Abstract
Thermal-stress events have changed the structure, biodiversity, and functioning of coral reefs. But how these disturbances affect the dynamics of individual coral colonies remains unclear. By tracking the fate of 1069 individual Acropora and massive Porites coral colonies for up to 5 years, spanning three bleaching events, we reveal striking genus-level differences in their demographic response to bleaching (mortality, growth, and recruitment). Although Acropora colonies were locally extirpated, substantial local recruitment and fast growth revealed a marked capacity for apparent recovery. By contrast, almost all massive Porites colonies survived and the majority grew in area; yet no new colonies were detected over the 5 years. Our results highlight contrasting dynamics of boom-and-bust vs. protracted declines in two major coral groups. These dangerous demographics emphasise the need for caution when documenting the susceptibility and perceived resistance or recovery of corals to disturbances.
Similar content being viewed by others
Introduction
Climate change is rapidly transforming global ecosystems1,2. On coral reefs, bleaching-induced coral mortality has led to abrupt changes in their structure, biodiversity, productivity and functioning3,4,5,6,7. However, the majority of studies examining coral population dynamics have been based on coral cover or colony counts1,6,8,9,10,11. Only rarely is the fate of individual colonies considered over multiple years, especially during the critical post-bleaching ‘recovery’ period12,13,14,15. Long term evaluations of colony level changes enable the separation of immediate vs. delayed and partial vs. total colony mortality16,17. Furthermore, if considered across multiple bleaching events, colony-tracking may reveal cumulative impacts and allow the identification of genus and colony-level variation in the response to bleaching impacts.
Using an extensive spatial design of fixed photo-quadrat locations (Fig. 1), we tracked the fate of 1069 coral colonies (in 362 quadrats spread across 16 km2 on the Lizard Island reef complex) over 5 years (2016–2021), encompassing three mass bleaching events on the Great Barrier Reef (GBR). Lizard Island was at the epicenter of the first of these bleaching events on the GBR, and represents a critical arena in which to explore long-term responses of corals to bleaching1,18. We focus on colonies within two dominant coral genera, with contrasting life-histories and differences in bleaching susceptibility: massive Porites, which are slow-growing19 and resistant to bleaching20, and Acropora (all growth forms), which are fast growing but susceptible to bleaching19,21,22. Our goal was to evaluate the extent, magnitude and variability of colony-level susceptibility to successive bleaching events, as well as the potential demographic consequences and their implications for recovery.
Results and discussion
There were dramatic differences in the response to successive bleaching between the two coral types investigated (Fig. 2). Acropora colonies underwent complete local extirpation (i.e., 100% loss across all quadrats) in the 2 years following the first bleaching episode. Remarkably, however, there was also massive recruitment (i.e., the appearance of previously undetected colonies greater than 3 cm2) of Acropora starting 2 years after the first bleaching, resulting in a 1000% increase in the number of colonies relative to the start of the study (Fig. 2b). New colonies showed rapid growth, with an average 201% increase in colony size per year by the end of the study period (Fig. 3). Despite a tenfold increase in numbers and rapid growth, mean Acropora cover only increased from approximately 1% to 3%. Thus, it still remained low (< 3%) compared to historical levels of Acropora cover (from ~ 15 to 30% between 1995 and 201410, likely reflecting an early ‘recovery’ trajectory (Fig. 2a).
By contrast, the number of massive Porites colonies remained stable: there was only a 2.3% loss of colonies (2 colonies). But no new colonies were detected over the 5 years (Fig. 2). Surviving colonies showed an average increase in colony area of 21%, however, there was extensive among-colony variation in live tissue area changes (Fig. 3). Indeed, approximately half of the colonies suffered tissue loss. The extent of tissue loss was relatively well predicted by bleaching severity at the individual level (i.e., relative area of bleached tissue in the April 2016 bleaching event, Fig. 4). Thus, Acropora corals appear to be responding with a pronounced boom-and-bust pattern23,24, while massive Porites colonies exhibit a precarious degree of resilience, increasing in area but with an underlying recruitment deficit and a strong negative response in tissue area to bleaching severity (Fig. 4b).
