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Small spatial scale effects of wave action exposure on morphological traits of the limpet Lottia subrugosa

Published online by Cambridge University Press:  27 March 2019

Edson A. Vieira  and
Marília Bueno
Edson A. Vieira*
Affiliation:
Departamento de Biologia Animal, Instituto de Biologia, CP 6109, Universidade Estadual de Campinas – UNICAMP, CEP 13083-970, Campinas, SP, Brazil
Marília Bueno
Affiliation:
Departamento de Biologia Animal, Instituto de Biologia, CP 6109, Universidade Estadual de Campinas – UNICAMP, CEP 13083-970, Campinas, SP, Brazil
*
Author for correspondence: Edson A. Vieira, Email: [email protected]
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Abstract

Many studies have already assessed how wave action may affect morphology of intertidal species among sites that vary in wave exposure, but few attempted to look to this issue in smaller scales. Using the most common limpet of the Brazilian coast, Lottia subrugosa, and assuming position on rocky boulders as a proxy for wave action at small scale, we tested the hypothesis that waves may also influence limpet morphology at a smaller spatial scale by investigating how individual size, foot area and shell shape vary between sheltered and exposed boulder sides on three shores in the coast of Ubatuba, Brazil. Limpets consistently showed a proportionally larger foot on exposed boulder sides for all shores, indicating that stronger attachment is an important mechanism to deal with wave action dislodgement at a smaller scale. Shell shape also varied in the scale investigated here, with more conical (dissipative) shells occurring in exposed boulder sides in one exposed shore across time and in the other exposed shore in one year. Shell shape did not vary regarding boulder sides across time in the most sheltered shore. Although we did not assess large spatial scale effects of wave action in this study, variations of the effect of waves at small spatial scale observed for shell shape suggest that it may be modulated by the local wave exposure regime. Our work highlights the importance of wave action at small spatial scales, and may help to understand the ecological variability of limpets inhabiting rocky shores.

Keywords

Dislodgementenergy dissipationgastropod attachmentrocky shoreshell shape
Type
Research Article
Information
Journal of the Marine Biological Association of the United Kingdom , Volume 99 , Issue 6 , September 2019 , pp. 1309 - 1315
Copyright
Copyright © Marine Biological Association of the United Kingdom 2019 

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Footnotes

*

Current Address: Departamento de Oceanografia e Limnologia, Universidade Federal do Rio Grande do Norte, Av Via Costeira Senador Dinarte Medeiros Mariz, 59014-002, Natal, RN, Brazil.

