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This article is about the distinguishing trait in sexually reproducing organisms. For activities, see Human sexual activity and Animal sexual behavior. For other uses, see Sex (disambiguation).
"Male and female" redirects here. For other uses, see Male and female (disambiguation).

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Sex
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Sexuality
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Sex is the biological trait that determines whether a sexually reproducing organism produces male or female gametes.[1][2][3][4][5] During sexual reproduction, a male and a female gamete fuse to form a zygote, which develops into an offspring that inherits traits from each parent. By convention, organisms that produce smaller, more mobile gametes (spermatozoa, sperm) are called male, while organisms that produce larger, non-mobile gametes (ova, often called egg cells) are called female.[6] An organism that produces both types of gamete is hermaphrodite.[3][7]

In non-hermaphroditic species, the sex of an individual is determined through one of several biological sex-determination systems. Most mammalian species have the XY sex-determination system, where the male usually carries an X and a Y chromosome (XY), and the female usually carries two X chromosomes (XX). Other chromosomal sex-determination systems in animals include the ZW system in birds, and the XO system in some insects.[8] Various environmental systems include temperature-dependent sex determination in reptiles and crustaceans.[9]

The male and female of a species may be physically alike (sexual monomorphism) or have physical differences (sexual dimorphism). In sexually dimorphic species, including most birds and mammals, the sex of an individual is usually identified through observation of that individual's sexual characteristics. Sexual selection or mate choice can accelerate the evolution of differences between the sexes.

The terms male and female typically do not apply in sexually undifferentiated species in which the individuals are isomorphic (look the same) and the gametes are isogamous (indistinguishable in size and shape), such as the green alga Ulva lactuca. Some kinds of functional differences between individuals, such as in fungi,[10] may be referred to as mating types.[11]

Sexual reproduction

Main article: Sexual reproduction
Further information: Isogamy and Anisogamy
The life cycle of a sexually reproducing species cycles through haploid and diploid stages

Sexual reproduction, in which two individuals produce an offspring that possesses a selection of the genetic traits of each parent, is exclusive to eukaryotes. Genetic traits are encoded in the deoxyribonucleic acid (DNA) of chromosomes. The eukaryote cell has a set of paired homologous chromosomes, one from each parent, and this double-chromosome stage is called "diploid". During sexual reproduction, a diploid organism produces specialized haploid sex cells called gametes via meiosis,[12] each of which has a single set of chromosomes. Meiosis involves a stage of genetic recombination via chromosomal crossover, in which regions of DNA are exchanged between matched pairs of chromosomes, to form new chromosomes, each with a new combination of the genes of the parents. Then the chromosomes are separated into single sets in the gametes. When gametes fuse during fertilization, the resulting zygote has half of the genetic material of the mother and half of the father.[13] The combination of chromosomal crossover and fertilization, bringing the two single sets of chromosomes together to make a new diploid zygote, results in a new organism that contains a different set of the genetic traits of each parent.

In animals, the haploid stage only occurs in the gametes, the sex cells that fuse to form a zygote that develops directly into a new diploid organism. In a plant species, the diploid organism produces a type of haploid spore by meiosis that is capable of undergoing repeated cell division to produce a multicellular haploid organism. In either case, the gametes may be externally similar (isogamy) as in the green alga Ulva or may be different in size and other aspects (anisogamy).[14] The size difference is greatest in oogamy, a type of anisogamy in which a small, motile gamete combines with a much larger, non-motile gamete.[15]

In anisogamic organisms, by convention, the larger gamete (called an ovum, or egg cell) is considered female, while the smaller gamete (called a spermatozoon, or sperm cell) is considered male. An individual that produces large gametes is female, and one that produces small gametes is male.[16] An individual that produces both types of gamete is a hermaphrodite. In some species, a hermaphrodite can self-fertilize and produce an offspring on its own.

Animals

Main article: Sexual reproduction § Animals
Simosyrphus grandicornis mating

Most sexually reproducing animals spend their lives as diploid, with the haploid stage reduced to single-cell gametes.[17] The gametes of animals have male and female forms—spermatozoa and egg cells, respectively. These gametes combine to form embryos which develop into new organisms.

The male gamete, a spermatozoon (produced in vertebrates within the testes), is a small cell containing a single long flagellum which propels it.[18] Spermatozoa are extremely reduced cells, lacking many cellular components that would be necessary for embryonic development. They are specialized for motility, seeking out an egg cell and fusing with it in a process called fertilization.

