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 development1) place coral reefs as the most endangered ecosystems on earth2. Rapid reversals in their health have been reported globally3, including reefs from the Caribbean region, where declines of the live hard coral cover of ~80% between 1975 and 2000 have been documented4,5,6. 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 disease7. Furthermore, the mass mortality of black sea urchins (Diadema antillarum), overfishing and eutrophication8 have resulted in a proliferation of more opportunistic, fast-growing organisms such as (macro)algae that outcompete reef-building corals8,9,10,11. 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 shifts11,12,13,14,15. Efforts to mitigate or reverse phase shifts and reef degradation in the Caribbean include the development of new coral reef monitoring and managing strategies16,17,18.
Monitoring efforts of Caribbean reefs began in the late 1970s at various reef locations for short durations19. It was until 1980 when coral reef monitoring programs first began for some countries due to the evident reef degradation and increasing threats19. In the Mesoamerican Reef System (MAR), the monitoring officially began in 2005 with the Healthy Reefs for Healthy People Initiative20. The MAR is recognized by the World Wildlife Fund (WWF) as one of 200 global priority ecoregions whose biodiversity protection is essential21. This ecoregion within the Caribbean spans 1600 km along the coasts of Mexico, Guatemala, Belize, and Honduras and has experienced rapid changes within the last decades22,23. In the Mexican part, in particular, in Cozumel and the northern part of Quintana Roo (Fig. 1), the 2005 bleaching event and subsequent hurricane impacts affected more than 50% of coral colonies19,24. In 2007, hurricane Dean (category 5) hit the Southern Quintana Roo reefs affecting Mahahual and Chinchorro Bank19. In the following years, i.e., 2009–2011 and 2014–2017, Mexican Caribbean (MC) coral reefs were less affected by increasing sea surface temperatures (SST)25 and hurricane impacts26. Nonetheless, the rapid increases in macroalgae and the growing local threats diminish the capacity of the coral reefs to recover11.
Reefs in the MC are threatened since the establishment of Cancun as an international tourist destination in the 1970s27. Tourism industry rapidly expanded through the region and has impacted reefs and other ecosystems through the constructions of piers to receive massive tourist cruise ships28, the clearing of vegetation to construct roads, houses, restaurants and hotels29,30, and recreational activities. Recreational activities provide the leading services for tourism industry31. However, they also pose potential threats to reef communities, e.g. breakage of corals by divers and snorkelers, trampling, taking fishes for aquaria, oil contamination due to shipping, among others32. Indeed, there are additional threats of the MC coral communities such as invading species (e.g. lionfish [Pterois volitans])33 and the recent large floating mats of Atlantic Sargassum species reaching Western Caribbean coasts34. The disintegration of these Sargassum mats not only releases nutrients and consumes oxygen, but also decreases light availability at the seafloor, thereby affecting ecosystem functions such as benthic photosynthesis35. All these threats impacted MC reefs, but their extent is still unknown.
Taken together, the current degradation of MC reefs makes it necessary to set a detailed knowledge baseline of its ecological history in a regional context, e.g. changes in coral and macroalgae cover. Even though monitoring and research efforts have been regularly conducted in the MC since the early 1980s, this only permitted to roughly understand the history of change for this region20. Despite existing efforts, a quantitative long-term spatiotemporal analysis of the condition of MC reefs is still lacking. Hard coral and macroalgae development trends are essential to understand the current status of these reefs and to identify patterns of occurred changes. In the last decade, meta-analysis has been a widely used tool applied in coral reef studies, since it allows to systematically combine a wide range of information including monitoring and experimental field exploration to provide an integrative view across time36. Here, a meta-analysis of data from monitoring programs, peer-reviewed scientific publications, and grey literature was performed to describe the large-scale and long-term changes in MC coral reefs. This study aims to answer the following questions: 1) What is the extent of hard coral and macroalgae (calcareous and fleshy) benthic cover change in the MC over the last 38 years? 2) Are there temporal and spatial patterns of change?
Hard coral and macroalgae cover between 1978 and 2016
When considering the effect of time on the cover percentage, the region-wide hard coral cover declined by more than half during the last 38 years (from ~30% in the 1970s to ~12% in 2016; p < 0.0001; Figs. 2A and 3). In contrast, macroalgae cover increased for the study region from ~17% in the late 1980s to ~25% in 2016 (p < 0.05; Fig. 2B and 3). In 2005, hard coral cover and macroalgae cover were lower compared to the previous available data point, except for hard coral cover in the Center region (Fig. 4C). Whereas macroalgae increased and/or stabilized in subsequent years, hard coral cover only showed modest signs of recovery, especially in the Cozumel and Center regions, however maintaining low coverage during the following years (Fig. 4B and 4C).
The spatial patterns of hard coral and macroalgae cover present some differences between regions (Fig. 4). Around the 2000s, macroalgae became the dominant biotic component in the North, Center, and South subregions, with a mean cover close to 30% (Fig. 4). While the hard coral cover was consistently low (<15%) for the North and South subregions; data for the Center of the MC was more sparse and was not possible to depict clear temporal trends for any of the two variables. However, for this region, macroalgae cover has been consistently and significantly higher than hard coral cover since 2010. For the Cozumel subregion, temporal trends show a decline, for both macroalgae and hard coral cover in 2006, and subsequently a slight recovery for both variables. Cozumel is the only subregion in which the cover of macroalgae and hard coral have not yet diverged; nevertheless, macroalgae cover peaked in 2014 and 2016.
Meta-analysis: temporal rates of change for the overall MC
Temporal patterns of hard coral change varied along the two analyzed periods for the overall MC, presenting trajectories of decline and recovery (Fig. 5). The mean effect size for annual rate of change (ARC) in the hard coral cover decreased over the first period (1978–2004) and was significantly negative (ARC = ~−12%, p = 0.0094, n = 35; Fig. 5A), meaning that on average there was a net loss of hard coral cover in the overall MC. Conversely, the annual rate of change in the second period (2005–2016) was 5% (p < 0.001, n = 92) for the overall MC (Fig. 5A), meaning that there was a slight recovery in hard coral cover. However, when combined, the mean effect size for ARC remained stable throughout the entire study period (ARC = ~1%, p = 0.656, n = 125; Fig. 5A). The macroalgae mean effect size for ARC presented an increase in the whole period analyzed (1989–2016) by ~11% (p < 0.0001, n = 94; Fig. 5B). See Supplementary Table S1 and S2 for all spatiotemporal statistics.
