Skip to main content
Log in

The social organization of the common vampire bat

II. Mating system, genetic structure, and relatedness

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

Summary

Variability at seven polymorphic allozyme loci and observations of dispersal and mating provide evidence for nonrandom genetic structure among adult female groups of the highly social bat, Desmodus rotundus. The average degree of relatedness, estimated by allelic correlations at each locus, within three and six groups of females is 0.018 (SE=0.013) and 0.032 (SE=0.023), respectively. Even though these estimates do not differ significantly from zero, a multivariate analysis of variance of individual allele frequencies reveals that three of six pairwise comparisons of groups reach significance. This genetic heterogeneity within a population does not lead to increased genetic subdivision between populations. Mean classificatory ability of the discriminant functions drops from 84% for assignment to group to 56% for assignment to population. This pattern of genetic variability is due to recruitment of female offspring into their natal groups and forced male dispersal. Occasional movements of unrelated females between groups lead to the formation of multiple matrilines within groups. Although males fight viciously for access to the top of preferred female roosting sites and top males mate preferentially with females in that roost, mean maximum paternity for top males is only 46%. Consequently, male mating success is sufficiently random to maintain gametic equilibria among all pairs of loci. Given an infant mortality of 54%, mean male tenure of 17 months, and a birth interval of 10 months, females are unlikely to be related through common male ancestors. In one group, the average degree of relatedness, derived from matrilineal pedigrees, is 0.11 (SD=0.17). Computer simulations of the growth of a group of female D. routundus show that the low level of relatedness within groups is expected even if the proportion of unrelated females allowed into a group decreases. This pattern holds for any animal which recruits one sex into its social group and has relatively high juvenile mortality followed by low adult mortality.

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

Access this article

Subscribe and save

Springer+ Basic
$34.99 /Month
  • Get 10 units per month
  • Download Article/Chapter or eBook
  • 1 Unit = 1 Article or 1 Chapter
  • Cancel anytime
Subscribe now

Buy Now

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

Instant access to the full article PDF.

Similar content being viewed by others

References

  • Boorman SA, Levitt PR (1980) The genetics of altruism. Academic Press, New York

    Google Scholar 

  • Boyd R, Richardson PJ (1980) Effect of phenotypic variation on kin selection. Proc Natl Acad Sci USA 77:7506–7509

    Google Scholar 

  • Brown JS, Sanderson MJ, Michod RE (1982) Evolution of social behavior by reciprocation. J Theor Biol 99:319–339

    Google Scholar 

  • Bush GL, Case SM, Wilson AC, Patton JL (1977) Rapid speciation and chromosomal evolution in mammals. Proc Natl Acad Sci USA 74:3942–3946

    Google Scholar 

  • Chakraborty R (1982) Allocation versus variation: the issue of genetic differences between human racial groups. Am Nat 120:403–404

    Google Scholar 

  • Charlesworth B (1979) A note on the evolution of altruism in structured demes. Am Nat 111:1010–1014

    Google Scholar 

  • Chesser RK (1983) Genetic variability within and among populations of the black-tailed prairie dog. Evolution 37:320–331

    Google Scholar 

  • Craig R, Crozier RH (1979) Relatedness in the polygynous ant Mymecia pilosula. Evolution 31:335–341

    Google Scholar 

  • Daly JC (1981) Effects of social organization and environmental diversity on determining the genetic structure of a population of the wild rabbit, Oryctolagus cuniculus. Evolution 35:689–706

    Google Scholar 

  • De Groot MH, Li CC (1960) Simplified method of estimating the MNS gene frequencies. Ann Hum Genet 24:109–115

    Google Scholar 

  • Eshel I, Cavalli-Sforza LL (1982) Assortment of encounters and evolution of cooperativeness. Proc Natl Acad Sci USA 79:1331–1335

    Google Scholar 

  • Falconer DS (1981) Introduction to quantitative genetics. Longman, New York

    Google Scholar 

  • Fleming TH, Hooper ET, Wilson DE (1972) Three central american bat communities: structure, reproductive cycles, and movement patterns. Ecology 53:555–569

