Information

Parthenogenesis in Bees


Parthenogenesis is defined as:

"A type of asexual reproduction in which egg develops without fertilization to form a new individual."

If parthenogenesis takes place in bees, a drone or male bee is produced.

My question is that parthenogenesis is the development of EGG into new individual so, how can egg be developed into male because egg won't have that "Y" chromosome required for male offspring?


Because the "Y chromosome" has nothing to do with sex determination in bees. Instead, the number of X chromosomes determines the sex. With only one X chromosome, the egg will develop into a male. This is called a haplodiploid system of sex determination (the male bees are haploid, having only half the number of chromosomes).

EDIT: I should add that there are many systems of sex determination, not just XY or the haplodiploid system. See the Z-W system (males are ZZ and females are ZW), the X0 system (the males are diploid for all but the sex chromosome), and temperature-dependent system of sex determination.


The Cape honey bee in South Africa can create female offspring without the queen being mated. Female stick insects can also produce female offspring without males, all daughters will however be clones of the mother. I guess this is a last resort to ensure survival in difficult times until a male is found to mate with.


Parthenogenesis

Origins

Origins of parthenogenesis are not well understood in mechanistic terms. One recurring pattern is that obligately parthenogenetic lineages are often of hybrid origin. Possibly this is related to the disruption of meiosis and to the sexual sterility that frequently results from hybridization. A related pattern is that parthenogenetic lineages are often polyploid: polyploidy might disrupt meiosis but is fully compatible with apomictic parthenogenesis. In recent decades, it has become clear that many origins of obligate parthenogenesis in invertebrates have been induced by Wolbachia and other intracellular bacteria. Because Wolbachia are transmitted vertically from mother to offspring through eggs – but not transmitted through sperm – the bacteria clearly benefit from distorting the sex ratios of their hosts toward production of more female offspring, and parthenogenesis induction is one of several means the bacteria have evolved to accomplish this, though the mechanisms remain largely unclear. Some groups clearly have a much lower rate of origin of parthenogenetic lineages than other groups, with a stark example being the total lack of successful parthenogenesis in mammals. It has now been shown that this is due to the genomic imprinting system of mammals – experiments show that parthenogenetic mice are viable if imprinted loci are suitably manipulated.


WHAT IS PARTHENOGENESIS?

Parthenogenesis is a type of asexual reproduction in which the offspring comes from a non-fertilized ovum. Without fertilization (union of the oocyte’s and the sperm’s genetic material) the offspring won’t have any part of the father’s DNA (if there is a father). The resulting babies will be genetic copies (clones) of their mother.

In parthenogenetic animals, the lack of paternal genetic material must be compensated because in many species haploid foetuses are non-viable. In these species diploidy (2n chromosomes) is usually re-established through a process called automixis. Yet in some species, haploid individuals with parthenogenetic origins are viable and have no problems in surviving.

It is impossible to pose a general example for asexual reproduction, as it is widely distributed through very different animal groups and there are many cases with many differences among them. Bellow, we’ll present you some examples of different strategies used by animals to reproduce asexually.


References

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Butler, C G, Callow, R K, and Johnston, N C. 1961. The isolation and synthesis of queen substance, 9-oxodec-2-enoic acid, a honeybee pheromone. Proc Roy Soc Lond, B155, 417–432.

Cohn, N S. 1969. Elements of Cytology, 2nd edn. Harcourt, Brace and World, New York.

Dupraw, E J. 1967. The honeybee embryo. In: Wilt, F. H. and Wessels, N. K. (eds) Methods in Developmental Biology, pp. 183–217. Crowell, New York.

Epplen, J T. 1988. On simple repeated GATA/GACA sequences: a critical reappraisal. J Hered, 79, 409–417.

Epplen, J T, and Zischler, H. 1989. DNA Fingerprinting with Oligonucleotides. Fresenius, Oberursel.

Greeff, J M, and Villet, M H. 1993. Deducing the coefficient of relationship by the amount of recombination produced during automictic parthenogenesis. Heredity, 70, 499–502.

Haberl, M, and Moritz, R F A. 1994. Estimation of intracolonial worker relationship in a honeybee colony (Apis mellifera L.) using DNA fingerprinting. Insect Soc. (in press).

Hearne, E M, and Huskins, C L. 1935. Chromosome pairing in Melanoplus femur-rubrum. Cytologia, 6, 123–147.

Huskins, C L, and Newcombe, H B. 1941. An analysis of chiasma pairs showing chromatid interference in Trillium erectum L. Genetics, 26, 101–127.

Kauhausen, D. 1978. Genetische Analyse der thelytoken Parthenogenese bei der Kap-Honigbiene (Apis mellifera capensis Esch.). Unpublished Thesis, J. W. Goethe Universität, Frankfurt/Main.

Moritz, R F A. 1990. Natural and artificial selection in the Cape honeybee Apis mellifera capensis. In: Anderson, R. H. and Buys, B. (eds) Bees and Beekeeping in Southern Africa, pp. 63–73. POSA & WPBA Cape Town.

Moritz, R F A, and Klepsch, A. 1985. Estimating heritabilities of worker characters: a new approach using laying workers of the Cape honeybee (Apis mellifera capensis Esch.). Apidologie, 16, 47–56.

Moritz, R F A, Meusel, M, and Haberl, M. 1991. Oligonucleotide DNA fingerprinting discriminates super and half-sisters in honeybee colonies (Apis mellifera L.). Naturwissenschaften, 78, 422–424.

Onions, G W. 1912. South-African ‘fertile worker bees’. Agric J Union S Africa, 3, 720–728.

Page, R E, and Erickson, E E. 1988. Reproduction by worker honey bees (Apis mellifera). Behav Ecol Sociobiol, 23, 117–126.

Sambrook, J, Fritsch, E F, and Maniatis, T. 1989. Molecular Cloning — a Laboratory Manual, 2nd edn. Cold Spring Harbor Laboratory Press, New York.

Snodgrass, R E. 1925. Anatomy and Physiology of the Honeybee. McGraw-Hill, New York.

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Sybenga, J. 1975. Meiotic Configurations. Springer Verlag, Berlin.

Sylvester, H A. 1986. Biochemical genetics. In: Rinderer, T. E. (ed.) Bee Genetics and Breeding, pp. 177–203. Academic Press, Orlando.

Tucker, K W. 1958. Automictic parthenogenesis in the honeybee. Genetics, 43, 299–316.

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Verma, S, and Ruttner, F. 1983. Cytological analysis of the thelytokous parthenogenesis in the Cape honeybee, (Apis mellifera capensis Escholtz). Apidologie, 14, 41–57.

