Abstract
Habitat structure is often assumed to be a predictor of habitat function. However, habitat structure may be insufficient to predict the functional significance of a habitat if the level of resources in the habitat is a consequence of the interaction between the habitat structure and physical or biological factors. In this study, we investigated whether depressions in tidal flat sediments generated by stout razor clams, Tagelus plebeius, affect the spatial patterns of pit digging by deposit-feeding burrowing crabs, Chasmagnathus granulata. The pits dug by crabs while feeding overlapped with clam siphon holes at a frequency higher than expected at random, and measurements of pit-digging by crabs integrated over several days indicated a higher frequency of feeding in the sediment of depressions. The daily frequency of pit-digging by crabs in depressions was positively related to the organic matter content of their sediments, but was significantly higher than the frequency of pit-digging away from clam siphon holes only after events of high bedload sediment transport, when the organic matter in the sediments of these depressions peaked. This example demonstrates the conditional nature of the relationship between habitat structure and function by illustrating how a physical process—bedload sediment transport—may introduce variation in the function that depressions play as feeding sites for burrowing crabs. Published information suggests that such conditional responses of organisms to habitat structure: (1) occur in a variety of habitats; (2) involve a variety of structures either of biotic or abiotic origin; and (3) are the consequence of either physical or biological controls that vary in importance according to the general mechanism through which habitat structure affect resources. This broad experimental evidence suggests that the accuracy of predictive models linking habitat structure and function can be improved by incorporating a mechanistic perspective that allows recognition of the potential for conditional responses of organisms to habitat structure.
Similar content being viewed by others
References
Alpert P (1991) Microtopography as habitat structure for mosses on rocks. In: Bell SS, McCoy ED, Mushinsky HR (eds) Habitat structure: the physical arrangements of objects in space. Chapman and Hall, New York, pp 120–140
Botto F (2001) Efectos directos e indirectos de la bioturbacion producida por el cangrejo cavador Chamagnathus granulata en ambientes estuariales. PhD thesis, Universidad Nacional de Mar del Plata, Mar del Plata, Argentina
Botto F, Iribarne OO (2000) Contrasting effects of two burrowing crabs (Chasmagnathus granulata and Uca uruguayensis) on sediment composition and transport in estuarine environments. Estuar Coast Shelf Sci 51:141–151
Crisp DJ (1971) Energy flow measurements. In: Holme NA, McIntyre AD (eds) Methods for the study of marine benthos. IBP handbook no. 16. Blackwell, Oxford, pp 197–279
Downes BJ, Lake PS, Schreiber ESG, Glaister A (1998) Habitat structure and regulation of local species diversity in a stony, upland stream. Ecol Monogr 68:237–257
Eckman JE, Thistle D (1991) Effects of flow about a biologically produced structure on harpacticoid copepods in San Diego trough. Deep Sea Res 38:1397–1416
Emerson CW (1991) A method for the measurement of bedload sediment transport and passive faunal transport on intertidal sandflats. Estuaries 14:361–371
Gee JM, Warwick RM (1994) Body-size distribution in a marine metazoan community and the fractal dimensions of macroalgae. J Exp Mar Biol Ecol 178:247–259
Griffis RB, Suchanek TH (1991) A model of burrow architecture and trophic modes in thalassinidean shrimp (Decapoda, Thalassinidea). Mar Ecol Prog Ser 79:171–183
Gunnarsson B (1992) Fractal dimension of plants and body size distribution in spiders. Funct Ecol 6:636–641
Gutiérrez JL, Iribarne OO (1998) The occurrence of juveniles of the grapsid crab Chasmagnathus granulata into siphon holes of the stout razor clam Tagelus plebeius. J Shellfish Res 17:925–929
Gutiérrez JL, Iribarne OO (1999) Role of Holocene beds of the stout razor clam Tagelus plebeius in structuring present benthic communities. Mar Ecol Prog Ser 185:213–228
Gutiérrez JL, Jones CG, Strayer DL, Iribarne OO (2003) Mollusks as ecosystem engineers: the role of shell production in aquatic habitats. Oikos 101:79–90
Hacker SD, Steneck RS (1990) Habitat architecture and the abundance and body-size-dependent habitat selection of a phytal-amphipod. Ecology 71:2269–2285
Heck KL, Crowder LB (1991) Habitat structure and predator-prey interactions in vegetated aquatic systems. In: Bell SS, McCoy ED, Mushinsky HR (eds) Habitat structure: the physical arrangements of objects in space. Chapman and Hall, New York, pp 231–299
Holland AF, Dean JM (1977) The biology of the stout razor clam Tagelus plebeius. I. Animal-sediment relationships, feeding mechanism, and community biology. Chesapeake Sci 18:58–66
Iribarne OO, Bortolus A, Botto F (1997) Between-habitat differences in burrow characteristics and trophic modes in the southwestern Atlantic burrowing crab Chasmagnathus granulata. Mar Ecol Prog Ser 155:137–145
