Caroline S. Rogers

Scleractinian Coral Recruitment Patterns at Salt River Submarine Canyon, St. Croix, U.S. Virgin Islands

Scleractinian coral recruitment patterns were studied at depths of 9, 18, 27 and 37 m on the east and west walls of Salt River submarine canyon, St. Croix, U.S. Virgin Islands, by censusing coral juveniles which settled on experimental settling plates placed on the reef for 3–26 months as well as coral juveniles within quadrats on the reef. The most common species in the juvenile population within quadrats were Agaricia agaricites, Porites astreoides, Madracis decactis, Stephanocoenia michelinii, and A. lamarcki. The only species settling on settling plates were Agaricia spp., Madracis decactis, Porites spp., Stephanocoenia michelinii and Favia fragum. A total of 271 corals settled on 342 plates, with 51% of the juveniles on the east wall and 49% on the west wall. Of these 34% settled on horizontal surfaces and 66% on vertical surfaces. Based on results from quadrats, Agaricia agaricites and Porites astreoides had high recruitment rates relative to their abundance on the reef. In contrast, Agaricia lamarcki, Montastraea annularis, M. cavernosa and Siderastrea siderea had high amounts of cover compared to their abundance as juveniles within quadrats. The mean number of juveniles per m2 within quadrats ranged from 3 to 42. In general, there was a decrease in the mean number of juveniles and the number of species with depth. Total number of juveniles on settling plates was highest at 18 m on both walls. The largest number within quadrats was at 18 m on the east wall, followed by 9 m and 18 m on the west wall. High rates of coral recruitment tended to be associated with low algal biomass and relatively high grazing pressure by urchins and fishes.

Degradation of marine ecosystems and decline of fishery resources in marine protected areas in the US Virgin Islands

The large number of marine protected areas (MPAs) in the Caribbean (over 100) gives a misleading impression of the amount of protection the reefs and other marine resources in this region are receiving. This review synthesizes information on marine resources in two of the first MPAs established in the USA, namely Virgin Islands National Park (1962) and Buck Island Reef National Monument (1961), and provides compelling evidence that greater protection is needed, based on data from some of the longest running research projects on coral reefs, reef fish assemblages, and seagrass beds for the Caribbean. Most of the stresses affecting marine resources throughout the Caribbean (e.g. damage from boats, hurricanes and coral diseases) are also causing deterioration in these MPAs. Living coral cover has decreased and macroalgal cover has increased. Seagrass densities have decreased because of storms and anchor damage. Intensive fishing in the US Virgin Islands has caused loss of spawning aggregations and decreases in mean fish size and abundance. Groupers and snappers are far less abundant and herbivorous fishes comprise a greater proportion of samples than in the 1960s. Effects of intensive fishing are evident even within MPA boundaries. Although only traditional fishing with traps of ‘conventional design’ is allowed, commercial trap fishing is occurring. Visual samples of fishes inside and outside Virgin Islands National Park showed no significant differences in number of species, biomass, or mean size of fishes. Similarly, the number of fishes per trap was statistically similar inside and outside park waters. These MPAs have not been effective because an unprecedented combination of natural and human factors is assaulting the resources, some of the greatest damage is from stresses outside the control of park managers (e.g. hurricanes), and enforcement of the few regulations has been limited. Fully functioning MPAs which prohibit fishing and other extractive uses (e.g. no-take marine reserves) could reverse some of the degradation, allowing replenishment of the fishery resources and recovery of benthic habitats.

