Skip to main content

Thank you for visiting nature.com. You are using a browser version with limited support for CSS. To obtain the best experience, we recommend you use a more up to date browser (or turn off compatibility mode in Internet Explorer). In the meantime, to ensure continued support, we are displaying the site without styles and JavaScript.

Advertisement

Scientific Reports
  • View all journals
  • Search
  • My Account Login
  • Content Explore content
  • About the journal
  • Publish with us
  • Sign up for alerts
  • RSS feed
  1. nature
  2. scientific reports
  3. articles
  4. article
Exploring spatial relationships of male wild Turkeys during the breeding season
Download PDF
Download PDF
  • Article
  • Open access
  • Published: 09 January 2026

Exploring spatial relationships of male wild Turkeys during the breeding season

  • Erin E. Ulrey1,
  • Nicholas W. Bakner2,
  • John C. Kilgo3,
  • Bret A. Collier4 &
  • …
  • Michael J. Chamberlain1 

Scientific Reports , Article number:  (2026) Cite this article

  • 652 Accesses

  • Metrics details

We are providing an unedited version of this manuscript to give early access to its findings. Before final publication, the manuscript will undergo further editing. Please note there may be errors present which affect the content, and all legal disclaimers apply.

Subjects

  • Behavioural ecology
  • Ecology

Abstract

Leks are characterized as clusters of displaying males that females visit primarily for the purpose of mating, and represent complex mating systems observed across various species, including birds, mammals, and insects. Male wild turkeys (Meleagris gallopavo) use reproductive strategies that involve visual and acoustic displays to compete for mates. However, there is ambiguity as to whether the mating system of eastern wild turkeys (M. g. silvestris) is a form of lekking. Our objective was to evaluate the potential that eastern wild turkeys use a form of a lek mating system via a movement based recursive analysis to identify if areas were revisited by males during the breeding season, and whether selection of revisited areas was related to resources or female distribution. Using GPS locations collected from 151 male and 261 female wild turkeys from 2014 to 2023 across the southeastern United States, we identified 6,565 locations that occurred within revisited areas during the breeding season and examined resource selection by males at those revisited areas. We found that average size of revisited areas was 49.89 ha and comprised approximately 8.12% of male breeding season home ranges. Male wild turkeys traveled greater distances from their winter home ranges to revisited areas, than did females from their winter home ranges to pre-laying ranges. Male wild turkeys selected revisited areas that were closer to hardwood forests and open areas. Additionally, we found that selection of revisited areas was positively associated with an increase in the relative probability of female presence and visibility of males. We encourage research to further elucidate the dynamics of wild turkey mating behaviors relative to potential forms of lekking that wild turkeys may use throughout their geographic range.

Data availability

The datasets generated during and/or analyzed during the current study are available from the corresponding author on reasonable request.

References

  1. Wiley, R. H. Evolution of social organization and life-history patterns among grouse. Q. R. Biol. 49, 201–227 (1974).

    Google Scholar 

  2. Wittenberger, J. F. The evolution of mating systems in grouse. Condor 80, 126–137 (1978).

    Google Scholar 

  3. Höglund, J., and R. V. Alatalo. 1995. Leks. Princeton University Press, Princeton, New Jersey, USA.

  4. Crawford, J. A. et al. Ecology and management of sage-grouse and sage-grouse habitat. J. Range Manag. 57, 2–19 (2004).

    Google Scholar 

  5. Larsson, L. C., Pruett, C. L., Wolfe, D. H. & Patten, M. A. Fine-scale selection of habitat by the lesser prairie-chicken. Southwestern Naturalist 58, 135–149 (2013).

    Google Scholar 

  6. Emlen, S. & Oring, L. Ecology, sexual selection, and the evolution of mating systems. Science 197, 215–223 (1977).

    Google Scholar 

  7. Wegge, P., Rolstad, J. & Storaunet, K. O. On the spatial relationship of males on “exploded” leks: the case of Capercaillie grouse Tetrao urogallus examined by GPS satellite telemetry. Ornis Fennica 90, 222–235 (2013).

    Google Scholar 

  8. Cornec, C., Hingrat, Y., Aubin, T. & Rybak, F. Booming far: the long-range vocal strategy of a lekking bird. Royal Society Open Science 4, 170594 (2017).

