, Volume 165, Issue 3, pp 629–637 | Cite as

Fit females and fat polygynous males: seasonal body mass changes in the grey-headed flying fox

  • Justin A. Welbergen
Behavioral ecology - Original Paper


When females and males differ in their timing of maximum reproductive effort, this can result in sex-specific seasonal cycles in body mass. Such cycles are undoubtedly under strong selection, particularly in bats, where they affect flying ability. Flying foxes (Old World fruit bats, Pteropus spp.) are the largest mammals that can sustain powered flight and therefore face critical trade-offs in managing body reserves for reproduction, yet little is known about body mass dynamics in this group. I investigated body mass changes in relation to reproductive behaviour in a large colony of grey-headed flying foxes (Pteropus poliocephalus). In this polygynous mammal, females were predicted to maximise reproductive effort during lactation and males during the breeding season. As predicted, female body condition declined during the nursing period, but did not vary in relation to sexual activity. By contrast, males accumulated body reserves prior to the breeding season, but subsequently lost over 20% of their body mass on territory defence and courtship, and lost foraging opportunities as they also defended their day roost territories at night. Males in better condition had larger testes, particularly during territory establishment, prior to maximum sexual activity. Thus, the seasonality of female mass reflected the high metabolic load that lactation imposes on mothers. However, male mass followed a pattern akin to the “fatted male phenomenon”, which is commonly observed in large polygynous mammals with seasonal reproduction, but not in bats. This shows the importance of body reserves for reproduction in flying foxes, despite their severe constraints on body mass.


Bats Fat deposition Pteropus poliocephalus Reproductive investment Sex differences 



I am very grateful to N. Davies, T. H. Clutton-Brock, and P. Racey for their constructive comments on earlier versions of the manuscript. I thank S. Klose and T. Sinclair-Taylor for their help in the field; A. Goldizen for her academic support; and G. H. Williams for access to the Dallis Park property. This work was supported in part by studentships from the Natural Environment Research Council, King’s College, the Isaac Newton Trust, and the Cambridge European Trust. All procedures used in this study were under permit and in accordance with the principles and guidelines of the Australian Bird and Bat Banding Scheme, NSW Parks and Wildlife Service, and NSW Department of Agriculture.