    Google Scholar 

  • Foltz DW, Hoogland JL (1981) Analysis of the mating system in the black-tailed prairie dog (Cynomys ludovicianus) by likelihood of paternity. J Mammal 62:706–712

    Google Scholar 

  • Foltz DW, Hoogland JL (1983) Genetic evidence of outbreeding in the black-tailed prairie dog (Cynomys ludovicianus). Evolution 37:273–281

    Google Scholar 

  • Frankie GW, Baker HG, Opler PA (1974) Comparative phenological studies of trees in tropical wet and dry forests in the lowlands of Costa Rica. J Ecol 62:881–919

    Google Scholar 

  • Hamilton WD (1964) The genetical evolution of social behavior. J Theor Biol 7:1–52

    Google Scholar 

  • Hankin J, Sherman P (1981) Multiple paternity in Belding's ground squirrel litters. Science 212:351–353

    Google Scholar 

  • Harris H, Hopkinson DA (1978) Handbook of enzyme electrophoresis in human genetics. American Elsevier, New York

    Google Scholar 

  • Hedrick PW (1975) Genetic similarity and distance: comments and comparisons. Evolution 29:362–366

    Google Scholar 

  • Hoogland JL (1983) Black-tailed prairie dog coteries are cooperatively breeding units. Am Nat 121:275–280

    Google Scholar 

  • Janzen DH (1983) Costa rican natural history. University of Chicago Press, Chicago, Ill

    Google Scholar 

  • Lester LJ, Selander RK (1981) Genetic relatedness and the social organization of Polistes colonies. Am Nat 117:147–166

    Google Scholar 

  • McCracken GF (1984) Social dispersion and genetic variation in two species of emballonurid bats. Z Tierpsychol 66:55–69

    Google Scholar 

  • McCracken GF, Bradbury JW (1977) Paternity and genetic heterogeneity in the polygynous bat, Phyllostomus hastatus. Science 198:303–306

    Google Scholar 

  • McCracken GF, Bradbury JW (1981) Social organization and kinship in the polygynous bat, Phyllostomus hastatus. Behav Ecol Sociobiol 8:11–34

    Google Scholar 

  • Metcalf RA, Whitt GS (1977) Intra-nest relatedness in the social wasp Polistes metricus. Behav Ecol Sociobiol 2:339–351

    Google Scholar 

  • Nei M (1977) F-statistics and analysis of gene diversity in subdivided populations. Am Hum Genet 41:225–233

    Google Scholar 

  • Nie NH, Hull CH, Jenkins JG, Steinbrenner K, Bent DH (1975) Statistical package for the social sciences, 2nd edn. McGraw Hill, New York

    Google Scholar 

  • Olivier TJ, Ober C, Buettner-Janusch J, Sade DS (1981) Genetic differentiation among matrilines in social groups of rhesus monkeys. Behav Ecol Sociobiol 8:279–285

    Google Scholar 

  • Packer C (1979) Inter-troop transfer and inbreeding avoidance in Papio anubis. Anim Behav 27:1–36

    Google Scholar 

  • Pamilo P (1981) Genetic organization of Formica sanguinea populations. Behav Ecol Sociobiol 9:45–50

    Google Scholar 

  • Pamilo P (1982) Genetic population structure in polygynous Formica ants. Heredity 48:95–106

    Google Scholar 

  • Pamilo P (1983) Genetic differentiation within subdivided populations of Formica ants. Evolution 37:1010–1022

    Google Scholar 

  • Pamilo P (1984) Genotypic correlation and regression in social groups: multiple alleles, multiple loci and subdivided populations. Genetics 107:307–320

    Google Scholar 

  • Pamilo P, Crozier RH (1982) Measuring genetic relatedness in natural populations: methodology. Theor Popul Biol 21:171–193

    Google Scholar 

  • Pamilo P, Varvio-Aho S (1979) Genetic structure of nests in the ant Formica sanguinea. Behav Ecol Sociobiol 6:91–98

