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Interesting Images

New Records of Heliopora hiberniana from SE Asia and the Central Indian Ocean

1
Coral Conservation and Research Group, School of Molecular and Life Sciences, Curtin University, Bentley, WA 6102, Australia
2
Western Australian Museum, Welshpool, WA 6106, Australia
3
Conservation Diver, Sunset Beach, Gili Air, East Nusa Nenggara 83355, Indonesia
4
Laboratory of Animal Biology, University of Lille, Sciences and Technologies, CEDEX, 59 650 Villeneuve d’Ascq, France
5
Doris Group Diver, 58a Rue du Dessous des Berges, 75013 Paris, France
*
Author to whom correspondence should be addressed.
Diversity 2020, 12(9), 328; https://doi.org/10.3390/d12090328
Submission received: 6 August 2020 / Revised: 26 August 2020 / Accepted: 26 August 2020 / Published: 28 August 2020
(This article belongs to the Collection Interesting Images from the Sea)

Graphical Abstract

Coral reefs are among the most diverse ecosystems on the planet. They provide spawning sites for fishes and habitat for a myriad of fauna and flora. They protect coastlines from waves and storms and have important socio-economic value. However, coral reefs, as we know them, are seriously threatened by globalization and climate change [1]. The widespread bleaching of scleractinian corals threatens to destabilize critical ecosystem functions such as reef-building [2], and a growing body of data indicates that coral reefs are being transformed [3,4]. Future reefs are predicted to be dominated by non-constructional taxa [5,6], and the retreat of scleractinians threatens to cripple coral reef ecosystem functioning and endanger the lives of the millions of people that rely on coral reefs for protection, income and nutrition [7]. To detect coral community responses to climate change, and to identify which species may perform critical functional roles on future reefs, accurate taxonomic and systematic information is needed.
Heliopora is a genus of hermatypic octocoral that is a major contributor to reef accretion in tropical Indo-Pacific locations [8]. Up until recently, Heliopora coerulea was the only extant species in the genera, however in 2018, a new reef-building octocoral species, Heliopora hiberniana was described from four locations in north Western Australia [7]. The newly described species is morphologically distinguished from H. coerulea by its thin branches and white skeleton. Colonies of H. hiberniana survived the 2016 coral bleaching event at Scott Reef, sparking suggestions that non-scleractinian reef builders may have a higher probability of persisting through future climate regimes [7]. Hence it has been hypothesized that Heliopora may become increasingly important in the reconfiguration of tropical Indo-Pacific coral reefs [7]. The ability to accurately detect such compositional changes on future reefs is contingent upon a good understanding of current species distribution patterns.
Here we report new photographic evidence (Figure 1A–E) that extends the known range of Heliopora hiberniana from the north-west shelf of Western Australia to the Maldives and the Wakatobi and Gili Islands in Indonesia (Figure 2). The visual records are augmented by the re-discovery of a specimen in the Smithsonian Museum, collected from Kur Island in Indonesia in 1979, which matches the description of H. hiberniana (Figure 1E). These new records extend the distribution of H. hiberniana from NW Australia to the Central Indian Ocean and the Bali and Banda Seas in SE Asia. It is possible H. hiberniana also occurs from the Philippines through to Taiwan and Japan as two morphologically and reproductively differentiated lineages have been described along the Kuroshio Current [9,10]; however, the relationship between these lineages and H. hiberniana remains to be clarified.
Colonies at the Gili Islands in Indonesia were commonly observed to have white rings with healthy, intact tissue in the centre (Figure 1G). The rings are presumed to be a feeding scar because similar annular lesions observed on Acropora palmata in the Atlantic Ocean, and Psammocora albopicta in South Korea, were formed by the foraging activity of cowfish (Ostraciidae) [11,12]. Further observational studies are needed to determine if a member of the Ostraciidae family is responsible for the Heliopora lesions. These new records advance our understanding of the distribution of this species, but little information is available about its reproductive behaviour or symbiont composition. Further demographic data, along with experimental and post-bleaching survivorship studies are needed to test the hypothesis that this species may play an increased functional role on future reefs as a result of higher tolerance to heat stress.

Author Contributions

Conceptualization, research and plate preparation, Z.T.R.; fieldwork and photography L.H., D.A.; writing—review and editing, Z.T.R, P.S. All authors have read and agreed to the published version of the manuscript.

Funding

Z.T.R. was supported in the write-up phase by a Thomas Davies Research Grant and an Australian Biological Resources Study Grant. Indonesian and Maldives fieldwork was supported by Blue Marlin Dive, Gili Air and Soneva Fushi Resort.

Acknowledgments

Thanks to Tim Coffer for communications regarding specimen #79530. Thanks to George Roff and Vianney Denis for information regarding the possible source of the lesions. Thanks to Rodrigo Garcia for assistance preparing the map.

Conflicts of Interest

The authors declare no conflict of interest.

