Skip to main content
Log in

Bird song and parasites

  • Review
  • Published:
Behavioral Ecology and Sociobiology Aims and scope Submit manuscript

Abstract

Bird song is a typical sexual trait that may have evolved at least partly to reflect health and vigor. However, the role of pathogens in modulating acoustic communication systems in birds is still less than clear as studies testing the relationship between parasites and song have provided inconsistent results both within and among species. It is often neglected that avian song is complex trait consisting of numerous and variable features with potentially different biological backgrounds. By using meta-analytic approaches to the available intraspecific evidence I demonstrate that different roles are applicable to song traits with different signal design, which could explain, to some extent, the inconsistency of results. I found that condition-dependent, performance-related traits are more closely related to immediate health status, whereas condition-independent features are more likely to be associated with intrinsically determined parasite resistance. Hence, parasitism may mediate the evolution of different acoustic features. Considering the signal function of songs, a communication system depends on the reaction of the receivers, but little is known about how mate choice and male–male competition are affected by parasite-mediated song production. This review of the literature thus suggests that receivers of songs may benefit by responding to these acoustic signals of health through the acquisition of resistance genes, paternal care of superior assistance, success in territory disputes, and the avoidance of directly transmitted parasites.

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.

Figure 1.

Similar content being viewed by others

References

  • Able DJ (1996) The contagion indicator hypothesis for parasite-mediated sexual selection. Proc Natl Acad Sci USA 93:2229–2233

    Article  PubMed  CAS  Google Scholar 

  • Airey DC, Buchanan KL, Székely T, Catchpole CK, DeVoogd TJ (2000a) Song, sexual selection, and song control nucleus (HVC) in the brains of European sedge warblers. J Neurobiol 44:1–6

    Article  PubMed  CAS  Google Scholar 

  • Airey DC, Castillo-Juarez H, Casella G, Pollak EJ, DeVoogd TJ (2000b) Variation in the volume of zebra finch song control nuclei is heritable: developmental and evolutionary implications. Proc R Soc Lond B267: 2099–2104

    Article  Google Scholar 

  • Appleby BM, Anwar MA, Petty SJ (1999) Short-term and long-term effects of food supply on parasite burdens in Tawny Owls, Strix aluco. Func Ecol 13:315–321

    Article  Google Scholar 

  • Appleby BM, Redpath SM (1997) Indicators of male quality in the hoots of Tawny Owls (Strix aluco). J Raptor Res 31:65–70

    Google Scholar 

  • Birkhead TR, Fletcher F, Pellatt EJ (1998) Sexual selection in the zebra finch Taeniopygia guttata: condition, sex traits and immune capacity. Behav Ecol Sociobiol 44:179–191

    Article  Google Scholar 

  • Blount JD, Metcalfe NB, Birkhead TR, Surai PF (2003) Carotenoid modulation of immune function and sexual attractiveness in zebra finches. Science 300:125–127

    Article  PubMed  CAS  Google Scholar 

  • Bonneaud C, Mazuc J, Gonzalez G, Haussy C, Chastel O, Faivre B, Sorci G (2003) Assessing the cost of mounting an immune response. Am Nat 161:367–379

    Article  PubMed  Google Scholar 

  • Borgia G (1986) Satin bowerbird parasites—a test of the bright male hypothesis. Behav Ecol Sociobiol 19:355–358

    Article  Google Scholar 

  • Borgia G, Collis K (1989) Female choice for parasite-free male satin bowerbirds and the evolution of bright male plumage. Behav Ecol Sociobiol 25:445–453

    Article  Google Scholar 

  • Boulinier T, Sorci G, Monnat JY, Danchin E (1997) Parent-offspring regression suggests heritable susceptibility to ectoparasites in a natural population of kittiwake Rissa tridactyla. J Evol Biol 10:77–85

    Article  Google Scholar 

  • Bouslama Z, Lambrechts MM, Ziane N, Djenidi RD, Chabi Y (2002) The effect of nest ectoparasites on parental provisioning in a north-African population of the Blue Tit Parus caeruleus. Ibis 144:E73–E78