    Google Scholar 

  • Patton JL, Feder JH (1981) Microspatial genetic heterogeneity in pocket gophers: nonrandom breeding and drift. Evolution 35:912–920

    Google Scholar 

  • Pearson B (1982) Relatedness of normal queens (macrogynes) in nests of the polygynous ant Myrmecia rubra Latreille. Evolution 36:107–112

    Google Scholar 

  • Rogers JS (1972) Measures of genetic similarity and genetic distance. Studies in genetics VII. Univ Texas Publ 7213:145–153

    Google Scholar 

  • Sassaman C (1978) Mating systems in porcellionid isopods multiple paternity and sperm mixing in Porcellio scaber Latr Heredity 41:385–397

    Google Scholar 

  • Schmidt U (1974) Die Tragezeit der Vampirfledermause (Desmodus rotundus). Z Saugetierkd 39:129–132

    Google Scholar 

  • Schmidt U (1978) Vampifledermause. Ziemsen, Wittenburg

    Google Scholar 

  • Schmidt U, Schmidt C, Lopez-Forment W, Crespo RF (1978) Banding experiment on vampire bats (Desmodus rotundus) in Mexico. Z Saugetierkd 43:70–75

    Google Scholar 

  • Schwartz OA, Armitage KB (1980) Genetic variation in social mammals: the marmot model. Science 207:665–667

    Google Scholar 

  • Selander RK, Smith MH, Yang SV, Johnson WE, Gentry JB (1971) Biochemical polymorphism and systematics in the genus Peromyscus. I. Variation in the old field mouse. Studies in genetics VI. Univ Texas Publ 7103:49–90

    Google Scholar 

  • Smouse PE, Spielman RS, Park MH (1982) Multiple-locus allocation of individuals to groups as a function of the genetic variation within and differences among human populations. Am Nat 119:445–463

    Google Scholar 

  • Sokal RR, Rohlf FJ (1981) Biometry. Freeman, San Fransisco, Calif

    Google Scholar 

  • Spiess EB (1977) Genes in populations. Wiley, New York

    Google Scholar 

  • Stanton RG (1960) Genetic correlations with multiple alleles. Biometrics 16:235–244

    Google Scholar 

  • Turner DC (1975) The vampire bat. Johns Hopkins University Press, Baltimore, Md

    Google Scholar 

  • Wade MJ (1978) A critical review of the models of group selection. Q Rev Biol 53:101–114

    Google Scholar 

  • Wade MJ (1980) Kin selection: its components. Science 210:665–667

    Google Scholar 

  • Ward PS (1983) Genetic relatedness and colony organization in a species complex of ponerine ants. I. Phenotypic and genotypic composition of colonies. Behav Ecol Sociobiol 12:285–299

    Google Scholar 

  • Weir BS, Cockerham CC (1978) Testing hypotheses about linkage disequilibrium with multiple alleles. Genetics 88:633–842

    Google Scholar 

  • Wilkinson GS (1984) Reciprocal food sharing in vampire bats. Nature 308:181–184

    Google Scholar 

  • Wilkinson GS (1985) The social organization of the common vampire bat. I. Pattern and cause of association. Behav Ecol Sociobiol 17:111–121

    Google Scholar 

  • Wilson DS (1980) The natural selection of populations and communities. Cummings, Menlo Park, Calif

    Google Scholar 

  • Wright S (1968) Evolution and the genetics of populations, vol 1. University of Chicago Press, Chicago, Ill

    Google Scholar 

  • Wright S (1978) Evolution and the genetics of populations, vol 4. University of Chicago Press, Chicago, Ill

    Google Scholar 

Download references

Author information

Authors and Affiliations

Authors

Rights and permissions

Reprints and permissions

About this article

Cite this article

Wilkinson, G.S. The social organization of the common vampire bat. Behav Ecol Sociobiol 17, 123–134 (1985). https://doi.org/10.1007/BF00299244

Download citation

  • Received:

  • Accepted:

  • Issue Date:

  • DOI: https://doi.org/10.1007/BF00299244

Keywords