Skip to main content
Log in

Effects of colony size and polyp position on polyp fecundity in the scleractinian coral genus Acropora

  • Report
  • Published:
Coral Reefs Aims and scope Submit manuscript

Abstract

This study examined the effects of colony size and polyp position on six variables of polyp fecundity [egg number, egg size, total egg volume, total testis volume, total gonad volume, and gonad ratio (egg volume/testis volume)] in three tabular Acropora corals (Scleractinia), A. hyacinthus, A. japonica, and A. solitaryensis. Samples were collected from various colony sizes (n = 21–30 colonies species−1), just before the predicted spawning at Kochi, Japan, in 2009. Five replicate polyps were sampled at three positions (center, middle, and outer) from the center to the marginal area in each tabular colony. Results indicated effects of colony size and polyp position on both male and female gonads polyp−1. A positive effect of colony size was observed on variables of female gonads polyp−1 (egg number, total egg volume) in A. hyacinthus only, while the positive effect on the variable of male gonads polyp−1 (total testis volume) was common in all Acropora species, with total testis volume polyp−1 increasing 2–4-fold from the small (200–400 cm2) to the large size class (5,000–9,000 cm2). Among the polyp positions, lower values were observed mostly in center polyps in A. hyacinthus, while lower values were observed only in outer polyps in the other Acropora species. The distinct patterns between A. hyacinthus and the other two Acropora species suggest different reproductive strategies at the species level. Further studies are needed to confirm the prevalence of these effects in scleractinian corals, which will broaden our understanding of reproductive life history strategies and improve the estimation of reproductive performance.

This is a preview of subscription content, log in via an institution to check access.

Access this article

Price excludes VAT (USA)
Tax calculation will be finalised during checkout.

Instant access to the full article PDF.

Fig. 1
Fig. 2
Fig. 3
Fig. 4
Fig. 5

References

  • Babcock RC (1984) Reproduction and distribution of two species of Goniastrea (Scleractinia) from the Great Barrier Reef province. Coral Reefs 2:187–195

    Google Scholar 

  • Babcock RC (1991) Comparative demography of three species of scleractinian corals using age- and size-dependent classifications. Ecol Monogr 61:225–244

    Article  Google Scholar 

  • Bayer MM, Todd CD (1997) Evidence for zooid senescence in the marine bryozoan Electra pilosa. Invertebr Biol 116:331–340

    Article  Google Scholar 

  • Beazley LI, Kenchington EL (2012) Reproductive biology of the deep-water coral Acanella arbuscula (Phylum Cnidaria: Class Anthozoa: Order Alcyonacea), northwest Atlantic. Deep Sea Res Part I Oceanogr Res Pap 68:92–104

    Article  Google Scholar 

  • Beiring EA, Lasker HR (2000) Egg production by colonies of a gorgonian coral. Mar Ecol Prog Ser 196:169–177

    Article  Google Scholar 

  • Brazeau DA, Lasker HR (1990) Sexual reproduction and external brooding by the Caribbean gorgonian Briareum asbestinum. Mar Biol 104:465–474

    Article  Google Scholar 

  • Chadwick-Furman NE, Goffredo S, Loya Y (2000) Growth and population dynamic model of the reef coral Fungia granulosa Klunzinger, 1879 at Eilat, northern Red Sea. J Exp Mar Biol Ecol 249:199–218

    Article  PubMed  Google Scholar 

  • Coma R, Zabala M, Gili JM (1995) Sexual reproductive effort in the Mediterranean gorgonian Paramuricea clavata. Mar Ecol Prog Ser 117:185–192

    Article  Google Scholar 

  • Cupido R, Cocito S, Manno V, Ferrando S, Peirano A, Iannelli M, Bramanti L, Santangelo G (2012) Sexual structure of a highly reproductive, recovering gorgonian population: quantifying reproductive output. Mar Ecol Prog Ser 469:25–36