    Article  Google Scholar 

  • Brenowitz EA, Kroodsma DE (1996) The neuroethology of birdsong. In: Kroodsma DE, Miller EH (eds) Ecology and evolution of acoustic communication in birds. Cornell University Press, Ithaca, pp 285–305

    Google Scholar 

  • Buchanan KL, Catchpole CK (1997) Female choice in the sedge warbler, Acrocephalus schoenobaenus: multiple cues from song and territory quality. Proc R Soc Lond B 264:521–526

    Article  Google Scholar 

  • Buchanan KL, Catchpole CK (2000) Song as an indicator of male parental effort in the sedge warbler. Proc R Soc Lond B 267:321–326

    Article  CAS  Google Scholar 

  • Buchanan KL, Catchpole CK, Lewis JW, Lodge A (1999) Song as an indicator of parasitism in the sedge warbler. Anim Behav 57:307–314

    Article  PubMed  Google Scholar 

  • Catchpole CK (1980) Sexual selection and the evolution of complex songs among European warblers of the genus Acrocephalus. Behaviour 74:149–166

    Article  Google Scholar 

  • Cheng S, Rotschild MF, Lamont ST (1991) Estimates of quantitative genetic-parameters of immunological traits in the chicken. Poultry Sci 70:2023–2027

    CAS  Google Scholar 

  • Christe P, Møller AP, Saino N, de Lope F (2000) Genetic and environmental components of phenotypic variation in immune response and body size of a colonial bird, Delichon urbica (the house martin). Heredity 85:75–83

    Article  PubMed  Google Scholar 

  • Cichoñ M (2000) Costs of incubation and immunocompetence in the collared flycatcher. Oecologia 125:453–457

    Article  Google Scholar 

  • Cichoñ M, Dubiec A, Chadzinska M (2001) The effect of elevated reproductive effort on humoral immune function in collared flycather females. Acta Oecolog 22:71–76

    Article  Google Scholar 

  • Cichoñ M, Sendecka J, Gustafsson L (2003) Age-related decline in humoral immune function in Collared Flycatchers. J Evol Biol 16:1205–1210

    Article  PubMed  Google Scholar 

  • Clark L (1991) The nestprotection hypothesis: the adaptive use of plant secondary compounds by European starlings. In: Loye JE, Zuk M (eds) Bird-parasite interaction. Oxford University Press, Oxford, pp 205–221

    Google Scholar 

  • Clayton DH (1991) The influence of parasites on host sexual selection. Parasitol Today 7:329–334

    Article  PubMed  CAS  Google Scholar 

  • Collins SA, Hubbard C, Houtman AM (1994) Female mate choice in the zebra finch—the effect of male beak color and male song. Behav Ecol Sociobiol 35:21–25

    Article  Google Scholar 

  • Cooper H, Hedges V (1994) The handbook of research synthesis. Russell Sage Foundation, New York

    Google Scholar 

  • Darolova A, Hoi H, Kristofik J, Hoi C (2001) Horizontal and vertical ectoparasite transmission of three species of malophaga, and individual variation in European bee-eaters (Merops apiaster). J Parasitol 87:256–262

    PubMed  CAS  Google Scholar 

  • Darolova A, Hoi H, Schleicher B (1997) The effect of ectoparasite nest load on the breeding biology of the Penduline Tit Remiz pendulinus. Ibis 139:115–120

    Article  Google Scholar 

  • de Lope F, Møller AP (1993) Effects of ectoparasites on reproduction of their swallow hosts—a cost of being multi-brooded. Oikos 67:557–562

    Article  Google Scholar 

  • Deerenberg C, Arpanius V, Daan S, Bos N (1997) Reproductive effort decreases antibody responsiveness. Proc R Soc Lond B 264:1021–1029

    Article  Google Scholar 

  • Duffy DL, Ball GF (2002) Song predicts immunocompetence in male European starlings (Sturnus vulgaris). Proc R Soc Lond B 269:847–852

    Article  Google Scholar 

  • Eens M (1997) Understanding the complex song of the European starling: an itegrated ethological approach. Adv Study Behav 26:355–434

    Article  Google Scholar 

  • Eens M, Pinxten R, Verheyen RF (1991) Male song as a cue for mate choice in the European starling. Behaviour 116:210–238

