Sexual reproduction is a form of reproduction where two morphologically distinct types of specialized reproductive cells called gametes fuse together, involving a female's large ovum (or egg) and a male's smaller sperm. Each gamete contains half the number of chromosomes of normal cells. They are created by a specialized type of cell division, which only occurs in eukaryotic cells, known as meiosis. The two gametes fuse during fertilization to produce DNA replication and the creation of a single-celled zygote which includes genetic material from both gametes. In a process called genetic recombination, genetic material (DNA) joins up so that homologous chromosome sequences are aligned with each other, and this is followed by exchange of genetic information. Two rounds of cell division then produce four daughter cells with half the number of chromosomes from each original parent cell, and the same number of chromosomes as both parents, though self-fertilization can occur. For instance, in human reproduction each human cell contains 46 chromosomes, 23 pairs, except gamete cells, which only contain 23 chromosomes, so the child will have 23 chromosomes from each parent genetically recombined into 23 pairs. Cell division initiates the development of a new individual organism in multicellular organisms, including animals and plants, for the vast majority of whom this is the primary method of reproduction.
The evolution of sexual reproduction is a major puzzle because asexual reproduction should be able to outcompete it as every young organism created can bear its own young. This implies that an asexual population has an intrinsic capacity to grow more rapidly with each generation. This 50% cost is a fitness disadvantage of sexual reproduction. The two-fold cost of sex includes this cost and the fact that any organism can only pass on 50% of its own genes to its offspring. One definite advantage of sexual reproduction is that it prevents the accumulation of genetic mutations.
Sexual selection is a mode of natural selection in which some individuals out-reproduce others of a population because they are better at securing mates for sexual reproduction. It has been described as "a powerful evolutionary force that does not exist in asexual populations."
Prokaryotes, whose initial cell has additional or transformed genetic material, reproduce through asexual reproduction but may, in lateral gene transfer, display processes such as bacterial conjugation, transformation and transduction, which are similar to sexual reproduction although they do not lead to reproduction.
Biologists studying evolution propose several explanations for why sexual reproduction developed and why it is maintained. These reasons include reducing the likelihood of the accumulation of deleterious mutations, increasing rate of adaptation to changing environments, dealing with competition, and masking deleterious mutations. All of these ideas about why sexual reproduction has been maintained are generally supported, but ultimately the size of the population determines if sexual reproduction is entirely beneficial. Larger populations appear to respond more quickly to benefits obtained through sexual reproduction than do smaller population sizes.
Maintenance of sexual reproduction has been explained by theories that work at several levels of selection, though some of these models remain controversial. However, newer models presented in recent years suggest a basic advantage for sexual reproduction in slowly reproducing complex organisms.
In order to sexually reproduce, both males and females need to find a mate. Generally in animals mate choice is made by females while males compete to be chosen. This can lead organisms to extreme efforts in order to reproduce, such as combat and display, or produce extreme features caused by a positive feedback known as a Fisherian runaway. Thus sexual reproduction, as a form of natural selection, has an effect on evolution. Sexual dimorphism is where the basic phenotypic traits vary between males and females of the same species. Dimorphism is found in both sex organs and in secondary sex characteristics, body size, physical strength and morphology, biological ornamentation, behavior and other bodily traits. However, sexual selection is only implied over an extended period of time leading to sexual dimorphism.
Apart from some eusocial wasps, organisms which reproduce sexually have a 1:1 sex ratio of male and female births. The English statistician and biologist Ronald Fisher outlined why this is so in what has come to be known as Fisher's principle. This essentially says the following:
- Suppose male births are less common than female.
- A newborn male then has better mating prospects than a newborn female, and therefore can expect to have more offspring.
- Therefore parents genetically disposed to produce males tend to have more than average numbers of grandchildren born to them.
- Therefore the genes for male-producing tendencies spread, and male births become more common.
- As the 1:1 sex ratio is approached, the advantage associated with producing males dies away.
- The same reasoning holds if females are substituted for males throughout. Therefore 1:1 is the equilibrium ratio.
