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At least 595 records · Page 33Linked to original sources

Chemically-mediated interactions between macroalgae Dictyota spp. and multiple life-history stages of the coral Porites astreoides

Competition between corals and macroalgae is often assumed to occur on reefs, especially those that have undergone shifts from coral to algal dominance; however, data examining these competitive interactions, especially during the early life-history stages of corals, are scarce. We conducted a series of field and outdoor seawater-table experiments to test the hypothesis that allelopathy (chemical inhibition) mediates interactions between 2 common brown macroalgae, Dictyota pulchella and D. pinnatifida , and the coral Porites astreoides at different life-history stages of the coral. D. pinnatifida significantly reduced larval survival and larval recruitment. The extracts of both D. pinnatifida and D. pulchella significantly reduced larval survival, and the extract of D. pulchella also negatively influenced larval recruitment. There was no measurable effect of the crude extracts from Dictyota spp. on the photophysiology of adult corals. Our results provide evidence that these Dictyota species chemically compete with P. astreoides by negatively affecting larval settlement and recruitment as well as the survival of larvae and new recruits. Macroalgae may perpetuate their dominance on degraded reefs by chemically inhibiting the process of coral recruitment.

Marine Ecology Progress Series↗

Temporal and spatial variability in the flow and dispersal of suspended-sediment on a fringing reef flat, Molokai, Hawaii

A multi-year study was conducted on a shallow fringing reef flat on Molokai, Hawaii to determine the temporal and spatial dispersal patterns of terrigenous suspended sediment. During this study, trade-wind conditions existed for the majority of the year on the reef flat. The trade-wind conditions produced strong currents and resuspended moderate amounts of sediment on the reef flat on a daily basis during the year of study, resulting in an overwhelming contribution to the total sediment flux. The magnitude and direction of the trade winds relative to the orientation of the coastline, the shallow-relief and broad morphology, and tidal elevation, provided the primary control of the physical processes that resuspended and transported sediment on the reef flat over the period of record. Spatial data indicate that much of the terrigenous sediment resuspended on the reef flat is transported predominantly alongshore and is confined to the inner- to mid-reef flat. Evidence for the limited across-shore mixing and transport is provided by the dominantly alongshore wind-driven currents during trade-wind conditions and the well-defined across-shore gradient in percentage calcium carbonate of the suspended sediment. Regions of slightly offshore suspended-sediment transport along the reef flat can be attributed to the circulation pattern set up by the interaction between the trade winds, coastal morphology, and anthropogenic coastal structures (i.e., fish ponds and wharf). The regions in which sediment were seen to move offshore provide the strongest link between the sediment dynamics on reef flat and fore reef, and qualitatively appears to be correlated with low coral coverage on the fore reef. ?? 2005 Elsevier Ltd. All rights reserved.

Estuarine, Coastal and Shelf Science↗

Coral Diseases Following Massive Bleaching in 2005 Cause 60 Percent Decline in Coral Cover and Mortality of the Threatened Species, Acropora Palmata, on Reefs in the U.S. Virgin Islands

Record-high seawater temperatures and calm seas in the summer of 2005 led to the most severe coral bleaching (greater than 90 percent bleached coral cover) ever observed in the U.S. Virgin Islands (USVI) (figs. 1 and 2). All but a few coral species bleached, including the threatened species, Acropora palmata. Bleaching was seen from the surface to depths over 20 meters.

Fact Sheet↗

Paleoclimate ocean conditions shaped the evolution of corals and their skeletal composition through deep time

Identifying how past environmental conditions shaped the evolution of corals and their skeletal traits provides a framework for predicting their persistence and that of their non-calcifying relatives under impending global warming and ocean acidification. Here we show that ocean geochemistry, particularly aragonite–calcite seas, drives patterns of morphological evolution in anthozoans (corals, sea anemones) by examining skeletal traits in the context of a robust, time-calibrated phylogeny. The lability of skeletal composition among octocorals suggests a greater ability to adapt to changes in ocean chemistry compared with the homogeneity of the aragonitic skeleton of scleractinian corals. Pulses of diversification in anthozoans follow mass extinctions and reef crises, with sea anemones and proteinaceous corals filling empty niches as tropical reef builders went extinct. Changing environmental conditions will likely diminish aragonitic reef-building scleractinians, but the evolutionary history of the Anthozoa suggests other groups will persist and diversify in their wake.