    Google Scholar 

  9. DuVal, E. H. & Kempenaers, B. Sexual selection in a lekking bird: the relative opportunity for selection by female choice and male competition. Proceedings of the Royal Society B: Biological Sciences 275, 1995–2003 (2008).

    Google Scholar 

  10. Bradbury, J. W. The evolution of leks. In Natural selection and social behavior: recent research and theory (eds Alexander, R. D. & Tinkle, D. W.) 138–169 (Chiron Press, 1981).

    Google Scholar 

  11. Nooker, J. K. & Sandercock, B. K. Phenotypic correlates and survival consequences of male mating success in lek-mating greater prairie-chickens (Tympanuchus cupido). Behav. Ecol. Sociobiol. 62, 1377–1388 (2008).

    Google Scholar 

  12. Widemo, F. The social implications of traditional use of lek sites in the ruff Philomachus pugnax. Behav. Ecol. 8, 211–217 (1997).

    Google Scholar 

  13. Alonso, J. C., Magaña, M. & Álvarez-Martínez, J. M. Male display areas in exploded leks: the importance of food resources for male mating success. Behav. Ecol. 23, 1296–1307 (2012).

    Google Scholar 

  14. Alonso, J. C., Álvarez-Martínez, J. M. & Palacín, C. Leks in ground-displaying birds: hotspots or safe places?. Behav. Ecol. 23, 491–501 (2012).

    Google Scholar 

  15. Ucero, A., Alonso, J. C., Palacín, C., Abril-Colón, I. & Álvarez-Martínez, J. M. Display site selection in a ground dwelling bird: the importance of viewshed. Behav. Ecol. 34, 223–235 (2022).

    Google Scholar 

  16. Andersson, M. B. Sexual selection (Princeton University Press, 1994).

    Google Scholar 

  17. Bradbury, J. W. & Vehrencamp, S. L. Principles of animal communication 2nd edn. (Oxford University Press, 2011).

    Google Scholar 

  18. Aspbury, A. S. & Gibson, R. M. Long-range visibility of greater sage grouse leks: a GIS-based analysis. Anim. Behav. 67, 1127–1132 (2004).

    Google Scholar 

  19. Marten, K. & Marler, P. Sound transmission and its significance for animal vocalization. Behav. Ecol. Sociobiol. 2, 271–290 (1977).

    Google Scholar 

  20. Delgado, M. M. & Penteriani, V. Vocal behaviour and neighbour spatial arrangement during vocal displays in eagle owls (Bubo bubo). J. Zool. 271, 3–10 (2006).

    Google Scholar 

  21. Boyko, A. R., Gibson, R. M. & Lucas, J. R. How predation risk affects the temporal dynamics of avian leks: greater sage grouse versus golden eagles. Am. Nat. 163, 154–165 (2004).

    Google Scholar 

  22. Krams, I. Perch selection by singing chaffinches: a better view of surroundings and the risk of predation. Behav. Ecol. 12, 295–300 (2001).

    Google Scholar 

  23. Gibson, R. M., Aspbury, A. S. & McDaniel, L. L. Active formation of mixed-species grouse leks: a role for predation in lek evolution?. Proceedings of the Royal Society B: Biological Sciences 269, 2503–2507 (2002).

    Google Scholar 

  24. Miller, D. A., Hurst, G. A. & Leopold, B. D. Chronology of wild turkey nesting, gobbling, and hunting in Mississippi. J. Wildl. Manag. 61, 840–845 (1997).

    Google Scholar 

  25. Krakauer, A. H. Sexual selection and the genetic mating system of wild turkeys. The Condor 110, 1–12 (2008).

    Google Scholar 

  26. Bevill, W. V. Jr. Some factors influencing gobbling activity among turkeys. Proceedings of the Southeastern Association of Game and Fish Commissioners 27, 62–73 (1973).

    Google Scholar 

  27. Healy, W. M. Behavior. In The wild turkey: biology and management (ed. Dickson, J. G.) 46–65 (Stackpole Books, 1992).

    Google Scholar 

  28. Buchholz, R. Female choice, parasite load and male ornamentation in wild turkeys. Anim. Behav. 50, 929–943 (1995).

    Google Scholar 

  29. Miller, D. A., Hurst, G. A. & Leopold, B. D. Factors affecting gobbling activity of wild turkeys in central Mississippi. Proceedings of the Southeastern Association of Fish and Wildlife Agencies 51, 353–361 (1997).

