11th ICRS Abstract book - Nova Southeastern University
11th ICRS Abstract book - Nova Southeastern University
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 />
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