After centuries of human-mediated disturbances, Caribbean reef communities are vastly different from those described in the 1950s. Many are functionally dominated by macroalgae, but this community state represents only one of several possibilities into which present-day coral reefs can transition. Octocorals have always been abundant on Caribbean reefs, but increases in their abundance over the last few decades suggest that arborescent octocorals have the potential to expand their populations on reefs that hitherto had been dominated by scleractinians. Here we show that octocoral-dominated communities at three sites on the fringing reefs of St. John, US Virgin Islands, were resilient to the effects of two Category 5 hurricanes in 2017. We describe the dynamics of octocoral communities over five years at three sites on shallow reefs (~9-m depth), and test for the effects of Hurricanes Irma and Maria. The hurricanes depressed the densities of juvenile and adult octocoral colonies as much as 47%. However, there were only weak effects on species richness and the relative abundances of the octocoral species. The hurricanes did not alter patterns of spatial variability in octocoral community structure that existed among sites prior to the storms. The density of octocoral recruits (individuals ≤ 5 cm high) was reduced in the year following the hurricanes, mainly due to a decline in abundance of recruits <0.5 cm, but returned to pre-storm densities in 2019. Persistently high octocoral recruitment provides a mechanism supporting ecological resilience of these communities. Continuing environmental degradation is a threat to all tropical marine communities, but the reefs of St. John illustrate how “octocoral forests” can persist as the structurally dominant community on Caribbean reefs.
Most present-day coral reefs greatly differ from the reefs described by ecologists in the 1950s and 1960s1,2,3,4, and are strikingly different from those encountered by European explorers in the 15th Century5. These changes have been attributed to a diversity of natural and anthropogenic disturbances6, but the emergence of climate change and ocean acidification7 has created the possibility that reefs dominated by scleractinian corals might cease to exist within decades8. Over the last four decades, Caribbean coral reefs have undergone marked declines in the abundance of scleractinian corals9,10,11. These losses typically have been recorded as stepwise incremental reductions in cover attributed to pulse disturbances caused by hurricanes9 and bleaching12,13, that overlie the chronic effects of press disturbances such as diseases14, depressed rates of growth15, and reduced recruitment16.
The declining abundances of scleractinians have generally been characterized as a trade-off in both the abundance and functional importance of scleractinians and macroalgae17,18,19. However, it has also become apparent that other sessile benthic invertebrates have increased in abundance20, and at some sites, where quantitative data are available, octocorals have increased as scleractinians have declined21,22,23,24. Octocorals have always been abundant on Caribbean reefs25,26, but unlike scleractinians, which have undergone marked declines in abundance, octocorals have increased in abundance on shallow reefs (i.e., <30 m depth) at sites ranging from the oceanic, southwest Caribbean24, to the U.S. Virgin Islands22, and the Florida Keys23. The temporal scope of these studies have spanned historic bleaching events and hurricanes, suggesting octocoral communities may be resistant and/or resilient to disturbances that have had strong negative effects on scleractinians. In this study we report on the resistance and resilience of octocorals on three reefs on the south shore of St. John, U.S. Virgin Islands (Fig. 1), following the passage of Hurricanes Irma and Maria in September 2017.
The frequency and severity of coral bleaching events has increased in the last few decades4,13,27,28,29, but prior to the first global scale mass bleaching in 198330, hurricanes were regarded as the major disturbance affecting reefs. The effects of hurricanes on coral reefs have been reported in the scientific literature since the early 20th century31,32,33 and the geologic record reveals that they have been important agents of disturbance on coral reefs for at least 125ky34. The presence of tropical reefs from the Pleistocene on which the scleractinian fauna mirrors the taxonomic composition of 20th century reefs35,36 is testimony to the historic ability of coral reefs to recover from disturbance. In more recent decades, however, populations of scleractinians on Caribbean reefs have not recovered from major hurricanes9. Debate has continued as to whether present day coral reef communities, especially those dominated by macroalgae, represent readily reversed phase transitions or alternative stable states17,37,38,39,40, and even the generality of the observation and the meaning of “dominance”, have been challenged18. However, the extent to which the shift in dominance from scleractinians to other taxa is representative of a stable change has not been discussed. An important determinant of the future of reef communities dominated by taxa other than scleractinians is their stability38 and resilience following disturbance.