Nature Ecology & Evolution↗

El Nino influence on Holocene reef accretion in Hawai'i

New observations of reef accretion from several locations show that in Hawai'i accretion during early to middle Holocene time occurred in areas where today it is precluded by the wave regime, suggesting an increase in wave energy. Accretion of coral and coralline algae reefs in the Hawaiian Islands today is largely controlled by wave energy. Many coastal areas in the main Hawaiian Islands are periodically exposed to large waves, in particular from North Pacific swell and hurricanes. These are of sufficient intensity to prevent modern net accretion as evidenced by the antecedent nature of the seafloor. Only in areas sheltered from intense wave energy is active accretion observed. Analysis of reef cores reveals patterns of rapid early Holocene accretion in several locations that terminated by middle Holocene time, ca. 5000 yr ago. Previous analyses have suggested that changes in Holocene accretion were a result of reef growth "catching up" to sea level. New data and interpretations indicate that the end of reef accretion in the middle Holocene may be influenced by factors in addition to sea level. Reef accretion histories from the islands of Kaua'i, O'ahu, and Moloka'i may be interpreted to suggest that a change in wave energy contributed to the reduction or termination of Holocene accretion by 5000 yr ago in some areas. In these cases, the decrease in reef accretion occurred before the best estimates of the decrease in relative sea-level rise during the mid-Holocene high stand of sea level in the main Hawaiian Islands. However, reef accretion should decrease following the termination of relative sea-level rise (ca. 3000 yr ago) if reef growth were "catching up" to sea level. Evidence indicates that rapid accretion occurred at these sites in early Holocene time and that no permanent accretion is occurring at these sites today. This pattern persists despite the availability of hard substrate suitable for colonization at a wide range of depths between -30 m and the intertidal zone. We infer that forcing other than relative sea-level rise has altered the natural ability to support reef accretion on Hawaiian insular shelves. The limiting factor in these areas today is wave energy. Numbers of both large North Pacific swell events and hurricanes in Hawai'i are greater during El Nino years. We infer that if these major reef-limiting forces were suppressed, net accretion would occur in some areas in Hawai'i that are now wave-limited. Studies have shown that El Nino/Southern Oscillation (ENSO) was significantly weakened during early-mid Holocene time, only attaining an intensity similar to the current one ca. 5000 yr ago. We speculate that this shift in ENSO may assist in explaining patterns of Holocene Hawaiian reef accretion that are different from those of the present and apparently not related to relative sen-level rise.

Hawaii↗

A new towed platform for the unobtrusive surveying of benthic habitats and organisms

Maps of coral ecosystems are needed to support many conservation and management objectives, as well as research activities. Examples include ground-truthing aerial and satellite imagery, characterizing essential habitat, assessing changes, and monitoring the progress of restoration efforts. To address some of these needs, the U.S. Geological Survey developed the Along-Track Reef-Imaging System (ATRIS), a boat-based sensor package for mapping shallow-water benthic environments. ATRIS consists of a digital still camera, a video camera, and an acoustic depth sounder affixed to a moveable pole. This design, however, restricts its deployment to clear waters less than 10 m deep. To overcome this limitation, a towed version has been developed, referred to as Deep ATRIS. The system is based on a light-weight, computer-controlled, towed vehicle that is capable of following a programmed diving profile. The vehicle is 1.3 m long with a 63-cm wing span and can carry a wide variety of research instruments, including CTDs, fluorometers, transmissometers, and cameras. Deep ATRIS is currently equipped with a high-speed (20 frames · s-1) digital camera, custom-built light-emitting-diode lights, a compass, a 3-axis orientation sensor, and a nadir-looking altimeter. The vehicle dynamically adjusts its altitude to maintain a fixed height above the seafloor. The camera has a 29° x 22° field-of-view and captures color images that are 1360 x 1024 pixels in size. GPS coordinates are recorded for each image. A gigabit ethernet connection enables the images to be displayed and archived in real time on the surface computer. Deep ATRIS has a maximum tow speed of 2.6 m · s-1and a theoretical operating tow-depth limit of 27 m. With an improved tow cable, the operating depth can be extended to 90 m. Here, we present results from the initial sea trials in the Gulf of Mexico and Biscayne National Park, Florida, USA, and discuss the utility of Deep ATRIS for map-ping coral reef habitats. Several example mosaics illustrate the high-quality imagery that can be obtained with this system. The images also reveal the potential for unobtrusive animal observations; fish and sea turtles are unperturbed by the presence of Deep ATRIS

Florida↗

Sedimentary petrology of a declining reef ecosystem, Florida reef tract (U.S.A.)