Female gametes are egg cells. In vertebrates, they are produced within the ovaries. They are large, immobile cells that contain the nutrients and cellular components necessary for a developing embryo.[19] Egg cells are often associated with other cells which support the development of the embryo, forming an egg. In mammals, the fertilized embryo instead develops within the female, receiving nutrition directly from its mother.

Animals are usually mobile and seek out a partner of the opposite sex for mating. Animals which live in the water can mate using external fertilization, where the eggs and sperm are released into and combine within the surrounding water.[20] Most animals that live outside of water, however, use internal fertilization, transferring sperm directly into the female to prevent the gametes from drying up.

In most birds, both excretion and reproduction are done through a single posterior opening, called the cloaca—male and female birds touch cloaca to transfer sperm, a process called "cloacal kissing".[21] In many other terrestrial animals, males use specialized sex organs to assist the transport of sperm—these male sex organs are called intromittent organs. In humans and other mammals, this male organ is known as the penis, which enters the female reproductive tract (called the vagina) to achieve insemination—a process called sexual intercourse. The penis contains a tube through which semen (a fluid containing sperm) travels. In female mammals, the vagina connects with the uterus, an organ which directly supports the development of a fertilized embryo within (a process called gestation).

Because of their motility, animal sexual behavior can involve coercive sex. Traumatic insemination, for example, is used by some insect species to inseminate females through a wound in the abdominal cavity—a process detrimental to the female's health.

Plants

Main article: Plant reproduction
Flowers contain the sexual organs of flowering plants. They are usually hermaphrodite, containing both male and female parts.

Like animals, land plants have specialized male and female gametes.[22][23] In seed plants, male gametes are produced by reduced male gametophytes that are contained within pollen which have hard coats that protect the male gamete forming cells during transport from the anthers to the stigma. The female gametes of seed plants are contained within ovules. Once fertilized, these form seeds which, like eggs, contain the nutrients necessary for the initial development of the embryonic plant.

Female (left) and male (right) cones contain the sex organs of pines and other conifers.

The flowers of flowering plants contain their sexual organs. Most flowering plants are hermaphroditic, with both male and female parts in the same flower or on the same plant in single sex flowers, about 5% of plant species have individual plants that are one sex or the other.[24] The female parts, in the center of a hermaphroditic or female flower, are the pistils, each unit consisting of a carpel, a style and a stigma. Two or more of these reproductive units may be merged to form a single compound pistil, the fused carpels forming an ovary. Within the carpels are ovules which develop into seeds after fertilization. The male parts of the flower are the stamens: these consist of long filaments arranged between the pistil and the petals that produce pollen in anthers at their tips. When a pollen grain lands upon the stigma on top of a carpel's style, it germinates to produce a pollen tube that grows down through the tissues of the style into the carpel, where it delivers male gamete nuclei to fertilize an ovule that eventually develops into a seed.

Some hermaphroditic plants are self-fertile, but plants have evolved multiple different self-incompatibility mechanisms to avoid self-fertilization, involving sequential hermaphroditism, molecular recognition systems and morphological mechanisms such as heterostyly.[25]: 73, 74 

In pines and other conifers, the sex organs are produced within cones that have male and female forms. Male cones are smaller than female ones and produce pollen, which is transported by wind to land in female cones. The larger and longer-lived female cones are typically more durable, and contain ovules within them that develop into seeds after fertilization.

Because seed plants are immobile, they depend upon passive methods for transporting pollen grains to other plants. Many, including conifers and grasses, produce lightweight pollen which is carried by wind to neighboring plants. Some flowering plants have heavier, sticky pollen that is specialized for transportation by insects or larger animals such as hummingbirds and bats, which may be attracted to flowers containing rewards of nectar and pollen. These animals transport the pollen as they move to other flowers, which also contain female reproductive organs, resulting in pollination.

Fungi

Main article: Mating in fungi
Mushrooms are produced as part of fungal sexual reproduction.

Most species of fungus can reproduce sexually and have life cycles with both haploid and diploid phases. These species of fungus are typically isogamous, i.e. lacking male and female specialization. One haploid fungus grows into contact with another, and then they fuse their cells. In some cases, the fusion is asymmetric, and the cell which donates only a nucleus (and no accompanying cellular material) could arguably be considered male.[26] Fungi may also have more complex allelic mating systems, with other sexes not accurately described as male, female, or hermaphroditic.[27]

Some fungi, including baker's yeast, have mating types that determine compatibility. Yeasts with the same mating types will not fuse with each other to form diploid cells, only with yeast carrying another mating type.[28]

Many species of higher fungi produce mushrooms as part of their sexual reproduction. Within the mushroom, diploid cells are formed, later dividing into haploid spores.

