Coral reefs in the wider Caribbean declined in hard coral cover by ~80% since the 1970s, but spatiotemporal analyses for sub-regions are lacking. Here, we explored benthic change patterns in the Mexican Caribbean reefs through meta-analysis between 1978 and 2016 including 125 coral reef sites. Findings revealed that hard coral cover decreased from ~26% in the 1970s to 16% in 2016, whereas macroalgae cover increased to ~30% in 2016. Both groups showed high spatiotemporal variability. Hard coral cover declined in total by 12% from 1978 to 2004 but increased again by 5% between 2005 and 2016 indicating some coral recovery after the 2005 mass bleaching event and hurricane impacts. In 2016, more than 80% of studied reefs were dominated by macroalgae, while only 15% were dominated by hard corals. This stands in contrast to 1978 when all reef sites surveyed were dominated by hard corals. This study is among the first within the Caribbean region that reports local recovery in coral cover in the caribbean, while other caribbean reefs have failed to recover. Most Mexican caribbean coral reefs are now no longer dominated by hard corals. in order to prevent further reef degradation, viable and reliable conservation alternatives are required. Monitoring change in coral reef ecosystems is essential in an era when humanity is having a widespread and long-term impact on nature. Current anthropogenic climate change and local stressors (such as overfishing and a mix of pollution and sedimentation from coastal development 1) place coral reefs as the most endangered ecosystems on earth 2. Rapid reversals in their health have been reported globally 3 , including reefs from the Caribbean region, where declines of the live hard coral cover of ~80% between 1975 and 2000 have been documented 4-6. In the late 1970s, entire populations of reef-building coral species (i.e. Acropora palmata and Acropora cervicornis) collapsed as a result of the white-band disease 7. Furthermore, the mass mortality of black sea urchins (Diadema antillarum), overfishing and eutrophication 8 have resulted in a proliferation of more opportunistic, fast-growing organisms such as (macro)algae that outcompete reef-building corals 8-11. As a result, many Caribbean benthic coral reef communities changed drastically from low coral cover to persistent states of high cover (macro)algae in the process of so-called phase shifts 11-15. Efforts to mitigate or reverse phase shifts and reef degradation in the Caribbean include the development of new coral reef monitoring and managing strategies 16-18. Monitoring efforts of Caribbean reefs began in the late 1970s at various reef locations for short durations 19. It was until 1980 when coral reef monitoring programs first began for some countries due to the evident reef degradation and increasing threats 19. In the Mesoamerican Reef System (MAR), the monitoring officially began in 2005 with the Healthy Reefs for Healthy People Initiative 20. The MAR is recognized by the World Wildlife Fund (WWF) as one of 200 global priority ec...
Documenting post-bleaching trajectories of coral reef communities is crucial to understand their resilience to climate change. We investigated reef community changes following the 2015/16 bleaching event at Aldabra Atoll, where direct human impact is minimal. We combined benthic data collected pre- (2014) and post-bleaching (2016–2019) at 12 sites across three locations (lagoon, 2 m depth; seaward west and east, 5 and 15 m depth) with water temperature measurements. While seaward reefs experienced relative hard coral reductions of 51–62%, lagoonal coral loss was lower (− 34%), probably due to three-fold higher daily water temperature variability there. Between 2016 and 2019, hard coral cover did not change on deep reefs which remained dominated by turf algae and Halimeda, but absolute cover on shallow reefs increased annually by 1.3% (east), 2.3% (west) and 3.0% (lagoon), reaching, respectively, 54%, 68% and 93% of the pre-bleaching cover in 2019. Full recovery at the shallow seaward locations may take at least five more years, but remains uncertain for the deeper reefs. The expected increase in frequency and severity of coral bleaching events is likely to make even rapid recovery as observed in Aldabra’s lagoon too slow to prevent long-term reef degradation, even at remote sites.
Coral recruitment and successive growth are essential for post-disturbance reef recovery. As coral recruit and juvenile abundances vary across locations and under different environmental regimes, their assessment at remote, undisturbed reefs improves our understanding of early life stage dynamics of corals. Here, we first explored changes in coral juvenile abundance across three locations (lagoon, seaward west and east) at remote Aldabra Atoll (Seychelles) between 2015 and 2019, which spanned the 2015/16 global coral bleaching event. Secondly, we measured variation in coral recruit abundance on settlement tiles from two sites (lagoon, seaward reef) during August 2018–August 2019. Juvenile abundance decreased from 14.1 ± 1.2 to 7.4 ± 0.5 colonies m-2 (mean ± SE) during 2015–2016 and increased to 22.4 ± 1.2 colonies m-2 during 2016–2019. Whilst juvenile abundance increased two- to three-fold at the lagoonal and seaward western sites during 2016–2018 (from 7.7–8.3 to 17.3–24.7 colonies m-2), increases at the seaward eastern sites occurred later (2018–2019; from 5.8–6.9 to 16.6–24.1 colonies m-2). The composition of coral recruits on settlement tiles was dominated by Pocilloporidae (64–92% of all recruits), and recruit abundance was 7- to 47-fold higher inside than outside the lagoon. Recruit abundance was highest in October–December 2018 (2164 ± 453 recruits m-2) and lowest in June–August 2019 (240 ± 98 recruits m-2). As Acroporid recruit abundance corresponded to this trend, the results suggest that broadcast spawning occurred during October–December, when water temperature increased from 26 to 29°C. This study provides the first published record on coral recruit abundance in the Seychelles Outer Islands, indicates a rapid (2–3 years) increase of juvenile corals following a bleaching event, and provides crucial baseline data for future research on reef resilience and connectivity within the region.
In frugivorous insects, the physiological state of the female (e.g. age, egg load) as well as environmental parameters like fruit availability and characteristics may affect oviposition decision, host choice and the resulting clutch size. We studied host acceptance and clutch size decision as a function of fly egg load as physiological state and mango variety and ripeness stage as the environmental parameter in two major mango pests in subSaharan Africa, Bactrocera invadens and Ceratitis cosyra, under laboratory conditions. In addiction, egg maturation dynamics were investigated because for both species, egg production had never been explored before. Female egg load was the most important factor influencing host acceptance in both species. With respect to fruit characteristics, ripeness stage was significant for oviposition decisions only in C. cosyra. In particular, ripe and fully ripe fruits had more probability of oviposition than unripe ones. In contrast, fruit variety affected clutch size in B. invadens, with, respectively, the local variety Ngowe receiving the biggest clutches and the export Kent the smallest. Moreover, the invasive species showed a significantly higher egg production compared with the native species. Implications in terms of competitive displacement between the two species are also discussed.
scite is a Brooklyn-based organization that helps researchers better discover and understand research articles through Smart Citations–citations that display the context of the citation and describe whether the article provides supporting or contrasting evidence. scite is used by students and researchers from around the world and is funded in part by the National Science Foundation and the National Institute on Drug Abuse of the National Institutes of Health.
hi@scite.ai
10624 S. Eastern Ave., Ste. A-614
Henderson, NV 89052, USA
Copyright © 2024 scite LLC. All rights reserved.
Made with 💙 for researchers
Part of the Research Solutions Family.