The shallow reefs on the south shore of St. John, U.S. Virgin Islands, have recently undergone a shift in benthic community structure that favors octocorals21,22,41,42,43,44. The decline in abundance of scleractinians has been recorded in detail45,46,47. Although octocorals have been less thoroughly studied, octocorals also are known to be negatively affected by hurricanes22,48 and bleaching49, but the available evidence suggests their populations can recover in only a few years22. Tsounis and Edmunds21 hypothesized that, unlike scleractinians, the shift in abundances of octocorals has been driven by the resilience of octocorals to major disturbances. In September 2017 Hurricane Irma passed over St. John, U.S. Virgin Islands, as category 5 hurricane followed two weeks later by Hurricane Maria, also a category 5 storm which passed south of St. John; together, these storms are unprecedented within human memory for the region. The waves, heavy rainfall, and resultant terrestrial runoff associated with these storms provided an opportunity to assess the effects of the hurricanes on the emerging octocoral-dominated communities we have been studying for six years. If present-day octocoral-dominated communities in the Caribbean are resistant and resilient to disturbance, then the trend towards community dominance by octocorals may create a “new normal” for shallow reefs in the region: a persistent transition from scleractinian reefs to octocoral forests (sensu Rossi et al.50).
Starting in 2014, we conducted annual surveys of octocoral abundance at three sites on the south shore of St. John, U.S. Virgin Islands. Those surveys have continued through 2019 and include an additional survey in November 2017, two months after Hurricanes Irma and Maria. Surveys differentiated between recruits (1 polyp to colonies 5 cm tall), and all colonies >5 cm tall that included juveniles (i.e., colonies that are not sexually mature), and adult colonies (i.e., colonies that are sexually mature). In 2014, the abundances and richness of juvenile and adult colonies differed among sites, with 30 taxa and 15.9 ± 0.5 colonies m−2 in East Cabritte, 31 taxa and 7.6 ± 0.2 colonies m−2 in Europa Bay, and 20 taxa and 3.4 ± 0.2 colonies m−2 in Tektite (mean ± SE). The mean densities at any one site differed 1–11% between any pair of years between 2014 and July 2017, and did not significantly differ among times at any site prior to the hurricanes (Fig. 2, Supplementary Information Table 1). Hurricanes Irma and Maria struck St. John in September 2017, causing reductions of 23–47% in mean octocoral densities (pooled among taxa) of juvenile and adult colonies at all sites, with the largest effect at Tektite. Abundances in November 2017 and July 2018 were the lowest observed at each site and comparisons of estimated marginal means for each site and census show that abundances in the November 2017 and/or 2018 were lower than all other censuses at each site (Supplementary Information Table 1). Post-hoc comparisons of abundances in each year showed that the November 2017 densities were lower than densities recorded in all other censuses (Supplementary Information Table 1). The decline in abundance that was associated with the hurricanes affected colonies across the entire range of colony heights. Size frequency distributions of octocorals differed among sites. However, the size frequency distributions did not significantly differ before and after the hurricanes (Supplementary Information Fig. 1), indicating that effects on structural complexity created by different size colonies and biomass (which is related to colony size) paralleled the changes in colony abundances.
Multivariate analysis of community structure based on juvenile and adult colonies identified large differences among sites and much smaller differences associated with the hurricanes (Fig. 3). Prior to the hurricanes, the octocoral communities at each site were 77–89% similar in sequential years (based on Bray-Curtis dissimilarities), while similarities among pairs of the three sites varied from 42% (in November 2017, Tektite vs East Cabritte) to 68% (Europa Bay vs East Cabritte in August 2018). The hurricanes had small but significant effects on the community structure of each site (SIMPROF, P-perm ≤ 0.05). However, differences among sites remained consistent following the hurricanes, and Bray-Curtis dissimilarities of the communities before and after the hurricanes indicate they were 75 to 84% similar. Octocoral species richness in the two post-hurricane surveys (November 2017 and August 2018) was similar to that recorded in all surveys before the hurricanes (East Cabritte, 36 vs 33 taxa; Europa Bay, 34 vs 31; and Tektite, 25 vs 24). Species that were not found after the hurricanes had been uncommon and had not regularly been recorded in the earlier surveys (Supplementary Information Table 2).