Bleaching increases likelihood of disease on Acropora palmata (Lamarck) in Hawksnest Bay, St John, US Virgin Islands

Anomalously high water temperatures may enhance the likelihood of coral disease outbreaks by increasing the abundance or virulence of pathogens, or by increasing host susceptibility. This study tested the compromised-host hypothesis, and documented the relationship between disease and temperature, through monthly monitoring of Acropora palmata colonies from May 2004 to December 2006, in Hawksnest Bay, St John, US Virgin Islands (USVI). Disease prevalence and the rate of change in prevalence showed a positive linear relationship with water temperature and rate of change in water temperature, respectively, but only in 2005 during prolonged periods of elevated temperature. Both bleached and unbleached colonies showed a positive relationship between disease prevalence and temperature in 2005, but the average area of disease-associated mortality increased only for bleached corals, indicating host susceptibility, rather than temperature per se, influenced disease severity on A. palmata.

Coral bleaching and disease combine to cause extensive mortality on reefs in US Virgin Islands

Coral Reefs (2006) 25: 418 DOI 10.1007/s00338-006-0125-6 Reef sites Reefs in the US Virgin Islands experienced extensive bleaching in September 2005 with >90% coral cover bleached (n = 20 video transects at each of five reef sites). Mean reef water temperatures from April 2005 to September 2005 were significantly higher than the previous 14 years. Corals began regaining color in October as water temperatures decreased, and minimal coral mortality was observed. Monitoring from November 2005 to April 2006 revealed significant coral mortality following distinct White Plague disease signs, resulting in unprecedented 26–48% losses in coral cover (Fig. 1). Chronic mortality from this disease has occurred monthly at one monitoring site since 1997, but with prevalence rates not related to elevated temperatures or previous bleaching events (Miller et al. 2003). While coral mortality from bleaching events has been well documented (Hoegh-Guldberg 1999) this study shows that only with frequent monitoring would these post-bleaching mortality patterns and presence of pathogenic disease be detected.

Coral Reef Diseases in the Atlantic-Caribbean

Coral reefs are the jewels of the tropical oceans. They boast the highest diversity of all marine ecosystems, aid in the development and protection of other important, productive coastal marine communities, and have provided millions of people with food, building materials, protection from storms, recreation and social stability over thousands of years, and more recently, income, active pharmacological compounds and other benefits. These communities have been deteriorating rapidly in recent times. The continuous emergence of coral reef diseases and increase in bleaching events caused in part by high water temperatures among other factors underscore the need for intensive assessments of their ecological status and causes and their impact on coral reefs.

Management implications of fish trap effectiveness in adjacent coral reef and gorgonian habitats

A combination of visual census and trap sampling in St. John, USVI indicated that traps performed better in gorgonian habitat than in adjacent coral reef habitat. Although most families were seen more commonly in coral habitat, they were caught more often in gorgonian areas. Traps probably fished more effectively in gorgonian habitats, especially for migrating species, because traps provided shelter in the relatively topographically uniform environment of gorgonian dominated habitats. Recently, trap fishermen on St. John have been moving effort away from traditionally fished nearshore coral reefs and into a variety of more homogeneous habitats such as gorgonian habitat. Consequently, exploitation rates of the already over-harvested reef fish resources may be increasing. Reef fish managers and marine reserve designers should consider limiting trap fishing in gorgonian habitats to slow the decline of reef fisheries.

The habitats exploited and the species trapped in a Caribbean island trap fishery

We visually observed fish traps in situ to identify the habitats exploited by the U.S. Virgin Islands fishery and to document species composition and abundance in traps by habitat. Fishers set more traps in algal plains than in any other habitat around St. John. Coral reefs, traditionally targeted by fishers, accounted for only 16 % of traps. Traps in algal plain contained the highest number of fishes per trap and the greatest numbers of preferred food species. Traps on coral reefs contained the most species, 41 of the 59 taxa observed in the study. Acanthurus coeruleus was the most abundant species and Acanthuridae the most abundant family observed in traps. Piscivore numbers were low and few serranids were observed. Traps in algal plain contained the most fishes as a result of: ecological changes such as shifts in habitat use, mobility of species and degradation of nearshore habitat (fishery independent); and, catchability of fishes and long-term heavy fishing pressure (fishery dependent). The low number of serranids per trap, dominance of the piscivore guild by a small benthic predator, Epinephelus guttatus, and dominance of trap contents overall by a small, fast-growing species of a lower trophic guild, Acanthurus coeruleus, all point to years of intense fishing pressure.

