Fertilisation

Fertilisation or fertilization (see spelling differences), also known as generative fertilisation, insemination, pollination,[1] fecundation, syngamy and impregnation,[2] is the fusion of gametes to initiate the development of a new individual organism or offspring.[3] This cycle of fertilisation and development of new individuals is called sexual reproduction. During double fertilisation in angiosperms the haploid male gamete combines with two haploid polar nuclei to form a triploid primary endosperm nucleus by the process of vegetative fertilisation.

This article is about fertilisation in animals and plants. For fertilisation in humans specifically, see Human fertilization. For soil improvement, see Fertilizer.
"Conceive" redirects here. For the health magazine, see Conceive magazine. For philosophical abstraction, see Concept. For other uses, see Conception (disambiguation).
"impregnate" and "impregnation" redirect here. For the process of making materials water-resistant, see waterproofing.

Sperm and ovum fusing

History

In Antiquity, Aristotle conceived the formation of new individuals through fusion of male and female fluids, with form and function emerging gradually, in a mode called by him as epigenetic.[4]

In 1784, Spallanzani established the need of interaction between the female's ovum and male's sperm to form a zygote in frogs.[5] In 1827, von Baer observed a therian mammalian egg for the first time.[4] Oscar Hertwig (1876), in Germany, described the fusion of nuclei of spermatozoa and of ova from sea urchin.[5]

Evolution

The evolution of fertilisation is related to the origin of meiosis, as both are part of sexual reproduction, originated in eukaryotes. There are two conflicting theories on how the couple meiosis–fertilisation arose. One is that it evolved from prokaryotic sex (bacterial recombination) as eukaryotes evolved from prokaryotes. The other is that mitosis originated meiosis.[6]

Fertilisation in plants
In the Bryophyte land plants, fertilisation takes place within the archegonium. This moss has been genetically modified so that the unfertilised egg within the archegonium produces a blue colour.

The gametes that participate in fertilisation of plants are the pollen (male), and the egg (female) cell. Various families of plants have differing methods by which the female gametophyte is fertilized. In Bryophyte land plants, fertilisation takes place within the archegonium. In flowering plants a second fertilisation event involves another sperm cell and the central cell which is a second female gamete. In flowering plants there are two sperm from each pollen grain.

In seed plants, after pollination, a pollen grain germinates, and a pollen tube grows and penetrates the ovule through a tiny pore called a micropyle.The sperm are transferred from the pollen through the pollen tube to the ovule.

Pollen tube growth

Unlike animal sperm which is motile, plant sperm is immotile and relies on the pollen tube to carry it to the ovule where the sperm is released.[7] The pollen tube penetrates the stigma and elongates through the extracellular matrix of the style before reaching the ovary. Then near the receptacle, it breaks through the ovule through the micropyle (an opening in the ovule wall) and the pollen tube "bursts" into the embryo sac, releasing sperm.[8] The growth of the pollen tube has been believed to depend on chemical cues from the pistil, however these mechanisms were poorly understood until 1995. Work done on tobacco plants revealed a family of glycoproteins called TTS proteins that enhanced growth of pollen tubes.[8] Pollen tubes in a sugar free pollen germination medium and a medium with purified TTS proteins both grew. However, in the TTS medium, the tubes grew at a rate 3x that of the sugar-free medium.[8] TTS proteins were also placed on various locations of semi in vevo pollinated pistils, and pollen tubes were observed to immediately extend toward the proteins. Transgenic plants lacking the ability to produce TTS proteins exhibited slower pollen tube growth and reduced fertility.[8]

Rupture of pollen tube

The rupture of the pollen tube to release sperm in Arabidopsis has been shown to depend on a signal from the female gametophyte. Specific proteins called FER protein kinases present in the ovule control the production of highly reactive derivatives of oxygen called reactive oxygen species (ROS).[9] ROS levels have been shown via GFP to be at their highest during floral stages when the ovule is the most receptive to pollen tubes, and lowest during times of development and following fertilization.[7] High amounts of ROS activate Calcium ion channels in the pollen tube, causing these channels to take up Calcium ions in large amounts. This increased uptake of calcium causes the pollen tube to rupture, and release its sperm into the ovule.[7] Pistil feeding assays in which plants were fed diphenyl iodonium chloride (DPI) suppressed ROS concentrations in Arabidopsis, which in turn prevented pollen tube rupture.[7]

Bryophytes

Bryophyte is a traditional name used to refer to all embryophytes (land plants) that do not have true vascular tissue and are therefore called "non-vascular plants". Some bryophytes do have specialised tissues for the transport of water; however, since these do not contain lignin, they are not considered true vascular tissue.