Densities of octocoral recruits at the three sites on St. John were quite variable during the 3 years prior to Hurricanes Irma and Maria, ranging from 6.1 (±0.9 SE) to 9.32 (±1.3) recruits 0.25 m−2 at East Cabritte, 2.8 (±0.4) to 3.3 (±0.5) at Europa and 1.0 (±0.1) to 1.6 (±0.2) at Tektite (Fig. 4). Numbers of recruits found in any single quadrat ranged from 0 to 41 with a median of 2 recruits and a mode of 0. The hurricanes had the greatest effect on recruit densities at East Cabritte. Recruit densities at East Cabritte were lower in November 2017 than in all other censuses, (Fig. 4, Supplementary Information Tables 3 and 4). Recruitment in 2018, the following summer, was still lower than 2017 prior to the hurricanes, but not significantly different from 2015 or 2016. Recruitment in 2019 was greater than in 2018 but not significantly greater than in 2017. Examination of recruit size frequency distributions (Supplementary Information Fig. 2) indicate that most of the decline and recovery in recruitment following the hurricanes can be attributed to changes in number of ≤1 cm recruits. Recruit densities at Europa followed a somewhat similar pattern to that observed at East Cabritte. The lowest number of recruits were observed in November 2017 (2.4 ± 0.3) and the greatest in 2019 (4.5 ± 0.5). However, both the recruit densities and the magnitude of the differences in recruitment between years were lower than at East Cabritte. The only significant pairwise differences among the Europa recruit censuses were the comparisons of 2019 with 2015, 2018 and November 2017 (Supplementary Information Table 4). Recruitment at Tektite was the lowest of the three sites and there was no significant difference among the censuses (Supplementary Information Table 4).
Understanding the stability of octocoral communities relative to disturbance is a critical component in assessing whether octocoral “animal forests” are the stable successor to the scleractinian dominated communities that preceded them. Although monitoring that also follows octocoral abundances is relatively rare, increased abundances of octocorals have now been documented on shallow reefs in the Caribbean such as the Florida Keys23, Virgin Islands21,22 and the southwest Caribbean24. Disturbance events and whether octocoral communities are affected (i.e. resistance) and/or whether they can rebound from the disturbance (i.e., resilience51) provide opportunities to assess the longer term stability of the octocoral forests. The octocoral communities that we studied on St. John suffered dramatic declines in abundances in association with the passage of Hurricanes Irma and Maria, and in that sense, were not resistant to the effects of severe storms. However, they showed resistance in species composition as the effects on the relative abundances of octocoral species were small (Fig. 3), and the differences between species composition before and after Hurricanes Irma and Maria were much smaller than the differences between the three sites.
Octocoral recruitment following the hurricanes facilitates the resilience of the octocoral community. The number of recruits found in the November 2017 census at East Cabritte was 82% of the number found in 2017 and 64% of the average of the preceding 3 years. However, much of that decline was among the smallest (≤1 cm) recruits (Supplementary Information Fig. 2) and that drop may reflect the high mortality that naturally occurs among recruits52,53 that would have settled in the summer. The more meaningful comparison is between pre-hurricane recruit abundances with the numbers of recruits observed in 2018 and 2019. In July 2018, recruit densities were lower than in 2016 and 2017 by 21% and 47%, respectively. That change was driven by a decline in the density of the smallest size class recruits (<0.5 cm) which declined by 77% in 2018 (Supplementary Information Fig. 2). In 2019, densities of recruits <0.5 cm recovered to levels similar to the years previous to the hurricanes with 1.82 ± 0.37 (mean ± SE) recruits 0.25 m−2.
