Dimethylsulfoniopropionate in corals and its interrelations with bacterial assemblages in coral surface mucus

Corals produce copious amounts of dimethylsulfoniopropionate (DMSP), a sulfur compound thought toplay a role in structuring coral-associated bacterial communities. We tested the hypothesis that a linkage exists betweenDMSP availability in coral tissues and the community dynamics of bacteria in coral surface mucus. We determinedDMSP concentrations in three coral species (Meandrina meandrites, Porites astreoides and Siderastrea siderea) at twosampling depths (5 and 25 m) and times of day (dawn and noon) at Curac¸ao, Southern Caribbean. DMSP concentration(4–409 nmol cm?2 coral surface) varied with host species-specific traits such as Symbiodinium cell abundance, but notwith depth or time of sampling. Exposure of corals to air caused a doubling of their DMSPconcentration. The phylogeneticaffiliation of mucus-associated bacteria was examined by clone libraries targeting three main subclades of the bacterialDMSP demethylase gene (dmdA). dmdA gene abundance was determined by quantitative Polymerase Chain Reaction(qPCR) against a reference housekeeping gene (recA). Overall, a higher availability of DMSP corresponded to a lowerrelative abundance of the dmdA gene, but this pattern was not uniform across all host species or bacterial dmdA subclades,suggesting the existence of distinct DMSP microbial niches or varying dmdA DMSP affinities. This is the first studyquantifying dmdA gene abundance in corals and linking related changes in the community dynamics of DMSP-degradingbacteria to DMSP availability. Our study suggests that DMSP mediates the regulation of microbe

Sharing the slope: depth partitioning of agariciid corals and associated <i>Symbiodinium</i> across shallow and mesophotic habitats (2-60 m) on a Caribbean reef

Background: Scleractinian corals and their algal endosymbionts (genus Symbiodinium) exhibit distinct bathymetric distributions on coral reefs. Yet, few studies have assessed the evolutionary context of these ecological distributions by exploring the genetic diversity of closely related coral species and their associated Symbiodinium over large depth ranges. Here we assess the distribution and genetic diversity of five agariciid coral species (Agaricia humilis, A. agaricites, A. lamarcki, A. grahamae, and Helioseris cucullata) and their algal endosymbionts (Symbiodinium) across a large depth gradient (2-60 m) covering shallow to mesophotic depths on a Caribbean reef.<br>Results: The five agariciid species exhibited distinct depth distributions, and dominant Symbiodinium associations were found to be species-specific, with each of the agariciid species harbouring a distinct ITS2-DGGE profile (except for a shared profile between A. lamarcki and A. grahamae). Only A. lamarcki harboured different Symbiodinium types across its depth distribution (i.e. exhibited symbiont zonation). Phylogenetic analysis (atp6) of the coral hosts demonstrated a division of the Agaricia genus into two major lineages that correspond to their bathymetric distribution ("shallow": A. humilis / A. agaricites and "deep": A. lamarcki / A. grahamae), highlighting the role of depth-related factors in the diversification of these congeneric agariciid species. The divergence between "shallow" and "deep" host species was reflected in the relatedness of the associated Symbiodinium (with A. lamarcki and A. grahamae sharing an identical Symbiodinium profile, and A. humilis and A. agaricites harbouring a related ITS2 sequence in their Symbiodinium profiles), corroborating the notion that brooding corals and their Symbiodinium are engaged in coevolutionary processes.<br>Conclusions: Our findings support the hypothesis that the depth-related environmental gradient on reefs has played an important role in the diversification of the genus Agaricia and their associated Symbiodinium, resulting in a genetic segregation between coral host-symbiont communities at shallow and mesophotic depths

Distribution and photobiology of Symbiodinium types in different light environments for three colour morphs of the coral Madracis pharensis: Is there more to it than total irradiance?

The role of symbiont variation in the photobiology of reef corals was addressed by investigating the links among symbiont genetic diversity, function and ecological distribution in a single host species, Madracis pharensis. Symbiont distribution was studied for two depths (10 and 25 m), two different light habitats (exposed and shaded) and three host colour morphs (brown, purple and green). Two Symbiodinium genotypes were present, as defined by nuclear internal transcribed spacer 2 ribosomal DNA (ITS2-rDNA) variation. Symbiont distribution was depth- and colour morph-dependent. Type B15 occurred predominantly on the deeper reef and in green and purple colonies, while type B7 was present in shallow environments and brown colonies. Different light microhabitats at fixed depths had no effect on symbiont presence. This ecological distribution suggests that symbiont presence is potentially driven by light spectral niches. A reciprocal depth transplantation experiment indicated steady symbiont populations under environment change. Functional parameters such as pigment composition, chlorophyll a fluorescence and cell densities were measured for 25 m and included in multivariate analyses. Most functional variation was explained by two photobiological assemblages that relate to either symbiont identity or light microhabitat, suggesting adaptation and acclimation, respectively. Type B15 occurs with lower cell densities and larger sizes, higher cellular pigment concentrations and higher peridinin to chlorophyll a ratio than type B7. Type B7 relates to a larger xanthophyll-pool size. These unambiguous differences between symbionts can explain their distributional patterns, with type B15 being potentially more adapted to darker or deeper environments than B7. Symbiont cell size may play a central role in the adaptation of coral holobionts to the deeper reef. The existence of functional differences between B-types shows that the clade classification does not necessarily correspond to functional identity. This study supports the use of ITS2 as an ecological and functionally meaningful marker in Symbiodinium

Studies on the Manufacturing Conditions of Hardboard from HIMESHARA (Stewartia monadelpha Sieb. et Zucc.). Part 2. : The Variation of the Chemical Components in the Manufacturing Process of Hardwood

A major challenge in coral biology is to find the most adequate and phylogenetically informative characters that allow for distinction of closely related coral species. Therefore, data on corallite morphology and genetic data are often combined to increase phylogenetic resolution. In this study, we address the question to which degree genetic data and quantitative information on overall coral colony morphologies identify similar groupings within closely related morphospecies of the Caribbean coral genus Madracis. Such comparison of phylogenies based on colony morphology and genetic data will also provide insight into the degree to which genotype and phenotype overlap. We have measured morphological features of three closely related Caribbean coral species of the genus Madracis (M. formosa, M. decactis and M. carmabi). Morphological differences were then compared with phylogenies of the same species based on two nuclear DNA markers, i.e. ATPS alpha and SRP54. Our analysis showed that phylogenetic trees based on (macroscopical) morphological properties and phylogenetic trees based on DNA markers ATPS alpha and SRP54 are partially similar indicating that morphological characteristics at the colony level provide another axis, in addition to commonly used features such as corallite morphology and ecological information, to delineate genetically different coral species. We discuss this new method that allows systematic quantitative comparison between morphological characteristics of entire colonies and genetic data