Resilience of coral reefs

The resilience of coral reefs is the biological ability of coral reefs to recover from natural and anthropogenic disturbances such as storms and bleaching episodes.^[1] Resilience refers to the ability of biological or social systems to overcome pressures and stresses by maintaining key functions through resisting or adapting to change.^[2] Reef resistance measures how well coral reefs tolerate changes in ocean chemistry, sea level, and sea surface temperature.^[3] Reef resistance and resilience are important factors in coral reef recovery from the effects of ocean acidification. Natural reef resilience can be used as a recovery model for coral reefs and an opportunity for management in marine protected areas (MPAs).

Thermal tolerance

Many corals rely on a symbiotic algae called zooxanthellae for nutrient uptake through photosynthesis. Corals obtain about 60-85% of their total nutrition from symbiotic zooxanthellae.^[4] Slight increases in sea surface temperature can cause zooxanthellae to die. Coral hosts become bleached when they lose their zooxanthellae. Differences in symbionts, determined by genetic groupings (clades A-H), may explain thermal tolerance in corals.^[5] Research has shown that some corals contain thermally-resistant clades of zooxanthellae. Corals housing primarily clade D symbionts, and certain types of thermally resistant clade C symbionts, allow corals to avoid bleaching as severely as others experiencing the same stressor.^[6] Scientists remain in debate if thermal resistance in corals is due to mixing or shifting of symbionts, or thermally resistant vs. thermally-sensitive types of zooxanthellae. Species of coral housing multiple types of zooxanthellae can withstand a 1-1.5 °C change in temperature.^[6] However, few species of coral are known to house multiple types of zooxanthellae. Corals are more likely to contain clade D symbionts after multiple coral bleaching events.^[6]

Reef recovery

 

Corals "seeded" with thermally-resistant zooxanthellae may become more resilient and able to resist coral bleaching

Research studies of the Mediterranean species of coral Oculina patagonica^[7] reveal that the presence of endolithic algae in coral skeletons may provide additional energy which can result in post-bleaching recovery.^[8] During bleaching, the loss of zooxanthellae decreases the amount of light absorbed by coral tissue, which allows increased amounts of photosynthetically active radiation to penetrate the coral skeleton. Greater amounts of photosynthetically active radiation in coral skeletons cause an increase in endolithic algae biomass and production of photoassimilates.^[8] During bleaching, the energy input to the coral tissue of phototrophic endoliths expand as the energy input of the zooxanthellae dwindles. This additional energy could explain the survival and rapid recovery of O. patagonica after bleaching events.^[8] A study by the Australian Research Council proposed that the loss of fast-growing coral could lead to less resilience of the remaining coral. The study was undertaken in both the Caribbean and the Indo-Pacific and reached the conclusion that the latter may be more resilient than the former based on several factors; the process of herbivory and the rates of algal blooms forming.^[9]

Coral bleaching effects on biodiversity

 

Parrot Fish

Coral bleaching is a major consequence of stress on coral reefs. Bleaching events due to distinct temperature changes, pollution, and other shifts of environmental conditions are detrimental to coral health, but corals can restore from bleaching events if the stress is not chronic.^[10] When corals are exposed to a long period of severe stress, death may occur due to the loss of zooxanthellae, which are vital to the coral's survival because of the nutrients they supply.^[11] Coral bleaching, degradation, and death have a great effect on the surrounding ecosystem and biodiversity. Coral reefs are important, diverse ecosystems that host a plethora of organisms that contribute different services to maintain reef health. For example, herbivorous reef fish, like the parrotfish, maintain levels of macro algae. The upkeep of seaweed contributes to decreasing space competition for substrate-seeking organisms, like corals, to establish and propagate, creating a stronger, more resilient reef.^[12] However, when corals become bleached, organisms often leave the coral reef habitat which in turn takes away the services that they were previously supplying. Reefs also administer many ecosystem services such as food provision for many people around the world who are dependent on fishing reefs to sustain themselves. There is evidence that some species of coral are resilient to elevated sea surface temperatures for a short period of time.^[13]

Natural disturbances

Natural forces such as disease and storms degrade corals. The frequency of coral disease caused by microbial pathogens has increased over the years, contributing to coral reef mortality.^[14] Bacterial, fungal, viral, and parasitic infections can result in physiological and morphological effects. Some of the most common coral diseases include black band disease, white pox disease, white plague, and white band disease, all of which involve tissue degradation and exposure of the coral skeleton.^[15] Diseases such as these can quickly spread among healthy coral reefs, potentially making them more susceptible to injury from disturbances like storms. Storms, including cyclones and hurricanes, can cause mechanical destruction to reefs and a change in sedimentation.^[16] The strong waves that result from these disturbances can strike corals, causing them to dislodge, and can also cause the reef to come into contact with released sediments and freshwater.