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Triaeris stenaspis is a spider species belonging to the Oonopidae family. Triaeris stenaspis can be found in the subtropical and tropical parts of the world including Australia, Madagascar, Argentina, the United States, and various isolated islands like Cook, Marquesas, Hawaii, and the Galapagos Islands. The Triaeris stenaspis is believed to be parthenogenetic since no male species has ever been found. Parthenogenesis has been proven in various Triaeris stenaspis species that were kept in laboratory-conditions. The spiders were reared since they were hatched until they died. All the spiders were female, and they laid fertile eggs which hatched into female offspring. Another spider species that is believed to be parthenogenetic is the Heteroonops spinimanus.

Brahminy blind snake, also known as Indotyphlops braminus, is a non-poisonous blind snake that is native to Asia and Africa. Brahminy blind snakes have been introduced in other parts of the world like Oceania, the Americas, and Australia. Brahminy blind snakes are fossorial creatures that resemble earthworms. These blind snakes are parthenogenetic, and so far all the specimens collected are females. These snakes can lay eggs or give birth to female offspring that are genetically identical.


Contents

Some species reproduce exclusively by parthenogenesis (such as the bdelloid rotifers), while others can switch between sexual reproduction and parthenogenesis. This is called facultative parthenogenesis (other terms are cyclical parthenogenesis, heterogamy [9] [10] or heterogony [11] [12] ). The switch between sexuality and parthenogenesis in such species may be triggered by the season (aphid, some gall wasps), or by a lack of males or by conditions that favour rapid population growth (rotifers and cladocerans like Daphnia). In these species asexual reproduction occurs either in summer (aphids) or as long as conditions are favourable. This is because in asexual reproduction a successful genotype can spread quickly without being modified by sex or wasting resources on male offspring who won't give birth. In times of stress, offspring produced by sexual reproduction may be fitter as they have new, possibly beneficial gene combinations. In addition, sexual reproduction provides the benefit of meiotic recombination between non-sister chromosomes, a process associated with repair of DNA double-strand breaks and other DNA damages that may be induced by stressful conditions. [13]

Many taxa with heterogony have within them species that have lost the sexual phase and are now completely asexual. Many other cases of obligate parthenogenesis (or gynogenesis) are found among polyploids and hybrids where the chromosomes cannot pair for meiosis.

The production of female offspring by parthenogenesis is referred to as thelytoky (e.g., aphids) while the production of males by parthenogenesis is referred to as arrhenotoky (e.g., bees). When unfertilized eggs develop into both males and females, the phenomenon is called deuterotoky. [14]

Parthenogenesis can occur without meiosis through mitotic oogenesis. This is called apomictic parthenogenesis. Mature egg cells are produced by mitotic divisions, and these cells directly develop into embryos. In flowering plants, cells of the gametophyte can undergo this process. The offspring produced by apomictic parthenogenesis are full clones of their mother. Examples include aphids.

Parthenogenesis involving meiosis is more complicated. In some cases, the offspring are haploid (e.g., male ants). In other cases, collectively called automictic parthenogenesis, the ploidy is restored to diploidy by various means. This is because haploid individuals are not viable in most species. In automictic parthenogenesis, the offspring differ from one another and from their mother. They are called half clones of their mother.

Automictic Edit

Automixis [15] is a term that covers several reproductive mechanisms, some of which are parthenogenetic. [16]

Diploidy might be restored by the doubling of the chromosomes without cell division before meiosis begins or after meiosis is completed. This is referred to as an endomitotic cycle. This may also happen by the fusion of the first two blastomeres. Other species restore their ploidy by the fusion of the meiotic products. The chromosomes may not separate at one of the two anaphases (called restitutional meiosis) or the nuclei produced may fuse or one of the polar bodies may fuse with the egg cell at some stage during its maturation.

Some authors consider all forms of automixis sexual as they involve recombination. Many others classify the endomitotic variants as asexual and consider the resulting embryos parthenogenetic. Among these authors, the threshold for classifying automixis as a sexual process depends on when the products of anaphase I or of anaphase II are joined together. The criterion for "sexuality" varies from all cases of restitutional meiosis, [17] to those where the nuclei fuse or to only those where gametes are mature at the time of fusion. [16] Those cases of automixis that are classified as sexual reproduction are compared to self-fertilization in their mechanism and consequences.

The genetic composition of the offspring depends on what type of apomixis takes place. When endomitosis occurs before meiosis [18] [19] or when central fusion occurs (restitutional meiosis of anaphase I or the fusion of its products), the offspring get all [18] [20] to more than half of the mother's genetic material and heterozygosity is mostly preserved [21] (if the mother has two alleles for a locus, it is likely that the offspring will get both). This is because in anaphase I the homologous chromosomes are separated. Heterozygosity is not completely preserved when crossing over occurs in central fusion. [22] In the case of pre-meiotic doubling, recombination -if it happens- occurs between identical sister chromatids. [18]

If terminal fusion (restitutional meiosis of anaphase II or the fusion of its products) occurs, a little over half the mother's genetic material is present in the offspring and the offspring are mostly homozygous. [23] This is because at anaphase II the sister chromatids are separated and whatever heterozygosity is present is due to crossing over. In the case of endomitosis after meiosis, the offspring is completely homozygous and has only half the mother's genetic material.

This can result in parthenogenetic offspring being unique from each other and from their mother.

Sex of the offspring Edit

In apomictic parthenogenesis, the offspring are clones of the mother and hence (except for aphids) are usually female. In the case of aphids, parthenogenetically produced males and females are clones of their mother except that the males lack one of the X chromosomes (XO). [24]

When meiosis is involved, the sex of the offspring will depend on the type of sex determination system and the type of apomixis. In species that use the XY sex-determination system, parthenogenetic offspring will have two X chromosomes and are female. In species that use the ZW sex-determination system the offspring genotype may be one of ZW (female), [20] [21] ZZ (male), or WW (non-viable in most species [23] but a fertile, [ dubious – discuss ] viable female in a few (e.g., boas)). [23] ZW offspring are produced by endoreplication before meiosis or by central fusion. [20] [21] ZZ and WW offspring occur either by terminal fusion [23] or by endomitosis in the egg cell.

In polyploid obligate parthenogens like the whiptail lizard, all the offspring are female. [19]

In many hymenopteran insects such as honeybees, female eggs are produced sexually, using sperm from a drone father, while the production of further drones (males) depends on the queen (and occasionally workers) producing unfertilized eggs. This means that females (workers and queens) are always diploid, while males (drones) are always haploid, and produced parthenogenetically.