  1. Adkins-Regan E (2005) Hormones and animal social behavior. Princeton University Press, PrincetonGoogle Scholar
  2. Archer J (2006) Testosterone and human aggression: an evaluation of the challenge hypothesis. Neurosci Biobehav Rev 30:319–345CrossRefPubMedGoogle Scholar
  3. Atkinson SN, Ramsay MA (1995) The effects of prolonged fasting of the body composition and reproductive success of female polar bears (Ursus maritimus). Funct Ecol 9:559–567CrossRefGoogle Scholar
  4. Baptista TL, Richardson CS, Kunz TH (2000) Post-natal growth and age estimation in free-ranging bats: a comparison of longitudinal and cross-sectional sampling methods. J Mammal 81:709–718CrossRefGoogle Scholar
  5. Barclay RMR, Harder LD (2003) Life histories of bats: life in the slow lane. In: Fenton MB (ed) Ecology of bats. University of Chicago Press, Chicago, pp 209–253Google Scholar
  6. Beck CA, Bowen WD, Iverson SJ (2003) Sex differences in the seasonal patterns of energy storage and expenditure in a phocid seal. J Anim Ecol 72:280–291CrossRefGoogle Scholar
  7. Bell G (1980) The costs of reproduction and their consequences. Am Nat 116:45–76CrossRefGoogle Scholar
  8. Brody S (1974) Bioenergetics and growth: with special reference to the efficiency complex in domestic animals. Hafner/Collier Macmillan, New York/LondonGoogle Scholar
  9. Clutton-Brock TH, Parker GA (1992) Potential reproductive rates and the operation of sexual selection. Q Rev Biol 67:437–456CrossRefGoogle Scholar
  10. Clutton-Brock TH, Albon SD, Guinness FE (1989) Fitness costs of gestation and lactation in wild mammals. Nature 337:260–262CrossRefPubMedGoogle Scholar
  11. Crichton EG, Krutzsch PH (eds) (2000) Reproductive biology of bats. Academic, San DiegoGoogle Scholar
  12. Deutsch CJ, Haley MP, Le Boeuf BJ (1990) Reproductive effort of male northern elephant seals: estimates from mass loss. Can J Zool 68:2580–2593CrossRefGoogle Scholar
  13. Du Mond FV, Hutchinson TC (1967) Squirrel monkey reproduction: the “fatted” male phenomenon and seasonal spermatogenesis. Science 158:1067–1070CrossRefPubMedGoogle Scholar
  14. Duncan A, Baker GB, Montgomery N (1999) The action plan for Australian bats. Environment Australia, CanberraGoogle Scholar
  15. Eby P (1991) Seasonal movements of grey-headed flying foxes, Pteropus poliocephalus (Chiroptera: Pteropodidae), from two maternity camps in northern New South Wales. Wildl Res 18:547–549CrossRefGoogle Scholar
  16. Eby P, Lunney D (2002) Managing the grey-headed flying fox, Pteropus poliocephalus as a threatened species: a context for the debate. In: Eby P, Lunney D (eds) Managing the grey-headed flying fox Pteropus poliocephalus as a threatened species in NSW. Royal Zoological Society of New South Wales, Mosman, pp 1–15Google Scholar
  17. Encarnação JA, Dietz M, Kierdorf U, Wolters V (2004) Body mass changes in male Daubenton’s bats Myotis daubentonii (Chiroptera, Vespertilionidae) during the seasonal activity period. Mammalia 68:291–297CrossRefGoogle Scholar
  18. Forsyth DM, Duncan RP, Tustin KG, Gaillard J-M (2005) A substantial energetic cost to male reproduction in a sexually dimorphic ungulate. Ecology 86:2154–2163CrossRefGoogle Scholar
  19. Fujita MS, Tuttle MD (1991) Flying-foxes (Chiroptera: Pteropodidae): threatened animals of key ecological and economic importance. Conserv Biol 5:455–463CrossRefGoogle Scholar
  20. Gittleman JL, Thompson SD (1988) Energy allocation in mammalian reproduction. Am Zool 28:863–875Google Scholar
  21. Gopalakrishna A, Chaudhari PN (1977) Breeding habits and associated phenomena in some Indian bats. Part 1. Rousettus leschenaulti (Desmarest). Megachiroptera. J Bombay Nat Hist Soc 74:1–16Google Scholar
  22. Hall LS, Richards GC (2000) Flying foxes: fruit and blossom bats. University of New South Wales Press, SydneyGoogle Scholar
  23. Hamilton IM, Barclay RMR (1998) Ontogenetic influences on foraging and mass accumulation by big brown bats (Eptesicus focus). J Anim Ecol 67:930–940CrossRefGoogle Scholar
  24. Hayssen V, Kunz TH (1996) Allometry of litter mass in bats: maternal size, wing morphology, and phylogeny. J Mammal 77:476–490CrossRefGoogle Scholar
  25. Hosken DJ (1998) Testes mass in megachiropteran bats varies in accordance with sperm competition theory. Behav Ecol Sociobiol 44:169–178CrossRefGoogle Scholar
  26. Hosken DJ, O’Shea JE (2001) Sperm production and immune function in two Australian bats, Chalinolobus morio and Nyctophilus geoffroyi. Ethol Ecol Evol 13:173–180CrossRefGoogle Scholar
  27. Kenagy GC (1976) The periodicity of daily activity and its seasonal changes in free-ranging and captive kangaroo rats. Oecologia 24:105–140CrossRefGoogle Scholar