Spatiotemporal rates of change for each subregion
In the Northern region, temporal differences in the mean effect size for ARC were found only for macroalgae, while the mean effect size of ARC for hard coral cover remained stable (Fig. 5A). In the whole period analyzed (1989–2016), the mean effect size for ARC for macroalgae cover was ~6%, (p = 0.0489, n = 29; Fig. 5B). Similarly, during the last period (2005–2016), the mean effect size for ARC for macroalgae cover was also ~6% (p = 0.0365, n = 28; Fig. 5B).
Temporal differences in the hard coral cover were found only for Cozumel over 11 years (2005–2016), where the mean effect size for ARC was ~9% (p < 0.0001, n = 35; Fig. 5A). In contrast, the mean effect size for ARC during the whole study period (1989–2016) for macroalgae was positive (~12%, p < 0.0001, n = 40; Fig. 5B). Similarly, for the period of 2005–2016 the mean effect size for ARC was also positive (16%, p < 0.0001, n = 34; Fig. 5B).
For the whole period analyzed (1978–2016) in the Center region, the mean effect size for ARC on hard coral cover was negative (~−14%, p = 0.045, n = 17; Fig. 5A). Likewise, the temporal analysis from 1978–2004 revealed a negative mean effect size for ARC on hard coral cover of ~−68% (p < 0.0001, n = 4; Fig. 5A).
In the period 1989–2016, the macroalgae mean effect size for ARC presented an overall increase of ~15% (p = 0.0014, n = 13; Fig. 5B). Temporal analysis also revealed significant differences. In the period 1989–2004, the macroalgae mean effect size for ARC presented a positive increase of ~28% (p = 0.02, n = 2; Fig. 5B), whereas in 2005–2016 it increased by ~14% (p = 0.0034, n = 12; Fig. 5B).
In the Southern region, the mean effect size for ARC on hard coral cover for the first period analyzed (1978–2004) was negative (~−23%, p = 0.0082, n = 4; Fig. 5A). In contrast, the mean effect size for ARC on macroalgae cover increased over the whole period of study by ~13% (p = 0.007, n = 12; Fig. 5B). Additionally, the macroalgae mean effect size for ARC in 1989–2004 increased by ~35% (p < 0.0001, n = 2; Fig. 5B). Finally, from 2005 to 2016, the macroalgae mean effect size for ARC continued increasing by ~10% (p = 0.0506, n = 11; Fig. 5B).
Our meta-analysis of ecological changes in the Mexican Caribbean showed that, on a regional scale, hard coral cover experienced a steady rate of decline between 1978 and 2004, mainly driven by hard coral cover loss in the Center and South regions, and a slow relative increase in the second period (2005–2016), mainly driven by Cozumel (Fig. 5A). On the contrary, macroalgae cover consistently increased across time and for most of the subregions in the MC (Fig. 2B and 5B). However, different trajectories of change for both hard coral and macroalgae were found with high spatiotemporal variability (Fig. 5). It is important also to mention that regional trends in hard coral cover during the late 1970s and 1980s were of low resolution compared to the period of 2000s onwards because of the earlier lack in monitoring efforts (Fig. 3). Historically, the Northern and Cozumel regions were most exhaustively sampled over time, whereas in the Center and Southern regions, fewer monitoring surveys were performed. The Center and South regions experienced the greatest rates of hard coral cover decline and highly significant increases of macroalgae cover between 1978 and 2004. For the second period (2005–2016), the same regions did not show signs of hard coral recovery; and as in the rest of the regions, macroalgae cover continued on an increasing trend (Fig. 5B). A different trend was observed for Cozumel and the North regions. Between 1978 and 2004, only non-significant declines were observed for hard coral cover (Fig. 5A), and macroalgae cover remained relatively stable in these regions (Fig. 5B). Yet, it was not until the second period where the increase of macroalgae became more evident in the Cozumel and North regions.
Since macroalgae compete with corals for space37, macroalgae in the overall MC likely rapidly proliferated in response to declining hard coral cover. Phase shifts can occur in response to various factors, including the loss of crucial herbivores and eutrophication that enhances benthic algal biomass38. The results presented here reveal a phase shift from hard coral towards macroalgae domination in the overall MC (Fig. 3) with high and significant variability among regions and periods of analysis (Fig. 4). Certain conditions can modulate macroalgae increase, such as nutrient enrichment, especially in reefs located near highly populated areas39. Surprisingly, in the current study, the meta-analysis revealed a higher macroalgae increase in the more sparsely populated Center and Southern regions between 1989 and 2004 (Fig. 5B). Between 2001 and 2013, the Southern region has been subject to ~90% of forest cover loss due to human settlement, agriculture, and livestock farming40, which may have caused increased sediment run-off. High sediment run-off can affect corals through increasing suspended sediment and nutrient levels thus favoring macroalgae growth41.
Phase shifts from coral towards algae-dominated states have been widely reported in the Caribbean42. From 1978 to 2004, results reported here suggest that, on average, hard coral cover declined across the MC, and macroalgae increased (Fig. 5). These results correspond with what was found in other local-scale and regional studies in the Caribbean4,5,43,44. Different successive biotic and abiotic impacts in the wider Caribbean may explain these outcomes. First, the diseases of hard coral species (i.e., A. palmata and A. cervicornis)7 impacted the overall coral coverage and compromised the architectural complexity of these reefs45. Secondly, the hurricane impacts, especially in shallow reefs, changed the physical structure of the benthos, as well as the local species distribution, and habitat diversity46. However, macroalgae colonization in the MC is likely to be related to mortality events after the 1998 ENSO, resulting in mass bleaching and exacerbated by hurricane impacts, when opportunistic macroalgae began to colonize the free available space and continued increasing in MC reefs (Fig. 2). Our findings suggest that the phase shift from hard coral towards macroalgae domination in MC started around the mid-2000s (Fig. 3). First, an overall increase in macroalgae and a decrease in hard coral cover, and later, a marked phase shift from hard coral to macroalgae domination, where hard coral cover halved, and macroalgae cover increased (Fig. 2). This regional-scale phase shift corresponds with the timing reported by previous studies that have assessed recent ecological changes at a local scale in the MC47,48.