Anthropogenic disturbances

Anthropogenic forces contribute to coral reef degradation, reducing their resiliency. Some anthropogenic forces that degrade corals include pollution, sedimentation from coastal development, and ocean acidification due to increased fossil fuel emissions. Carbon emissions cause ocean surface waters to warm and acidify.^[17] The combustion of fossil fuels results in the emission of greenhouse gases, such as carbon dioxide into the atmosphere. The ocean uptakes some of the emitted carbon dioxide, injurious to the natural processes that occur in the ocean. Ocean acidification results in a lower ocean water pH, negatively affecting the formation of calcium carbonate structures which are imperative to coral development.^[18] Developing coastal areas has the potential for chemical and nutrient pollution to run off into surrounding waters. Nutrient pollution causes the overgrowth of aquatic vegetation which has the ability to out-compete corals for space, nutrients, and other resources.^[19] Overfishing can also have devastating effects on coral reefs. Due to the food security that reefs hold, they are often overfished, which can cause reef ecosystems to be unable to reconstruct after damage has been done.^[20] Restoration can be challenging due to the direct harm that fishing activities can have on coral reefs through damage caused by fishing gear, including nets, lines, and traps. Additionally, noticeable changes in marine life, such as the loss of herbivorous fish that offer valuable services to coral reefs, can reduce ecosystem function as a whole.^[21] Another anthropogenic force that degrades coral reefs is bottom trawling; a fishing practice that scrapes coral reef habitats and other bottom substrate-dwelling organisms off the ocean floor. Bottom trawling results in physical wreckage and stress that leads to corals being broken and zooxanthellae expelled. Similar to bottom trawling, rock anchoring used for fishing can cause physical damage to these fragile reefs due to the heavy weight of the anchor, cables, and chains.^[22] If coral reefs are exposed to physical damage like rock anchoring regularly, it can result in less resiliency to ocean acidification. Ecotourism is another anthropogenic factor that contributes to coral reef degradation. During ecotourism, humans can cause stress to the corals by accidentally touching, polluting, or breaking off parts of the reef, often resulting in coral bleaching as they attempt to fight off the intrusion.^[23] However, ecotourism is not only harmful when humans are close enough to touch the coral. Less direct impacts, such as harmful chemicals in sunscreen and sedimentation driven by the tourism industry, can have irreversible effects as well.^[23]

Managing coral reefs

In an attempt to prevent coral bleaching, scientists are experimenting by "seeding" corals that can host multiple types of zooxanthellae with thermally-resistant zooxanthellae.^[1] MPAs have begun to apply reef resilience management techniques in order to improve the 'immune system' of coral reefs and promote reef recovery after bleaching.^[3]

The Nature Conservancy has developed, and is continually refining, a model to help manage and promote reef resilience. Although this model does not guarantee reef resilience, it is a comprehensible management model to follow. The principles outlined in their model are:^[3]

• Representation and replication: Coral survivorship is ensured by representing and replicating resilient species and habitats in an MPA network. The presence of resilient species in management in MPAs will help protect corals from bleaching events and other natural disturbances.
• Critical areas: Conservation priority areas provide protection to critical marine areas, such as sources of larvae for coral reef regeneration or nursery habitats for fish spawning.
• Connectivity: Preserving the connectivity between coral reefs and surrounding habitats provides healthy coral communities and fish habitat.
• Effective management: Resilience based strategies are based on reducing threats to maintain healthy reefs. Measurements of effective management of MPAs allows for adaptive management.

