Parthenogenesis is a form of asexual reproduction in which the embryo develops directly from an egg without need for fertilization. It occurs in many eukaryote taxa. [1] [2]
Apomixis appears to occur in Phytophthora , 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. [3]
No males of Epiperipatus imthurni have been found, and specimens from Trinidad were shown to reproduce parthenogenetically, making it the only velvet worm known to use parthenogenesis. [4]
In bdelloid rotifers, females reproduce exclusively by parthenogenesis (obligate parthenogenesis), [5] 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. [6]
At least two species of flatworms in the genus Dugesia , include polyploid individuals that reproduce by parthenogenesis. [7] 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.[ citation needed ]
Several species of parthenogenetic gastropods have been studied, especially with respect to their status as invasive species. These include the New Zealand mud snail (Potamopyrgus antipodarum), [8] the red-rimmed melania (Melanoides tuberculata), [9] and the Quilted melania (Tarebia granifera). [10]
Parthenogenesis in insects can cover a wide range of mechanisms. [11] The offspring produced by parthenogenesis may be of both sexes, only female (thelytoky, e.g., aphids and some hymenopterans [12] ) or only male (arrhenotoky, e.g., most hymenopterans). Both true parthenogenesis and pseudogamy (gynogenesis or sperm-dependent parthenogenesis) are known to occur. [13] The egg cells, depending on the species may be produced without meiosis (apomictically) or by one of the several automictic mechanisms.[ citation needed ]
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. [11] 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. [11] 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. [11] Parasitic bacteria like Wolbachia induce automictic thelytoky in many insect species with haplodiploid systems. They cause gamete duplication in unfertilized eggs causing them to develop into female offspring. [11]
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.[ citation needed ]
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 .[ citation needed ]
The workers in five [14] 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. [14]
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. As a consequence, the males only have fathers and the queens only mothers, while the sterile workers are the only ones with both parents of both sexes. [15] 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. [14] [15]
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. [16]
Crustacean reproduction varies both across and within species. The water flea Daphnia pulex alternates between sexual and parthenogenetic reproduction. [17] 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. [18] Offspring are genetically identical to the parent, indicating it reproduces by apomixis, i.e. parthenogenesis in which the eggs did not undergo meiosis. [19] Spinycheek crayfish ( Orconectes limosus ) can reproduce both sexually and by parthenogenesis. [20] The Louisiana red swamp crayfish ( Procambarus clarkii ), which normally reproduces sexually, has also been suggested to reproduce by parthenogenesis, [21] 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. [22]
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. [23]
Parthenogenesis in sharks has been confirmed in at least three species, the bonnethead, [24] the blacktip shark, [25] and the zebra shark. [26]
A bonnethead, a type of small hammerhead shark, was found to have produced a pup, born live in 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. It was concluded after DNA testing that the reproduction was parthenogenetic, as the female pup's DNA matched only one female who lived in the tank, and 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 not in cartilaginous fish such as sharks. [27]
In the same year, a female Atlantic blacktip shark in Virginia reproduced via parthenogenesis. [28] On 10 October 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. [25]
In 2002, two white-spotted bamboo sharks were born at the Belle Isle Aquarium in Detroit. They hatched 15 weeks after being laid in an aquarium containing only two female sharks. [29]
In 2011, recurring shark parthenogenesis over several years was demonstrated in a captive zebra shark, a type of carpet shark. [26] [30] DNA genotyping demonstrated that individual zebra sharks can switch from sexual to parthenogenetic reproduction. [31]
A female round stingray (Urobatis halleri) held in captivity from all males for eight years was reported pregnant in 2024. [32] In June 2024, the aquarium where the ray resided reported that she was not pregnant, and instead had a rare reproductive disease. [33]
In June 2023, discovery was made at a zoo in Costa Rica, where researchers identified the first documented case of a self-pregnant crocodile. This female American crocodile, housed at Parque Reptilania, produced a genetically identical foetus, with a 99.9% similarity to herself. The scientists speculate that this unique ability might be inherited from an evolutionary ancestor, suggesting that even dinosaurs could have possessed the capability for self-reproduction. The 18-year-old crocodile laid the egg in January 2018, the fully formed foetus did not hatch and was stillborn. Notably, this crocodile had been kept separated from other crocodiles throughout her entire life since being acquired at the age of two. [34] [35]
