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Morphological differences associated with colour morphs of the auger snail Hastula cinerea (Conoidea: Terebridae) from north-east Brazil

Published online by Cambridge University Press:  04 September 2012

Wagner Franco Molina ,
Paulo Augusto de Lima Filho ,
Vivianne Fernandes Ribeiro Dantas ,
Clóvis Coutinho da Motta-Neto  and
Luiz Antonio Carlos Bertollo
Wagner Franco Molina*
Affiliation:
Department of Cellular and Genetic Biology, Biosciences Center, Federal University of Rio Grande do Norte, Natal, Rio Grande do Norte, Brazil
Paulo Augusto de Lima Filho
Affiliation:
Department of Cellular and Genetic Biology, Biosciences Center, Federal University of Rio Grande do Norte, Natal, Rio Grande do Norte, Brazil
Vivianne Fernandes Ribeiro Dantas
Affiliation:
Department of Cellular and Genetic Biology, Biosciences Center, Federal University of Rio Grande do Norte, Natal, Rio Grande do Norte, Brazil
Clóvis Coutinho da Motta-Neto
Affiliation:
Department of Cellular and Genetic Biology, Biosciences Center, Federal University of Rio Grande do Norte, Natal, Rio Grande do Norte, Brazil
Luiz Antonio Carlos Bertollo
Affiliation:
Department of Genetics and Evolution, São Carlos Federal University, São Carlos, São Paulo, Brazil
*
Correspondence should be addressed to: W.F. Molina, Departamento de Biologia Celular e Genética, Centro de Biociências, Universidade, Federal do Rio Grande  do Norte, Campus Universitário, CEP 59.078-970, Natal, Rio Grande do  Norte, Brazil email: [email protected]
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Abstract

Chromatic polymorphisms in shells may be associated with adaptive characteristics in molluscs. Colouring among Hastula cinerea reveals different patterns in large aggregations of individuals. Although the impacts of temperature are considered critical in the intertidal region, selective effects associated with colouring in H. cinerea shells, in addition to possible physiological consequences, remain an open issue. In this context, H. cinerea is a viable evolutionary model for investigating selective processes related to chromatic polymorphism in shells given its abundance and biological characteristics. Individuals from the same population were classified into three groups according to shell colour: light, reddish and dark. They were then examined with regard to frequency of colour morphs and morphological patterns in each group. Reddish and light-coloured specimens were the most abundant, while those with dark coloration were less common and morphologically distinct from the first two colour morphs. Morphological differences in the anterior region of dark shells, which may be associated with movement ability and lower frequencies in these specimens, suggest possible selective effects on types that are less reflective to light in the intertidal zone.

Keywords

chromatic polymorphismadaptationnatural selection
Type
Research Article
Information
Journal of the Marine Biological Association of the United Kingdom , Volume 93 , Issue 4 , June 2013 , pp. 1035 - 1039
Copyright
Copyright © Marine Biological Association of the United Kingdom 2012 