    Article  Google Scholar 

  • Eens M, Pinxten R, Verheyen RF (1992) Song learning in captive European starlings, Sturnus vulgaris. Anim Behav 44:1131–1143

    Article  Google Scholar 

  • Eshel I, Hamilton WD (1984) Parent-offspring correlation in fitness under fluctuating selection. Proc R Soc Lond B 222:1–14

    Google Scholar 

  • Espmark Y, Amundsen T, Rosenqvist G (2000) Animal signals: signaling and signal design in animal communication. Tapir Academic Press, Trondheim

    Google Scholar 

  • Folstad I, Karter AJ (1992) Parasites, bright males, and immunocompetence handicap. Am Nat 139:603–622

    Article  Google Scholar 

  • Freeland WJ (1976) Pathogens and the evolution of primate sociality. Biotropica 8:12–24

    Article  Google Scholar 

  • Galeotti P (1998) Correlates of hoot rate and structure in male Tawny Owls Strix aluco: implications for male rivalry and female mate choice. J Avian Biol 29:25–32

    Article  Google Scholar 

  • Garamszegi LZ, Eens M, Erritzøe J, Møller AP (2005a) Sexually size dimorphic brains and song complexity in passerine birds. Behav Ecol 16:335–345

    Article  Google Scholar 

  • Garamszegi LZ, Heylen D, Møller AP, Eens M, de Lope F (2005b) Age-dependent health status and song characteristics in the barn swallow. Behav Ecol 16:580–591

    Article  Google Scholar 

  • Garamszegi LZ, Møller AP, Erritzøe J (2003) The evolution of immune defense and song complexity in birds. Evolution 57:905–912

    Article  PubMed  Google Scholar 

  • Garamszegi LZ, Møller AP, Török J, Michl G, Péczely P, Richard M (2004) Immune challenge mediates vocal communication in a passerine bird: an experiment. Behav Ecol 15:148–157

    Article  Google Scholar 

  • Gentner TQ, Hulse SH (2000) Female European starling preference and choice for variation in conspecific male song. Anim Behav 59:443–458

    Article  PubMed  Google Scholar 

  • Gil D, Cobb JLS, Slater PJB (2001) Song characteristics are age dependent in the willow warbler, Phylloscopus trochilus. Anim Behav 62:689–694

    Article  Google Scholar 

  • Gil D, Gahr M (2002) The honesty of bird song: multiple constraints for multiple traits. Trends Ecol Evol 17:133–141

    Article  Google Scholar 

  • Glick B (1983) Bursa of Fabricius. In: Farner DS, King JR (eds) Avian Biology, vol 7. Academic Press, New York, pp 443–500

    Google Scholar 

  • Grafen A (1990) Biological signals as handicaps. J Theor Biol 144:517–546

    Article  PubMed  CAS  Google Scholar 

  • Greigsmith PW (1982) Song rates and parental care by individual male stonechats (Saxicola torquata). Anim Behav 30:245–252

    Article  Google Scholar 

  • Gustafsson L, Nordling D, Andersson MS, Sheldon BC, Qvarnström A (1994) Infectious diseases, reproductive effort and the cost of reproduction in birds. Phil Trans R Soc Lond B 346:323–331

    Article  CAS  Google Scholar 

  • Hamilton WD (1984) Pathogens as causes of genetic diversity in their host populations. In: Andersson MR, May RM (eds) Population biology of infectious disease agents. Verlag-Chemie, Weinheim, pp 269–296

    Google Scholar 

  • Hamilton WD (1990) Mate choice near and far. Am Zool 30:341–352

    Google Scholar 

  • Hamilton WD, Zuk M (1982) Heritable true fitness and bright birds: a role for parasites. Science 218:384–387

    Article  PubMed  CAS  Google Scholar 

  • Hasselquist D (1994) Male attractiveness, mating tactics and realized fitness in the polygynous Great Reed Warbler. Lund University, Lund

    Google Scholar 

  • Hasselquist D, Bensch S, von Schantz T (1996) Correlation between male song repertoire, extra-pair paternity and offspring survival in the great reed warbler. Nature 381:229–232

