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Reproduction patterns of four Antarctic octocorals in the Weddell Sea: an inter-specific, shape, and latitudinal comparison

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Abstract

The reproductive patterns of four Antarctic gorgonian species have been investigated. Two of them, Dasystenella acanthina and Thouarella sp., present the bottle-brush-shape type; the other two, Fannyella rossii and Fannyella spinosa, are fan-shaped. Two different reproductive patterns have been observed in D. acanthina and Thouarella sp., which point to two size classes in the frequency distribution of oocytes. This feature indicates a reproduction cycle with overlapping generations, being each of them of more than one year, probably with seasonal spawning. F. rossii and F. spinosa show only one size class of oocytes, which could point towards an annual reproductive cycle. The presence of larvae in the gastrovascular cavities in both Fanyella species and Thoaurella sp. is a sign of a possible larvae release during austral summer. The number of oocytes per polyp ranges from 1.1 ± 0.10 SE to 1.5 ± 0.06 SE, and the size ranges from 50 to 1200 μm. The number of spermatic cysts ranges from 2.6 ± 0.19 SE to 5.0 ± 0.21SE, and their sizes range from 50 to 800 μm. These values are comparable to the reproductive trends and features found in gorgonians from other latitudes, which correspond in some cases with similar morphotypes. These coincident strategies could be related to morphological similarities rather than with latitude or water temperature. The results of this study indicate that octocoral morphology may play a crucial role in determining the reproductive output of these organisms.

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References

  • Aliño PM, Coll JC (1989) Observations of the synchronised mass spawning and post-settlement activity of octocorals on the Great Barrier Reef, Australia: biological aspects. Bull Mar Sci 45:697–707

    Google Scholar 

  • Arnaud PM (1974) Contribution à la binomie marine benthique des régions antarctiques et subantarctiques. Téthys 6:465–656

    Google Scholar 

  • Arntz WE, Gili JM (2001) A case for tolerance in marine ecology: let us put out the baby with the bath water. In: Gili JM, Pretus JL, Packard TT (eds) A marine science odissey into the 21st century. Sci Mar 65(Suppl 2):283–299

  • Arntz WE, Gutt J (1997) The expedition Antarktis XIII/3 (EASIZ I) of RV “Polarstern” to the eastern Weddell Sea in 1996. Ber Polarforsch 249:148

    Google Scholar 

  • Arntz WE, Gutt J (1999) The expedition Antarktis XV/3 (EASIZ II) of RV “Polarstern” to the eastern Weddell Sea in 1998. Ber Polarforsch 301:229

    Google Scholar 

  • Arntz WE, Brey T, Gerdes D, Gorny M, Gutt J, Hain S, Klages M (1992) Patterns of life history and population dynamics of benthic invertebrates under the high Antarctic conditions of the Weddell Sea. In: Olson, Olson (eds) Proceedings of the 27th EMB symposium, Ferrara, September 1990, vol 370 pp 221–230

  • Arntz WE, Brey T, Gallardo VA (1994) Antarctic zoobenthos. Oceanogr Mar Biol Ann Rev 32:241–304

    Google Scholar 

  • Barnes DKA (1996) Low levels of colonisation in Antarctica: the role of bryozoans in early community development. In: Gordon DP, Smith AM, Grant-Mackie JA (eds) Bryozoans in space and time. NIWA, Wellington, pp 19–28

    Google Scholar 

  • Barnes DKA, Clarke A (1998) Seasonality of polypide recycling and sexual reproduction in some erect Antarctic bryozoans. Mar Biol 131:647–658

    Article  Google Scholar 

  • Barthel D, Gutt J (1992) Sponge associations in the eastern Weddell Sea. Ant Sci 4:137–150

    Google Scholar 

  • Bayer FM (1996) New primnoid gorgonians (Coelenterata: Octocorallia) from Antarctic waters. Bull Mar Sci 58(2):511–530

    Google Scholar 

  • Behety-González PA, Guardiola M (1979) Ciclo reproductivo de Plexaura homomalla (Esper, 1792) forma kuekenthali Moser, 1921 (Gorgonacea). Acad Ser Cien Cuba Biol 3:99–104

    Google Scholar 

  • Benayahu Y (1989) Reproductive cycle and developmental processes during embryogenesis of Clavularia hamra (Cnidaria: Octocorallia). Acta Zool Stockh 70(1):29–36