Ferns

A fern is a member of a group of roughly 12,000 species of vascular plants that reproduce via spores and have neither seeds nor flowers. They differ from mosses by being vascular (i.e. having water-conducting vessels). They have stems and leaves, like other vascular plants. Most ferns have what are called fiddleheads that expand into fronds, which are each delicately divided.

Gymnosperms

The gymnosperms are a group of seed producing plants that includes conifers, Cycads, Ginkgo, and Gnetales. The term "gymnosperm" comes from the Greek composite word γυμνόσπερμος (γυμνός gymnos, "naked" and σπέρμα sperma, "seed"), meaning "naked seeds", after the unenclosed condition of their seeds (called ovules in their unfertilised state). Their naked condition stands in contrast to the seeds and ovules of flowering plants (angiosperms), which are enclosed within an ovary. Gymnosperm seeds develop either on the surface of scales or leaves, often modified to form cones, or at the end of short stalks as in Ginkgo.

Flowering plants

After being fertilised, the ovary starts to swell and develop into the fruit.[10] With multi-seeded fruits, multiple grains of pollen are necessary for syngamy with each ovule. The growth of the pollen tube is controlled by the vegetative (or tube) cytoplasm. Hydrolytic enzymes are secreted by the pollen tube that digest the female tissue as the tube grows down the stigma and style; the digested tissue is used as a nutrient source for the pollen tube as it grows. During pollen tube growth towards the ovary, the generative nucleus divides to produce two separate sperm nuclei (haploid number of chromosomes)[11] – a growing pollen tube therefore contains three separate nuclei, two sperm and one tube.[12] The sperms are interconnected and dimorphic, the large one, in a number of plants, is also linked to the tube nucleus and the interconnected sperm and the tube nucleus form the "male germ unit".[13]

Double fertilisation is the process in angiosperms (flowering plants) in which two sperm from each pollen tube fertilise two cells in a female gametophyte (sometimes called an embryo sac) that is inside an ovule. After the pollen tube enters the gametophyte, the pollen tube nucleus disintegrates and the two sperm cells are released; one of the two sperm cells fertilises the egg cell (at the bottom of the gametophyte near the micropyle), forming a diploid (2n) zygote. This is the point when fertilisation actually occurs; pollination and fertilisation are two separate processes. The nucleus of the other sperm cell fuses with two haploid polar nuclei (contained in the central cell) in the centre of the gametophyte. The resulting cell is triploid (3n). This triploid cell divides through mitosis and forms the endosperm, a nutrient-rich tissue, inside the seed.

The two central-cell maternal nuclei (polar nuclei) that contribute to the endosperm arise by mitosis from the single meiotic product that also gave rise to the egg. Therefore, maternal contribution to the genetic constitution of the triploid endosperm is double that of the embryo.

One primitive species of flowering plant, Nuphar polysepala, has endosperm that is diploid, resulting from the fusion of a sperm with one, rather than two, maternal nuclei. It is believed that early in the development of angiosperm linages, there was a duplication in this mode of reproduction, producing seven-celled/eight-nucleate female gametophytes, and triploid endosperms with a 2:1 maternal to paternal genome ratio.[14]

In many plants, the development of the flesh of the fruit is proportional to the percentage of fertilised ovules. For example, with watermelon, about a thousand grains of pollen must be delivered and spread evenly on the three lobes of the stigma to make a normal sized and shaped fruit.