Irlandi EA, Peterson CH (1991) Modification of animal habitat by large plants: mechanisms by which seagrasses influence clam growth. Oecologia 87:307–318
Isla FI (1997) Seasonal behavior of Mar Chiquita tidal inlet in relation to adjacent beaches, Argentina. J Coast Res 13:1221–1232
Jones CG, Lawton JH, Shachak M (1994) Organisms as ecosystem engineers. Oikos 69:373–386
Jumars PA (1993) Gourmands of mud: diet selection in marine deposit feeders. In: Hughes RN (ed) Diet selection: an interdisciplinary approach to foraging behaviour. Blackwell, Oxford, pp 124–256
Kohn AJ, Leviten PJ (1976) Effect of habitat complexity on population-density and species richness in tropical intertidal predatory gastropod assemblages. Oecologia 25:199–210
Leonard GH (2000) Latitudinal variation in species interactions: a test in the New England rocky intertidal zone. Ecology 81:1015–1030
Lohse DP (1993) The importance of secondary substratum in a rocky intertidal community. J Exp Mar Biol Ecol 166:1–17
Lopez GR, Levinton JS (1987) Ecology of deposit-feeding animals in marine sediments. Q Rev Biol 62:235–260
Martinetto P (2001) Efecto de los cangrejales sobre el epibentos y organismos que viven en la columna de agua. Licenciado Degree thesis, Universidad Nacional de Mar del Plata, Mar del Plata, Argentina
McCoy ED, Bell SS, Mushinsky HR (1991) Habitat structure: synthesis and perspectives. In: Bell SS, McCoy ED, Mushinsky HR (eds) Habitat structure: the physical arrangements of objects in space. Chapman and Hall, New York, pp 428–430
Morse DR, Lawton JH, Dodson MM, Williamson MH (1985) Fractal dimension of the vegetation and the distribution of arthropod body lengths. Nature 314:731–732
Neter J, Wasserman W, Kutner MH (1991) Applied linear statistical models. Regression, analysis of variance, and experimental designs. Irwin, Homewood, Ill.
Nowell ARM, Jumars PA (1984) Flow environments of aquatic benthos. Annu Rev Ecol Syst 15:303–328
Palmer MA, Ambrose RF, Poff NL (1997) Ecological theory and community restoration ecology. Restor Ecol 5:291–300
Rigg LS, Enright NJ, Perry GLW, Miller BP (2002) The role of cloud combing and shading by isolated trees in the succession from maquis to rain forest in New Caledonia. Biotropica 34:199–210
Sebens KP (1991) Habitat structure and community dynamics in marine benthic systems. In: Bell SS, McCoy ED, Mushinsky HR (eds) Habitat structure: the physical arrangements of objects in space. Chapman and Hall, New York, pp 211–234
Shachak M, Brand S, Gutterman Y (1991) Porcupine disturbances and vegetation pattern along a resource gradient in a desert. Oecologia 88:141–147
Sogard SM, Olla BL (1993) The influence of predator presence on utilization of artificial seagrass habitats by juvenile walleye pollock, Theragra chalcogramma. Environ Biol Fish 37:57–65
Spivak E, Anger K, Luppi T, Bas C, Ismael D (1994) Distribution and habitat preferences in two grapsid crab species in Mar Chiquita Lagoon (Province of Buenos Aires, Argentina). Helgol Meeresunters 48:59–78
Stewart TW, Gafford JC, Miner JG, Lowe RL (1999) Dreissena-shell habitat and antipredator behavior: combined effects on survivorship of snails co-occurring with molluscivorous fish. J N Am Benthol Soc 18:274–283
Stoner AW (2003) What constitutes essential nursery habitat for a marine species? A case study of habitat form and function for queen conch. Mar Ecol Prog Ser 257:275–289
Sun B, Fleeger JW (1994) Field experiments on the colonization of meiofauna into sediment depressions. Mar Ecol Prog Ser 110:167–175
Taniguchi H, Nakano S, Tokeshi M (2003) Influences of habitat complexity on the diversity and abundance of epiphytic invertebrates on plants. Freshw Biol 48:718–728
Underwood AJ (1997) Experiments in ecology: their logical design and interpretation using analysis of variance. Cambridge University Press, Cambridge
Van Blaricom GR (1982) Experimental analysis of structural regulation in a marine sand community exposed to ocean swell. Ecol Monogr 52:283–305
Yager PL, Nowell ARM, Jumars PA (1993) Enhanced deposition to pits: a local food source for benthos. J Mar Res 51:209–236
Yang LH (2000) Effects of body size and plant structure on the movement ability of a predaceous stinkbug, Podisus maculiventris (Heteroptera: Pentatomidae). Oecologia 125:85–90
Zar JH (1984) Biostatistical analysis. Prentice-Hall, Englewood Cliffs, N.J.
Acknowledgements
We thank Gabriela Palomo and Betina Lomovasky for field assistance and Pablo Ribeiro for statistical advice. This article benefited from the critical reading of Mark Bertness, Clive Jones, Gabriela Palomo, Charles Peterson, Pablo Ribeiro, Maria Uriarte, and two anonymous reviewers. This project was supported by grants from Universidad Nacional de Mar del Plata, CONICET, FONDECyT, and Fundación Antorchas. J.L.G. was supported by scholarships from CONICET and this article is part of his Doctoral thesis.
Author information
Authors and Affiliations
Corresponding author
Rights and permissions
About this article
Cite this article
Gutiérrez, J.L., Iribarne, O.O. Conditional responses of organisms to habitat structure: an example from intertidal mudflats. Oecologia 139, 572–582 (2004). https://doi.org/10.1007/s00442-004-1533-3
Received:
Accepted:
Published:
Issue Date:
DOI: https://doi.org/10.1007/s00442-004-1533-3