Skip to main content
Log in

Background and temperature effects on Uca panacea color change

  • Original Paper
  • Published:
Marine Biology Aims and scope Submit manuscript

Abstract

Organismal coloration is used for communication, camouflage, and thermoregulation. These functions of body coloration may impose conflicting demands upon color-changing organisms. Here, we examined interacting thermoregulatory and camouflage color change responses when fiddler crabs Uca panacea were subject to simultaneously changing temperatures (10, 25, 40 °C) and backgrounds (black, white). Crab coloration lightened on a white background and at high temperatures and darkened on a black background and at low temperatures, reflecting the camouflage and thermoregulatory functions of color change. Synergistic background and temperature treatments (i.e., hot/white or cold/black) induced strong color change responses. When temperature and background were in conflict (i.e., hot/black or cold/white), responses to background coloration constrained thermoregulatory color change such that carapace coloration did not change. Such conflicts are likely to be common in nature, especially in highly heterogeneous environments. Throughout the experiment, males remained lighter than females and showed a greater response to the hot/white treatment, driven by a stronger response to high temperatures. These differences may reflect the physiological, morphological, and behavioral differences associated with sexual selection and sexual dimorphism in this species.

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

Similar content being viewed by others

References

  • Allen BJ (2007) Costs of sexual selection in the sand fiddler crab, Uca pugilator. Ph.D. Dissertation, Stony Brook, New York

  • Barnwell FH, Thurman CL (1984) Taxonomy and biogeography of the fiddler crabs (Ocypodidae: Genus Uca) of the Atlantic and Gulf coasts of eastern North America. Zool J Linn Soc 81:23–87

    Article  Google Scholar 

  • Bildstein KL, McDowell SG, Brisbin IL (1989) Consequences of sexual dimorphism in sand fiddler crabs, Uca pugilator: differential vulnerability to avian predation. Anim Behav 37:133–139

    Article  Google Scholar 

  • Brown FA, Sandeen MI (1948) Responses of the chromatophores of the fiddler crab, Uca, to light and temperature. Physiol Zool 21:361–371

    Google Scholar 

  • Campbell GS, Norman JM (1998) Introduction to environmental biophysics. Springer, New York

    Book  Google Scholar 

  • Caravello HE, Cameron GN (1987a) The effects of sexual selection on the foraging behavior of the Gulf Coast fiddler crab Uca panacea. Anim Behav 35:1864–1874

    Article  Google Scholar 

  • Caravello HE, Cameron GN (1987b) Foraging time allocation in relation to sex by the Gulf Coast fiddler crab Uca panacea. Oecologia 72:123–126

    Article  Google Scholar 

  • Caravello HE, Cameron GN (1991) Time activity budgets of the Gulf Coast fiddler crab Uca panacea. Am Midl Nat 126:403–407

    Article  Google Scholar 

  • Chiao C-C, Hanlon RT (2001) Cuttlefish cue visually on area, not shape or aspect ratio, of light objects in the substrate to produce disruptive body patterns for camouflage. Biol Bull 201:269–270

    Article  CAS  Google Scholar 

  • Christy JH, Backwell PRY, Goshima S, Kreuter T (2002) Sexual selection for structure building by courting male fiddler crabs: an experimental study of behavioral mechanisms. Behav Ecol 13:366–374

    Article  Google Scholar 

  • Clusella-Trullas S, Terblanche JS, Blackburn TM, Chown SL (2008) Testing the thermal melanism hypothesis: a macrophysiological approach. Funct Ecol 22:232–238

    Article  Google Scholar 

  • Couldridge VCK, Alexander GJ (2002) Color patterns and species recognition in four closely related species of Lake Malawi cichlid. Behav Ecol 13:59–64

    Article  Google Scholar 

  • Crane J (1975) Fiddler crabs of the world (Ocypodidae: genus Uca). Princeton University Press, Princeton

    Google Scholar 

  • Croll GA, McClintock JB (2000) An evaluation of lekking behavior in the fiddler crab Uca spp. J Exp Mar Biol Ecol 254:109–121

    Article  Google Scholar 

  • Crothers L, Gering E, Cummings M (2011) Aposematic signal variation predicts male–male interactions in a polymorphic poison frog. Evolution 65:599–605

    Article  Google Scholar 

  • Cummings ME, Jordao JM, Cronin TW, Oliveira RF (2008) Visual ecology of the fiddler crab, Uca tangeri: effects of sex, viewer and background on conspicuousness. Anim Behav 75:175–188

    Article  Google Scholar 

  • Cuthill IC, Stevens M, Sheppard J, Maddocks T, Parraga CA, Troscianko TS (2005) Disruptive coloration and background pattern matching. Nature 434:72–74

    Article  CAS  Google Scholar 

  • Darnell MZ (2012) Ecological physiology of the circadian pigmentation rhythm in the fiddler crab Uca panacea. J Exp Mar Biol Ecol 426–427:39–47

    Article  Google Scholar 

  • Darnell MZ, Munguia P (2011) Thermoregulation as an alternate function of the sexually dimorphic fiddler crab claw. Am Nat 178:419–428