Cross-fertilisation and self-fertilisation represent different strategies with differing benefits and costs. An estimated 48.7% of plant species are either dioecious or self-incompatible obligate out-crossers.[15] It is also estimated that about 42% of flowering plants exhibit a mixed mating system in nature.[16]

In the most common kind of mixed mating system, individual plants produce a single type of flower and fruits may contain self-fertilised, out-crossed or a mixture of progeny types. The transition from cross-fertilisation to self-fertilisation is the most common evolutionary transition in plants, and has occurred repeatedly in many independent lineages.[17] About 10-15% of flowering plants are predominantly self-fertilising.[17]

Self-pollination
Main article: Self-pollination
See also: Cleistogamy and Autogamy

Under circumstances where pollinators or mates are rare, self-fertilisation offers the advantage of reproductive assurance.[17] Self-fertilisation can therefore result in improved colonisation ability. In some species, self-fertilisation has persisted over many generations. Capsella rubella is a self-fertilisating species that became self-compatible 50,000 to 100,000 years ago.[18] Arabidopsis thaliana is a predominantly self-fertilising plant with an out-crossing rate in the wild of less than 0.3%;[19] a study suggested that self-fertilisation evolved roughly a million years ago or more in A. thaliana.[20] In long-established self-fertilising plants, the masking of deleterious mutations and the production of genetic variability is infrequent and thus unlikely to provide a sufficient benefit over many generations to maintain the meiotic apparatus. Consequently, one might expect self-fertilisation to be replaced in nature by an ameiotic asexual form of reproduction that would be less costly. However the actual persistence of meiosis and self-fertilisation as a form of reproduction in long-established self-fertilising plants may be related to the immediate benefit of efficient recombinational repair of DNA damage during formation of germ cells provided by meiosis at each generation.

Fertilisation in animals
See also: Sexual reproduction in animals and Animal sexual behaviour

The mechanics behind fertilisation has been studied extensively in sea urchins and mice. This research addresses the question of how the sperm and the appropriate egg find each other and the question of how only one sperm gets into the egg and delivers its contents. There are three steps to fertilisation that ensure species-specificity:

  1. Chemotaxis
  2. Sperm activation/acrosomal reaction
  3. Sperm/egg adhesion

Internal vs. external

Consideration as to whether an animal (more specifically a vertebrate) uses internal or external fertilisation is often dependent on the method of birth. Oviparous animals laying eggs with thick calcium shells, such as chickens, or thick leathery shells generally reproduce via internal fertilisation so that the sperm fertilises the egg without having to pass through the thick, protective, tertiary layer of the egg. Ovoviviparous and viviparous animals also use internal fertilisation. It is important to note that although some organisms reproduce via amplexus, they may still use internal fertilisation, as with some salamanders. Advantages to internal fertilisation include: minimal waste of gametes; greater chance of individual egg fertilisation, relatively "longer" time period of egg protection, and selective fertilisation; many females have the ability to store sperm for extended periods of time and can fertilise their eggs at their own desire.

Oviparous animals producing eggs with thin tertiary membranes or no membranes at all, on the other hand, use external fertilisation methods. Advantages to external fertilisation include: minimal contact and transmission of bodily fluids; decreasing the risk of disease transmission, and greater genetic variation (especially during broadcast spawning external fertilisation methods).

Sea urchins
Acrosome reaction on a sea urchin cell.

Sperm find the eggs via chemotaxis, a type of ligand/receptor interaction. Resact is a 14 amino acid peptide purified from the jelly coat of A. punctulata that attracts the migration of sperm.

After finding the egg, the sperm penetrates the jelly coat through a process called sperm activation. In another ligand/receptor interaction, an oligosaccharide component of the egg binds and activates a receptor on the sperm and causes the acrosomal reaction. The acrosomal vesicles of the sperm fuse with the plasma membrane and are released. In this process, molecules bound to the acrosomal vesicle membrane, such as bindin, are exposed on the surface of the sperm. These contents digest the jelly coat and eventually the vitelline membrane. In addition to the release of acrosomal vesicles, there is explosive polymerisation of actin to form a thin spike at the head of the sperm called the acrosomal process.

The sperm binds to the egg through another ligand reaction between receptors on the vitelline membrane. The sperm surface protein bindin, binds to a receptor on the vitelline membrane identified as EBR1.

Fusion of the plasma membranes of the sperm and egg are likely mediated by bindin. At the site of contact, fusion causes the formation of a fertilisation cone.