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References

REFERENCES

Bergamini, L.L. (2011) Navegar é preciso: o tamanho do gastrópode H. cinerea (Mollusca) determina seu comportamento de seleção de hábitat? In Machado, G. and Prado, P.I.K.L. (eds) Ecologia da mata Atlântica. São Paulo: Universidade de São Paulo.Google Scholar
Bratcher, T. and Cernohorsky, W.O. (1987) Living Terebras of the world. New York: American Malacologists, Inc.Google Scholar
Brown, A.C., Stenton-Dozey, J.M.E. and Trueman, E.R. (1989) Sandy beach bivalves and gastropods: a comparison between Donax serra and Bullia digitalis. Advances in Marine Biology 23, 179–247.CrossRefGoogle Scholar
Defeo, O. and De Alava, A. (1995) Effects of human activities on long-term trends in sandy beach populations: the wedge clam Donax hanleyanus in Uruguay. Marine Ecology Progress Series 123, 73–82.CrossRefGoogle Scholar
Dryden, I.L. and Mardia, K.V. (1998) Statistical shape analysis. New York: John Wiley & Sons.Google Scholar
Efford, I.E. (1965) Aggregation in the sand crab Emerita analoga (Stimpson). Journal of Animal Ecology 34, 63–75.CrossRefGoogle Scholar
Endler, J.A. (1978) A predator's view of animal color patterns. Evolutionary Biology 11, 319–364.Google Scholar
Etter, R.J. (1988) Physiological stress and colour polymorphism in the intertidal snail Nucella lapillus. Evolution 42, 660–680.CrossRefGoogle ScholarPubMed
Gibson, A.R. and Falls, J.B. (1979) Thermal biology of the common garter snake Thamnophis sirtalis (L.) II. The effects of melanism. Oecologia 43, 99–109.CrossRefGoogle Scholar
Hayashi, M. and Chiba, S. (2004) Enhanced colour polymorphisms in island populations of the land snail Euhadra peliomphala. Biological Journal of the Linnean Society 81, 417–425.CrossRefGoogle Scholar
Heath, D.J. (1975) Colour, sunlight and internal temperatures in the land-snail Cepaea nemoralis (L.). Oecologia 19, 29–38.CrossRefGoogle ScholarPubMed
Helmuth, B.S.T. (1998) Intertidal mussel microclimates: predicting the body temperature of a sessile invertebrate. Ecological Monographs 68, 29–52.CrossRefGoogle Scholar
Helmuth, B.S.T. (1999) Thermal biology of rocky intertidal mussels: quantifying body temperatures using climatological data. Ecology 80, 15–34.CrossRefGoogle Scholar
Hughes, J.M. and Jones, M.P. (1985) Shell colour polymorphism in a mangrove snail Littorina sp. (Prosobranchia: Littorinidae). Biological Journal of the Linnean Society 25, 365–378.CrossRefGoogle Scholar
Jawor, J.M. and Breitwisch, R. (2003) Melanin ornaments, honesty, and sexual selection. Auk 120, 249–265.CrossRefGoogle Scholar
Johannesson, K. and Ekendahl, A. (2003) Selective predation favoring cryptic individuals of marine snails (Littorina). Biological Journal of the Linnean Society 76, 137–144.CrossRefGoogle Scholar
Klingenberg, C.P. (2011) MORPHOJ: an integrated software package for geometric morphometrics. Molecular Ecology Resources 11, 353–357.CrossRefGoogle ScholarPubMed
Kovach, R.P. and Tallmon, D.A. (2010) Strong influence of microhabitat on survival for an intertidal snail, Nucella lima. Hydrobiologia 652, 49–56.CrossRefGoogle Scholar
Lai, C.H., Morley, S.A., Tan, K.S. and Peck, L.S. (2011) Thermal niche separation in two sympatric tropical intertidal Laternula (Bivalvia: Anomalodesmata). Journal of Experimental Marine Biology and Ecology 405, 68–72.CrossRefGoogle Scholar
Marcus, E. and Marcus, E. (1960) On Hastula cinerea. Boletim da Faculdade de Filosofia, Ciências e Letras, São Paulo (Zoologia) 23, 25–66.CrossRefGoogle Scholar
Manríquez, P.H., Lagos, N.A., Jara, M.E. and Castilla, J.C. (2009) Adaptive shell color plasticity during the early ontogeny of an intertidal keystone snail. Proceedings of the National Academy of Sciences of the United States of America 106, 16298–16303.CrossRefGoogle ScholarPubMed
