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11th ICRS Abstract book - Nova Southeastern University

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Oral Mini-Symposium 26: Biodiversity and Diversification of Reef Organisms<br />

26-29<br />

Evolution Of The Zoanthid Genus zoanthus (Hexacorallia: Anthozoa) And<br />

Associated symbiodinium in The Atlantic And Pacific Oceans<br />

James REIMER* 1,2 , Frederic SINNIGER 1 , Kiyotaka TAKISHITA 2<br />

1 Department of Chemistry, Biology and Marine Science, <strong>University</strong> of the Ryukyus,<br />

Nishihara, Okinawa, Japan, 2 Extremobiosphere Research Center, Japan Agency for<br />

Marine-Earth Science and Technology, Yokosuka, Kanagawa, Japan<br />

Zooxanthellate zoanthids (=Order Zoantharia) of the order Zoanthus are commonly<br />

found in coral reef ecosystems throughout the world’s tropical and sub-tropical oceans,<br />

but until recently remained relatively neglected in terms of research. Recent work using a<br />

combination of molecular and more traditional morphological and ecological techniques<br />

have led to a more concise understanding of true levels of Zoanthus species diversity. In<br />

this study DNA sequences (cytochrome oxidase subunit I, 16S ribosomal DNA, and<br />

internal transcribed spacer of ribosomal DNA) from Zoanthus spp. specimens from<br />

numerous locations in the Atlantic and Pacific were obtained in order to investigate<br />

evolutionary patterns in this genus. The results show two separate clades of apparently<br />

“ancient” species groups that existed before the separation of the Atlantic and Pacific by<br />

the Isthmus of Panama. Within each clade are two species of Zoanthus, one from each<br />

ocean. Additionally, both species within each of the clades associate with the same<br />

unique subclade of Symbiodinium (zooxanthellae), suggesting that in Zoanthus<br />

associations with Symbiodinium may be apparently stable over relatively long<br />

(~millions of years) periods of time. Attempts to estimate the age of the divergence of<br />

these two “ancient” species clades using molecular clock calculations will be introduced.<br />

26-30<br />

Phylogenetical Analysis Of Zoanthus (Zoanthidea) Morphotypes From Brazilian<br />

Coast<br />

Leila LONGO* 1 , Erika SCHLENZ 2 , Maria Cristina ARIAS 3<br />

1 Genética e Biologia Evolutiva, Instituto de Biociências USP, São Paulo, Brazil,<br />

2 Zoologia, Instituto de Biociências USP, São Paulo, Brazil, 3 Genética e Biologia<br />

evolutiva, Instituto de Biociências USP, São Paulo, Brazil<br />

The Zoanthidae (Anthozoa) presents morphological plasticity which constitute a<br />

constraint for species identification. This study presents the morphological variability<br />

within the genus Zoanthus and an evaluation of the taxonomical status of different<br />

morphotypes, by the association of morphological and molecular data. Twenty one<br />

morphological atributes were analysed from 235 samples comprising 20 collecting sites<br />

along Brazilian coast, and submitted to a cluster analysis to detect the morphological<br />

similarities. A canonical correspondence analysis was conducted to evaluate the<br />

morphological character contribution to each group. These data were submitted to<br />

phylogenetic analysis. Tissues from these morphotypes were used for molecular analysis<br />

of 16S and COI mitochondrial genes using heterologous primers for PCR amplification.<br />

The sequences were submitted to a phylogenetic analysis. The cluster analyses resulted in<br />

12 different morphotypes. The correspondence analysis showed three most important<br />

characters distinguishing the morphotypes. The phylogenetic analysis based on<br />

morphological data evidenced the following three clades grouping: one - morphotypes 1,<br />

2, 3, 4 and 5; two – morphotypes 6, 7, 8 and 9; three - 10 and 12, once they always<br />

clustered together. However the morphotype 11 did not cluster in any of the former<br />

groups. Molecular analysis from the 16S gene corroborates the cluster number and<br />

composition based on the morphological traits, except for morphotype 12. The data from<br />