The drop in abundance of the smallest size class following the hurricanes could have occurred through a variety of mechanisms. There may have been a reduced supply of larvae, perhaps due to lower fecundity following the hurricanes. Such effects are known from bleaching in scleractinians54,55. Whether stress from hurricanes might cause similar effects is not known, but the allocation of resources to repair colony damage should affect resources available for reproduction56. Alternatively, the hurricanes may have altered the substratum making it less suitable for successful settlement. Grazing and browsing affect recruit survival52,53 and changes in the abundance of predators or in the ratio of predator abundance and prey could have depressed the abundance of recruits following the hurricanes. Indirect effects such as the reduction of predators of the taxa that feed on octocorals57 could also account for the lack of the smallest recruits in 2018. Any explanation must also account for the differences in responses at the three reefs. Regardless of the causation of the reduced numbers of recruits in 2018, the return to pre-hurricane recruitment will, barring other disturbances, regenerate the populations over time. The rapid recovery of recruitment rates following the hurricanes plays a critical role in supporting the resilience of the octocoral community. Reduced adult densities might also stimulate growth of all colonies through a reduction in resource competition58 and reduced interference created by abrasion of colonies against each other59.
Under the environmental and biotic conditions prevailing on present-day shallow Caribbean reefs, octocoral communities have exhibited resilience and some resistance51,60 to major disturbances including hurricanes (present data), bleaching61, eutrophication24, diseases62 and early signs of the effects of ocean acidification on seawater pH63,64. At high population densities, Caribbean octocorals form underwater forests50 that alter environmental conditions, such as light, currents, and sedimentation, beneath their canopy, and create habitat utilized by many species50,65,66. Octocoral forests, unlike scleractinians, do not build hard, wave resistant structures, but they provide some of the ecosystem services formerly supported by scleractinians (e.g., providing fish habitat67, acting as a carbon sink68 and generating sediments69). In the present environmental conditions, octocoral-dominated communities may constitute the “new normal” for shallow Caribbean reefs. However, it is important to recognize that the resilience that these communities currently exhibit may decline with future intensification of hurricanes, bleaching events, and other disturbances, making the current communities a temporary state in a longer term sequence that has been described as a “slope to slime”8.
Materials and methods
Juvenile and adult surveys of octocorals in St. John have been previously described42. The three sites, East Cabritte (18° 18.360′N, 64° 43.140′W), Europa Bay (18° 19.016′N, 64° 43.798′W) and Tektite (18° 18.796′N, 64 43.356′W) are located on the southern shore of St. John, within the Virgin Islands National Park. All three sites are fringing reefs. Quantitative assessments of the environments at East Cabritte and Europa have previously been discussed42. The substratum at East Cabritte is a mix of igneous boulders and scleractinian-generated carbonate mounds. The reefs at Europa and Tektite are all carbonate with a mix of carbonate rock (living and mostly dead coral heads) and sand patches. East Cabritte is more exposed to wave action, which dominantly comes out of the east and southeast, than Europa42. Those differences affect light levels and sedimentation with East Cabritte having lower rates of sedimentation than Europa. Tektite is the most protected of the three sites, but there was extensive evidence of mobilization of loose rubble at the site during the hurricanes.
Censuses of juvenile and adult colonies were conducted annually in the summers of 2014 through 2018. Those data were supplemented with additional surveys in November 2017, two months after Hurricanes Irma and Maria. At each site, abundances of juveniles and adult octocorals were monitored along 6 permanently marked 10-m long transects, spaced at 10 m intervals. Transects were oriented perpendicular to the shore, and ranged in depth from 5.6 to 9 m. During each juvenile and adult census, 1 m2 positions along the transects were randomly chosen, each on a randomly selected side of the transect. Ten quadrats were censused on each transect at Europa and Tektite. At East Cabritte, where octocoral densities were high, 6 quadrats per transect were sampled during the 2015–2017 censuses. Rarefaction analysis indicates the sample sizes were suitable for assessing species richness42. The identity and height of all arborescent octocoral colonies that were ≥5-cm tall were recorded. Erythropodium caribeorum and encrusting Briareum asbestinum were not included in the surveys. Eunicea laxispica, E. mammosa and E. succinea could not be unambiguously distinguished in the field and those counts were pooled into a single operational taxon, as were Pseudoplexaura flexuosa and P. wagenaari. Recruit censuses were conducted in July from 2015 to 2019. Recruits (1 polyp – 5 cm tall) were enumerated, and when possible were identified to genus in separate 0.25 m2 quadrats randomly placed (n = 8) along each transect at each site (48 quadrats per site). Multivariate analyses were conducted with Primer version 670. Using quadrats as replicates, recruit density and adult/juvenile density data were analyzed using the Generalized Linear Methods function in SPSS (v 26).
