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11th ICRS Abstract book - Nova Southeastern University

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Poster Mini-Symposium 5: Functional Biology of Corals and Coral Symbiosis: Molecular Biology, Cell Biology and Physiology<br />

5.100<br />

The Effect Of Different Flow Regimes On The Long-Term Skeletal Growth And<br />

Physiology Of The Scleractinian Coral Galaxea Fascicularis in A Closed Aquarium<br />

System<br />

Miriam SCHUTTER* 1,2 , Max JANSE 3 , Ronald OSINGA 1 , Johan VERRETH 1 , René<br />

WIJFFELS 2<br />

1 Aquaculture and Fisheries, Wageningen <strong>University</strong>, Wageningen, Netherlands,<br />

2 Bioprocess Engineering Group, Wageningen <strong>University</strong>, Wageningen, Netherlands,<br />

3 Burgers Zoo, Arnhem, Netherlands<br />

Water flow is one of the most important abiotic factors influencing the growth of<br />

scleractinian corals. Different aspects of flow, such as speed, turbulence and direction,<br />

affect prey capture efficiency, exchange rate of dissolved gasses and nutrients, and<br />

removal of sediment or mucus.<br />

A long term experiment was performed in a closed aquarium system (Burgers Ocean, the<br />

Netherlands) to examine the effect of different flow regimes (1 cm/s, 10 cm/s, 20 cm/s<br />

and 25 cm/s, alternating, bidirectional flow) on long-term growth. Ten nubbins (single<br />

polyp clones of a coral colony) of Galaxea fascicularis were used for each treatment.<br />

Growth of these nubbins was measured for a 42 week period by determination of buoyant<br />

weight and by making polyp counts (every six weeks), and by image analysis for surface<br />

area (every three weeks).<br />

In concurrent short-term incubation experiments, the feeding efficiency (uptake of<br />

Artemia nauplii) and the metabolic rates (photosynthesis and respiration) of these corals<br />

under the selected flow regimes was studied in a respirometric flow cell. These short term<br />

experiments may provide an explanation for the observed differences in growth.<br />

So far, it is found that the coral nubbins grow less in the zero flow regime, while they<br />

grow most at 25 cm/s. Not much difference is found in growth between 10 and 20 cm/s.<br />

Water flow speed seems to have little effect on photosynthetic rate and a much larger<br />

effect on respiration rate. Feeding seems neither enhanced nor impaired at higher flow<br />

speeds.<br />

5.101<br />

Segmented Gastric Cavity Of The Stony Coral<br />

Michal RAZ BAHAT* 1 , Zehava UNI 2 , Buki RINKEVICH 1<br />

1 zoology, National Institute of Oceanography, Israel Oceanographic and Limnological<br />

Research, Haifa, Israel, 2 Zoology, Faculty of Agriculture, Hebrew <strong>University</strong>, P.O. Box<br />

12, Rehovot, Israel, Rehovo, Israel<br />

The digestive system of the stony coral has not been yet investigated thoroughly. The<br />

literature describes the polyp’s digestive system schematically, as a blind sac divided into<br />

compartments by mesenteries lined with the gastrodermis tissue and with numerous<br />

mucus cells. This study investigates, in various methods, the detailed morphology and the<br />

enzymatic function of coral’s digestive cavity.<br />

Observing histological sections along the gastric cavity of the small-polyp coral<br />

Stylophora pistillata, by light microscopy, we found that the polyp’s digestive system<br />

along the oral-aboral axis, is divided into several segments of different cell types and<br />

distribution. Using SAM, we investigated the structure and surface area of the gastric<br />

cavity walls, and found that they change, gradually, from the pharynx towards the basal<br />

plate. In order to elucidate whether the observed morphological characteristics are<br />

functional as well, we tested the activities of some digestive enzymes and found a<br />

differential abundance along the gastric cavity. This insight into the segmented gastric<br />

cavity provides a new perspective of the coral’s digestive system.<br />

5.102<br />

The Tropical Sea Anemone aiptasia Pallida As A Lab Model For The Study Of Coral<br />

Bleaching<br />

Ophélie LADRIÈRE* 1 , Stéphane ROBERTY 1 , Charlotte BAUDESSON 1 , Philippe<br />