Sexual systems

Main article: Sexual system

A sexual system is a distribution of male and female functions across organisms in a species.[29]

Animals

Approximately 95% of animal species have separate male and female individuals, and are said to be gonochoric. About 5% of animal species are hermaphroditic.[29] This low percentage is partially attributable to the very large number of insect species, in which hermaphroditism is absent.[30] About 99% of vertebrates are gonochoric, and the remaining 1% that are hermaphroditic are almost all fishes.[31]

Plants

The majority of plants are bisexual,[32]: 212  either hermaphrodite (with both stamens and pistil in the same flower) or monoecious.[33][34] In dioecious species male and female sexes are on separate plants.[35] About 5% of flowering plants are dioecious, resulting from as many as 5000 independent origins.[36] Dioecy is common in gymnosperms, in which about 65% of species are dioecious, but most conifers are monoecious.[37]

Evolution of sex

Main article: Evolution of sexual reproduction
Different forms of anisogamy:
A) anisogamy of motile cells, B) oogamy (egg cell and sperm cell), C) anisogamy of non-motile cells (egg cell and spermatia).
Different forms of isogamy:
A) isogamy of motile cells, B) isogamy of non-motile cells, C) conjugation.

It is generally accepted that isogamy was ancestral to anisogamy[38] and that anisogamy evolved several times independently in different groups of eukaryotes, including protists, algae, plants, and animals.[30] The evolution of anisogamy is synonymous with the origin of male and the origin of female.[39] It is also the first step towards sexual dimorphism[40] and influenced the evolution of various sex differences.[41]

It is unclear whether anisogamy first led to the evolution of hermaphroditism or the evolution of gonochorism,[32]: 213  and the evolution of sperm and eggs has left no fossil evidence.[42]

A 1.2 billion year old fossil from Bangiomorpha pubescens has provided the oldest fossil record for the differentiation of male and female reproductive types and shown that sexes evolved early in eukaryotes.[43] Studies on green algae have provided genetic evidence for the evolutionary link between sexes and mating types.[44]

The original form of sex was external fertilization. Internal fertilization, or sex as we know it, evolved later[45] and became dominant for vertebrates after their emergence on land.[46]

Adaptive function of sex

The most basic role of meiosis appears to be conservation of the integrity of the genome that is passed on to progeny by parents.[47][48] The two most fundamental aspects of sexual reproduction, meiotic recombination and outcrossing, are likely maintained respectively by the adaptive advantages of recombinational repair of genomic DNA damage and genetic complementation which masks the expression of deleterious recessive mutations.[49] Genetic variation, often produced as a byproduct of these processes, may provide long-term advantages in those sexual lineages that favor outcrossing.[49]

Sex-determination systems

Main article: Sex-determination system
Sex helps the spread of advantageous traits through recombination. The diagrams compare the evolution of allele frequency in a sexual population (top) and an asexual population (bottom). The vertical axis shows frequency and the horizontal axis shows time. The alleles a/A and b/B occur at random. The advantageous alleles A and B, arising independently, can be rapidly combined by sexual reproduction into the most advantageous combination AB. Asexual reproduction takes longer to achieve this combination because it can only produce AB if A arises in an individual which already has B or vice versa.

The biological cause of an organism developing into one sex or the other is called sex determination. The cause may be genetic, environmental, haplodiploidy, or multiple factors.[30] Within animals and other organisms that have genetic sex-determination systems, the determining factor may be the presence of a sex chromosome. In plants that are sexually dimorphic, such as Ginkgo biloba,[25]: 203  the liverwort Marchantia polymorpha or the dioecious species in the flowering plant genus Silene, sex may also be determined by sex chromosomes.[50] Non-genetic systems may use environmental cues, such as the temperature during early development in crocodiles, to determine the sex of the offspring.[51]

Sex determination is often distinct from sex differentiation. Sex determination is the designation for the development stage towards either male or female while sex differentiation is the pathway towards the development of the phenotype.[52]

Genetic

XY sex determination

The common fruit fly has an XY sex-determination system, as do humans and most mammals.