Goreau, T. F. The ecology of Jamaican coral reefs I. Species composition and zonation. Ecol. 40, 67–89 (1959).
Storr, J. F. Ecology and Oceanography of the Coral Reef Tract, Abaco Is., Bahamas. Geol. Soc. Amer. Sp. Paper, 79 (1964).
Stoddart, D. R. Ecology and morphology of recent coral reefs. Biol. Rev. 44, 433–498 (1969).
Oliver, J. K., Berkelmans, R. & Eakin, C. M. In Coral Bleaching (eds. van Oppen M. & Lough J.) 27–49 (Springer, 2018).
Jackson, J. B. C. Reefs since Columbus. Coral Reefs 16, S23–S32 (1997).
Hughes, T. P. et al. Coral reefs in the Anthropocene. Nat. 546, 82–90, https://doi.org/10.1038/nature22901 (2017).
Hoegh-Guldberg, O. et al. Coral reefs under rapid climate change and ocean acidification. Sci. 318, 1737–1742, https://doi.org/10.1126/science.1152509 (2007).
Pandolfi, J. M. et al. Ecology - Are US coral reefs on the slippery slope to slime? Sci. 307, 1725–1726, https://doi.org/10.1126/science.1104258 (2005).
Gardner, T. A., Cote, I. M., Gill, J. A., Grant, A. & Watkinson, A. R. Hurricanes and Caribbean coral reefs: Impacts, recovery patterns, and role in long-term decline. Ecol. 86, 174–184 (2005).
Gardner, T. A., Cote, I. M., Gill, J. A., Grant, A. & Watkinson, A. R. Long-term region-wide declines in Caribbean corals. Sci. 301, 958–960, https://doi.org/10.1126/science.1086050 (2003).
Jackson, J., Donovan, M., Cramer, K. & Lam, V. Status and trends of Caribbean coral reefs: 1970-2012. 306 (Washington, D.C., 2014).
Glynn, P. W. Coral-Reef Bleaching - Ecological Perspectives. Coral Reefs 12, 1–17 (1993).
Hoegh-Guldberg, O. Climate change, coral bleaching and the future of the world’s coral reefs. Mar. Freshw. Res. 50, 839–866, https://doi.org/10.1071/mf99078 (1999).
Weil, E., Smith, G. & Gil-Agudelo, D. L. Status and progress in coral reef disease research. Dis. Aquat. Org. 69, 1–7, https://doi.org/10.3354/dao069001 (2006).
Edmunds, P. J. & Elahi, R. The demographics of a 15-year decline in cover of the Caribbean reef coral Montastraea annularis. Ecol. Monogr. 77, 3–18 (2007).
Price, N. N. et al. Global biogeography of coral recruitment: tropical decline and subtropical increase. Mar. Ecol. Prog. Ser. 621, 1–17, https://doi.org/10.3354/meps12980 (2019).
Hughes, T. P. Catastrophes, phase shifts, and large-scale degradation of a Caribbean coral reef. Sci. 265, 1547–1551 (1994).
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. Ecol. 90, 1478–1484, https://doi.org/10.1890/08-1781.1 (2009).
Roff, G. & Mumby, P. J. Global disparity in the resilience of coral reefs. Trends in Ecology &. Evolution 27, 404–413, https://doi.org/10.1016/j.tree.2012.04.007 (2012).
Norstrom, A. V., Nystrom, M., Lokrantz, J. & Folke, C. Alternative states on coral reefs: beyond coral-macroalgal phase shifts. Mar. Ecol. Prog. Ser. 376, 295–306, https://doi.org/10.3354/meps07815 (2009).