Facultative Edit

Facultative parthenogenesis is the term for when a female can produce offspring either sexually or via asexual reproduction. [25] Facultative parthenogenesis is extremely rare in nature, with only a few examples of animal taxa capable of facultative parthenogenesis. [25] One of the best-known examples of taxa exhibiting facultative parthenogenesis are mayflies presumably, this is the default reproductive mode of all species in this insect order. [26] Facultative parthenogenesis is believed to be a response to a lack of a viable male. A female may undergo facultative parthenogenesis if a male is absent from the habitat or if it is unable to produce viable offspring.

In aphids, a generation sexually conceived by a male and a female produces only females. The reason for this is the non-random segregation of the sex chromosomess X and O during spermatogenesis. [27]

Facultative parthenogenesis is often used to describe cases of spontaneous parthenogenesis in normally sexual animals. [28] For example, many cases of spontaneous parthenogenesis in sharks, some snakes, Komodo dragons and a variety of domesticated birds were widely attributed to facultative parthenogenesis. [29] These cases are examples of spontaneous parthenogenesis. [25] [28] The occurrence of such asexually produced eggs in sexual animals can be explained by a meiotic error, leading to eggs produced via automixis. [28] [30]

Obligate Edit

Obligate parthenogenesis is the process in which organisms exclusively reproduce through asexual means. [31] Many species have been shown to transition to obligate parthenogenesis over evolutionary time. Well documented transitions to obligate parthenogenesis have been found in numerous metazoan taxa, albeit through highly diverse mechanisms. These transitions often occur as a result of inbreeding or mutation within large populations. [32] There are a number of documented species, specifically salamanders and geckos, that rely on obligate parthenogenesis as their major method of reproduction. As such, there are over 80 species of unisex reptiles (mostly lizards but including a single snake species), amphibians and fishes in nature for which males are no longer a part of the reproductive process. [33] A female will produce an ovum with a full set (two sets of genes) provided solely by the mother. Thus, a male is not needed to provide sperm to fertilize the egg. This form of asexual reproduction is thought in some cases to be a serious threat to biodiversity for the subsequent lack of gene variation and potentially decreased fitness of the offspring. [31]

Some invertebrate species that feature (partial) sexual reproduction in their native range are found to reproduce solely by parthenogenesis in areas to which they have been introduced. [34] [35] Relying solely on parthenogenetic reproduction has several advantages for an invasive species: it obviates the need for individuals in a very sparse initial population to search for mates, and an exclusively female sex distribution allows a population to multiply and invade more rapidly, potentially up to twice as fast. Examples include several aphid species [34] and the willow sawfly, Nematus oligospilus, which is sexual in its native Holarctic habitat but parthenogenetic where it has been introduced into the Southern Hemisphere. [35]

Parthenogenesis is seen to occur naturally in aphids, Daphnia, rotifers, nematodes and some other invertebrates, as well as in many plants. Among vertebrates, strict parthenogenesis is only known to occur in lizards, snakes, [36] birds [37] and sharks, [38] with fish, amphibians and reptiles exhibiting various forms of gynogenesis and hybridogenesis (an incomplete form of parthenogenesis). [39] The first all-female (unisexual) reproduction in vertebrates was described in the fish Poecilia formosa in 1932. [40] Since then at least 50 species of unisexual vertebrate have been described, including at least 20 fish, 25 lizards, a single snake species, frogs, and salamanders. [39] Other usually sexual species may occasionally reproduce parthenogenetically the Komodo dragon and hammerhead and blacktip sharks are recent additions to the known list of spontaneous parthenogenetic vertebrates. As with all types of asexual reproduction, there are both costs (low genetic diversity and therefore susceptibility to adverse mutations that might occur) and benefits (reproduction without the need for a male) associated with parthenogenesis.

Parthenogenesis is distinct from artificial animal cloning, a process where the new organism is necessarily genetically identical to the cell donor. In cloning, the nucleus of a diploid cell from a donor organism is inserted into an enucleated egg cell and the cell is then stimulated to undergo continued mitosis, resulting in an organism that is genetically identical to the donor. Parthenogenesis is different, in that it originates from the genetic material contained within an egg cell and the new organism is not necessarily genetically identical to the parent.

Parthenogenesis may be achieved through an artificial process as described below under the discussion of mammals.

Oomycetes Edit

Apomixis can apparently occur in Phytophthora, [41] an oomycete. Oospores from an experimental cross were germinated, and some of the progeny were genetically identical to one or other parent, implying that meiosis did not occur and the oospores developed by parthenogenesis.

Velvet worms Edit

No males of Epiperipatus imthurni have been found, and specimens from Trinidad were shown to reproduce parthenogenetically. This species is the only known velvet worm to reproduce via parthenogenesis. [42]

Rotifers Edit

In bdelloid rotifers, females reproduce exclusively by parthenogenesis (obligate parthenogenesis), [43] while in monogonont rotifers, females can alternate between sexual and asexual reproduction (cyclical parthenogenesis). At least in one normally cyclical parthenogenetic species obligate parthenogenesis can be inherited: a recessive allele leads to loss of sexual reproduction in homozygous offspring. [44]

Flatworms Edit

At least two species in the genus Dugesia, flatworms in the Turbellaria sub-division of the phylum Platyhelminthes, include polyploid individuals that reproduce by parthenogenesis. [45] This type of parthenogenesis requires mating, but the sperm does not contribute to the genetics of the offspring (the parthenogenesis is pseudogamous, alternatively referred to as gynogenetic). A complex cycle of matings between diploid sexual and polyploid parthenogenetic individuals produces new parthenogenetic lines.

Snails Edit

Several species of parthenogenetic gastropods have been studied, especially with respect to their status as invasive species. Such species include the New Zealand mud snail (Potamopyrgus antipodarum), [46] the red-rimmed melania (Melanoides tuberculata), [47] and the Quilted melania (Tarebia granifera). [48]

Insects Edit

Parthenogenesis in insects can cover a wide range of mechanisms. [49] The offspring produced by parthenogenesis may be of both sexes, only female (thelytoky, e.g. aphids and some hymenopterans [50] ) or only male (arrhenotoky, e.g. most hymenopterans). Both true parthenogenesis and pseudogamy (gynogenesis or sperm-dependent parthenogenesis) are known to occur. [25] The egg cells, depending on the species may be produced without meiosis (apomictically) or by one of the several automictic mechanisms.