Mammals

Mammals internally fertilise through copulation. After a male ejaculates, many sperm move to the upper vagina (via contractions from the vagina) through the cervix and across the length of the uterus to meet the ovum. In cases where fertilisation occurs, the female usually ovulates during a period that extends from hours before copulation to a few days after; therefore, in most mammals it is more common for ejaculation to precede ovulation than vice versa.

When sperm are deposited into the anterior vagina, they are not capable of fertilization (i.e., non-capacitated) and are characterized by slow linear motility patterns. This motility, combined with muscular contractions enables sperm transport towards the uterus and fallopian tubes.[21] There is a pH gradient within the micro-environment of the female reproductive tract such that the pH near the vaginal opening is lower (approximately 5) than the fallopian tubes (approximately 8).[22] The sperm-specific pH-sensitive calcium transport protein called CatSper increases the sperm cell permeability to calcium as it moves further into the reproductive tract. Intracellular calcium influx contributes to sperm capacitation and hyperactivation, causing a more violent and rapid non-linear motility pattern as sperm approach the oocyte. The capacitated spermatozoon and the oocyte meet and interact in the ampulla of the fallopian tube. Rheotaxis, thermotaxis and chemotaxis are known mechanisms that guide sperm towards the egg during the final stage of sperm migration.[23] Spermatozoa respond (see Sperm thermotaxis) to the temperature gradient of ~2 °C between the oviduct and the ampulla,[24] and chemotactic gradients of progesterone have been confirmed as the signal emanating from the cumulus oophorus cells surrounding rabbit and human oocytes.[25] Capacitated and hyperactivated sperm respond to these gradients by changing their behaviour and moving towards the cumulus-oocyte complex. Other chemotactic signals such as formyl Met-Leu-Phe (fMLF) may also guide spermatozoa.[26]

The zona pellucida, a thick layer of extracellular matrix that surrounds the egg and is similar to the role of the vitelline membrane in sea urchins, binds the sperm. Unlike sea urchins, the sperm binds to the egg before the acrosomal reaction. ZP3, a glycoprotein in the zona pellucida, is responsible for egg/sperm adhesion in mice. The receptor galactosyltransferase (GalT) binds to the N-acetylglucosamine residues on the ZP3 and is important for binding with the sperm and activating the acrosome reaction. ZP3 is sufficient though unnecessary for sperm/egg binding. Two additional sperm receptors exist: a 250kD protein that binds to an oviduct secreted protein, and SED1, which independently binds to the zona. After the acrosome reaction, the sperm is believed to remain bound to the zona pellucida through exposed ZP2 receptors. These receptors are unknown in mice but have been identified in guinea pigs.

In mammals, the binding of the spermatozoon to the GalT initiates the acrosome reaction. This process releases the hyaluronidase that digests the matrix of hyaluronic acid in the vestments around the oocyte. Additionally, heparin-like glycosaminoglycans (GAGs) are released near the oocyte that promote the acrosome reaction.[27] Fusion between the oocyte plasma membranes and sperm follows and allows the sperm nucleus, the typical centriole, and atypical centriole that is attached to the flagellum, but not the mitochondria, to enter the oocyte.[28] The protein CD9 likely mediates this fusion in mice (the binding homolog). The egg "activates" itself upon fusing with a single sperm cell and thereby changes its cell membrane to prevent fusion with other sperm. Zinc atoms are released during this activation.

This process ultimately leads to the formation of a diploid cell called a zygote. The zygote divides to form a blastocyst and, upon entering the uterus, implants in the endometrium, beginning pregnancy. Embryonic implantation not in the uterine wall results in an ectopic pregnancy that can kill the mother.

In such animals as rabbits, coitus induces ovulation by stimulating the release of the pituitary hormone gonadotropin; this release greatly increases the likelihood of pregnancy.

Humans
Fertilisation in humans. The sperm and ovum unite through fertilisation, creating a zygote that (over the course of 8-9 days) implants in the uterine wall, where it resides for nine months.

Fertilisation in humans is the union of a human egg and sperm, usually occurring in the ampulla of the fallopian tube, producing a zygote cell, or fertilized egg, initiating prenatal development. Scientists discovered the dynamics of human fertilization in the nineteenth century.