Tsounis, G. & Edmunds, P. J. Three decades of coral reef community dynamics in St. John, USVI: a contrast of scleractinians and octocorals. Ecosphere 8, https://doi.org/10.1002/ecs2.1646 (2017).
Lenz, E. A., Bramanti, L., Lasker, H. & Edmunds, P. J. Long-term variation of octocoral populations in St. John, US Virgin Islands. Coral Reefs 34, 1–11, https://doi.org/10.1007/s00338-015-1315-x (2015).
Ruzicka, R. R. et al. Temporal changes in benthic assemblages on Florida Keys reefs 11 years after the 1997/1998 El Nino. Mar. Ecol. Prog. Ser. 489, 125–141, https://doi.org/10.3354/meps10427 (2013).
Sanchez, J. A. et al. Steady Decline of Corals and Other Benthic Organisms in the SeaFlower Biosphere Reserve (Southwestern Caribbean). Frontiers in Marine Science 6, https://doi.org/10.3389/fmars.2019.00073 (2019).
Kinzie, R. A. I. The zonation of West Indian gorgonians. Bull. Mar. Sci. 23, 93–155 (1973).
Cary, L. R. Observations Upon the Growth and Ecology of Gorgonians. Carnegie Inst. Wash. Pop. Tortugas Lab, publ.182 5, 81–90 (1914).
Donner, S. D., Skirving, W. J., Little, C. M., Oppenheimer, M. & Hoegh-Guldberg, O. Global assessment of coral bleaching and required rates of adaptation under climate change. Glob. Change Biol. 11, 2251–2265 (2005).
Hughes, T. P. et al. Spatial and temporal patterns of mass bleaching of corals in the Anthropocene. Sci. 359, 80–+, https://doi.org/10.1126/science.aan8048 (2018).
Hughes, T. P. et al. Global warming and recurrent mass bleaching of corals. Nat. 543, 373–+, https://doi.org/10.1038/nature21707 (2017).
Glynn, P. W. Widespread Coral Mortality And The 1982-83 El Nino Warming Event. Environ. Conserv. 11, 133–146 (1984).
Stoddart, D. R. Catastrophic storm effects on British Honduras reefs and cays. Nat. 196, 512–515, https://doi.org/10.1038/196512a0 (1962).
Hedley, C. The natural destruction of a coral reef. Rep. Gt. Barrier Reef. Comm. 1, 25–40 (1925).
Blumenstock, D. I. Typhoon effects at Jaluit Atoll in the Marshall Islands. Nat. 182, 1267–1269 (1958).
Vernhet, E., Conesa, G. & Bruna, P. O. Reworking processes and deposits in coral reefs during (very) high-energy events: Example from a Pleistocene coral formation (125 ka), La Desirade Island, Lesser Antilles. Palaeogeography Palaeoclimatology Palaeoecology 490, 293–304, https://doi.org/10.1016/j.palaeo.2017.11.008 (2018).
Pandolfi, J. M. Limited membership in Pleistocene reef coral assemblages from the Huon Peninsula, Papua New Guinea: Constancy during global change. Paleobiology 22, 152–176 (1996).
Pandolfi, J. M. & Jackson, J. B. C. Community structure of Pleistocene coral reefs of Curacao, Netherlands Antilles. Ecol. Monogr. 71, 49–67 (2001).
Schmitt, R. J., Holbrook, S. J., Davis, S. L., Brooks, A. J. & Adam, T. C. Experimental support for alternative attractors on coral reefs. Proc. Natl Acad. Sci. U S Am. 116, 4372–4381, https://doi.org/10.1073/pnas.1812412116 (2019).
Dudgeon, S. R., Aronson, R. B., Bruno, J. F. & Precht, W. F. Phase shifts and stable states on coral reefs. Mar. Ecol. Prog. Ser. 413, 201–216, https://doi.org/10.3354/meps08751 (2010).