A related phenomenon, polyembryony is a process that produces multiple clonal offspring from a single egg cell. This is known in some hymenopteran parasitoids and in Strepsiptera. [49]

In automictic species the offspring can be haploid or diploid. Diploids are produced by doubling or fusion of gametes after meiosis. Fusion is seen in the Phasmatodea, Hemiptera (Aleurodids and Coccidae), Diptera, and some Hymenoptera. [49]

In addition to these forms is hermaphroditism, where both the eggs and sperm are produced by the same individual, but is not a type of parthenogenesis. This is seen in three species of Icerya scale insects. [49]

Parasitic bacteria like Wolbachia have been noted to induce automictic thelytoky in many insect species with haplodiploid systems. They also cause gamete duplication in unfertilized eggs causing them to develop into female offspring. [49]

Among species with the haplo-diploid sex-determination system, such as hymenopterans (ants, bees and wasps) and thysanopterans (thrips), haploid males are produced from unfertilized eggs. Usually, eggs are laid only by the queen, but the unmated workers may also lay haploid, male eggs either regularly (e.g. stingless bees) or under special circumstances. An example of non-viable parthenogenesis is common among domesticated honey bees. The queen bee is the only fertile female in the hive if she dies without the possibility of a viable replacement queen, it is not uncommon for the worker bees to lay eggs. This is a result of the lack of the queen's pheromones and the pheromones secreted by uncapped brood, which normally suppress ovarian development in workers. Worker bees are unable to mate, and the unfertilized eggs produce only drones (males), which can mate only with a queen. Thus, in a relatively short period, all the worker bees die off, and the new drones follow if they have not been able to mate before the collapse of the colony. This behavior is believed to have evolved to allow a doomed colony to produce drones which may mate with a virgin queen and thus preserve the colony's genetic progeny.

A few ants and bees are capable of producing diploid female offspring parthenogenetically. These include a honey bee subspecies from South Africa, Apis mellifera capensis, where workers are capable of producing diploid eggs parthenogenetically, and replacing the queen if she dies other examples include some species of small carpenter bee, (genus Ceratina). Many parasitic wasps are known to be parthenogenetic, sometimes due to infections by Wolbachia.

The workers in five [22] ant species and the queens in some ants are known to reproduce by parthenogenesis. In Cataglyphis cursor, a European formicine ant, the queens and workers can produce new queens by parthenogenesis. The workers are produced sexually. [22]

In Central and South American electric ants, Wasmannia auropunctata, queens produce more queens through automictic parthenogenesis with central fusion. Sterile workers usually are produced from eggs fertilized by males. 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. [51] As a consequence, the males will only have fathers and the queens only mothers, while the sterile workers are the only ones with both parents of both genders.

These ants get both the benefits of both asexual and sexual reproduction [22] [51] —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.

Other examples of insect parthenogenesis can be found in gall-forming aphids (e.g., Pemphigus betae), where females reproduce parthenogenetically during the gall-forming phase of their life cycle and in grass thrips. In the grass thrips genus Aptinothrips there have been, despite the very limited number of species in the genus, several transitions to asexuality. [52]

Crustaceans Edit

Crustacean reproduction varies both across and within species. The water flea Daphnia pulex alternates between sexual and parthenogenetic reproduction. [53] Among the better-known large decapod crustaceans, some crayfish reproduce by parthenogenesis. "Marmorkrebs" are parthenogenetic crayfish that were discovered in the pet trade in the 1990s. [54] Offspring are genetically identical to the parent, indicating it reproduces by apomixis, i.e. parthenogenesis in which the eggs did not undergo meiosis. [55] Spinycheek crayfish (Orconectes limosus) can reproduce both sexually and by parthenogenesis. [56] The Louisiana red swamp crayfish (Procambarus clarkii), which normally reproduces sexually, has also been suggested to reproduce by parthenogenesis, [57] although no individuals of this species have been reared this way in the lab. Artemia parthenogenetica is a species or series of populations of parthenogenetic brine shrimps. [58]

Spiders Edit

At least two species of spiders in the family Oonopidae (goblin spiders), Heteroonops spinimanus and Triaeris stenaspis, are thought to be parthenogenetic, as no males have ever been collected. Parthenogenetic reproduction has been demonstrated in the laboratory for T. stenaspis. [59]

Sharks Edit

Parthenogenesis in sharks has been confirmed in at least three species, the bonnethead, [38] the blacktip shark, [60] and the zebra shark, [61] and reported in others.

A bonnethead, a type of small hammerhead shark, was found to have produced a pup, born live on December 14, 2001 at Henry Doorly Zoo in Nebraska, in a tank containing three female hammerheads, but no males. The pup was thought to have been conceived through parthenogenesis. The shark pup was apparently killed by a stingray within days of birth. [62] The investigation of the birth was conducted by the research team from Queen's University Belfast, Southeastern University in Florida, and Henry Doorly Zoo itself, and it was concluded after DNA testing that the reproduction was parthenogenetic. The testing showed the female pup's DNA matched only one female who lived in the tank, and that no male DNA was present in the pup. The pup was not a twin or clone of her mother, but rather, contained only half of her mother's DNA ("automictic parthenogenesis"). This type of reproduction had been seen before in bony fish, but never in cartilaginous fish such as sharks, until this documentation.

In the same year, a female Atlantic blacktip shark in Virginia reproduced via parthenogenesis. [63] On October 10, 2008 scientists confirmed the second case of a "virgin birth" in a shark. The Journal of Fish Biology reported a study in which scientists said DNA testing proved that a pup carried by a female Atlantic blacktip shark in the Virginia Aquarium & Marine Science Center contained no genetic material from a male. [60]

In 2002, two white-spotted bamboo sharks were born at the Belle Isle Aquarium in Detroit. They hatched 15 weeks after being laid. The births baffled experts as the mother shared an aquarium with only one other shark, which was female. The female bamboo sharks had laid eggs in the past. This is not unexpected, as many animals will lay eggs even if there is not a male to fertilize them. Normally, the eggs are assumed to be inviable and are discarded. This batch of eggs was left undisturbed by the curator as he had heard about the previous birth in 2001 in Nebraska and wanted to observe whether they would hatch. Other possibilities had been considered for the birth of the Detroit bamboo sharks including thoughts that the sharks had been fertilized by a male and stored the sperm for a period of time, as well as the possibility that the Belle Isle bamboo shark is a hermaphrodite, harboring both male and female sex organs, and capable of fertilizing its own eggs, but that is not confirmed. [64]

In 2008, a Hungarian aquarium had another case of parthenogenesis after its lone female shark produced a pup without ever having come into contact with a male shark.

The repercussions of parthenogenesis in sharks, which fails to increase the genetic diversity of the offspring, is a matter of concern for shark experts, taking into consideration conservation management strategies for this species, particularly in areas where there may be a shortage of males due to fishing or environmental pressures. Although parthenogenesis may help females who cannot find mates, it does reduce genetic diversity.