    Google Scholar 

  30. Healy, W. M., and S. M. Powell. 1999. Wild turkey harvest management: biology, strategies, and techniques. U.S. Fish and Wildlife Service Biological Technical Publication BTP-R5001–1999. U.S. Fish and Wildlife Service, Washington, D. C., USA.

  31. Weir, L. K., Grant, J. W. A. & Hutchings, J. A. The influence of operational sex ratio on the intensity of competition for mates. Am. Nat. 177, 167–176 (2011).

    Google Scholar 

  32. Watts, C. H. & Stokes, A. W. The social order of turkeys. Sci. Am. 224, 112–119 (1971).

    Google Scholar 

  33. Eaton, S. W., Evans, J. W., Glidden, J. W. & Penrod, B. D. Annual range of wild turkeys in southwestern New York. New York Fish and Game Journal 23, 20–33 (1976).

    Google Scholar 

  34. Williams, L. E. & Austin, D. H. Studies of the wild turkey in Florida (University of Florida Press, 1988).

    Google Scholar 

  35. Watts, C. H. Rio Grande turkeys in the mating season. Proceedings of the North American Wildlife and Natural Resources Conference 23, 205–210 (1968).

    Google Scholar 

  36. Avise, J. C. Three fundamental contributions of molecular genetics to avian ecology and evolution. Ibis 138, 16–25 (1996).

    Google Scholar 

  37. Watts, C. H. The social organization of wild turkeys on the Welder Wildlife Refuge (Thesis, Utah State University, Logan, USA, 1969).

    Google Scholar 

  38. Wakefield, C. T. et al. Hunting and nesting phenology influence gobbling of wild turkeys. J. Wildl. Manag. 84, 448–457 (2020).

    Google Scholar 

  39. Imm, D. W. & McLeod, K. W. Plant communities. In Ecology and management of a forested landscape: fifty years of natural resource stewardship on the Savannah River Site (eds Kilgo, J. C. & Blake, J. I.) 106–161 (Island Press, 2005).

    Google Scholar 

  40. White, D. L. 2005. Land-use history. Page 2–12 in J. C. Kilgo and J. I. Blake, editors. Ecology and management of a forested landscape: fifty years of natural resource stewardship on the Savannah River Site. Island Press, Washington, D. C., USA.

  41. Wightman, P. H. et al. Gobbling chronology of eastern wild turkeys in South Carolina. J. Wildl. Manag. 83, 325–333 (2019).

    Google Scholar 

  42. Guthrie, J. D. et al. Evaluation of a global positioning system backpack transmitter for wild turkey research. J. Wildl. Manag. 75, 539–547 (2011).

    Google Scholar 

  43. Cohen, B. S., Prebyl, T. J., Collier, B. A. & Chamberlain, M. J. Home range estimator method and GPS sampling schedule affect habitat selection inferences for wild turkeys. Wildl. Soc. Bull. 42, 150–159 (2018).

    Google Scholar 

  44. Lott, H. et al. Male mating season rang expansion results from an increase in scale of daily movements for a polygynous-promiscuous bird. Ecol. Evol. 14, e11302 (2024).

    Google Scholar 

  45. Collier, B. A., Wightman, P. H., Cantrell, J. R. & Ruth, C. R. Hunting activity and male wild turkey movements in South Carolina. Journal of the Southeastern Association of Fish and Wildlife Agencies 4, 85–93 (2017).

    Google Scholar 

  46. Wightman, P. H. et al. Impact of supplemental feeding for Northern Bobwhite on movement ecology of Eastern wild turkeys in South Carolina. Journal of Southeastern Association of Fish and Wildlife Agencies 5, 114–124 (2018).

    Google Scholar 

  47. Wightman, P. H., Henrichs, D. W., Collier, B. A. & Chamberlain, M. J. Comparisons of methods for automated identification of wild turkey gobbles. Wildl. Soc. Bull. 46, e1246 (2022).

    Google Scholar 

  48. Berger-Tal, O. & Bar-David, S. Recursive movement patterns: review and synthesis across species. Ecosphere 6, 1–12 (2015).

    Google Scholar 

  49. Bracis, C., Bildstein, K. L. & Mueller, T. Revisitation analysis uncovers spatio-temporal patterns in animal movement data. Ecography 41, 1801–1811 (2018).