Humans and most other mammals have an XY sex-determination system: the Y chromosome carries factors responsible for triggering male development, making XY sex determination mostly based on the presence or absence of the Y chromosome. It is the male gamete that determines the sex of the offspring.[53] In this system XX mammals typically are female and XY typically are male.[30] However, individuals with XXY or XYY are males, while individuals with X and XXX are females.[9] Unusually, the platypus, a monotreme mammal, has ten sex chromosomes; females have ten X chromosomes, and males have five X chromosomes and five Y chromosomes. Platypus egg cells all have five X chromosomes, whereas sperm cells can either have five X chromosomes or five Y chromosomes.[54]

XY sex determination is found in other organisms, including insects like the common fruit fly,[55] and some plants.[56] In some cases, it is the number of X chromosomes that determines sex rather than the presence of a Y chromosome.[9] In the fruit fly individuals with XY are male and individuals with XX are female; however, individuals with XXY or XXX can also be female, and individuals with X can be males.[57]

ZW sex determination

In birds, which have a ZW sex-determination system, the W chromosome carries factors responsible for female development, and default development is male.[58] In this case, ZZ individuals are male and ZW are female. It is the female gamete that determines the sex of the offspring. This system is used by birds, some fish, and some crustaceans.[9]

The majority of butterflies and moths also have a ZW sex-determination system. Females can have Z, ZZW, and even ZZWW.[59]

XO sex determination

In the XO sex-determination system, males have one X chromosome (XO) while females have two (XX). All other chromosomes in these diploid organisms are paired, but organisms may inherit one or two X chromosomes. This system is found in most arachnids, insects such as silverfish (Apterygota), dragonflies (Paleoptera) and grasshoppers (Exopterygota), and some nematodes, crustaceans, and gastropods.[60][61]

In field crickets, for example, insects with a single X chromosome develop as male, while those with two develop as female.[62]

In the nematode Caenorhabditis elegans, most worms are self-fertilizing hermaphrodites with an XX karyotype, but occasional abnormalities in chromosome inheritance can give rise to individuals with only one X chromosome—these XO individuals are fertile males (and half their offspring are male).[63]

ZO sex determination

In the ZO sex-determination system, males have two Z chromosomes whereas females have one. This system is found in several species of moths.[64]

Environmental

Main article: Environmental sex determination

For many species, sex is not determined by inherited traits, but instead by environmental factors such as temperature experienced during development or later in life.[65]

In the fern Ceratopteris and other homosporous fern species, the default sex is hermaphrodite, but individuals which grow in soil that has previously supported hermaphrodites are influenced by the pheromone antheridiogen to develop as male.[50] The bonelliidae larvae can only develop as males when they encounter a female.[30]

Sequential hermaphroditism

Clownfishes are initially male; the largest fish in a group becomes female.

Some species can change sex over the course of their lifespan, a phenomenon called sequential hermaphroditism.[66]

Teleost fishes are the only vertebrate lineage where sequential hermaphroditism occurs. In clownfish, smaller fish are male, and the dominant and largest fish in a group becomes female; when a dominant female is absent, then her partner changes sex from male to female. In many wrasses the opposite is true: the fish are initially female and become male when they reach a certain size.[67]

Sequential hermaphroditism also occurs in plants such as Arisaema triphyllum.

Temperature-dependent sex determination

pile of eggs in the sand, with a newly hatched crocodile looking over the top
Crocodiles do not have sex chromosomes.[68] Instead, whether these eggs will produce male or female crocodiles depends on the temperature of the eggs.

Many reptiles, including all crocodiles and most turtles, have temperature-dependent sex determination. In these species, the temperature experienced by the embryos during their development determines their sex.[30]

In some turtles, for example, males are produced at lower temperatures than females; but Macroclemys females are produced at temperatures lower than 22 °C or above 28 °C, while males are produced in between those temperatures.[69]

Haplodiploidy

Certain insects, such as honey bees and ants, use a haplodiploid sex-determination system.[70] Diploid bees and ants are generally female, and haploid individuals (which develop from unfertilized eggs) are male. This sex-determination system results in highly biased sex ratios, as the sex of offspring is determined by fertilization (arrhenotoky or pseudo-arrhenotoky resulting in males) rather than the assortment of chromosomes during meiosis.[71]

Sex ratio

This section is an excerpt from Sex ratio.[edit]

A sex ratio is the ratio of males to females in a population. As explained by Fisher's principle, for evolutionary reasons this is typically about 1:1 in species which reproduce sexually.[72][73] However, many species deviate from an even sex ratio, either periodically or permanently. Examples include parthenogenic and androgenetic[74] species, periodically mating organisms such as aphids, some eusocial wasps, bees, ants, and termites.[75]

