams discard zooxanthella that are still alive and have been observed being able to recover them<ref name=":0" />. This not only has positive indications for the clams themselves, but also the surrounding ecosystem<ref name=":0" />. For many organisms, clams are a vital part of the food chain. Not only can they themselves be eaten, but excrement from giant clams contains live zooxanthella<ref name=":0" />. Opportunistic feeders and clams alike use excreted zooxanthella as a nutrient source<ref name=":0" /> . The consumption of zooxanthella is especially vital for a clam in its veliger stage as it encourages growth<ref name=":0" />.   Zooxanthella are not only found in clam excrement, but in the mantle tissue as well where they take up ammonia and nitrate<ref>{{Cite journal |last=Fitt |first=W. |last2=Rees |first2=T. |last3=Yellowlees |first3=D. |date=1995 |title=Relationship between pH and the availability of dissolved inorganic nitrogen in the zooxanthella-giant clam symbiosis |url=https://www.semanticscholar.org/paper/Relationship-between-pH-and-the-availability-of-in-Fitt-Rees/ceea8a21d9a7d1fe51989e7031d1c59ff2a8c392 |doi=10.4319/LO.1995.40.5.0976}}</ref>. They are also found in the eyes of clams like ''Tridacna'' where they act as a lens<ref>{{Cite journal |last=Fankboner |first=P. V. |date=1981-01-01 |title=Siphonal eyes of giant clams and their relationship to adjacent zooxanthellae |url=https://www.osti.gov/biblio/6701276 |journal=Veliger; (United States) |language=English |volume=23:3}}</ref>. Different clades of zooxanthella have an impact on clam morphology<ref name=":1">{{Cite journal |last=Long |first=Chao |last2=Zhang |first2=Yuehuan |last3=Li |first3=Yunqing |last4=Li |first4=Jun |last5=Zhou |first5=Zihua |last6=Qin |first6=Yanping |last7=Li |first7=Xingyou |last8=Ma |first8=Haitao |last9=Wei |first9=Jinkuan |last10=Zhou |first10=Yinyin |last11=Noor |first11=Zohaib |date=2021 |title=Effects of Symbiodiniaceae Phylotypes in Clades A–E on Progeny Performance of Two Giant Clams (Tridacna squamosa and T. crocea) During Early History Life Stages in the South China Sea |url=https://www.frontiersin.org/article/10.3389/fmars.2021.633761 |journal=Frontiers in Marine Science |volume=8 |doi=10.3389/fmars.2021.633761 |issn=2296-7745}}</ref>. Clade E1 of zooxanthella seems to influence or favor smaller offspring from clams when compared to clams harboring other clades and all five clades appear to be needed in order for larval settlement to occur<ref name=":1" />.

