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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Oral Mini-Symposium 11: From Molecules to Moonbeams: How is Reproductive Timing Regulated in Coral Reef Organisms?<br />
11-1<br />
Sex Change In Fungiid Corals<br />
Yossi LOYA* 1 , Kazuhiko SAKAI 2<br />
1 Zoology, Tel Aviv <strong>University</strong>, Tel Aviv, Israel, 2 Sesoko Station, <strong>University</strong> of the<br />
Ryukyus, Okinawa, Sesoko, Motobu-Cho, Japan<br />
Sex change in animals has been the subject of a variety of theoretical and empirical<br />
evolutionary studies. The direction of sex change in animals has been reported occurring<br />
mainly from M to F (males to females; protandry) and visa versa (protogyny) and in<br />
some cases as bidirectional. Our knowledge of the various modes of sexual reproduction<br />
in scleractinian corals has increased greatly during the last two decades, but is far from<br />
encompassing the wide plasticity of reproductive strategies exhibited by this group. Here<br />
we report on novel observations of sex change in two coral species, where tagged<br />
individuals have been monitored during 3 years in the field and experimental aquaria at<br />
Sesoko, Okinawa: Fungia repanda (exhibiting protandry), and Ctenactis echinata,<br />
revealing novel bidirectional mode of sex change: (M-F-M and F-M-F). Our study<br />
exemplifies the view that models that can be applied on the scale of individuals may<br />
provide important insights to the factors underlying the evolution of sex change in<br />
animals.<br />
11-2<br />
Behavioural Endocrinology Of Bi-Directional Sex Change in Coral-Dwelling Gobies<br />
Frederieke KROON* 1 , Philip MUNDAY 2 , David WESTCOTT 1 , Luke GARDNER 3 ,<br />
Abigail ELIZUR 4,5<br />
1 CSIRO Sustainable Ecosystems, Atherton, Australia, 2 James Cook <strong>University</strong>, School of<br />
Marine and Tropical Biology, Townsville, Australia, 3 Queensland Department of Primary<br />
Industries & Fisheries, Woorim, Bribie Island, Australia, 4 <strong>University</strong> of the Sunshine<br />
Coast, School of Science and Education, Maroochydore DC, Australia, 5 Queensland<br />
Department of Primary Industries & Fisheries, Woorim, Australia<br />
The discovery of bi-directional sex change (i.e. the ability to change sex repeatedly in<br />
both directions) in various fish species provides a unique opportunity to study the<br />
endocrine mechanisms underlying female and male sex differentiation. We examined a<br />
potential causal relationship between behaviour, endocrine pathways, and natural sex<br />
change in coral-dwelling gobies of the genus Gobiodon. These species generally live in<br />
heterosexual pairs and natural sex change occurs as a result of changes in social<br />
conditions. If adult sex change in coral-dwelling gobies is a result of changes in<br />
behavioural interactions perceived by an individual fish, then we predict the following:<br />
that in heterosexual pairs males are behaviourally dominant;<br />
that in heterosexual pairs cortisol levels are higher in females than in males;<br />
that in heterosexual pairs aromatase expression is higher in females than in males;<br />
that in heterosexual pairs estradiol levels are higher in females than in males;<br />
that an increase in cortisol levels results in protandrous sex change, and a decrease in<br />
cortisol levels results in protogynous sex change.<br />
To test these predictions, we observed behavioural interactions in existing heterosexual<br />
pairs in the laboratory, and conducted field experiments under natural social conditions.<br />
The results suggest that, in coral dwelling gobies, behavioural interactions mediates sex<br />
change in each direction via the aromatase pathway.<br />
11-3<br />
Light Sensing And The Coordination Of Coral Broadcast Spawning Behavior<br />
Dan HILTON 1 , Peter VIZE* 2<br />
1 Biological Sciences, <strong>University</strong> of Calgary, Calgary, AB, Canada, 2 Biological Sceinces,<br />
<strong>University</strong> of Calgary, Calgary, AB, Canada<br />
While lunar cycles establish the day of spawning in corals, sunlight driven systems control the<br />
hour and minute of spawning. The two lines of evidence supporting this contention are: 1. coral<br />
spawning times change from year to year corresponding to changes in sunset time 2. artificially<br />
changing sunset time results in a corresponding change to spawn time. This later point also<br />
indicates that the solar control is not an entrained circadian system or it would not respond in<br />
this manner. Our research is exploring the cellular pathways by which solar light regulates<br />
spawning behavior through a combination of proteomics and candidate pathway analysis. We<br />
are mapping coral protein phosphorylation oscillations in response to different levels of<br />
illumination. As most light transduction systems result in changes in such patterns this approach<br />
will identify phosphoprotein signatures that can be used as markers of signal perception. Such<br />
signatures can then be used to test the role of different signaling pathways in the response to<br />
light, to compare responses in species with different spawning times, to measure the importance<br />
of zooxanthellae in the response etc. A second approach is identifying coral orthologs of genes<br />
involved in regulating either circadian cycles or light responses. These candidates are then<br />
tested for responsiveness to lunar and solar light at both the transcriptional and posttranscriptional<br />
level. Through a combination of these two approaches we hope to map the<br />
pathways by which lunar and solar light independently regulate coral spawning behavior. We<br />
are particularly interested in how these two different systems intersect to select the exact<br />
moment of gamete release and how changes in the dynamics of the molecular sensing systems<br />
generates distinct species-specific spawning windows.<br />
11-4<br />
Light-Responsive Cryptochromes From A Simple Multicellular Animal, The Coral<br />
Acropora Millepora<br />
Oren LEVY* 1 , Lior APPELBAUM 2 , William LEGGAT 3 , Yoav GOTHILF 4 , David<br />
HAYWARD 5 , David MILLER 6 , Ove HOEGH-GULDBERG 7<br />
1 Department of Environmental Sciences, The Weizmann Institute of Science, Rehovot, Israel,<br />
2 Center For Narcolepsy, Stanford <strong>University</strong>, Palo Alto, CA, 3 Biochemistry and Molecular<br />
Biology, James Cook <strong>University</strong>, Townsville, Australia, 4 Department of Neurobiochemistry,<br />
Tel Aviv <strong>University</strong>, Tel Aviv, Israel, 5 Molecular Genetics and Evolution Group, Australian<br />
National <strong>University</strong>, Canberra ACT, Australia, 6 Comparative Genomics Centre, James Cook<br />
<strong>University</strong>, Townsville, Australia, 7 Centre for Marine Studies, The <strong>University</strong> of Queensland,<br />
Brisbane, Australia<br />
Hundreds of species of reef-building corals spawn synchronously over a few nights each year,<br />
and moonlight regulates this spawning event. However, the molecular elements underpinning<br />
the detection of moonlight remain unknown. Here we report the presence of an ancient family<br />
of blue-light–sensing photoreceptors, cryptochromes, in the reef-building coral Acropora<br />
millepora. In addition to being cryptochrome genes from one of the earliest-diverging<br />
eumetazoan phyla, cry1 and cry2 were expressed preferentially in light. Consistent with<br />
potential roles in the synchronization of fundamentally important behaviors such as mass<br />
spawning, cry2 expression increased on full moon nights versus new moon nights. Our results<br />
demonstrate phylogenetically broad roles of these ancient circadian clock–related molecules in<br />
the animal kingdom.<br />
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