Eusociality is a term in animal behaviour for the more complex kinds of social organisation. The term "eusocial" was introduced in 1966 by Suzanne Batra. E.O. Wilson gave it a more precise meaning.
Meaning of the term [change]
- Different animals have different jobs to do. There is a division of labour. Some castes may be sterile.
- Animal generations overlap. There are different generations in the hive or nest.
- Animals cooperate to care for the young.
The most familiar examples of eusociality are insects such as ants, bees, wasps, and termites. All of these are colonial animals which have queens for reproduction. The animals that are workers or soldiers are usually sterile--they cannot have offspring.
Reproductive specialization usually means involves the production of sterile members of the species. They do specialized tasks, often caring for the reproductive members. It includes individuals whose behaviour, body shape and function is modified for group defence, including self-sacrifice (altruism).
Definition debates [change]
||The English used in this article may not be easy for everybody to understand. (April 2012)|
Evolution means that those animals that are better adapted to their environment have a better chance of passing on their genes. In colonies of eusocial animals, some animals are sterile. They can not pass on their genes at all. How can these animals evolve and persist? Since they do not breed, their fitness should be zero and any genes causing this condition should be eliminated from the population immediately. In Origin of Species (first edition, Ch. 8), Darwin called this behavior the "one special difficulty, which at first appeared to me insuperable, and actually fatal to my theory". Darwin thought that the resolution to the paradox would lie in the close family relationship.
Darwin could not say more because he did no know what the mechanism of heredity was. The first explanations were kin selection, and inclusive fitness. Both rely on the discovery of how genes are inherited. This discovery was made after Darwin had published On the Origin of Species, and not understood until after 1900.
Early ideas on eusociality included suggestions that trophallaxis or food sharing was a basis for sociality. The most widely accepted model to explain eusociality is based on W.D. Hamilton's idea of inclusive fitness.
Inclusive fitness [change]
In this system, sex is determined by the number of sets of chromosomes an individual receives. An offspring formed from the union of a sperm and an egg develops as a female, and an unfertilized egg develops as a male. This means that the males have half the number of chromosomes that a female has, and so are haploid.
The haplodiploid sex-determination system has a number of peculiarities. Most importantly, the relatedness between the sisterhood of worker bees in a hive or nest is 0.75. This means the workers are significantly more closely related than siblings in other sex determination systems. It is this point which drives the kin selection theory of how eusociality evolved.p465
If the theory of inclusive fitness is accurate, the haplodiploidy makes kin selection easier. Sisters are more related to each other than to any offspring they might have. Hamilton called them supersisters. On average, two supersisters have 75 percent of the same genes. If they breed, they would share only half of their genome with their offspring. From the selfish gene's point-of-view, it is better to raise more sisters. Even though workers often do not reproduce, they are potentially passing on more of their genes by caring for sisters than they would by having their own offspring.
This unusual situation may explain why eusociality evolved several times in the haplodiploid group Hymenoptera — ants, bees and wasps. As of 2009, 11 separate cases are known. However, Hymenoptera is a large group and the majority of its species are not social. Furthermore, highly developed eusociality also exists in non-hymenopterans, perhaps most obviously in termites. Most such cases involve organisms that display high levels of inbreeding, so that colony members share more than half of their genes. Therefore the same model is considered to apply to these species.
Reeve and Holldobler put forward a theory of a superorganism. They look at competition and co-operation between groups as well as within groups. In their model, an individual's inclusive fitness varies according to how much it invests in within-group competition (e.g. hoarding a private food cache) versus between-group competition (e.g. contributing to common foraging); and on its relatedness to the other group members.
In a colony with one breeder (queen) and many workers, the evolutionarily stable state is for each individual to invest entirely in helping the group. This leads to a perfect "superorganism". In other words, the eusociality is stable, a result that agrees with Hamilton's findings. Also, they show that the effect is reinforced if there are many groups competing for the same resources.
Other examples [change]
Recently, some species of gall-making aphids (Order Hemiptera) and thrips (Order Thysanoptera) were found to be eusocial, with many separate origins of the state (convergent evolution). These species have extremely high relatedness among individuals due to their partially asexual mode of reproduction (sterile soldier castes being of the same clone as the reproducing female), but the gall-inhabiting behavior gives these species a defensible resource that sets them apart from related species with similar genetics. In these groups, therefore, high relatedness alone does not lead to the evolution of social behavior, but requires that groups occur in a restricted, shared area.
Similarly, eusociality has been found among some crustaceans and other arthropods. On some tropical reefs, several species of minute Synalpheus pistol shrimp that depend on certain sponges for the survival of their colony, live eusocially, with a single breeding female and a preponderance of male defenders, armed with enlarged snapping claws. Again, there is a single shared domicile for the colony members, and the non-breeding members act to defend it.
Related pages [change]
- Batra S.W.T. 1966. Nests and social behavior of halictine bees of India (Hymenoptera: Halictidae). Indian J. Entomol 28 375-393.
- Wilson E.O. 1971. The insect societies. Harvard University Press. Cambridge. Massachusetts.
- Michener C.D. 1969. Ann. Rev. Entomol. 14, 299-342.
- Gadagkar, Raghavendra 1993. And now... eusocial thrips!. Current Science 64(4) 215-216. PDF
- Burda H. Honeycutt R.L. Begall S. Locker-Grutjen O & Scharff A. 2000. Are naked and common mole-rats eusocial and if so, why? Behavioral Ecology and Sociobiology 47 293-303 Abstract
- Crespi B.J. and Yanega D. 1995. The definition of eusociality. Behav. Ecol. 6, 109–115
- Kevin R. Foster & Francis L.W. Ratnieks 2005. A new eusocial vertebrate? Trends in Ecology and Evolution 20(7):363-364 PDF
- James T. Costa & Terrence D. Fitzgerald 2005. Social terminology revisited: where are we ten years later? Ann. Zool. Fennici 42:559-564 PDF
- Wheeler W.M. 1918. A study of some ant larvae with a consideration of the origin and meaning of social habits among insects. Proc. Am. Phil. Soc. 57, 293-343.
- Grimaldi D. and Engel M.S. 2005. The evolution of the insects. Cambridge University Press. ISBN 0-521-82149-5
- The relatedness of siblings is usually 0.5.
- Hamilton W.D. 1964. The genetical evolution of social behaviour, I and II. Journal of Theoretical Biology 7, 1–52. Reprinted with comments in Hamilton W.D. 1996. Narrow roads of geneland, volume I Evolution of social behaviour. Freeman/Spektrum, Oxford. ISBN 0-7167-4530-5
- Hughes W.O.H. et al (2008). "Ancestral monogamy shows kin selection is key to the evolution of eusociality". Science 320 (5880): 1213–1216. doi:10.1126/science.1156108. PMID 18511689. http://www.sciencemag.org/cgi/content/abstract/320/5880/1213. Retrieved 2008-08-04.
- Reeve H.K. and Hölldobler B. 2007. The emergence of a superorganism through intergroup competition. Proceedings of the National Academy of Sciences 104: 9736-9740
- Crespi. B.J. 1992 Eusociality in Australian gall thrips. Nature 359: 724-726.
- Duffy, J. Emmett; Cheryl L. Morrison and Ruben Rios (2000). "Multiple origins of eusociality among sponge-dwelling shrimps (Synalpheus)". Evolution 54 (2): 503-516.
- Duffy, J. E (1998). "On the frequency of eusociality in snapping shrimps (Decapoda : Alpheidae), with description of a second eusocial species". Bulletin of marine science 63 (2): 387-400.