Coral Reef Resilience through Biodiversity

Irrefutable evidence of coral reef degradation worldwide and increasing pressure from rising seawater temperatures and ocean acidification associated with climate change have led to a focus on reef resilience and a call to “manage” coral reefs for resilience. Ideally, global action to reduce emission of carbon dioxide and other greenhouse gases will be accompanied by local action. Effective management requires reduction of local stressors, identification of the characteristics of resilient reefs, and design of marine protected area networks that include potentially resilient reefs. Future research is needed on how stressors interact, on how climate change will affect corals, fish, and other reef organisms as well as overall biodiversity, and on basic ecological processes such as connectivity. Not all reef species and reefs will respond similarly to local and global stressors. Because reef-building corals and other organisms have some potential to adapt to environmental changes, coral reefs will likely persist in spite of the unprecedented combination of stressors currently affecting them. The biodiversity of coral reefs is the basis for their remarkable beauty and for the benefits they provide to society. The extraordinary complexity of these ecosystems makes it both more difficult to predict their future and more likely they will have a future.

Extensive coral mortality in the US Virgin Islands in 2005/2006: A review of the evidence for synergy among thermal stress, coral bleaching and disease

Abstract. In the summer/fall of 2005, extensive coral bleaching on reefs in the US Virgin Islands (USVI) was associated with sea water temperatures exceeding 30°C. Almost all coral species bleached, including Acropora palmata, which bleached for the first time on record in the USVI. As water temperatures cooled, corals began to regain their normal coloration. However, a severe disease outbreak then occurred on deeper, non-acroporid reefs. The disease demonstrated signs consistent with white plague. Monitoring of coral cover along previously established long-term transects on several reefs in St. John and St. Croix was intensified. Data on bleaching and disease were collected before, during and after this bleaching/disease episode. Average coral cover declined by over 50%, from 21.4% to 10.3% at the long-term study sites, within one year of the onset of bleaching, declining further to 8.3% after two years. This loss of coral cover was greater than from all other stressors affecting the USVI reefs in preceding years, and no significant recovery is evident. Disease prevalence increased on bleached A. palmata colonies that were being monitored as well as on the colonies of other species on the deeper reefs. Bleached A. palmata colonies had more disease (primarily white pox and other un-described diseases) than unbleached colonies. The non-acroporid corals that bleached most severely suffered the highest mortality from disease. Although the research summarized in this paper is not conclusive, the results suggest that high water temperatures lead to bleaching, which weakens corals and makes them more vulnerable to diseases.

Words matter: Recommendations for clarifying coral disease nomenclature and terminology

Coral diseases have caused significant losses on Caribbean reefs and are becoming a greater concern in the Pacific. Progress in coral disease research requires collaboration and communication among experts from many different disciplines. The lack of consistency in the use of terms and names in the recent scientific literature reflects the absence of an authority for naming coral diseases, a lack of consensus on the meaning of even some of the most basic terms as they apply to corals, and imprecision in the use of descriptive words. The lack of consensus partly reflects the complexity of this newly emerging field of research. Establishment of a nomenclature committee under the Coral Disease and Health Consortium (CDHC) could lead to more standardized definitions and could promote use of appropriate medical terminology for describing and communicating disease conditions in corals. This committee could also help to define disease terminology unique to corals where existing medical terminology is not applicable. These efforts will help scientists communicate with one another and with the general public more effectively. Scientists can immediately begin to reduce some of the confusion simply by explicitly defining the words they are using. In addition, digital photographs can be posted on the CDHC website and included in publications to document the macroscopic (gross) signs of the conditions observed on coral colonies along with precisely written characterizations and descriptions.