McLachlan, A. and Brown, A.C. (2006) The ecology of sandy shores. San Diego, CA: Academic Press.Google Scholar
Menge, B.A. and Olson, A.M. (1990) Role of scale and environmental factors in regulation of community structure. Trends in Ecology and Evolution 5, 52–57.CrossRefGoogle ScholarPubMed
Miller, B.A. (1979) The biology of Hastula inconstans (Hinds, 1844) and a discussion of life history similarities among other hastulas of similar proboscis type. Pacific Science 33, 289–306.Google Scholar
Miller, B.A. and Croker, R.A. (1970) Distribution and abundance of an isolated population of Terebra gouldi (Gastropoda: Terebridae) on a Hawaiian subtidal sand flat. Ecology 53, 1120–1126.CrossRefGoogle Scholar
Miller, L.P. and Denny, M.W. (2011) Importance of behavior and morphological traits for controlling body temperature in littorinid snails. Biological Bulletin. Marine Biological Laboratory, Woods Hole 220, 209–223.CrossRefGoogle Scholar
Nybakken, J.W. (1993) Marine biology: an ecological approach. New York: Harper Collins College Publishers.Google Scholar
Ozgo, M. (2005) Cepaea nemoralis (l.) in southeastern Poland: association of morph frequencies with habitat. Journal of Molluscan Studies 71, 93–103.CrossRefGoogle Scholar
Perry, D.M. (1980) Factors influencing aggregation patterns in the sand crab Emerita analoga (Crustacea: Hippidae). Oecologia 45, 379–384.CrossRefGoogle ScholarPubMed
Robinson, B.W. and Wilson, D.S. (1996) Genetic variation and phenotypic plasticity in a trophically polymorphic population of pumpkinseed sunfish (Lepomis gibbosus). Evolutionary Ecology 10, 631–652.CrossRefGoogle Scholar
Rohlf, F.J. (2004) TpsDig, version 1.40. Stony Brook: State University of New York, Department of Ecology and Evolution.Google Scholar
Rohlf, F.J. and Slice, D.E. (1990) Extensions of the Procrustes method for the optimal superimposition of landmarks. Systematic Zoology 39, 40–59.CrossRefGoogle Scholar
Schluter, D. (2000) The ecology of adaptive radition. Oxford: Oxford University Press.CrossRefGoogle Scholar
Silva, V.P.R., Pereira, E.R.R., Azevedo, P.V., Sousa, F.A.S. and Sousa, I.F. (2011) Análise da pluviometria e dias chuvosos na região Nordeste do Brasil. Revista Brasileira de Engenharia Agrícola e Ambiental 15, 131–138.CrossRefGoogle Scholar
Simone, L.R.L. (1999) Comparative morphology and systematics of Brazilian Terebridae (Mollusca, Gastropoda, Conoidea), with descriptions of three new species. Zoosystema 21, 199–248.Google Scholar
Tattersfield, P. (2008) Variation in foot size and shape in some British land snails and its functional significance. Biological Journal of the Linnean Society 36, 365–376.CrossRefGoogle Scholar
Taylor, J.D. (1990) The anatomy of the foregut and relationships in Terebridae. Malacologia 32, 19–34.Google Scholar
Terryn, Y. (2007) A collectors guide to recent Terebridae (Mollusca: Neogastropoda). Hackenheim, Germany and Ghent, Belgium: ConchBooks and NaturalArt.Google Scholar
Trueman, E.R. (1971) The control of burrowing and the migratory behavior of Donax denticulatus (Bivalvia: Tellinacea). Journal of Zoology 165, 453–469.CrossRefGoogle Scholar
Veloso, V.G., Cardoso, R.S. and Fonseca, D.B. (1997) Adaptações e biologia da macrofauna de praias arenosas expostas com ênfase nas espécies da região entre-marés do litoral fluminense. Oecologia Brasiliensis 3, 135–154.CrossRefGoogle Scholar
Wilbur, A.K. and Steneck, R.S. (1999) Polychromatic patterns of Littorina obtusata on Ascophyllum nodosum: are snails hiding in intertidal seaweed? Northeastern Naturalist 6, 189–198.CrossRefGoogle Scholar
Williams, G.A. and Morritt, D. (1995) Habitat partitioning and thermal tolerance in a tropical limpet, Cellana grata. Marine Ecology Progress Series 124, 89–103.CrossRefGoogle Scholar