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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 />

5.141<br />

Effect Of Irradiance And Increased Temperature On Differential Gene Expression<br />

In Dinoflagellate<br />

Nedeljka ROSIC 1 , Mauricio RODRIGUEZ-LANETTY 1 , William LEGGAT 1 , Ove<br />

HOEGH-GULDBERG* 1<br />

1 The <strong>University</strong> of Queensland, Brisbane, Australia<br />

Using microarray technology, with over 3000 ESTs, we assessed gene expression profiles<br />

in symbiotic dinoflagellate from culture after exposure to elevated temperature and light<br />

level. Cultures of the coral symbionts, Symbiodinium sp. from clade C1 have been<br />

exposed to elevated temperatures (29ºC and 32ºC) under high (100 µmole quantum/m2/s<br />

Photosynthetic Active Radiation) and low (15 µmole quantum/m2/s) light level. As a<br />

result we discovered some interesting genes involved in stress respond in dinoflagellate.<br />

Heat shock proteins such as DnaJ molecular chaperone (HSP 40), which is involved in<br />

protein translation and folding, then serine/threonine-protein kinase have been up<br />

regulated with increased temperature. Light level effected expression of various genes<br />

such as actin, ammonium and nitrate transporters. Also, a list of potential house keeping<br />

genes has been established from this sequence as a good basis for further gene expression<br />

studies in symbiotic dinoflagellate. These preliminary microarray data should provide<br />

more information and highlight future directions towards better understanding of the<br />

process involved in the breakdown of coral-algal symbiosis.<br />

5.142<br />

Genetic Diversity Of The Zooxanthellae Symbionts Of Corals From Reunion Island<br />

Fabien GUÉRIN* 1 , Laury DIJOUX 2 , Xavier HOENNER 2,3 , Vianney DENIS 2 , Henrich<br />

BRUGGEMANN 2 , Mireille GUILLAUME 2,4<br />

1 UMR PVBMT, Université de la Réunion, Saint Denis, Reunion, 2 ECOMAR, Université<br />

de la Réunion, Saint Denis, Reunion, 3 Te mana o te moana, Moorea, French Polynesia,<br />

4 Milieux et Peuplements Aquatiques, UMR 5178 CNRS-UPMC-MNHN, Muséum<br />

National d'Histoire Naturelle, Paris, France<br />

In the Western Indian Ocean extinction of coral reefs in response to global change has<br />

been predicted within the next 50 years. Reefs at Reunion, a high island in an exposed<br />

oceanic setting at high latitude (21° S), were hitherto little affected by the strong 1997-98<br />

ENSO event. Although recurrent bleaching events are occurring since, they probably still<br />

contain ‘naïve’ coral communities with original species composition, locally dominated<br />

by Acropora. The future of these communities depends of the capacity of corals to adapt<br />

or acclimatize to climate change. Zooxanthellae clade D has been shown to impart greater<br />

tolerance to high temperatures.<br />

This is the first study of genetic diversity and distribution of zooxanthellae at Reunion<br />

Island, aiming to better understand the potential of its coral reefs to cope with the SST<br />

increase. From January to April 2007 a minimum of ten replicate coral colonies of some<br />

abundant species was sampled on both top and side parts from each colony. After<br />

holobiont DNA extraction, samples were analysed by PCR-RFLP (Polymerase Chain<br />

Reaction – Restriction Fragment Length Polymorphism) on small and long subunit<br />

ribosomal nRNA of symbionts using TaqI and HhaI as restriction enzymes.<br />

Zooxanthellae RFLPs were classified in clades according to Rowan and Powers (1991)<br />

and Baker et al. (1997). Clade C was dominant in Acropora austera, A. gemmifera, A.<br />

muricata, Porites lutea and P. (Synarea) rus. Branch tips in three colonies of A.<br />

gemmifera were bicladic, harbouring clade C and A. Clade D was also found in<br />