Most reptiles of the squamata (lizards and snakes) reproduce sexually, but parthenogenesis occurs naturally in certain whiptails, some geckos, rock lizards, [36] [37] [38] Komodo dragons, [39] and snakes. [40] 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, [41] and some species of boas, [42] [43] [44] pythons, [45] [46] filesnakes, [47] [48] gartersnakes, [49] and rattlesnakes [50] [51] were previously considered as cases of facultative parthenogenesis, but may be cases of accidental parthenogenesis. [52]
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. [53] The Komodo dragon, which normally reproduces sexually, has also been found able to reproduce asexually by parthenogenesis. [54] A case has been documented of a Komodo dragon reproducing via sexual reproduction after a known parthenogenetic event, [55] highlighting that these cases of parthenogenesis are reproductive accidents, rather than adaptive, facultative parthenogenesis. [52]
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. [56]
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. [57] 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.[ citation needed ]
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. [58]
Some lizard parthenogens show a pattern of geographic parthenogenesis, occupying high mountain areas where their ancestral forms have an inferior competition ability. [59] In Caucasian rock lizards of genus Darevskia , which have six parthenogenetic forms of hybrid origin [37] [38] [60] 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. [61]
Parthenogenesis in birds is known mainly from studies of domesticated turkeys and chickens, although it has also been noted in the domestic pigeon. [62] In most cases the egg fails to develop normally or completely to hatching. [62] [63] 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. [62]
Parthenogenesis in turkeys appears to result from a conversion of haploid cells to diploid; [63] 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, [64] but male turkeys produced from parthenogenesis have smaller testes and reduced fertility. [65]
In 2021, the San Diego Zoo reported that they had two unfertilized eggs from their California condor breeding program hatch. This is the first known example of parthenogenesis in this species, as well as one of the only known examples of parthenogenesis happening where males are still present. [66]
There are no known cases of naturally occurring mammalian parthenogenesis in the wild. Parthenogenetic progeny of mammals would have two X chromosomes, and would therefore be genetically female.[ citation needed ] In 1936, Gregory Goodwin Pincus inducing parthenogenesis in a rabbit. [67] In 2004, scientists at Tokyo University of Agriculture used parthenogenesis 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 [68] and subsequently show that fatherless mice have enhanced longevity. [69]
Asexual reproduction is a type of reproduction that does not involve the fusion of gametes or change in the number of chromosomes. The offspring that arise by asexual reproduction from either unicellular or multicellular organisms inherit the full set of genes of their single parent and thus the newly created individual is genetically and physically similar to the parent or an exact clone of the parent. Asexual reproduction is the primary form of reproduction for single-celled organisms such as archaea and bacteria. Many eukaryotic organisms including plants, animals, and fungi can also reproduce asexually. In vertebrates, the most common form of asexual reproduction is parthenogenesis, which is typically used as an alternative to sexual reproduction in times when reproductive opportunities are limited. Some monitor lizards, including Komodo dragons, can reproduce asexually.
Reproduction is the biological process by which new individual organisms – "offspring" – are produced from their "parent" or parents. There are two forms of reproduction: asexual and sexual.
In botany, apomixis is asexual development of seed or embryo without fertilization. However, other definitions include replacement of the seed by a plantlet or replacement of the flower by bulbils.
Teiidae is a family of Lacertoidean lizards native to the Americas. Members of this family are generally known as whiptails or racerunners; however, tegus also belong to this family. Teiidae is sister to the Gymnopthalmidae, and both families comprise the Teiioidea. The Teiidae includes several parthenogenic species – a mode of clonal reproduction. Presently, the Teiidae consists of approximately 150 species in eighteen genera.
Cnemidophorus is a genus of lizards in the family Teiidae. Species in the genus Cnemidophorus are commonly referred to as whiptail lizards or racerunners. The genus is native to South America, Central America, and the West Indies.
Pseudocopulation is a behavior similar to copulation that serves a reproductive function for one or both participants but does not involve actual sexual union between the individuals. It is most generally applied to a pollinator attempting to copulate with a flower adapted to mimic a potential female mate. The resemblance may be visual, but the key stimuli are often chemical and tactile. The form of mimicry in plants that deceives an insect into pseudocopulation is called Pouyannian mimicry after the French lawyer and amateur botanist Maurice-Alexandre Pouyanne.
Fish reproductive organs include testes and ovaries. In most species, gonads are paired organs of similar size, which can be partially or totally fused. There may also be a range of secondary organs that increase reproductive fitness. The genital papilla is a small, fleshy tube behind the anus in some fishes, from which the sperm or eggs are released; the sex of a fish can often be determined by the shape of its papilla.
