Asexual reproduction

While all prokaryotes reproduce without the formation and fusion of gametes, mechanisms for lateral gene transfer such as conjugation, transformation and transduction can be likened to sexual reproduction in the sense of genetic recombination in meiosis.

Types of asexual reproduction

Fission

Prokaryotes (Archaea and Bacteria) reproduce asexually through binary fission, in which the parent organism divides in two to produce two genetically identical daughter organisms. Eukaryotes (such as protists and unicellular fungi) may reproduce in a functionally similar manner by mitosis; most of these are also capable of sexual reproduction.

Multiple fission at the cellular level occurs in many protists, e.g. sporozoans and algae. The nucleus of the parent cell divides several times by mitosis, producing several nuclei. The cytoplasm then separates, creating multiple daughter cells.

In apicomplexans, multiple fission, or schizogony appears either as merogony, sporogony or gametogony. Merogony results in merozoites, which are multiple daughter cells, that originate within the same cell membrane, sporogony results in sporozoites, and gametogony results in microgametes.

Budding

Some cells divide by budding (for example baker's yeast), resulting in a "mother" and a "daughter" cell that is initially smaller than the parent. Budding is also known on a multicellular level; an animal example is the hydra, which reproduces by budding. The buds grow into fully matured individuals which eventually break away from the parent organism.

Internal budding is a process of asexual reproduction, favoured by parasites such as Toxoplasma gondii. It involves an unusual process in which two (endodyogeny) or more (endopolygeny) daughter cells are produced inside a mother cell, which is then consumed by the offspring prior to their separation.

Also, budding (external or internal) occurs in some worms like Taenia or Echinococcus; these worms produce cysts and then produce (invaginated or evaginated) protoscolex with budding.

Vegetative propagation

Vegetative propagation is a type of asexual reproduction found in plants where new individuals are formed without the production of seeds or spores and thus without syngamy or meiosis. Examples of vegetative reproduction include the formation of miniaturized plants called plantlets on specialized leaves, for example in kalanchoe (Bryophyllum daigremontianum) and many produce new plants from rhizomes or stolon (for example in strawberry). Some plants reproduce by forming bulbs or tubers, for example tulip bulbs and Dahlia tubers. In these examples, all the individuals are clones, and the clonal population may cover a large area.

Spore formation

Many multicellular organisms produce spores during their biological life cycle in a process called sporogenesis. Exceptions are animals and some protists, which undergo meiosis immediately followed by fertilization. Plants and many algae on the other hand undergo sporic meiosis where meiosis leads to the formation of haploid spores rather than gametes. These spores grow into multicellular individuals called gametophytes, without a fertilization event. These haploid individuals produce gametes through mitosis. Meiosis and gamete formation therefore occur in separate multicellular generations or "phases" of the life cycle, referred to as alternation of generations. Since sexual reproduction is often more narrowly defined as the fusion of gametes (fertilization), spore formation in plant sporophytes and algae might be considered a form of asexual reproduction (agamogenesis) despite being the result of meiosis and undergoing a reduction in ploidy. However, both events (spore formation and fertilization) are necessary to complete sexual reproduction in the plant life cycle.

Fungi and some algae can also utilize true asexual spore formation, which involves mitosis giving rise to reproductive cells called mitospores that develop into a new organism after dispersal. This method of reproduction is found for example in conidial fungi and the red algae Polysiphonia, and involves sporogenesis without meiosis. Thus the chromosome number of the spore cell is the same as that of the parent producing the spores. However, mitotic sporogenesis is an exception and most spores, such as those of plants and many algae, are produced by meiosis.

Fragmentation

Fragmentation is a form of asexual reproduction where a new organism grows from a fragment of the parent. Each fragment develops into a mature, fully grown individual. Fragmentation is seen in many organisms. Animals that reproduce asexually include planarians, many annelid worms including polychaetes and some oligochaetes, turbellarians and sea stars. Many fungi and plants reproduce asexually. Some plants have specialized structures for reproduction via fragmentation, such as gemmae in mosses and liverworts. Most lichens, which are a symbiotic union of a fungus and photosynthetic algae or cyanobacteria, reproduce through fragmentation to ensure that new individuals contain both symbionts. These fragments can take the form of soredia, dust-like particles consisting of fungal hyphae wrapped around photobiont cells.

Clonal Fragmentation in multicellular or colonial organisms is a form of asexual reproduction or cloning where an organism is split into fragments. Each of these fragments develop into mature, fully grown individuals that are clones of the original organism. In echinoderms, this method of reproduction is usually known as fissiparity. Due to many environmental and epigenetic differences, clones originating from the same ancestor might actually be genetically and epigenetically different.

Agamogenesis

Agamogenesis is any form of reproduction that does not involve any union of gametes. Examples are parthenogenesis and apomixis.

Parthenogenesis

Parthenogenesis is a form of agamogenesis in which an unfertilized egg develops into a new individual. It has been documented in over 2,000 species. Parthenogenesis occurs in the wild in many invertebrates (e.g. water fleas, rotifers, aphids, stick insects, some ants, bees and parasitic wasps) and vertebrates (mostly reptiles, amphibians, and fish). It has also been documented in domestic birds and in genetically altered lab mice. Plants can engage in parthenogenesis as well through a process called apomixis. However this process is considered by many to not be an independent reproduction method, but instead a breakdown of the mechanisms behind sexual reproduction. Parthenogenetic organisms can be split into two main categories: facultative and obligate.