=== '''Jellyfish and Zooxanthella''' ===
Jellyfish and zooxanthella have a history together in the scientific world as ''Symbiodinium'' was first cultured from the jellyfish ''Cassiopea,'' a model  jellyfish species<ref name=":2">{{Cite journal |last=Djeghri |first=Nicolas |last2=Pondaven |first2=Philippe |last3=Stibor |first3=Herwig |last4=Dawson |first4=Michael N. |date=2019-10-10 |title=Review of the diversity, traits, and ecology of zooxanthellate jellyfishes |url=https://doi.org/10.1007/s00227-019-3581-6 |journal=Marine Biology |language=en |volume=166 |issue=11 |pages=147 |doi=10.1007/s00227-019-3581-6 |issn=1432-1793}}</ref>. Many different types of zooxanthella have been observed forming relationships with jellyfish across many different phylogenetic branches, and the roles they play will change throughout the jellyfish’s life cycle<ref name=":2" />. However, as the jellyfishes ages, the diversity of zooxanthella attaching to them decreases, suggesting that zooxanthella compete with each other to form relationships with the jellyfish<ref name=":2" />. Not all jellyfish form relationships with these microbes and for the most part the ones that do are found in tropic and subtropic waters<ref name=":2" />. The relationship between jellyfish and zooxanthella is affected a little differently than coral in terms of climate change despite both of them being a part of the cnidaria family<ref name=":2" />. One study suggested that certain species of jellyfish and their symbiotic zooxanthella may have some type of resistance to decreasing pH caused by climate change to a certain point<ref>{{Cite journal |last=Weeks |first=Chelsea |last2=Meagher |first2=Shawn |last3=Willink |first3=Philip |last4=McCravy |first4=Kenneth W. |date=2019-09 |title=Does seawater acidification affect zooxanthellae density and health in the invasive upside‐down jellyfish, Cassiopea spp.? |url=https://onlinelibrary.wiley.com/doi/10.1111/ivb.12255 |journal=Invertebrate Biology |language=en |volume=138 |issue=3 |doi=10.1111/ivb.12255 |issn=1077-8306}}</ref>. Although, jellyfish bleaching events have been documented during extreme heat events<ref name=":2" />.  While the causal factors that normally seem to affect the relationship between zooxanthella and their host may not apply to jellyfish, light intensity does<ref name=":3">{{Cite journal |last=Mortillaro |first=J. M. |last2=Pitt |first2=K. A. |last3=Lee |first3=S. Y. |last4=Meziane |first4=T. |date=2009-09-30 |title=Light intensity influences the production and translocation of fatty acids by zooxanthellae in the jellyfish Cassiopea sp. |url=https://www.sciencedirect.com/science/article/pii/S0022098109002718 |journal=Journal of Experimental Marine Biology and Ecology |language=en |volume=378 |issue=1 |pages=22–30 |doi=10.1016/j.jembe.2009.07.003 |issn=0022-0981}}</ref>. Light availability can affect the lipid production of zooxanthella that the jellyfish then utilize<ref name=":3" />. To maximize their light uptake, jellyfish will both swim near the surface and do very specific migrations<ref name=":2" />.  The migration patterns also assist with helping the zooxanthella access specific nutrients.  Many of these jellyfish appear to be mixotrophic consuming both live prey and utilizing phototrophy<ref name=":2" />.  This may be what helps jellyfish survive climate change and bleaching as they could switch feeding methods rather than attempting to recover lost zooxanthella quickly<ref name=":2" />. There are many unknowns in when it comes to the relationship between zooxanthella and jellyfish that scientists look to answer<ref name=":2" />.


==References==
==References==

Revision as of 17:42, 25 April 2022

Yellow-brown zooxanthellae

Zooxanthellae is a colloquial term for single-celled dinoflagellates that are able to live in symbiosis with diverse marine invertebrates including demosponges, corals, jellyfish, and nudibranchs. Most known zooxanthellae are in the genus Symbiodinium,[1] but some are known from the genus Amphidinium, and other taxa, as yet unidentified, may have similar endosymbiont affinities.[2] The true Zooxanthella K.brandt is a mutualist of the radiolarian Collozoum inerme (Joh.Müll., 1856)[3] and systematically placed in Peridiniales.[4] Another group of unicellular eukaryotes that partake in similar endosymbiotic relationships in both marine and freshwater habitats are green algae zoochlorellae.[5]

Zooxanthellae are photosynthetic organisms, which contain chlorophyll a and chlorophyll c, as well as the dinoflagellate pigments peridinin and diadinoxanthin. These provide the yellowish and brownish colours typical of many of the host species.[2] During the day, they provide their host with the organic carbon products of photosynthesis, sometimes providing up to 90% of their host's energy needs for metabolism, growth and reproduction. In return, they receive nutrients, carbon dioxide, and an elevated position with access to sunshine.[6][7]

Morphology and classification

Zooxanthellae can be grouped in the classes of Bacillariophyceae, Cryptophyceae, Dinophyceae, and Rhodophycaeae and of the genera Amphidinium, Gymnodinium, Aureodinium, Gyrodinium, Prorocentrum, Scrippsiella, Gloeodinium, and most commonly, Symbiodinium.[8] Zooxanthellae of genus Symbiodinium belong to a total of eight phylogenetic clades A-H, differentiated via their nuclear ribosomal DNA and chloroplast DNA.[9]

