Literature DB >> 14601413

Coral bleaching--capacity for acclimatization and adaptation.

S L Coles1, Barbara E Brown.   

Abstract

Coral bleaching, i.e., loss of most of the symbiotic zooxanthellae normally found within coral tissue, has occurred with increasing frequency on coral reefs throughout the world in the last 20 years, mostly during periods of El Nino Southern Oscillation (ENSO). Experiments and observations indicate that coral bleaching results primarily from elevated seawater temperatures under high light conditions, which increases rates of biochemical reactions associated with zooxanthellar photosynthesis, producing toxic forms of oxygen that interfere with cellular processes. Published projections of a baseline of increasing ocean temperature resulting from global warming have suggested that annual temperature maxima within 30 years may be at levels that will cause frequent coral bleaching and widespread mortality leading to decline of corals as dominant organisms on reefs. However, these projections have not considered the high variability in bleaching response that occurs among corals both within and among species. There is information that corals and their symbionts may be capable of acclimatization and selective adaptation to elevated temperatures that have already resulted in bleaching resistant coral populations, both locally and regionally, in various areas of the world. There are possible mechanisms that might provide resistance and protection to increased temperature and light. These include inducible heat shock proteins that act in refolding denatured cellular and structural proteins, production of oxidative enzymes that inactivate harmful oxygen radicals, fluorescent coral pigments that both reflect and dissipate light energy, and phenotypic adaptations of zooxanthellae and adaptive shifts in their populations at higher temperatures. Such mechanisms, when considered in conjunction with experimental and observational evidence for coral recovery in areas that have undergone coral bleaching, suggest an as yet undefined capacity in corals and zooxanthellae to adapt to conditions that have induced coral bleaching. Clearly, there are limits to acclimatory processes that can counter coral bleaching resulting from elevated sea temperatures, but scientific models will not accurately predict the fate of reef corals until we have a better understanding of coral-algal acclimatization/adaptation potential. Research is particularly needed with respect to the molecular and physiological mechanisms that promote thermal tolerance in corals and zooxanthellae and identification of genetic characteristics responsible for the variety of responses that occur in a coral bleaching event. Only then will we have some idea of the nature of likely responses, the timescales involved and the role of 'experience' in modifying bleaching impact.

Entities:  

Mesh:

Year:  2003        PMID: 14601413     DOI: 10.1016/s0065-2881(03)46004-5

Source DB:  PubMed          Journal:  Adv Mar Biol        ISSN: 0065-2881            Impact factor:   5.143


  46 in total

Review 1.  The effects of habitat on coral bleaching responses in Kenya.

Authors:  Gabriel Grimsditch; Jelvas M Mwaura; Joseph Kilonzo; Nassir Amiyo
Journal:  Ambio       Date:  2010-06       Impact factor: 5.129

Review 2.  Paths toward algal genomics.

Authors:  Arthur R Grossman
Journal:  Plant Physiol       Date:  2005-02       Impact factor: 8.340

3.  Outbreak and persistence of opportunistic symbiotic dinoflagellates during the 2005 Caribbean mass coral 'bleaching' event.

Authors:  Todd C LaJeunesse; Robin T Smith; Jennifer Finney; Hazel Oxenford
Journal:  Proc Biol Sci       Date:  2009-09-09       Impact factor: 5.349

4.  Effects of flow and colony morphology on the thermal boundary layer of corals.

Authors:  Isabel M Jimenez; Michael Kühl; Anthony W D Larkum; Peter J Ralph
Journal:  J R Soc Interface       Date:  2011-05-20       Impact factor: 4.118

5.  Response of coral assemblages to thermal stress: are bleaching intensity and spatial patterns consistent between events?

Authors:  Lucie Penin; Jeremie Vidal-Dupiol; Mehdi Adjeroud
Journal:  Environ Monit Assess       Date:  2012-10-11       Impact factor: 2.513

6.  Host-symbiont recombination versus natural selection in the response of coral-dinoflagellate symbioses to environmental disturbance.

Authors:  Todd C LaJeunesse; Robin Smith; Mariana Walther; Jorge Pinzón; Daniel T Pettay; Michael McGinley; Matthew Aschaffenburg; Pedro Medina-Rosas; Amilcar L Cupul-Magaña; Andrés López Pérez; Hector Reyes-Bonilla; Mark E Warner
Journal:  Proc Biol Sci       Date:  2010-05-05       Impact factor: 5.349

7.  Intraspecific and interspecific variation in thermotolerance and photoacclimation in Symbiodinium dinoflagellates.

Authors:  Erika M Díaz-Almeyda; C Prada; A H Ohdera; H Moran; D J Civitello; R Iglesias-Prieto; T A Carlo; T C LaJeunesse; M Medina
Journal:  Proc Biol Sci       Date:  2017-12-06       Impact factor: 5.349

8.  Activation of the cnidarian oxidative stress response by ultraviolet radiation, polycyclic aromatic hydrocarbons and crude oil.

Authors:  A M Tarrant; A M Reitzel; C K Kwok; M J Jenny
Journal:  J Exp Biol       Date:  2014-01-16       Impact factor: 3.312

9.  Location-specific responses to thermal stress in larvae of the reef-building coral Montastraea faveolata.

Authors:  Nicholas R Polato; Christian R Voolstra; Julia Schnetzer; Michael K DeSalvo; Carly J Randall; Alina M Szmant; Mónica Medina; Iliana B Baums
Journal:  PLoS One       Date:  2010-06-23       Impact factor: 3.240

10.  The roles and interactions of symbiont, host and environment in defining coral fitness.

Authors:  Jos C Mieog; Jeanine L Olsen; Ray Berkelmans; Silvia A Bleuler-Martinez; Bette L Willis; Madeleine J H van Oppen
Journal:  PLoS One       Date:  2009-07-24       Impact factor: 3.240

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