Skip to main page content
U.S. flag

An official website of the United States government

Dot gov

The .gov means it’s official.
Federal government websites often end in .gov or .mil. Before sharing sensitive information, make sure you’re on a federal government site.

Https

The site is secure.
The https:// ensures that you are connecting to the official website and that any information you provide is encrypted and transmitted securely.

Access keys NCBI Homepage MyNCBI Homepage Main Content Main Navigation
. 2016 Jun 15;283(1832):20160196.
doi: 10.1098/rspb.2016.0196.

Facultative asexual reproduction and genetic diversity of populations in the humivorous termite Cavitermes tuberosus

Affiliations

Facultative asexual reproduction and genetic diversity of populations in the humivorous termite Cavitermes tuberosus

Denis Fournier et al. Proc Biol Sci. .

Abstract

Termite colonies are typically founded by a pair of sexually reproducing dispersers, which can sometimes be replaced by some of their offspring. Some Reticulitermes and Embiratermes species routinely practice asexual queen succession (AQS): the queen is replaced by neotenic daughters produced by parthenogenesis, which mate with the primary king. Here, to cast light on the evolution of AQS, we investigated another candidate species, Cavitermes tuberosus (Termitinae). Of 95 nests, 39 contained a primary queen and 28 contained neotenic females (2-667 individuals), usually with the primary king. Microsatellite analyses confirmed that colonies were initiated by single pairs after large dispersal flights. More than 80% of the neotenic females were of exclusively maternal origin and completely homozygous, suggesting automictic parthenogenesis with gamete duplication. Conversely, workers, soldiers, and most alates and primary reproductives were produced sexually. AQS often occurs late, after colonies have reached maturity, whereas early AQS in other species may boost the young colony's growth rate. We suggest additional benefits of AQS in C. tuberosus, related with a smaller size, lesser stability and higher mobility of colonies. Our data add to the phylogenetical dispersion and diversity of modalities of AQS in termites, supporting a multiple evolutionary origin of this process.

Keywords: Isoptera; Termitidae; gamete duplication; population structure; reproductive strategies; thelytokous parthenogenesis.

PubMed Disclaimer

Figures

Figure 1.
Figure 1.
Proportion of sexually (dark grey) and parthenogenetically (light grey) produced individuals for primary reproductives, neotenics, dispersers (i.e. alates and alate-destined fifth instar nymphs), workers, soldiers and nymphs (from instars 1 to 4) of C. tuberosus. Numbers of individuals indicated within bars (no indication = 0).

Similar articles

Cited by

References

    1. Bengtsson BO. 2009. Asex and evolution: a very large-scale overview. In Lost sex—the evolutionary biology of parthenogenesis (eds Schön I, Martens K, van Dijk P), pp. 1–19. Berlin, Germany: Springer.
    1. Simon J-C, Rispe C, Sunnucks P. 2002. Ecology and evolution of sex in aphids. Trends Ecol. Evol. 17, 34–39. (10.1016/S0169-5347(01)02331-X) - DOI
    1. Decaestecker E, De Meester L, Mergeay J. 2009. Cyclical parthenogenesis in Daphnia: sexual versus asexual reproduction. In Lost sex—the evolutionary biology of parthenogenesis (eds Schön I, Martens K, van Dijk P), pp. 295–316. Berlin, Germany: Springer.
    1. Fournier D, Aron S. 2009. No-male's land for an Amazonian ant. Curr. Biol. 19, R738–R740. (10.1016/j.cub.2009.07.021) - DOI - PubMed
    1. Wenseleers T, Van Oystaeyen A. 2011. Unusual modes of reproduction in social insects: shedding light on the evolutionary paradox of sex. BioEssays 33, 927–937. (10.1002/bies.201100096) - DOI - PubMed