Mumby, P. J. Phase shifts and the stability of macroalgal communities on Caribbean coral reefs. Coral Reefs 28, 761–773, https://doi.org/10.1007/s00338-009-0506-8 (2009).
Mumby, P. J., Steneck, R. S. & Hastings, A. Evidence for and against the existence of alternate attractors on coral reefs. Oikos 122, 481–491, https://doi.org/10.1111/j.1600-0706.2012.00262.x (2013).
Edmunds, P. J. & Lasker, H. R. Regulation of population size of arborescent octocorals on shallow Caribbean reefs. Mar. Ecol. Prog. Ser. 615, 1–14, https://doi.org/10.3354/meps12907 (2019).
Tsounis, G., Edmunds, P. J., Bramanti, L., Gambrel, B. & Lasker, H. R. Variability of size structure and species composition in Caribbean octocoral communities under contrasting environmental conditions. Mar. Biol. 165, 1–14, https://doi.org/10.1007/s00227-018-3286-2 (2018).
Edmunds, P. J., Tsounis, G. & Lasker, H. R. Differential distribution of octocorals and scleractinians around St. John and St. Thomas, US Virgin Islands. Hydrobiologia 767, 347–360, https://doi.org/10.1007/s10750-015-2555-z (2016).
Edmunds, P. J. & Lasker, H. R. Cryptic regime shift in benthic community structure on shallow reefs in St. John, US Virgin Islands. Mar. Ecol. Prog. Ser. 559, 1–12, https://doi.org/10.3354/meps11900 (2016).
Miller, M. W. et al. Alternate benthic assemblages on reef restoration structures and cascading effects on coral settlement. Mar. Ecology-Progress Ser. 387, 147–156, https://doi.org/10.3354/meps08097 (2009).
Edmunds, P. J. Three decades of degradation lead to diminished impacts of severe hurricanes on Caribbean reefs. Ecology 100, https://doi.org/10.1002/ecy.2587 (2019).
Edmunds, P. J. Decadal-scale changes in the community structure of coral reefs of St. John, US Virgin Islands. Mar. Ecol. Prog. Ser. 489, 107–117, https://doi.org/10.3354/meps10424 (2013).
Woodley, J. D. et al. Hurricane Allens Impact on Jamaican Coral Reefs. Sci. 214, 749–755, https://doi.org/10.1126/science.214.4522.749 (1981).
Prada, C., Weil, E. & Yoshioka, P. M. Octocoral bleaching during unusual thermal stress. Coral Reefs 29, 41–45, https://doi.org/10.1007/s00338-009-0547-z (2010).
Rossi, S., Bramanti, L., Gori, A. & Orejas, C. In Marine Animal Forests (ed. Rossi, S.) 1–26 (Springer International Publishing, 2017).
Holling, C. S. Resilience and stability of ecological systems. Annu. Rev. Ecol. Syst. 4, 1–23, https://doi.org/10.1146/annurev.es.04.110173.000245 (1973).
Lasker, H. R., Kim, K. & Coffroth, M. A. Production, settlement, and survival of plexaurid gorgonian recruits. Mar. Ecology-Progress Ser. 162, 111–123 (1998).
Evans, M. J., Coffroth, M. A. & Lasker, H. R. Effects of predator exclusion on recruit survivorship in an octocoral (Briareum asbestinum) and a scleractinian coral (Porites astreoides). Coral Reefs 32, 597–601, https://doi.org/10.1007/s00338-012-1001-1 (2013).
Baird, A. H. & Marshall, P. A. Mortality, growth and reproduction in scleractinian corals following bleaching on the Great Barrier Reef. Mar. Ecology-Progress Ser. 237, 133–141 (2002).
Levitan, D. R., Boudreau, W., Jara, J. & Knowlton, N. Long-term reduced spawning in Orbicella coral species due to temperature stress. Mar. Ecol. Prog. Ser. 515, 1–10, https://doi.org/10.3354/meps11063 (2014).
Tsounis, G. et al. Anthropogenic effects on reproductive effort and allocation of energy reserves in the Mediterranean octocoral Paramuricea clavata. Mar. Ecol. Prog. Ser. 449, 161–U193, https://doi.org/10.3354/meps09521 (2012).
