Haplodiploidy is a sex-determination system in which males develop from unfertilized eggs and are haploid, and females develop from fertilized eggs and are diploid. Haplodiploidy is sometimes called arrhenotoky.
Haplodiploidy determines the sex in all members of the insect order Hymenoptera (bees, ants, and wasps),p408 Coccidae, and the Thysanoptera ('thrips'). The system also occurs sporadically in some spider mites, Hemiptera, Coleoptera (bark beetles), and rotifers.
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 are haploid.
The haplodiploid sex-determination system has a number of peculiarities. For example, a male has no father and cannot have sons, but he has a grandfather and can have grandsons. Additionally, if a eusocial-insect colony has only one queen, and she has only mated once, then the relatedness between workers (diploid females) in a hive or nest is 0.75. This means the workers in such monogamous single-queen colonies are significantly more closely related than in other sex determination systems where the relatedness of siblings is usually no more than 0.5. It is this point which drives the kin selection theory of how eusociality evolved.:465 Whether haplodiploidy did in fact pave the way for the evolution of eusociality is still a matter of debate.
Another feature of the haplodiploidy system is that recessive lethal and deleterious alleles will be removed from the population rapidly because they will automatically be expressed in the males (dominant lethal and deleterious alleles are removed from the population every time they arise, as they kill any individual they arise in).
Haplodiploidy is not the same thing as an XO sex-determination system. In Haplodiploidy, males receive one half of the chromosomes that female receive, including autosomes. In an XO sex-determination system, males and females receive an equal number of autosomes, but when it comes to sex chromosomes, females will receive two X chromosomes while males will receive only a single X chromosome.
Several models have been proposed for the genetic mechanisms of haplodiploid sex-determination. The model most commonly referred to is the complementary allele model. According to this model, if an individual is heterozygous for a certain locus, it develops into a female, whereas hemizygous and homozygous individuals develop into males. In other words, diploid offspring develop from fertilized eggs, and are normally female, while haploid offspring develop into males from unfertilized eggs. Diploid males would be infertile, as their cells would not undergo meiosis to form sperm. Therefore the sperm would be diploid, which means that their offspring would be triploid. Since hymenopteran mother and sons share the same genes, they may be especially sensitive to inbreeding: Inbreeding reduces the number of different sex alleles present in a population, hence increasing the occurrence of diploid males.
After mating, each fertile hymenopteran female stores sperm in an internal sac called the spermatheca. The mated female controls the release of stored sperm from within the organ: If she releases sperm as an egg passes down her oviduct, the egg is fertilized. Social bees, wasps, and ants can modify sex ratios within colonies which maximizes relatedness among members and generates a workforce appropriate to surrounding conditions. In other solitary hymenopterans, the females lay unfertilized male eggs on poorer food sources while laying the fertilized female eggs on better food sources, possibly because the fitness of females will be more adversely affected by shortages in their early life. Sex ratio manipulation is also practiced by haplodiploid ambrosia beetles, who lay more male eggs when the chances for males to disperse and mate with females in different sites are greater.
Sex-determination in honey bees
In honeybees the drones (males) are entirely derived from the queen, their mother. The diploid queen has 32 chromosomes and the haploid drones have 16 chromosomes. Drones produce sperm cells that contain their entire genome, so the sperm are all genetically identical except for mutations. The male bees' genetic makeup is therefore entirely derived from the mother, while the genetic makeup of the female worker bees is half derived from the mother, and half from the father. Thus, if a queen bee mates with only one drone, any two of her daughters will share, on average, 3/4 of their genes. The diploid queen's genome is recombined for her daughters, but the haploid father's genome is inherited by his daughters "as is".
There are rare instances of diploid drone larvae. This phenomenon usually arises when there is more than two generations of brother-sister mating. Sex determination in honey bees is initially due to a single locus, called the complementary sex determiner (csd) gene. In developing bees, if the conditions are that the individual is heterozygous for the csd gene, they will develop into females. If the conditions are so that the individual is hemizygous or homozygous for the csd gene, they will develop into males. The instances where the individual is homozygous at this gene are the instances of diploid males. Diploid males do not survive to adulthood, as the nurse worker bees will cannibalize the diploid males upon hatching.
While workers can lay unfertilized eggs that become their sons, haplodiploid sex-determination system increases the individual's fitness due to indirect selection. Since the worker is more related to the queen's daughters (her sisters) than to her own offspring, helping the queen's offspring to survive aids the spread of the same genes that the worker possesses more efficiently than direct reproduction.  Batches of worker bees are short lived and are constantly being replaced by the next batch, so this kin selection is possibly a strategy to ensure the proper working of the hive. However, since queens usually mate with a dozen drones or more, not all workers are full sisters. Due to the separate storage of drone sperm, a specific batch of brood may be more closely related than a specific batch of brood laid at a later date.
Relatedness ratios in haplodiploidy
Relatedness is used to calculate the strength of kin selection (via Hamilton's rule). The haplodiploidy hypothesis proposes that the unusual 3/4 relatedness coefficient amongst full haplodiploid sisters is responsible for the frequency of evolution of eusocial behavior in hymenopterans.