Thelytoky is a type of parthenogenesis and is the absence of mating and subsequent production of all female diploid offspring as for example in aphids. Thelytokous parthenogenesis is rare among animals and reported in about 1,500 species, about 1 in 1000 of described animal species, according to a 1984 study. It is more common in invertebrates, like arthropods, but it can occur in vertebrates, including salamanders, fish, and reptiles such as some whiptail lizards.
The desert grassland whiptail lizard is an all-female species of reptiles in North America. It was formerly placed in the genus Cnemidophorus. A common predator of the whiptail lizard is the leopard lizard that preys on A. uniparens by using ambush and stalk hunting tactics. These reptiles reproduce by parthenogenesis. In this process, eggs undergo a chromosome doubling after meiosis, developing into lizards without being fertilized. However, ovulation is enhanced by female-female courtship and mating (pseudo-copulation) rituals that resemble the behavior of closely related species that reproduce sexually.
Arrhenotoky, also known as arrhenotokous parthenogenesis, is a form of parthenogenesis in which unfertilized eggs develop into males. In most cases, parthenogenesis produces exclusively female offspring, hence the distinction.
The New Mexico whiptail is a female-only species of lizard found in New Mexico and Arizona in the southwestern United States, and in Chihuahua in northern Mexico. It is the official state reptile of New Mexico. It is one of many lizard species known to be parthenogenetic. Individuals of the species can be created either through the hybridization of the little striped whiptail and the western whiptail, or through the parthenogenetic reproduction of an adult New Mexico whiptail.
Parthenogenesis is a natural form of asexual reproduction in which the embryo develops directly from an egg without need for fertilization. In animals, parthenogenesis means development of an embryo from an unfertilized egg cell. In plants, parthenogenesis is a component process of apomixis. In algae, parthenogenesis can mean the development of an embryo from either an individual sperm or an individual egg.
Sexual reproduction is a type of reproduction that involves a complex life cycle in which a gamete with a single set of chromosomes combines with another gamete to produce a zygote that develops into an organism composed of cells with two sets of chromosomes (diploid). This is typical in animals, though the number of chromosome sets and how that number changes in sexual reproduction varies, especially among plants, fungi, and other eukaryotes.
Automixis is the fusion of nuclei or gametes derived from the same individual. The term covers several reproductive mechanisms, some of which are parthenogenetic.
In biology, a klepton and synklepton is a species that requires input from another biological taxon to complete its reproductive cycle. Specific types of kleptons are zygokleptons, which reproduce by zygogenesis; gynokleptons which reproduce by gynogenesis, and tychokleptons, which reproduce by a combination of both systems.
Nauphoeta cinerea, the speckled cockroach, lobster cockroach, or (small) cinereous cockroach, is a species of cockroach in the family Blaberidae. It is the sole species in the genus Nauphoeta.
Parthenogenesis is a mode of asexual reproduction in which offspring are produced by females without the genetic contribution of a male. Among all the sexual vertebrates, the only examples of true parthenogenesis, in which all-female populations reproduce without the involvement of males, are found in squamate reptiles. There are about 50 species of lizard and 1 species of snake that reproduce solely through parthenogenesis. It is unknown how many sexually reproducing species are also capable of parthenogenesis in the absence of males, but recent research has revealed that this ability is widespread among squamates.
Muscidifurax uniraptor is a species of wasp in the family Pteromalidae. The species does not currently have a common name. M. uniraptor is a pupal parasitoid of synanthropic filth-breeding Diptera and is a natural enemy of the housefly Musca domestica and the stable fly Stomoxys calcitrans.
Gynogenesis, a form of parthenogenesis, is a system of asexual reproduction that requires the presence of sperm without the actual contribution of its DNA for completion. The paternal DNA dissolves or is destroyed before it can fuse with the egg. The egg cell of the organism is able to develop, unfertilized, into an adult using only maternal genetic material. Gynogenesis is often termed "sperm parasitism" in reference to the somewhat pointless role of male gametes. Gynogenetic species, "gynogens" for short, are unisexual, meaning they must mate with males from a closely related bisexual species that normally reproduces sexually.
Androgenesis is a system of asexual reproduction that requires the presence of eggs and occurs when a zygote is produced with only paternal nuclear genes. During standard sexual reproduction, one female and one male parent each produce haploid gametes, which recombine to create offspring with genetic material from both parents. However, in androgenesis, there is no recombination of maternal and paternal chromosomes, and only the paternal chromosomes are passed down to the offspring. The offspring produced in androgenesis will still have maternally inherited mitochondria, as is the case with most sexually reproducing species.
Some female birds, reptiles, and other animals can make a baby on their own. But for mammals like us, eggs and sperm need each other.