Burkepile, D. E. & Hay, M. E. Predator release of the gastropod Cyphoma gibbosum increases predation on gorgonian corals. Oecologia 154, 167–173, https://doi.org/10.1007/s00442-007-0801-4 (2007).
Kim, K. & Lasker, H. R. Flow-mediated resource competition in the suspension feeding gorgonian Plexaura homomalla (Esper). J. Exp. Mar. Biol. Ecol. 215, 49–64 (1997).
Gambrel, B. & Lasker, H. R. Interactions in the canopy among Caribbean reef octocorals. Mar. Ecol. Prog. Ser. 546, 85–95, https://doi.org/10.3354/meps11670 (2016).
Connell, J. H. & Sousa, W. P. On The Evidence Needed To Judge Ecological Stability Or Persistence. Am. Naturalist 121, 789–824 (1983).
McWilliams, J. P., Cote, I. M., Gill, J. A., Sutherland, W. J. & Watkinson, A. R. Accelerating impacts of temperature-induced coral bleaching in the Caribbean. Ecol. 86, 2055–2060 (2005).
Weil, E. & Rogers, C. S. In Coral Reefs: An Ecosystem in Transition (eds. Dubinsky, Z. & Stambler, N.) 465–491 (Springer, 2011).
Gomez, C. E. et al. Responses of the tropical gorgonian coral Eunicea fusca to ocean acidification conditions. Coral Reefs 34, 451–460, https://doi.org/10.1007/s00338-014-1241-3 (2015).
Enochs, I. C., Manzello, D. P., Wirshing, H. H., Carlton, R. & Serafy, J. Micro-CT analysis of the Caribbean octocoral Eunicea flexuosa subjected to elevated pCO(2). Ices J. Mar. Sci. 73, 910–919, https://doi.org/10.1093/icesjms/fsv159 (2016).
Fava, F., Ponti, M., Scinto, A., Calcinai, B. & Cerrano, C. Possible effects of human impacts on epibenthic communities and coral rubble features in the marine Park of Bunaken (Indonesia). Estuar. Coast. Shelf Sci. 85, 151–156, https://doi.org/10.1016/j.ecss.2009.02.028 (2009).
Valisano, L., Notari, F., Mori, M. & Cerrano, C. Temporal variability of sedimentation rates and mobile fauna inside and outside a gorgonian garden. Mar. Ecology-an Evolut. Perspect. 37, 1303–1314, https://doi.org/10.1111/maec.12328 (2016).
Tsounis, G., Steele, M. & Edmunds, P. J. Effects of octocorals on the feeding behavior of herbivorous coral reef fishes in the Caribbean. Coral Reefs (in review).
Coppari, M., Zanella, C. & Rossi, S. The importance of coastal gorgonians in the blue carbon budget. Sci. Rep. 9, 13550 (2019).
Cary, L. R. The Gorgonacea as a Factor in the Formation of Coral Reefs. Carnegie Inst. Wash. Pop. Tortugas Lab, Publ.213. 9, 341–362 (1918).
Clarke, K. R. & Gorley, R. N. P. 192 p. PRIMER V6: User Manual/Tutorial. PRIMER-E. 192 p. (2006).
Research was supported by U.S. National Science Foundation Grants OCE-1334052, OCE-1801475, OCE-1756381 to HRL; OCE-1756678 to PJE; and Project GORGOSHIFT (PICS-CNRS 2017–2020 n. 279738) to LB. B. Gambrel, J. Krawiecki and A. Cerpovicz assisted with data collection on St. John. We thank the crew of the R/V F.G. Walton Smith and A. Potter, S. Zimmermann and G. Tsounis for assistance on research cruises following Hurricanes Irma and Maria, and the Virgin Islands Ecological Research Station for logistical support.
The authors declare no competing interests.
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Lasker, H.R., Martínez-Quintana, Á., Bramanti, L. et al. Resilience of Octocoral Forests to Catastrophic Storms. Sci Rep 10, 4286 (2020). https://doi.org/10.1038/s41598-020-61238-1
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