The human sex ratio is of particular interest to anthropologists and demographers. In human societies, sex ratios at birth may be considerably skewed by factors such as the age of mother at birth[76] and by sex-selective abortion and infanticide. Exposure to pesticides and other environmental contaminants may be a significant contributing factor as well.[77] As of 2024, the global sex ratio at birth is estimated at 107 boys to 100 girls (1,000 boys per 934 girls).[78] By old age, the sex ratio reverses, with 81 older men for every 100 older women; across all ages, the global population is nearly balanced, with 101 males for every 100 females.[78]

Sex differences

See also: Sex differences in medicine, Sex differences in intelligence, Neuroscience of sex differences, and Sex differences in human physiology

Anisogamy is the fundamental difference between male and female.[79][80] Richard Dawkins has stated that it is possible to interpret all the differences between the sexes as stemming from this.[81]

Sexual characteristics

This section is an excerpt from Sexual characteristics.[edit]
Sexual characteristics are physical traits of an organism (typically of a sexually dimorphic organism) which are indicative of or resultant from biological sexual factors. These include both primary sex characteristics, such as gonads, and secondary sex characteristics.

Sexual dimorphism

Main article: Sexual dimorphism
Common pheasants are sexually dimorphic in both size and appearance.
The common hill myna is sexually monomorphic, meaning that the external appearance of males and females is very similar.[82]

In many animals and some plants, individuals of male and female sex differ in size and appearance, a phenomenon called sexual dimorphism.[83] Sexual dimorphism in animals is often associated with sexual selection: the mating competition between individuals of one sex vis-à-vis the opposite sex.[84] Other examples demonstrate that it is the preference of females that drives sexual dimorphism, such as in the case of the stalk-eyed fly.[85]

Sex differences in humans include a generally larger size and more body hair in men, while women have larger breasts, wider hips, and a higher body fat percentage. In other species, there may be differences in coloration or other features, and may be so pronounced that the different sexes may be mistaken for two entirely different taxa.[84]

Females are the larger sex in a majority of animals.[83] For instance, female southern black widow spiders are typically twice as long as the males.[86] This size disparity may be associated with the cost of producing egg cells, which requires more nutrition than producing sperm: larger females are able to produce more eggs.[87][83] In many other cases, the male of a species is larger than the female. Mammal species with extreme sexual size dimorphism, such as elephant seals, tend to have highly polygynous mating systems, presumably due to selection for success in competition with other males.

Sexual dimorphism can be extreme, with males, such as some anglerfish, living parasitically on the female. Some plant species also exhibit dimorphism in which the females are significantly larger than the males, such as in the moss genus Dicranum[88] and the liverwort genus Sphaerocarpos.[89] There is some evidence that, in these genera, the dimorphism may be tied to a sex chromosome,[89][90] or to chemical signaling from females.[91]

In birds, males often have a more colorful appearance and may have features (like the long tail of male peacocks) that would seem to put them at a disadvantage (e.g. bright colors would seem to make a bird more visible to predators). One proposed explanation for this is the handicap principle.[92] This hypothesis argues that, by demonstrating he can survive with such handicaps, the male is advertising his genetic fitness to females—traits that will benefit daughters as well, who will not be encumbered with such handicaps.

Sex differences in behavior

See also: Sex differences in psychology, Animal sexual behaviour, Non-reproductive sexual behavior in animals, and Sex differences in cognition

The sexes across gonochoric species usually differ in behavior. In most animal species, females invest more in parental care,[93] although in some species, such as some coucals, the males invest more parental care.[94] Females also tend to be more choosy for who they mate with,[95] such as most bird species.[96] Males tend to be more competitive for mating than females.[39]

Distinction from gender

This section is an excerpt from Sex–gender distinction.[edit]
While in ordinary speech, the terms sex and gender are often used interchangeably, in contemporary academic literature, the terms often have distinct meanings, especially when referring to people.[97][98] Sex generally refers to an organism's biological sex, while gender usually refers to either social roles typically associated with the sex of a person (gender role) or personal identification of one's own gender based on their own personal sense of it (gender identity).[99][100][101][102] Most contemporary social scientists,[103][104][105] behavioral scientists and biologists,[106][107] many legal systems and government bodies and intergovernmental agencies such as the WHO make a distinction between gender and sex.[108][109]

