Corallite

Abstract: Scanning electron microscopy and serial petrographic thin sections were used to investigate skeletal elongation and mineralization in the perforate coral, Acropora cervicornis. The axial corallite extends by the formation of randomly oriented fusiform crystals which are deposited on its distal edge. Aragonitic needle-like crystals grow in random directions from the surface of these fusiform crystals. Only those needle-like crystals growing toward the calicoblastic epithelium (i.e. crystals whose growth axis is perpendicular to the plane of the calicoblastic cell membrane) continue to elongate. Groups of these growing crystals join to form well-defined fasciculi which make up the primary skeletal elements comprising the septotheca. The resulting skeleton is highly porous with all surfaces covered by the continuous calicoblastic epithelium. This cell layer is separated by thin mesoglea from the flagellated gastrodermis which lines the highly ramified coelenteron. Porosity and permeability of the skeleton decrease with distance from the tip. Density correspondingly increases due to the addition of aragonite to the fasciculi whose boundaries become less distinct as channels fill with calcium carbonate.

Abstract: The occurrence of zooxanthellae in Recent scleractinian corals is strongly correlated with their growth form, corallite size, and degree of morphological integration of corallites. The great majority of zooxanthellate corals are multiserial with small, highly integrated corallites, whereas most corals lacking zooxanthellae are solitary or uniserial colonial forms with large, poorly integrated corallites. Beginning in the Jurassic, fossil scleractinian faunas are morphologically similar to Recent faunas dominated by zooxanthellate species, strongly implying that most scleractinians contained zooxanthellae by that time. Evidence for Siluro–Devonian tabulates and Triassic scleractinians is equivocal but still suggests the presence of zooxanthellae in these corals. In contrast, morphological evidence suggests that rugosan corals lacked zooxanthellae.Most populations of Recent zooxanthellate corals contribute to reef formation, but many do not. Similarly, fossil corals interpreted to contain zooxanthellae on morphological grounds did not always form reefs. Recent reef formation depends upon a host of environmental factors that have little to do with the possession of zooxanthellae per se. Coral morphology should be a better predictor of the presence of zooxanthellae in fossil corals than their association with reefs.

Abstract: Patterns of growth lines and the composition of stable oxygen and carbon isotopes were studied in skeletons of the deep-water scleractinian Lophelia pertusa in longitudinal and transverse sections of corallites. δ180 showed a significant, positive linear correlation with δ13C. A gradual depletion of δ180 and BC was found in the theca, both towards the corallite edge within single growth layers, and across growth layers from the theca surface. δ18O was negatively correlated with the rate of linear extension. These results indicated that isotopic fractionation in Lophelia is controlled by kinetic isotope effects. The range of δ180 was 3.5 times larger than expected for aragonite precipitating in isotopic equilibrium with ambient sea water. However, the shape of the δ180 curve along the growth axis in the septa was almost parallel with the curve of sea water temperatures. This correspondence may be caused by a relation between growth rate and temperature or other environmental variables correlated w...