  28. Klose SM, Welbergen JA, Goldizen AW, Kalko EKV (2009a) Spatio-temporal vigilance architecture of an Australian flying-fox colony. Behav Ecol Sociobiol 63:371–380CrossRefGoogle Scholar
  29. Klose SM, Welbergen JA, Kalko EKV (2009b) Testosterone is associated with harem maintenance ability in free-ranging grey-headed flying-foxes, Pteropus poliocephalus. Biol Lett 5:758–761CrossRefPubMedGoogle Scholar
  30. Koprowski JL (2005) Annual cycles in body mass and reproduction of endangered Mt. Graham red squirrels. J Mammal 86:309–313CrossRefGoogle Scholar
  31. Korine C, Speakman J, Arad Z (2004) Reproductive energetics of captive and free-ranging Egyptian fruit bats (Rousettus aegyptiacus). Ecology 85:220–230CrossRefGoogle Scholar
  32. Kunz TH, Parsons S (eds) (2009) Ecological and behavioral methods for the study of bats. Johns Hopkins Press, BaltimoreGoogle Scholar
  33. Kunz TH, Stern AA (1995) Maternal investment and post-natal growth in bats. In: Swift SM, Racey PA (eds) Symposia of the Zoological Society of London, vol 67. Clarendon, Oxford, pp 123–138Google Scholar
  34. Kunz TH, Wrazen JA, Burnett CD (1998) Changes in body mass and fat reserves in prehibernating little brown bats (Myotis lucifugus). Ecoscience 5:8–17Google Scholar
  35. Kurta A, Kunz TH, Nagy KA (1990) Energetics and water flux of free-ranging Big Brown Bats (Eptesicus fuscus) during pregnancy and lactation. J Mammal 71:59–65CrossRefGoogle Scholar
  36. Lindstedt SL, Boyce MS (1985) Seasonality, fasting endurance, and body size in mammals. Am Nat 125:873–878CrossRefGoogle Scholar
  37. Loudon ASI, Racey PA (eds) (1987) Reproductive energetics of mammals. Oxford University Press, OxfordGoogle Scholar
  38. Lunney D, Richards G, Dickman C (2008) Pteropus poliocephalus. In: IUCN (ed) IUCN Red List of Threatened Species. IUCN, GlandGoogle Scholar
  39. Maina JN (2000) What it takes to fly: the structural and functional respiratory refinements in birds and bats. J Exp Biol 203:3045–3064PubMedGoogle Scholar
  40. Malo AF et al (2009) What does testosterone do for red deer males? Proc R Soc Biol Sci Ser B 276:971–980CrossRefGoogle Scholar
  41. Markus N (2002) Behaviour of the black flying fox Pteropus alecto. 2. Territoriality and courtship. Acta Chiropt 4:153–166Google Scholar
  42. Markus N, Blackshaw JK (2002) Behaviour of the black flying fox, Pteropus alecto. 1. An ethogram of behaviour, and preliminary characterisation of mother-infant interactions. Acta Chiropt 4:137–152Google Scholar
  43. Martin L et al (1995) The reproductive biology of Australian flying-foxes (genus Pteropus). In: Swift SM, Racey PA (eds) Symposia of the Zoological Society of London, vol 67. Clarendon, Oxford, pp 167–184Google Scholar
  44. McGuckin MA, Blackshaw AW (1987) Seasonal changes in spermatogenesis (including germ cell degeneration) and plasma testosterone concentration in the Grey-headed fruit bat, Pteropus poliocephalus. Aust J Biol Sci 40:211–220Google Scholar
  45. McGuckin MA, Blackshaw AW (1991a) Mating-associated peak in plasma testosterone concentration in wild male grey-headed flying foxes (Pteropus poliocephalus). J Reprod Fert 92:347–352CrossRefGoogle Scholar
  46. McGuckin MA, Blackshaw AW (1991b) Seasonal changes in testicular size, plasma testosterone concentration and body weight in captive flying foxes (Pteropus poliocephalus and P. scapulatus). J Reprod Fert 92:339–346CrossRefGoogle Scholar
  47. McLean JA, Speakman JR (1999) Energy budgets of lactating and non-reproductive brown long-eared bats (Plecotus auritus) suggest females use compensation in lactation. Funct Ecol 13:360–372CrossRefGoogle Scholar
  48. McNab BK (1976) Seasonal fat reserves of bats in two tropical environments. Ecology 57:332–338CrossRefGoogle Scholar
  49. Michener GR, Locklear L (1990) Differential costs of reproductive effort for male and female Richardson’s ground squirrels. Ecology 71:855–868CrossRefGoogle Scholar
  50. Miquelle DG (1990) Why don’t bull moose eat during the rut? Behav Ecol Sociobiol 27:145–151CrossRefGoogle Scholar
  51. Mitchell B, McCowan D, Nicholson IA (1976) Annual cycles of body weight and condition in Scottish red deer, Cervus elaphus. J Zool (Lond) 180:107–127CrossRefGoogle Scholar
  52. Nelson JEW (1964) Vocal communication in Australian flying foxes (Pteropodidae; Megachiroptera). Z Tierpsychol 27:857–870Google Scholar
  53. Nelson JEW (1965a) Behavior of Australian pteropodidae (Megachiroptera). Anim Behav 13:544–557CrossRefPubMedGoogle Scholar
  54. Nelson JEW (1965b) Movements of Australian flying foxes (Pteropodidae: Megachiroptera). Aust J Zool 13:53–73CrossRefGoogle Scholar
  55. Norberg UM, Rayner JMV (1987) Ecological morphology and flight in bats (Mammalia; Chiroptera): wing adaptations, flight performance, foraging strategy and echolocation. Philos Trans R Soc Lond B Biol Sci 316:335–427CrossRefGoogle Scholar