    Article  Google Scholar 

  • Benayahu Y, Loya Y (1983) Surface brooding in the red sea soft coral Parerythropodium fulvum fulvum (Forskal, 1775). Biol Bull Mar Biol Lab Woods Hole 165:353–369

    Google Scholar 

  • Benayahu Y, Loya Y (1984) Life history studies on the Red Sea soft coral X. macrospiculata Gohar, 1940. I. Annual dynamics of gonadal development. Biol Bull (Woods Hole Mass) 166:32–43

    Google Scholar 

  • Benayahu Y, Loya Y (1986) Sexual reproduction of a soft coral: synchronous and brief annual spawning of Sarcophyton glaucum (Quoy and Gaimard, 1833). Biol Bull 170:32–42

    Google Scholar 

  • Benayahu Y, Berner T, Achituv Y (1989) Development of planulae within a mesogleal coat in the soft coral Heteroxenia fuscescens. Mar Biol 100:203–210

    Article  Google Scholar 

  • Benayahu Y, Weil D, Kleinman M (1990) Radiation of broadcasting and brooding patterns in coral reef alcyonaceans. In: Hoshi M, Yamashita O (eds) Advances in invertebrate reproduction, vol 5. Elsevier, Amsterdam, pp 323–328

    Google Scholar 

  • Berkman PA, Waller TR, Alexander SP (1991) Unprotected larval development in the Antarctic scallop Adamussium colbecki (Mollusca: Bivalvia: Pectinidae). Ant Sci 3:7–151

    Google Scholar 

  • Brazeau DA, Lasker HR (1989) The reproductive cycle and spawning in a Caribbean gorgonian. Biol Bull 176:1–7

    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 

  • Brito TAS, Tyler PA, Clarke A (1997) Reproductive biology of the Antarctic octocoral Thouarella variabilis Wright and Studer 1889. In: Proceedings of the sixth international conference on coelenterate biology, 1995, pp 63–69

  • Chia FS, Crawford BJ (1973) Some observations on gametogenesis, larval development and susbtratum selection of the sea-pen Ptilosarcus guerneyi. Mar Biol 23:73–82

    Article  Google Scholar 

  • Chornesky EA, Peters EC (1987) Sexual reproduction and colony growth in the scleractinian coral Porites astreoides. Biol Bull 172:161–177

    Google Scholar 

  • Clarke A (1992) Reproduction in the cold: Thorson revisited. Invert Reprod Dev 22:175–184

    Google Scholar 

  • Coma R, Lasker HR (1997) Effects of spatial distribution and reproductive biology on in situ fertilisation rates of a broadcast-spawning invertebrate. Biol Bull 193:20–29

    Google Scholar 

  • Coma R, Ribes M, Zabala M, Gili JM (1995a) Reproduction and cycle of gonadal development in the Mediterranean gorgonian Paramuricea clavata. Mar Ecol Progr Ser 117:173–183

    Google Scholar 

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

    Google Scholar 

  • Connell JH (1973) Population ecology of reef-building corals. In: Jones OA, Endean R (eds) Biology and geology of coral reefs II Biology. Academic, New York, pp 205–245

    Google Scholar 

  • Dahan M, Benayahu Y (1997) Reproduction of Dendronephthya hemprichi (Cnidaria: Octocorallia): year-round spawning in an azooxanthellae soft coral. Mar Biol 129:David and Mooi 1990

  • Fadlallah YH (1983) Sexual reproduction, development and larval biology in scleractinian corals. Coral Reefs 2:129–150

    Article  Google Scholar 

  • FadlallahYH, Pearse JS (1982a) Sexual reproduction in solitary corals: overlapping oogenic and brooding cycles, and benthic planulas in Balanophyllia elegans. Mar Biol 71:223–231

    Article  Google Scholar 

  • FadlallahYH, Pearse JS (1982b) Sexual reproduction in solitary corals: synchronous gametogenesis and broadcast spawning in Paracyathus stearnsii. Mar Biol 71:233–239

    Article  Google Scholar 

  • Fautin DG, Mariscal RN (1991) Cnidaria: Anthozoa. In: Harrison FH (ed) Microscopic anatomy of invertebrates, vol 2: Placozoa, porifera, cnidaria, and ctenophora. Wiley, New York, pp 267–358

    Google Scholar 

  • Galéron J, Herman RL, Arnaud PM, Arntz WE, Hain S, Klages M (1992) Macrofaunal communities on the continental shelf and slope of the southeastern Weddell Sea, Antarctica. Polar Biol 12(2):283–290

