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From brooding to hatching: new insights from a female Octopus vulgaris in the wild

Published online by Cambridge University Press:  21 December 2015

Manuel E. Garci
Affiliation:
Instituto de Investigaciones Marinas (CSIC), Eduardo Cabello 6, 36208 Vigo, Spain
Jorge Hernández-Urcera
Affiliation:
Instituto de Investigaciones Marinas (CSIC), Eduardo Cabello 6, 36208 Vigo, Spain
Miguel Gilcoto
Affiliation:
Instituto de Investigaciones Marinas (CSIC), Eduardo Cabello 6, 36208 Vigo, Spain
Raquel Fernández-Gago
Affiliation:
Universidad de Vigo, Facultad de Ciencias del Mar, Lagoas s/n, 36310 Vigo, Spain
Ángel F. González
Affiliation:
Instituto de Investigaciones Marinas (CSIC), Eduardo Cabello 6, 36208 Vigo, Spain
Ángel Guerra
Affiliation:
Instituto de Investigaciones Marinas (CSIC), Eduardo Cabello 6, 36208 Vigo, Spain
Corresponding
E-mail address:

Abstract

A brooding Octopus vulgaris female was monitored for 128 days in her natural habitat. The main reproductive events and embryonic development in relation to the temperature inside the spawning den, which was recorded by long-battery-life mini-data loggers, are described in the wild. The den temperature ranged from 12.9 to 19.3°C. The total number of egg strings was 160, and the total number of eggs spawned ranged between 139,040 and 241,760 (mean 190,400). The brooding period, the egg laying interval and the duration of the hatching course lasted 128, 35 and 43 days, respectively. Both egg laying and hatching were intermittent processes. The time taken for embryonic development was variable (85–128 d) and depended on the laying date, temperature and position of the string in the egg cluster and the position of the egg in the egg string. The first hatching observed occurred after a progressive and gradual increase of the temperature from 14.9 to 19.3°C. The 280 min of video recordings taken by scuba divers showed that several times, this female opened and closed a small window in the obstructions of the den entrance to facilitate a way out for the hatchling batches.

Type
Research Article
Copyright
Copyright © Marine Biological Association of the United Kingdom 2015 