In 2011, recurring shark parthenogenesis over several years was demonstrated in a captive zebra shark, a type of carpet shark. [61] [65] DNA genotyping demonstrated that individual zebra sharks can switch from sexual to parthenogenetic reproduction. [66]

Amphibians Edit

Squamata Edit

Most reptiles of the squamatan order (lizards and snakes) reproduce sexually, but parthenogenesis has been observed to occur naturally in certain species of whiptails, some geckos, rock lizards, [5] [67] [68] Komodo dragons [69] and snakes. [70] Some of these like the mourning gecko Lepidodactylus lugubris, Indo-Pacific house gecko Hemidactylus garnotii, the hybrid whiptails Cnemidophorus, Caucasian rock lizards Darevskia, and the brahminy blindsnake, Indotyphlops braminus are unisexual and obligately parthenogenetic. Other reptiles, such as the Komodo dragon, other monitor lizards, [71] and some species of boas, [8] [23] [72] pythons, [21] [73] filesnakes, [74] [75] gartersnakes [76] and rattlesnakes [77] [78] were previously considered as cases of facultative parthenogenesis, but are in fact cases of accidental parthenogenesis. [28]

In 2012, facultative parthenogenesis was reported in wild vertebrates for the first time by US researchers amongst captured pregnant copperhead and cottonmouth female pit-vipers. [79] The Komodo dragon, which normally reproduces sexually, has also been found able to reproduce asexually by parthenogenesis. [80] A case has been documented of a Komodo dragon reproducing via sexual reproduction after a known parthenogenetic event, [81] highlighting that these cases of parthenogenesis are reproductive accidents, rather than adaptive, facultative parthenogenesis. [28]

Some reptile species use a ZW chromosome system, which produces either males (ZZ) or females (ZW). Until 2010, it was thought that the ZW chromosome system used by reptiles was incapable of producing viable WW offspring, but a (ZW) female boa constrictor was discovered to have produced viable female offspring with WW chromosomes. [82]

Parthenogenesis has been studied extensively in the New Mexico whiptail in the genus Aspidoscelis of which 15 species reproduce exclusively by parthenogenesis. These lizards live in the dry and sometimes harsh climate of the southwestern United States and northern Mexico. All these asexual species appear to have arisen through the hybridization of two or three of the sexual species in the genus leading to polyploid individuals. The mechanism by which the mixing of chromosomes from two or three species can lead to parthenogenetic reproduction is unknown. Recently, a hybrid parthenogenetic whiptail lizard was bred in the laboratory from a cross between an asexual and a sexual whiptail. [83] Because multiple hybridization events can occur, individual parthenogenetic whiptail species can consist of multiple independent asexual lineages. Within lineages, there is very little genetic diversity, but different lineages may have quite different genotypes.

An interesting aspect to reproduction in these asexual lizards is that mating behaviors are still seen, although the populations are all female. One female plays the role played by the male in closely related species, and mounts the female that is about to lay eggs. This behaviour is due to the hormonal cycles of the females, which cause them to behave like males shortly after laying eggs, when levels of progesterone are high, and to take the female role in mating before laying eggs, when estrogen dominates. Lizards who act out the courtship ritual have greater fecundity than those kept in isolation, due to the increase in hormones that accompanies the mounting. So, although the populations lack males, they still require sexual behavioral stimuli for maximum reproductive success. [84]

Some lizard parthenogens show a pattern of geographic parthenogenesis, occupying high mountain areas where their ancestral forms have an inferior competition ability. [85] In Caucasian rock lizards of genus Darevskia, which have six parthenogenetic forms of hybrid origin [67] [68] [86] hybrid parthenogenetic form D. "dahli" has a broader niche than either of its bisexual ancestors and its expansion throughout the Central Lesser Caucasus caused decline of the ranges of both its maternal and paternal species. [87]

Birds Edit

Parthenogenesis in birds is known mainly from studies of domesticated turkeys and chickens, although it has also been noted in the domestic pigeon. [37] In most cases the egg fails to develop normally or completely to hatching. [37] [88] The first description of parthenogenetic development in a passerine was demonstrated in captive zebra finches, although the dividing cells exhibited irregular nuclei and the eggs did not hatch. [37]

Parthenogenesis in turkeys appears to result from a conversion of haploid cells to diploid [88] most embryos produced in this way die early in development. Rarely, viable birds result from this process, and the rate at which this occurs in turkeys can be increased by selective breeding, [89] however male turkeys produced from parthenogenesis exhibit smaller testes and reduced fertility. [90]

Mammals Edit

There are no known cases of naturally occurring mammalian parthenogenesis in the wild. Though claims of that happening date back to antiquity, including in humans (for example, Virgin Mary, mother of Jesus), this has never been observed in a controlled environment. Parthenogenetic progeny of mammals would have two X chromosomes, and would therefore be female.

In 1936, Gregory Goodwin Pincus reported successfully inducing parthenogenesis in a rabbit. [91]

In April 2004, scientists at Tokyo University of Agriculture used parthenogenesis successfully to create a fatherless mouse. Using gene targeting, they were able to manipulate two imprinted loci H19/IGF2 and DLK1/MEG3 to produce bi-maternal mice at high frequency [92] and subsequently show that fatherless mice have enhanced longevity. [93]

Induced parthenogenesis in mice and monkeys often results in abnormal development. This is because mammals have imprinted genetic regions, where either the maternal or the paternal chromosome is inactivated in the offspring in order for development to proceed normally. A mammal created by parthenogenesis would have double doses of maternally imprinted genes and lack paternally imprinted genes, leading to developmental abnormalities. It has been suggested [94] that defects in placental folding or interdigitation are one cause of swine parthenote abortive development. As a consequence, research on human parthenogenesis is focused on the production of embryonic stem cells for use in medical treatment, not as a reproductive strategy.

Use of an electrical or chemical stimulus can produce the beginning of the process of parthenogenesis in the asexual development of viable offspring. [95]

During oocyte development, high metaphase promoting factor (MPF) activity causes mammalian oocytes to arrest at the metaphase II stage until fertilization by a sperm. The fertilization event causes intracellular calcium oscillations, and targeted degradation of cyclin B, a regulatory subunit of MPF, thus permitting the MII-arrested oocyte to proceed through meiosis.