References

Argüelles, A, Álvarez, F and Alcaraz, G (2009) Shell architecture and its relation to shell occupation by the hermit crab Clibanarius antillensis under different wave action conditions. Scientia Marina 73, 717–723.Google Scholar
Arsenault, DJ, Marchinko, KB and Palmer, AR (2001) Precise tuning of barnacle leg length to coastal wave action. Proceedings of the Royal Society B – Biological Sciences 268, 2149–2154.Google Scholar
Boulding, EG, Holst, M and Pilon, V (1999) Changes in selection on gastropod shell size and thickness with wave-exposure on Northeastern Pacific shores. Journal of Experimental Marine Biology and Ecology 232, 217–239.Google Scholar
Branch, GM (1978) The response of South African patellid limpets to invertebrate predators. Zoologica Africana 13, 221–232.Google Scholar
Branch, GM and Marsh, AC (1978) Tenacity and shell shape in six patella species: adaptive features. Journal of Experimental Marine Biology and Ecology 34, 111–130.Google Scholar
Branch, GM and Odendaal, F (2003) The effects of marine protected areas on the population dynamics of a South African limpet, Cymbula oculus, relative to the influence of wave action. Biological Conservation 114, 255–269.Google Scholar
Brown, KM and Quinn, JF (1988) The effect of wave action on growth in three species of intertidal gastropods. Oecologia 75, 420–425.Google Scholar
Burrows, MT, Harvey, R and Robb, L (2008) Wave exposure indices from digital coastlines and the prediction of rocky shore community structure. Marine Ecology Progress Series 353, 1–12.Google Scholar
Carstens, T (1968) Wave forges on boundaries and submerged surfaces. Sarsia 34, 37–60.Google Scholar
Chapman, MG (1997) Relationships between shell shape, water reserves, survival and growth of high shore littorinids under experimental conditions in New South Wales, Australia. Journal of Molluscan Studies 63, 511–529.Google Scholar
Christofoletti, RA, Takahashi, CK, Oliveira, DN and Flores, AAV (2011) Abundance of sedentary consumers and sessile organisms along the wave exposure gradient of subtropical rocky shores of the south-west Atlantic. Journal of the Marine Biological Association of the United Kingdom 91, 961–967.Google Scholar
Cook, SB (1971) A study of homing behavior in the limpet Siphonaria alternata. Biological Bulletin 141, 449–457.Google Scholar
Cusson, M and Bourget, E (1997) Influence of topographic heterogeneity and spatial scales on the structure of the neighbouring intertidal endobenthic macrofaunal community. Marine Ecology Progress Series 150, 181–193.Google Scholar
Dayton, PK (1971) Competition, disturbance, and community organization: the provision and subsequent utilization of space in a rocky intertidal community. Ecological Monographs 41, 351–389.Google Scholar
Denny, MW (1985) Wave forces on intertidal organisms: a case study. Limnology and Oceanography 30, 1171–1187.Google Scholar
Denny, MW (1995) Predicting physical disturbance: mechanistic approaches to the study of survivorship on wave-swept shores. Ecological Monographs 65, 371–418.Google Scholar
Denny, MW (2000) Limits to optimization: fluid dynamics, adhesive strength and the evolution of shape in limpet shells. Journal of Experimental Biology 203, 2603–2622.Google Scholar
Denny, MW (2006) Ocean waves, nearshore ecology, and natural selection. Aquatic Ecology 40, 439–461.Google Scholar
Denny, MW and Blanchette, CA (2000) Hydrodynamics, shell shape, behavior and survivorship in the owl limpet Lottia gigantea. Journal of Experimental Biology 203, 2623–2639.Google Scholar
Denny, MW, Daniel, TL and Koehl, MAR (1985) Mechanical limits to size in wave-swept organisms. Ecological Monographs 55, 69–102.Google Scholar
Etter, RJ (1988) Asymmetrical developmental plasticity in an intertidal snail. Evolution 42, 322–334.Google Scholar
Fenberg, PB (2013) Intraspecific home range scaling: a case study from the owl limpet (Lottia gigantea). Evolutionary Ecology Research 15, 103–110.Google Scholar
Frid, CLJ and Fordham, E (1994) The morphology of the sub-littoral gastropod Gibbula cineraria (L.) along a gradient of wave action. Ophelia 40, 135–146.Google Scholar
Gray, DR and Hodgson, AN (1998) Foraging and homing behavior in the high-shore, crevice-dwelling limpet Helcion pectunculus (Prosobranchia: Patellidae). Marine Biology 132, 283–294.Google Scholar
Gibbs, PE (1993) Phenotypic changes in the progeny of Nucella lapillus (Gastropoda) transplanted from an exposed shore to sheltered inlets. Journal of Molluscan Studies 59, 187–194.Google Scholar
Grahame, J and Mill, PJ (1986) Relative size of the foot of two species of Littorina on a rocky shore in Wales. Journal of Zoology 208, 229–236.Google Scholar
Guichard, F and Bourget, E (1998) Topographic heterogeneity, hydrodynamics, and benthic community structure: a scale-dependent cascade. Marine Ecology Progress Series 171, 59–70.Google Scholar
Harley, CDG, Denny, MW, Mach, KJ and Miller, LP (2009) Thermal stress and morphological adaptations in limpets. Functional Ecology 23, 292–301.Google Scholar
Hartnoll, RG and Wright, JR (1977) Foraging movements and homing in the limpet Patella vulgata L. Animal Behavior 25, 806–810.Google Scholar
Hayne, KJR and Palmer, AR (2013) Intertidal sea stars (Pisaster ochraceus) alter body shape in response to wave action. Journal of Experimental Biology 216, 1717–1725.Google Scholar