    Article  Google Scholar 

  • Gambi MC, Giangrande A, Patti FP (2000) Comparative observations on reproductive biology of four species of Perkinsiana (Polychaeta: Sabellidae: Sabellinae). Bull Mar Sci 67(1):299–309

    Google Scholar 

  • Goldberg W, Hamilton R (1974) The sexual cycle in Plexaura homomalla. In: Bayer FM, Weinheimer AJ (eds) Prostaglandins from Plexaura homomalla: ecology, utilization, and conservation of a major medical marina resource. University of Florida Press, Coral Gables

    Google Scholar 

  • Gorny M, George MR (1997) Oocyte development and gonadal production of Nematocarcinus lanceopes (Decapoda: Caridea) in the eastern Weddell Sea (Antarctica). Polar Biol 17(3):191–198

    Article  Google Scholar 

  • Gorny M, Arntz WE, Clarke A, Gore DJ (1992) Reproductive biology of caridean decapods from the Weddell Sea. Polar Biol 12(1):111–120

    Article  Google Scholar 

  • Gorny M, Brey T, Arntz W, Bruns T (1993) Growth, development and productivity of Chorismus antarcticum (Pfeffer) (Crustacea: Decapoda: Natantia) in the eastern Weddell Sea (Antarctica). J Exp Mar Biol Ecol 174(2):261–275

    Article  Google Scholar 

  • Grigg RW (1977) Population dynamics of two gorgonian corals. Ecology 58:278–290

    Article  Google Scholar 

  • Gutt J (1991) On the distribution and ecology of holothurians in the Weddell Sea (Antarctica). Polar Biol 11:145–155

    Article  Google Scholar 

  • Gutt J, Gerdes D, Klages M (1992) Seasonality and spatial variability in the reproduction of two Antarctic holothurians (Echinodermata). Polar Biol 11(8):533–544

    Article  Google Scholar 

  • Hain S, Arnaud PM (1992) Notes on the reproduction of high Antarctic molluscs from the Weddell Sea. Polar Biol 12(2):303–312

    Article  Google Scholar 

  • Hall VR, Hughes TP (1996) Reproductive strategies of modular organisms: comparative studies of reef-building corals. Ecology 77(3):950–963

    Article  Google Scholar 

  • Harper JL (1977) Population biology of plants. Academic, London

    Google Scholar 

  • Harrison PL, Wallace CC (1990) Reproduction, dispersal and recruitment of scleractinian corals. In: Dubinsky Z (ed) Ecosystems of the world. Elsevier, Amsterdam, pp 133–204

    Google Scholar 

  • Hughes DJ (1989) Variation in reproductive strategy among clones of the bryozoan Celleporella hyalina. Ecol Monogr 59:387–403

    Article  Google Scholar 

  • Hughes TP, Jackson JBC (1980) Do corals lie about their age? Some demographic consequences of partial predation, fission and fusion. Science 209:713–715

    Article  PubMed  Google Scholar 

  • Kapela W, Lasker HR (1999) Size-dependent reproduction in the Caribbean gorgonian Pseudoplexaura porosa. Mar Biol 135(1):107–114

    Article  Google Scholar 

  • Kinzie RA (1970) The ecology of the gorgonians (Cnidaria, Octocorallia) of Discovery Bay, Jamaica. Ph.D. Thesis, Yale University, New Haven

    Google Scholar 

  • Kinzie RA (1974) Plexaura homomalla: the biology and ecology of a harvestable marine resource. In: Bayer FM, Weinheimer AJ (eds) Prostaglandins from Plexaura homomalla. Studies in Tropical Oceanography No. 12. Coral Gables, Florida, pp 22–38

    Google Scholar 

  • Klages M (1993) Distribution, reproduction and population dynamics of the Antarctic gammaridean amphipod Eusirus perdentatus Chevreux, 1912 (Crustacea). Ant Sci 5(4):349–359

    Google Scholar 

  • Kojis BL, Quinn NJ (1982) Reproductive ecology of two faviid corals (Coelenterata: Scleractinia). Mar Ecol Progr Ser 8:251–255

    Google Scholar 

  • Kruger A, Schleyer MH, Benayahu Y (1998) Reproduction in Anthelia glauca (Octocorallia: Xeniidae). I. Gametogenesis and larval brooding. Mar Biol 131:423–432

