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Marine Biology

, Volume 148, Issue 2, pp 319–326 | Cite as

Age and growth of the naticid gastropod Polinices pulchellus (Gastropoda: Naticidae) based on length frequency analysis and statolith growth rings

  • C. A. Richardson
  • P. R. Kingsley-Smith
  • R. Seed
  • E. Chatzinikolaou
Research Article

Abstract

In Red Wharf Bay, UK the naticid gastropod, Polinices pulchellus, was more abundant and more highly aggregated during the summer months (June–August 2001) than during the winter (December 2000). Whilst small numbers of juvenile P. pulchellus (4–6 mm shell length) were present throughout the year the population consisted mainly of individuals of 12–14 mm shell length. Juvenile snails grew rapidly in size during the winter and early spring; growth then virtually ceased between May and June, following which there was a further period of rapid growth between August and February. Densities ranged between 57 and 4,073 ha−1 and the largest individual collected during this investigation measured 16.2 mm in shell length. Statoliths from adult P. pulchellus revealed the presence of a settlement ring and two prominent growth rings (rings 1 and 2). A curvilinear relationship exists between statolith diameter and shell length in snails up to 16 mm in length. Settlement rings ranged in diameter from 19.7 to 45.2 μm (mean 29.8 μm; SE=0.41) giving an estimated shell length of the settled juvenile of 1.1 mm. The diameter of ring 1 and ring 2 were significantly correlated indicating that rapid growth during the first year is maintained during year 2. Shell lengths estimated from the diameters of the prominent statolith rings and those obtained from length frequency data analysis (LFDA), were broadly congruent strongly suggesting an annual periodicity to the statolith rings. The largest snails (>15 mm) present within this population were estimated to be between 2 and 3 years old. Von Bertallanfy seasonal growth curves obtained from the LFDA predicted values of L∞, K and t0 of 14.32 mm, 1.54 and −0.14 years, respectively, suggesting that P. pulchellus rapidly attains its maximum asymptotic size.

Keywords

Shell Length Growth Ring Muddy Sand Annual Periodicity Length Frequency Distribution 
These keywords were added by machine and not by the authors. This process is experimental and the keywords may be updated as the learning algorithm improves.

Notes

Acknowledgements

We are grateful to Gwynn Parry Jones and Berwyn Roberts for their continued help in obtaining the naticid gastropods used in this study. The help of Jessica Taylor and Camille Saurel in refining the techniques for sectioning the statoliths is gratefully acknowledged.