    Article  Google Scholar 

  • Darnell MZ, Fowler KK, Munguia P (2013) Sex-specific thermal constraints on fiddler crab behavior. Behav Ecol. doi:10.1093/beheco/art006

  • Detto T (2007) The fiddler crab Uca mjoebergi uses colour vision in mate choice. Proc R Soc B-Biol Sci 274:2785–2790

    Article  Google Scholar 

  • Detto T, Backwell PRY (2009) The fiddler crab Uca mjoebergi uses ultraviolet cues in mate choice but not aggressive interactions. Anim Behav 78:407–411

    Article  Google Scholar 

  • Detto T, Backwell PRY, Hemmi JM, Zeil J (2006) Visually mediated species and neighbour recognition in fiddler crabs (Uca mjoebergi and Uca capricomis). Proc R Soc B-Biol Sci 273:1661–1666

    Article  Google Scholar 

  • Detto T, Hemmi JM, Backwell PRY (2008) Colouration and colour changes of the fiddler crab, Uca capricornis: a descriptive study. PLoS ONE 3:e1629

    Article  Google Scholar 

  • Fleishman LJ, Leal M, Sheehan J (2006) Illumination geometry, detector position and the objective determination of animal signal colours in natural light. Anim Behav 71:463–474

    Article  Google Scholar 

  • Fletcher DJ, Underwood AJ (2002) How to cope with negative estimates of components of variance in ecological field studies. J Exp Mar Biol Ecol 273:89–95

    Article  Google Scholar 

  • Garcia TS, Sih A (2003) Color change and color-dependent behavior in response to predation risk in the salamander sister species Ambystoma barbouri and Ambystoma texanum. Oecologia 137:131–139

    Article  Google Scholar 

  • Godin J-GJ, McDonough HE (2003) Predator preference for brightly colored males in the guppy: a viability cost for a sexually selected trait. Behav Ecol 14:194–200

    Article  Google Scholar 

  • Guilford T (1988) The evolution of conspicuous coloration. Am Nat 131:S7–S21

    Article  Google Scholar 

  • Haskell DG (1996) Do bright colors at nests incur a cost due to predation? Evol Ecol 10:285–288

    Article  Google Scholar 

  • Heinen JT (1994) The significance of color change in newly metamorphosed American toads (Bufo a. americanus). J Herpetol 28:87–93

    Article  Google Scholar 

  • Hemmi JM, Marshall J, Pix W, Vorobyev M, Zeil J (2006) The variable colours of the fiddler crab Uca vomeris and their relation to background and predation. J Exp Biol 209:4140–4153

    Article  Google Scholar 

  • King RB, Hauff S, Phillips JB (1994) Physiological color change in the green tree frog: responses to background brightness and temperature. Copeia 1994:422–432

    Article  Google Scholar 

  • Koga T, Backwell PRY, Christy JH, Murai M, Kasuya E (2001) Male-biased predation of a fiddler crab. Anim Behav 62:201–207

    Article  Google Scholar 

  • Marshall NJ (2000) Communication and camouflage with the same ‘bright’ colours in reef fishes. Philos Trans R Soc Lond B Biol Sci 355:1243–1248

    Article  CAS  Google Scholar 

  • Merilaita S (1998) Crypsis through disruptive coloration in an isopod. Proc R Soc Lond B Biol Sci 265:1059–1064

    Article  Google Scholar 

  • Munguia P, Levinton JS, Silbiger NJ (2013) Latitudinal differences in thermoregulatory color change in Uca pugilator. J Exp Mar Biol Ecol 440:8–14

    Article  Google Scholar 

  • Norris KS (1967) Color adaptation in desert reptiles and its thermal relationships. In: Milstead WW (ed) Lizard ecology- a symposium. University of Missouri Press, Columbia, pp 162–229

    Google Scholar 

  • O’Connor KI, Metcalfe NB, Taylor AC (1999) Does darkening signal submission in territorial contests between juvenile Atlantic salmon, Salmo salar? Anim Behav 58:1269–1276

    Article  Google Scholar 

  • Patterson HD, Thompson R (1971) Recovery of inter-block information when block sizes are unequal. Biometrika 58:545–554

    Article  Google Scholar 

  • Pope DS (2000) Testing function of fiddler crab claw waving by manipulating social context. Behav Ecol Sociobiol 47:432–437

    Article  Google Scholar 

  • Porter WP (1967) Solar radiation through the living body walls of vertebrates with emphasis on desert reptiles. Ecol Monogr 37:274–296

    Article  Google Scholar 

  • Powers LW (1975) Fiddler crabs in a nontidal environment. Contrib Mar Sci 19:67–78

    Google Scholar 

  • Powers LW, Cole JF (1976) Temperature variation in fiddler crab microhabitats. J Exp Mar Biol Ecol 21:141–157

    Article  Google Scholar 

  • Rao KR (1985) Pigmentary effectors. In: Bliss DE, Mantel LH (eds) The biology of crustacea integuments, pigments, and hormonal processes. Academic Press, New York, pp 395–462