The term conception commonly refers to "the process of becoming pregnant involving fertilization or implantation or both".[29] Its use makes it a subject of semantic arguments about the beginning of pregnancy, typically in the context of the abortion debate. Upon gastrulation, which occurs around 16 days after fertilisation, the implanted blastocyst develops three germ layers, the endoderm, the ectoderm and the mesoderm, and the genetic code of the father becomes fully involved in the development of the embryo; later twinning is impossible. Additionally, interspecies hybrids survive only until gastrulation and cannot further develop. However, some human developmental biology literature refers to the conceptus and such medical literature refers to the "products of conception" as the post-implantation embryo and its surrounding membranes.[30] The term "conception" is not usually used in scientific literature because of its variable definition and connotation.

Insects
Red-veined darters (Sympetrum fonscolombii) flying "in cop" (male ahead), enabling the male to prevent other males from mating. The eggs are fertilised as they are laid, one at a time.

Insects in different groups, including the Odonata (dragonflies and damselflies) and the Hymenoptera (ants, bees, and wasps) practise delayed fertilisation. Among the Odonata, females may mate with multiple males, and store sperm until the eggs are laid. The male may hover above the female during egg-laying (oviposition) to prevent her from mating with other males and replacing his sperm; in some groups such as the darters, the male continues to grasp the female with his claspers during egg-laying, the pair flying around in tandem.[31] Among social Hymenoptera, honeybee queens mate only on mating flights, in a short period lasting some days; a queen may mate with eight or more drones. She then stores the sperm for the rest of her life, perhaps for five years or more.[32][33]

Fertilisation in fungi
Main article: Mating in fungi

In many fungi (except chytrids), as in some protists, fertilisation is a two step process. First, the cytoplasms of the two gamete cells fuse (called plasmogamy), producing a dikaryotic or heterokaryotic cell with multiple nuclei. This cell may then divide to produce dikaryotic or heterokaryotic hyphae. The second step of fertilisation is karyogamy, the fusion of the nuclei to form a diploid zygote.

In chytrid fungi, fertilisation occurs in a single step with the fusion of gametes, as in animals and plants.

Fertilisation in protists

Fertilisation in protozoa

There are three types of fertilisation processes in protozoa:[34]

  • gametogamy;
  • autogamy;[35][36]
  • gamontogamy.

Fertilisation in algae

Fertilisation in algae occurs by binary fission. The pseudopodia is first withdrawn and the nucleus starts dividing. When the cytoplasm is divided, the cytoplasm is also divided into two equal parts for each daughter cell. Two daughter cells are produced by one parent cell. It involves the process of mitosis.

Fertilisation in fungi-like protists
See also: Mating in fungi

Fertilisation in fungi. In many fungi (except chytrids), as in some protists, fertilisation is a two step process. ... In chytrid fungi, fertilisation occurs in a single step with the fusion of gametes, as in animals and plants.

Fertilisation and genetic recombination

Meiosis results in a random segregation of the genes that each parent contributes. Each parent organism is usually identical save for a fraction of their genes; each gamete is therefore genetically unique. At fertilisation, parental chromosomes combine. In humans, (2²²)² = 17.6x1012 chromosomally different zygotes are possible for the non-sex chromosomes, even assuming no chromosomal crossover. If crossover occurs once, then on average (4²²)² = 309x1024 genetically different zygotes are possible for every couple, not considering that crossover events can take place at most points along each chromosome. The X and Y chromosomes undergo no crossover events and are therefore excluded from the calculation. The mitochondrial DNA is only inherited from the maternal parent.

Parthenogenesis
Main article: parthenogenesis

Organisms that normally reproduce sexually can also reproduce via parthenogenesis, wherein an unfertilised female gamete produces viable offspring. These offspring may be clones of the mother, or in some cases genetically differ from her but inherit only part of her DNA. Parthenogenesis occurs in many plants and animals and may be induced in others through a chemical or electrical stimulus to the egg cell. In 2004, Japanese researchers led by Tomohiro Kono succeeded after 457 attempts to merge the ova of two mice by blocking certain proteins that would normally prevent the possibility; the resulting embryo normally developed into a mouse.[37]

Allogamy and autogamy

Allogamy, which is also known as cross-fertilisation, refers to the fertilisation of an egg cell from one individual with the male gamete of another.

