Parthenogenesis

Ants have a haplodiploid sex-determination system, where females are diploid and develop from fertilized eggs (sexually) and males are haploid and develop from unfertilized eggs (arrhenotokous parthenogenesis). However, a handful of ant species can produce female offspring parthenogenetically. In these, asexual reproduction produces a diploid embryo which develops from an unfertilized egg (thelytokous parthenogensis). Facultative parthenogenesis occurs when a female can produce offspring either sexually or asexually, although this ability is extremely rare.

With thelytoky, female offspring may or may not be complete clones of their mothers, depending on the type of parthenogenesis that takes place (automixis or apomixis) (Fournier et al., 2005; Rabling & Kronauer, 2013), and these offspring can develop into either queens or workers. Examples of such species included Mycocepurus smithii and clonal raider ant, Ooceraea biroi.

The workers in some species and the queens in others are known to reproduce by parthenogenesis. In Cataglyphis cursor, a European formicine ant, queens and workers can produce new queens by parthenogenesis while workers are produced sexually (Pearcy et al., 2004).

In Central and South American little fire ants, Wasmannia auropunctata, queens produce more queens through automictic parthenogenesis with central fusion. Sterile workers are usually produced from fertilized eggs. In some of the eggs fertilized by males, however, the fertilization can cause the female genetic material to be ablated from the zygote. In this way, males pass on only their genes to become fertile male offspring. This is the first recognized example of an animal species where both females and males can reproduce clonally resulting in a complete separation of male and female gene pools (Fournier et al., 2005). As a consequence, the males will only have fathers and the queens only mothers, while the sterile workers are the only ones with parents of both genders.

These ants get the benefits of both asexual and sexual reproduction - the daughters who can reproduce (the queens) have all of the mother's genes, while the sterile workers whose physical strength and disease resistance are important are produced sexually.

Reproductive strategy can vary across populations within a single species. Workers of Platythyrea punctata from the Caribbean are fully capable of parthenogenesis and produce diploid female offspring from unfertilized eggs, and mated females and males are rare. In contrast, workers in one colony from Costa Rica were incapable of thelytoky; instead mated workers produced all female offspring while the northernmost population from Texas show sexual reproduction, and individuals were incapable of reproduction by thelytoky (Kellner et al., 2013).

Taxa Known to be Parthenogenetic

Taxonomic Distribution

Subfamily placement (in red) of species known to reproduce using parthenogenesis.

	Leptanillinae

	Martialinae

Proceratiinae

	Amblyoponinae

	Apomyrminae

Ponerinae - 1 genus, 1 species

	Agroecomyrmecinae

	Paraponerinae

Dorylinae - 1 genus, 1 species

	Aneuretinae

	Dolichoderinae

	Myrmeciinae

	Pseudomyrmecinae

Formicinae - 2 genera, 3 species

Myrmicinae - 8 genera, 14 species

	Ectatomminae

	Heteroponerinae

References

Fournier, D., Estoup, A., Orivel, J., Foucaud, J., Jourdan, H., Le Breton, J., Keller, L. 2005. Clonal reproduction by males and females in the little fire ant. Nature (London) 435(7046): 1230-1234 (doi:10.1038/nature03705).
Gadagkar, R. 2004. Sex...Only if really necessary in a feminine monarchy. Science 306(5702): 1694-1695 (doi:10.1126/science.1106673).
Heinze, J. and Hölldobler, B. (1995). Thelytokous parthenogenesis and dominance hierarchies in the ponerine ant, Platythyrea punctata. Naturwissenschaften 82, 40-41 (doi:10.1007/BF01167871).
Kellner, K., Heinze, J. 2010. Mechanism of facultative parthenogenesis in the ant Platythyrea punctata. Evolutionary Ecology 25: 77-89 (doi:10.1007/s10682-010-9382-5).
Kellner, K., Seal, J.N., Heinze, J. 2013. Sex at the margins: parthenogenesis vs. facultative and obligate sex in a Neotropical ant. Journal of Evolutionary Biology 26, 108-117 (doi:10.1111/jeb.12025).
Lee, C.C., Hsu, S.H., Yang, C.C., Lin, C.C. 2017. Thelytokous parthenogenesis in the exotic dacetine ant Strumigenys rogeri (Hymenoptera: Formicidae) in Taiwan. Entomological Science 21: 28–33.
Masuko, K. 2013. Thelytokous parthenogenesis in the ant Strumigenys hexamera (Hymenoptera: Formicidae). Annals of the Entomological Society of America 106: 479–484.
Masuko, K. 2014. Thelytokous parthenogenesis in the ant Myrmecina nipponica. Zoological Science 31: 582–586 (doi:10.2108@zs140050).
Oxley, P.R., Ji, L., Fetter-Pruneda, I., McKenzie, S.K., Li, C., Hu, H., Zhang, G., Kronauer, D.J. 2014. The genome of the clonal raider ant Cerapachys biroi. Current Biology 24: 451–458 (doi:10.1016/j.cub.2014.01.018).
Pearcy, M., Aron, S., Doums, C., Keller, L. 2004. Conditional use of sex and parthenogenesis for worker and queen production in ants. Science. 306 (5702): 1780–1783 (doi:10.1126/science.1105453).
Rabeling, C., Kronauer, D.J.C. 2013. Evolution of thelytokous parthenogenesis in eusocial Hymenoptera. Annual Review of Entomology 58: 273-292 (doi:10.1146/annurev-ento-120811-153710).
Rey, O., Loiseau, A., Facon, B., Foucaud, J., Orivel, J., Cornuet, J.-M., Robert, S., Dobigny, G., Delabie, J.H.C., Mariano, C.D.S.F., Estoup, A. 2011. Meiotic recombination dramatically decreased in thelytokous aueens of the Little Fire Ant and their sexually produced workers. Molecular Biology and Evolution 28, 2591–2601 (doi:10.1093/molbev/msr082).
Wang, C., Sung, P.-J., Lin, C.-C., Ito, F., Billen, J. 2023. Parthenogenetic reproduction in Strumigenys ants: An update. Insects 14, 195 (doi:10.3390/insects14020195).