Epibiont and basibiont relationships can have positive and negative effects on both organisms involved, ranging in intensity from minor to major effects. Limpets of species Lottia pelta are commonly found with two algal species growing on their backs, Ulva lactuca and Acrosiphonia spp. Previous research has shown that basibionts (substrate organism) and epibionts (organism growing on the surface) have complex interactions that can be positive, negative, or neutral. A force transducer and flume were used to measure the drag forces experienced by a limpet at various water velocities. Presence of either epiphyte significantly increased limpet drag. Acrosiphonia produced a greater drag effect than U. lactuca, increasing the force substantially. When dropped in a tank, limpets with algal growth landed foot-down significantly more often than limpets without algal growth. Acrosiphonia spp. had a greater effect than Ulva lactuca. Lastly, limpets in a wind tunnel with algal growth (especially Acrosiphonia) had cooler body temperatures than limpets without algal growth. In conclusion, the effects on the basibiont of this relationship were found to be both positive and negative. 1. Introduction In the rocky intertidal environment, primary space is often a limiting resource. Because of this, many organisms have developed a life-history strategy of growing on the surface of another organism. The basibiont (substrate organism) and the epibiont (organism growing on the surface) often have complex direct and indirect interspecific associations [1]. The effects of epibionts on the basibiont may show positive, neutral, or negative consequences [1–4]. The mechanical effects of epizoic growth are of particular concern for the basibiont in a marine system. Hydrodynamic effects of epibionts have been well studied in a number of epibiont-basibiont systems. Epibionts may increase drag and lift in environments with high water flow, such as wave-swept intertidal zones [5]. Mytilus byssus receives a 2- to 6.7-fold increase in stress induced by drag forces from epibiotic kelp [6]. Epibiotic algae on Mytilus mussels increased dislodgement during storms, regardless of the size of the algae [4]. Indeed, mussel dislodgment due to algae may be more important than predation in certain systems [6, 7]. Hydrodynamic effects on the basibiont are not the only possible negative impacts of epizoic organisms. In Littorina littorea, for instance, the presence of barnacles growing on the shell causes an increase in the snail’s volume and weight and a decrease in the locomotionspeed and
References
[1]
M. Wahl, “Marine epibiosis.1. Fouling and antifouling: some basic aspects,” Marine Ecology, vol. 58, pp. 175–189, 1989.
[2]
J. D. Witman and T. H. Suchanek, “Mussels in flow: drag and dislodgement by epizoans,” Marine Ecology, vol. 16, pp. 259–268, 1984.
[3]
C. Buschbaum and K. Reise, “Effects of barnacle epibionts on the periwinkle Littorina littorea (L.),” Helgoland Marine Research, vol. 53, no. 1, pp. 56–61, 1999.
[4]
N. E. O'Connor, T. P. Crowe, and D. McGrath, “Effects of epibiotic algae on the survival, biomass and recruitment of mussels, Mytilus L. (Bivalvia: Mollusca),” Journal of Experimental Marine Biology and Ecology, vol. 328, no. 2, pp. 265–276, 2006.
[5]
M. W. Denny, “Lift as a mechanism of patch initiation in mussel beds,” Journal of Experimental Marine Biology and Ecology, vol. 113, no. 3, pp. 231–245, 1987.
[6]
J. D. Witman, “Subtidal coexistence: storms, grazing, mutualism, and the zonation of kelps and mussels,” Ecological Monographs, vol. 57, no. 2, pp. 167–187, 1987.
[7]
A. A. Lachance, B. Myrand, R. Tremblay, V. Koutitonsky, and E. Carrington, “Biotic and abiotic factors influencing attachment strength of blue mussels Mytilus edulis in suspended culture,” Aquatic Biology, vol. 2, no. 2, pp. 119–129, 2008.
[8]
E. C. Bell and J. M. Gosline, “Strategies for life in flow: tenacity, morphometry, and probability of dislodgment of two Mytilus species,” Marine Ecology, vol. 159, pp. 197–208, 1997.
[9]
M. W. Denny and C. A. Blanchette, “Hydrodynamics, shell shape, behavior and survivorship in the owl limpet Lottia gigantea,” Journal of Experimental Biology, vol. 203, no. 17, pp. 2623–2639, 2000.
[10]
G. K. Ellem, J. E. Furst, and K. D. Zimmerman, “Shell clamping behaviour in the limpet Cellana tramoserica,” Journal of Experimental Biology, vol. 205, no. 4, pp. 539–547, 2002.
[11]
F. P. Lima and D. S. Wethey, “Robolimpets: measuring intertidal body temperatures using biomimetic loggers,” Limnology and Oceanography, vol. 7, pp. 347–353, 2009.
[12]
W. G. Wright and J. W. Nybakken, “Effect of wave action on movement in the owl limpet, Lottia gigantea, in Santa Cruz, California,” Bulletin of Marine Science, vol. 81, no. 2, pp. 235–244, 2007.
[13]
R. B. Lowell, “Crab predation on limpets—predator behavior and defensive features of the shell morphology of the prey,” Biological Bulletin, vol. 171, pp. 577–596, 1986.
[14]
J. R. Voight and J. D. Sigwart, “Scarred limpets at hydrothermal vents: evidence of predation by deep-sea whelks,” Marine Biology, vol. 152, no. 1, pp. 129–133, 2007.
[15]
M. W. Denny, “Limits to optimization: fluid dynamics, adhesive strength and the evolution of shape in limpet shells,” Journal of Experimental Biology, vol. 203, no. 17, pp. 2603–2622, 2000.
[16]
M. R. Evans and G. A. Williams, “Time partitioning of foraging in the limpet Patella vulgata,” Journal of Animal Ecology, vol. 60, no. 2, pp. 563–575, 1991.
[17]
C. D. G. Harley, M. W. Denny, K. J. MacH, and L. P. Miller, “Thermal stress and morphological adaptations in limpets,” Functional Ecology, vol. 23, no. 2, pp. 292–301, 2009.
[18]
M. W. Denny, L. P. Miller, and C. D. G. Harley, “Thermal stress on intertidal limpets: long-term hindcasts and lethal limits,” Journal of Experimental Biology, vol. 209, no. 13, pp. 2420–2431, 2006.
[19]
M. Wahl, “Fouled snails in flow: potential of epibionts on Littorina littorea to increase drag and reduce snail growth rates,” Marine Ecology, vol. 138, no. 1–3, pp. 157–168, 1996.
[20]
L. Tomanek and B. Helmuth, “Physiological ecology of rocky intertidal organisms: a synergy of concepts,” Integrative and Comparative Biology, vol. 42, no. 4, pp. 771–775, 2002.
[21]
M. W. Denny, “Wave forces on intertidal organisms: a case study,” Limnology and Oceanography, vol. 30, no. 6, pp. 1171–1187, 1985.
[22]
F. J. Hidalgo, F. N. Firstater, B. J. Lomovasky, P. Gallegos, P. Gamero, and O. O. Iribarne, “Macroalgal fouling on the intertidal mole crab Emerita analoga facilitates bird predation,” Helgoland Marine Research, vol. 64, no. 4, pp. 367–376, 2010.
[23]
M. Wahl, “Ecological lever and interface ecology: epibiosis modulates the interactions between host and environment,” Biofouling, vol. 24, no. 6, pp. 427–438, 2008.