Autogamy which is also known as self-fertilisation, occurs in such hermaphroditic organisms as plants and flatworms; therein, two gametes from one individual fuse.

Other variants of bisexual reproduction

Some relatively unusual forms of reproduction are:[38][39]

Gynogenesis: A sperm stimulates the egg to develop without fertilisation or syngamy. The sperm may enter the egg.

Hybridogenesis: One genome is eliminated to produce haploid eggs.

Canina meiosis: (sometimes called "permanent odd polyploidy") one genome is transmitted in the Mendelian fashion, others are transmitted clonally.

Benefits of cross-fertilisation
Main articles: Allogamy and Heterosis

The major benefit of cross-fertilisation is generally thought to be the avoidance of inbreeding depression. Charles Darwin, in his 1876 book The Effects of Cross and Self Fertilisation in the Vegetable Kingdom (pages 466-467) summed up his findings in the following way.[40]

“It has been shown in the present volume that the offspring from the union of two distinct individuals, especially if their progenitors have been subjected to very different conditions, have an immense advantage in height, weight, constitutional vigour and fertility over the self-fertilised offspring from one of the same parents. And this fact is amply sufficient to account for the development of the sexual elements, that is, for the genesis of the two sexes.”

In addition, it is thought by some,[41] that a long-term advantage of out-crossing in nature is increased genetic variability that promotes adaptation or avoidance of extinction (see Genetic variability).

gollark: Of course not.
gollark: People accessing the remote debugging service connect on `potatOS` as admins. This requires a key with the right perms.
gollark: PotatOS devices listen on the `potatOS` channel as unprivileged clients.
gollark: Basically, access is divided into "channels".
gollark: Well, it uses a somewhat limited permission model.