Following the 2005 bleaching event and hurricane impacts, hard coral and macroalgae cover in the overall MC initially responded with similar declines in absolute cover, while their long-term responses displayed different trajectories defined by the fast (i.e., 11 years) recovery of macroalgae during the second period of study (2005–2016; Fig. 3). Despite this increase in macroalgae cover, in the second period, hard coral cover in the overall MC exhibited a modest recovery (i.e. 5%; Fig. 5A). This increase was driven mostly by the Cozumel region as this region was the only one where the mean effect size of ARC was significantly positive (Fig. 5A). However, the average hard coral mean effect size of ARC for the Northern, Center, and Southern regions were all positive thus supporting the mean effect size for ARC for the overall MC towards a positive trend (2005-2016; Fig. 5A). Generally, it is more common to find recovery rates after mass mortality events in areas far away from anthropogenic impacts such as the Seychelles islands49 and the archipelagos in the Central Pacific Ocean50. Here, the coral settlement, calcification, and reproduction has been successful in comparison with reefs located near highly populated areas. However, current investigations in the Chagos Archipelago report that coral growth still did not recover completely from warming events, thus keeping reefs in a low coral cover state51. Likewise, in remote islands in the Central Equatorial Pacific, corals and reef fish species biomass were severely reduced after the 2015/16 bleaching event52. In the Great Barrier Reef, the coral community was recovering at a slow growth rate compared with previous bleaching events and pre-disturbance status53.
MC reefs are directly exposed to chronic stressors. However, this study is one of the first within the Caribbean region that reports recovery. In the last decades, other Caribbean coral reefs have failed to recover after bleaching events54,55. This recovery does not necessarily suggest that the assemblage has recovered or maintained its previous diversity richness. Moreover, the recovery reported here, 5% between 2005 and 2016, is still less than half of what was lost in 2005 and is slow compared with recovery rates found in reefs of the Pacific after widespread mortality49,56,57. There are three potential explanations for the unexpected recovery in MC reefs: 1) The protection due to 13 Marine Protected Areas (MPAs) in the MC may have promoted the reported recovery47,58, 2) these management actions may have helped to increase resilience of MC reefs59, and 3) the dynamic of the water circulation and currents especially in the Northern region60 may help to flush and diminish the adverse effects of land-based pollution sources61.
The Northern region of the MC had experienced more rapid rates of coastal modification since the 1970s when Cancun was conceived as an international tourist destination62. Furthermore, this region has, potentially, the highest pressure of coastal development in the MC63. Surprisingly, this region had the lowest macroalgae increase (i.e., ~6%) for the entire study period (Fig. 5B). Three reasons may explain this result: first, this region had an older history of reef degradation; the reefs were already impacted by the time the first surveys began64. Second, the MPAs actions helped to conserve those systems during the last 20 years, and coupled with rehabilitation efforts, may have helped the reefs inside of the reserves to become more resistant47. One key example is Limones reefs in Puerto Morelos National Park which is the Cancun area of influence but also has the highest coral cover (mainly A. palmata) within the Northern region65. Third, the geology and local oceanographic conditions in the Northern region favor the formations of seasonal eddies66. Recirculating eddies may damage macroalgae production because of their velocities and turbulence67. Also, eddies favor coral larval retention and recruitment patterns68.
Coral reefs in Cozumel presented ~9% hard coral cover increase from 2005 to 2016. The high hard coral cover in this area suggests a higher resilience, even though extensive unsustainable tourism activities have taken place since the late 1970s. The creation of Cozumel as a National Park in 1980 was a significant effort that may have helped to build reef resilience and to cope with local anthropogenic impacts69. The best-developed reefs in this area are located in the leeward of Cozumel coast. According to Fenner70, the reef development in Cozumel in a sheltered area permitted a better reef growth. Regardless of the good shape of Cozumel reefs, macroalgae cover remains high as in the rest of MC reefs (Fig. 4B) and exhibits an increasing trend (Fig. 5B) similar to other reefs around the globe71. This may be attributed to increasing nutrient uptake on the island due to the human population growth in the last decades72. However, water quality studies are still lacking.
The Center area in the MC encompasses one of the largest protected areas in the region: The Biosphere Reserve of Sian Ka’an, with protection on the sea and land since 1986, experiencing little local anthropogenic impacts73. Surprisingly, coral reefs in this area experienced the most drastic decrease in hard coral cover and a substantial increase of macroalgae. Nevertheless, these results should be interpreted with caution due to the small sample size. Thus, for the first period analyzed (1978–2004), the sample size is reduced to 3 time-series studies. Observational studies noted the importance of the size of protected areas and stated that protected areas itself could improve coral reef health by protecting herbivorous fish, thus reducing macroalgae74,75. However, due to management measures in MC reefs, the herbivorous fish biomass has increased in the last decade11. Therefore, the most reliable explanation for the reported reef degradation in this area may be caused by the natural water circulation carrying nutrients and pollutants stressing the corals in different ways60,76. Gondwe et al.77 suggested through geochemical and phreatic analyses that Sian Ka’an has an entirely different groundwater system compared to, i.e., the Northern region. Indeed, systems surrounding Sian Ka’an experience a higher groundwater discharge of freshwater compared to the other coasts76. Moreover, this higher influx increases nutrient concentrations in the otherwise oligotrophic coastal wetlands of Sian Ka’an78. Consequently, nearby coral reefs may now be exposed to higher nutrient enrichment, sedimentation, and turbidity, resulting in a degraded state potentially favoring macroalgae overgrowth39,79,80,81,82.
Recent studies have described the Southern part as a focal point for mass tourism development without proper selective management strategies, possibly causing a more rapid increase in the macroalgae coverage28,30. As mentioned, herbivores are an essential biotic factor in regulating macroalgae83. However, this is not the case in these reefs. Evidence suggests that in the Southern region macroalgae increase is not related to a reduction in herbivores48. This may indicate that it did not increase sufficiently to control and restrict macroalgae growth, or that macroalgae are unpalatable. It has been suggested that different fish species have specific preferences for certain types of algae84, thus impacting the benthic community differently. Besides, critical grazers such as the sea urchin, D. antillarum, continues to be rare on most reefs since its region-wide die-off in the 1980s85,86, and although the populations of herbivorous fishes have increased, its biomass is likely far below historical baselines due to the impacts of decades of overfishing and habitat degradation87. Further anthropogenic local impacts, i.e. the pier construction (2000–2006) to receive massive cruise ships, fragmented the ecosystem facilitating coral degradation and overgrow of macroalgae. The lack of adequate management in the reefs in the Southern region pose higher local pressure to the coral reefs.