    Google Scholar 

  50. Youngmann, J. L., Hinton, J. W., Bakner, N. W., Chamberlain, M. J. & D’Angelo, G. J. Recursive use of home ranges and seasonal shifts in foraging behavior by a generalist carnivore. Ecol. Evol. 12, e9540 (2022).

    Google Scholar 

  51. Yeldell, N. A., Cohen, B. S., Prebyl, T. J., Collier, B. A. & Chamberlain, M. J. Prescribed fire influences habitat selection of female eastern wild turkeys. J. Wildl. Manag. 81, 1287–1297 (2017).

    Google Scholar 

  52. Conner, L. M., Smith, M. D. & Burger, L. W. A comparison of distance-based and classification-base analyses of habitat use. Ecology 84, 526–531 (2003).

    Google Scholar 

  53. Manly, B. F. J., McDonald, L. L., Thomas, D. L., McDonald, T. L. & Erickson, W. P. Resource selection by animals: statistical design and analysis for field studies 2nd edn. (Kluwer Academic Publishers, 2002).

    Google Scholar 

  54. Law, M. & Collins, A. Getting to know ArcGIS Pro 2nd edn. (Esri Press, 2019).

    Google Scholar 

  55. Godwin, K. D., Hurst, G. A. & Kelly, R. L. Movements of wild turkey gobblers in central Mississippi. Proceedings of the Southeastern Association of Fish and Wildlife Agencies 44, 260–267 (1994).

    Google Scholar 

  56. Chamberlain, M. J., Wightman, P. H., Cohen, B. S. & Collier, B. A. Gobbling activity of eastern wild turkeys relative to male movements and female nesting phenology in South Carolina. Wildl. Soc. Bull. 42, 632–642 (2018).

    Google Scholar 

  57. Kranstauber, B., Kays, R., Lapoint, S. D., Wikelski, M. & Safi, K. A dynamic Brownian bridge movement model to estimate utilization distributions for heterogeneous animal movement: the dynamic Brownian bridge movement model. J. Anim. Ecol. 81, 738–746 (2012).

    Google Scholar 

  58. Byrne, M. E., McCoy, J. C., Hinton, J. W., Chamberlain, M. J. & Collier, B. A. Using dynamic Brownian bridge movement modeling to measure temporal patterns of habitat selection. J. Anim. Ecol. 83, 1234–1243 (2014).

    Google Scholar 

  59. Badyaev, A. V., Etges, W. J. & Martin, T. E. Ecological and behavioral correlates of variation in seasonal home ranges of wild turkeys. Journal Wildlife Management 60, 154–164 (1996).

    Google Scholar 

  60. Miller, D. A., Hurst, G. A. & Leopold, B. D. Habitat use of eastern wild turkeys in central Mississippi. J. Wildl. Manag. 63, 210–222 (1999).

    Google Scholar 

  61. Chamberlain, M. J. & Leopold, B. Habitat sampling and selection by female wild turkeys during preincubation. Wilson and Bulletin 112, 326–331 (2000).

    Google Scholar 

  62. Benson, J. F. Improving rigour and efficiency of use-availability habitat selection analyses with systematic estimation of availability. Methods in Ecology Evolution 4, 244–251 (2013).

    Google Scholar 

  63. Dormann, C. F. et al. Collinearity: a review of methods to deal with it and a simulation study evaluating their performance. Ecography 36, 27–46 (2013).

    Google Scholar 

  64. Johnson, C. J., Nielsen, S. E., Merrill, E. H., McDonald, T. L. & Boyce, M. S. Resource selection functions based on use-availability data: theoretical motivation and evaluation methods. J. Wildl. Manag. 70, 347–357 (2006).

    Google Scholar 

  65. Muff, S., Signer, J. & Fieberg, J. Accounting for individual-specific variation in habitat selection studies: efficient estimation of mixed-effects models using Bayesian or frequentist computation. J. Anim. Ecol. 89, 80–96 (2020).

    Google Scholar 

  66. Bates, D., Mächler, M., Bolker, B. M. & Walker, S. C. Fitting linear mixed-effects models using lme4. J. Stat. Softw. 67, 1–48 (2014).

    Google Scholar 

  67. Gelman, A. Scaling regression inputs by dividing by two standard deviations. Stat. Med. 27, 2865–2873 (2008).

    Google Scholar 

  68. Akaike, H. Information theory and an extension of the maximum likelihood principle. Proceedings of the International Symposium on Information Theory 2, 267–281 (1973).