    Article  CAS  Google Scholar 

  • Hedges LV, Olkin I (1985) Statistical methods for meta-analysis. Academic Press., London

    Google Scholar 

  • Hillgarth N (1990) Parasites and female choice in the Ring-necked Pheasant. Am Zool 30:227–233

    Google Scholar 

  • Hillgarth N (1996) Ectoparasite transfer during mating in ring-necked pheasants Phasianus colchicus. J Avian Biol 27:260–262

    Article  Google Scholar 

  • Hillgarth N, Wingfield J (1997) Parasite-mediated sexual selection: endocrine-aspects. In: Clayton DH, Moore J (eds) Host-parasite evolution: general principles and avian models. Oxford University Press, Oxford, pp 78–104

    Google Scholar 

  • Hoi-Leitner M, Nechtelberger H, Dittami J (1993) The relationship between individual-differences in male song frequency and parental care in blackcaps. Behaviour 126:1–12

    Article  Google Scholar 

  • Houtman AM (1992) Female zebra finches choose extra-pair copulations with genetically attractive males. Proc R Soc Lond B 249:3–6

    Article  Google Scholar 

  • Hurtrez-Boussès S, Blondel J, Perret P, Fabreguettes J, Renaud F (1998) Chick parasitism by blowflies affects feeding rates in a Mediterranean population of blue tits. Ecol Letters 1:17–20

    Article  Google Scholar 

  • Ilmonen P, Hakkarainen H, Koivunen V, Korpimaki E, Mullie A, Shutler D (1999) Parental effort and blood parasitism in Tengmalm's owl: effects of natural and experimental variation in food abundance. Oikos 86:79–86

    Article  Google Scholar 

  • Kean RP, Cahaner A, Freeman AE, Lamont SJ (1994) Direct and correlated responses to multitrait, divergent selection for immunocompetence. Poultry Sci 73:18–32

    CAS  Google Scholar 

  • Kotiaho JS (2002) Meta-analysis, can it ever fail? Oikos 96:551–553

    Article  Google Scholar 

  • Krebs JR, Kroodsma DE (1980) Repertoires and geographical variation in birdsong. Adv Study Behav 11:143–177

    Article  Google Scholar 

  • Kurtz J, Sauer KP (1999) The immunocompetence handicap hypothesis: testing the genetic predictions. Proc R Soc Lond B 266:2515–2522

    Article  Google Scholar 

  • Lambrechts MM (1996) Organization of birdsong and constraints on performance. In: Kroodsma DE, Miller EH (eds) Ecology and evolution of acoustic communication in birds. Cornell University Press, Ithaca, pp 305–320

    Google Scholar 

  • Liker A, Markus M, Vozar A, Zemankovics E, Rózsa L (2001) Distribution of Carnus hemapterus in a starling colony. Can J Zool 79:574–580

    Article  Google Scholar 

  • Maynard-Smith J, Harper DGC (1995) Animal signals models and terminology. J Theor Biol 177:305–311

    Article  Google Scholar 

  • Mazgajski TD, Kedra AH (1998) Endoparasite Isospora sp. (Coccidia, Eimeriidae) affects the growth of starling Sturnus vulgaris nestling. Acta Parasitolog 43:214–216

    Google Scholar 

  • Merino S, Moreno J, Sanz JJ, Arriero E (2000) Are avian blood parasites pathogenic in the wild? A medication experiment in blue tits (Parus caeruleus). Proc R Soc Lond B 267:2507–2510

    Article  CAS  Google Scholar 

  • Møller AP (1990a) Effects of a hematophagous mite on the barn swallow (Hirundo rustica)—a test of the Hamilton and Zuk hypothesis. Evolution 44:771–784

    Article  Google Scholar 

  • Møller AP (1990b) Effects of parasitism by a hematophagous mite on the reproduction in barn swallow. Ecology 71:2345–2357

    Article  Google Scholar 

  • Møller AP (1990c) Parasites and sexual selection: Current status of the Hamilton and Zuk hypothesis. J Evol Biol 3:319–328

    Article  Google Scholar 

  • Møller AP (1991) Parasite load reduces song output in a passerine bird. Anim Behav 41:723–730