References

  1. Ambrose WG Jr (1991) Are infaunal predators important in structuring marine soft-bottom communities? Am Zool 31:849–860CrossRefGoogle Scholar
  2. Ansell AD (1960) Observations on predation of Venus striatula (da Costa) by Natica alderi (Forbes). Proc Malac Soc Lond 34:157–164Google Scholar
  3. Barroso CM, Nunes M, Richardson CA, Moreira MH (2005) The gastropod statolith: a tool for determining the age of Nassarius reticulatus. Mar Biol 146:1139–1144CrossRefGoogle Scholar
  4. Bell JL (1982) Daily increments in the statoliths of gastropod larvae: their use in age determination. Am Zool 22:861Google Scholar
  5. Bell JL (1983) Deposition of increments in the statoliths of gastropod larvae; effects of environmental conditions. Am Zool 23:989Google Scholar
  6. Bell JL (1984) Statoliths as age indicators in gastropod larvae: application to measurement of field growth rates. Pac Sci 38:357Google Scholar
  7. Berry AJ (1982) Predation by Natica maculosa Lamarck (Naticidae: Gastropoda) upon the trochacean gastropod Umbonium vestiarium (L.) on a Malaysian shore. J Exp Mar Biol Ecol 64:71–89CrossRefGoogle Scholar
  8. Broom MJ (1982) Size-selection, consumption rates and growth of the gastropods Natica maculosa (Lamarck) and Thais carinifera (Lamarck) preying on the bivalve, Anadara granosa (L.). J Exp Mar Biol Ecol 56:213–233CrossRefGoogle Scholar
  9. Clarke MR (1978) The cephalopod statolith—an introduction to its form. J Mar Biol Ass UK 58:701–712CrossRefGoogle Scholar
  10. Commito JA, Ambrose WG Jr (1985) Predatory infauna and trophic complexity in soft bottom communities. In: Gibbs PE (ed) Proceedings of the nineteenth European marine biology symposium. Cambridge University Press, Cambridge, pp 323–333Google Scholar
  11. Edwards DG, Huebner JD (1977) Feeding and growth rates of Polinices duplicatus preying on Mya arenaria at Barnstable Harbour, Massachusetts, USA. Ecology 58:1218–1236CrossRefGoogle Scholar
  12. Elliott JM (1971) Some methods for the statistical analysis of samples of benthic invertebrates. Freshwat Biol Assoc Sci Publ 25:37–49Google Scholar
  13. Freeman SM (1999) The ecology of Astropecten irregularis and its potential role as a benthic predator in structuring a soft-sediment community. PhD Thesis, University of Wales, BangorGoogle Scholar
  14. Freeman SM, Richardson CA, Seed R (2001) Seasonal abundance, spatial distribution, spawning and growth of Astropecten irregularis (Echinodermata: Asteroidea) in the Irish Sea. Est Coast Shelf Sci 53:39–49CrossRefGoogle Scholar
  15. Fretter V, Graham A (1994) British Prosobranch Molluscs: their functional anatomy and ecology. Printed for the Ray Society, London. Revised and updated editionGoogle Scholar
  16. Grana-Raffucci FA, Appeldoorn RS (1997) Age determination of larval strombid gastropods by means of increment counts in statoliths. Fish Bull 95:857–862Google Scholar
  17. Griffiths RJ (1981) Predation on the bivalve Choromytilus meridionalis (Kr.) by the gastropod Natica (Tectonatica) tecta Anton. J Moll Stud 47:112–120CrossRefGoogle Scholar
  18. Hayward PJ, Wigham GD, Yonow N (1995) Molluscs (Phylum Mollusca). In: Hayward PJ, Ryland JS (eds) Handbook of the marine fauna of north-west Europe. Oxford University Press, Oxford, pp 484–628Google Scholar
  19. Hoenig JM, Hanumara RC (1982) A statistical study of a seasonal growth model for fishes. University of Rhode Island, Department of Computer Science, Technical Report, NarragansettGoogle Scholar
  20. Hurley GV, Odense PH, O’Dor RK, Dawe EG (1985) Strontium labelling for verifying daily growth increments in the statolith of the short-finned squid (Illex illecebrosus). Can J Fish Aquat Sci 42:380–383CrossRefGoogle Scholar
  21. Jackson GD (1994) Application and future potential of statolith increment analysis in squids and sepioids. Can J Fish Aquat Sci 51:2612–2625CrossRefGoogle Scholar
  22. Jensen KT, Jensen JN (1985) The importance of some epibenthic predators on the density of juvenile benthic macrofauna in the Danish Wadden Sea. J Exp Mar Biol Ecol 89:157–174CrossRefGoogle Scholar
  23. Kingsley-Smith PR, Richardson CA, Seed R (2003a) Stereotypic and size-selective predation in Polinices pulchellus (Gastropoda: Naticidae) Risso 1826. J Exp Mar Biol Ecol 295:173–190CrossRefGoogle Scholar
  24. Kingsley-Smith PR, Richardson CA, Seed R (2003b) Size-related patterns of egg collar production in Polinices pulchellus (Gastropoda: Naticidae) Risso 1826. J Exp Mar Biol Ecol 295:91–206CrossRefGoogle Scholar
  25. Kingsley-Smith PR, Richardson CA, Seed R (2005) Growth and development of the veliger larva and juveniles of Polinices pulchellus (Gastropoda: Naticidae) Risso 1826. J Mar Biol Ass UK 85:171–174CrossRefGoogle Scholar
  26. Kirkwood GP, Aukland R, Zara SJ (2001) Length frequency distribution analysis (LFDA), version 5.0. MRAG Ltd, LondonGoogle Scholar
  27. Lipinski M (1980) Statoliths as a possible tool for squid age determination. Bulletin de L’academie Pol des Sci Biol 28:569–582Google Scholar
  28. Menge BA, Berlow EI, Blanchette CA, Navarrette SA, Yamada SB (1994) The keystone species concept: variation in interaction strength in a rocky intertidal habitat. Ecol Monogr 64:249–286CrossRefGoogle Scholar
  29. Peterson CH (1979) Predation, competitive exclusion, and diversity in the soft-sediment communities of estuaries and lagoons. In: Livingston RJ (ed) Ecological processes in coastal and marine processes. Plenum Press, New York, pp 233–264Google Scholar
  30. Richardson CA (2001) Molluscs as archives of environmental change. Oceanogr Mar Biol Ann Rev 39:103–164Google Scholar
  31. Richardson CA, Saurel C, Barroso CM, Thain J (2005) Evaluation of the age of Neptunea antiqua using statoliths, opercula and element ratios in the shell. J Exp Mar Biol Ecol (published on-line June 2005)Google Scholar
  32. Russell-Hunter W, Grant DC (1966) Estimates of population density and dispersal in the naticid gastropod, Polinices duplicatus, with a discussion of computational methods. Biol Bull 131:292–307CrossRefGoogle Scholar
  33. Wiltse WI (1980a) Effects of Polinices duplicatus (Gastropoda: Naticidae) on infaunal community structure at Barnstable Harbour, Massachusetts, USA. Mar Biol 56:301–310CrossRefGoogle Scholar
  34. Wiltse WI (1980b) Predation by juvenile Polinices duplicatus (Say) on Gemma gemma (Totten). J Exp Mar Biol Ecol 42:187–199CrossRefGoogle Scholar

Copyright information

© Springer-Verlag 2005

Authors and Affiliations

  • C. A. Richardson
    • 1
  • P. R. Kingsley-Smith
    • 1
    • 2
  • R. Seed
    • 1
  • E. Chatzinikolaou
    • 1
  1. 1.School of Ocean SciencesUniversity of Wales BangorWalesUK
  2. 2.Eastern Shore laboratoryVirginia Institute of Marine ScienceWachapreagueUSA

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