Scientists have also developed a new technique by Smithsonian’s National Zoo and Conservation Biology Institute and funded by a conservation organization called Revive and Restore. This technique is referred to as cryopreservation and involves freezing and thawing entire fragments of coral, resulting in slowing the loss of coral species and restoring damaged reefs. Previous coral cryopreservation techniques relied on largely freezing sperm and larvae, making collection difficult, as spawning events only occur a few days a year. This previous technique was also difficult because frequent marine heatwaves and warm waters can cause corals to be biologically stressed, resulting in their reproductive material being too weak to be frozen or thawed. The new technique is easier and works more rapidly, as it allows researchers and preservations to work throughout the year, rather than waiting for a certain species to spawn and put stress on coral's reproductive materials.^[24] Scientists have also looked deeper into energy reserves and coral feeding. Feeding on zooplankton, brine shrimp, and algae may serve as a buffer for the harsh effects of climate change. Feeding corals can help them sustain tissue biomass and energy reserves and enhance nitrogen content, allowing for a higher zooxanthellae concentration and increased photosynthesis.^[25][26] Increased feeding rates can also allow certain species of bleached and recovering coral to exceed their daily metabolic energy requirements. These results suggest that coral species with a high CHAR (percent contribution of heterotrophically acquired carbon to daily animal respiration) capability may be more resilient to bleaching events, becoming the dominant species, and helping to safeguard affected reefs from extinction.^[27]