To initiate parthenogenesis of swine oocytes, various methods exist to induce an artificial activation that mimics sperm entry, such as calcium ionophore treatment, microinjection of calcium ions, or electrical stimulation. Treatment with cycloheximide, a non-specific protein synthesis inhibitor, enhances parthenote development in swine presumably by continual inhibition of MPF/cyclin B. [96] As meiosis proceeds, extrusion of the second polar is blocked by exposure to cytochalasin B. This treatment results in a diploid (2 maternal genomes) parthenote [94] Parthenotes can be surgically transferred to a recipient oviduct for further development, but will succumb to developmental failure after ≈30 days of gestation. The swine parthenote placentae often appears hypo-vascular: see free image (Figure 1) in linked reference. [94]

Humans Edit

On June 26, 2007, International Stem Cell Corporation (ISCC), a California-based stem cell research company, announced that their lead scientist, Dr. Elena Revazova, and her research team were the first to intentionally create human stem cells from unfertilized human eggs using parthenogenesis. The process may offer a way for creating stem cells that are genetically matched to a particular female for the treatment of degenerative diseases that might affect her. In December 2007, Dr. Revazova and ISCC published an article [97] illustrating a breakthrough in the use of parthenogenesis to produce human stem cells that are homozygous in the HLA region of DNA. These stem cells are called HLA homozygous parthenogenetic human stem cells (hpSC-Hhom) and have unique characteristics that would allow derivatives of these cells to be implanted into millions of people without immune rejection. [98] With proper selection of oocyte donors according to HLA haplotype, it is possible to generate a bank of cell lines whose tissue derivatives, collectively, could be MHC-matched with a significant number of individuals within the human population.

On August 2, 2007, after an independent investigation, it was revealed that discredited South Korean scientist Hwang Woo-Suk unknowingly produced the first human embryos resulting from parthenogenesis. Initially, Hwang claimed he and his team had extracted stem cells from cloned human embryos, a result later found to be fabricated. Further examination of the chromosomes of these cells show indicators of parthenogenesis in those extracted stem cells, similar to those found in the mice created by Tokyo scientists in 2004. Although Hwang deceived the world about being the first to create artificially cloned human embryos, he did contribute a major breakthrough to stem cell research by creating human embryos using parthenogenesis. [99] The truth was discovered in 2007, long after the embryos were created by him and his team in February 2004. This made Hwang the first, unknowingly, to successfully perform the process of parthenogenesis to create a human embryo and, ultimately, a human parthenogenetic stem cell line.

Helen Spurway, a geneticist specializing in the reproductive biology of the guppy, Lebistes reticulatus, claimed, in 1955, that parthenogenesis, which occurs in the guppy in nature, may also occur (though very rarely) in the human species, leading to so-called "virgin births". This created some sensation among her colleagues and the lay public alike. [100] Sometimes an embryo may begin to divide without fertilisation but it cannot fully develop on its own, so while it may create some skin and nerve cells, it cannot create others (such as skeletal muscle) and becomes a type of benign tumor called an ovarian teratoma. [101] Spontaneous ovarian activation is not rare and has been known about since the 19th century. Some teratomas can even become primitive fetuses (fetiform teratoma) with imperfect heads, limbs and other structures but these are non-viable. However, in 1995 there was a reported case of partial-parthenogenesis a boy was found to have some of his cells (such as white blood cells) to be lacking in any genetic content from his father. Scientists believe that in the boy's case, an unfertilised egg began to self-divide but then had some (but not all) of its cells fertilised by a sperm cell this must have happened early in development, as self-activated eggs quickly lose their ability to be fertilised. The unfertilised cells eventually duplicated their DNA, boosting their chromosomes to 46. When the unfertilised cells hit a developmental block, the fertilised cells took over and developed that tissue. The boy had asymmetrical facial features and learning difficulties but was otherwise healthy. This would make him a parthenogenetic chimera (a child with two cell lineages in his body). [102] While over a dozen similar cases have been reported since then (usually discovered after the patient demonstrated clinical abnormalities), there have been no scientifically confirmed reports of a non-chimeric, clinically healthy human parthenote (i.e. produced from a single, parthenogenetic-activated oocyte). [101]

Gynogenesis Edit

A form of asexual reproduction related to parthenogenesis is gynogenesis. Here, offspring are produced by the same mechanism as in parthenogenesis, but with the requirement that the egg merely be stimulated by the presence of sperm in order to develop. However, the sperm cell does not contribute any genetic material to the offspring. Since gynogenetic species are all female, activation of their eggs requires mating with males of a closely related species for the needed stimulus. Some salamanders of the genus Ambystoma are gynogenetic and appear to have been so for over a million years. It is believed [ by whom? ] that the success of those salamanders may be due to rare fertilization of eggs by males, introducing new material to the gene pool, which may result from perhaps only one mating out of a million. In addition, the amazon molly is known to reproduce by gynogenesis. [103]

Hybridogenesis Edit

Hybridogenesis is a mode of reproduction of hybrids. Hybridogenetic hybrids (for example AB genome), usually females, during gametogenesis exclude one of parental genomes (A) and produce gametes with unrecombined [104] genome of second parental species (B), instead of containing mixed recombined parental genomes. First genome (A) is restored by fertilization of these gametes with gametes from the first species (AA, sexual host, [104] usually male). [104] [105] [106]

So hybridogenesis is not completely asexual, but instead hemiclonal: half of genome is passed to the next generation clonally, unrecombined, intact (B), other half sexually, recombined (A). [104] [107]

This process continues, so that each generation is half (or hemi-) clonal on the mother's side and has half new genetic material from the father's side.

This form of reproduction is seen in some live-bearing fish of the genus Poeciliopsis [105] [108] as well as in some of the Pelophylax spp. ("green frogs" or "waterfrogs"):


Komodo Dragon Virgin Birth

A Komodo Dragon was born at the Chester Zoo in England, the result of a parthenogenetic birth. Komodo Dragons will have male offspring as the result of parthenogenesis.


Parthenogenesis in Insects

It has Greek origin as “parthenos” which means “virgin birth”. Virgin birth means development of egg cell into an embryo without being fertilized by sperm. Hence parthenogenesis has been defined as the asexual reproduction in which organism developes from an unfertilized egg. Many insects reproduce by this mode of reproduction. This may occur due to lack of viable male to fertilise eggs.

  • Parthenogenesis can be broadly grouped on the three bases:
    • Based on natural occurrence
    • Based on sex of offspring
    • Based on division of germ cells

    BASED ON NATURAL OCCURRENCE

    (A) FACULTATIVE PARTHENOGENESIS

    • Female can reproduce via sexual or asexual mode.
    • Sexually reproducing female switch to asexual reproduction as the viable male is absent from the habitat.
    • Automixis during reductional division i.e. meiosis enable the sexual animal to reproduce asexually.
    • Mayfly exhibits facultative parthenogenesis.