  56. O’Brien GM (1993) Seasonal reproduction in flying foxes, reviewed in the context of other tropical mammals. Reprod Fertil Dev 5:499–521CrossRefPubMedGoogle Scholar
  57. Olsson M, Madsen T, Shine R (1997) Is sperm really so cheap? Costs of reproduction in male adders, Vipera berus. Proc R Soc Lond B Biol Sci 264:455–459CrossRefGoogle Scholar
  58. Parry-Jones KA, Augee ML (1992) Movements of grey-headed flying-foxes (Pteropus poliocephalus) to and from a colony site on the central coast of New South Wales. Wildl Res 19:331–340CrossRefGoogle Scholar
  59. Puddicombe R (1981) A behavioural study of the Grey-Headed Flying Fox, Pteropus poliocephalus (Megachiroptera) (BSc Hons thesis). University of New England, Armidale Google Scholar
  60. Racey PA (1982) The ecology of bat reproduction. In: Kunz TH (ed) The ecology of bats. Plenum, New York, pp 57–104Google Scholar
  61. Racey PA, Speakman JR (1987) The energy costs of pregnancy and lactation in heterothermic bats. Symp Zool Soc Lond 54:107–125Google Scholar
  62. Ratcliffe F (1932) Notes on the fruit bats (Pteropus spp.) of Australia. J Anim Ecol 1:32–57CrossRefGoogle Scholar
  63. Reeder DM, Kosteczko NS, Kunz TH, Widmaier EP (2006) The hormonal and behavioral response to group formation, seasonal changes, and restraint stress in the highly social Malayan Flying Fox (Pteropus vampyrus) and the less social Little Golden-mantled Flying Fox (Pteropus pumilus) (Chiroptera: Pteropodidae). Horm Behav 49:484–500Google Scholar
  64. Schulte-Hostedde AI, Millar JS, Hickling GJ (2005a) Condition dependence of testis size in small mammals. Evol Ecol Res 7:143–149Google Scholar
  65. Schulte-Hostedde AI, Zinner B, Millar JS, Hickling GJ (2005b) Restitution of mass-size residuals: validating body condition indices. Ecology 86:155–163CrossRefGoogle Scholar
  66. Speakman J, Racey P (1986) The influence of body condition on sexual development of male brown long-eared bats (Plecotus auritus) in the wild. J Zool (Lond) 210:515–525CrossRefGoogle Scholar
  67. Speakman JR, Rowland A (1999) Preparing for inactivity: how insectivorous bats deposit a fat store for hibernation. Proc Nutr Soc 58:123–131CrossRefPubMedGoogle Scholar
  68. Spencer HJ, Palmer C, Parry-Jones K (1991) Movements of fruit bats in eastern Australia, determined by using radio-tracking. Wildl Res 18:463–468CrossRefGoogle Scholar
  69. Stearns SC (1992) The evolution of life histories. Oxford University Press, OxfordGoogle Scholar
  70. Temminck CJ (1825) Vues générales sur l’ordre des cheiroptères. In: Temminck CJ (ed) Monographies de mammalogie, ou description de quelques genres de mammifères, dont les espèces dont été observées dans les différens musées de l’Europe. G. Dufour & E. D’Ocagne, Paris, pp 157–204Google Scholar
  71. Thomas DW, Marshall AG (1984) Reproduction and growth in three species of West African fruit bats. J Zool (Lond) 202:265–281CrossRefGoogle Scholar
  72. Vardon MJ, Tidemann CR (1998) Reproduction, growth and maturity in the black flying-fox, Pteropus alecto (Megachiroptera: Pteropodidae). Aust J Zool 46:329–344CrossRefGoogle Scholar
  73. Voigt CC (2003) Reproductive energetics of the nectar-feeding bat Glossophaga soricina (Phyllostomidae). J Comp Physiol B Biochem Syst Environ Physiol 173:79–85Google Scholar
  74. Welbergen JA (2005) The social organisation of the grey-headed flying-fox (Ph.D thesis). University of Cambridge, CambridgeGoogle Scholar
  75. Welbergen JA (2006) Timing of the evening emergence from day roosts of the grey-headed flying-fox, Pteropus poliocephalus: the effects of predation risk, foraging needs and social context. Behav Ecol Sociobiol 60:311–322CrossRefGoogle Scholar
  76. Welbergen JA (2008) Variation in twilight predicts the duration of the evening emergence of fruit bats from a mixed-species roost. Anim Behav 75:1543–1550CrossRefGoogle Scholar
  77. Welbergen JA (2010) Growth, bimaturation and sexual size dimorphism in wild gray-headed flying-foxes (Pteropus poliocephalus). J Mammal 91:38–47CrossRefGoogle Scholar
  78. Welbergen JA, Klose SM, Markus N, Eby P (2008) Climate change and the effects of temperature extremes on Australian flying-foxes. Proc R Soc Biol Sci Ser B 275:419–425CrossRefGoogle Scholar
  79. Wolff JO (1998) Breeding strategies, mate choice, and reproductive success in American bison. Oikos 83:529–544CrossRefGoogle Scholar

Copyright information

© Springer-Verlag 2010

Authors and Affiliations

  1. 1.Department of ZoologyUniversity of CambridgeCambridgeUK
  2. 2.Division of Evolution, Ecology and Genetics, Research School of BiologyAustralian National UniversityCanberraAustralia

Personalised recommendations