Petrologic evaluation of biogenic sediments collected shelf-wide along the Florida reef tract in 1989 revealed three principal components: coral, the calcareous green alga Halimeda, and mollusc. The dominant grain was dependent in part upon local morphology that controlled composition and vitality of the biota. Either Halimeda or mollusc grains prevailed in sands off the upper Keys. In the middle and lower Keys, Halimeda grains prevailed nearshore and coral grains offshore. Comparison with similar analyses of samples collected in 1952 and 1963 indicates that, over 37 years, the relative abundance of molluscan grains more than doubled in the upper Keys and that of particulate coral tripled in the middle Keys. These changes can be interpreted in the context of physical and biological events that affected Florida Keys reefs over that period of time. In the 1970s, outbreaks of extremely cold water killed even representatives of the hardiest coral species. In the 1980s, black-band and white-band diseases decimated the major reef-building acroporid corals, and the pivotal herbivore, Diadema antillarum, disappeared. Although Diadema is a major coral bioeroder, the sea urchin is also essential to healthy reef growth. The increase in coral debris in the middle Keys may be related to Hurricane Donna in 1960, but it is also consistent with the prediction of accelerated bioerosion by boring organisms in response to increased plankton productivity. Plankton productivity is stimulated by nutrients from Florida Bay and by well-documented eutrophication of nearshore environments. In the upper Keys, where reefs are somewhat removed from bay and nearshore influence, a relative decrease in coral debris over the 37 years may reflect proliferation of algae and algae-grazing molluscs as well as suppressed rates of bioerosion in the absence of Diadema. Human activities have substantially increased the natural flux of fixed nitrogen to coastal systems worldwide. Waters in the Florida Keys are no exception. Spatial and temporal trends in sediment constituents are compared to a previously published model that predicts the response of benthic biota to changes in nutrient supply. As adapted to interpret changes observed in reef-tract sediments, the model provides insights into the natural nutrient gradient along the Florida reef tract.

Journal of Coastal Research↗

An integrated approach to benthic habitat mapping using remote sensing and GIS: An example from the Hawaiian Islands

This chapter documents our effort to map benthic habitats within the KalokoHonokohau National Historic Park, Hawai`i, USA. We produce detailed benthichabitat maps by using a combination of color aerial photography, high-resolution bathymetry, and georeferenced underwater video and still photography. We classify individual habitat polygons using five basic attributes and additional information regarding geology, morphology, and coral species. Derivative data sets including isobaths, hillshades, and slope maps are also generated. The mapping shows that benthic habitat and seafloor morphology varies greatly throughout the study area. Nearly 73% of the study area consists of a hardbottom structure that is potentially available for coral habitation; the remaining 27% includes unconsolidated sediment and artificial or historical features. Coral cover is generally low and increases with water depth. The offshore geology is predominantly composed of smooth to undulating pahoehoe-type basalt flows that form flat to gently sloping benches, vertical walls, and steep escarpments. In some locations the basalt surface is irregular and mounded into ridges, pinnacles, and arches. Large rounded basaltic boulders and smaller scattered rocks are common throughout the marine portions of the park. Coral or accreted carbonate reef obscures the underlying volcanic surface in only a few areas. The underlying geologic framework and morphology of the submerged volcanic flows within Kaloko-Honokohau National Historical Park provide the primary control on benthic habitats within the park. The habitat maps and associated data can be used as a stand-alone product or in a GIS to provide useful baseline information to scientists, managers and the general public.