See also

References

  1. ^ Stevenson A, Waite M (2011). "Sex". Concise Oxford English Dictionary: Book & CD-ROM Set. OUP Oxford. p. 1302. ISBN 978-0-19-960110-3. Retrieved 23 March 2018. Sex: Either of the two main categories (male and female) into which humans and most other living things are divided on the basis of their reproductive functions. The fact of belonging to one of these categories. The group of all members of either sex.
  2. ^ Mills A (1 January 2018). "Sex and Reproduction". Biology of Sex. University of Toronto Press. pp. 43–45. ISBN 978-1-4875-9337-7. Retrieved 3 October 2023.
  3. ^ a b Purves WK, Sadava DE, Orians GH, Heller HC (2000). Life: The Science of Biology. Macmillan. p. 736. ISBN 978-0-7167-3873-2. Retrieved 23 March 2018. A single body can function as both male and female. Sexual reproduction requires both male and female haploid gametes. In most species, these gametes are produced by individuals that are either male or female. Species that have male and female members are called dioecious (from the Greek for 'two houses'). In some species, a single individual may possess both female and male reproductive systems. Such species are called monoecious ("one house") or hermaphroditic.
  4. ^ De Loof A (31 January 2018). "Only two sex forms but multiple gender variants: How to explain?". Communicative & Integrative Biology. 11 (1): e1427399. doi:10.1080/19420889.2018.1427399. ISSN 1942-0889. PMC 5824932. PMID 29497472.
  5. ^ Goymann W, Brumm H, Kappeler PM (February 2023). "Biological sex is binary, even though there is a rainbow of sex roles: Denying biological sex is anthropocentric and promotes species chauvinism". BioEssays. 45 (2). doi:10.1002/bies.202200173. PMID 36543364. Retrieved 23 November 2024.
  6. ^ Kokko H, Jennions M (2012). "Sex differences in parental care". In Royle NJ, Smiseth PT, Kölliker M (eds.). The Evolution of Parental Care. Oxford University Press. p. 103. ISBN 978-0-19-969257-6. The answer is that there is an agreement by convention: individuals producing the smaller of the two gamete types – sperm or pollen – are males, and those producing larger gametes – eggs or ovules – are females.
  7. ^ Avise JC (2011). "Two sexes in one". Hermaphroditism: A Primer on the Biology, Ecology, and Evolution of Dual Sexuality. Columbia University Press. pp. 1–7. ISBN 978-0-231-52715-6. Retrieved 18 September 2020.
  8. ^ Blackmon H, Ross L, Bachtrog D (January 2017). "Sex Determination, Sex Chromosomes, and Karyotype Evolution in Insects". The Journal of Heredity. 108 (1): 78–93. doi:10.1093/jhered/esw047. ISSN 0022-1503. PMC 6281344. PMID 27543823.
  9. ^ a b c d Hake L, O'Connor C (2008). "Genetic Mechanisms of Sex Determination | Learn Science at Scitable". Nature Education. 1 (1): 25. Archived from the original on 19 August 2017. Retrieved 13 April 2021.
  10. ^ Moore D, Robson JD, Trinci AP (2020). 21st Century guidebook to fungi (2 ed.). Cambridge University Press. pp. 211–228. ISBN 978-1-108-74568-0.
  11. ^ Kumar R, Meena M, Swapnil P (2019). "Anisogamy". In Vonk J, Shackelford T (eds.). Encyclopedia of Animal Cognition and Behavior. Cham: Springer International Publishing. pp. 1–5. doi:10.1007/978-3-319-47829-6_340-1. ISBN 978-3-319-47829-6. Anisogamy can be defined as a mode of sexual reproduction in which fusing gametes, formed by participating parents, are dissimilar in size.
  12. ^ Alberts B, Johnson A, Lewis J, Raff M, Roberts K, Walter P (2002). "Meiosis". Molecular Biology of the Cell (4th ed.). New York: Garland Science. ISBN 978-0-8153-3218-3. Archived from the original on 25 January 2017.
  13. ^ Alberts B, Johnson A, Lewis J, Raff M, Roberts K, Walter P (2002). "The Benefits of Sex". Molecular Biology of the Cell (4th ed.). New York: Garland Science. ISBN 978-0-8153-3218-3.