See also

References
  1. "Fertilization". Merriam-Webster. Retrieved July 10, 2018.
  2. http://www.oxfordlearnersdictionaries.com/definition/english/impregnation%5B%5D%5B%5D
  3. {], or outside (external fertilisation)
  4. Maienschein J. 2017. The first century of cell theory: From structural units to complex living systems. In: Stadler F. (eds.), Integrated History and Philosophy of Science. Vienna Circle Institute Yearbook. Institute Vienna Circle, University of Vienna, Vienna Circle Society, Society for the Advancement of Scientific World Conceptions, vol 20. Springer, Cham. link.
  5. Birkhead, T.R. & Montgomerie, R. (2009). Three centuries of sperm research, pp 1-42 in: Birkhead, T. R., Hosken, D. J. & Pitnick, S. Sperm Biology: An Evolutionary Perspective. Elsevier/Academic Press, Amsterdam. 642 pp., .
  6. Wilkins AS, Holliday R (January 2009). "The evolution of meiosis from mitosis". Genetics. 181 (1): 3–12. doi:10.1534/genetics.108.099762. PMC 2621177. PMID 19139151.
  7. Duan, Qiaohong; Kita, Daniel; Johnson, Eric A; Aggarwal, Mini; Gates, Laura; Wu, Hen-Ming; Cheung, Alice Y (2014). "Reactive oxygen species mediate pollen tube rupture to release sperm for fertilization in Arabidopsis". Nature Communications. 5: 3129. Bibcode:2014NatCo...5.3129D. doi:10.1038/ncomms4129. PMID 24451849.
  8. Cheung, Alice Y; Wang, Hong; Wu, Hen-Ming (1995). "A floral transmitting tissue-specific glycoprotein attracts pollen tubes and stimulates their growth". Cell. 82 (3): 383–93. doi:10.1016/0092-8674(95)90427-1. PMID 7634328.
  9. Maejima, Yasuhiro (2012). "Reactive oxygen species". Science Direct. Retrieved April 25, 2018.
  10. Johnstone, Adam (2001). Biology: facts & practice for A level. Oxford University Press. p. 95. ISBN 0-19-914766-3.
  11. Handbook of plant science. Chichester, West Sussex, England: John Wiley. 2007. p. 466. ISBN 978-0-470-05723-0.
  12. Kirk, David; Starr, Cecie (1975). Biology today. Del Mar, Calif.: CRM. p. 93. ISBN 978-0-394-31093-0.
  13. Raghavan, Valayamghat (2006). Double fertilization: embryo and endosperm development in flowering plant. Berlin: Springer-Verlag. p. 12. ISBN 978-3-540-27791-0.
  14. Friedman, William E; Williams, Joseph H (2003). "Modularity of the Angiosperm Female Gametophyte and Its Bearing on the Early Evolution of Endosperm in Flowering Plants". Evolution. 57 (2): 216–30. doi:10.1111/j.0014-3820.2003.tb00257.x. PMID 12683519.
  15. Igic B, Kohn JR (2006). "The distribution of plant mating systems: study bias against obligately outcrossing species". Evolution. 60 (5): 1098–103. doi:10.1554/05-383.1. PMID 16817548.
  16. Goodwillie C, Kalisz S, Eckert CG (2005). "The evolutionary enigma of mixed mating systems in plants: Occurrence, theoretical explanations, and empirical evidence". Annu. Rev. Ecol. Evol. Syst. 36: 47–79. doi:10.1146/annurev.ecolsys.36.091704.175539. S2CID 3755371.
  17. Wright, S. I; Kalisz, S; Slotte, T (2013). "Evolutionary consequences of self-fertilization in plants". Proceedings of the Royal Society B: Biological Sciences. 280 (1760): 20130133. doi:10.1098/rspb.2013.0133. PMC 3652455. PMID 23595268.
  18. Brandvain, Yaniv; Slotte, Tanja; Hazzouri, Khaled M; Wright, Stephen I; Coop, Graham (2013). "Genomic Identification of Founding Haplotypes Reveals the History of the Selfing Species Capsella rubella". PLOS Genetics. 9 (9): e1003754. arXiv:1307.4118. Bibcode:2013arXiv1307.4118B. doi:10.1371/journal.pgen.1003754. PMC 3772084. PMID 24068948.
  19. Abbott, RJ; Gomes, MF (1989). "Population genetic structure and outcrossing rate of Arabidopsis thaliana (L.) Heynh". Heredity. 62 (3): 411–418. doi:10.1038/hdy.1989.56.
  20. Tang C, Toomajian C, Sherman-Broyles S, Plagnol V, Guo YL, Hu TT, Clark RM, Nasrallah JB, Weigel D, Nordborg M (2007). "The evolution of selfing in Arabidopsis thaliana". Science. 317 (5841): 1070–2. Bibcode:2007Sci...317.1070T. doi:10.1126/science.1143153. PMID 17656687.
  21. Suarez, S.S.; Pacey, A. A. (2006). "Sperm transport in the female reproductive tract". Human Reproduction Update. 12 (1): 23–37. doi:10.1093/humupd/dmi047. PMID 16272225.