Hawaii↗

Seafloor morphology and coral habitat variability in a volcanic environment: Kaloko-Honokohau National Park, Hawaii, USA

Kaloko–Honokohau National Historical Park (KAHO) is one of three National Park lands along the leeward, west, or Kona, coast of the island of Hawaii, USA. The park includes 596 acres (2.4 km2) of submerged lands and marine resources within its official boundaries. The offshore region of KAHO, part of the insular shelf of the island of Hawaii, comprises a volcanic embayment that extends nearly 3.5 km alongshore and varies in width between 120 and 875 m from the shoreline to the 40 m isobath, the limit of the high-resolution bathymetry. Multiple Holocene volcanic flows coalesce within Kaloko-Honokohau National Historical Park (KAHO) on the island of Hawaii to create a complex offshore morphology. The volcanic-dominated morphology includes flat to gently sloping volcanic benches, boulder fields, cliffs and ledges, pinnacles, ridges, arches, and steep shelf escarpments. Each of these environments provide distinct habitat zones for coral species, ranging from isolated heads of Porites lobata and Pocillopora meandrina to dense thickets of Porites compressa . In contrast to coral habitat elsewhere in the Hawaiian Islands, where coral typically populates relict carbonate platforms, coral cover in KAHO is typically only a thin veneer of live coral and rubble on exposed volcanic pavement. In only a few locations does coral or accreted carbonate reef obscure the underlying volcanic surface.

Book chapter↗

Water in St. John, U.S. Virgin Islands

Water for domestic and municipal supply on St. John, in the past, has been obtained from rain catchments, dug wells, and barge shipments from St. Thomas and Puerto Rico. As a result of this study, small ground-water supplies have been developed for the Virgin Islands National Park. Ground water occurs in significant but limited quantities in the fractured volcanic rock throughout most of the Island. Yield of wells in this aquifer ranges from less than 100 to about 2,000 gpd (gallons per day). The average long-term yield of the three drilled wells in use by the National Park Service in 1967 was about 1,000 gpd. Yield ofl,000 to 5,000 gpd may be expected in the Coral Bay and the Reef Bay areas. Estimated total recharge of the fractured volcanic rock on St. John, based on a recharge of 1 to 3 inches per year, is 1,000,000 to 3,000,000 gpd. Perhaps as much as a quarter to a third of this water could be developed practically, depending on the rainfall in a given year. The chemical quality of the ground water in the fractured-rock aquifer in areas uncontaminated by sea water ranges from 600 to 2,000 mg/l (milligrams per liter) or more dissolved solids. Water from-formations in the higher altitudes is of better quality than that in the lower formations. Small quantities of ground water are available from beach sand, alluvium, and fractured rock near the sea. However, these sources tend to be brackish and are subject to salt-water encroachment. There are no perennial streams on St. John. There are a few spring-fed pools in stream channels, however, that are sustained, except in severe drought. Storm runoff is estimated to average 1 inch over the island annually, and evaporation from open water surfaces is about 70 inches per year. Ponds can be developed, but because of the high .evaporation they may be unreliable during droughts. Rain water collected in cisterns from roofs and catchments yield about 50 gpd per 1,000 square feet of catch area during an average year of rainfall. This is the main method of Water supply for domestic use on the Island; it will probably be continued even if a public distribution system is made available, because of the limited quantity of other natural water.