Zooxanthellae are autotrophs containing chloroplasts composed of thylakoids present in clusters of three.[8] A pyrenoid protrudes from each chloroplast and is encased along with the chloroplast by a thick, starchy covering. Within the cell’s cytoplasm also exists lipid vacuoles, calcium oxalate crystals, dictyosomes, and mitochondria.[8] The cell wall of zooxanthellae varies in structure across species. One structure consists of an outer membrane, middle layer compact with electrons, and a thin inner layer. In other species, the characteristics of this low-density inner layer make up the cell wall’s entire structure.[8] Beneath the cell wall is the cell membrane, and beneath the cell membrane are thecal vesicles.[8]

DNA in the cell exists in the form of chromatin coils tightly compacted together.[8] It is condensed in the nucleus alongside an atypical histone complement.[10][11][12] The DNA possesses ribosomal RNA (rRNA) that is folded and of similar morphology to rRNA in archaeobacteria. This indicates that RNA is important for DNA packaging in zooxanthellae.[10] Zooxanthellae, in addition to all other dinoflagellates, possess 5-hydroxymethylmuracil and thymidine in their genomes, unlike any other eukaryotic genome.[10]

Life history

Zooxanthellae alternate between life phases expressed as cysts and as motile organisms in the water column.[13][14] In zooxanthellae of the genus Gymnodinium, one possible life cycle of the cell begins as an immature cyst which reaches maturity then divides to form an immature cyst once more. Once growing into an older cell, it becomes no longer useful. In the life cycle of a motile zooxanthellae cell, its youngest stage is known as a zoosporangium, which matures into a zoospore capable of motility. This motile cell produces and releases gametes for reproduction.[14]

Vegetative phase

The vegetative phase in the life cycle of a zooxanthellae is the predominant form of the organism.[13] In this form, the single-celled organism has a thin cell wall. As opposed to the zoospore, the zooxanthella contains numerous chloroplasts. Once the cell continues growing, however, chloroplasts decrease in abundance.[13] The vegetative cell will either divide into two separate daughter cells or transition into a cyst stage.[13]

Cyst stages

The most common phases in the life history of zooxanthellae following the vegetative phase are cysts, dividing cysts, and degenerate cysts.[14] Cysts possess a thick cell wall yet retain the composition of the cytoplasm and constitute the majority of clustered zooxanthellae in host tissues. This stage of the cell provides the host with a reddish-brown hue.[14] Dividing cysts make up a fourth of the composition of zooxanthellae clusters in host tissues and are expressed as cell stages where two daughter cells remain adjoined but possess individual cell walls. Degenerate cysts are present in clusters, though rare, and lose much of their mutualistic benefit to the host they reside in due to a decrease in photosynthetic efficiency.[14] The young zoosporangium and motile zoospore stages, though seen in zooxanthellae life cycles, are much rarer amongst clades. The zoospore resides in the zoosporangium until the cell wall of the cyst bursts. Zooxanthellae is only motile if it originates as a zoospore.[14]

Motility

Zooxanthellae in the zoospore stage exhibit motility as forward movement or gyratory movement.[14] In moving forward, the organism rotates on the posterior flagellum’s axis whilst simultaneously propelling through the water column. The zoospore gyrates through the water column via attachment of the posterior flagellum to a substrate.[14]

Ecology

Endosymbiont acquisition

Zooxanthellae are particularly associated with reef-building corals but they also inhabit other invertebrates and protists; their hosts include many sea anemones, jellyfish, nudibranchs, certain bivalve molluscs like the giant clam Tridacna, sponges and flatworms as well as some species of radiolarians and foraminiferans.[15] Many different species of zooxanthellae are present in host organisms, each species with its own adaptive capabilities and degree of tolerance of varying environmental factors.[2]

A juvenile organism or newly established colony can acquire its zooxanthellae via sexual reproduction or directly from the environment. The egg from which the individual developed may have already been infected by zooxanthellae at the time of fertilization, or cells of the symbiont may have been transferred from the mother in a period during which the larva was brooded by its parent. Alternatively, the new individual may acquire the zooxanthellae direct from sea water in which the dinoflagellates freely live at some stages of their life cycle. Some stony corals use chemotaxis, with infection occurring as a result of the emission by the coral of a chemical attractant. Infection may also occur after ingestion of infected faecal matter by the host, or of prey that already houses the symbionts. Such indirect acquisition can result in the new host being infected by a species of zooxanthella different from that present in its parent.[2]