Our findings agree with previous studies that show a high-susceptibility to thermal stress in Acropora25,26,27 and a degree of resistance to thermal stress in Porites25,28. These contrasting responses to disturbances play an important role in structuring coral communities and are now more apparent than ever given the frequency and severity of disturbances impacting coral reefs24,29. While the devastating effects of climate change on corals have been emphasized numerous times1,6,10,26,30, the fate of individual coral colonies has rarely been tracked over multiple bleaching events over multiple years, particularly in conjunction with key demographics traits such as recruitment and growth. Quantifying these dynamics is critical to understand future trajectories of coral populations subject to changing disturbance regimes, especially in a scenario of shortening ‘recovery’ windows31,32,33.
Acropora colony density at the start of the study was relatively low (85 trackable colonies, > 3 cm, across 362 quadrats (521.2 m2) in 2016). This was primarily due to two back-to-back cyclones in 2014 and 201510. Following these disturbances, the severe bleaching events in 2016 and 2017 led to complete loss of Acropora in our censused area. After this widespread mortality period, we documented a > tenfold increase in colony numbers between 2018 and 2021 (relative to the first sampling period), with 897 new colonies by 2021 (1.72 new colonies m−2). These seemingly high levels of population replenishment were observed despite large (89%) declines in coral settlement across GBR, especially in Acropora, following the bleaching events in 2016 and 201732. It was anticipated that the GBR-wide decline in settlement would have severely compromised the recovery capacity of these corals, as it was estimated that recovery would take at least a decade, even for faster-growing corals such as Acropora32. Although coral replenishment can be highly variable across spatial scales32,36, the rate of appearance of new colonies in our study, especially following such a sharp decline in coral numbers, offers some hope for the future of coral reefs.
Not only did new colonies of Acropora recruit in substantial numbers, but they also rapidly increased in size. Colonies initially detected in January 2018 had grown, on average, by 393% over 24 months. Peak detection of new colonies occurred in January 2020, and new colonies detected in 2020 and 2018 grew, on average, 211% between January 2020 and January 2021 (Fig. 3). Such fast growth is likely to underpin the perceived ‘potential recovery’ of Acropora, even as these ‘recovery’ windows between disturbances become shorter and shorter32. However, the realized long-term recovery of reef systems will depend on the capacity of these corals to persist in a scenario of increased frequency of extreme thermal events over the coming years24,37. The growth we observed resulted in a mean Acropora cover of just 3%, far below pre-bleach levels of coral cover. It may represent, therefore, just a short-term boom in a new Anthropocene configuration, where fast-growing corals persist but are unlikely to attain their former abundance due to successive disturbances and suppression of recovery dynamics6,24,38. Nevertheless, the responses we observed over five years highlight the remarkable potential for ‘boom and bust’ dynamics in Acropora, providing evidence that degraded coral reefs may still maintain some potential for apparent Acropora recovery, at least for a limited time and at the colony level.
However, our findings also highlight the need for caution. Although massive Porites shows ecosystem-level resistance to bleaching, responses of individual colonies are highly variable24,25. Indeed, individual bleaching susceptibility (indicated by the maximum proportion of colony area observed to bleach) was able to predict long-term (60 month) individual massive Porites colony tissue loss (Fig. 4a). Colonies that bleached more intensely also suffered heavier tissue loss, while those that bleached less intensely often grew in tissue area (Fig. 4b). Nevertheless, even when massive Porites colonies suffered intermediate to high bleaching (in proportion to live colony area), their likelihood of recovery was much higher than Acropora colonies as noted previously25. Most importantly, however, despite censusing 521.2 m2 of reef in extreme detail over 5 years, we did not record a single new massive Porites colony. This lack of apparent recruitment over half a decade suggests that massive Porites could be rare, a pattern supported by the examination of coral recruitment on tiles across large spatial scales post-bleaching18. However, the apparent rarity of Porites recruits could also be magnified by the difficulty of detecting Porites recruits in photos. Indeed, due to a combination of cryptic colouration, small size and slow growth, Porites recruits are likely to be harder to detect than Acropora recruits in photographs, potentially leading to an underestimation of relative recruitment in Porites32,39. Nevertheless, the scarcity of massive Porites recruitment throughout our study highlights the potential for protracted declines and storage effects40,41. Such protracted declines may be even more concerning than sudden dynamic shifts, as in Acropora abundance, as they may be easier to overlook or ignore, and harder to reverse42.