COI gene showed two major clades, and high genetic divergence between the sequences<br />

from morphotype 7 and 8. Our morphological and molecular results were congruent and<br />

enabled us to stablish the following: morphotypes 1, 2, 3, 4 and 5 constitute<br />

morphological variations of Zoanthus sociatus species; morphotypes 6, 7, 8 and 9<br />

represent intraspecific polymorfism of Zoanthus solanderi; morphotypes 10 and 12 are<br />

variations of Zoanthus nymphaeus; and morphotype 11 must be consider a new Zoanthus<br />

species.<br />

26-31<br />

Coral Geographic: A Progress Report<br />

J. VERON* 1 , L. DEVANTIER 2 , E. TURAK 3 , S. KININMONTH 4<br />

1 Coral Reef Research, Townsville, Australia, 2 private, Noosaville, Australia, 3 private, Paris,<br />

France, 4 AIMS, Townsville, Australia<br />

Coral Geographic is a GIS database that has been in the building for a decade, during which<br />

time it has been used extensively for reef conservation planning. The extent of this usage<br />

prompted a major revision, which will remain on-going. The first product was a composite<br />

global map of coral diversity that delineated a revised “Coral Triangle”. This, in turn, became<br />

the basis for “The Coral Triangle Initiative”, a multi-million dollar international conservation<br />

effort, launched at the Bali summit on climate change in December, 2007. Coral Geographic is<br />

continuing towards a target product which will allow all users to download coral distribution<br />

and environmental data in GIS format. These products will be amenable to detailed<br />

interrogation and interfacing with other datasets.<br />

26-32<br />

"Species Richness and Morphological Diversity of the Genus Porites in the Pacific Ocean"<br />

Alonso MOHEDANO - NAVARRETE* 1 , Hector REYES-BONILLA 2 , Ramon Andres<br />

LOPÉZ-PÉREZ 3,4<br />

1 Biologia Marina, Universidad Autonoma de Baja California Sur, La Paz, Mexico, 2 Biologia<br />

Marina, Universidad Autonom de Baja California Sur, La Paz, Mexico, 3 Instituto de recursos,<br />

Universidad del Mar, Oaxaca, Mexico, 4 Universidad del Mar, Oaxaca, Mexico<br />

Biological diversity has been usually measured using species richness, but unfortunately this<br />

parameter only shows a partial view of the communities. Studies on fossil and recent species<br />

showed that morphological diversity can reflect functional aspects of the system more<br />

efficiently than richness. The objective of this paper was to compare patterns of species richness<br />

and morphological diversity in the genus Porites, recognized for its ecological relevance and<br />

skeletal plasticity. Distribution data of 52 species were arranged in quadrants of 20° of latitude<br />

and longitude, covering the entire Pacific Ocean (N=48). Nine morphological characters were<br />

measured or considered for each species (maximum and minimum corallite diameter,<br />

presence/absence of collumella, presence/absence of pali, proportion between wall width and<br />

maximum diameter of corallites, type of septa, proportion between depth and maximum<br />

diameter of corallites, presence/absence of ramifications, presence/absence of triplet). The set of<br />

measurements was standardized and processed with a principal component analysis, and<br />

estimation of the morphospace occupied by Porites at each quadrant was obtained by<br />

calculation of the geometric mean of the morphological eigenvalues of the species. The results<br />

show that there is no lineal relationship between species richness and diversity of forms for the<br />

genus Porites along the Pacific Ocean; this occurs because in areas with mid to high richness<br />

(from 20 to 31 species), morphological diversity is almost stable. We propose that the detected<br />

morphospace limitations may indicate saturation in niche availability, or is caused by phyletic<br />

limitations in this genus. In contrast, regions with low richness (16 to 6 species) have the<br />

highest morphological diversity, and are usually located in peripheral areas such as Japan and<br />

the eastern Pacific. Finally, there is no difference in morphological variability between<br />

hemispheres or among latitudes.<br />

249

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