    Google Scholar 

  69. Burnham, K. P. & Anderson, D. R. Model Selection and multimodal inference: a practical information-theoretic approach 2nd edn. (Springer-Verlag, 2002).

    Google Scholar 

  70. Zipkin, E. F., Grant, E. H. C. & Fagan, W. F. Evaluating the predictive abilities of community occupancy models using AUC while accounting for imperfect detection. Ecol. Appl. 22, 1962–1972 (2012).

    Google Scholar 

  71. Silva, J. P., Moreira, F. & Palmeirim, J. M. Spatial and temporal dynamics of lekking behaviour revealed by high-resolution GPS tracking. Anim. Behav. 129, 197–204 (2017).

    Google Scholar 

  72. Ponjoan, A., Bota, G. & Mañosa, S. Ranging behaviour of little bustard males, Tetrax tetrax, in the lekking grounds. Behav. Proc. 91, 35–40 (2012).

    Google Scholar 

  73. Alonso, J. C., Morales, M. B. & Alonso, J. A. Partial migration, and lek and nesting area fidelity in female great bustards. Condor 102, 127–136 (2000).

    Google Scholar 

  74. Morales, M. B., Jiguet, F. & Arroyo, B. Exploded leks: what bustards can teach us. Ardeola 48, 85–98 (2001).

    Google Scholar 

  75. Castro-Astor, I. N., Alves, M. A. S. & Cavalcanti, R. B. Display behavior and spatial distribution of the red-headed manakin in the Atlantic forest of Brazil. Condor 106, 320–335 (2004).

    Google Scholar 

  76. Hingrat, Y., Saint Jalme, M., Chalah, T., Orhant, N. & Lacroix, F. Environmental and social constraints on breeding site selection. Does the exploded-lek and hotspot model apply to the Houbara bustard Chlamydotis undulata undulata?. J. Avian Biol. 39, 393–404 (2008).

    Google Scholar 

  77. Gross, J. T., Cohen, B. S., Collier, B. A. & Chamberlain, M. J. Influences of hunting on movements of male wild turkeys during the spring. National Wild Turkey Symposium 11, 175–185 (2015).

    Google Scholar 

  78. Roth, A. P. et al. Sex-specific resource use by wild turkeys in response to hunting activity. J. Wildl. Manag. 88, e22567 (2024).

    Google Scholar 

  79. Forsgren, E. & Magnhagen, C. Conflicting demands in sand gobies: predators influence reproductive behaviour. Behaviour 126, 125–135 (1993).

    Google Scholar 

  80. Candolin, U. Reproduction under predation risk and the trade-off between current and future reproduction in the threespine stickleback. Proc. R. Soc. Lond. B 265, 1171–1175 (1998).

    Google Scholar 

  81. Winder, V. L., Gregory, A. J., McNew, L. B. & Sandercock, B. K. Responses of male Greater Prairie-Chickens to wind energy development. Ornithological Applications 117, 284–296 (2015).

    Google Scholar 

  82. Lautenbach, J. M. et al. Lesser prairie-chicken avoidance of trees in a grassland landscape. Rangel. Ecol. Manage. 70, 78–86 (2017).

    Google Scholar 

  83. Brenner, S. J., Buffum, B., Tefft, B. C. & McWilliams, S. R. Landscape context matters when American woodcock select singing grounds: results form a reciprocal transplant experiment. Condor 121, 1–11 (2019).

    Google Scholar 

  84. Hurst, G. A. Foods and feeding. In The wild turkey: biology and management (ed. Dickson, J. G.) 66–83 (Stackpole Books, 1992).

    Google Scholar 

  85. Ryan, C. W., Pack, J. C., Igo, W. K., Rieffenberger, J. C. & Billings, A. B. Relationships of mast production to big-game harvests in West Virginia. Wildl. Soc. Bull. 32, 786–794 (2004).

    Google Scholar 

  86. Little, A. R., Chamberlain, M. J., Conner, L. M. & Warren, R. J. Habitat selection of wild turkeys in burned longleaf pine Savannas. J. Wildl. Manag. 80, 1280–1289 (2016).

    Google Scholar 

  87. Bakner, N. W. et al. Spatial roost networks and resource selection of female wild turkeys. Royal Society Open Science 11, 231938 (2024).