Thus, our data has revealed how the colony-level population dynamics of two archetypical coral types, massive Porites and Acropora, have responded in distinctly different manners over multiple disturbances events caused by thermal stress and a short-term ‘recovery’ window. For weedy, fast-growing Acropora colonies, high susceptibility to bleaching and complete mortality was followed by substantial recruitment and fast growth, revealing a marked capacity for apparent ‘recovery’. However, the lifespan of these new colonies is already being tested as a fourth bleaching event began to unfold in January/February 2021, with marked paling of these new Acropora colonies (Supplementary Fig. 1). We also demonstrated the well-documented resistance of stress-tolerant colonies of massive Porites, with net positive growth over five years. However, the complete lack of new colonies over this same time frame (despite intensive sampling) suggests that recruitment is rare and, potentially, unpredictable. Without replacement, increasing repetitive bleaching events30,43, may drive a slow, protracted decline of massive Porites that could be easily overlooked. These markedly different demographic patterns offer grounds for both optimism and concern. Massive Porites are resistant, but potentially compromised in the long-term, while Acropora are vulnerable, but have greater capacity to recover in the aftermath of major disturbances24,31. In both cases their dangerous demographics require caution when interpreting the susceptibility and perceived resistance of corals to disturbances.
Methods
Study area and sampling
Tracking of individual colonies was based on a comprehensive photo-quadrat census at Lizard Island, (14°40′ S, 145°28′E) in the northern region of the Great Barrier Reef (GBR), described in Wismer et al.44,45. This region experienced two prolonged thermal events between February and April 2016, as well as between January and March 2017, leading to extensive coral bleaching1,10. During the first sampling period, a total of 19 permanent transects (between 50 and 210 m in length, as constrained by reef morphology) along the reef ‘crest’ (at 0–4 m below chart-datum) were established around Lizard Island (Supplementary Fig. 2). Along each transect, between 12 and 38 quadrats (1 m2 area), approximately 5 m apart, were sampled. These transects were revisited five times: in April 2016 (2–3 months after first sampling); October 2016 (9 months after first sampling); January 2018 (after 24 months); January 2020 (after 48 months) and January/February 2021 (after 60 months).
Using SCUBA, each quadrat was photographed in each of the six sampling periods (Camera: Nikon Coolpix AW130) from a planar ‘bird's-eye’ view between 09:00 and 16:00 h. To survey each transect on subsequent trips, the starting location was identified based on a GPS mark taken on the first sampling trip. The same quadrat area was relocated during each sampling trip using a second underwater camera containing all previous images from each quadrat ordered from the start to the end of the transect (see Wismer et al.44 for a sensitivity analysis of this method). A total of 362 photo-quadrats were sampled across the entire study. Around each quadrat there was also a buffer area (Fig. 1) where individual colonies could be located and followed. We therefore tracked and quantified the fate of individual colonies within the quadrats and in the 10 cm wide buffer area around each quadrat. This resulted in a censused area of 1.44 m2 per quadrat, and a total censused area of 521.2 m2. All colonies from the two studied groups (Acropora spp. and massive Porites spp.) within the photo-quadrats and within the buffering area were recorded, identified (to species level whenever possible) and had their live tissue area determined from the photographs (please see Supplementary Fig. 3). Live tissue area of each colony was determined by tracing around the visible live coral tissue to obtain the planar area in cm2 relative to the quadrat area (10,000 cm2). All images were processed using the software ImageJ46.