Montipora circumvallata, a species characteristic of degraded coral reef flat communities.<br />

So far, these results suggest a higher potential for resilience to SST increase in<br />

A.gemmifera and M. circumvallata than in other coral species.<br />

5.143<br />

Seasonal Acclimation in Photosynthetic Efficiency Of Coral Holobiont Photosynthesis<br />

Angela LAWTON* 1<br />

1 Centre for Marine Studies, <strong>University</strong> of Queensland, St Lucia, Australia<br />

Faced with current predictions of 2 C warming by 2050, many people hope that corals will be<br />

able to acclimate to the increased temperature, but little is known about the acclimatory ability<br />

of the coral holobiont.<br />

In order to determine if the coral holobiont is able to acclimate its photosystems and<br />

metabolism to seasonally varying environmental conditions, PI curves from Pavona decussata<br />

and Stylophora pistallata were measured at the end of summer (February) and the end of winter<br />

(August) for 3 years using fast-responding microsensors and the light-dark shift method of<br />

Revsbech (1989). The gross and net photosynthetic rates of nubbins of Pavona decussata and<br />

Stylophora pistilata were measured over a range of temperatures during both the summer and<br />

winter to determine if the effect of temperature of the gross and net photosynthetic rates was<br />

different from summer to winter.<br />

It was determined that corals are able to adjust their metabolisms in order to maximize the<br />

amount of photosynthesis occurring in both the summer and winter. Also, the tolerance to<br />

extreme temperature was reduced in the winter. These results indicate that the coral holobiont<br />

does use acclimatory mechanisms to maximize the amount of C gained seasonally. The<br />

mechanisms of seasonal acclimation may be able to be used to acclimate to warmer conditions,<br />

but there is no indication what the maximum range of acclimation is.<br />

5.144<br />

Survival At The Surface: Enhanced Photoprotection Pathways in Shallow Water<br />

symbiodinium<br />

Jennifer McCabe REYNOLDS* 1 , Brigitte BRUNS 2 , William FITT 1 , Gregory SCHMIDT 2<br />

1 Odum School of Ecology, <strong>University</strong> of Georgia, Athens, GA, 2 Department of Plant Biology,<br />

<strong>University</strong> of Georgia, Athens, GA<br />

Photoprotections are necessary for the survival of the coral-dinoflagellate symbiosis. However,<br />

not all symbiont phylotypes display the same sensitivity to the enhancement of photosynthetic<br />

loss at high light and temperatures. We have found that members of different clades in the<br />

genus Symbiodinium exhibit distinct physiological responses as measured by a novel serial<br />

irradiation pulse (SIP) PAM fluorometry method. We monitored fluorescence patterns<br />

indicative of photoprotections using the SIP method from March 2006 to August 2007 in three<br />

coral species in symbiosis with different Symbiodinium clades to determine seasonal changes in<br />

photosynthetic physiology as ocean temperatures fluctuated naturally and light intensity was<br />

increased artificially.<br />

The synergism of sustained high light and increased temperature underlies damage to the coraldinoflagellate<br />

symbiosis by causing photosynthetic loss in Symbiodinium cells. Unlike Clades B<br />

and C, Clade A Symbiodinium, in culture and in hospice, show enhanced capabilities for<br />

alternative photosynthetic electron transport pathways including cyclic and/or chlororespiratory<br />

electron transport. Clade A Symbiodinium also undergo pronounced light-induced dissociation<br />

of antennae complexes from Photosystem II reaction centers as a major component of nonphotochemical<br />

quenching. Cnidarians harboring Clade A Symbiodinium exhibit sustained cyclic<br />

activities coincidental with diminished bleaching during periods of elevated temperature and<br />

high light.<br />

Supported by NSF grant OCE-0137007 to Fitt and Schmidt and a NOAA Dr. Nancy Foster<br />

Scholarship to J.C.M. Reynolds.<br />

293

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