Symbiosis with coral

A zooxanthella in symbiosis with coral is contained in vacuoles of the host’s gastrodermal cells and is of the genus Symbiodinium.[16] Zooxanthellae provide nutrients to their host cnidarians in the form of sugars, glycerol, and amino acids and in return gain carbon dioxide, phosphates, and nitrogen compounds.[17][16] A coral exposed to environmental stressors can result in expulsion of zooxanthellae from host tissues. This in turn strips the coral of its color in this phenomenon, known as coral bleaching, where the now transparent tissues of the coral reveal its internal, white skeletal structure.[16] Variations in salinity, light intensity, temperature, pollution, sedimentation, and disease can all impact the photosynthetic efficiency of zooxanthellae or result in expulsion from their mutualistic relationships.[16]

The physiological mechanisms behind endosymbiont expulsion remain under research but are speculated to involve various means of detachment of zooxanthellae or gastrodermal cells from host corals.[16] During a bleaching event, entire gastrodermal cells containing zooxanthellae may leave the host. In other cases, gastrodermal cells will remain in the host tissues, but zooxanthellae contained in vacuoles may separately undergo damage or may physically leave the cells and enter the surrounding environment.[16]

Clams and Zooxanthella

Coral is not the only aquatic organism to be affected by bleaching and the expulsion of zooxanthella; clams have also been found to undergo a similar process when temperatures become too high[18].  However, clams discard zooxanthella that are still alive and have been observed being able to recover them[18]. This not only has positive indications for the clams themselves, but also the surrounding ecosystem[18]. For many organisms, clams are a vital part of the food chain. Not only can they themselves be eaten, but excrement from giant clams contains live zooxanthella[18]. Opportunistic feeders and clams alike use excreted zooxanthella as a nutrient source[18] . The consumption of zooxanthella is especially vital for a clam in its veliger stage as it encourages growth[18].   Zooxanthella are not only found in clam excrement, but in the mantle tissue as well where they take up ammonia and nitrate[19]. They are also found in the eyes of clams like Tridacna where they act as a lens[20]. Different clades of zooxanthella have an impact on clam morphology[21]. Clade E1 of zooxanthella seems to influence or favor smaller offspring from clams when compared to clams harboring other clades and all five clades appear to be needed in order for larval settlement to occur[21].

Jellyfish and Zooxanthella

Jellyfish and zooxanthella have a history together in the scientific world as Symbiodinium was first cultured from the jellyfish Cassiopea, a model  jellyfish species[22]. Many different types of zooxanthella have been observed forming relationships with jellyfish across many different phylogenetic branches, and the roles they play will change throughout the jellyfish’s life cycle[22]. However, as the jellyfishes ages, the diversity of zooxanthella attaching to them decreases, suggesting that zooxanthella compete with each other to form relationships with the jellyfish[22]. Not all jellyfish form relationships with these microbes and for the most part the ones that do are found in tropic and subtropic waters[22]. The relationship between jellyfish and zooxanthella is affected a little differently than coral in terms of climate change despite both of them being a part of the cnidaria family[22]. One study suggested that certain species of jellyfish and their symbiotic zooxanthella may have some type of resistance to decreasing pH caused by climate change to a certain point[23]. Although, jellyfish bleaching events have been documented during extreme heat events[22].  While the causal factors that normally seem to affect the relationship between zooxanthella and their host may not apply to jellyfish, light intensity does[24]. Light availability can affect the lipid production of zooxanthella that the jellyfish then utilize[24]. To maximize their light uptake, jellyfish will both swim near the surface and do very specific migrations[22].  The migration patterns also assist with helping the zooxanthella access specific nutrients.  Many of these jellyfish appear to be mixotrophic consuming both live prey and utilizing phototrophy[22].  This may be what helps jellyfish survive climate change and bleaching as they could switch feeding methods rather than attempting to recover lost zooxanthella quickly[22]. There are many unknowns in when it comes to the relationship between zooxanthella and jellyfish that scientists look to answer[22].