    Article  Google Scholar 

  • Møller AP (1993) Ectoparasites increase the cost of reproduction in their hosts. J Anim Ecol 62:309–322

    Article  Google Scholar 

  • Møller AP (1994) Parasite infestation and parental care in the Barn Swallow Hirundo rustica—a test of the resource-provisioning model of parasite-mediated sexual selection. Ethology 97:215–225

    Article  Google Scholar 

  • Møller AP, Biard C, Blount JD, Houston DC, Ninni P, Saino N, Surai PF (2000a) Carotenoid-dependent signals: indicators of foraging efficiency, immunocompetence or detoxification ability? Avian Poultry Biol Rev 11:137–159

    Google Scholar 

  • Møller AP, Christe P, Lux E (1999) Parasitism, host immune function, and sexual selection. Quart Rev Biol 74:3–20

    Article  PubMed  Google Scholar 

  • Møller AP, Henry P-Y, Erritzøe J (2000b) The evolution of song repertoires and immune defense in birds. Proc R Soc Lond B 267:165–169

    Article  Google Scholar 

  • Møller AP, Pomiankowski A (1993) Punctuated equilibria or gradual evolution: the importance of fluctuating asymmetry. J Theor Biol 161:359–367

    Article  PubMed  Google Scholar 

  • Møller AP, Saino N, Taramino G, Galeotti P, Ferrario S (1998) Paternity and multiple signaling: effects of a secondary sexual character and song on paternity in the barn swallow. Am Nat 151:236–242

    Article  PubMed  Google Scholar 

  • Mountjoy DJ, Lemon RE (1991) Song as an attractant for male and female European starlings, and the influence of song complexity on their response. Behav Ecol Sociobiol 28:97–100

    Article  Google Scholar 

  • Mountjoy DJ, Lemon RE (1995) Extended song learning in wild European starlings. Anim Behav 49:357–366

    Article  Google Scholar 

  • Mountjoy DJ, Lemon RE (1996) Female choice for complex song in the European starling: a field experiment. Behav Ecol Sociobiol 38:65–71

    Article  Google Scholar 

  • Mountjoy DJ, Lemon RE (1997) Male song complexity and parental care in the European starling. Behaviour 134:661–675

    Article  Google Scholar 

  • Mundinger PC (1995) Behaviour-genetic analysis of canary song: inter-strain differences in sensory learning, and epigenetic rules. Anim Behav 50:1491–1511

    Article  Google Scholar 

  • Nordling D, Andersson M, Zohari S, Gustafsson L (1998) Reproductive effort reduces specific immune response and parasite resistance. Proc R Soc Lond B 265:1291–1298

    Article  Google Scholar 

  • Norris K, Evans MR (2000) Ecological immunology: life history trade-offs and immune defense in birds. Behav Ecol 11:19–26

    Article  Google Scholar 

  • Oberweger K, Goller F (2001) The metabolic cost of birdsong production. J Exp Biol 204:3379–3388

    PubMed  CAS  Google Scholar 

  • Potti J, Merino S (1995) Louse loads of Pied Flycatchers—effects of hosts sex, age, condition and relatedness. J Avian Biol 26:203–208

    Article  Google Scholar 

  • Price T, Schluter D, Heckman NE (1993) Sexual selection when the female directly benefits. Biol J Linn Soc 48:187–211

    Article  Google Scholar 

  • Råberg L, Nilsson J-A, Ilmonen P, Stjernman M, Hasselquist D (2000) The cost of an immune response: vaccination reduces parental effort. Ecol Letters 3:382–386

    Article  Google Scholar 

  • Råberg L, Stjernman M, Hasselquist D (2003) Immune responsiveness in adult blue tits: heritability and effects of nutritional status during ontogeny. Oecologia 136:360–364

    Article  PubMed  Google Scholar 

  • Read AF, Weary DM (1990) Sexual selection and the evolution of bird song: A test of the Hamilton-Zuk hypothesis. Behav Ecol Sociobiol 26:47–56

    Article  Google Scholar 

  • Redpath SM, Appleby MB, Petty SJ (2000) Do male hoots betray parasite loads in Tawny Owls? J Avian Biol 31:457–462