COMPÈRE 2 , Fabrice FRANCK 3 , Mathieu POULICEK 1<br />

1 Unit of Marine Ecology, Laboratory of Animal Ecology and Ecotoxicology, <strong>University</strong> of<br />

Liège, Liège, Belgium, 2 Unit of Ultrastructural Morphology, Laboratory of Functional and<br />

Evolutive Morphology, <strong>University</strong> of Liège, Liège, Benin, 3 Unit of Plant Biochemistry,<br />

<strong>University</strong> of Liège, Liège, Belgium<br />

Bleaching is still among major events threatening coral reefs. New tools have to be developped<br />

to better understand the mechanisms leading to this pathology : we studied the use of the<br />

hermatypic anemone Aiptasia pallida as experimental model for coral bleaching. Aiptasia<br />

appears as a good candidate as it is easy to maintain in aquarium and subjected to bleaching like<br />

corals.<br />

Both morphological and physiological approaches were performed to investigate the<br />

ultrastructure of the anemone tissues (TEM) and the zooxanthellae photophysiology<br />

(chlorophyll a fluorescence, respiration and pigmentation).<br />

Experiments under light and dark stress reveal that anemone tissues ultrastructure can be<br />

differently affected. In darkness, the ectoderm activity is reoriented to capture prey by<br />

increasing cnidocyte density. In contrast, intense light affects especially the gastroderm :<br />

intercellular spaces increase, the expulsion of intact algae in the gastric cavity and the<br />

degradation of zooxanthellae inside vacuoles seem to reduce the zooxanthellae density,<br />

chloroplast thylakoids lose their parallel arrangement.<br />

The analysis of the fluorescence induction curve appears as a powerful tool to analyse the<br />

physiological events series previous to bleaching. Although no significant zooxanthellae density<br />

reduction was observed, the decrease of pigments concentrations indicates that light or dark<br />

stresses induce anemone bleaching. Under strong light intensity, A. pallida zooxanthellae show<br />

an increased proportion of PSII QB non reducing, leading to partial photoinhibition. This<br />

phenomenon favours the ROS production that damages cellular structures of host and<br />

zooxanthellae. In darkness, there is no photosynthesis; anemones have therefore to find other<br />

feeding sources, as suggested by the ultrastructural approach.<br />

As the present results confirm some of those obtained on scleractinians, A. pallida can be<br />

regarded as a good model for coral bleaching studies and has numerous advantages for<br />

experimentation.<br />

5.103<br />

The Tissue-Skeleton Interface in the Scleractinian Coral Stylophora pistillata<br />

Eric TAMBUTTÉ* 1 , Denis ALLEMAND 1 , Didier ZOCCOLA 1 , Anders MEIBOM 2 , Severine<br />

LOTTO 3 , Natacha CAMINITI 1 , Sylvie TAMBUTTÉ 1<br />

1 Centre Scientifique de Monaco, Monaco, Monaco, 2 Laboratoire d'Etude de la Matière<br />

Extraterrestre, Museum National d'Histoire Naturelle, paris, France, 3 Centre Scientifique de<br />

Monaco, Monaco, France<br />

Stylophora pistillata is a coral for which numerous physiological data on calcification are<br />

available through detailed laboratory studies. However, for this species, as well as for most<br />

other species, the cellular tissue is poorly described at the microscopic level. The aim of the<br />

present work is to provide histological observations of the coral tissue at the interface with the<br />

skeleton, using Stylophora pistillata as a model, and to discuss these observations in the context<br />

of the morpho-functional aspects of biomineralization. The approach is top-down, i.e., it starts<br />

from a macroscopic level with observations made on a microcolony-level and proceeds to a<br />

sub-microscopic level with observations made on the cells and the corresponding skeletal<br />

surface. Several important observations can be made: 1) At all scales of observation, there is a<br />

precise morphological correspondence between the tissues and the skeleton. 2) The distribution<br />

and density of desmocyte cells, which anchor the calicoblastic ectoderm to the skeletal surface,<br />

vary spatially and temporally during skeletal growth stages 3) The calicoblastic cell layer differs<br />

dramatically between regions corresponding to different ultra-structural components of the<br />

skeleton. From the base to the tip of coenosteal spines, the histology of coral tissues changes<br />

from four epithelial layers to two epithelial layers that completely lack endoderms. These<br />

findings have important implications for models for vital effects in coral skeletal chemistry and<br />

isotope composition.<br />

283

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