Hobday, A (1995) Body-size variation exhibited by an intertidal limpet: influence of wave exposure, tidal height and migratory behavior. Journal of Experimental Marine Biology and Ecology 189, 29–45.Google Scholar
Hollander, J and Butlin, RK (2010) The adaptive value of phenotypic plasticity in two ecotypes of a marine gastropod. BMC Evolutionary Biology 10, 333.Google Scholar
Iwasaki, K (1993) Analysis of limpet defense and predator offense in the field. Marine Biology 116, 277–289.Google Scholar
Iwasaki, K (1999) Short- and long-term movements of the patellid limpet Patella flexuosa within gaps in intertidal mussel beds. Journal of Molluscan Studies 65, 295–301.Google Scholar
Joseph, S, Vakani, B and Kundu, R (2018) Molecular phylogenetic study on few morphotypes of a patellogastropod Cellana karachiensis from northern Arabian Sea reveals unexpected genetic diversity. Mitochondrial DNA Part A 29, 181–191.Google Scholar
Kitching, JA (1976) Distribution and changes in shell form of Thais spp. (Gastropoda) near Bamfield, B.C. Journal of Experimental Marine Biology and Ecology 23, 109–126.Google Scholar
Lowell, RB (1987) Safety factors of tropical vs temperate limpet shells: multiple selection pressures on a single structure. Evolution 41, 638–650.Google Scholar
Machado, GEM, Nassar, CAG and Széchy, MTM (2011) Flora ficológica da região sublitorânea rasa de costões rochosos do Núcleo Picinguaba, Parque Estadual da Serra do mar, Ubatuba, São Paulo. Acta Botanica Brasilica 25, 71–82.Google Scholar
Martinez, MM (2001) Running in the surf: hydrodynamics of the shore crab Grapsus tenuicrustatus. Journal of Experimental Biology 204, 3097–3112.Google Scholar
Miller, SL (1974) Adaptive design of locomotion and foot form in prosobranch gastropods. Journal of Experimental Marine Biology and Ecology 14, 99–156.Google Scholar
Paine, RT and Levin, SA (1981) Intertidal landscapes: disturbance and the dynamics of pattern. Ecological Monographs 51, 145–178.Google Scholar
Pais, A, Azurro, E and Guidetti, P (2007) Spatial variability of fish fauna in sheltered and exposed shallow rocky reefs from a recently established Mediterranean Marine Protected Area. Italian Journal of Zoology 74, 277–287.Google Scholar
Paresque, K, Alves, MM, Stein, EM and Gonçalves, JLO (2007) Avaliação do comportamento de homing em Collisella subrugosa (Orbigore, 1846) (Mollusca: Archaeogastropoda). Proceedings of the VIII Congresso de Ecologia do Brasil, Caxambu, 23–28 September 2007.Google Scholar
Paula, EJ and Oliveira-Filho, EC (1982) Wave exposure and ecotypical differentiation in Sargassum cymosum (Phaeophyta – Fucales). Phycologia 21, 145–153.Google Scholar
Raffaelli, D and Hawkins, S (1996) Intertidal Ecology. London: Chapman and Hall, 356 pp.Google Scholar
Rios, EC (2009) Compendium of Brazilian Sea Shells. Rio Grande do Sul: Evangraf.Google Scholar
Rosário, NA and Ourives, TMS (2007) Estudo preliminar do comportamento de ‘homing’ de Collisella subrugosa (Gastropoda: Acmaeidae) na Praia do Pé da Serra, Uruçuca, BA, Brasil. Proceedings of the VIII Congresso de Ecologia do Brasil, Caxambu, 23–28 September 2007.Google Scholar
Sebastián, CR, Steffani, CN and Branch, GM (2002) Homing and movement patterns of a South African limpet Scutellastra argenvillei in an area invaded by an alien mussel Mytilus galloprovincialis. Marine Ecology Progress Series 243, 111–122.Google Scholar
Silva, ACF, Hawkins, SJ, Boaventura, DM, Brewster, E and Thompson, RC (2010) Use of the intertidal zone by mobile predators: influence of wave exposure, tidal phase and elevation on abundance and diet. Marine Ecology Progress Series 406, 197–210.Google Scholar
Somero, GN (2002) Thermal physiology and vertical zonation of intertidal animals: optima, limits, and costs of living. Integrative and Comparative Biology 42, 780–789.Google Scholar
Steffani, CN and Branch, GM (2003) Growth rate, condition, and shell shape of Mytilus galloprovincialis: responses to wave exposure. Marine Ecology Progress Series 246, 197–209.Google Scholar
Széchy, MTM and Paula, EJ (2000) Padrões estruturais quantitativos de bancos de Sargassum (phaeophyta, Fucales) do litoral dos estados do Rio de Janeiro e São Paulo, Brasil. Revista Brasileira de Botânica 23, 121–132.Google Scholar
Tanaka, MO and Magalhães, CA (2002) Edge effects and succession dynamics in Brachidontes mussel beds. Marine Ecology Progress Series 237, 151–158.Google Scholar
Tanaka, MO, Duque-Estrada, TEM and Magalhães, CA (2002) Dynamics of the acmaeid limpet Collisella subrugosa and vertical distribution of size and abundance along a wave exposure gradient. Journal of Molluscan Studies 68, 55–64.Google Scholar
Teske, PR, Barker, NP and McQuaid, CD (2007) Lack of genetic differentiation among four sympatric southeast African intertidal limpets (Siphonariidae): phenotypic plasticity in a single species? Journal of Molluscan Studies 73, 223–228.Google Scholar
Trussell, GC (1997) Phenotypic selection in an intertidal snail: effects of a catastrophic storm. Marine Ecology Progress Series 151, 73–79.Google Scholar
Trussell, GC, Johnson, AS, Rudolph, SG and Gilfillan, ES (1993) Resistance to dislodgement: habitat and size-specific differences in morphology and tenacity in an intertidal snail. Marine Ecology Progress Series 100, 135–144.Google Scholar
Underwood, AJ (1997) Experiments in Ecology: Their Logical Design and Interpretation Using Analysis of Variance. Cambridge: Cambridge University Press, 504 pp.Google Scholar