The current coral reef crisis is represented not only by a shift in species composition but also in the ecosystem functions and services88. Meta-analyses benefit coral reef research due to the synthesis of a large amount of data under specific objectives of the analysis. Primary information deriving from monitoring campaigns is highly valuable. However, if this information is not integrated and analysed into the bigger picture, likely, researchers will not be able to detect and predict the consequences of the occurred changes89. Moreover, identifying the significant factors impacting the coral reef health along the MC would be helpful to determine which areas require the most protection from anthropogenic activities. Even with the high number of MPAs and the creation of the MC MPA in 2016, monitoring active management and resources are still limited20,90. Meta-analyses enable long-term coral and algae cover assessment to set the baseline for a monitoring strategy based on science-based management that ensures coral reef biodiversity not only in the MC but also in the wider Caribbean.
In summary, coral disturbance regimes continue to intensify, while recovery capacities are now also dependent on human impacts91. The potential use of this study is to set the basis aimed to understand how the reefs have changed through time and what measures should be taken to respond and counter those changes. The use of individual studies integrated into a whole long-term longitudinal research can be used as a management tool. However, standardized future monitoring methods are highly recommended for the MC to follow up on the further development of these ecosystems.
Material and Methods
Reefs in the MC occur along the coast of the state of Quintana Roo (Fig. 1) and consist of various reef formations in terms of location, type and degree of development20,92. The MC can be divided into five main regions, i.e. Northern, Center, Southern, Cozumel, and Banco Chinchorro, each with its particular characteristics and features20. The Northern region spans from Isla Contoy to Tulum (Fig. 1). The fore reef zones in this area are generally flat and gently sloped93. It includes three MPAs, namely Isla Contoy, Puerto Morelos, the Costa Occidental de Isla Mujeres, Punta Cancun & Punta Nizuc. Cozumel region is an island also located in the North in front of the coastline of the Yucatan Peninsula (Fig. 1). The Center region is part of the Sian Ka’an Biosphere Reserve (Fig. 1), one of Mexico’s largest protected areas, which is a UNESCO world heritage site. The Southern region consists of ridges with a clear zonation of reef crest, front, slope, and terrace. This area also encompasses Arrecifes de Xcalak National Park (Fig. 1). The last region is Banco Chinchorro atoll and is also located in the Southern part (Fig. 1). However, due to a lack of monitoring information, it was omitted from the analysis. The MC region has an extensive network of MPAs that by 2016, nearly all the coral reefs have a protection status with the creation of the Mexican Caribbean Biosphere Reserve20.
Data selection and extraction
The hard coral and macroalgae cover databases were collated by a wide variety of sources, including published literature, research protocols, grey literature, and monitoring programs (Supplementary Table S3 and S4). For this study, the category of macroalgae included both fleshy and calcareous macroalgae; many of the used sources did not report the type of macroalgae and combined them into one single group. Literature searches were conducted using standard search engines (e.g. ISI Web of Science and Google Scholar) using specific terms (e.g., coral reef AND hard*coral* OR coral* AND algae* OR macroalgae* AND benthic* AND Mexico* AND Mesoamerican*reef* AND Mexican*Caribbean*). All the information was curated, systemized and is now included in the Caribbean Reef Information System (CRIS), from the Biodiversity and Reef Conservation Lab, UNAM. The criteria for the potential inclusion of the study were as follows: (i) percentage cover of live hard coral and/or macroalgae; (ii) replicated measurements over time (not necessarily consecutive); (iii) if the authors use the same location of survey; (iv) the year of survey; (v) reports of the number and/or length of transects covered; and/or (vi) other variables e.g. water depth and reef zonation reported. If the studies reported monitoring and multi-temporal information, all sites defined in each study were used as a separate site. Care was taken not to double count coverage published in more than one study. If cover data were presented in graphical form, GetData94 was used to extract the percent cover. The raw monitoring information contributed a large number of sites to the dataset. The Northern region was sampled far more exhaustively than others (e.g. Center and Southern regions). Therefore, not all selected reef sites were surveyed in all years, although each reef site was visited at least two times. The monitoring database included 2,458 coral cover surveys on 125 reef sites between 1978 and 2016. Macroalgae cover was measured in 2391 surveys on 94 reef sites between 1989 and 2016. From all the included studies, 32% used the Atlantic and Gulf Rapid Reef Assessment (AGRRA) protocol to measure the benthic cover, 36% used the Synoptic Monitoring for the Mesoamerican Reef System (SAM) protocol, and 32% did not mention the use of a monitoring protocol but the use of other sampling methodologies (mainly Linear Intercept Transect). Both protocols focus on specific monitoring sites; one of the main differences is the methodology to monitor benthic organisms. SAM protocol uses point intercept methodology with 30 m length transects, whereas AGRRA protocol uses line intercept methodology with 10 m length transect95,96. The majority of data analyzed in this study was obtained during the same season of the year (May to October) following recommendations of the monitoring protocols (e.g. AGRAA, SAM).
A regression analysis was performed to test the effect of time on overall yearly means of hard coral and macroalgae cover. Meta-analysis was used to analyze the temporal change in macroalgae and hard coral cover and how that change differed in the Northern, Cozumel, Center, and Southern regions of the MC.
The mean cover for hard coral and macroalgae for each year was calculated, pulling all the regions together. Since the cover of both the hard coral and the macroalgae were not normally distributed, the data were tested using a Generalized Linear Model (GLM) with Gamma error distribution and log link function, which best fit these data.
