scholarly journals Correction: Ocean acidification at a coastal CO2 vent induces expression of stress-related transcripts and transposable elements in the sea anemone Anemonia viridis

PLoS ONE ◽  
2020 ◽  
Vol 15 (3) ◽  
pp. e0230397
Author(s):  
PLoS ONE ◽  
2019 ◽  
Vol 14 (5) ◽  
pp. e0210358 ◽  
Author(s):  
Ilona Urbarova ◽  
Sylvain Forêt ◽  
Mikael Dahl ◽  
Åse Emblem ◽  
Marco Milazzo ◽  
...  

2012 ◽  
Vol 65 (2) ◽  
pp. 269-276 ◽  
Author(s):  
Dalit Meron ◽  
Maria-Cristina Buia ◽  
Maoz Fine ◽  
Ehud Banin

Toxins ◽  
2022 ◽  
Vol 14 (1) ◽  
pp. 27
Author(s):  
Ainara Ballesteros ◽  
Janire Salazar ◽  
Macarena Marambio ◽  
José Tena ◽  
José Rafael García-March ◽  
...  

Anemonia viridis is an abundant and widely distributed temperate sea anemone that can form dense congregations of individuals. Despite the potential severity of its sting, few detailed cases have been reported. We report a case of a severe toxic reaction following an A. viridis sting in a 35-year-old oceanographer. She developed severe pain, itching, redness, and burning sensation, which worsened one week after treatment with anti-inflammatories, antihistamines and corticosteroids. Prompted by this event, and due to the insufficient risk prevention, lack of training for marine-environment users, and lack of research into sting-specific first-aid protocols, we evaluated the cnidocyst response to five different compounds commonly recommended as rinse solutions in first-aid protocols (seawater, vinegar, ammonia, baking soda, and freshwater) by means of the Tentacle Solution Assay. Vinegar and ammonia triggered an immediate and massive cnidocyst discharge after their application and were classified as activator solutions. Baking soda and freshwater were also classified as activator solutions, although with a lower intensity of discharge. Only seawater was classified as a neutral solution and therefore recommended as a rinse solution after A. viridis sting, at least until an inhibitory solution is discovered.


2018 ◽  
Vol 28 ◽  
pp. 13-23
Author(s):  
Suharsono

The zooxanthella, Symbiodinum microadriaticum, an endosymbiotic dinoflagellate shows variation in its ultrastructure within its population in the sea anemone, Anemonia viridis. Such variation included the number of thylakoid, the structure of inclusions and the structure of amphiesma. The string-like structure was also found in the nucleoplasm. Some zooxanthellae have a branching or double pyrenoid with two or three stalks. Under certain condition, which are not clearly understood, two or three zooxanthellae are enclosed within one very thick membrane.