References

  1. ^ LaJeunesse, Todd C.; Parkinson, John Everett; Gabrielson, Paul W.; Jeong, Hae Jin; Reimer, James Davis; Voolstra, Christian R.; Santos, Scott R. (20 August 2018). "Systematic Revision of Symbiodiniaceae Highlights the Antiquity and Diversity of Coral Endosymbionts". Current Biology. 28 (16): 2570–2580.e6. doi:10.1016/j.cub.2018.07.008. PMID 30100341.
  2. ^ a b c d Birkeland, Charles (1997). Life and Death of Coral Reefs. Springer Science & Business Media. pp. 98–99. ISBN 978-0-412-03541-8.
  3. ^ Brandt, K. (1881). "Über das Zusammenleben von Thieren und Algen" [About the coexistence of animals and algae]. Archiv für Anatomie und Physiologie / Physiologische Abteilung (in German). 1881: 570–574.
  4. ^ Gottschling, M.; McLean, T.I. (2013). "New home for tiny symbionts: Dinophytes determined as Zooxanthella are Peridiniales and distantly related to Symbiodinium". Molecular Phylogenetics and Evolution. 67 (1): 217–222. doi:10.1016/j.ympev.2013.01.003. PMID 23333735.{{cite journal}}: CS1 maint: multiple names: authors list (link)
  5. ^ Hoek, Christiaan; Mann, David; Jahns, H. M. (1995). Algae: An Introduction to Phycology. Cambridge University Press. p. 278. ISBN 978-0-521-31687-3.
  6. ^ Ruppert, Edward E.; Fox, Richard, S.; Barnes, Robert D. (2004). Invertebrate Zoology, 7th edition. Cengage Learning. p. 122. ISBN 978-81-315-0104-7.{{cite book}}: CS1 maint: multiple names: authors list (link)
  7. ^ Lohr, Jayme; Munn, Colin B.; Wilson1, William H. (2007). "Characterization of a Latent Virus-Like Infection of Symbiotic Zooxanthellae". Applied and Environmental Microbiology. 73 (9): 2976–2981. doi:10.1128/AEM.02449-06. PMC 1892877. PMID 17351090.{{cite journal}}: CS1 maint: multiple names: authors list (link) CS1 maint: numeric names: authors list (link)
  8. ^ a b c d e f Wakefield, Timothy; Farmer, Mark; Kempf, Stephen (2000). "Revised Description of the Fine Structure of in situ "Zooxanthellae" Genus Symbiodinium". The Biological Bulletin. 199 (1): 76–84. doi:10.2307/1542709. JSTOR 1542709. PMID 10975645.
  9. ^ Berkelmans, Ray; van Oppen, Madeleine J.H. (2006). "The role of zooxanthellae in the thermal tolerance of corals: a 'nugget of hope' for coral reefs in an era of climate change". Proceedings of the Royal Society B. 273 (1599): 2305–2312. doi:10.1098/rspb.2006.3567. PMC 1636081. PMID 16928632.
  10. ^ a b c Stat, Michael; Carter, Dee; Hoegh-Guldberg, Ove (2006). "The evolutionary history of Symbiodinium and scleractinian hosts--Symbiosis, diversity, and the effect of climate change". Perspectives in Plant Ecology, Evolution and Systematics. 8: 23–43. doi:10.1016/j.ppees.2006.04.001.
  11. ^ Herzog, M.; Soyer-Gobillard, M. (1981). "Distinctive features of dinoflagellate chromatin. Absence of nucleosomes in a primitive species Prorocentrum micans". European Journal of Cell Biology. 23 (2): 295–302. PMID 6258920.
  12. ^ Rizzo, P.J. (1981). "Comparative aspects of basic chromatin proteins in dinoflagellates". BioSystems. 14 (3–4): 433–443. doi:10.1016/0303-2647(81)90048-4. PMID 6175358.
  13. ^ a b c d Freudenthal, Hugo (1962). "Symbiodinium gen. nov. and Symbiodinium microadriaticum sp. Nov., a Zooxanthella: Taxonomy, Life Cycle, and Morphology*". The Journal of Protozoology. 9 (1): 45–52. doi:10.1111/j.1550-7408.1962.tb02579.x.
