Skip to main content

Advertisement

Log in

Body and resource size at the land–sea interface

  • Research Article
  • Published:
Marine Biology Aims and scope Submit manuscript

Abstract

Body size in animals varies with many parameters, amongst them taxonomic affiliation, lifestyle and ambient environment oxygen levels. Size has considerable implication to possibilities for animals; for example, parasites need to be small and top predators large. Body size and resource requirements (shell size) were investigated across the land–sea interface in hermit crabs (Crustacea: Malacostraca: Decapoda) and snails (Mollusca: Gastropoda: Prosobranchia). These are two of the few taxa to occur in the sea, on the shore and on land as residents. Both taxa are also appropriate for such an analysis as they are abundant, speciose, cohabit the same environments and are linked—gastropod shells are a critical resource to hermit crabs. Both the maximum and mean sizes of hermit crab species showed parabolic relationships with shore height, decreasing from the sublittoral and supralittoral to the eulittoral. Average maximum size of gastropods exhibited a similar intertidal minimum although variability was high. It is suggested that this pattern is robust: not only did two distantly related taxa show the same pattern, but neither region nor site contributed significantly to total variability. The mass of resources (gastropod shells) used by hermit crabs, however, showed a converse pattern. The smallest shells (relative to hermit crab body size) were used in the sublittoral and supralittoral. Response to environmental stress and predation pressure are offered as two alternate theories to explain the observed body dwarfism and resource gigantism in the intertidal zone.

This is a preview of subscription content, log in via an institution to check access.

Access this article

Price excludes VAT (USA)
Tax calculation will be finalised during checkout.

Instant access to the full article PDF.

Fig. 1
Fig. 2
Fig. 3
Fig. 4a, b

Similar content being viewed by others

References

  • Anderson RP, Handley CO (2002) Dwarfism in insular sloths: biogeography, selection and evolutionary rate. Evolution 56:1045–1058

    PubMed  Google Scholar 

  • Atkinson D, Sibley RM (1997) Why are organisms usually bigger in colder environments? Making sense of a life history puzzle. Trends Ecol Evol 12:235–239

    Article  Google Scholar 

  • Barnes DKA (1997) Ecology of tropical hermit crabs at Quirimba Island, Mozambique: distribution, abundance and activity. Mar Ecol Prog Ser 154:133–142

    Google Scholar 

  • Barnes DKA (1999) Ecology of tropical hermit crabs at Quirimba Island, Mozambique: shell characteristics and utilisation. Mar Ecol Prog Ser 183:241–251

    Google Scholar 

  • Barnes DKA, Arnold RJ (2001) Competition, sublethal mortality and diversity on Southern Ocean coastal boulder communities. Polar Biol 24:447–454

    Article  Google Scholar 

  • Barnes DKA, DeGrave S (2002) Temporospatial constraints in resources available to and used by hermit crabs: tests of models. Funct Ecol 16:714–726

    Article  Google Scholar 

  • Barnes RSK (1973) The intertidal lamellibranchs of Southampton Water, with particular reference to Cerastoderma edule and C. glaucum. Proc Malacol Soc Lond 40:413–433

    Google Scholar 

  • Bell JJ, Barnes DKA, Turner J (2002) The importance of macro- and micro-morphological variation in the adaptation of a sublittoral demosponge to current extremes. Mar Biol 140:75–81

    Article  Google Scholar 

  • Bertness MD (1982) Shell utilization, predation pressure, and thermal stress in Panamanian hermit crabs: an interoceanic comparison. J Exp Mar Biol Ecol 64:159–187

    Article  Google Scholar 

  • Borjesson DL, Szelistowski WA (1989) Shell selection, utilization and predation in the hermit crab Clibanarius panamensis Stimpson in a tropical mangrove estuary. J Exp Mar Biol Ecol 133:213–228

    Article  Google Scholar 

  • Burness GP, Diammond J, Flannery T (2001) Dinosaurs, dragons and dwarfs: the evolution of maximal body size. Proc Natl Acad Sci 98:14518–14523

    Article  CAS  PubMed  Google Scholar 

  • Chapelle G, Peck LS (1999) Polar gigantism dictated by oxygen availability. Nature 399:114–115

    Article  CAS  Google Scholar 

  • Damuth J (1993) Cope’s rule, the island rule and the scaling of mammalian population density. Nature 365:748–750

    Article  CAS  PubMed  Google Scholar 

  • De Boer WF (1999) Between the tides. Universal Press, Veenedaal, The Netherlands