    Article  Google Scholar 

  • Elahi R, Edmunds PJ (2007) Determinate growth and the scaling of photosynthetic energy intake in the solitary coral Fungia concinna (Verrill). J Exp Mar Biol Ecol 349:183–193

    Article  Google Scholar 

  • Fine M, Oren U, Loya Y (2002) Bleaching effect on regeneration and resource translocation in the coral Oculina patagonica. Mar Ecol Prog Ser 234:119–125

    Article  Google Scholar 

  • Hall V, Hughes TP (1996) Reproductive strategies of modular organisms: comparative studies of reef-building corals. Ecology 77:950–963

    Article  Google Scholar 

  • Johnson KG (1992) Population dynamics of a free-living coral: recruitment, growth and survivorship of Manicina areolata (Linnaeus) on the Caribbean coast of Panama. J Exp Mar Biol Ecol 164:171–191

    Article  Google Scholar 

  • Kapela W, Lasker HR (1999) Size-dependent reproduction in the Caribbean gorgonian Pseudoplexaura porosa. Mar Biol 135:107–114

    Article  Google Scholar 

  • Kojis BL, Quinn NJ (1981) Aspects of sexual reproduction and larval development in the shallow water hermatypic coral, Goniastrea australensis (Edwards and Haime, 1857). Bull Mar Sci 31:558–573

    Google Scholar 

  • Kojis BL, Quinn N (1985) Puberty in Goniastrea favulus. Age or size limited. Proc 5th Int Coral Reef Symp 4:289–293

  • Levitan DR, Petersen C (1995) Sperm limitation in the sea. Trends Ecol Evol 10:228–231

    Article  CAS  PubMed  Google Scholar 

  • Meesters EH, Bak RPM (1995) Age-related deterioration of a physiological function in the branching coral Acropora palmata. Mar Ecol Prog Ser 121:203–209

    Article  Google Scholar 

  • Mezaki T, Hayashi T, Iwase F, Nozawa Y, Miyamoto M, Tominaga M (2007) Spawning patterns of high latitude scleractinian corals from 2002 to 2006 at Nishidomari, Otsuki, Kochi, Japan. Kuroshio Biosphere 3:33–47

    Google Scholar 

  • Nozawa Y (2012) Annual variation in the timing of coral spawning in a high-latitude environment: influence of temperature. Biol Bull 222:192–202

    PubMed  Google Scholar 

  • Orejas C, López-González PJ, Gili JM, Teixidó N, Gutt J, Arntz WE (2002) Distribution and reproductive ecology of the Antarctic octocoral Ainigmaptilon antarcticum in the Weddell Sea. Mar Ecol Prog Ser 231:101–114

    Article  Google Scholar 

  • Oren U, Rinkevich B, Loya Y (1997) Oriented intra-colonial transport of 14C labeled materials during coral regeneration. Mar Ecol Prog Ser 161:117–122

    Article  Google Scholar 

  • Oren U, Brickner I, Loya Y (1998) Prudent sessile feeding by the corallivore snail, Coralliophila violacea on coral energy sinks. Proc R Soc Lond B Biol Sci 265:2043–2050

    Article  Google Scholar 

  • Palumbi SR, Jackson JBC (1983) Aging in modular organisms: ecology of zooid senescence in Steginoporella sp. (Bryozoa; Cheilostomata). Biol Bull 164:267–278

    Article  Google Scholar 

  • Pearse VB, Muscatine L (1971) Role of symbiotic algae (zooxanthellae) in coral calcification. Biol Bull 141:350–363

    Article  CAS  Google Scholar 

  • Pires DO, Castro CB, Silva JC (2009) Reproductive biology of the deep-sea pennatulacean Anthoptilum murrayi (Cnidaria, Octocorallia). Mar Ecol Prog Ser 397:103–112

    Article  Google Scholar 

  • Rinkevich B (1996) Do reproduction and regeneration in damaged corals compete for energy allocation? Mar Ecol Prog Ser 143:297–302