Open-File Report↗

Rapid broad-scale ecosystem changes and their consequences for biodiversity

Biodiversity contributes to and depends on ecosystem structure and associated function. Ecosystem structure, such as the amount and type of tree cover, influences fundamental abiotic variables such as near-ground incoming solar radiation (e.g., Royer et al. 2011), which in turn affects species and associated biodiversity (e.g., Trotter et al. 2008). In many systems, foundational, dominant, or keystone species (or species groups) are important in determining biodiversity, often because of their role in determining ecosystem structure. At spatial scales ranging from ecosystems to regions and larger, structural characteristics of vegetation or other structurally dominant organisms such as corals can influence species diversity, whether focused on alpha diversity (mean species diversity at the habitat level), beta diversity (differentiation among habitats), or gamma diversity (total species diversity across a landscape; Whittaker 1960). Climate change is projected to alter ecosystems at broad scales. In many cases, this will be due to extreme climate events such as droughts, floods and hurricanes, the effects of which can be rapid (IPCC 2012). Consequently, rapid broad-scale changes in ecosystems are of increasing concern. Climate change can directly affect species physiology, phenology, and distribution, as highlighted throughout this book (e.g. Citations to chapters in this volume to be added). Changes in one species can also affect other species (Cahill et al. 2013), particularly when dominant or co-dominant species that collectively provide habitat for other species are impacted (e.g. tree canopy architecture in many forest ecosystems; coral species via their reefs). Several rapid ecological changes have occurred at spatial scales that are sufficiently broad enough to represent biome changes (Gonzalez et al. 2010, Settele et al. 2014; Fig. 1 A). Rapid broad-scale changes differ from other patterns of vegetation dynamics in that they result in a “crash” in one or more populations (Breshears et al. 2008) over large areas of the affected region. Rapid broad-scale changes triggered by climate can include mega-fires; drought-triggered tree die-off and associated pest and pathogen outbreaks (Breshears et al. 2005, Safranyik et al. 2007); and hurricanes and wind-throw events (IPCC 2012, 2014). These rapid broad-scale changes can rapidly alter other factors such as resultant microclimate, which in turn can affect numerous other species and associated biodiversity (Royer et al. 2011; Fig. 1B). Many examples of broad-scale changes are documented in the paleoecology literature (Settele et al. 2014), although the temporal resolution at which those events can be resolved is relatively coarse (often centuries or longer). Such broad-scale changes documented in the paleoecology literature provide examples of types of change are likely to be of increasing concern in the future (Settele et al. 2014). Contemporary events have highlighted that broad-scale changes can occur rapidly (years or less; Breshears et al. 2005, Gonzalez et al. 2010, Settele et al. 2014). These rapid broad-scale changes will have important consequences for biodiversity beyond the direct impacts of climate change through the cascading effects associated with ecosystem structural and functional changes. The objective of this chapter is to alert readers to recent and projected rapid ecosystem changes and their potential consequences for biodiversity at ecosystem, landscape and regional scales.

Book chapter↗

Sea-level history of past interglacial periods: New evidence from uranium-series dating of corals from Curaçao, Leeward Antilles islands

Curaçao has reef terraces with the potential to provide sea-level histories of interglacial periods. Ages of the Hato (upper) unit of the “Lower Terrace” indicate that this reef dates to the last interglacial period, Marine Isotope Stage (MIS) 5.5. On Curaçao, this high sea stand lasted at least 8000 yr (~ 126 to ~ 118 ka). Elevations and age of this reef show that late Quaternary uplift rates on Curaçao are low, 0.026–0.054 m/ka, consistent with its tectonic setting. Ages of ~ 200 ka for corals from the older Cortalein unit of the Lower Terrace correlate this reef to MIS 7, with paleo-sea level estimates ranging from − 3.3 m to + 2.3 m. The estimates are in agreement with those for MIS 7 made from other localities and indicate that the penultimate interglacial period was a time of significant warmth, on a par with the present interglacial period. The ~ 400 ka (MIS 11) Middle Terrace I on Curaçao, dated by others, may have formed from a paleo-sea level of + 8.3 to + 10.0 m, or (less likely) + 17 m to + 20 m. The lower estimates are conservative compared to previous studies, but still require major ice sheet loss from Greenland and Antarctica.

Leeward Antilles↗

Seasonal microbial and environmental parameters at Crocker Reef, Florida Keys, 2014–2015

Crocker Reef, located on the outer reef tract of the Florida Keys (fig. 1), was the site of an integrated “reefscape characterization” effort focused on calcification and related biogeochemical processes as part of the U.S. Geological Survey (USGS) C oral R eef E cosystem ST udies (CREST) project. It is characterized as a senile or dead reef, with only scattered stony coral colonies and areas of sand and rubble. It was chosen as an end-member for later comparison to sites with a healthy, growing reef framework. The CREST reefscape characterization included two intensive seasonal sampling trips to capture summer (July 8–17, 2014) and winter (January 29–February 5, 2015) conditions. This report presents water column microbial and environmental data collected for use as metadata in future publications examining reef metabolic processes via metagenomes derived from water samples and fine-scale temporal and spatial carbonate chemistry measurements. Microbial measurements included enumeration of total bacteria, enumeration of virus-like particles, and plate counts of Vibrio spp. colony-forming units (CFU). These measurements were intended to give a sense of any seasonal changes in the total microbial load and to provide an indication of water quality. Additional environmental parameters measured included water temperature, salinity, dissolved oxygen, and pH. Four sites (table 1) were intensively sampled for periods of approximately 48 hours during summer (July 2014) and winter (January–February 2015), during which water samples were collected every 4 hours for analysis, except when prevented by weather conditions.

