With in situ and laboratory chamber incubations we demonstrate that coral mucus, an important component of particulate organic matter in reef ecosystems, is a valuable substrate for microbial communities in the water column and sandy sediments of coral reefs. The addition of coral mucus to the water of benthic chambers placed on lagoon sands in the coral cay Heron Island, Australia, resulted in a rapid and significant increase in both O 2 consumption and DIC production in the chambers. The permeable coral sands permitted the transport of mucus into the sediment with interfacial water flows, resulting in the mucus being mainly (> 90%) degraded in the sediment and not in the water column of the chambers. A low ratio of 0.48 (in situ) to 0.64 (laboratory) for O 2 consumption/DIC production after the addition of coral mucus, and high sulfate reduction rates (SRR) in natural sediments which were exposed to coral mucus, suggest a large contribution of anaerobic processes to the degradation of coral mucus. Oxygen penetrated less than 5 mm deep into these sediments. The microbial reaction to mucus addition was rapid, with a calculated in situ C turnover rate ranging from 7 to 18% h -1 . The degradation of coral mucus showed a dependency on the permeability of the carbonate sediments, with faster degradation and remineralization in coarse sands. This indicates the importance of permeable reef sediments for the trapping and degradation of organic matter. We suggest that coral mucus may have a function as a carrier of energy to the benthic microbial consumers.KEY WORDS: Coral mucus · POM · Degradation · Permeable carbonate sands · O 2 consumption · DIC production · C turnover
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BackgroundCiguatera is a type of fish poisoning that occurs throughout the tropics, particularly in vulnerable island communities such as the developing Pacific Island Countries and Territories (PICTs). After consuming ciguatoxin-contaminated fish, people report a range of acute neurologic, gastrointestinal, and cardiac symptoms, with some experiencing chronic neurologic symptoms lasting weeks to months. Unfortunately, the true extent of illness and its impact on human communities and ecosystem health are still poorly understood.MethodsA questionnaire was emailed to the Health and Fisheries Authorities of the PICTs to quantify the extent of ciguatera. The data were analyzed using t-test, incidence rate ratios, ranked correlation, and regression analysis.ResultsThere were 39,677 reported cases from 17 PICTs, with a mean annual incidence of 194 cases per 100,000 people across the region from 1998–2008 compared to the reported annual incidence of 104/100,000 from 1973–1983. There has been a 60% increase in the annual incidence of ciguatera between the two time periods based on PICTs that reported for both time periods. Taking into account under-reporting, in the last 35 years an estimated 500,000 Pacific islanders might have suffered from ciguatera.ConclusionsThis level of incidence exceeds prior ciguatera estimates locally and globally, and raises the status of ciguatera to an acute and chronic illness with major public health significance. To address this significant public health problem, which is expected to increase in parallel with environmental change, well-funded multidisciplinary research teams are needed to translate research advances into practical management solutions.
Extensive coral bleaching occurred intertidally in early August 2003 in the Capricorn Bunker group (Wistari Reef, Heron and One Tree Islands; southern Great Barrier Reef). The affected intertidal coral had been exposed to unusually cold (minimum ϭ 13.3ЊC; wet bulb temperature ϭ 9ЊC) and dry winds (44% relative humidity) for 2 d during predawn low tides. Coral bleached in the upper 10 cm of their branches and had less than 0.2 ϫ 10 6 cell cm Ϫ2 as compared with over 2.5 ϫ 10 6 cell cm Ϫ2 in nonbleached areas. Dark-adapted quantum yields did not differ between symbionts in bleached and nonbleached areas. Exposing symbionts to light, however, led to greater quenching of Photosystem II in symbionts in the bleached coral. Bleached areas of the affected colonies had died by September 2003, with areas that were essentially covered by more than 80% living coral decreasing to less than 10% visible living coral cover. By January 2004, coral began to recover, principally from areas of colonies that were not exposed during low tide (i.e., from below dead, upper regions). These data highlight the importance of understanding local weather patterns as well as the effects of longer term trends in global climate.
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