    Article  Google Scholar 

  • Rinden H, Lampe HM, Slagsvold T, Espmark YO (2000) Song quality does not indicate male parental abilities in the pied flycatcher Ficedula hypoleuca. Behaviour 137:809–823

    Article  Google Scholar 

  • Roberts ML, Buchanan KL, Evans MR (2004) Testing the immunocompetence handicap hypothesis: a review of the evidence. Anim Behav 68:227–239

    Article  Google Scholar 

  • Rosenthal R (1991) Meta-analytic procedures for social research. Sage Publications, Thousand Oaks

    Google Scholar 

  • Ryder JJ, Siva-Jothy MT (2000) Male calling song provides a reliable signal of immune function in a cricket. Proc R Soc Lond B 267:1171–1175

    Article  CAS  Google Scholar 

  • Ryder JJ, Siva-Jothy MT (2001) Quantitative genetics of immune function and body size in the house cricket, Acheta domesticus. J Evol Biol 14:646–653

    Article  Google Scholar 

  • Saino N, Calza S, Møller AP (1997a) Immunocompetence of nestling barn swallows in relation to brood size and parental effort. J Anim Ecol 66:827–836

    Article  Google Scholar 

  • Saino N, Calza S, Møller AP (1998) Effects of a dipteran ectoparasite on immune response and growth trade-offs in barn swallow, Hirundo rustica, nestlings. Oikos 81:217–228

    Article  Google Scholar 

  • Saino N, Calza S, Ninni P, Møller AP (1999) Barn swallows trade survival against offspring condition and immunocompetence. J Anim Ecol 68:999–1009

    Article  Google Scholar 

  • Saino N, Ferrari RP, Romano M, Ambrosini R, Møller AP (2002) Ectoparasites and reproductive trade-offs in the barn swallow (Hirundo rustica). Oecologia 133:139–145

    Article  Google Scholar 

  • Saino N, Ferrari RP, Romano M, Rubolini D, Møller AP (2003) Humoral immune response in relation to senescence, sex and sexual ornamentation in the barn swallow (Hirundo rustica). J Evol Biol 16:1127–1134

    Article  PubMed  CAS  Google Scholar 

  • Saino N, Galeotti P, Sacchi R, Møller AP (1997b) Song and immunological conditions in male barn swallows (Hirundo rustica). Behav Ecol 8:364–371

    Article  Google Scholar 

  • Saino N, Incagli M, Martinelli R, Ambrosini R, Møller AP (2001) Immunity, growth and begging behaviour of nestling Barn Swallows Hirundo rustica in relation to hatching order. J Avian Biol 32:263–270

    Article  Google Scholar 

  • Schmid-Hempel P (2003) Variation in immune defense as a question of evolutionary ecology. Proc R Soc Lond B 270:357–366

    Article  Google Scholar 

  • Schmid-Hempel P, Ebert D (2003) On the evolutionary ecology of specific immune defense. Trends Ecol Evol 18:27–32

    Article  Google Scholar 

  • Searcy WA, Andersson M (1986) Sexual selection and the evolution of song. Ann Rev Ecol Syst 17:507–533

    Article  Google Scholar 

  • Searcy WA, Nowicki S (2000) Male–male competition and female choice in the evolution of vocal signaling. In: Espmark Y, Amundsen T, Rosenqvist G (eds) Animal signals: signaling and signal design in animal communication. Tapir Academic Press, Trondheim, pp 301–315

    Google Scholar 

  • Searcy WA, Yasukawa K (1990) Use of the song repertoire in intersexual and intrasexual contexts by male red-winged blackbirds. Behav Ecol Sociobiol 27:123–128

    Article  Google Scholar 

  • Searcy WA, Yasukawa K (1996) Song and female choice. In: Kroodsma DE, Miller EH (eds) Ecology and evolution of acoustic communication in birds. Cornell University Press, Ithaca, pp 454–473

    Google Scholar 

  • Thomas F, Renaud F, DeMeeüs T, Cezilly F (1995) Parasites, age and the Hamilton-Zuk hypothesis: Inferential fallacy? Oikos 74:305–309