Insect species make up more than two-thirds of all extant animal species. Most insect species reproduce sexually, though some species are facultatively parthenogenetic. Many insects species have sexual dimorphism, while in others the sexes look nearly identical. Typically they have two sexes with males producing spermatozoa and females ova. The ova develop into eggs that have a covering called the chorion, which forms before internal fertilization. Insects have very diverse mating and reproductive strategies most often resulting in the male depositing spermatophore within the female, which she stores until she is ready for egg fertilization. After fertilization, and the formation of a zygote, and varying degrees of development, in many species the eggs are deposited outside the female; while in others, they develop further within the female and are born live.
There are three extant kinds of mammals: monotremes, placentals and marsupials, all with internal fertilization. In placental mammals, offspring are born as juveniles: complete animals with the sex organs present although not reproductively functional. After several months or years, depending on the species, the sex organs develop further to maturity and the animal becomes sexually mature. Most female mammals are only fertile during certain periods during their estrous cycle, at which point they are ready to mate. Individual male and female mammals meet and carry out copulation. For most mammals, males and females exchange sexual partners throughout their adult lives.
The vast majority of fish species lay eggs that are then fertilized by the male, some species lay their eggs on a substrate like a rock or on plants, while others scatter their eggs and the eggs are fertilized as they drift or sink in the water column.
Some fish species use internal fertilization and then disperse the developing eggs or give birth to live offspring. Fish that have live-bearing offspring include the guppy and mollies or Poecilia. Fishes that give birth to live young can be ovoviviparous, where the eggs are fertilized within the female and the eggs simply hatch within the female body, or in seahorses, the male carries the developing young within a pouch, and gives birth to live young. Fishes can also be viviparous, where the female supplies nourishment to the internally growing offspring. Some fish are hermaphrodites, where a single fish is both male and female and can produce eggs and sperm. In hermaphroditic fish, some are male and female at the same time while in other fish they are serially hermaphroditic; starting as one sex and changing to the other. In at least one hermaphroditic species, self-fertilization occurs when the eggs and sperm are released together. Internal self-fertilization may occur in some other species. One fish species does not reproduce by sexual reproduction but uses sex to produce offspring; Poecilia formosa is a unisex species that uses a form of parthenogenesis called gynogenesis, where unfertilized eggs develop into embryos that produce female offspring. Poecilia formosa mate with males of other fish species that use internal fertilization, the sperm does not fertilize the eggs but stimulates the growth of the eggs which develops into embryos.
Animals typically produce gametes directly by meiosis. Male gametes are called sperm, and female gametes are called eggs or ova. In animals, fertilization follows immediately after meiosis. Plants on the other hand have mitosis occurring in spores, which are produced by meiosis. The spores germinate into the gametophyte phase. The gametophytes of different groups of plants vary in size; angiosperms have as few as three cells in pollen, and mosses and other so called primitive plants may have several million cells. Plants have an alternation of generations where the sporophyte phase is succeeded by the gametophyte phase. The sporophyte phase produces spores within the sporangium by meiosis.
Flowering plants are the dominant plant form on land and they reproduce either sexually or asexually. Often their most distinguishing feature is their reproductive organs, commonly called flowers. The anther produces pollen grains which contain the male gametophytes (sperm). For pollination to occur, pollen grains must attach to the stigma of the female reproductive structure (carpel), where the female gametophytes (ovules) are located inside the ovary. After the pollen tube grows through the carpel's style, the sex cell nuclei from the pollen grain migrate into the ovule to fertilize the egg cell and endosperm nuclei within the female gametophyte in a process termed double fertilization. The resulting zygote develops into an embryo, while the triploid endosperm (one sperm cell plus two female cells) and female tissues of the ovule give rise to the surrounding tissues in the developing seed. The ovary, which produced the female gametophyte(s), then grows into a fruit, which surrounds the seed(s). Plants may either self-pollinate or cross-pollinate.
In 2013, flowers dating from the Cretaceous (100 million years before present) were found encased in amber, the oldest evidence of sexual reproduction in a flowering plant. Microscopic images showed tubes growing out of pollen and penetrating the flower's stigma. The pollen was sticky, suggesting it was carried by insects.