References

  1. Darling, E.S.; McClanahan, T.R.; Maina, J.; Gurney, G.G.; Graham, N.A.; Januchowski-Hartley, F.; Cinner, J.E.; Mora, C.; Hicks, C.C.; Maire, E.; et al. Social-environmental drivers inform strategic management of coral reefs in the Anthropocene. Nat. Ecol. Evol. 2019, 3, 1341–1350. [Google Scholar] [CrossRef] [PubMed]
  2. Perry, C.T.; Alvarez-Filip, L.; Graham, N.A.; Mumby, P.J.; Wilson, S.K.; Kench, P.S.; Manzello, D.P.; Morgan, K.M.; Slangen, A.B.; Thomson, D.P.; et al. Loss of coral reef growth capacity to track future increases in sea level. Nature 2018, 396–400. [Google Scholar] [CrossRef]
  3. Hughes, T.P.; Kerry, J.T.; Baird, A.H.; Connolly, S.R.; Dietzel, A.; Eakin, C.M.; Heron, S.F.; Hoey, A.S.; Hoogenboom, M.O.; Liu, G.; et al. Global warming transforms coral reef assemblages. Nature 2018, 556, 492–496. [Google Scholar] [CrossRef]
  4. Graham, N.A.; Jennings, S.; MacNeil, M.A.; Mouillot, D.; Wilson, S.K. Predicting climate-driven regime shifts versus rebound potential in coral reefs. Nature 2015, 518, 94–97. [Google Scholar] [CrossRef]
  5. Inoue, S.; Kayanne, H.; Yamamoto, S.; Kurihara, H. Spatial community shift from hard to soft corals in acidified water. Nat. Clim. Chang. 2013, 3, 683–687. [Google Scholar] [CrossRef]
  6. Enochs, I.C.; Manzello, D.P.; Donham, E.M.; Kolodziej, G.; Okano, R.; Johnston, L.; Young, C.; Iguel, J.; Edwards, C.B.; Fox, M.D.; et al. Shift from coral to macroalgae dominance on a volcanically acidified reef. Nat. Clim. Chang. 2015, 5, 1083–1088. [Google Scholar] [CrossRef]
  7. Richards, Z.T.; Yasuda, N.; Kikuchi, T.; Foster, T.; Mitsuyuki, C.; Stat, M.; Suyama, Y.; Wilson, N.G. Integrated evidence reveals a new species in the ancient blue coral genus Heliopora (Octocorallia). Sci. Rep. 2018, 8, 15875. [Google Scholar] [CrossRef] [PubMed] [Green Version]
  8. Zann, L.P.; Bolton, L. The distribution, abundance and ecology of the blue coral Heliopora coerulea (Pallas) in the Pacific. Coral Reefs 1985, 4, 125–134. [Google Scholar] [CrossRef]
  9. Yasuda, N.; Taquet, C.; Nagai, S.; Fortes, M.; Fan, T.Y.; Phongsuwan, N.; Nadaoka, K. Genetic structure and cryptic speciation in the threatened reef-building coral Heliopora coerulea along Kuroshio Current. Bull. Mar. Sci. 2014, 90, 233–255. [Google Scholar] [CrossRef]
  10. Villanueva, R.D. Cryptic speciation in the stony octocoral Heliopora coerulea: Temporal reproductive isolation between two growth forms. Mar. Biodivers. 2016, 46, 503–507. [Google Scholar] [CrossRef]
  11. Williams, D.E.; Bright, A.J. White rings on the threatened coral, Acropora palmata, associated with foraging activity of the honeycomb cowfish, Acanthostracion polygonius (Ostraciidae). Coral Reefs 2013, 32, 651. [Google Scholar] [CrossRef] [Green Version]
  12. Denis, V.; Ribas Deulofeu, L.; De Palmas, S.; Chen, C.A. First record of the scleractinian coral Psammocora albopicta from Korean waters. Mar. Biodivers. 2014, 44, 157–158. [Google Scholar] [CrossRef]
Figure 1. New photographic evidence increases the known distribution of Heliopora hiberniana. (A). Kunfunadhoo Island, Baa Atoll, Maldives, 12 m; (B,C). Wangiwangi Island, Wakatobi Islands, Indonesia, 10–12 m. The red arrow points to a broken branch showing the white skeleton; (D). Gili Islands, Indonesia, 8 m; (E). Specimen #79530 Smithsonian Institute. Collected by Gordon Hendler on the Helix-79 expedition in 1979, station M-99, Kur Island, Moluccas, 8–16 m; (F). Gili Islands, 10 m with annular lesions.
Figure 1. New photographic evidence increases the known distribution of Heliopora hiberniana. (A). Kunfunadhoo Island, Baa Atoll, Maldives, 12 m; (B,C). Wangiwangi Island, Wakatobi Islands, Indonesia, 10–12 m. The red arrow points to a broken branch showing the white skeleton; (D). Gili Islands, Indonesia, 8 m; (E). Specimen #79530 Smithsonian Institute. Collected by Gordon Hendler on the Helix-79 expedition in 1979, station M-99, Kur Island, Moluccas, 8–16 m; (F). Gili Islands, 10 m with annular lesions.
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Figure 2. The current known distribution of Heliopora hiberniana extends from the Central Indian Ocean to SE Asia and NW Australia (red dots).
Figure 2. The current known distribution of Heliopora hiberniana extends from the Central Indian Ocean to SE Asia and NW Australia (red dots).
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MDPI and ACS Style

Richards, Z.T.; Haines, L.; Scaps, P.; Ader, D. New Records of Heliopora hiberniana from SE Asia and the Central Indian Ocean. Diversity 2020, 12, 328. https://doi.org/10.3390/d12090328

AMA Style

Richards ZT, Haines L, Scaps P, Ader D. New Records of Heliopora hiberniana from SE Asia and the Central Indian Ocean. Diversity. 2020; 12(9):328. https://doi.org/10.3390/d12090328

Chicago/Turabian Style

Richards, Zoe T., Leon Haines, Patrick Scaps, and Denis Ader. 2020. "New Records of Heliopora hiberniana from SE Asia and the Central Indian Ocean" Diversity 12, no. 9: 328. https://doi.org/10.3390/d12090328

APA Style

Richards, Z. T., Haines, L., Scaps, P., & Ader, D. (2020). New Records of Heliopora hiberniana from SE Asia and the Central Indian Ocean. Diversity, 12(9), 328. https://doi.org/10.3390/d12090328

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