    Article  Google Scholar 

  • Vehrencamp SL (2000) Handicap, index, and conventional signal elements of bird song. In: Espmark Y, Amundsen T, Rosenqvist G (eds) Animal signals: signaling and signal design in animal communication. Tapir Academic Press, Trondheim, pp 277–300

    Google Scholar 

  • Wakelin D (1996) Immunity to parasites, 2nd edn. Cambridge University Press, Cambridge

    Google Scholar 

  • Wakelin D, Blackwell JM (1988) Genetics and resistance to bacterial and parsaitic infection. Taylor and Francis, London

    Google Scholar 

  • Ward S, Lampe HM, Slater PJB (2004) Singing is not energetically demanding for pied flycatchers, Ficedula hypoleuca. Behav Ecol 15:477–484

    Article  Google Scholar 

  • Ward S, Speakman JR, Slater PJB (2003) The energy cost of song in the canary, Serinus canaria. Anim Behav 66:893–902

    Article  Google Scholar 

  • Weatherhead PJ, Bennett GF (1991) Ecology of red-winged blackbird parasitism by hematozoa. Can J Zool 69:2352–2359

    Article  Google Scholar 

  • Weatherhead PJ, Metz KJ, Bennett GF, Irwin RE (1993) Parasite faunas, testosterone and secondary sexual traits in male red-winged blackbirds. Behav Ecol Sociobiol 33:13–23

    Article  Google Scholar 

  • Wedekind C (1994a) Handicaps not obligatory in sexual section for resistance genes. J Theor Biol 170:57–62

    Article  PubMed  CAS  Google Scholar 

  • Wedekind C (1994b) Mate choice and maternal selection for specific parasite resistances before, during and after fertilization. Phil Trans R Soc Lond B 346:303–311

    Article  CAS  Google Scholar 

  • Welling PP, Rytkonen SO, Koivula KT, Orell MI (1997) Song rate correlates with paternal care and survival in willow tits: Advertisement of male quality? Behaviour 134:891–904

    Article  Google Scholar 

  • Wesolowski T (2001) Host-parasite interactions in natural holes: marsh tits (Parus palustris) and blow flies (Protocalliphora falcozi). J Zool 255:495–503

    Google Scholar 

  • Westneat DF, Hasselquist D, Wingfield JC (2003) Tests of association between the humoral immune response of red-winged blackbirds (Agelaius phoeniceus) and male plumage, testosterone, or reproductive success. Behav Ecol Sociobiol 53:315–323

    Google Scholar 

  • Williams TD, Christians JK, Aiken JJ, Evanson M (1999) Enhanced immune function does not depress reproductive output. Proc R Soc Lond B 266:753–757

    Article  Google Scholar 

  • Yasukawa K (1981) Song and territory defense in the red-winged blackbird. Auk 98:185–187

    Google Scholar 

  • Yasukawa K, Blank JL, Patterson CB (1980) Song repertoires and sexual selection in the red-winged blackbird. Behav Ecol Sociobiol 7:233–238

    Article  Google Scholar 

  • Zahavi A (1975) Mate selection—a selection for a handicap. J Theor Biol 53:205–214

    Article  PubMed  CAS  Google Scholar 

  • Zahavi A, Zahavi A (1997) The handicap principle. Oxford University Press, Oxford

    Google Scholar 

  • Zuk M, Stoehr AM (2002) Immune defense and host life history. Am Nat 160 Supplement:9–22

    Article  Google Scholar 

  • Zuk M, Thornhill R, Ligon JD, Johnson K (1990) Parasites and mate choice in Red Jungle Fowl. Am Zool 30:235–244

    Google Scholar 

Download references

Author information

Authors and Affiliations

Authors

Corresponding author

Correspondence to László Zsolt Garamszegi.

Additional information

Communicated by A. Cockburn

Rights and permissions

Reprints and permissions

About this article

Cite this article

Garamszegi, L.Z. Bird song and parasites. Behav Ecol Sociobiol 59, 167–180 (2005). https://doi.org/10.1007/s00265-005-0041-8

Download citation

  • Received:

  • Revised:

  • Accepted:

  • Published:

  • Issue Date:

  • DOI: https://doi.org/10.1007/s00265-005-0041-8

Keywords

Navigation