  22. Cheong, Ying; MacKlon, Nick; Morgan, Hywel; Mingels, Roel; Ng, Ka Ying Bonnie (January 2018). "In vivo oxygen, temperature and pH dynamics in the female reproductive tract and their importance in human contraception: a systemic review". Human Reproduction Update. 24 (1): 15–34. doi:10.1093/humupd/dmx028. PMID 29077897.
  23. Li, Shuai; Winuthayanon, Wipawee (2016). "Oviduct: Roles in fertilization and early embryo development". Journal of Endocrinology. 232 (1): R1–R26. doi:10.1530/JOE-16-0302. PMID 27875265.
  24. Bahat, Anat; Eisenbach, Michael (2006). "Sperm thermotaxis". Molecular and Cellular Endocrinology. 252 (1–2): 115–9. doi:10.1016/j.mce.2006.03.027. PMID 16672171.
  25. Teves, Maria E; Guidobaldi, Hector A; Uñates, Diego R; Sanchez, Raul; Miska, Werner; Publicover, Stephen J; Morales Garcia, Aduén A; Giojalas, Laura C (2009). "Molecular Mechanism for Human Sperm Chemotaxis Mediated by Progesterone". PLOS ONE. 4 (12): e8211. Bibcode:2009PLoSO...4.8211T. doi:10.1371/journal.pone.0008211. PMC 2782141. PMID 19997608.
  26. Gnessi L, Fabbri A, Silvestroni L, Moretti C, Fraioli F, Pert CB, Isidori A (1986). "Evidence for the presence of specific receptors for N-formyl chemotactic peptides on human spermatozoa". J Clin Endocrinol Metab. 63 (4): 841–846. doi:10.1210/jcem-63-4-841. PMID 3018025.
  27. Ax, R. L.; First, N. L.; Bushmeyer, S. M.; Clayton, M. K.; Lee, C. N. (1986-09-01). "Glycosaminoglycans in Ewe Reproductive Tracts and Their Influence on Acrosome Reactions in Bovine Spermatozoa in Vitro". Journal of Animal Science. 63 (3): 861–867. doi:10.2527/jas1986.633861x. ISSN 0021-8812. PMID 3759713. S2CID 853558.
  28. Fishman, Emily L; Jo, Kyoung; Nguyen, Quynh P. H; Kong, Dong; Royfman, Rachel; Cekic, Anthony R; Khanal, Sushil; Miller, Ann L; Simerly, Calvin; Schatten, Gerald; Loncarek, Jadranka; Mennella, Vito; Avidor-Reiss, Tomer (2018). "A novel atypical sperm centriole is functional during human fertilization". Nature Communications. 9 (1): 2210. Bibcode:2018NatCo...9.2210F. doi:10.1038/s41467-018-04678-8. PMC 5992222. PMID 29880810.
  29. "Conception". Merriam-Webster. Retrieved January 27, 2019.
  30. Moore, K. L.; T. V. M. Persaud (2003). The Developing Human: Clinically Oriented Embryology. W. B. Saunders Company. ISBN 0-7216-6974-3.
  31. Dijkstra, Klaas-Douwe B. (2006). Field Guide to the Dragonflies of Britain and Europe. British Wildlife Publishing. pp. 8–9. ISBN 0-9531399-4-8.
  32. Waldbauer, Gilbert (1998). The Birder's Bug Book. Harvard University Press.
  33. Agriculture and Consumer Protection. "Beekeeping in Africa: Colony life and social organization". FAO.
  34. Fertilization in protozoa and metazoan animals: cellular and molecular aspects. Juan J. Tarín; Antonio Cano (eds.). Springer-Verlag, 2000.
  35. Reproduction#Autogamy
  36. "Autogamy | biology".
  37. Kono, Tomohiro; Obata, Yayoi; Wu, Quiong; Niwa, Katsutoshi; Ono, Yukiko; Yamamoto, Yuji; Park, Eun Sung; Seo, Jeong-Sun; Ogawa, Hidehiko (2004). "Birth of parthenogenetic mice that can develop to adulthood". Nature. 428 (6985): 860–4. Bibcode:2004Natur.428..860K. doi:10.1038/nature02402. PMID 15103378. Lay summary – National Geographic (2004-04-21).
  38. Stenberg, P; Saura, A (2013). "Meiosis and Its Deviations in Polyploid Animals". Cytogenetic and Genome Research. 140 (2–4): 185–203. doi:10.1159/000351731. PMID 23796636.
  39. Stock, M; Ustinova, J; Betto-Colliard, C; Schartl, M; Moritz, C; Perrin, N (2011). "Simultaneous Mendelian and clonal genome transmission in a sexually reproducing, all-triploid vertebrate". Proceedings of the Royal Society B: Biological Sciences. 279 (1732): 1293–1299. doi:10.1098/rspb.2011.1738. PMC 3282369. PMID 21993502.
  40. Darwin CR (1876). The effects of cross and self fertilisation in the vegetable kingdom. London: John Murray. http://darwin-online.org.uk/converted/published/1881-Worms-CrossandSelfFertilisation-F1249/1876-F1249.html%5B%5D see page 466-467
  41. Otto, S.P; Gerstein, A.C (2006). "Why have sex? The population genetics of sex and recombination". Biochemical Society Transactions. 34 (4): 519–22. doi:10.1042/BST0340519. PMID 16856849. S2CID 14542950.
This article is issued from Wikipedia. The text is licensed under Creative Commons - Attribution - Sharealike. Additional terms may apply for the media files.