Meta-analysis is one method of research synthesis supported by statistical procedures to merge the findings of individual primary studies (Supplementary Table S597)98. The fundamental statistical parameter is the ‘effect size’. It standardizes the outcomes of different studies99, such that initially different measures can be combined and compared. There are different effect size methods to choose, depending on the availability of the data from primary studies99,100. Meta-analysis was used to detect overall changes at different spatial and temporal scales and sub-grouped by the three regions. Percentages of hard coral and macroalgae coverage for MC reefs were extracted from all available data that met the inclusion criteria. The random-effects meta-analysis was conducted in R using the “metaphor” package98. A random-effect model was used to represent the probability that any particular effect size is the best-approximating model to detect changes in coral reefs ecosystems. The relative annual rate of change (ARC) was the effect size used to measure the change in percentage cover for both hard coral and macroalgae percentage over time. Because of the principle of compounding, the annual rate of change is calculated over a period. In this study, the ARC is implemented by comparing the percentage cover in the same reef site at two different times to finally obtain an average mean for the period of interest, and it is computed as follows:
where Start and End are the percentages hard coral cover or macroalgae at the start and end of the time series, respectively, a is the time in years elapsed between both measures87,101. Traditional meta-analysis weights within- and between-study sampling errors. However, the survey area has been found to produce more biologically realistic weightings for coral reef benthic data5.
For this reason, the weighting method for individual effect sizes was estimated by using the spatial area covered in each survey101,102. The mean effect size (MES) input for the meta-analyses are yi, which corresponds to the individual effect size per reef site and vi, which corresponds to the weighting method, defined as follows:
where rma is the function to fit the general linear models via mixed-effects in meta-analyses98.
All data points were pooled per year and averaged regardless of the method used in the surveys. The temporal heterogeneity was examined in two periods, before and after the 2005 mass bleaching event and hurricane impacts. The 2005 coral bleaching event was chosen as a cut-off point for data analyses because it was the warmest year in the Northern Hemisphere on average since reliable records in 1880103 and also because insufficient data were available for previous bleaching events in the MC (small sample size between 1978 and 2004). Reef monitoring efforts in MC increased considerably after this bleaching event. Because the individual effect sizes were log-transformed, they were back-transformed to percentages of coral/algae cover for interpretation purposes. Finally, a subset was made by grouping the surveyed sites by areas, i.e. (1) Northern, (2) Cozumel, (3) Center and (4) Southern (Fig. 1).
Previous research has established that independent effect sizes are a significant statistical premise of meta-analysis. Monitoring data are non-independent because various measures over time are conducted of the same experimental object. This non-independence is addressed in the meta-analysis by “treating each period as an individual study and the original studies as groups104.” Thus, each effect size constitutes a separate unit of information100,105. The data was ranked by the magnitude of effect size (independent of the direction) to assess the potential bias in this analysis. The largest effect size magnitude of each reef site was removed stepwise to define the number of studies that need to be removed to change the significance of the results5. If the exclusion of the largest effect size altered the significance of the results, that site was omitted from the analysis.
Several analyses were performed to determine the meta-analysis’ sensitivity. The funnel plot is the most commonly used method to visually inspect the data106. This method assumes that the results from smaller studies will mainly spread around the bottom because of more substantial random error, and the more robust studies will spread towards the top107. In ecological studies, results are inclined to be published if they show significant effects108. In this regard, the database used includes a large sample of monitoring data and grey literature, so the sample of studies is not only drawn from those studies that were already published.
All data analyses were implemented and analyzed in the R Core Team (2018) software. The map of sites (Fig. 1) was produced with the software QGIS (Development Team, 2019). The remaining graphical representations were produced using R Statistics (R Development Core Team) and Sigmaplot 12.0 (Systat software) for Windows.
Raw data of the current study are available from the corresponding authors on reasonable request.
Carilli, J. E., Norris, R. D., Black, B. A., Walsh, S. M. & McField, M. Local stressors reduce coral resilience to bleaching. Plos one 4, e6324 (2009).
Bellwood, D. R., Hughes, T. P., Folke, C. & Nyström, M. Confronting the coral reef crisis. Nature 429, 827–833 (2004).
Mercado-Molina, A. E., Ruiz-Diaz, C. P., Pérez, M. E., Rodríguez-Barreras, R. & Sabat, A. M. Demography of the threatened coral Acropora cervicornis: implications for its management and conservation. Coral Reefs 34, 1113–1124 (2015).
Gardner, T. A., Côté, I. M., Gill, J. A., Grant, A. & Watkinson, A. R. Long-term region-wide declines in Caribbean corals. Science (80-.). 301, 958–960 (2003).
Côté, I. M., Gill, J. A., Gardner, T. A. & Watkinson, A. R. Measuring coral reef decline through meta-analyses. Philos. Trans. R. Soc. B Biol. Sci. 360, 385–395 (2005).
Schutte, V. G. W., Selig, E. R. & Bruno, J. F. Regional spatio-temporal trends in Caribbean coral reef benthic communities. Mar. Ecol. Prog. Ser. 402, 115–122 (2010).
Aronson, R. B. & Precht, W. F. White-band disease and the changing face of Caribbean coral reefs. Hydrobiologia 460, 25–38 (2001).
Hughes, T. P. Catastrophes, phase shifts, and large-scale degradation of a Caribbean Coral Reef. Science (80-). 265, 1547–1551 (1994).
Aronson, R. B. & Precht, W. F. Conservation, precaution, and Caribbean reefs. Coral Reefs 25, 441–450 (2006).
Dubinsky, Z. & Stambler, N. Coral Reefs: An Ecosystem in Transition. https://doi.org/10.1007/978-94-007-0114-4 (Springer Science & Business Media, 2010).
Suchley, A., McField, M. D. & Alvarez-Filip, L. Rapidly increasing macroalgal cover not related to herbivorous fishes on Mesoamerican reefs. PeerJ 4, e2084 (2016).
McManus, J. W. & Polsenberg, J. F. Coral-algal phase shifts on coral reefs: Ecological and environmental aspects. Prog. Oceanogr. 60, 263–279 (2004).
Hughes, T. P. & Tanner, J. E. Recruitment failure, life histories, and long-term decline of Caribbean corals. Ecology 81, 2250–2263 (2000).
Aronson, R. B., Macintyre, I. G., Wapnick, C. M. & O’Neill, M. W. Phase shifts, alternative states, and the unprecedented convergence of two reef systems. Ecology 85, 1876–1891 (2004).
Roff, G. & Mumby, P. J. Global disparity in the resilience of coral reefs. Trends Ecol. Evol. 27, 404–413 (2012).
Ladd, M. C. & Collado-Vides, L. Practical applications of monitoring results to improve managing for coral reef resilience: A case study in the Mexican Caribbean. Biodivers. Conserv. 22, 1591–1608 (2013).
Flower, J. et al. Interpreting coral reef monitoring data: A guide for improved management decisions. Ecol. Indic. 72, 848–869 (2017).