    Article  Google Scholar 

  • Levitan DR (1993) The importance of sperm limitation to the evolution of egg size in marine invertebrates. Am Nat 141:517–536

    Article  PubMed  CAS  Google Scholar 

  • Levitan DR (1996a) Effects of gamete traits on fertilization in the sea and the evolution of sexual dimorphism. Nature 382:153–155

    Article  CAS  Google Scholar 

  • Levitan DR (1996b) Predicting optimal and unique egg sizes in free spawning marine invertebrates. Am Nat 148:174–188

    Article  Google Scholar 

  • Luxmoore RA (1982) The reproductive biology of some serolid isopods from the Antarctic. Polar Biol 1:3–11

    Article  Google Scholar 

  • Marsh AG, Leong PKK, Manahan DT (1999) Energy metabolism during embryonic development and larval growth of an Antarctic sea urchin. J Exp Biol 202:2041–2050

    PubMed  CAS  Google Scholar 

  • Martin E (1982) Ciclo reproductivo, proporción sexual y fecundidad del coral blando Plexaura homomalla (Esper.) en el mar Caribe Mexicano (Octocorallia: Plexauridae). An Inst Cien Mar Limnol Univ Natl Autón México 9:359–380

    Google Scholar 

  • McClintock JB, Baker BJ (1997) Palatability and chemical defence of eggs, embryos and larvae of shallow-water Antarctic marine Invertebrata. Mar Ecol Prog Ser 154:121–131

    Google Scholar 

  • Meidlinger K, Tyler PA, Peck LS (1998) Reproductive patterns in the Antarctic brachiopod Liothyrella uva. Mar Biol 132(1):153–162

    Article  Google Scholar 

  • Mileikowsky SA (1971) Types of larval development in marine bottom invertebrates, their distribution and ecological significance: a re-evaluation. Mar Biol 10:193–213

    Article  Google Scholar 

  • Mühlenhardt-Siegel U (1988) Some results on quantitative investigations of macrozoobenthos in the Scotia Arc (Antarctica). Polar Biol 8:241–248

    Article  Google Scholar 

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

    Google Scholar 

  • Pearse JS, Lockhart SJ (2004) Reproduction in cold water: paradigm changes in the 20th century and role for cidaroid sea urchins. Deep-Sea Res II 51:1533–1549

    Article  Google Scholar 

  • Pearse JS, McClintock JB, Bosch I (1991) Reproduction of Antarctic marine invertebrates: tempos, modes and timing. Am Zool 31:65–80

    Google Scholar 

  • Peck LS, Robinson K (1994) Pelagic larval development in the brooding brachiopod Liothyrella uva. Mar Biol 120(2):279–286

    Article  Google Scholar 

  • Pörtner HO (2002) Climate variations and the physilogical basis of temperature dependent biogeography: systemic to molecular hierarchy of thermal tolerance in animals. Comp Bioch Physiol 132A:739–761

    Article  Google Scholar 

  • Pörtner HO, van Dijk P, Hardewig I, Sommer A (2000) Levels of metabolic cold adaptation, tradeoffs in eurythermal and stenothermal ecotherms. In: Davison W, Howard-Williams C, Broady P (eds) Antarctic ecosystems: models for wider ecological understanding. Caxton, Christchurch, pp 109–122

    Google Scholar 

  • Poulin E, Féral JP (1996) Why are there so many species of brooding Antarctic echinoids? Evolution 50(2):820–830

    Article  Google Scholar 

  • Rice AL, Tyler PA, Paterson GJL (1992) The pennatulacean Kophobelemnon stelliferum (Cnidaria: Octocorallia) in the Porcupine Seabight (North-east Atlanctic Ocean). J Mar biol Ass UK 72:417–434

    Article  Google Scholar 

  • Rinkevich B, Loya Y (1979) The reproduction of the Red Sea coral Stylophora pistillata. I. Gonads and planulae. Mar Ecol Progr Ser 1:133–144

    Google Scholar 

  • Sará A, Cerrano C, Sará M (2002) Viviparous development in the Antarctic sponge Stylocordyla borealis Loven, 1868. Pol Biol 25(6):425–431

    Google Scholar 

  • Slattery M, McClintock J (1997) An overview of the population biology and chemical ecology of three species of Antarctic soft corals. SCAR Proc pp 309–315

