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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7-17<br />
Spatial variation in aspergillosis and the mycoflora associated to Gorgonia ventalina<br />
in Puerto Rico.<br />
Anabella ZULUAGA-MONTERO* 1 , Carlos TOLEDO-HERNÁNDEZ 1 , Jose Antonio<br />
RODRÍGUEZ 1 , Paul BAYMAN 1 , Alberto SABAT 1<br />
1 Biology, <strong>University</strong> of Puerto Rico, San Juan, Puerto Rico<br />
Most of the coral disease literature has focused on identifying potential pathogens or<br />
environmental factors linked to disease. However, to better understand the etiology of<br />
coral diseases it is also necessary to increase our knowledge of the basic ecology of<br />
marine microorganisms. Many fungal species reported in marine organisms are common<br />
in land, but very little is known about their distribution in marine ecosystems. The<br />
objectives of this study were to determine the spatial variation in prevalence of<br />
aspergillosis, and relate it to the mycoflora associated with healthy and diseased colonies.<br />
We measured prevalence at three times during one year at six reefs sites. Colonies were<br />
tagged, photographed and categorized as healthy or diseased. The mycoflora associated<br />
to G. ventalina was identified by morphology and sequencing of the ITS region. We<br />
found significant differences in aspergillosis prevalence among sites. We also found<br />
significant spatial variation in the composition of the fungi community, and between<br />
healthy and diseased sea fans. However, sites with high or low prevalence did not have a<br />
distinctive mycoflora. Aspergillus flavus was an ubiquitous isolate at almost all sites, as<br />
well as in diseased and healthy colonies. A. sydowii was not isolated from diseased<br />
colonies. The main cause of colony death was detachment, followed by colonies that<br />
were overgrown by fouling organisms, and least by aspergillosis. The significant spatial<br />
variation in the fungi community suggests that local environmental factors are<br />
influencing the fungal composition of sea fans. The fact that A. sydowii was not isolated<br />
from diseased tissue from any reef site supports the argument that aspergillosis may be<br />
caused by a polymicrobial consortium. The data also indicates that aspergillosis is not a<br />
significant cause of mortality for sea fans in Puerto Rico.<br />
7-18<br />
Emerging Infectious Diseases Of Coral Reef Sponges: aplysina Red Band<br />
Syndrome On Caribbean Reefs<br />
Deborah J. GOCHFELD* 1,2 , Robert W. THACKER 3 , Julie B. OLSON 4<br />
1 National Center for Natural Products Research, <strong>University</strong> of Mississippi, <strong>University</strong>,<br />
MS, 2 Environmental Toxicology Research Program, <strong>University</strong> of Mississippi,<br />
3<br />
<strong>University</strong>, Department of Biology, <strong>University</strong> of Alabama at Birmingham,<br />
Birmingham, AL, 4 Department of Biological Sciences, <strong>University</strong> of Alabama,<br />
Tuscaloosa, AL<br />
A substantial and increasing number of reports have documented dramatic changes and<br />
continuing declines in the health of Caribbean coral reef communities over the past few<br />
decades. Disease is often implicated as a major factor contributing to these declines. To<br />
date, most disease reports have focused on scleractinian corals, whereas sponge diseases<br />
have been less frequently documented. Here we describe Aplysina Red Band Syndrome<br />
(ARBS), which affects Caribbean rope sponges. Visible signs of disease presence<br />
include one or more rust-colored leading edges, with a trailing area of necrotic tissue,<br />
such that the lesion forms a contiguous band around a portion or the entire sponge<br />
branch. Microscopic examination of the leading edge of the disease margin indicates that<br />
filamentous cyanobacteria are responsible for the coloration. Although the presence of<br />
this distinctive coloration is used to characterize the diseased state, it is not yet known<br />
whether this cyanobacterium is directly responsible for disease causation. Approximately<br />
10% of the Aplysina cauliformis sponges on reefs near Lee Stocking Island, Bahamas,<br />
are affected by ARBS, and the disease has also been observed on reefs at other Caribbean<br />
sites. Transmission studies in the lab and field demonstrated that contact with an active<br />
lesion's leading edge was sufficient to spread ARBS to a healthy sponge, suggesting that<br />
the etiologic agent, currently undescribed, is contagious. Population studies indicate<br />
clumping of diseased individuals on the reef, but the presence of affected individuals in<br />
isolation suggests that waterborne transmission is also likely. Studies to elucidate the<br />
