Coral micro- and macro-morphological skeletal properties in response to life-long acclimatization at CO2 vents in Papua New Guinea

This study investigates the effects of long-term exposure to OA on skeletal parameters of four tropical zooxanthellate corals naturally living at CO2 seeps and adjacent control sites from two locations (Dobu and Upa Upasina) in the Papua New Guinea underwater volcanic vent system. The seeps are characterized by seawater pH values ranging from 8.0 to about 7.7. The skeletal porosity of Galaxea fascicularis, Acropora millepora, massive Porites, and Pocillopora damicornis was higher (up to ~ 40%, depending on the species) at the seep sites compared to the control sites. Pocillopora damicornis also showed a decrease of micro-density (up to ~ 7%). Thus, further investigations conducted on this species showed an increase of the volume fraction of the larger pores (up to ~ 7%), a decrease of the intraskeletal organic matrix content (up to ~ 15%), and an increase of the intraskeletal water content (up to ~ 59%) at the seep sites. The organic matrix related strain and crystallite size did not vary between seep and control sites. This multi-species study showed a common phenotypic response among different zooxanthellate corals subjected to the same environmental pressures, leading to the development of a more porous skeletal phenotype under OA.

Photosymbiosis in Late Triassic scleractinian corals from the Italian Dolomites

During the Carnian, oligotrophic shallow-water regions of the western Tethys were occupied by small, coral-rich patch reefs. Scleractinian corals, which already contributed to the formation of the reef structure, owed their position most probably to the symbiosis with dinoflagellate algae (zooxanthellae). Using microstructural (regularity of growth increments) and geochemical (oxygen and carbon stable isotopes) criteria of zooxanthellae symbiosis, we investigated whether this partnership was widespread among Carnian scleractinians from the Italian Dolomites (locality Alpe di Specie). Although corals from this locality are renowned from excellent mineralogical preservation (aragonite), their skeletons were rigorously tested against traces of diagenesis Irrespective of their growth forms, well preserved skeletons of corals from the Dolomites, most frequently revealed regular growth bands (low values of coefficient of variation) typical of modern zooxanthellate corals. Paradoxically, some Carnian taxa (Thamnasteriomorpha frechi and Thamnasteriomorphasp.)with highly integrated thamnasterioid colonies which today are formed exclusively by zooxanthellate corals, showed irregular fine-scale growth bands (coefficient of variation of 40% and 41% respectively) that could suggest their asymbiotic status. However, similar irregular skeletal banding is known also in some modern agariciids (Leptoseris fragilis) which are symbiotic with zooxanthellae. This may point to a similar ecological adaptation of Triassic taxa with thamnasterioid colonies. Contrary to occasionally ambiguous interpretation of growth banding, all examined Carnian corals exhibited lack of distinct correlation between carbon (δ13C range between 0.81‰ and 5.81‰) and oxygen (δ18O values range between −4.21‰ and −1.06‰) isotope composition of the skeleton which is consistent with similar pattern in modern zooxanthellates. It is therefore highly likely, that Carnian scleractinian corals exhibited analogous ecological adaptations as modern symbiotic corals and that coral-algal symbiosis that spread across various clades of Scleractinia preceded the reef bloom at the end of the Triassic.

Coexistence of the reef-building coral Cladocora caespitosa and the canopy-forming alga Treptacantha ballesterosii: Description of a new Mediterranean habitat

Shallow Mediterranean rocky environments are usually dominated by macroalgae, but the stony colonial zooxan­thellate coral Cladocora caespitosa is able to build extensive banks in some particular areas. Although zooxanthellate corals and benthic macroalgae are expected to compete for light and space when overlapping in the same habitat, there is previous evidence that C. Caespitosa and Mediterranean macroalgae do not suffer from competitive exclusion when living together. Here we characterize a new and unique Mediterranean habitat where the reef-building coral C. Caespitosa and erect seaweeds of the order Fucales (Cystoseira s.l.) coexist. In this new habitat C. Caespitosa reaches 34% cover and densities of Cystoseira s.l. (mainly Treptacantha ballesterosii) are much higher than values reported from other sites. Interestingly, abundances of T. Ballesterosii and C. Caespitosa show a positive relationship, suggesting that some kind of facilitation mechanism is taking place. These findings challenge the theory of competitive exclusion between corals and macroalgae and launch a wide array of possible open discussions on coral-macroalgae interactions.

Early Miocene shallow-water corals from La Guajira, Colombia: Part II, Mussidae–Siderastreidae and Milleporidae

In this contribution we describe and illustrate 14 coral morphospecies collected from the early Miocene Siamaná (Aquitanian–Burdigalian) and Jimol (late Burdigalian) formations of the Cocinetas Basin in La Guajira Peninsula, northern Colombia. Eleven were identified as already established species including seven genera belonging to the families Mussidae, Pocilloporidae, Poritidae, Siderastreidae, and Milleporidae; the other three remain in open nomenclature. Nine of the 11 species identified (81%) are extinct. The remaining two living species,Siderastrea sidereaandMillepora alcicornis, are common on modern Caribbean reefs. Their presence in the Siamaná Formation extends their temporal range in the Caribbean region to the early Miocene. Most of the taxa described here were hermatypic and zooxanthellate corals of the order Scleractinia, with the exception of the fire coralMillepora alcicornis, of the order Anthothecata, family Milleporidae. The coral fauna recorded in the Siamaná and Jimol formations is typical of shallow and calm waters of the Oligocene–Miocene transition.