» Articles » PMID: 27087927

Noninvasive Genetic Sampling Reveals Intrasex Territoriality in Wolverines

Overview
Journal Ecol Evol
Date 2016 Apr 19
PMID 27087927
Citations 6
Authors
Affiliations
Soon will be listed here.
Abstract

Due to its conspicuous manifestations and its capacity to shape the configuration and dynamics of wild populations, territorial behavior has long intrigued ecologists. Territoriality and other animal interactions in situ have traditionally been studied via direct observations and telemetry. Here, we explore whether noninvasive genetic sampling, which is increasingly supplementing traditional field methods in ecological research, can reveal territorial behavior in an elusive carnivore, the wolverine (Gulo gulo). Using the locations of genotyped wolverine scat samples collected annually over a period of 12 years in central Norway, we test three predictions: (1) male home ranges constructed from noninvasive genetic sampling data are larger than those of females, (2) individuals avoid areas used by other conspecifics of the same sex (intrasexual territoriality), and (3) avoidance of same-sex territories diminishes or disappears after the territory owner's death. Each of these predictions is substantiated by our results: sex-specific differences in home range size and intrasexual territoriality in wolverine are patently reflected in the spatial and temporal configuration of noninvasively collected genetic samples. Our study confirms that wildlife monitoring programs can utilize the spatial information in noninvasive genetic sampling data to detect and quantify home ranges and social organization.

Citing Articles

Environmental variability across space and time drives the recolonization pattern of a historically persecuted large carnivore.

Moqanaki E, Milleret C, Dupont P, Mattisson J, Dey S, Broseth H Proc Natl Acad Sci U S A. 2025; 122(5):e2401679122.

PMID: 39869793 PMC: 11804516. DOI: 10.1073/pnas.2401679122.


An experimental design for obtaining DNA of a target species and its diet from a single non-invasive genetic protocol.

Paul S, Shahar N, Seifan M, Bar-David S Ecol Evol. 2023; 13(10):e10616.

PMID: 37877104 PMC: 10590962. DOI: 10.1002/ece3.10616.


Development of short-target primers for species identification in biological studies of Carnivora.

Liu H, Wang D, Zhang C, Pu T, Xiong L, Wei F Ecol Evol. 2023; 13(5):e10135.

PMID: 37250442 PMC: 10212699. DOI: 10.1002/ece3.10135.


Landscape genetics of wolverines (): scale-dependent effects of bioclimatic, topographic, and anthropogenic variables.

Balkenhol N, Schwartz M, Inman R, Copeland J, Squires J, Anderson N J Mammal. 2020; 101(3):790-803.

PMID: 32665742 PMC: 7333878. DOI: 10.1093/jmammal/gyaa037.


Population genetics reveals high connectivity of giant panda populations across human disturbance features in key nature reserve.

Qiao M, Connor T, Shi X, Huang J, Huang Y, Zhang H Ecol Evol. 2019; 9(4):1809-1819.

PMID: 30847074 PMC: 6392360. DOI: 10.1002/ece3.4869.


References
1.
Kohn M, York E, Kamradt D, Haught G, Sauvajot R, Wayne R . Estimating population size by genotyping faeces. Proc Biol Sci. 1999; 266(1420):657-63. PMC: 1689828. DOI: 10.1098/rspb.1999.0686. View

2.
Taberlet , Waits , Luikart . Noninvasive genetic sampling: look before you leap. Trends Ecol Evol. 1999; 14(8):323-327. DOI: 10.1016/s0169-5347(99)01637-7. View

3.
Waits L, Luikart G, Taberlet P . Estimating the probability of identity among genotypes in natural populations: cautions and guidelines. Mol Ecol. 2001; 10(1):249-56. DOI: 10.1046/j.1365-294x.2001.01185.x. View

4.
Balkenhol N, Waits L . Molecular road ecology: exploring the potential of genetics for investigating transportation impacts on wildlife. Mol Ecol. 2009; 18(20):4151-64. DOI: 10.1111/j.1365-294X.2009.04322.x. View

5.
Kohn M, Wayne R . Facts from feces revisited. Trends Ecol Evol. 2011; 12(6):223-7. DOI: 10.1016/s0169-5347(97)01050-1. View