  • Sokal RR, Rohlf FJ (1995) Biometry. Freeman, San Francisco, p 859

    Google Scholar 

  • Stanwell-Smith D, Clarke A (1998) The timing of reproduction in the Antarctic limpet Nacella concinna (Strebel, 1908) (Patellidae) at Signy Island, in relation to environmental variables. J Mollusc Stud 64:123–127

    Google Scholar 

  • Stanwell-Smith D, Peck LS (1998) Temperature and embryonic development in relation to spawning and field occurrence of larvae of three Antarctic echinoderms. Biol Bull 194:44–52

    Google Scholar 

  • Starmans A, Gutt J, Arntz WE (1999) Mega-epibenthic communities in Arctic and Antarctic shelf areas. Mar Biol 135:269–280

    Article  Google Scholar 

  • Stiller M (1996) Distribution and biology of the aphroditides and polynoids (Polychaeta) in the eastern Weddell Sea and the Lazarev Sea (Antarctica). Ber Polarforsch 185:1–200

    Google Scholar 

  • Stimson JS (1978) Mode and timing of reproduction in some common hermatypic corals of Hawaii and Enewetak. Mar Biol 48:173–184

    Article  Google Scholar 

  • Szmant AM (1986) Reproductive ecology of Caribbean reef corals. Coral Reefs 5:43–54

    Article  Google Scholar 

  • Szmant-Froehlich A (1985) The effect of colony size on the reproductive ability of the Caribbean coral Montastrea annularis (Ellis and Solander). In: Proceedings of the fifth international coral reef congress, Tahiti, vol 158, pp 295–300

  • Thorson G (1950) Reproductive and larval ecology of marine bottom invertebrates. Biol Rev 25:1–45

    Article  Google Scholar 

  • Vighi M (1972) Etude sur la reproduction du Corallium rubrum (L). Vie et Milieu XXIII(1):21–32

    Google Scholar 

  • Voß J (1988) Zoogeographie und Gemeinschaftsanalyse des Makrozoobenthos des Weddellmeeres (Antarktis). Ber Polarforsch 45:1–145

    Google Scholar 

  • Wallace CC (1985) Reproduction, recruitment and fragmentation in nine sympatric species of the coral genus Acropora. Mar Biol 88:217–233

    Article  Google Scholar 

  • Wasson K, Newberry AT (1997) Modular metazoans: gonochoric, hermaphroditic, or both at once? Inv Rep Dev 31(1–3):159–175

    Google Scholar 

  • Weinberg S, Weinberg F (1979) The life cycle of a gorgonian: Eunicella singularis (Esper 1794). Bijdr Dierk 48:127–140

    Google Scholar 

  • White MG (1977) Ecological adaptations by Antarctic poikilotherms to the polar marine environment. In: Llano GA (ed) Adaptations within Antarctic ecosystems. The Smithsonian Institution, Washington, pp 197–208

    Google Scholar 

  • White MG (1984) Marine benthos. In: Laws RM (ed) Antarctic ecology, vol 2. Academic, London, pp 421–461

    Google Scholar 

  • Yamazo KM, Sato M, Yamashiro H (1981) Reproductive biology of an alcyonacean coral Lobophytum crassum Marenzeller. In: Proceedings of the fourth international coral reef symposium, vol 2, pp 671–678

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Acknowledgments

Financial support for this study was provided by a European Comission fellowship within the programme “Training and Mobility of Researchers” (TMR-CT97-2813), by CICYT (Spanisch Antarctic Research Programme) grants ANT98-1739-E and ANT099-1608-E, and by the programme “Acciones integradas hispano-alemanas” (314-Al-e-dr/ia. “Ministerio de Educación y Ciencia” and DAAD (Deutscher Akademischer Austauschdienst). We are indebted to Andrew Clarke, Miriam Fernández, and two anonymous referees whose comments improved very much the end version of the manuscript. We also thank Nuria Teixidó, Patricia Pinto, and Kerstin Beyer for their laboratory assistance. The authors are grateful to many colleagues who helped onboard, and especially to officers and crew of RV “Polarstern” for their cooperation and hospitality during the EASIZ II cruise.

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Communicated by O. Kinne, Oldendorf/Luhe

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Orejas, C., Gili, J.M., López-González, P.J. et al. Reproduction patterns of four Antarctic octocorals in the Weddell Sea: an inter-specific, shape, and latitudinal comparison. Mar Biol 150, 551–563 (2007). https://doi.org/10.1007/s00227-006-0370-9

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