2021 ◽  
Author(s):  
◽  
Michael Doherty

<p>Ocean acidification has the potential to drastically alter the coral reef ecosystem by reducing the calcification rate of corals and other reef-builders, and hence a considerable amount of research is now focused on this issue. It also is conceivable that acidification may affect other physiological processes of corals. In particular, acidification may alter photosynthetic physiology and hence the productivity of the coraldinoflagellate symbiosis that is pivotal to the reef's survival and growth. However, very little is known about the impacts of acidification on the photophysiology of corals or, indeed, other invertebrate-algal symbioses. This gap in our knowledge was addressed here by measuring the impacts of acidification (pH 7.6 versus pH 8.1) on the photophysiology and health of the tropical coral Stylophora pistillata and its isolated dinoflagellate symbionts ('zooxanthellae'), and the temperate sea anemone Anthopleura aureoradiata. The comparative nature of this study allowed for any differences between tropical and temperate symbioses, and zooxanthellae in a symbiotic or free-living state, to be assessed. Corals, anemones and cultured zooxanthellae were maintained in flowthrough seawater systems, and treated either with non-acidified (control) seawater at pH 8.1, or seawater acidified with CO2 or HCl to pH 7.6. A variety of parameters, including zooxanthellar density, chlorophyll content, photosynthetic health (Yi), and the ratio of gross photosynthetic production to respiration (P:R) were measured via cell counts, spectrophotometry, respirometry and PAM fluorometry, at a series of time-points up to a maximum of 42 days. Acidification generated by the addition of CO2 had no discernible effect on Yi of either the corals or anemones. However, in the coral, chlorophyll content per zooxanthella cell increased by 25%, which was countered by a near-significant decline (22%) in the rate of gross photosynthesis per unit chlorophyll; as zooxanthellar density remained unchanged, this led to a constant P:R ratio. When acidified via CO2, the isolated zooxanthellae exhibited no impacts in recorded Yi or chlorophyll levels. The response of the anemone to acidification via CO2 was different to that observed in the coral, as the density of zooxanthellae increased, rather than the chlorophyll content per cell, leading to an increased rate of gross photosynthesis. However P:R again remained constant as the increased photosynthesis was matched by an increased rate of respiration. In contrast to the impacts of CO2, HCl adversely impacted the chlorophyll content per cell in both the isolated zooxanthellae and sea anemone, and Yi, gross photosynthesis per cell, and overall gross photosynthesis in the sea anemone; however, despite the decline in gross photosynthesis, P:R remained constant due to the concurrent decline in respiration. Unfortunately, the corals in the HCl experiment died due to technical issues. There are two plausible reasons for this difference between CO2 and HCl. Firstly, HCl may have caused intracellular acidosis which damaged chloroplast structure and photosynthetic function. Secondly, the increased levels of aqueous CO2 stimulated photosynthetic function and hence mitigated for the effects of lowered pH. In addition, evidence is presented for a pH threshold for A. aureoradiata of between pH 6 and pH 6.75 (acidified with HCl), at which point photosynthesis 'shuts-down'. This suggests that, even without the potentially beneficial effects from increased CO2 levels, it is likely that oceanic pH would need to decrease to less than pH 6.75 for any acidosis effects to compromise the productivity of this particular symbiosis. Since acidification will have the benefits of increased CO2 and will reach nowhere near such low pH levels as those extremes tested here, it is proposed that ocean acidification via increased dissolution of CO2 into our oceans will have no impact on the photosynthetic production of symbiotic cnidarians. Indeed, it is entirely likely that increased CO2 will add some benefit to the usually carbon-limited symbiotic zooxanthellae. Ocean acidification is not likely to benefit corals however, with compromised calcification rates likely to undermine the viability of the coral. Symbiotic sea anemones, which do not bio-mineralise CaCO3, are better placed to take advantage of the increased CO2 as we move toward more acidic oceans.</p>


Marine Drugs ◽  
2018 ◽  
Vol 16 (4) ◽  
pp. 134 ◽  
Author(s):  
Erwann Loret ◽  
José Luis ◽  
Christopher Nuccio ◽  
Claude Villard ◽  
Pascal Mansuelle ◽  
...  

1998 ◽  
Vol 274 (2) ◽  
pp. R303-R310 ◽  
Author(s):  
Paola Furla ◽  
Sylvie Bénazet-Tambutté ◽  
Jean Jaubert ◽  
Denis Allemand

The oral epithelial layers of anthozoans have a polarized morphology: photosynthetic endosymbionts live within endodermal cells facing the coelenteric cavity and are separated from the external seawater by the ectodermal layer and the mesoglea. To study if this morphology plays a role in the supply of inorganic carbon for symbiont photosynthesis, we measured the change in pH and the rate of OH−(H+) fluxes induced by each cell layer on a tentacle of the sea anemone Anemonia viridis. Light-induced pH increase of the medium bathing the endodermal layers led to the generation of a transepithelial pH gradient of ∼0.8 pH units across the tentacle, whereas darkness induced acidification of this medium. The light-induced pH change was associated with an increase of total alkalinity. Only the endodermal layer was able to induce a net OH− secretion (H+ absorption). The light-induced OH− secretion by the endodermal cell layer was dependent on the presence of[Formula: see text] in the compartment facing the ectoderm and was sensitive to several inhibitors of ion transport. [14C][Formula: see text]incorporation into photosynthates confirmed the ectodermal supply, the extent of which varied from 25 to >90%, according to[Formula: see text] availability. Our results suggest that the light-induced OH−secretion by the endodermal cell layer followed the polarized transport of [Formula: see text] and its subsequent decarboxylation within the endodermal cell layer. This polarity may play a significant role both in inorganic carbon absorption and in the control of light-enhanced calcification in scleractinian corals.


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