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 />
5.83<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