In normal sexual reproduction, the father has two sets of chromosomes, and crossing over takes place between the chromatids of each pair during the meiosis which produces the sperm. Therefore, the sperms are not identical, because in each chromosome of a pair there will be different alleles at many of the loci. But when the father is haploid all the sperm will be identical (except for a small number where gene mutations have taken place in the germ line). So, as long as a female has mated with only one male, all of her female offspring will inherit the male's chromosomes 100% intact. In Hymenoptera, the males generally produce enough sperm to last the female for her whole lifetime after a single mating event with that male.
Relatedness coefficients in haplodiploid organisms are as follows, assuming that a female has only mated once.
|Sex||Daughter||Son||Mother||Father||Full Sister||Full Brother|
Under this assumption that mothers only mate once, sisters are more strongly related to each other than to their own daughters. This fact has been used to explain the evolution of eusociality in many hymenopterans. However, colonies which have workers from multiple queens or queens which have mated multiple times will have worker-to-worker relatedness which is less than worker-to-daughter relatedness.
- Green-beard effect
- Sex-determination system
- Sexual differentiation
- Worker policing
- X chromosome
- Y chromosome
- King R.C; Stansfield W.D. and Mulligan P.K. 2006. A dictionary of genetics. 7th ed, Oxford University Press, p194. ISBN 0-19-530761-5
- Grimaldi D. and Engel M.S. 2005. The evolution of the insects. Cambridge University Press. ISBN 0-521-82149-5
- Gullan, P.J. and Cook, L.G. (2007) Phylogeny and higher classification of the scale insects Zootaxa 1668: 413–425
- White, Michael J.D. (1984). "Chromosomal mechanisms in animal reproduction". Bolletino di zoologia (free full text)doi:10.1080/11250008409439455. ISSN 0373-4137. 51 (1-2): 1–23.
- 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. Retrieved 2008-08-04.
- Edward O. Wilson (2005). "Kin Selection as the Key to Altruism: Its Rise and Fall". Social Research 72 (1): 159–166. Retrieved 2013-09-22.
- van Wilgenburg, Ellen; Driessen, Gerard & Beukeboom, Leo W. Single locus complementary sex determination in Hymenoptera: an "unintelligent" design? Frontiers in Zoology 2006, 3:1
- Mahowald, Michael; von Wettberg, Eric Sex determination in the Hymenoptera Swarthmore College (1999)
- Chow, A.; MacKauer, M. (1996). "Sequential allocation of offspring sexes in the hyperparasitoid wasp,Dendrocerus carpenteri". Animal Behaviour 51 (4): 859. doi:10.1006/anbe.1996.0090.
- Van Alphen, J. J. M.; Thunnissen, I. (1982). "Host Selection and Sex Allocation by Pachycrepoideus Vindemiae Rondani (Pteromalidae) as a Facultative Hyperparasitoid of Asobara Tabida Nees (Braconidae; Alysiinae) and Leptopilina Heterotoma (Cynipoidea; Eucoilidae)". Netherlands Journal of Zoology 33 (4): 497. doi:10.1163/002829683X00228.
- Peer, K.; Taborsky, M. (2004). "Female ambrosia beetles adjust their offspring sex ratio according to outbreeding opportunities for their sons". Journal of Evolutionary Biology 17 (2): 257–264. doi:10.1111/j.1420-9101.2003.00687.x. PMID 15009259.
- Sinervo, Barry Kin Selection and Haplodiploidy in Social Hymenoptera 1997
- Woyka, J.; Pszczelnictwa, Zaklad; Drone Larvae from Fertilized Eggs of the Honey Bee Journal of Apiculture Research, (1963), pages 19-24
- Weinstock, George M.; Robinson, Gene E., & the Honeybee Genome Sequencing Consortium Insights into social insects from the genome of the honeybee Apis mellifera Nature, volume "'443'" (2006), pages 931-949
- Santomauro, Giulia; Oldham, Neil J.; Boland, Wilhelm; Engels Wolf; Cannibalism of Diploid Drone Larvae in the Honey Bee (Apis mellifera) is Released by Odd Pattern of Circular Substance Journal of Apiculture Research, volume "'43'" (2004), pages 69-74
- Foster, Kevin R.; Ratnieks, Francis L. W. The effect of sex-allocation biasing on the evolution of worker policing in hymenopteran societies The American Naturalist, volume 158 (2001), pages 615–623
- 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
- Kevin R. Foster, Tom Wenseleers and Francis L.W. Ratnieks (2006). "Kin selection is the key to altruism". Trends in ecology & evolution 21 (2): 57–60. doi:10.1016/j.tree.2005.11.020.
- Beye, Martin et al 1999. Unusually high recombination rate detected in the sex locus region of the honey bee (Apis mellifera) Genetics, 153, 1701-1708.
- Wu Z. et al. 2005. Single-locus complementary sex determination absent in Heterospilus prosopidis (Hymenoptera: Braconidae) Heredity 95, 228–234
- Ratnieks, Francis 1988. Reproductive harmony via mutual policing by workers in eusocial hymenoptera American Naturalist 132(2) 217-236.