Genome-wide assessment reveals opposing patterns of vertical connectivity in two depth-generalist coral species.

Profound ecological changes are occurring on coral reefs throughout the tropics, with marked coral cover losses and concomitant algal increases, particularly in the Caribbean region. Historical declines in the abundance of large Caribbean reef fishes likely reflect centuries of overexploitation. However, effects of drastic recent degradation of reef habitats on reef fish assemblages have yet to be established. By using meta-analysis, we analyzed time series of reef fish density obtained from 48 studies that include 318 reefs across the Caribbean and span the time period 1955-2007. Our analyses show that overall reef fish density has been declining significantly for more than a decade, at rates that are consistent across all subregions of the Caribbean basin (2.7% to 6.0% loss per year) and in three of six trophic groups. Changes in fish density over the past half-century are modest relative to concurrent changes in benthic cover on Caribbean reefs. However, the recent significant decline in overall fish abundance and its consistency across several trophic groups and among both fished and nonfished species indicate that Caribbean fishes have begun to respond negatively to habitat degradation.

Protecting a Thalassia testudinum-dominated seagrass meadow from grazing by sea turtles for 1 yr caused an increase in the biomass of seagrasses and an increase in the structural complexity of the seagrass canopy, as the length and width of the seagrass blades increased in comparison to grazed plots. Plots from which turtles were excluded had higher rates of primary production on a per-shoot or areal basis, but the relative growth rate was not affected. The leaves of seagrasses protected from grazing had lower concentrations of nitrogen and phosphorus than grazed blades, but the storage of soluble carbohydrates in the rhizomes increased markedly in the protected plots, suggesting that reduced carbon fixation caused by the removal of photosynthetic leaves is the mechanism for seagrass decline in heavily grazed meadows, not nutrient limitation as has been suggested in the literature. The continued grazing of sea turtles in our plots did not lead to significant changes in seagrass shoot density or nutrient content over the 1 yr duration of our experiments. The decreased canopy cover and the shorter, thinner seagrass leaves induced by sea turtle grazing in our experimental plots suggest that the progressive narrowing and thinning of seagrasses observed before the collapse of 2 offshore seagrass beds in Bermuda during the 1990s may have been in response to repeated and intense grazing of those seagrass beds. KEY WORDS: Caribbean Coastal Marine Productivity Program · CARICOMP · Thalassia testudinum · Nutrient content · Soluble carbohydrates · Productivity Resale or republication not permitted without written consent of the publisherMar Ecol Prog Ser 419: [223][224][225][226][227][228][229][230][231][232] 2010 (Williams 1988, Bjorndal 1997. Whether to reject the relatively low nutrient content of old seagrass leaves (Bjorndal 1980) or to avoid the calcareous encrusting epiphyte communities on those old blades , green sea turtles often clip seagrass shoots to within approximately 1 cm of the sediment surface, allowing the leaves to float away; they then repeatedly graze the newly-produced, unepiphytized, high nutrient-content seagrass leaves that grow after the clipping (Bjorndal 1997). Thayer et al. (1984) surmised that these repeated grazing events would stress the seagrasses, so that leaf widths would decrease, short shoot density would decline, leaf production would decline, and recycling of nutrients through a local detritus cycle would be interrupted. Further, they suggested that internal stores of carbohydrates and proteins would be mobilized from the rhizomes to grow new leaves, and that the repeated cropping of new leaves would eventually lead to a decline in the nutrient content of the seagrass as stores were depleted, resulting in poor food quality and decreased food production for the turtles. These declines would then cause the turtles to abandon that grazing patch and begin the cultivation of a new grazing site. However, recent experimental work has shown that growth rates (Moran & Bjorndal 2...

[1] Strontium to calcium ratios (Sr/Ca) are reported for a massive brain coral Diploria labyrinthiformis collected from the south shore of Bermuda and are strongly correlated with both sea surface temperature (SST) and mean annual skeletal growth rate. High Sr/Ca ratios correspond with cold SSTs and slow skeletal growth rate and vice versa. We provide a quantitative calibration of Sr/Ca to extension rate and SST along the axis of maximum growth and derive a growth-dependent Sr/Ca-SST calibration equation to reconstruct western subtropical North Atlantic SSTs for the past 223 years. When the influence of growth rate is excluded from the calibration, Sr/Ca ratios yield SSTs that are too cold during cool anomalies and too warm during warm anomalies. Toward the end of the Little Ice Age ($1850), SST changes derived using a calibration that is not growth-dependent are exaggerated by a factor of 2 relative to those from the growth-corrected model that yields SSTs $1.5°C cooler than today. Our results indicate that incorporation of growth rate effects into coral Sr/Ca calibrations may improve the accuracy of SSTs derived from living and fossil corals.