  • Foster JB (1964) Evolution of mammals on islands. Nature 202:234–235

    Google Scholar 

  • Garrity SD (1984) Some adaptations of gastropods to physical stress on a tropical rocky shore. Ecology 65:559–574

    Google Scholar 

  • Hazlett BA (1981) The behavioural ecology of hermit crabs. Annu Rev Ecol Syst 12:1–22

    Article  Google Scholar 

  • Helmuth B (1999) Thermal ecology of rocky intertidal mussels: quantifying body temperatures using climatological data. Ecology 80:15–34

    Google Scholar 

  • Hoffman GE (1999) Ecologically relevant variation in induction and function of heat shock proteins in marine organisms. Am Zool 39:889–900

    Google Scholar 

  • Hoffman GE, Somero GN (1999) Evidence for protein damage at environmental temperatures: seasonal changes in levels of ubiquitin conjugates and Hsp70 in the intertidal mussel, Mytilus trosulus. J Exp Biol 198:1509–1518

    Google Scholar 

  • Ishimatsu A, Hishida Y, Takita T, Kanda T, Oikawa S, Takeda T, Huat KK (1998) Mudskippers store air in their burrows. Nature 391:237–238

    Article  CAS  Google Scholar 

  • Jensen K (1970) The interaction between Pagurus bernhardus (L.) and Hydractinia echinata (Fleming). Ophelia 8:135–144

    Google Scholar 

  • Kellogg CW (1976) Gastropod shells: a potentially limiting resource for hermit crabs. J Exp Mar Biol Ecol 22:101–111

    Article  Google Scholar 

  • Kreutzer U, Siegmund B, Grieshaber MK (1985) Role of coupled substrates and alternative end products in hypoxia tolerance of marine invertebrates. Mol Physiol 8:371–392

    CAS  Google Scholar 

  • Leite FPP, Turra A, Gandolfi SM (1998) Hermit crabs (Crustacea: Decapoda: Anomura), gastropod shells and environmental structure: their relationship in southeastern Brazil. J Nat Hist 32:1599–1608

    Google Scholar 

  • Maughan B, Barnes DKA (2000) A ‘minimum stress inflexion’ in relation to environmental and biological influences on the dynamics of subtidal encrusting communities. Hydrobiologia 440:101–109

    Article  Google Scholar 

  • McGuiness KA (1990) Physical variability, diversity gradients and the ecology of temperate and tropical reefs. Aust J Ecol 15:465–476

    Google Scholar 

  • Palmer (2002)

  • Peck LS (1993) The tissues of articulate brachiopods and their value to predators. Philos Trans R Soc Lond B Biol Sci339:17–32

    Google Scholar 

  • Pörtner HO, Kreutzer U, Siegmund B, Heisler N, Grieshaber MK (1984) Metabolic adaptations of the intertidal worm Sipunculus nudus to functional and environmental hypoxia. Mar Biol 79:237–247

    Google Scholar 

  • Remane A (1934) Die Brackwasserfauna. Verh Dtsch Zool Ges 36:34–74

    Google Scholar 

  • Turra A, Leite FPP (2001) Shell utilisation patterns of a tropical rocky intertidal hermit crab assemblage. 1. The case of Grande Beach. J Crustac Biol 21:393–406

    Google Scholar 

  • Vermeij GJ (1976) Interoceanic differences in vulnerability of shelled prey to crab predation. Nature 260:135–136

    Google Scholar 

  • Williams JD, McDermott JJ (2004) Hermit crab biocenoses: a worldwide review of the diversity and natural history of hermit crab associates. J Exp Mar Biol Ecol 305:1–128

    Article  Google Scholar 

  • Zipser E, Vermeij GJ (1978) Crushing behaviour of tropical and temperate crabs. J Exp Mar Biol Ecol 31:155–172

    Article  Google Scholar 

Download references

Acknowledgements

I would like to thank Dr P. Convey, Professor L. Peck and two anonymous referees for comments leading to an improved manuscript.

Author information

Authors and Affiliations

Authors

Corresponding author

Correspondence to D. K. A. Barnes.

Additional information

Communicated by J.P. Thorpe, Port Erin

Rights and permissions

Reprints and permissions

About this article

Cite this article

Barnes, D.K.A. Body and resource size at the land–sea interface. Marine Biology 146, 625–632 (2005). https://doi.org/10.1007/s00227-004-1451-2

Download citation

  • Received:

  • Accepted:

  • Published:

  • Issue Date:

  • DOI: https://doi.org/10.1007/s00227-004-1451-2

Keywords

Navigation