References

1. Coral reef conservation program: Addressing key threats NOAA. Retrieved 7 December 2011.
2. Holling, C.S. (1973) "Resilience and stability of ecological systems" Annual Review of Ecology and Systematics, 4: 1–23.
3. Reef resilience toolkit model: Introduction The Nature Conservancy Retrieved 7 December 2011.
4. Fujise, L., Yamashita, H., Suzuki, G., Sasaki, K., Liao, L.M., Koike, K. (2014) Moderate thermal stress causes active and immediate expulsion of photosynthetically damaged zooxanthellae (Symbiodinium) from corals PLoS ONE, 9(12): 1-18.
5. Sampayo, E.M., Ridgway, T., Bongaerts, P., Hoegh-Guldberg, O. (2008) "Bleaching susceptibility and mortality of corals are determined by fine-scale differences in symbiont type" PNAS Environmental Sciences, 105 (30): 10444–10449.
6. Berkelmans, R. and M.J.H. van Oppen (2006) "The role of zooxanthellae in the thermal tolerance of corals: a 'nugget of hope' for coral reefs in an era of climate change" Proceedings of the Royal Society of London Series B, 273: 2305–2312
7. Palomares ML, Pauly D, eds. (2011). "Oculina patagonica" in SeaLifeBase. December 2011 version.
8. Fine, Maoz, Loya, Yossi (2002) "Endolithic algae: an alternative source of photoassimilates during coral bleaching" Proceedings of the Royal Society, 269 (1497): 1205–1210.
9. Roff, George; Mumby, Peter J. (2012-07-01). "Global disparity in the resilience of coral reefs". Trends in Ecology & Evolution. 27 (7): 404–413. doi:10.1016/j.tree.2012.04.007. ISSN 0169-5347. PMID 22658876.
10. US Department of Commerce, National Oceanic and Atmospheric Administration. "What is coral bleaching?". oceanservice.noaa.gov. Retrieved 2020-08-25.
11. "Zooxanthellae and Coral Bleaching | Smithsonian Ocean". ocean.si.edu. Retrieved 2020-08-25.
12. Pratchett, Morgan S.; Hoey, Andrew S.; Wilson, Shaun K.; Messmer, Vanessa; Graham, Nicholas A. J. (September 2011). "Changes in Biodiversity and Functioning of Reef Fish Assemblages following Coral Bleaching and Coral Loss". Diversity. 3 (3): 424–452. doi:10.3390/d3030424. hdl:10754/334624.
13. Curran, Sara R.; Agardy, Tundi (June 2002). "Common Property Systems, Migration, and Coastal Ecosystems". Ambio: A Journal of the Human Environment. 31 (4): 303–305. Bibcode:2002Ambio..31..303C. doi:10.1579/0044-7447-31.4.303. ISSN 0044-7447. PMID 12174600. S2CID 24074727.
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15. Sharma, Diksha; Ravindran, Chinnarajan (2020-06-01). "Diseases and pathogens of marine invertebrate corals in Indian reefs". Journal of Invertebrate Pathology. 173: 107373. doi:10.1016/j.jip.2020.107373. ISSN 0022-2011. PMID 32272136. S2CID 215726552.
16. Harmelin-Vivien, Mireille L. (1994). "The Effects of Storms and Cyclones on Coral Reefs: A Review". Journal of Coastal Research: 211–231. ISSN 0749-0208. JSTOR 25735600.
17. Brace, Claire (2018). "Climate Change Below the Surface: The Impact of Ocean Acidification on Reef Corals". Reinvention. 11 (2): 1 – via Academic Search Complete.
18. US EPA, OW (2017-01-30). "Threats to Coral Reefs". US EPA. Retrieved 2020-08-25.
19. US Department of Commerce, National Oceanic and Atmospheric Administration. "Anthropogenic Threats to Corals - Corals: NOAA's National Ocean Service Education". oceanservice.noaa.gov. Retrieved 2020-08-25.
20. Cinner, Joshua (2014-04-01). "Coral reef livelihoods". Current Opinion in Environmental Sustainability. Environmental change issues. 7: 65–71. Bibcode:2014COES....7...65C. doi:10.1016/j.cosust.2013.11.025. ISSN 1877-3435.
21. McLean, Matthew; Cuetos-Bueno, Javier; Nedlic, Osamu; Luckymiss, Marston; Houk, Peter (2016-11-30). "Local Stressors, Resilience, and Shifting Baselines on Coral Reefs". PLOS ONE. 11 (11): e0166319. Bibcode:2016PLoSO..1166319M. doi:10.1371/journal.pone.0166319. ISSN 1932-6203. PMC 5130202. PMID 27902715.
22. Maynard, Jeffrey A.; Anthony, Kenneth R. N.; Afatta, Siham; Dahl-Tacconi, Nancy; Hoegh-Guldberg, Ove (2010-03-19). "Making a Model Meaningful to Coral Reef Managers in a Developing Nation: a Case Study of Overfishing and Rock Anchoring in Indonesia: Overfishing and Rock Anchoring in Indonesia". Conservation Biology. 24 (5): 1316–1326. doi:10.1111/j.1523-1739.2010.01487.x. PMID 20337685. S2CID 11512144.
23. Cossio, Camila (2016-04-18). "Coral Reefs and the Unintended Impact of Tourism". Earthjustice. Retrieved 2023-10-25.
24. "New Technique Could Facilitate Rapid Cryopreservation of All Coral Species". Smithsonian's National Zoo. 2023-08-23. Retrieved 2023-10-25.
25. Grottoli, Andréa G.; Martins, Paula Dalcin; Wilkins, Michael J.; Johnston, Michael D.; Warner, Mark E.; Cai, Wei-Jun; Melman, Todd F.; Hoadley, Kenneth D.; Pettay, D. Tye; Levas, Stephen; Schoepf, Verena (2018-01-16). "Coral physiology and microbiome dynamics under combined warming and ocean acidification". PLOS ONE. 13 (1): e0191156. Bibcode:2018PLoSO..1391156G. doi:10.1371/journal.pone.0191156. ISSN 1932-6203. PMC 5770069. PMID 29338021.
26. Grottoli, Andréa G. (2002-06-01). "Effect of light and brine shrimp on skeletal δ13C in the Hawaiian coral Porites compressa: a tank experiment". Geochimica et Cosmochimica Acta. 66 (11): 1955–1967. Bibcode:2002GeCoA..66.1955G. doi:10.1016/S0016-7037(01)00901-2. ISSN 0016-7037.
27. Grottoli, Andréa G.; Rodrigues, Lisa J.; Palardy, James E. (April 2006). "Heterotrophic plasticity and resilience in bleached corals". Nature. 440 (7088): 1186–1189. Bibcode:2006Natur.440.1186G. doi:10.1038/nature04565. ISSN 1476-4687. PMID 16641995. S2CID 4422247.

Further references

• Oliver, Thomas Andrew (2009) The role of coral's algal symbionts in coral reef adaptation to climate change ProQuest. ISBN 978-0-549-98995-0.

External links

• Reef resilience – coral reef conservation site of The Nature Conservancy