    Google Scholar 

  88. Watson, J. W., Duff, A. A. & Davies, R. W. Home range and resource selection by GPS monitored adult golden eagles in the Columbia Plateau Ecoregion: implications for wind power development. J. Wildl. Manag. 78, 1012–1021 (2014).

    Google Scholar 

  89. Domenech, R., Bedrosian, B. E., Crandall, R. H. & Slabe, V. A. Space use and habitat selection by adult migrant Golden Eagles wintering in the western United States. Journal of Raptor Research 49, 429–440 (2015).

    Google Scholar 

  90. Gerhardt, H. C., and R. S. Larry. 2009. Signal design rules in animal communication. Pages 791–798 in L. R. Squire, editor. Encyclopedia of Neuroscience. Academic Press.

  91. Caves, E. M., Brandley, N. C. & Johnsen, S. Visual acuity and the evolution of signals. Trends Ecol. Evol. 33, 358–372 (2018).

    Google Scholar 

  92. Yang, W., Qiao, J., Combreau, O., Gao, X. & Zhong, W. Display-sites selection by houbara bustard (Chlamydotis [undulata] macqueenii) in Mori, Xinjiang, People’s Republic of China. Journal Arid Environment 51, 625–631 (2002).

    Google Scholar 

  93. Koshkin, M. A. et al. Effects of habitat and land use on breeding season density of male Asian Houbara Chlamydotis macqueenii. J. Ornithol. 157, 811–823 (2016).

    Google Scholar 

  94. Geary, M., Cooper, J. R. & Collar, N. J. Anthropogenic influences on habitat use by African houbaras Chlamydotis undulata on Lanzarote, Canary Islands. J. Nat. Conserv. 68, 126–231 (2022).

    Google Scholar 

  95. Théry, M. The evolution of leks through female choice: differential clustering and space utilization in 6 sympatric manakins. Behav. Ecol. Sociobiol. 30, 227–237 (1992).

    Google Scholar 

  96. Drummer, T. D., Corace, R. G. III. & Sjogren, S. J. Sharp-tailed grouse lek attendance and fidelity in upper Michigan. J. Wildl. Manag. 75, 311–318 (2011).

    Google Scholar 

  97. Wiley, R. H. Territoriality and non-random mating in sage grouse (Centrocercus urophasianus). Animal Behavior Monographs 6, 85–169 (1973).

    Google Scholar 

  98. Gibson, R. M. & Bradbury, J. W. Sexual selection in lekking sage grouse: phenotypic correlates of male mating success. Behav. Ecol. Sociobiol. 18, 117–123 (1985).

    Google Scholar 

  99. Payne, R. B. Sexual selection, lek, and arena behavior, and sexual size dimorphism in birds. Ornithol. Monogr. 33, 1–52 (1984).

    Google Scholar 

Download references

Acknowledgements

We thank M. Bellamy, C. Parenti, C. Ruth Jr., H. Lott, A. P. Roth, A. K. Lohr, C. J. Wakefield, P. H. Wightman, S. D. Nelson, S. Watkins, P. Goodman, N. Gulotta, J. White, and J. W. Wood for their assistance with fieldwork.

Author information

Authors and Affiliations

  1. Warnell School of Forestry and Natural Resources, University of Georgia, Athens, GA, 30602, USA

    Erin E. Ulrey & Michael J. Chamberlain

  2. Department of Entomology and Wildlife Ecology, University of Delaware, Newark , DE, 19716, USA

    Nicholas W. Bakner

  3. United States Department of Agriculture Forest Service, Southern Research Station, New Ellenton, SC, USA

    John C. Kilgo

  4. School of Renewable Natural Resources, Louisiana State University Agricultural Center, Baton Rouge, LA, 70803, USA

    Bret A. Collier

Authors
  1. Erin E. Ulrey
    View author publications

    Search author on:PubMed Google Scholar

  2. Nicholas W. Bakner
    View author publications

    Search author on:PubMed Google Scholar

  3. John C. Kilgo
    View author publications

    Search author on:PubMed Google Scholar

  4. Bret A. Collier
    View author publications

    Search author on:PubMed Google Scholar

  5. Michael J. Chamberlain
    View author publications

    Search author on:PubMed Google Scholar

Contributions

EEU: Conceptualization, Data curation, Formal analysis, Methodology, Writing- Original draft.NWB: Data curation, Formal analysis, Methodology, Writing-review and editing.JCK: Resources, Project administration, supervision, Writing-review and editing.BAC: Conceptualization, Project administration, Funding acquisition, Writing-review and editingMJC: Conceptualization, Project administration, Funding acquisition, Supervision, Writing-review and editing.