  14. ^ Gilbert SF (2000). "Multicellularity: Evolution of Differentiation". Developmental Biology (6th ed.). Sunderland (MA): Sinauer Associates. ISBN 978-0-87893-243-6. Archived from the original on 8 March 2021. Retrieved 17 April 2021.
  15. ^ Allaby M (2012). A Dictionary of Plant Sciences. OUP Oxford. p. 350. ISBN 978-0-19-960057-1.
  16. ^ Gee H (22 November 1999). "Size and the single sex cell". Nature. Archived from the original on 11 October 2017. Retrieved 4 June 2018.
  17. ^ Alberts B, Johnson A, Lewis J, Raff M, Roberts K, Walter P (2002). "Mendelian genetics in eukaryotic life cycles". Molecular Biology of the Cell (4th ed.). New York: Garland Science. ISBN 978-0-8153-3218-3. Archived from the original on 2 April 2017.
  18. ^ Alberts B, Johnson A, Lewis J, Raff M, Roberts K, Walter P (2002). "Sperm". Molecular Biology of the Cell (4th ed.). New York: Garland Science. ISBN 978-0-8153-3218-3. Archived from the original on 29 June 2009.
  19. ^ Alberts B, Johnson A, Lewis J, Raff M, Roberts K, Walter P (2002). "Eggs". Molecular Biology of the Cell (4th ed.). New York: Garland Science. ISBN 978-0-8153-3218-3. Archived from the original on 29 June 2009.
  20. ^ Alberts B, Johnson A, Lewis J, Raff M, Roberts K, Walter P (2002). "Fertilization". Molecular Biology of the Cell (4th ed.). New York: Garland Science. ISBN 978-0-8153-3218-3. Archived from the original on 19 December 2008.
  21. ^ Ritchison G. "Avian Reproduction". Eastern Kentucky University. Archived from the original on 12 April 2008. Retrieved 3 April 2008.
  22. ^ Gilbert SF (2000). "Gamete Production in Angiosperms". Developmental Biology (6th ed.). Sunderland (MA): Sinauer Associates. ISBN 978-0-87893-243-6. Archived from the original on 21 April 2021. Retrieved 17 April 2021.
  23. ^ Dusenbery DB (2009). Living at Micro Scale: The Unexpected Physics of Being Small. Harvard University Press. pp. 308–326. ISBN 978-0-674-03116-6.
  24. ^ Wilton P (12 March 2009). "Plants, sex & Darwin". OxSciBlog. University of Oxford. Retrieved 10 January 2024.
  25. ^ a b Judd WS, Campbell CS, Kellogg EA, Stevens PF, Donoghue MJ (2002). Plant systematics, a phylogenetic approach (2nd ed.). Sunderland MA: Sinauer Associates Inc. ISBN 0-87893-403-0.
  26. ^ Nick Lane (2005). Power, Sex, Suicide: Mitochondria and the Meaning of Life. Oxford University Press. pp. 236–237. ISBN 978-0-19-280481-5.
  27. ^ Watkinson SC, Boddy L, Money N (2015). The Fungi. Elsevier Science. p. 115. ISBN 978-0-12-382035-8. Retrieved 18 February 2018.
  28. ^ Lodish H, Berk A, Zipursky SL, Matsudaira P, Baltimore D, Darnell J (2000). "Cell-Type Specification and Mating-Type Conversion in Yeast". Molecular Cell Biology (Fourth ed.). W.H. Freeman and Co. ISBN 978-0-7167-4366-8. Archived from the original on 1 July 2009.
  29. ^ a b Leonard JL (22 August 2013). "Williams' Paradox and the Role of Phenotypic Plasticity in Sexual Systems". Integrative and Comparative Biology. 53 (4): 671–688. doi:10.1093/icb/ict088. ISSN 1540-7063. PMID 23970358.
  30. ^ a b c d e f Bachtrog D, Mank JE, Peichel CL, Kirkpatrick M, Otto SP, Ashman TL, et al. (July 2014). "Sex determination: why so many ways of doing it?". PLOS Biology. 12 (7): e1001899. doi:10.1371/journal.pbio.1001899. PMC 4077654. PMID 24983465.
  31. ^ Kuwamura T, Sunobe T, Sakai Y, Kadota T, Sawada K (1 July 2020). "Hermaphroditism in fishes: an annotated list of species, phylogeny, and mating system". Ichthyological Research. 67 (3): 341–360. Bibcode:2020IchtR..67..341K. doi:10.1007/s10228-020-00754-6. ISSN 1616-3915. S2CID 218527927.
  32. ^ a b Kliman RM (2016). Encyclopedia of Evolutionary Biology. Vol. 2. Academic Press. pp. 212–224. ISBN 978-0-12-800426-5. Archived from the original on 6 May 2021. Retrieved 14 April 2021.