    (B) OBLIGATE PARTHENOGENESIS

    • Female can reproduce only via asexual mode of reproduction.
    • Few invertebrates solely reproduce asexually.
    • Nematus oligospilus reproduce via parthenogenesis when it has been placed in Southern Hemisphere

    BASED ON SEX OF OFFSPRING

    (A) ARRHENOTOKY – The resultant of parthenogenesis is male offspring.
    Example- Hymenoptera
    (B) THELYTOKY – The resultant of parthenogenesis is female offspring.
    Example- Aphids.
    (C) DEUTEROTOKY – Male and female, both can me the resultants of parthenogenesis. Example- Cynipid wasp.

    BASED ON DIVISION OF GERM CELLS

    (A) HAPLO-DIPLOIDY – Germ cells undergoes complete meiosis to form oocyte which either fertilises to form female embryo or unfertilise to form male.
    Example- Hymenoptera (Bees)
    (B) APOMICTIC – Meiosis is absent. The egg cell is the resultant of mitotic division, thus egg has diploid genetic makeup and develops a diploid embryo.
    Example- Aphids
    (C) AUTOMICTIC – Germ cell undergoes Meiosis but chromosomes unable to separate at Anaphase -II or two nuclei fuse and diploid chromosome number is restored. Female produce as the resultant.
    Example- Phasmids (stick insects).


    Disadvantages of Parthenogenesis as a Form of Reproduction

    Parthenogenesis is a form of asexual reproduction. Thus, it is characterized by a lack of genetic diversity since the offspring gets all genetic material from one parent only. Lack of genetic diversity predisposes the offspring to the same diseases and same conditions as its parent. Moreover, negative mutations, as well as unfavorable traits, will persist in many generations. Furthermore, the offspring produced by parthenogenesis is a clone of the parent so it cannot adapt easily or survive when the condition changes and becomes unfavorable. That’s why parthenogenesis may produce a large number of organisms that cannot survive through any slight change in their environment.


    Parthenogenesis in insects: synthesis

    In order for them to multiply, nature has endowed living organisms with a wide diversity of reproductive systems. In insects, one of these strategies is parthenogenesis. This is based on the development of individuals from unfertilized gametes, thus without the need for fertilization. This strategy is interesting for more than one reason: it is evidenced by the declination of a multitude of forms (thelytokia, arrhenotokia and deuterotokia) and its appearance on multiple occasions during evolution, within unrelated and phylogenetically distant taxa and species.

    Description of the different types of parthenogenesis

    I) Thelytokia

    Corresponding to parthenogenesis sensu stricto, thelytokia is characterized by the fact that all the unfertilized eggs emitted by a female insect in turn only produce a female diploid progeny.

    Thelytoic parthenogenesis can result in two distinct genetic systems: one based on mitosis (apomixis) and the other on meiosis (automixis).

    • L’apomixie is the simplest system: female offspring are genetically similar to the mother, the absence of meiosis prevents any chromosomal rearrangement (genetic mixing). Mother and daughter can thus be considered as clones
    • L’automixie involves the meiosis process, diploidy is restored without the contribution of a gamete (without fertilization). This process can be carried out in several ways: 1) duplication of the genome before meiosis, creating a cell with 4n chromosomes (4 sets of chromosomes) 2) fusion of the two nuclei during meiosis 3) a haploid nucleus resulting from meiosis is duplicated by mitosis to fuse again with itself

    II) Arrhenotokism

    In arrhenotokic parthenogenesis, progeny from unfertilized eggs consist only of male individuals (opposite system to thelytokia). There are two distinct genetic systems: 1) haplodiploid, males are haploid (1 set of chromosomes) and females are diploid (2 sets of chromosomes) 2) diploid, males and females are derived from diploid eggs as for thelycan parthenesis.

    III) Deuterotokia

    Deutherotokic parthenogenesis produces unfertilized eggs from both males and females.

    Parthenogenetic reproduction modes ( Source : Rabeling & Kronauer, 2013)

    Appearance of parthenogenesis

    A parthenogenetic system can appear in various ways. The most singular case is based on the interaction between certain groups of insects and endosymbiotic bacteria such as Wolbachia, Rickettsia and Cardinium – the most widely represented being Wolbachia pipientis – causing cytoplasmic incompatibilities causing either the cessation of the development of diploid embryos, or the thelytokia, or the feminization of males, their death. These bacteria often play a role in sex conversion and modify the sex ratio in favour of females.

    Many insect species are monosexed (their population is composed of only one sex). These species occur in isolated environments such as islands or high-altitude regions. They perform a geographic parthenogenesis, demonstrating the adaptive power of this type of reproduction.

    >Parthenogenesis in hemimetaboles (or heterometaboles)

    Hemimetazole insects federate species whose metamorphosis is said to be incomplete: the adult stage is reached gradually during the development cycle by successive moulting, the larvae possessing most of the attributes of adults, except sexual and parasexual organs (link article).

    Odonata (dragonflies) : only the species Ischnura hastata (Caenagrionidae), found in the Azores, has been described as parthenogenetic (thelytoic type).

    Orthoptera (locusts, crickets and grasshoppers) : the species Locusta migratoria and Schistocerca gregaria have the ability to spontaneously generate female offspring from unfertilized eggs: thycoparthenogenesis. Haploid gametes become diploid gradually during development. For Loxoblemmus frontalis, the only species in the Gryllidae family to practice parthenogenesis, thelytokia is induced by the presence of bacteria Wolbachia. It is without intervention of Wolbachia in grasshoppers Saga pedo (Tettigonidae).

    Phasme du genre Timema – Santa Barbara – Californie ( Source : Alice Abela )

    Phasmatodea (Phasms) : parthenogenesis is quite common. For example, the genus Timema, endemic to California, is composed of 5 species all related and descended from the same lineage. However, rare fertile males could be collected, their presence being estimated at less than 0.2% of the population. The sexual determination of phasms is based on a system where individuals carrying a pair of autosome chromosomes (XX) are female and those with only one copy of the X are male (XO), (in humans the system is XX-XY), males develop via spontaneous loss of the X chromosome during oogenesis. Other species also reproduce only by parthenogenesis such as Bacillus rossius and Clonopsis gallica (species found in southern France).

    Blattoptera (formerly Isoptera) (termites) : several groups optionally use thelycan parthenogenesis through a ploidy restoration process similar to that found in Reticulitermes speratus and R. virginicus (automiscie). This type of termites is known to harbour Wolbachia, whether the colonies are parthenogenetic or bisexual, suggesting that there is no correlation between the two reproductive modes.

    Mantodea (mantes) (lien) : only two species, Miomantis savignyi and Bruneria borealis, carry out parthenogenesis (thelytoque), mandatory parthenogenesis in B. borealis.