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References

Anderson, R.C. (1996) Sedating and euthanizing octopuses. Drum and Croaker 27, 78.Google Scholar
Anderson, R.C., Mather, J.A. and Wood, J.B. (2010) Octopus: the ocean's intelligent invertebrate. Portland, OR: Timber Press.Google Scholar
Boal, J.G. (2011) Behavioral research methods for octopuses and cuttlefishes. Vie et Milieu 61, 203210.Google Scholar
Boletzky, S.v. (1987) Embryonic phase. In Boyle, P.R. (ed.) Cephalopod life cycles, volume 2. London: Academic Press, pp. 531.Google Scholar
Boyle, P.R. and Rodhouse, P.B. (2005) Cephalopods: ecology and fisheries. Oxford: Blackwell Science.CrossRefGoogle Scholar
Calow, P. (1987) Fact and theory – an overview. In Boyle, P.R. (ed.) Cephalopod life cycles, volume 2. London: Academic Press, pp. 351365.Google Scholar
Caverivière, A., Domain, F. and Diallo, M. (1999) Observations on the influence of temperature on the length of embryonic development in Octopus vulgaris (Senegal). Aquatic Living Resources 12, 151154.CrossRefGoogle Scholar
Chung, W.S. (2003) Effects of temperature, salinity and photoperiod on the deposition of growth increments in statoliths of the oval squid Sepioteuthis lessoniana Lesson, 1830 (Cephalopoda: Loliginidae) during early stages . MSc thesis, National Sun Yat-sen University, Kaohsiung City, Taiwan, 65 pp.Google Scholar
Cosgrove, J.A. (1993) Aspects of the natural history of Octopus dofleini, the giant Pacific octopus . MSc thesis. University of Victoria, Canada.Google Scholar
Cuccu, D., Mereu, M., Porcu, C., Follesa, M.C., Cau, A.L. and Cau, A. (2013) Development of sexual organs and fecundity in Octopus vulgaris Cuvier, 1797 from the Sardinian waters (Mediterranean Sea). Mediterranean Marine Science 14, 270277.CrossRefGoogle Scholar
Delgado, M., Gairin, J.I., Carbo, R. and Aguilera, C. (2011) Growth of Octopus vulgaris (Cuvier, 1797) in tanks in the Ebro Delta (NE Spain): effects of temperature, salinity and culture density. Scientia Marina 75, 5359.CrossRefGoogle Scholar
Gonçalves, I., Sendao, J. and Borges, T.C. (2002) Octopus vulgaris (Cephalopoda: Octopodidae) Gametogenesis: a histological approach to the verification to the macroscopic maturity scales. Abhandlungen der Geologishen Bundesanstalt 57, 7988.Google Scholar
Hanlon, R.T. and Messenger, J.B. (1996) Cephalopod behaviour. Cambridge: Cambridge University Press.Google ScholarPubMed
Harman, R.F., Young, R.E., Reid, S.B., Mangold, K.M., Suzuki, T. and Hixon, R.F. (1989) Evidence for multiple spawning in the tropical oceanic squid Stenoteuthis oualaniensis (Teuthoidea: Ommastrephidae). Marine Biology 101, 515519.CrossRefGoogle Scholar
Iglesias, J. and Fuentes, L. (2014) Octopus vulgaris, Paralarval culture. In Iglesias, J., Fuentes, L. and Villanueva, R. (eds) Cephalopod culture. New York, NY: Springer, pp. 427451.CrossRefGoogle Scholar
Iglesias, J., Otero, J.J., Moxica, C., Fuentes, L. and Sánchez, F.J. (2004) The completed life cycle of the octopus (Octopus vulgaris, Cuvier) under culture conditions: paralarval rearing using Artemia and zoeae, and first data on juvenile growth up to 8 months of age. Aquaculture International 12, 481487.CrossRefGoogle Scholar
Itami, K., Izawa, Y., Maeda, S. and Nakai, K. (1963) Notes on the laboratory culture of the octopus larvae. Bulletin of the Japanese Society of Scientific Fisheries 29, 514520.CrossRefGoogle Scholar
Katsanevakis, S. and Verriopoulus, G. (2006) Seasonal population dynamics of Octopus vulgaris in the eastern Mediterranean. Journal of Marine Science 63, 151160.Google Scholar
Khallahi, O.M.F. and Inejih, C.A.O. (2002) Proposition d'une échelle macroscopique de maturité sexuelle des femelles de poulpe Octopus vulgaris (Cuvier, 1797). Bulletin Scientifique du Centre National de Recherches Océanographiques et des Pêches 23, 5157.Google Scholar
Lewis, A.R. and Choat, J.H. (1993) Spawning mode and reproductive output of the tropical cephalopod Idiosepius pygmaeus . Canadian Journal of Fisheries and Aquatic Sciences 50, 2028.CrossRefGoogle Scholar