Florida↗

Empirical relationships among resilience indicators on Micronesian reefs

A process-orientated understanding of ecosystems usually starts with an exploratory analysis of empirical relationships among potential drivers and state variables. While relationships among herbivory, algal cover, and coral recruitment, have been explored in the Caribbean, the nature of such relationships in the Pacific appears to be variable or unclear. Here, we examine potential drivers structuring the benthos and herbivorous fish assemblages of outer-shelf reefs in Micronesia (Palau, Guam and Pohnpei). Surveys were stratified by wave exposure and protection from fishing. High biomass of most herbivores was favoured by high wave exposure. High abundance of large-bodied scarids was associated with low turf abundance, high coral cover, and marine reserves. The remaining herbivores were more abundant in reefs with low coral cover, possibly because space and hence food limitation occur in high-coral-cover reefs. Rugosity had no detectable effect on herbivorous fish abundance once differences in exposure and coral cover were accounted for. At identical depths, high wave exposure was associated with greater volumes (cover × canopy height) of macroalgae and algal turfs, which most likely resulted from high primary productivity driven by flow. In exposed areas, macroalgal cover declined as the acanthurid biomass increased. The volume of algal turfs was negatively associated with coral cover and herbivore biomass. In turn, high coral cover and herbivore biomass are likely to intensify grazing. The density of juvenile corals was variable where macroalgal cover was low but was confined to lower densities where macroalgal cover was high. High coral cover and density of juvenile corals were favoured in sheltered habitats. While a weak positive relationship was found between scarid biomass and juvenile coral density, we hypothesise that high scarid densities may hinder juvenile density through increased corallivory. New hypotheses emerged that will help clarify the role of acanthurids, wave exposure, and corallivory in driving the recovery of Pacific coral communities.

Pohnpei↗

20th century warming in the lower Florida Keys was dominated by increasing winter temperatures

Long-lived Atlantic coral species like Orbicella faveolata are important archives of oceanographic change in shallow, marine environments like the Florida Keys. Not only can coral-based records extend for multiple centuries beyond the limits of the instrumental record, but they can also provide a more accurate representation of in situ conditions than gridded interpolated sea-surface temperature (SST) products for nearshore reef environments. We use the coral Sr/Ca paleothermometer to produce a 150-year (1830–1980 C.E.) monthly SST reconstruction from an O . faveolata colony collected in the Marquesas Keys, FL, USA. An important feature of our record is a significant 20th-century warming trend in winter SSTs. We hypothesize that the winter warming trend was driven partially by a decrease in upwelling associated cyclonic eddies spinning off the Florida Current. A long-term weakening of winter Florida Current transport over the 20th century could be responsible for decreased cyclonic eddy formation in the Florida Straits. Another feature of the record is pronounced multidecadal fluctuations of mean annual warming and cooling in the record, which correspond to Atlantic Multidecadal Variability (AMV), with the AMV lagging behind western Florida Keys temperatures by 5–11 years. Strong coherence between coral-based SST reconstructions in the western Florida Keys with broader scale Atlantic oceanographic trends over the past century suggests a common driver of regional SST variability.

Florida↗

PhyloChipTM microarray comparison of sampling methods used for coral microbial ecology

Interest in coral microbial ecology has been increasing steadily over the last decade, yet standardized methods of sample collection still have not been defined. Two methods were compared for their ability to sample coral-associated microbial communities: tissue punches and foam swabs, the latter being less invasive and preferred by reef managers. Four colonies of star coral, Montastraea annularis , were sampled in the Dry Tortugas National Park (two healthy and two with white plague disease). The PhyloChip™ G3 microarray was used to assess microbial community structure of amplified 16S rRNA gene sequences. Samples clustered based on methodology rather than coral colony. Punch samples from healthy and diseased corals were distinct. All swab samples clustered closely together with the seawater control and did not group according to the health state of the corals. Although more microbial taxa were detected by the swab method, there is a much larger overlap between the water control and swab samples than punch samples, suggesting some of the additional diversity is due to contamination from water absorbed by the swab. While swabs are useful for noninvasive studies of the coral surface mucus layer, these results show that they are not optimal for studies of coral disease.

Dry Tortugas National Park↗

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.

Diseases of Aquatic Organisms↗