Dipsastraea speciosa

Dipsastraea speciosa (previously called Favia speciosa) is a species of colonial stony coral in the family Merulinidae. It is found in tropical waters of the Indian and Pacific oceans.

Dipsastraea speciosa
Dipsastraea speciosa on Kingman Reef, Line Islands
Scientific classification Edit this classification
Domain: Eukaryota
Kingdom: Animalia
Phylum: Cnidaria
Class: Hexacorallia
Order: Scleractinia
Family: Merulinidae
Genus: Dipsastraea
Species:
D. speciosa
Binomial name
Dipsastraea speciosa
(Dana, 1846)[2]
Synonyms[2]
  • Astrea speciosa Dana, 1846
  • Favia speciosa (Dana, 1846)

Description

Dipsastraea speciosa has rounded to very elongated corallites, with diameters of 10 to 15 mm. The corallites are separated by broad walls, with a distance of 3 to 6 mm between individual corallites.[3] This species can be distinguished from the more common Dipsastraea pallida, with which it has often been confused, by its septa, which are fine, numerous, and regularly spaced. Both the septa and costae have fine, evenly spaced teeth.

Colonies of Dipsastraea speciosa are massive in their growth habit. The corallites are crowded together, subcircular, with calices up to 12 mm in diameter. Their coloration ranges, including pale grey, green or brown, usually with calices of contrasting color. Colonies of Dipsastraea speciosa tend to be massive.

Habitat

It is a tropical coral found in all shallow, tropical reef environments in the Indian and Pacific Oceans. It can be found at depths ranging from 0 to 40m.[1] It can be found in all reef environments, sub-tidal on rocks, rocky reefs, outer reef channels, black and fore-slopes and in lagoons. Dipsastraea speciosa prefers waters ranging from 23° to 29 °C but can tolerate temperatures slightly above and below.

Feeding

Like most other corals, they contain photosynthetic algae, called zooxanthellae. Dipsastraea speciosa and the algae have a mutualistic relationship. The algae live within the coral polyps and use sunlight to make energy. The coral provides protection and the compounds needed for photosynthesis. In return, the algae produce oxygen and help the coral to remove waste. Most importantly, the zooxanthellae supply the coral with glucose, glycerol and amino acids. The coral then uses these to make proteins, fats, and carbohydrates which help produce their calcium carbonate skeleton. The relationship between the zooxanthellae and the coral polyp creates a tight recycling of nutrients in nutrient-poor tropical waters and is the driving force behind the growth and productivity of the reef.[4]

In addition, corals also eat through filter feeding. At night, coral polyps come out of their skeletons to feed, stretching their nematocysts to capture plankton floating by. The prey is then pulled into the polyps' mouths and digested in their stomach cavity.[5]

Life Cycle

Dipsastraea speciosa is a hermaphrodite meaning they produce both sperm and egg gametes for reproduction. Mature corals use energy to produce their gametes through meiosis. Dipsastraea speciosa then release their gametes into the water column. The gametes float to the surface and external fertilization takes place.[6] Once the egg is fertilized it becomes a zygote develops into a planktonic larva called planula and floats around the water column by currents. The planula is a type of zooplankton that is able to maneuver by cilia that cover its body. Eventually, the planula settles on a hard substrate and begins to undergo metamorphosis transforming it from a juvenile to an adult. The juvenile polyp begins to lay down a calcium carbonate corallite and begins early morphogenesis of tentacles, septa, and pharynx before larval settlement on the aboral end.[7] Since it is a colonial coral, the polyp then goes through asexual reproduction to form more polyps, expanding the size of the coral colony and increasing the number of coral polyps.

Dipsastraea speciosa is one of the types of corals that synchronizes its time of spawning. This reproductive synchrony increases the likelihood that male and female gametes will meet. Spawning tends to take place in the evening or at night, around the last quarter moon of the lunar cycle.[8][9][10] A full moon is equivalent to four to six hours of continuous dim light exposure, which can cause light-dependent reactions in protein.[8][11] Corals contain light-sensitive cryptochromes, proteins whose light-absorbing flavin structures are sensitive to different types of light. This allows corals such as Dipsastraea speciosa to detect and respond to changes in sunlight and moonlight.[8] Moonlight itself may actually suppress coral spawning. The most immediate cue to cause spawning appears to be the dark portion of the night between sunset and moonrise. Over the lunar cycle, moonrise shifts progressively later, occurring after sunset on the day of the full moon. The resulting dark period between day-light and night-light removes the suppressive effect of moonlight and enables coral to spawn.[8][9] Light pollution desynchronizes spawning in some coral species.[8]

The emergence of complex rhythms from solar and lunar cycles in marine ecosystems.[11]

Conservation and Protection

Dipsastraea speciosa was cited as "Least Concern" on the IUCN Red List in January 2008 although its population trend is decreasing.[1] It faces threats such as residential and commercial development, transportation and services through shipping lanes, fishing, and harvesting for aquatic resources like aquariums, human recreational activities, pollution such as domestic and urban wastewater and climate change.[12] Parts of the range of Dipsastraea speciosa fall within Marine Protected Areas providing them some protection.

