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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 />

5.83<br />

The Effects Of Salinity Stress On The Physiology And Protein Content Of The<br />

Hermatypic Coral - Acropora pruinosa In Hong Kong<br />

William BUT* 1<br />

1<br />

Swire Institute of Marine Science, The <strong>University</strong> of Hong Kong, Hong Kong, Hong<br />

Kong<br />

The effects of low salinity on the scleractinian coral Acropora pruinosa were investigated<br />

in this study. 100% coral mortality and significant drops in percentage protein content<br />

were observed in A. pruinosa exposed to the salinity of 15 psu. No mortality occurred in<br />

A. pruinosa fragments at 18 psu salinity level. The data suggested that 15 psu salinity<br />

level is the mortality threshold for A. pruinosa. The crude protein content measured in the<br />

18, 22 and 25 psu salinity treatment groups are not significantly different from that in the<br />

35 psu salinity control group. While no statistically significant difference in the amount<br />

of crude protein per unit surface area was detected, sub-lethal behavioural responses were<br />

observed at salinity level of 18 psu and above. Increasing tissue swelling and polyp<br />

retraction characterized salinities between 22 and 18 psu but were not observed at higher<br />

salinities, suggesting that these are traumatic, but not necessarily fatal salinity levels.<br />

Salinity is quite likely to be the major environmental factor that affecting the coral<br />

community distribution in a regional context. Freshwater excursions from the Pearl River<br />

and seasonal monsoon downpours establish a salinity gradient across Hong Kong waters.<br />

The sharp mortality threshold at low salinity in A. pruinosa might provide us insight into<br />

the spatial distribution patterns of corals in Hong Kong waters. On top of that, the data<br />

from this study might help us to predict the possible consequence of Hong Kong’s corals<br />

under the influence of global climate change.<br />

5.84<br />

Sources and metabolism of essential fatty acids in Scleractinian corals<br />

Mark TEECE* 1 , Diego LIRMAN 2 , Mary Alice COFFROTH 3<br />

1 Chemistry, SUNY-ESF, Syracuse, NY, 2 RSMAS/MBF, <strong>University</strong> of Miami, Miami,<br />

FL, 3 Geology, State <strong>University</strong> of New York at Buffalo, Buffalo, NY<br />

Invertebrates such as corals require essential fatty acids for growth and reproduction and<br />

can obtain them either through direct feeding on zooplankton and particulates, or through<br />

translocation from their symbiotic zooxanthellae. We used the naturally occurring stable<br />

isotopes of carbon to trace the sources and metabolism of essential fatty acids in four<br />

corals from varying water quality environments. Comparative analyses of symbionts and<br />

hosts from Siderastrea siderea, Porites astreoides, Montastrea faveolata, ,and Montastrea<br />

cavernosa collected in the Florida Keys, USA revealed considerable differences in the<br />

abundances of these essential compounds in individual symbiont-host associations. The<br />

relative abundances of these polyunsaturated fatty acids (PUFA) was significantly higher<br />

in P. astreoides than S. siderea and accounted for more than 38% of total fatty acids in<br />

this coral species. The high abundances of these PUFA attest to the importance of their<br />

function in corals. Concentrations of PUFA in cultured zooxanthellae clades spanned a<br />

considerable range, accounting for more than 45% of total fatty acids in specific clades.<br />

We measured the stable isotope compositions of individual fatty acids in corals and<br />

symbionts to determine metabolic routing of these essential compounds in the natural<br />

environment. Our analyses revealed that some corals, including P. astreoides, obtain<br />

fatty acids from both zooxanthellae and direct feeding, and may also be able to synthesize<br />

long chain length fatty acids from shorter precursors obtained from their symbionts.<br />

Other corals including S. siderea, rely to a greater extent on their symbionts for their<br />

source of essential fatty acid.<br />

5.85<br />

The Development Of Fluorescently-Labeled symbiodinium To Investigate Symbiont<br />

Acquisition And Flexibility in Coral-Algal Symbiosis<br />

Nitzan SOFFER* 1 , Patrick GIBBS 1 , Michael C. SCHMALE 1 , Andrew C. BAKER 1<br />

