25 research outputs found

    Climate warming, marine protected areas and the ocean-scale integrity of coral reef ecosystems

    Get PDF
    Coral reefs have emerged as one of the ecosystems most vulnerable to climate variation and change. While the contribution of a warming climate to the loss of live coral cover has been well documented across large spatial and temporal scales, the associated effects on fish have not. Here, we respond to recent and repeated calls to assess the importance of local management in conserving coral reefs in the context of global climate change. Such information is important, as coral reef fish assemblages are the most species dense vertebrate communities on earth, contributing critical ecosystem functions and providing crucial ecosystem services to human societies in tropical countries. Our assessment of the impacts of the 1998 mass bleaching event on coral cover, reef structural complexity, and reef associated fishes spans 7 countries, 66 sites and 26 degrees of latitude in the Indian Ocean. Using Bayesian meta-analysis we show that changes in the size structure, diversity and trophic composition of the reef fish community have followed coral declines. Although the ocean scale integrity of these coral reef ecosystems has been lost, it is positive to see the effects are spatially variable at multiple scales, with impacts and vulnerability affected by geography but not management regime. Existing no-take marine protected areas still support high biomass of fish, however they had no positive affect on the ecosystem response to large-scale disturbance. This suggests a need for future conservation and management efforts to identify and protect regional refugia, which should be integrated into existing management frameworks and combined with policies to improve system-wide resilience to climate variation and change

    Habitat Associations of Juvenile Fish at Ningaloo Reef, Western Australia: The Importance of Coral and Algae

    Get PDF
    Habitat specificity plays a pivotal role in forming community patterns in coral reef fishes, yet considerable uncertainty remains as to the extent of this selectivity, particularly among newly settled recruits. Here we quantified habitat specificity of juvenile coral reef fish at three ecological levels; algal meadows vs. coral reefs, live vs. dead coral and among different coral morphologies. In total, 6979 individuals from 11 families and 56 species were censused along Ningaloo Reef, Western Australia. Juvenile fishes exhibited divergence in habitat use and specialization among species and at all study scales. Despite the close proximity of coral reef and algal meadows (10's of metres) 25 species were unique to coral reef habitats, and seven to algal meadows. Of the seven unique to algal meadows, several species are known to occupy coral reef habitat as adults, suggesting possible ontogenetic shifts in habitat use. Selectivity between live and dead coral was found to be species-specific. In particular, juvenile scarids were found predominantly on the skeletons of dead coral whereas many damsel and butterfly fishes were closely associated with live coral habitat. Among the coral dependent species, coral morphology played a key role in juvenile distribution. Corymbose corals supported a disproportionate number of coral species and individuals relative to their availability, whereas less complex shapes (i.e. massive & encrusting) were rarely used by juvenile fish. Habitat specialisation by juvenile species of ecological and fisheries importance, for a variety of habitat types, argues strongly for the careful conservation and management of multiple habitat types within marine parks, and indicates that the current emphasis on planning conservation using representative habitat areas is warranted. Furthermore, the close association of many juvenile fish with corals susceptible to climate change related disturbances suggests that identifying and protecting reefs resilient to this should be a conservation priority

    Non-random habitat use by coral reef fish recruits in Mafia Island Marine Park, Tanzania

    No full text
    The habitat use by nearly 3 000 reef fish recruits, comprising 56 taxa, at seven sites in Mafia Island Marine Park, Tanzania, were examined. The study was carried out following the 1998 global coral bleaching event and all sites but one were dominated by dead coral and rubble. Mean recruit densities ranged between 0.1 m–2 and 0.7 m–2 among sites. Although live coral represented only 15% of the overall substrate composition, almost half of all observed recruits were found associated with this substrate. Pooled across all sites, 46% of the recruits used live coral cover in disproportion to availability. Principal component analyses were applied to explore microhabitat use by the 11 most common recruit taxa in comparison to availability. Among these taxa, 10 exhibited nonrandom microhabitat use and six associated with live coral in disproportion to availability. A comparison with the adult fish community revealed that adult abundances of four of the six coral selective recruit taxa were significantly correlated with live coral. The study demonstrated that reef fish recruits use microhabitats non-randomly and that a substantial proportion is selective towards live coral.African Journal of Marine Science 2007, 29(2): 187–19