Corresponding author

Correspondence to Erin E. Ulrey.

Ethics declarations

Competing interests

The authors declare no competing interests.

Additional information

Publisher’s note

Springer Nature remains neutral with regard to jurisdictional claims in published maps and institutional affiliations.

Supplementary Information

Below is the link to the electronic supplementary material.

Supplementary Material 1

Supplementary Material 2

Rights and permissions

Open Access This article is licensed under a Creative Commons Attribution-NonCommercial-NoDerivatives 4.0 International License, which permits any non-commercial use, sharing, distribution and reproduction in any medium or format, as long as you give appropriate credit to the original author(s) and the source, provide a link to the Creative Commons licence, and indicate if you modified the licensed material. You do not have permission under this licence to share adapted material derived from this article or parts of it. The images or other third party material in this article are included in the article’s Creative Commons licence, unless indicated otherwise in a credit line to the material. If material is not included in the article’s Creative Commons licence and your intended use is not permitted by statutory regulation or exceeds the permitted use, you will need to obtain permission directly from the copyright holder. To view a copy of this licence, visit http://creativecommons.org/licenses/by-nc-nd/4.0/.

Reprints and permissions

About this article

Check for updates. Verify currency and authenticity via CrossMark

Cite this article

Ulrey, E.E., Bakner, N.W., Kilgo, J.C. et al. Exploring spatial relationships of male wild Turkeys during the breeding season. Sci Rep (2026). https://doi.org/10.1038/s41598-025-34883-7

Download citation

  • Received: 17 April 2025

  • Accepted: 31 December 2025

  • Published: 09 January 2026

  • DOI: https://doi.org/10.1038/s41598-025-34883-7

Share this article

Anyone you share the following link with will be able to read this content:

Sorry, a shareable link is not currently available for this article.

Provided by the Springer Nature SharedIt content-sharing initiative

Keywords

  • Leks
  • Mating system
  • Movement ecology
  • Revisitation
  • Wild turkey
Download PDF

Advertisement

Explore content

  • Research articles
  • News & Comment
  • Collections
  • Subjects
  • Follow us on Facebook
  • Follow us on Twitter
  • Sign up for alerts
  • RSS feed

About the journal

  • About Scientific Reports
  • Contact
  • Journal policies
  • Guide to referees
  • Calls for Papers
  • Editor's Choice
  • Journal highlights
  • Open Access Fees and Funding

Publish with us

  • For authors
  • Language editing services
  • Open access funding
  • Submit manuscript

Search

Advanced search

Quick links

  • Explore articles by subject
  • Find a job
  • Guide to authors
  • Editorial policies

Scientific Reports (Sci Rep)

ISSN 2045-2322 (online)

nature.com sitemap

About Nature Portfolio

  • About us
  • Press releases
  • Press office
  • Contact us

Discover content

  • Journals A-Z
  • Articles by subject
  • protocols.io
  • Nature Index

Publishing policies

  • Nature portfolio policies
  • Open access

Author & Researcher services

  • Reprints & permissions
  • Research data
  • Language editing
  • Scientific editing
  • Nature Masterclasses
  • Research Solutions

Libraries & institutions

  • Librarian service & tools
  • Librarian portal
  • Open research
  • Recommend to library

Advertising & partnerships

  • Advertising
  • Partnerships & Services
  • Media kits
  • Branded content

Professional development

  • Nature Awards
  • Nature Careers
  • Nature Conferences

Regional websites

  • Nature Africa
  • Nature China
  • Nature India
  • Nature Japan
  • Nature Middle East
  • Privacy Policy
  • Use of cookies
  • Legal notice
  • Accessibility statement
  • Terms & Conditions
  • Your US state privacy rights
Springer Nature

© 2026 Springer Nature Limited

Nature Briefing Anthropocene

Sign up for the Nature Briefing: Anthropocene newsletter — what matters in anthropocene research, free to your inbox weekly.

Get the most important science stories of the day, free in your inbox. Sign up for Nature Briefing: Anthropocene