Data analysis
We considered ‘growth’ to be the difference in live tissue area of each colony between the first and subsequent sampling periods. For Acropora colonies, growth was calculated from recruitment onwards (for colonies that recruited in 2018 or 2020), and was expressed as increase in live tissue are per year. Because there were no recruits detected for Porites, all colonies were present at the start of the study. Thus, growth for massive Porites colonies represents growth over 5 years. To facilitate comparisons among colonies, we standardized live tissue area using the area from the first sampling period as the reference. The same method was used when we detected ‘recruit’ colonies (i.e., new colonies of a visible size in the quadrat) in the subsequent samples.
For massive Porites colonies that bleached, we also measured the proportion of bleached planar area on each colony during the 2016 bleaching event. We tested for the hypothesis that bleaching severity had an effect on the change in live tissue area (loss or gain) for massive Porites colonies following this event. ‘Bleaching severity’ was defined as the highest proportion of tissue area observed to bleach for each coral colony across all trips in which bleaching occurred. To test this hypothesis, we used a generalized linear mixed effects model (GLMM) with tissue area change as the response variable and ‘bleaching severity’ as the predictor. We also included quadrat, nested in transect, as random intercepts in the model to account for repeated sampling and any lack of spatial independence in the data. We used a Gamma error distribution with a log link function. Because the data was slightly right skewed, we used model selection to find the best error distribution to fit the model. We compared models fitted using the Gaussian distribution, the lognormal distribution (i.e., a Gaussian distribution with a log link), and the gamma distribution (also with a log link), using Akaike’s Information Criterion. Model selection showed that the gamma distribution model was the one that best balanced fit and parsimony, and therefore was the one chosen. Model fit and assumptions were assessed using residual plots, all of which were satisfactory. Statistical modelling was performed in the software R34, using the glmmTMB package35.
References
Hughes, T. P. et al. Global warming and recurrent mass bleaching of corals. Nature 543, 373–377 (2017).
Duarte, C. M. et al. Rebuilding marine life. Nature 580, 39–51 (2020).
Darling, E. S. et al. Relationships between structural complexity, coral traits, and reef fish assemblages. Coral Reefs 36, 561–575 (2017).
McWilliam, M., Chase, T. J. & Hoogenboom, M. O. Neighbor diversity regulates the productivity of coral assemblages. Curr. Biol. 28, 3634–3639 (2018).
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, 94–97 (2015).
Hughes, T. P. et al. Global warming transforms coral reef assemblages. Nature 556, 492–496 (2018).
Cornwall, C. E. et al. Global declines in coral reef calcium carbonate production under ocean acidification and warming. Proc. Natl. Acad. Sci. 118, e2015265118 (2021).
Gardner, T. A. Long-term region-wide declines in caribbean corals. Science 301, 958–960 (2003).
De’ath, G., Fabricius, K. E., Sweatman, H. & Puotinen, M. The 27—year decline of coral cover on the Great Barrier Reef and its causes. Proc. Natl. Acad. Sci. USA https://doi.org/10.1073/pnas.1208909109 (2012).
Madin, J. S. et al. Cumulative effects of cyclones and bleaching on coral cover and species richness at Lizard Island. Mar. Ecol. Prog. Ser. 604, 263–268 (2018).
Dietzel, A., Bode, M., Connolly, S. R. & Hughes, T. P. Long-term shifts in the colony size structure of coral populations along the Great Barrier Reef: Demographic change in Australia’s corals. Proc. R. Soc. B Biol. Sci. 287, 20201432 (2020).
Claar, D. C. et al. Dynamic symbioses reveal pathways to coral survival through prolonged heatwaves. Nat. Commun. 11, 1–10 (2020).
Claar, D. C. & Baum, J. K. Timing matters: Survey timing during extended heat stress can influence perceptions of coral susceptibility to bleaching. Coral Reefs 38, 559–565 (2019).
Edmunds, P. J. Vital rates of small reef corals are associated with variation in climate. Limnol. Oceanogr. 66, 901–913 (2021).
Hall, T. E. et al. Stony coral populations are more sensitive to changes in vital rates in disturbed environments. Ecol. Appl. 31, 1–11 (2021).
Madin, J. S., Baird, A. H., Dornelas, M. & Connolly, S. R. Mechanical vulnerability explains size-dependent mortality of reef corals. Ecol. Lett. 17, 1008–1015 (2014).