Research

Dipsastraea speciosa is often a subject of research because it is a good indicator of the overall health of the ecosystem. It has been studied to better understand reef formation and maintenance of coral reef ecosystems and their response to changing environments. In one study, Dipsastraea speciosa was tested to see how its morphological, physiological or behavioral expression of a genotype is effected by environment-dependent variation. To test this, plastic was transplanted into corals found at shallow and deep depths. It was found that the shallow water corals showed little to no change, but the deeper corals responded by changing dramatically. The oral disks lost their bright green pigmentation and the surrounding tissues turned pale brown. This showed that plasticity in color was evident and probably light-induced.[12]

References

  1. L. DeVantier; G. Hodgson; D. Huang; O. Johan; A. Licuanan; D. Obura; C. Sheppard; M. Syahrir & E. Turak (2008). "Favia speciosa". IUCN Red List of Threatened Species. 2008: e.T133210A3633217. doi:10.2305/IUCN.UK.2008.RLTS.T133210A3633217.en.
  2. Hoeksema, Bert (2014). "Dipsastraea speciosa (Dana, 1846)". WoRMS. World Register of Marine Species. Retrieved 14 December 2014.
  3. Veron, J. E. N. (1993). Corals of Australia and the Indo-Pacific (University of Hawaii Press ed.). Honolulu: University of Hawaii Press. ISBN 9780824815042.
  4. Barnes, Robert D. (December 1969). "Bibliography: Invertebrate Zoology". BioScience. 19 (12): 1131–1132. doi:10.2307/1294886. ISSN 0006-3568. JSTOR 1294886.
  5. Núñez-Pons, Laura (2014-12-15). "Stayin' alive: how do microbes help corals recover from bleaching?". doi:10.18258/4236. {{cite journal}}: Cite journal requires |journal= (help)
  6. Okubo, Nami; Mezaki, Takuma; Nozawa, Yoko; Nakano, Yoshikatsu; Lien, Yi-Ting; Fukami, Hironobu; Hayward, David C.; Ball, Eldon E. (2013-12-18). "Comparative Embryology of Eleven Species of Stony Corals (Scleractinia)". PLOS ONE. 8 (12): e84115. Bibcode:2013PLoSO...884115O. doi:10.1371/journal.pone.0084115. ISSN 1932-6203. PMC 3867500. PMID 24367633.
  7. Halanych, Kenneth M. (2004-08-01). "Invertebrates; Invertebrate Zoology: A Functional Evolutionary Approach". Systematic Biology. 53 (4): 662–664. doi:10.1080/10635150490472977. ISSN 1076-836X.
  8. Markandeya, Virat (22 February 2023). "How lunar cycles guide the spawning of corals, worms and more". Knowable Magazine. Annual Reviews. doi:10.1146/knowable-022223-2. Retrieved 6 March 2023.
  9. Lin, Che-Hung; Takahashi, Shunichi; Mulla, Aziz J.; Nozawa, Yoko (24 August 2021). "Moonrise timing is key for synchronized spawning in coral Dipsastraea speciosa". Proceedings of the National Academy of Sciences. 118 (34): e2101985118. doi:10.1073/pnas.2101985118. ISSN 0027-8424. PMC 8403928. PMID 34373318.
  10. Rosenberg, Yaeli; et al. (2022). "Urbanization comprehensively impairs biological rhythms in coral holobionts" (PDF). Glob Change Biol. 28 (10): 3349–3364. doi:10.1111/gcb.16144. PMID 35218086. S2CID 247130171.
  11. Häfker, N. Sören; Andreatta, Gabriele; Manzotti, Alessandro; Falciatore, Angela; Raible, Florian; Tessmar-Raible, Kristin (16 January 2023). "Rhythms and Clocks in Marine Organisms". Annual Review of Marine Science. 15 (1): 509–538. doi:10.1146/annurev-marine-030422-113038. ISSN 1941-1405. PMID 36028229. S2CID 251865474. Retrieved 6 March 2023.
  12. Todd, PA; Ladle, RJ; Lewin-Koh, NJI; Chou, LM (2004). "Genotype × environment interactions in transplanted clones of the massive corals Favia speciosa and Diploastrea heliopora". Marine Ecology Progress Series. 271: 167–182. Bibcode:2004MEPS..271..167T. doi:10.3354/meps271167. ISSN 0171-8630.
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