Facultative parthenogenesis

In facultative parthenogenesis, females can reproduce both sexually and asexually. Because of the many advantages of sexual reproduction, most facultative parthenotes only reproduce asexually when forced to. This typically occurs in instances when finding a mate becomes difficult. For example, female zebra sharks will reproduce asexually if they are unable to find a mate in their ocean habitats.

Parthenogenesis was previously believed to rarely occur in vertebrates, and only be possible in very small animals. However, it has been discovered in many more species in recent years. Today, the largest species that has been documented reproducing parthenogenically is the Komodo dragon at 10 feet long and over 300 pounds.

Heterogony is a form of facultative parthenogenesis where females alternate between sexual and asexual reproduction at regular intervals (see Alternation between sexual and asexual reproduction). Aphids are one group of organism that engages in this type of reproduction. They use asexual reproduction to reproduce quickly and create winged offspring that can colonize new plants and reproduce sexually in the fall to lay eggs for the next season. However, some aphid species are obligate parthenotes.

Obligate parthenogenesis

In obligate parthenogenesis, females only reproduce asexually. One example of this is the desert grassland whiptail lizard, a hybrid of two other species. Typically hybrids are infertile but through parthenogenesis this species has been able to develop stable populations.

Gynogenesis is a form of obligate parthenogenesis where a sperm cell is used to initiate reproduction. However, the sperm's genes never get incorporated into the egg cell. The best known example of this is the Amazon molly. Because they are obligate parthenotes, there are no males in their species so they depend on males from a closely related species (the Sailfin molly) for sperm.

Apomixis and nucellar embryony

Apomixis in plants is the formation of a new sporophyte without fertilization. It is important in ferns and in flowering plants, but is very rare in other seed plants. In flowering plants, the term "apomixis" is now most often used for agamospermy, the formation of seeds without fertilization, but was once used to include vegetative reproduction. An example of an apomictic plant would be the triploid European dandelion. Apomixis mainly occurs in two forms: In gametophytic apomixis, the embryo arises from an unfertilized egg within a diploid embryo sac that was formed without completing meiosis. In nucellar embryony, the embryo is formed from the diploid nucellus tissue surrounding the embryo sac. Nucellar embryony occurs in some citrus seeds. Male apomixis can occur in rare cases, such as in the Saharan Cypress Cupressus dupreziana, where the genetic material of the embryo is derived entirely from pollen.

Androgenesis

Androgenesis 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 (such as a sperm or egg cell, each containing only a single set of chromosomes), 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 inverse of this is gynogenesis, where only the maternal chromosomes are inherited, which is more common than androgenesis). The offspring produced in androgenesis will still have maternally inherited mitochondria, as is the case with most sexually reproducing species. Androgenesis occurs in nature in many invertebrates (for example, clams, stick insects, some ants, bees, flies and parasitic wasps) and vertebrates (mainly amphibians and fish). The androgenesis has also been seen in genetically modified laboratory mice.

One of two things can occur to produce offspring with exclusively paternal genetic material: the maternal nuclear genome can be eliminated from the zygote, or the female can produce an egg with no nucleus, resulting in an embryo developing with only the genome of the male gamete.

Male apomixis

Other type of androgenesis is the male apomixis or paternal apomixis is a reproductive process in which a plant develops from a sperm cell (male gamete) without the participation of a female cell (ovum). In this process, the zygote is formed solely with genetic material from the father, resulting in offspring genetically identical to the male organism. This has been noted in many plants like Nicotiana, Capsicum frutescens, Cicer arietinum, Poa arachnifera, Solanum verrucosum, Phaeophyceae, Pripsacum dactyloides, Zea mays, and occurs as the regular reproductive method in Cupressus dupreziana. This contrasts with the more common apomixis, where development occurs without fertilization, but with genetic material only from the mother.

There are also clonal species that reproduce through vegetative reproduction like Lomatia tasmanica and Pando, where the genetic material is exclusively male.

Other species where androgenesis has been observed naturally are the stick insects Bacillus rossius and Bassillus Grandii, the little fire ant Wasmannia auropunctata, Vollenhovia emeryi, Paratrechina longicornis, occasionally in Apis mellifera, the Hypseleotris carp gudgeons, the parasitoid Venturia canescens, and occasionally in fruit flies Drosophila melanogaster carrying a specific mutant allele. It has also been induced in many crops and fish via irradiation of an egg cell to destroy the maternal nuclear genome.

Obligate androgenesis

Obligate androgenesis is the process in which males are capable of producing both eggs and sperm, however, the eggs have no genetic contribution and the offspring come only from the sperm, which allows these individuals to self-fertilize and produce clonal offspring without the need for females. They are also capable of interbreeding with sexual and other androgenetic lineages in a phenomenon known as "egg parasitism." This method of reproduction has been found in several species of the clam genus Corbicula, many plants like, Cupressus dupreziana, Lomatia tasmanica, Pando and recently in the fish Squalius alburnoides.

Other species where androgenesis has been observed naturally are the stick insects Bacillus rossius and Bassillus Grandii, the little fire ant Wasmannia auropunctata, Vollenhovia emeryi, Paratrechina longicornis, occasionally in Apis mellifera, the Hypseleotris carp gudgeons, the parasitoid Venturia canescens, and occasionally in fruit flies Drosophila melanogaster carrying a specific mutant allele. It has also been induced in many crops and fish via irradiation of an egg cell to destroy the maternal nuclear genome.