    Google Scholar 

  • Rodrigues RR, Carvalho LN, Zuanon J, Del-Claro K (2009) Color changing and behavioral context in the Amazonian dwarf cichlid Apistogramma hippolytae (Perciformes). Neotrop Ichthyol 7:641–646

    Article  Google Scholar 

  • Silbiger N, Munguia P (2008) Carapace color change in Uca pugilator as a response to temperature. J Exp Mar Biol Ecol 355:41–46

    Article  Google Scholar 

  • Smith WK, Miller PC (1973) The thermal ecology of two South Florida fiddler crabs: Uca rapax Smith and U. pugilator Bosc. Physiol Zool 46:186–207

    Google Scholar 

  • Stegen JC, Gienger CM, Sun LX (2004) The control of color change in the Pacific tree frog, Hyla regilla. Can J Zool 82:889–896

    Article  Google Scholar 

  • Stevens M, Merilaita S (2009) Animal camouflage: current issues and new perspectives. Philos Trans R Soc B Biol Sci 364:423–427

    Article  Google Scholar 

  • Stevenson RD (1985) The relative importance of behavioral and physiological adjustments controlling body temperature in terrestrial ectotherms. Am Nat 126:362–386

    Article  Google Scholar 

  • Stuart-Fox D, Moussalli A (2009) Camouflage, communication and thermoregulation: lessons from colour changing organisms. Philos Trans R Soc B Biol Sci 364:463–470

    Article  Google Scholar 

  • Stuart-Fox DM, Moussalli A, Marshall NJ, Owens IPF (2003) Conspicuous males suffer higher predation risk: visual modelling and experimental evidence from lizards. Anim Behav 66:541–550

    Article  Google Scholar 

  • Thurman CL (1984) Ecological notes on fiddler crabs of south Texas, with special reference to Uca subcylindrica. J Crust Biol 4:665–681

    Article  Google Scholar 

  • Thurman CL (1990) Adaptive coloration in Texas fiddler crabs (Uca). In: Wicksten M (ed) Adaptive coloration in invertebrates. Texas A&M University Sea Grant College Program, College Station

    Google Scholar 

  • Thurman CL (2002) Osmoregulation in six sympatric fiddler crabs (genus Uca) from the northwestern Gulf of Mexico. Mar Ecol Prog Ser 23:269–284

    Google Scholar 

  • Tullberg BS, Merilaita S, Wiklund C (2005) Aposematism and crypsis combined as a result of distance dependence: functional versatility of the colour pattern in the swallowtail butterfly larva. Proc R Soc B-Biol Sci 272:1315–1321

    Article  Google Scholar 

  • Vroonen J, Vervust B, Fulgione D, Maselli V, Van Damme R (2012) Physiological colour change in the Moorish gecko, Tarentola mauritanica (Squamata: Gekkonidae): effects of background, light, and temperature. Biol J Linn Soc 107:182–191

    Article  Google Scholar 

  • Walton BM, Bennett AF (1993) Temperature-dependent color change in Kenyan chameleons. Physiol Zool 66:270–287

    Google Scholar 

  • Weis JS (1985) Cadmium acclimation and limb regeneration in the fiddler crab, Uca pugilator: sex differences. Mar Environ Res 16:199–214

    Article  CAS  Google Scholar 

  • Weissburg M (1993) Sex and the single forager: gender-specific energy maximization strategies in fiddler crabs. Ecology 74:279–291

    Article  Google Scholar 

  • Weissburg MJ, Derby CD (1995) Regulation of sex-specific feeding behavior in fiddler crabs: physiological properties of chemoreceptor neurons in claws and legs of males and females. J Comp Physiol A Neuroethol Sens Neural Behav Physiol 176:513–526

    CAS  Google Scholar 

  • Wiernasz DC, Kingsolver JG (1992) Wing melanin pattern mediates species recognition in Pieris occidentalis. Anim Behav 43:89–94

    Article  Google Scholar 

  • Wilkens JL, Fingerman M (1965) Heat tolerance and temperature relationships of the fiddler crab, Uca pugilator, with reference to coloration. Biol Bull 128:133–141

    Article  Google Scholar 

  • Zeil J, Hofmann M (2001) Signals from ‘crabworld’: cuticular reflections in a fiddler crab colony. J Exp Biol 204:2561–2569

    CAS  Google Scholar 

Download references

Acknowledgments

We would like to thank K. Darnell for her assistance in collecting crabs. M. Buckley, P. Gravinese, R. Tankersley, and A. Wassick provided comments and suggestions on an earlier version of this manuscript. S.M.K. was supported by the NSF Research Experiences for Undergraduates program.

Author information

Authors and Affiliations

Authors

Corresponding author

Correspondence to M. Zachary Darnell.

Additional information

Communicated by M. G. Chapman.

Rights and permissions

Reprints and permissions

About this article

Cite this article

Kronstadt, S.M., Darnell, M.Z. & Munguia, P. Background and temperature effects on Uca panacea color change. Mar Biol 160, 1373–1381 (2013). https://doi.org/10.1007/s00227-013-2189-5

Download citation

  • Received:

  • Accepted:

  • Published:

  • Issue Date:

  • DOI: https://doi.org/10.1007/s00227-013-2189-5

Keywords

Navigation