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Evidence for Rhythmicity Pacemaker in the Calcification Process of Scleractinian Coral

  • Eldad Gutner-Hoch
  • , Kenneth Schneider
  • , Jaroslaw Stolarski
  • , Isabelle Domart-Coulon
  • , Ruth Yam
  • , Anders Meibom
  • , Aldo Shemesh
  • , Oren Levy
  • Bar-Ilan University
  • Polish Academy of Sciences
  • Muséum national d'histoire naturelle
  • Weizmann Institute of Science
  • Swiss Federal Institute of Technology Lausanne
  • University of Lausanne

Research output: Contribution to journalArticlepeer-review

14 Scopus citations

Abstract

Reef-building scleractinian (stony) corals are among the most efficient bio-mineralizing organisms in nature. The calcification rate of scleractinian corals oscillates under ambient light conditions, with a cyclic, diurnal pattern. A fundamental question is whether this cyclic pattern is controlled by exogenous signals or by an endogenous 'biological-clock' mechanism, or both. To address this problem, we have studied calcification patterns of the Red Sea scleractinian coral Acropora eurystoma with frequent measurements of total alkalinity (AT) under different light conditions. Additionally, skeletal extension and ultra-structure of newly deposited calcium carbonate were elucidated with 86Sr isotope labeling analysis, combined with NanoSIMS ion microprobe and scanning electron microscope imaging. Our results show that the calcification process persists with its cyclic pattern under constant light conditions while dissolution takes place within one day of constant dark conditions, indicating that an intrinsic, light-entrained mechanism may be involved in controlling the calcification process in photosymbiotic corals.

Original languageEnglish
Article number20191
JournalScientific Reports
Volume6
DOIs
StatePublished - 5 Feb 2016

Bibliographical note

Funding Information:
This work was supported in part by the European Research Council Advanced Grant 246749 (BIOCARB) to AM and by the MNHN ATM ‘Biomineralization’ program to AM and IDC. NanoSIMS analyses were conducted at the MNHN platform funded by the CNRS and the Region Ile de France. We would like to thank the French Embassy in Israel for their financial support to EGH, and also thank the Interuniversity Institute (IUI) Marine Lab in Eilat for support the experiments conducted at the station. This work represents partial fulfillment of the requirements for a PhD thesis for Gutner-Hoch Eldad at Bar-Ilan University, Faculty of Life Sciences, Israel.

Funding

This work was supported in part by the European Research Council Advanced Grant 246749 (BIOCARB) to AM and by the MNHN ATM ‘Biomineralization’ program to AM and IDC. NanoSIMS analyses were conducted at the MNHN platform funded by the CNRS and the Region Ile de France. We would like to thank the French Embassy in Israel for their financial support to EGH, and also thank the Interuniversity Institute (IUI) Marine Lab in Eilat for support the experiments conducted at the station. This work represents partial fulfillment of the requirements for a PhD thesis for Gutner-Hoch Eldad at Bar-Ilan University, Faculty of Life Sciences, Israel.

FundersFunder number
French Embassy in Israel
Interuniversity Institute
Region Ile de France
Seventh Framework Programme246749
European Commission
Centre National de la Recherche Scientifique

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