etiologic agent of ARBS are ongoing. Sponges are an essential component of coral reef<br />
communities and emerging sponge diseases have the potential to impact benthic diversity<br />
and community structure on coral reefs.<br />
Oral Mini-Symposium 7: Diseases on Coral Reefs<br />
7-19<br />
The Pathological Studies Of Skeletal Anomaly in The Coral porites Australiensis<br />
Naoko YASUDA* 1 , Yoshikatsu NAKANO 2 , Hideyuki YAMASHIRO 3 , Michio HIDAKA 4<br />
1 Department of Marine and Environmental Science, Graduate School of Engineering and<br />
Science, <strong>University</strong> of the Ryukyus, Nishihara, Japan, 2 Sesoko Station, Tropical Biosphere<br />
Research Center, <strong>University</strong> of the Ryukyus, Motobu, Japan, 3 Department of Bioresources<br />
Engineering, Okinawa National College of Technology, Nago, Japan, 4 Department of<br />
Chemistry, Biology and Marine Science, Faculity of Science, <strong>University</strong> of the Ryukyus,<br />
Nishihara, Japan<br />
The skeletal anomalies (SAs) of the scleractinian corals have been reported from reefs<br />
throughout the world and have been commonly referred to as ‘tumors’. The SAs are<br />
characterized by swelled and abnormal skeletal structures, reduced number of polyps, and fewer<br />
zooxanthellae as compared with healthy parts. Causative agents of SAs have not been<br />
identified. In this study, the pathological characteristics of the SAs developed on a colony of<br />
Porites australiensis in the reef at Kayo, Okinawa, Japan were investigated. The polyp density<br />
was reduced in the SA due to enlargement of both calices and the coenosteum. Corallites in the<br />
SA region lost the skeletal architecture characteristic to Porites australiensis. The soft tissue in<br />
the SA region contained fewer and smaller spermaries and thinner gastrodermis containing<br />
lower density of zooxanthellae than the adjacent ordinary tissue. The gross production of SA<br />
tissues was lower than that of ordinary tissues and it decreased to almost 0 in 9 days after<br />
isolation. However, when SA fragments were brought into contact with ordinary fragments<br />
from the same colony, they fused and both SA and ordinary regions grew. The growth rate of<br />
ordinary regions was lower when they were fused with SA fragments than those fused with<br />
ordinary fragments. The present results suggest that SAs may be maintained by energy supply<br />
from the surrounding healthy tissue. The SAs of the coral may act as parasite for host corals and<br />
eventually decrease the fitness of the host coral.<br />
7-20<br />
Is Increased Scarring Of Hard Corals From Disease Associated With Subsequent Declines<br />
in Coral Cover On Reefs Of The Great Barrier Reef.<br />
Ian MILLER* 1 , Andrew DOLMAN 1<br />
1 Long Term Monitoring, Australian Institute of Marine Science, Townsville, Australia<br />
Increased reports of disease induced hard coral mortality in recent years have highlighted the<br />
emerging threat coral disease poses to reef ecosystems. To study the effects of coral disease on<br />
the Great Barrier Reef (GBR) the Australian Institute of Marine Science monitored causes of<br />
coral mortality on a suite of 48 reefs throughout the Great Barrier Reef (GBR) annually from<br />
1999 to 2005 and on a further 48 reefs biannually from 2006. Sampling consisted of<br />
categorising corals scars according to signs commonly associated with coral disease (white<br />
syndromes and black-band disease), crown-of-thorns starfish (COTS), Drupella spp. feeding<br />
activity and scars that could not be assigned directly to any of these categories. In 2005<br />
sampling was extended to include signs of recently defined disease formerly classified as white<br />
syndromes or band diseases (brown band disease, skeletal eroding band disease and<br />
atramentous necrosis). Of those categories recorded only increases in COTS scars were<br />
independently associated with subsequent declines in coral cover on survey reefs. Between<br />
1999 and 2005 there was no clear evidence to suggest there were any disease outbreaks that had<br />
a significant impact (above background levels) on live coral cover on survey reefs. This is<br />
despite the fact that scaring due to disease constitutes a relatively high proportion of the scars<br />
observed. This suggests that though disease plays an important role in GBR coral communities<br />
it mainly contributes to “background” levels of coral mortality. The relative proportion of scars<br />
recorded show that white syndrome and unknown scars make up the most common category of<br />
scars observed. The high proportion of scars from unknown sources suggests that the causes of<br />
many corals scars remain unexplained and highlights the difficulty classifying coral scars based<br />
on visual signs.<br />
50