    Episodic heterogeneous decline and recovery of coral cover in the Indian Ocean

    Get PDF
    Long-term changes in coral cover for the Caribbean and the Pacific/Southeast Asia regions (PSEA) have proven extremely useful in assessing the main drivers, magnitude and timescales of change. The one major coral reef region where such assessments have not been made is the Indian Ocean (IO). Here, we compiled coral cover survey data from across the IO into a database of similar to 2,000 surveys from 366 coral reef sites collected between 1977 and 2005. The compilation shows that the 1998 mass coral bleaching event was the single most important and widespread factor influencing the change in coral cover across the region. The trend in coral cover followed a step-type function driven by the 1998 period, which differs from findings in the Caribbean and the PSEA regions where declines have been more continuous and mostly began in the 1980s. Significant regional variation was observed, with most heterogeneity occurring during and after 1998. There was a significant relationship between cover and longitude for all periods, but the relationship became stronger in the period immediately after 1998. Before 1998, highest coral cover was observed in the central IO region, while this changed to the eastern region after 1998. Coral cover and latitude displayed a significant U-shaped relationship immediately after 1998, due to a large decrease in cover in the northern-central regions. Post-1998 coral cover was directly correlated to the impact of the disturbance; areas with the lowest mortality having the highest cover with India-Sri Lanka being an outlier due to its exceptionally high recovery. In 1998, reefs within Marine Protected Areas (MPAs) were more heavily impacted than unmanaged reefs, losing significantly greater total cover. MPA recovery was greater such that no differences were observed by 2001-2005. This study indicates that the regional patterns in coral cover distribution in the IO are driven mainly by episodic and acute environmental stress

    Appraisal of visual assessments of habitat complexity and benthic composition on coral reefs

    No full text
    Visual assessments of topographic habitat structure and benthos on coral reefs were appraised using quantitative data collected from 16 replicate surveys within each of 21 sites on Seychelles reefs. Results from visual assessments of reef benthos were similar to those obtained using techniques frequently used to assess benthic complexity and composition. Visual estimates of habitat topography were correlated with rugosity, reef height and holes of 10–70 cm diameter, whilst visual estimates of benthic composition were very similar to those obtained from line intercept transects. Visual estimates of topography correlated strongly with species richness of fish communities and explained 42% of the variation in these data. The relationship between visual estimates of topography and species richness is strongest with fish 10–30 cm total length (TL), abundance of fish within this size category also correlating positively with topographic visual assessments. Visual techniques are prone to observer bias, however with regular training they can be used to quickly provide a reliable and effective means of assessing habitat complexity and benthos on coral reefs

    Maintenance of fish diversity on disturbed coral reefs

    Get PDF
    Habitat perturbations play a major role in shaping community structure; however, the elements of disturbance-related habitat change that affect diversity are not always apparent. This study examined the effects of habitat disturbances on species richness of coral reef fish assemblages using annual surveys of habitat and 210 fish species from 10 reefs on the Great Barrier Reef (GBR). Over a period of 11 years, major disturbances, including localised outbreaks of crown-of-thorns sea star (Acanthaster planci), severe storms or coral bleaching, resulted in coral decline of 46–96% in all the 10 reefs. Despite declines in coral cover, structural complexity of the reef framework was retained on five and species richness of coral reef fishes maintained on nine of the disturbed reefs. Extensive loss of coral resulted in localised declines of highly specialised coral-dependent species, but this loss of diversity was more than compensated for by increases in the number of species that feed on the epilithic algal matrix (EAM). A unimodal relationship between areal coral cover and species richness indicated species richness was greatest at approximately 20% coral cover declining by 3–4 species (6–8% of average richness) at higher and lower coral cover. Results revealed that declines in coral cover on reefs may have limited short-term impact on the diversity of coral reef fishes, though there may be fundamental changes in the community structure of fishes
    corecore