  14. ^ a b c d e f g h Steele, Dunbar (1975). "Stages in the Life History of a Symbiotic Zooxanthella in Pellets Extruded by ITS Host Aiptasia Tagetes (Duch. And Mich.) (Coelenterata, Anthozoa)". The Biological Bulletin. 149 (3): 590–600. doi:10.2307/1540389. JSTOR 1540389. PMID 29324193.
  15. ^ Trench, R.K. (1997). "Diversity of symbiotic dinoflagellates and the evolution of microalgal-invertebrate symbioses". In Lessios, H.A.; MacIntyre, I.G. (eds.). Proceedings of the eighth International Coral Reef Symposium, Panama, June 24–29, 1996. Vol. 2. Balboa, Panama: Smithsonian Tropical Research Institute. pp. 1275–86. OCLC 833272061.
  16. ^ a b c d e f Ladrière, Ophélie; Compère, Philippe; Decloux, Nicole; Vandewalle, Pierre; Poulicek, Mathieu (2008). "Morphological alterations of zooxanthellae in bleached cnidarian hosts". Cahiers de Biologie Marine. 49 (3). hdl:2268/6020.
  17. ^ Muscatine, L; Porter, James W. (1977). "Reef Corals: Mutualistic Symbioses Adapted to Nutrient-Poor Environments". BioScience. 27 (7): 454–460. doi:10.2307/1297526. JSTOR 1297526.
  18. ^ a b c d e f Moore, David (2022), Moore, David; Heilweck, Matthias; Petros, Peter (eds.), "Farming Giant Clams in 2021: A Great Future for the 'Blue Economy' of Tropical Islands", Aquaculture: Ocean Blue Carbon Meets UN-SDGS, Cham: Springer International Publishing, pp. 131–153, doi:10.1007/978-3-030-94846-7_5.pdf, ISBN 978-3-030-94846-7, retrieved 2022-04-25
  19. ^ Fitt, W.; Rees, T.; Yellowlees, D. (1995). "Relationship between pH and the availability of dissolved inorganic nitrogen in the zooxanthella-giant clam symbiosis". doi:10.4319/LO.1995.40.5.0976. {{cite journal}}: Cite journal requires |journal= (help)
  20. ^ Fankboner, P. V. (1981-01-01). "Siphonal eyes of giant clams and their relationship to adjacent zooxanthellae". Veliger; (United States). 23:3.
  21. ^ a b Long, Chao; Zhang, Yuehuan; Li, Yunqing; Li, Jun; Zhou, Zihua; Qin, Yanping; Li, Xingyou; Ma, Haitao; Wei, Jinkuan; Zhou, Yinyin; Noor, Zohaib (2021). "Effects of Symbiodiniaceae Phylotypes in Clades A–E on Progeny Performance of Two Giant Clams (Tridacna squamosa and T. crocea) During Early History Life Stages in the South China Sea". Frontiers in Marine Science. 8. doi:10.3389/fmars.2021.633761. ISSN 2296-7745.{{cite journal}}: CS1 maint: unflagged free DOI (link)
  22. ^ a b c d e f g h i j Djeghri, Nicolas; Pondaven, Philippe; Stibor, Herwig; Dawson, Michael N. (2019-10-10). "Review of the diversity, traits, and ecology of zooxanthellate jellyfishes". Marine Biology. 166 (11): 147. doi:10.1007/s00227-019-3581-6. ISSN 1432-1793.
  23. ^ Weeks, Chelsea; Meagher, Shawn; Willink, Philip; McCravy, Kenneth W. (2019-09). "Does seawater acidification affect zooxanthellae density and health in the invasive upside‐down jellyfish, Cassiopea spp.?". Invertebrate Biology. 138 (3). doi:10.1111/ivb.12255. ISSN 1077-8306. {{cite journal}}: Check date values in: |date= (help)
  24. ^ a b Mortillaro, J. M.; Pitt, K. A.; Lee, S. Y.; Meziane, T. (2009-09-30). "Light intensity influences the production and translocation of fatty acids by zooxanthellae in the jellyfish Cassiopea sp". Journal of Experimental Marine Biology and Ecology. 378 (1): 22–30. doi:10.1016/j.jembe.2009.07.003. ISSN 0022-0981.
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