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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 />

11-29<br />

The Reproductive Biology And Recruitment Ecology Of Porites Bernardi<br />

Jonathan MARTINEZ* 1 , Robert RICHMOND 1 , Jorg ANSON 2 , Sean MCDUFF 3<br />

1 Pacific Biomedical Research Center, <strong>University</strong> of Hawaii at Manoa, Honolulu, HI,<br />

2 Kewalo Marine Laboratory, Honolulu, HI, 3 <strong>University</strong> of Hawaii at Manoa, Honolulu,<br />

HI<br />

Porites cf. bernardi is a scleractinian coral described by Vaughn 1904. Its worldwide<br />

distribution remains uncertain although it has been reported from locations in Japan,<br />

Hawai’i & São Tomé e Principe. In Hawai’i, this coral inconspicuously grows in<br />

encrusting forms rarely larger than 10 cm2 in areas of high wave motion, inhabiting the<br />

subtidal zone to depths of 13m. No previous data are available describing the<br />

reproductive biology and larval ecology of this species.<br />

P. bernardi is a brooding coral, which reproduces year-round. Colonies do not appear to<br />

be dependent on sperm from conspecifics for planulae production and release larvae most<br />

days of the year with peak planulation near the lunar third quarter. There is a positive<br />

relationship between adult size and reproductive output. A regression model predicts that<br />

adults larger than 0.7225 cm2 may be reproductively mature, and adults as small as 0.882<br />

cm2 have been observed to planulate. The larvae of P. bernardi have not been observed<br />

to swim in the water column under laboratory conditions, but rather only crawl along the<br />

substrata along a single axis Larval recruitment occurred mainly in response to coralline<br />

algal chemical metabolites although modest recruitment has been observed in presence of<br />

bacterial biofilms. In bioassays, almost all of the larvae settled within 48 hrs of exposure<br />

to appropriate crustose coralline algae.<br />

The availability of P. bernardi planulae throughout the year, and the larvae’s responses to<br />

metamorphic inducers makes this a good model organism for studies of the effects of<br />

anthropogenic stressors such as pollution, elevated temperatures, acidification and<br />

sedimentation on coral reproduction and recruitment.<br />

11-30<br />

A Review Of Sexual Reproduction in Octocorallia<br />

Samuel KAHNG* 1 , Yehuda BENAYAHU 2 , Howard LASKER 3<br />

1 College of Natural Science, Hawaii Pacific <strong>University</strong>, Kaneohe, HI, 2 Tel Aviv<br />

<strong>University</strong>, Tel Aviv, Israel, 3 <strong>University</strong> at Buffalo, Buffalo, NY<br />

Since its initial discovery on Oahu in 1966, the azooxanthellate octocoral, Carijoa riisei<br />

(Duchassaing and Michelotti, 1860), has spread across the main Hawaiian Islands and<br />

proliferated in abundance. To help understand the substantial ecological success of C.<br />

riisei in Hawaii, its sexual reproduction was examined. Carijoa riisei is gonochoric with<br />

a male to female ratio of one. Gametogenesis is asynchronous, continuous, and does not<br />

exhibit seasonal or lunar periodicity. Carijoa riisei spawns negatively buoyant eggs<br />

which suggest external fertilization and possibly benthic larvae. Under favorable<br />

conditions, C. riisei exhibits high polyp fecundity. Asynchronous, continuous spawning<br />

of gametes is an unusual mode of reproduction which forgoes the advantages of<br />

concentrating gametes in space and time and requires dense aggregations of male and<br />

female colonies in close proximity to ensure fertilization success. Other life history traits<br />

such as fast growth, early age of sexual maturity, vegetative propagation, and superior<br />

competitive ability enable C. riisei to form dense, multi-colony aggregations thereby<br />

facilitating sexual reproduction. Provided C. riisei can achieve a critical density, this<br />

unusual sexual reproductive strategy probably enables it to exploit the ephemeral<br />

availability of space across time with a high and continuous production of larvae.<br />

11-31<br />

Sexual Reproduction In The Soft Coral Lobophytum Sp. In Tung Ping Chau Marine<br />

Park, Hong Kong Sar, China<br />

Chung Wing YEUNG* 1 , Put ANG 1<br />

1 Marine Science Laboratory, Department of Biology, The Chinese <strong>University</strong> of Hong Kong,<br />

Hong Kong, Hong Kong<br />

The soft coral genus Lobophytum is a carpet-like encrusting coral and is commonly found in<br />

Hong Kong waters. The reproductive biology of Lobophytum, as well as that of other soft corals<br />

in Hong Kong has never been investigated. This study provides the first baseline information on<br />

the reproductive biology of soft corals in Hong Kong.<br />

The sampling site in this experiment was Lung Lok Shui in Tung Ping Chau Marine Park.<br />

Three samples from five marked Lobophytum aggregations were collected monthly from 16<br />

Aug 2006 to 7 Jul 2007. Histological sections of each sample were prepared and their gonadal<br />

development was observed under the microscope. All colonies in the same aggregation were<br />

assumed to come from the same mother colony, since Lobophytum was reported to undergo<br />

asexual reproduction and thus, its daughter colonies would remain in close proximity forming<br />

the aggregation.<br />

From the histological analysis of the samples, all colonies bore only eggs. As Lobophytum was<br />

reported to be gonochoric, all the colonies sampled were therefore female. Male colonies may<br />

be missed during sampling. Oocytes from the samples measured increased in mean (±SD)<br />

diameter from 116.5±18.8 µm in Aug 2006 to 239.3±82.2 µm in Jun 2007, and dropped back to<br />

93.0±23.2 µm in Jul 2007. This indicates that spawning of Lobophytum probably occurred in or<br />

before Jul 2007. The oocyte development appeared synchronized as shown in the simultaneous<br />

increase in their sizes. However, new oocytes likely developed before the release of the mature<br />

ones so that each cycle of development took more than one year to complete. Additional<br />

samples will be processed in order to confirm this initial observation.<br />

11-32<br />

Reproductive Biology Of Temperate Soft Corals (Alyonacea: Nephtheidae) in Korean<br />

Waters<br />

Sung-Jin HWANG* 1 , Jun-Im SONG 1<br />

1 Division of EcoScience, Ewha Womans <strong>University</strong>, Seoul, Korea, Republic of<br />

There was little information about the reproductive biology of family Nephtheidae. This study<br />

were examined the reproductive diversity on three soft coral species from 2003 to 2007, and<br />

two of them were belonged to genus Dendronephthya and one was to genus Scleronephthya.<br />

They are all sympatric species in the Jejudo Island area (33° 22′ N, 126° 33′ E), and highly<br />

distributed on the horizontal and vertical rocky substrata from 3 to 50 m in depth. One species,<br />

Dendronephthya castanea, was a gonochoric internal brooder and two, D. spinulosa and<br />

Scleronephthya gracillimum, were gonochoric broadcasters. They showed annual reproductive<br />

cycles and similar patterns in gametogenesis. Gametes of them were matured as seawater<br />

temperatures increased, reflecting a seasonal correlation in reproductive cycle. While oocytes<br />

were observed at all times of the year, spermaries were found during a short period. D. castanea<br />

released lecithotrophic planulae from July to September, and D. spinulosa and S. gracillimum<br />

spawned gametes asynchronously from August to December and in August, respectively. The<br />

ratio of female to male was 2.5: 1 in an internal brooder (D. castanea) and 1.5: 1 in broadcasters<br />

(D. spinulosa and S. gracillimum), suggesting the correlation to mode of reproduction.<br />

98

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