Mangold-Wirz, K. (1963) Biologie des céphalopodes benthiques et nectoniques de la Mer Catalane. Vie et Milieu, supplément 13. Banyuls-sur-Mer: Hermann.Google Scholar
Mangold, K. (1983) Octopus vulgaris . In Boyle, P.R. (ed.) Cephalopod life cycles, volume 1. London: Academic Press, pp. 335364.Google Scholar
Mangold, K. (1987) Reproduction. In Boyle, P.R. (ed.) Cephalopod life cycles, volume 2. London: Academic Press, pp. 157200.Google Scholar
Mangold, K. and Boletzky, S. (1973) New data on reproductive biology and growth of Octopus vulgaris . Marine Biology 19, 712.CrossRefGoogle Scholar
Mangold, K., Young, R.E. and Nixon, M. (1993) Growth versus maturation in cephalopods. In Okutani, T., O'Dor, R.K. and Kubodera, T. (eds) Recent advances in cephalopod fisheries biology. Tokyo: Tokai University Press, pp. 697703.Google Scholar
Mather, J.A., Anderson, R.C. and Wood, J.B. (2010) Octopus: the ocean's intelligent invertebrate. Portland, OR: Timber Press.CrossRefGoogle Scholar
Naef, A. (2000) Cephalopoda. Embryology. Monograph No. 35. Washington, DC: Smithsonian Institution Libraries. English translation by Boletzky S.v. of Die Cephalopoden (Embryologie). Fauna e Flora del Golfo di Napoli Rome: Dr. G. Bardi and Berlin: Friedländer & Sons, 1928.Google Scholar
Oosthuizen, A. and Smale, M.J. (2003) Population biology of Octopus vulgaris on the temperate south-eastern coast of South Africa. Journal of the Marine Biological Association of the United Kingdom 83, 535541.CrossRefGoogle Scholar
Otero, J., González, A.F., Sieiro, M.P. and Guerra, A. (2007) Reproductive cycle and energy allocation of Octopus vulgaris in Galician waters, NE Atlantic. Fisheries Research 85, 122129.CrossRefGoogle Scholar
Robin, J.P., Roberts, M., Zeidberg, L., Bloor, I., Rodriguez, A., Briceño, F., Downey, N., Mascaró, M., Navarro, M., Guerra, A., Hofmeister, J., Barcellos, D.D., Lourenço, S.A.P., Roper, C.F.E., Moltschaniwskyj, N.A., Green, C.P. and Mather, J. (2014) Transitions during cephalopod life history: the role of habitat, environment, functional morphology and behaviour. Advances in Marine Biology 67, 361404.CrossRefGoogle ScholarPubMed
Rocha, F., Guerra, A. and González, A.F. (2001) A review of reproductive strategies in cephalopods. Biological Reviews 76, 291304.CrossRefGoogle ScholarPubMed
Rodaniche, A.F. (1984) Iteroparity in the lesser Pacific Striped octopus Octopus chierchiae (Jatta, 1889). Bulletin of Marine Science 35, 99104.Google Scholar
Sieiro, M.P., Otero, J. and Guerra, A. (2014) Contrasting macroscopic maturity staging with histological characteristics of the gonads in female Octopus vulgaris . Hydrobiologia 730, 113125.CrossRefGoogle Scholar
Sobrino, I., Silva, L., Bellido, J.M. and Ramos, F. (2002) Rainfall, river discharges and sea temperature as factors affecting abundance of two coastal benthic cephalopod species in the Gulf of Cádiz (SW Spain). Bulletin of Marine Science 71, 851865.Google Scholar
Sonderblohm, C. P., Pereira, J. and Erzini, K. (2014) Environmental and fishery-driven dynamics of the common octopus (Octopus vulgaris) based on time-series analyses from leeward Algarve, southern Portugal. ICES Journal of Marine Science 71, 19891992.CrossRefGoogle Scholar
Steer, M.A., Moltschaniwskyj, N. and Jordan, A. R. (2003) Embryonic development of southern calamary (Sepioteuthis australis) within the constraints of an aggregated egg mass. Marine and Freshwater Research 54, 217226.CrossRefGoogle Scholar
Strathmann, R.R. and Strathmann, M.F. (1995) Oxygen supply and limits on aggregation of embryos. Journal of the Marine Biological Association of the United Kingdom 75, 413428.CrossRefGoogle Scholar
Villanueva, R. (1995) Experimental rearing and growth of planktonic Octopus vulgaris from hatching to settlement. Canadian Journal of Fisheries and Aquatic Sciences 52, 26392650.CrossRefGoogle Scholar
Villanueva, R. and Norman, M. (2008) Biology of the planktonic stages of benthic octopuses. Oceanography and Marine Biology: An Annual Review 46, 105202.Google Scholar
Zar, J.H. (1999) Biostatistical analysis, 4th edn. Upper Saddle River, NJ: Prentice Hall.Google Scholar

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