Melbourne-Thomas, J. et al. A multi-scale biophysical model to inform regional management of coral reefs in the western Philippines and South China Sea. Environ. Model. Softw. 26, 66–82 (2011).
Jackson, J., Donovan, M., Cramer, K. & Lam, V. Status and trends of Caribbean coral Reefs: 1970-2012. Global Coral Reef Monitoring Network, IUCN, Gland, Switzerland (2012).
Rioja-Nieto, R. & Álvarez-Filip, L. Coral reef systems of the Mexican Caribbean: Status, recent trends and conservation. Mar. Pollut. Bull. 140, 616–625 (2019).
Olson, D. M. & Dinerstein, E. The global 200: priority ecoregions for global conservation. Ann. Missouri Bot. Gard. 89, 199–224 (2002).
Almada-Villela, P., McField, M., Kramer, P. A., Richards, P. & Arias-Gonzalez, E. Status of coral reefs of Mesoamerica – Mexico, Belize, Guatemala, Honduras, Nicaragua and El Salvador. in Status of Coral Reefs of the World: 2002 (ed. Wilkinson, C. R.) 303–324 (GCRMN Report, Australian Institute of Marine Science, 2002).
Wilkinson, C. Status of Coral Reefs of the World: 2004 (Volume 2). (Australian Institute of Marine Science, 2004).
Álvarez-Filip, L., Millet-Encalada, M. & Reyes-Bonilla, H. Impact of hurricanes Emily and Wilma on the coral community of Cozumel Island, Mexico. Bull. Mar. Sci. 84, 295–306 (2009).
NOAA. Coral Reef Watch. (2018).
NOAA. Historical Hurricane Tracks. (2019).
Padilla, N. S. The environmental effects of tourism in Cancun, Mexico. Int. J. Environ. Sci. 6, 282–294 (2015).
Martínez-Rendis, A., González, G. A., Hernández-Stefanoni, J. L. & González, J. E. A. Quantifying the reefscape transformation of a coastal Caribbean coral reef during a phase shift and the associated coastal landscape change. Mar. Ecol. 37, 697–710 (2016).
Hirales-Cota, M., Espinoza-Avalos, J., Schmock, B., Ruiz-Luna, A. & Ramos-Reyes, R. Drivers of mangrove deforestation in Mahahual-Xcalak, Quintana Roo, southeast Mexico. Ciencias Mar. 36, 147–159 (2010).
Figueroa-Zavala, B., Correa-Sandoval, J., Ruiz-Zárate, M. Á., Weissenberger, H. & González-Solís, D. Environmental and socioeconomic assessment of a poorly known coastal section in the southern Mexican Caribbean. Ocean Coast. Manag. 110, 25–37 (2015).
Reyes-Bonilla, H. & Jordán-Dahlgren, E. Caribbean Coral Reefs: Past, Present, and Insights into the Future. in Marine Animal Forests: The Ecology of Benthic Biodiversity Hotspots (eds. Bramanti, R. S., Gori, A. & Orejas, C.) 31–72 (Springer, 2017). 10.1007/978-3-319-21012-4.
Gil, M. A., Renfro, B., Figueroa-Zavala, B., Penié, I. & Dunton, K. H. Rapid tourism growth and declining coral reefs in Akumal, Mexico. Mar. Biol. 162, 2225–2233 (2015).
Schofield, P. J. Geographic extent and chronology of the invasion of non-native lionfish (Pterois volitans [Linnaeus 1758] and P. miles [Bennett 1828]) in the Western North Atlantic and Caribbean Sea. Aquat. Invasions 4, 473–479 (2009).
Putman, N. F. et al. Simulating transport pathways of pelagic Sargassum from the Equatorial Atlantic into the Caribbean Sea. Prog. Oceanogr. 165, 205–214 (2018).
Wang, M. et al. Remote sensing of Sargassum biomass, nutrients, and pigments. Geophys. Res. Lett. 45(12), 359–12,367 (2018).
Arnqvist, G. & Wooster, D. Meta-analysis: synthesizing research findings in ecology and evolution. Trends Ecol. Evol. 10, 236–240 (1995).
Bozec, Y.-M. & Mumby, P. J. Synergistic impacts of global warming on the resilience of coral reefs. Philos. Trans. R. Soc. B Biol. Sci. 370, 20130267 (2015).
Lapointe, B. E. Nutrient thresholds for bottom-up control of macroalgal blooms on coral reefs in Jamaica and southeast Florida. Limnol. Oceanogr. 42, 1119–1131 (1997).
Szmant, A. M. Nutrient enrichment on coral reefs: Is it a major cause of coral reef decline? Estuaries 25, 743–766 (2002).
Ellis, E. A., Romero Montero, J. A. & Hernández Gómez, I. U. Evaluación y mapeo de los determinantes de la deforestación en la Península Yucatán. (2015).
Roberts, M., Hanley, N., Williams, S. & Cresswell, W. Terrestrial degradation impacts on coral reef health: Evidence from the Caribbean. Ocean Coast. Manag. 149, 52–68 (2017).
Bruno, J. F., Sweatman, H., Precht, W. F., Selig, E. R. & Schutte, V. G. W. Assessing evidence of phase shifts from coral to macroalgal dominance on coral reefs. Ecology 90, 1478–1484 (2009).
Somerfield, P. J. et al. Changes in coral reef communities among the Florida Keys, 1996-2003. Coral Reefs 27, 951–965 (2008).
de Bakker, D. M. et al. 40 Years of benthic community change on the Caribbean reefs of Curaçao and Bonaire: the rise of slimy cyanobacterial mats. Coral Reefs 36, 355–367 (2017).
Alvarez-Filip, L., Gill, J. A. & Dulvy, N. K. Complex reef architecture supports more small-bodied fishes and longer food chains on Caribbean reefs. Ecosphere 2, 1–17 (2011).
Rioja-Nieto, R., Chiappa-Carrara, X. & Sheppard, C. Effects of hurricanes on the stability of reef-associated landscapes. Ciencias Mar. 38, 47–55 (2012).
Suchley, A. & Alvarez-Filip, L. Local human activities limit marine protection efficacy on Caribbean coral reefs. Conserv. Lett. 11, e12571 (2018).
Arias-González, J. E. et al. A coral-algal phase shift in Mesoamerica not driven by changes in herbivorous fish abundance. Plos one 12, e0174855 (2017).
