Elsevier

Animal Behaviour

Volume 170, December 2020, Pages 111-118
Animal Behaviour

From quiet-night-in to party animal: sex ratio and density affect male/female aggregations in a ‘harem’ polygynous insect

https://doi.org/10.1016/j.anbehav.2020.10.019Get rights and content

Highlights

  • Tree wētā aggregations in roosts vary depending on sex ratio and population density.

  • Males with larger heads are associated with more females.

  • Males avoid roosting with other males unless females are present in the roosts also.

Varying forms of polygyny are observed across many animal groups. In some species, a male defends a group of females from other males, and successful defence leads to greater reproductive success. This is often referred to as harem polygyny and is most observed in mammals. A female-biased sex ratio has been associated with harem polygynous species. In such populations, formation of ‘harems’ may be an inevitable consequence of the relative lack of available males, rather than multiple females actively choosing to mate with a subset of specific males. Although a rare mating system for insects, harem polygyny has been described in several orders, including tree wētā (Orthoptera: Anostostomatidae: Hemideina) in New Zealand. Aggregations of multiple females have been found with a single male in their diurnal roosts. We aimed to determine how the sex ratio and local density of Hemideina thoracica affected the formation of harems in laboratory conditions. ‘Harems’ were observed when the sex ratio was female biased, but no more than would be expected by chance arrangement of individuals, although females preferred to associate with males rather than be alone. Conversely, when the sex ratio was male biased, females preferred to be alone. The number of females associated with each male was lowest when the sex ratio was even and local density was low. However, males and females did not associate randomly: when local density was high aggregations of multiple males with multiple females were observed more often than expected by chance, suggesting that, in contrast to classic ‘harem’ behaviour, males accepted other males being present as long as females were also found in the roost. Additionally, females were more likely to be associated with males than in low-density conditions. Individuals in this study showed much more flexibility in their mating behaviour than what would be expected in a harem polygynous species.

Section snippets

Methods

The sex ratio of a wild population of H. thoracica was measured during nocturnal observations at Matuku Reserve (-36.86, 174.48) in the Waitakere ranges near Auckland, New Zealand in January–March 2017 and 2018. Two observers walked down the track and carefully scanned the foliage up to 10 m into the bush from the track. The sex, life stage (juvenile or adult), weight (assessed using Toltec portable field scales), head length and lengths of the hind tibia (using Mako digital callipers measuring

Results

The sex ratio of H. thoracica at Matuku reserve over the two seasons was female biased for both adults and juveniles (Table 2). The adult sex ratio was not significantly different from even in 2017 (1:1.29 males: females; binomial test: N = 39, P = 0.522) and significantly female biased in 2018 (1:1.60 males: females; binomial test: N = 104, P = 0.024).

In the laboratory trials, females and males did not distribute themselves randomly, and there were significant differences between the observed and

Discussion

The manipulation of sex ratio and density showed that as the number and proportion of male and female wētā changed from an even sex ratio to male or female biased so did their aggregation behaviour. In all treatments empty roosts were observed much more commonly than expected. This suggests that individuals chose to aggregate rather than spreading themselves among the available roosts. In high-density/even sex ratio (6M6F) treatments, there was a higher incidence of aggregations of multiple

Acknowledgments

We thank the Royal Forest & Bird Protection Society and John Staniland for access to Matuku Reserve administered by the Waitakere Branch. M.J.G. was supported by Deakin University Centre for Integrated Ecology funding and a Deakin University Postgraduate Research Scholarship and received funding from the New Zealand Entomological Society 21st Anniversary Fund and the Royal Society of New Zealand Hutton Fund. Thanks are due to those who helped with fieldwork for this project: Leilani Walker,

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