    Hemiptera (cicadas, aphids and bedbugs) : this order offers an abundant diversity of parthenogenetic systems within a large number of families such as Aclerdidae, Diaspididae, Aphididae or Anthocoridae. For example, several species of Fulgores (Delphacidae) belonging to the genera Delphacodes and Ribautodelphax use thelytokia and pseudogamy (females mate with males but the offspring are entirely female). The intervention of Wolbachia in the parthenogenesis process has been demonstrated in Delphacodes kuscheli but not in other species. A multitude of forms of parthenogenesis occur between species of the Coccidae and Diapsididae families: arrhenotokism with males that may be diploid or haploid, and deuterotokism.

    Some aphid species (Aphidimorpha) have a cyclic reproductive mode, changing from bisexual to parthenogenetic depending on the season. Thus, in spring, a female aphid (founder) multiplies by parthenogenesis in order to rapidly colonize the environment, then, in autumn, reproduction becomes sexual, resulting in the production of fertilized eggs that overwinter in the vegetation.

    Aphid life cycle (Source: )

    With regard to “real” bedbugs, there are no cases of parthenogenesis revealed. However, two species have optional use of telytokism: Calliodis maculipennis (neotropical species of the Anthociridae family) and Campyloneura virgula (Miridae). Surprisingly, a parthenogenetic population of C. maculipennis located on the island of Trinidad has been discovered, while the populations of the mainland, Mexico and Guyana, are gendered.

    Life cycle of the aphid (english)

    Parthenogenesis in holometabolas

    The holometabol group characterizes species using a so-called complete metamorphosis phase where the passage to adulthood requires a chrysalis (butterfly) or pupa (flies) phase during which the larvae are totally transformed (lien article).

    Hollo-metabolas make up the vast majority of insect species diversity: 800,000 species divided into 11 orders such as Diptera, Coleoptera, Lepidoptera or Hymenoptera.

    The Hymenoptera (wasps, bees, ants), with nearly 150,000 species described, constitutes one of the most diversified insect orders. Parthenogenesis is common to all species of the order, thus encompassing the greatest diversity of types of parthenogenesis. The most common and ancestral is arrhenotokism combined with haplodiploidy. Females thus have the ability to fertilize or not their eggs and can adjust the sex ratio of their offspring: a diploid egg will give a sterile female or worker and a haploid egg a male (see illustration below). However, mechanisms may vary between taxa.

    The transition from arrhenotopic to thelytoic parthenogenesis is relatively frequent due to the absence of a sexual chromosome making it possible to restore diploidy through an apomictic or automictic process. For example, the species Diplolepis eglanteria (Cynipidae) is a small wasp that uses apomixis, and Apis mellifera capensis a, on the other hand, uses self-mixing.

    Queen Wasmannia auropunctata and sterile workers – As with many ants species, the queen is more imposing than the workers ( Source : Alex Wild )

    Cataglyphis hispanica, Paratrechina longicornis, Vollenhovia emeyri and Wasmannia auropunctata are derived from sexual reproduction while the new queens come from parthenogenetic thelycan eggs. The study of the reproductive mode of Wasmannia auropunctata revealed a unique case of a dual parthenogenetic system (arrhenotokic and thelytok). It was discovered in 2005 that males, derived from fertilized eggs, expressed only the paternal genome, with the maternal genome disappearing (except the mitochondrial genome) through a mechanism that remains partly unknown. This process indicates that male offspring are cloned (see illustration opposite).

    So far as these workers are sterile, this sexual reproduction does not lead to the mixing of male and female genomes in the next generation. This lack of gene flow between males and females leads to genetic differentiation and separate evolution of the two genomes. This raises the question as to the classification of a possible distinction between these two sexes as two distinct species, one of which would only consist of males! In addition, males can be considered as parasites exploiting females, where the production of sterile workers ensures the protection and supply of the colony.

    “Classic” reproductive system of social hymenoptera (A) and ant Wasmannia auropunctata (B) (Source: Erudit.org )

    At 30% of parasitoid wasp species (article link) Cynipidae and Chalcidoidea, thelytokia is caused by endosymbiotic microorganisms of the genus Wolbachia, Cardinium and Rickettsia.

    Life cycle of Micromalthus debilis ( Link article )

    The order of Coleoptera accounts for 30% of insect species, or 380,000 species of which only 600 species (20 families) are parthenogenetic. Thelytokia is more widespread than arrhenotokia: it is found in Alexiidae, Anobiidae, Cerambycidae, Dermestidae, Elateridae, Hydrophiliidae, Passalidae, Sphindidae or Staphylinidae, among others. The case of Micromalthus debilis is unique in its kind, the thelytokia is pushed to the extreme because the sterile males have almost disappeared from the populations (lire this article).

    So, the species Reesa vesopulae (Dermestidae), present throughout the nearctic region, is strictly parthenogenetic, as are the majority of North American populations of Cis fuscipes (Ciidae) and Aelus mellillus (Elateridae). In Chrysomelidae, the species Bromius obscurus is represented by diploid bisexual populations in North America and other apomictic triploids in Europe. The two European weevil species (Curculionidae), Polydrus mollis and Otiorhynchus scaber are mainly thelytoics, although some populations are bisexual diploids in small localities.

    In Lepidoptera, despite more than 170,000 species described, only two dozen species practice parthenogenesis. These species are mainly Lymantriidae and Psychidae (11 species). There is a gendered form of Dahlica triquetrella in Central Europe, while several diploid and tetraploid thelytok populations are widespread throughout Europe and North America.

    Flies (Dipteran Orders), parthenogenesis has appeared in at least 11 families with more than 150 000 species : Chironomidae, Hybotidae, Agromyzidae, Cecidomyiidae, Psychodidae, Sciaridae, Ctenostylidae, Lonchopteridae, Simuliidae, Ceratopogonidae and Chamaemyliidae. Half of the Chironomidae taxa studied appear parthenogenetic. This strategy seems to have been selected to survive extreme environmental conditions, particularly cold (altitude and latitude), such as Eretmoptera murphyi (Antarctica) and Micropsectra sedna (Canada). Others, such as Cladotanytarsus aeiparthenus and Paratanytarsus grimmii, live in polluted or acidic waters.

    Troglocladius hajdi and Lymnophyes minimus living in the Gough and Nightingale Islands south of the Atlantic Ocean, or Monopelopia caraguata, Phtytelmatocladius delarosai and Polypedilum parthenogeneticum which live in small puddles (water accumulated in the leaf axil, trunk cavity, etc.)) located on terrestrial plants: phytotelme, from ancient Greek phyto – plant telma – pond.


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