Graham, N. A. J., Jennings, S., MacNeil, M. A., Mouillot, D. & Wilson, S. K. Predicting climate-driven regime shifts versus rebound potential in coral reefs. Nature 518, 94–100 (2015).
Smith, J. E. et al. Re-evaluating the health of coral reef communities: baselines and evidence for human impacts across the central pacific. Proc. R. Soc. B Biol. Sci. 283, 20151985 (2016).
Sheppard, C. et al. Coral bleaching and mortality in the Chagos Archipelago. Atoll Res. Bull. 1–26 https://doi.org/10.5479/si.0077-5630.613 (2017).
Brainard, R. E. et al. Ecological impacts of the 2015/16 El Niño in the central equatorial Pacific [in “Explaining Extreme Events of 2016 from a Climate Perspective”]. Bull. Am. Meteorol. Soc. 99, S21–S26 (2018).
Sato, Y. et al. Early-phase dynamics in coral recovery following cyclone disturbance on the inshore Great Barrier Reef, Australia. Coral Reefs 37, 431–443 (2018).
Huntington, B. E., Karnauskas, M. & Lirman, D. Corals fail to recover at a Caribbean marine reserve despite ten years of reserve designation. Coral Reefs 30, 1077–1085 (2011).
Neal, B. P. et al. Caribbean massive corals not recovering from repeated thermal stress events during 2005–2013. Ecol. Evol. 7, 1339–1353 (2017).
Johns, K. A., Osborne, K. O. & Logan, M. Contrasting rates of coral recovery and reassembly in coral communities on the Great Barrier Reef. Coral Reefs 33, 553–563 (2014).
Gilmour, J. P., Smith, L. D., Heyward, A. J., Baird, A. H. & Pratchett, M. S. Recovery of an isolated coral reef system following severe disturbance. Science (80-.). 340, 69–71 (2013).
Mumby, P. J. & Harborne, A. R. Marine reserves enhance the recovery of corals on Caribbean reefs. Plos one 5, e8657 (2010).
Mellin, C., Macneil, M. A., Cheal, A. J., Emslie, M. J. & Caley, M. J. Marine protected areas increase resilience among coral reef communities. Ecol. Lett. 19, 629–637 (2016).
Cetina, P., Candela, J., Sheinbaum, J., Ochoa, J. & Badan, A. Circulation along the Mexican Caribbean coast. J. Geophys. Res. Ocean. 111, C08021 (2006).
Storlazzi, C. D., Cheriton, O. M., Messina, A. M. & Biggs, T. W. Meteorologic, oceanographic, and geomorphic controls on circulation and residence time in a coral reef-lined embayment: Faga’alu Bay, American Samoa. Coral Reefs 37, 457–469 (2018).
Murray, G. Constructing paradise: The impacts of big tourism in the Mexican coastal zone. Coast. Manag. 35, 339–355 (2007).
Baker, D. M., Rodríguez-Martínez, R. E. & Fogel, M. L. Tourism’s nitrogen footprint on a Mesoamerican coral reef. Coral Reefs 32, 691–699 (2013).
Jordan-Dahlgren, E. El ecosistema arrecifal coralino del Atlántico mexicano. Rev. Soc. Mex. Hist. Nat. 44, 157–175 (1993).
Rodríguez-Martínez, R. E., Banaszak, A. T., McField, M. D., Beltrán-Torres, A. U. & Álvarez-Filip, L. Assessment of Acropora palmata in the Mesoamerican reef system. Plos one 9, e96140 (2014).
Suárez-Morales, E. & Rivera Arriaga, E. Zooplancton e hidrodinámica en zonas litorales y arrecifales de Quintana Roo, México. Hidrobiológica 8, 19–32 (1998).
Hurd, C. L. Water motion, marine macroalgal physiology, and production. J. Phycol. 36, 453–472 (2000).
Harriott, V. J. & Fisk, D. A. Recruitment patterns of scleractinian corals: A study of three reefs. Mar. Freshw. Res. 39, 409–416 (1988).
Rioja-Nieto, R. & Sheppard, C. Effects of management strategies on the landscape ecology of a Marine Protected Area. Ocean Coast. Manag. 51, 397–404 (2008).
Fenner, D. P. Some leeward reefs and corals of Cozumel, Mexico. Bull. Mar. Sci. 42, 133–144 (1988).
Mumby, P. J. Embracing a world of subtlety and nuance on coral reefs. Coral Reefs 36, 1003–1011 (2017).
INEGI. Mexico en Cifras. (2015).
Walker, R., Ponce-Taylor, D., Smith, I. & Raines, P. Sian Ka’an Coral Reef Conservation Project Mexico 2003 – Summary Report. 44, (2004).
Halpern, B. S. The impact of marine reserves: Do reserves work and does reserve size matter? Ecol. Appl. 13, 117–137 (2003).
Mumby, P. J. The impact of exploiting grazers (Scaridae) on the dynamics of Caribbean coral reefs. Ecol. Appl. 16, 747–769 (2006).
Null, K. A. et al. Composition and fluxes of submarine groundwater along the Caribbean coast of the Yucatan Peninsula. Cont. Shelf Res. 77, 38–50 (2014).
Gondwe, B. R. N. et al. Hydrogeology of the south-eastern Yucatan Peninsula: New insights from water level measurements, geochemistry, geophysics and remote sensing. J. Hydrol. 389, 1–17 (2010).
Lagomasino, D. et al. Connecting groundwater and surface water sources in groundwater dependent coastal wetlands and estuaries: Sian Ka’an Biosphere Reserve, Quintana Roo, Mexico. Estuaries and Coasts 38, 1744–1763 (2015).
Pastorok, R. & Bilyard, G. Effects of sewage pollution on coral-reef communities. Mar. Ecol. Prog. Ser. 21, 175–189 (1985).
Fabricius, K. E. Effects of terrestrial runoff on the ecology of corals and coral reefs: review and synthesis. Mar. Pollut. Bull. 50, 125–146 (2005).
Carpenter, K. E. et al. One-third of reef-building corals face elevated extinction risk from climate change and local impacts. Science (80-.). 321, 560–563 (2008).
Harborne, A. R., Rogers, A., Bozec, Y.-M. & Mumby, P. J. Multiple stressors and the functioning of coral reefs. Ann. Rev. Mar. Sci. 9, 445–468 (2017).