1 Marine Biology and Fisheries, Rosenstiel School of Marine and Atmospheric science,<br />

<strong>University</strong> of Miami, Key Biscayne, FL<br />

Symbiosis is a defining characteristic of reef-building scleractinian corals. During times of<br />

environmental stress, such as increased temperature, these symbioses can break down,<br />

jeopardizing the survival of affected corals. Corals can recover from these “bleaching” events if<br />

their symbiont populations are able to recover. However, for scleractinian corals, the source of<br />

these symbionts remains debated: do symbionts proliferate from residual populations, or can<br />

they also acquire symbionts de novo from the environment? Answering this question fills a<br />

critical gap in our understanding of symbiont population dynamics, helps us understand<br />

recovery trajectories of corals, and has significant implication for corals’ response to continued<br />

climate change. To help answer this question, we are developing fluorescently-labeled<br />

Symbiodinium for use as tools to test hypotheses of symbiont acquisition and flexibility in<br />

scleractinian corals. Initial attempts to use viable stains to selectively visualize symbionts<br />

showed mixed success, and we have now begun transforming symbionts with DNA vectors.<br />

Cultured Symbiodinium in clades A, B, C and D have been electroporated with vectors<br />

containing Bactin, metallothionein and/or heat shock promoters driving expression of green and<br />

red fluorescent proteins (GFPs, RFPs), as well as neomycin resistance to help select successful<br />

transformants. To overcome problems associated with symbiont autofluorescence, other vectors<br />

containing sequences for cyan or yellow fluorescent proteins (CFPs, YFPs) and luciferase are<br />

also being targeted. We believe that the development of fluorescent or luminescent<br />

Symbiodinium will be of broad potential use in a variety of marine invertebrate symbioses, and<br />

will help address critical outstanding questions concerning the survivorship trajectories of reef<br />

corals in the current era of climate change.<br />

5.86<br />

The Influence Of Habitat On Nitrogen Acquisition And Status in A Temperate Cnidarian-<br />

Dinoflagellate Symbiosis<br />

Shyam MORAR 1 , Sarah BURY 2 , Simon DAVY* 1<br />

1 School of Biological Sciences, Victoria <strong>University</strong> of Wellington, Wellington, New Zealand,<br />

2 NIWA, Wellington, New Zealand<br />

Nitrogen deficiency is a well-known feature of tropical cnidarian-algal symbioses that inhabit<br />

oligotrophic seas. In contrast, temperate seas have plentiful supplies of nutrients, and a number<br />

of temperate symbiotic cnidarians inhabit high-sediment localities. The symbiotic sea anemone<br />

Anthopleura aureoradiata is abundant on mudflats around New Zealand where it lives attached<br />

to cockle shells, often buried under the sediment surface; it is also common on rocky shores.<br />

We tested whether the mudflat habitat provides a source of particulate matter that enriches the<br />

nitrogen status of the algal symbionts, and whether anemones living on rocky shores are<br />

nutritionally starved by comparison. 15 N-labelled sediment was provided to anemones, and 15 Nenrichment<br />

was detected for both anemone and algal partners. NH4 + enhancement of dark 14 C<br />

fixation showed that while sedimentary particulate nitrogen can ultimately be acquired by the<br />

algae there was no discernible effect of this uptake on their nitrogen status. Indeed anemones<br />

maintained in mud but otherwise unfed for up to 8 weeks contained algae that were as Ndeficient<br />

as those in anemones starved in the absence of mud. In contrast, symbiotic algae in the<br />

field were N-sufficient when on the mudflat but markedly N-deficient when on the rocky shore.<br />

Our results suggest that this symbiosis can assimilate particulate nitrogen from the surrounding<br />

mud but that this source is less important than other potential ones such as interstitial<br />

ammonium and nitrate. Furthermore, the nutrient-rich mudflat environment enhances the Nstatus<br />

of symbiotic algae far more than does the rocky shore. We will consider the implications<br />

of these trends for the functional biology of the symbiosis, and use our findings to speculate on<br />

the likely scenarios for those reef corals that live in relatively low sediment and more<br />

‘marginal’, high-sediment locations.<br />

296

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