Edmunds, P. J. & Riegl, B. Urgent need for coral demography in a world where corals are disappearing. Mar. Ecol. Prog. Ser. 635, 233–242 (2020).
Hughes, T. P. et al. Ecological memory modifies the cumulative impact of recurrent climate extremes. Nat. Clim. Chang. 9, 40–43 (2019).
Pratchett, M. et al. Spatial, temporal and taxonomic variation in coral growth—Implications for the structure and function of coral reef ecosystems. Oceanogr. Mar. Biol. Ann. Rev. 53, 215–295 (2015).
Cantin, N. E. & Lough, J. M. Surviving coral bleaching events: Porites growth anomalies on the great barrier reef. PLoS ONE 9, e88720 (2014).
Linares, C., Pratchett, M. S. & Coker, D. J. Recolonisation of Acropora hyacinthus following climate-induced coral bleaching on the Great Barrier Reef. Mar. Ecol. Prog. Ser. 438, 97–104 (2011).
Victor, S., Golbuu, Y., Yukihira, H. & Van Woesik, R. Acropora size-frequency distributions reflect spatially variable conditions on coral reefs of Palau. Bull. Mar. Sci. 85, 149–157 (2009).
Wilson, S. K., Robinson, J. P. W., Chong-Seng, K., Robinson, J. & Graham, N. A. J. Boom and bust of keystone structure on coral reefs. Coral Reefs 38, 625–635 (2019).
Pratchett, M. S., McWilliam, M. J. & Riegl, B. Contrasting shifts in coral assemblages with increasing disturbances. Coral Reefs 39, 783–793 (2020).
Loya, Y. et al. Coral bleaching: The winners and the losers. Ecol. Lett. 4, 122–131 (2001).
Van Woesik, R., Sakai, K., Ganase, A. & Loya, Y. Revisiting the winners and the losers a decade after coral bleaching. Mar. Ecol. Prog. Ser. 434, 67–76 (2011).
McWilliam, M., Pratchett, M. S., Hoogenboom, M. O. & Hughes, T. P. Deficits in functional trait diversity following recovery on coral reefs. Proc. R. Soc. B Biol. Sci. 287, 20192628 (2020).
Marshall, P. A. & Baird, A. H. Bleaching of corals on the Great Barrier Reef: Differential susceptibilities among taxa. Coral Reefs 19, 155–163 (2000).
Graham, N. A. J., Cinner, J. E., Norström, A. V. & Nyström, M. Coral reefs as novel ecosystems: Embracing new futures. Curr. Opin. Environ. Sustain. 7, 9–14 (2014).
Sully, S., Burkepile, D. E., Donovan, M. K., Hodgson, G. & van Woesik, R. A global analysis of coral bleaching over the past two decades. Nat. Commun. 10, 1–5 (2019).
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 340, 69–71 (2013).
Hughes, T. P. et al. Global warming impairs stock–recruitment dynamics of corals. Nature 568, 387–390 (2019).
Vercelloni, J. et al. Forecasting intensifying disturbance effects on coral reefs. Glob. Chang. Biol. 26, 2785–2797 (2020).
Team, R. C. R: A Language and Environment for Statistical Computing. (2020).
Brooks, M. E. et al. glmmTMB balances speed and flexibility among packages for zero-inflated generalized linear mixed modeling. R J. 9, 378 (2017).
Evans, R. D. et al. Early recovery dynamics of turbid coral reefs after recurring bleaching events. J. Environ. Manag. 268, 110666 (2020).
Carlot, J. et al. Juvenile corals underpin coral reef carbonate production after disturbance. Glob. Chang. Biol. 27, 2623–2632 (2021).
Bellwood, D. R. et al. Coral reef conservation in the Anthropocene: Confronting spatial mismatches and prioritizing functions. Biol. Conserv. 236, 604–615 (2019).
Baird, A., Emslie, M. & Lewis, A. Extended periods of coral recruitment on the Great Barrier Reef. In Proc. 12th Int. Coral Reef Symp. (2012).