Ferns mostly produce large diploid sporophytes with rhizomes, roots and leaves; and on fertile leaves called sporangium, spores are produced. The spores are released and germinate to produce short, thin gametophytes that are typically heart shaped, small and green in color. The gametophytes or thallus, produce both motile sperm in the antheridia and egg cells in separate archegonia. After rains or when dew deposits a film of water, the motile sperm are splashed away from the antheridia, which are normally produced on the top side of the thallus, and swim in the film of water to the archegonia where they fertilize the egg. To promote out crossing or cross fertilization the sperm are released before the eggs are receptive of the sperm, making it more likely that the sperm will fertilize the eggs of different thallus. A zygote is formed after fertilization, which grows into a new sporophytic plant. The condition of having separate sporephyte and gametophyte plants is called alternation of generations. Other plants with similar reproductive means include the Psilotum, Lycopodium, Selaginella and Equisetum.
The bryophytes, which include liverworts, hornworts and mosses, reproduce both sexually and vegetatively. They are small plants found growing in moist locations and like ferns, have motile sperm with flagella and need water to facilitate sexual reproduction. These plants start as a haploid spore that grows into the dominate form, which is a multicellular haploid body with leaf-like structures that photosynthesize. Haploid gametes are produced in antherida and archegonia by mitosis. The sperm released from the antherida respond to chemicals released by ripe archegonia and swim to them in a film of water and fertilize the egg cells thus producing a zygote. The zygote divides by mitotic division and grows into a sporophyte that is diploid. The multicellular diploid sporophyte produces structures called spore capsules, which are connected by seta to the archegonia. The spore capsules produce spores by meiosis, when ripe the capsules burst open and the spores are released. Bryophytes show considerable variation in their breeding structures and the above is a basic outline. Also in some species each plant is one sex while other species produce both sexes on the same plant.
Fungi are classified by the methods of sexual reproduction they employ. The outcome of sexual reproduction most often is the production of resting spores that are used to survive inclement times and to spread. There are typically three phases in the sexual reproduction of fungi: plasmogamy, karyogamy and meiosis. The cytoplasm of two parent cells fuse during plasmogamy and the nuclei fuse during karyogamy. New haploid gametes are formed during meiosis and develop into spores.
Bacteria and archaea
Three distinct processes in prokaryotes are regarded as similar to eukaryotic sex: bacterial transformation, which involves the incorporation of foreign DNA into the bacterial chromosome; bacterial conjugation, which is a transfer of plasmid DNA between bacteria, but the plasmids are rarely incorporated into the bacterial chromosome; and gene transfer and genetic exchange in archaea.
Bacterial transformation involves the recombination of genetic material and its function is mainly associated with DNA repair. Bacterial transformation is a complex process encoded by numerous bacterial genes, and is a bacterial adaptation for DNA transfer. This process occurs naturally in at least 40 bacterial species. For a bacterium to bind, take up, and recombine exogenous DNA into its chromosome, it must enter a special physiological state referred to as competence (see Natural competence). Sexual reproduction in early single-celled eukaryotes may have evolved from bacterial transformation, or from a similar process in archaea (see below).
On the other hand, bacterial conjugation is a type of direct transfer of DNA between two bacteria through an external appendage called the conjugation pilus. Bacterial conjugation is controlled by plasmid genes that are adapted for spreading copies of the plasmid between bacteria. The infrequent integration of a plasmid into a host bacterial chromosome, and the subsequent transfer of a part of the host chromosome to another cell do not appear to be bacterial adaptations.
Exposure of hyperthermophilic archaeal Sulfolobus species to DNA damaging conditions induces cellular aggregation accompanied by high frequency genetic marker exchange. Ajon et al. hypothesized that this cellular aggregation enhances species-specific DNA repair by homologous recombination. DNA transfer in Sulfolobus may be an early form of sexual interaction similar to the more well-studied bacterial transformation systems that also involve species-specific DNA transfer leading to homologous recombinational repair of DNA damage.
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