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Department of Biology, California State University, Northridge, California 91330-8303
* To whom correspondence should be addressed, at Department of Biology, University of Washington, Seattle, Washington 98195-1800. E-mail: elahi{at}u.washington.edu
In this study, two factorial experiments were used to investigate the role of tissue age in affecting the phenotypic expression of calcification in scleractinian corals. Both experiments tested whether calcification was altered by tissue age and whether corals of different ages exploit plasticity to differing degrees by altering calcification rates under new environmental conditions. To isolate age and size effects, branches of the Caribbean coral Madracis mirabilis were broken into a distal portion that was functionally young and a proximal portion that was functionally old. Fragments were transplanted from a deep (17 m) to a shallow (9 m) site in a Jamaican lagoon to test whether age affected the plasticity of calcification. Both experiments demonstrated that calcification scaled isometrically in the two age groups, and although scaling exponents were indistinguishable statistically among ages, young fragments calcified faster than old fragments. Thus, the effect of age on calcification rate was absolute and independent of size. However, the interactive effect of age and depth was not significant, demonstrating that ability to alter calcification rate (i.e., the extent of phenotypic plasticity for this trait) was unaffected by age. Together, these patterns are consistent with the hypothesis that the proximal modules (i.e., polyps) of M. mirabilis are subject to physiological senescence, as has been reported for other clonal organisms, including algae, fungi, plants, bryozoans, ascidians, and other cnidarians.
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