Foster, N. L., Baums, I. B. & Mumby, P. J. Sexual vs. asexual reproduction in an ecosystem engineer: The massive coral Montastraea annularis. J. Anim. Ecol. 76, 384–391 (2007).
Edmunds, P. J. Patterns in the distribution of juvenile corals and coral reef community structure in St. John, US Virgin Islands. Mar. Ecol. Prog. Ser. 202, 113–124 (2000).
Hughes, T. P., Linares, C., Dakos, V., van de Leemput, I. A. & van Nes, E. H. Living dangerously on borrowed time during slow, unrecognized regime shifts. Trends Ecol. Evol. 28, 149–155 (2013).
Hughes, T. P. et al. Spatial and temporal patterns of mass bleaching of corals in the Anthropocene. Science 359, 80–83 (2018).
Wismer, S., Tebbett, S. B., Streit, R. P. & Bellwood, D. R. Spatial mismatch in fish and coral loss following 2016 mass coral bleaching. Sci. Total Environ. 650, 1487–1498 (2019).
Wismer, S., Tebbett, S. B., Streit, R. P. & Bellwood, D. R. Young fishes persist despite coral loss on the Great Barrier Reef. Commun. Biol. 2, 1–7 (2019).
Abràmoff, M. D., Hospitals, I., Magalhães, P. J. & Abràmoff, M. Image processing with ImageJ. Biophotonics Int. 11, 36–42 (2004).
Acknowledgements
We thank R.P. Streit, J.A Schlaefer, M. Mihalitsis, C. Bowden, C.R. Hemingson, J. Grimm, P. O’Brien, C.H.R. Goatley and the Lizard Island Research Station staff for field support; V. Huertas for photographs; and the Australian Research Council (DRB: CE140100020 and FL190100062), the International Coral Reef Society (SBT), the Ian Potter Foundation (SBT), and the Australian Museum’s Lizard Island Research Station (SBT) for financial support.
Author information
Authors and Affiliations
Contributions
J.M., D.B., R.M., and S.B.T. conceived and designed the study. J.M., D.B., and S.B.T. collected the data. R.M. and J.M. performed the analysis. J.M., D.B., R.M., S.B.T. and M.P. wrote the manuscript. All authors reviewed the manuscript.
Corresponding author
Ethics declarations
Competing interests
The authors declare no competing interests.
Additional information
Publisher's note
Springer Nature remains neutral with regard to jurisdictional claims in published maps and institutional affiliations.
Supplementary Information
Rights and permissions
Open Access This article is licensed under a Creative Commons Attribution 4.0 International License, which permits use, sharing, adaptation, distribution and reproduction in any medium or format, as long as you give appropriate credit to the original author(s) and the source, provide a link to the Creative Commons licence, and indicate if changes were made. The images or other third party material in this article are included in the article's Creative Commons licence, unless indicated otherwise in a credit line to the material. If material is not included in the article's Creative Commons licence and your intended use is not permitted by statutory regulation or exceeds the permitted use, you will need to obtain permission directly from the copyright holder. To view a copy of this licence, visit http://creativecommons.org/licenses/by/4.0/.
About this article
Cite this article
Morais, J., Morais, R.A., Tebbett, S.B. et al. Dangerous demographics in post-bleach corals reveal boom-bust versus protracted declines. Sci Rep 11, 18787 (2021). https://doi.org/10.1038/s41598-021-98239-7
Received:
Accepted:
Published:
DOI: https://doi.org/10.1038/s41598-021-98239-7
- Springer Nature Limited
This article is cited by
-
Exploring benthic habitat assessments on coral reefs: a comparison of direct field measurements versus remote sensing
Coral Reefs (2024)
-
Changing dynamics of Great Barrier Reef hard coral cover in the Anthropocene
Coral Reefs (2024)
-
Studying functions on coral reefs: past perspectives, current conundrums, and future potential
Coral Reefs (2024)
-
Size structure of the coral Stylophora pistillata across reef flat zones in the central Red Sea
Scientific Reports (2022)
-
Unprecedented erosion of Mussismilia harttii, a major reef-building species in the Southwestern Atlantic, after the 2019 bleaching event
Coral Reefs (2022)