Holbrook, S. J., Schmitt, R. J., Adam, T. C. & Brooks, A. J. Coral reef resilience, tipping points and the strength of herbivory. Sci. Rep. 6, 35817 (2016).
Adam, T. C., Burkepile, D. E., Ruttenberg, B. I. & Paddack, M. J. Herbivory and the resilience of Caribbean coral reefs: Knowledge gaps and implications for management. Mar. Ecol. Prog. Ser. 520, 1–20 (2015).
Steneck, R. S. & Lang, J. C. Rapid assessment of Mexico’s Yucatan Reef in 1997 and 1999: pre- and post-1998 mass bleaching and hurricane Mitch (stony corals, algae and fishes). Atoll Res. Bull. 496, 294–317 (2003).
Lessios, H. A. The great Diadema antillarum die-off: 30 years later. Ann. Rev. Mar. Sci. 8, 267–283 (2016).
Paddack, M. J. et al. Recent region-wide declines in Caribbean reef fish abundance. Curr. Biol. 19, 590–595 (2009).
Woodhead, A. J., Hicks, C. C., Norström, A. V., Williams, G. J. & Graham, N. A. J. Coral reef ecosystem services in the Anthropocene. Funct. Ecol. 33, 1023–1034 (2019).
Hillebrand, H. et al. Decomposing multiple dimensions of stability in global change experiments. Ecol. Lett. 21, 21–30 (2018).
Carriquiry, J. D. et al. Conservation and sustainability of Mexican Caribbean coral reefs and the threats of a human-induced phase-shift. in Environmental Change and Sustainability 29–51 10.5772/54339 (InTech, 2013).
Birkeland, C. Coral Reefs in the Anthropocene. 10.1007/978-94-017-7249-5 (Springer, 2015).
Jordan-Dahlgren, E. & Rodriguez-Martinez, R. E. The Atlantic coral reefs of Mexico. in Latin American Coral Reefs 131–158 https://doi.org/10.1016/B978-044451388-5/50007-2 (Elsevier Science, 2003).
Rodríguez-Zaragoza, F. A. & Arias-González, J. E. Coral biodiversity and bio-construction in the northern sector of the mesoamerican reef system. Front. Mar. Sci. 2, 13 (2015).
Wiebe, D., Netterfield, C. & Kisner, T. GetData: A filesystem-based, column-oriented database format for time-ordered binary data. Astrophys. Source Code Libr.
Hill, J. & Wilkinson, C. Methods for ecological monitoring of coral reefs: A resource for managers. (Australian Institute of Marine Science, 2004).
Obura, D. Coral reef monitoring manual south-west Indian Ocean islands. Indian Ocean Comm. 68 (2014).
Moher, D. et al. Preferred reporting items for systematic reviews and meta-analyses: The PRISMA statement. Plos Med. 6, e1000097 (2009).
Viechtbauer, W. Conducting meta-analyses in R with the metafor package. J. Stat. Softw. 36, 1–48 (2010).
Cooper, H., Hedges, L. V. & Valentine, J. C. The handbook of research synthesis and meta-analysis 2nd edition. The Hand. of Res. Synthesis and Meta-Analysis, 2nd Ed. 10.7758/9781610448864 (Russell Sage Foundation, 2009).
Koricheva, J., Gurevitch, J. & Mengersen, K. Handbook of meta-analysis in ecology and evolution. Handbook of meta-analysis in ecology and evolution https://doi.org/10.23943/princeton/9780691137285.001.0001 (Princeton University Press, 2013).
Alvarez-Filip, L. et al. Drivers of region-wide declines in architectural complexity on Caribbean reefs. Coral Reefs 30, 1051–1060 (2011).
Magdaong, E. T. et al. Long-term change in coral cover and the effectiveness of marine protected areas in the Philippines: A meta-analysis. Hydrobiologia 733, 5–17 (2014).
McField, M. D. et al. Status of the Mesoamerican Reef after the 2005 coral bleaching event. in Status of Caribbean coral reefs after bleaching and hurricanes in 2005 (eds. Wilkinson, C. & Souter, D.) 45–60 (Reef and Rainforest Research Centre, 2005).
Lajeunesse, M. J. Achieving synthesis with meta-analysis by combining and comparing all available studies. Ecology 91, 2561–2564 (2010).
Mengersen, K., Schmid, C. H., Jennions, M. D., Koricheva, J. & Gurevitch, J. Statistical models and approaches to inference. in Handbook of Meta-analysis in Ecology and Evolution (eds. Koricheva, J., Gurevitch, J. & Mengersen, K.) 89–107 https://doi.org/10.1515/9781400846184-010 (Princeton University Press, 2013)..
Fragkos, K. C., Tsagris, M. & Frangos, C. C. Publication bias in meta-analysis: confidence intervals for Rosenthal’s fail-safe number. Int. Sch. Res. Not. 2014, 825383 (2014).
Sterne, J. A. C. et al. Recommendations for examining and interpreting funnel plot asymmetry in meta-analyses of randomised controlled trials. BMJ 343, d4002 (2011).
Gates, S. Review of methodology of quantitative reviews using meta-analysis in ecology. J. Anim. Ecol. 71, 547–557 (2002).
We are thankful to our colleagues Dieter Wolf-Gladrow and Carmen Villacañas, who provided statistics expertise.
The authors declare no competing interests.
Publisher’s note Springer Nature remains neutral with regard to jurisdictional claims in published maps and institutional affiliations.
About this article
Cite this article
Contreras-Silva, A.I., Tilstra, A., Migani, V. et al. A meta-analysis to assess long-term spatiotemporal changes of benthic coral and macroalgae cover in the Mexican Caribbean. Sci Rep 10, 8897 (2020). https://doi.org/10.1038/s41598-020-65801-8
This article is cited by
Stony coral tissue loss disease decimated Caribbean coral populations and reshaped reef functionality
Communications Biology (2022)
Rapid recovery of coral communities from a mass bleaching event in the summer of 2016, observed in Amitori Bay, Iriomote Island, Japan
Marine Biology (2022)
Cultivable bacteria associated with Caribbean octocorals are active against coral pathogens but exhibit variable bioactivity when grown under different temperature conditions
Coral Reefs (2022)
Increasing coral calcification in Orbicella faveolata and Pseudodiploria strigosa at Flower Garden Banks, Gulf of Mexico
Coral Reefs (2021)