    Article  Google Scholar 

  • Rinkevich B, Loya Y (1979) The reproduction of the Red Sea coral Stylophora pistillata. II. Synchronization in breeding and seasonality of planulae shedding. Mar Ecol Prog Ser 1:145–152

    Article  Google Scholar 

  • Rinkevich B, Loya Y (1984) Senescence and dying signals in a reef building coral. Experientia 42:320–322

    Article  Google Scholar 

  • Rinkevich B, Lauzon RJ, Brown BW, Weissman IL (1992) Evidence for a programmed life span in a colonial protochordate. Proc Natl Acad Sci USA 89:3546–3550

    Article  CAS  PubMed Central  PubMed  Google Scholar 

  • Rossi S, Gili J-M (2009) Reproductive features and gonad development cycle of the soft bottom-gravel gorgonian Leptogorgia sarmentosa (Esper, 1791) in the NW Mediterranean Sea. Invertebr Reprod Dev 53:175–190

    Article  Google Scholar 

  • Sakai K (1998a) Effect of colony size, polyp size, and budding mode on egg production in a colonial coral. Biol Bull 195:319–325

    Article  Google Scholar 

  • Sakai K (1998b) Delayed maturation in the colonial coral Goniastrea asper (Scleractinia): whole-colony mortality, colony growth and polyp egg production. Res Popul Ecol 40:287–292

    Article  Google Scholar 

  • Santangelo G, Carletti E, Maggi E, Bramanti L (2003) Reproduction and population sexual structure of the overexploited Mediterranean red coral Corallium rubrum. Mar Ecol Prog Ser 248:99–108

    Article  Google Scholar 

  • Suzuki G, Fukami H (2012) Evidence of genetic and reproductive isolation between two morphs of subtropical-dominant coral Acropora solitaryensis in the non-reef region of Japan. Zool Sci 29:134–140

    Article  PubMed  Google Scholar 

  • Tanner JE (1997) Interspecific competition reduces fitness in scleractinian corals. J Exp Mar Biol Ecol 214:19–34

    Article  Google Scholar 

  • Tsounis G, Rossi S, Aranguren M, Gili J-M, Arntz W (2006) Effects of spatial variability and colony size on the reproductive output and gonadal development cycle of the Mediterranean red coral (Corallium rubrum L.). Mar Biol 148:513–527

    Article  Google Scholar 

  • van Woesik R, Sakai K, Ganase A, Loya Y (2011) Revisiting the winners and the losers a decade after coral bleaching. Mar Ecol Prog Ser 434:67–76

    Article  Google Scholar 

  • Veron JEN (2002) New species described in corals of the world. Australian Institute of Marine Science, Townsville

    Google Scholar 

  • Yamashiro H, Nishihira M (1998) Experimental study of growth and asexual reproduction in Diaseris distorta (Michelin, 1843), a free-living fungiid coral. J Exp Mar Biol Ecol 225:253–267

    Article  Google Scholar 

Download references

Acknowledgments

The authors thank the staff at the Biological Institute on Kuroshio for the filed support, as well as A. Santacruz-Castro and T. Kawai for their comments that improved the manuscript. This study was supported by an internal research grant of the Biodiversity Research Center, Academia Sinica.

Author information

Authors and Affiliations

Authors

Corresponding author

Correspondence to Yoko Nozawa.

Additional information

Communicated by Biology Editor Dr. Mark Vermeij

Rights and permissions

Reprints and permissions

About this article

Check for updates. Verify currency and authenticity via CrossMark

Cite this article

Nozawa, Y., Lin, CH. Effects of colony size and polyp position on polyp fecundity in the scleractinian coral genus Acropora . Coral Reefs 33, 1057–1066 (2014). https://doi.org/10.1007/s00338-014-1185-7

Download citation

  • Received:

  • Accepted:

  • Published:

  • Issue Date:

  • DOI: https://doi.org/10.1007/s00338-014-1185-7

Keywords

Navigation