  33. ^ Sabath N, Goldberg EE, Glick L, Einhorn M, Ashman TL, Ming R, et al. (February 2016). "Dioecy does not consistently accelerate or slow lineage diversification across multiple genera of angiosperms". The New Phytologist. 209 (3): 1290–1300. doi:10.1111/nph.13696. PMID 26467174.
  34. ^ Beentje H (2016). The Kew plant glossary (2 ed.). Royal Botanic Gardens, Kew: Kew Publishing. ISBN 978-1-84246-604-9.
  35. ^ Leite Montalvão AP, Kersten B, Fladung M, Müller NA (2021). "The Diversity and Dynamics of Sex Determination in Dioecious Plants". Frontiers in Plant Science. 11: 580488. doi:10.3389/fpls.2020.580488. PMC 7843427. PMID 33519840.
  36. ^ Renner SS (October 2014). "The relative and absolute frequencies of angiosperm sexual systems: dioecy, monoecy, gynodioecy, and an updated online database". American Journal of Botany. 101 (10): 1588–1596. doi:10.3732/ajb.1400196. PMID 25326608.
  37. ^ Walas Ł, Mandryk W, Thomas PA, Tyrała-Wierucka Ż, Iszkuło G (2018). "Sexual systems in gymnosperms: A review" (PDF). Basic and Applied Ecology. 31: 1–9. Bibcode:2018BApEc..31....1W. doi:10.1016/j.baae.2018.05.009. S2CID 90740232. Archived (PDF) from the original on 27 January 2022. Retrieved 7 June 2021.
  38. ^ Awasthi AK. Textbook of Algae. Vikas Publishing House. p. 363. ISBN 978-93-259-9022-7.
  39. ^ a b Lehtonen J, Kokko H, Parker GA (October 2016). "What do isogamous organisms teach us about sex and the two sexes?". Philosophical Transactions of the Royal Society of London. Series B, Biological Sciences. 371 (1706). doi:10.1098/rstb.2015.0532. PMC 5031617. PMID 27619696.
  40. ^ Togashi T, Bartelt JL, Yoshimura J, Tainaka K, Cox PA (August 2012). "Evolutionary trajectories explain the diversified evolution of isogamy and anisogamy in marine green algae". Proceedings of the National Academy of Sciences of the United States of America. 109 (34): 13692–13697. Bibcode:2012PNAS..10913692T. doi:10.1073/pnas.1203495109. PMC 3427103. PMID 22869736.
  41. ^ Székely T, Fairbairn DJ, Blanckenhorn WU (2007). Sex, Size and Gender Roles: Evolutionary Studies of Sexual Size Dimorphism. OUP Oxford. pp. 167–169, 176, 185. ISBN 978-0-19-920878-4.
  42. ^ Pitnick SS, Hosken DJ, Birkhead TR (2008). Sperm Biology: An Evolutionary Perspective. Academic Press. pp. 43–44. ISBN 978-0-08-091987-4.
  43. ^ Hörandl E, Hadacek F (August 2020). "Oxygen, life forms, and the evolution of sexes in multicellular eukaryotes". Heredity. 125 (1–2): 1–14. doi:10.1038/s41437-020-0317-9. PMC 7413252. PMID 32415185.
  44. ^ Sawada H, Inoue N, Iwano M, eds. (2014). Sexual Reproduction in Animals and Plants. Springer. pp. 215–227. doi:10.1007/978-4-431-54589-7. ISBN 978-4-431-54589-7.
  45. ^ Black R (19 October 2014). "Armored Fish Pioneered Sex As You Know It". Animals. National Geographic. Archived from the original on 2 March 2021. Retrieved 10 July 2023.
  46. ^ "43.2A: External and Internal Fertilization". Biology LibreTexts. 17 July 2018. Archived from the original on 24 May 2022. Retrieved 9 November 2020.
  47. ^ Brandeis M (May 2018). "New-age ideas about age-old sex: separating meiosis from mating could solve a century-old conundrum". Biological Reviews of the Cambridge Philosophical Society. 93 (2): 801–810. doi:10.1111/brv.12367. PMID 28913952.
  48. ^ Hörandl E (June 2024). "Apomixis and the paradox of sex in plants". Annals of Botany. 134 (1): 1–18. doi:10.1093/aob/mcae044. PMC 11161571. PMID 38497809.
  49. ^ a b Bernstein H, Byerly HC, Hopf FA, Michod RE (September 1985). "Genetic damage, mutation, and the evolution of sex". Science. 229 (4719). New York, N.Y.: 1277–81. Bibcode:1985Sci...229.1277B. doi:10.1126/science.3898363. PMID 3898363.
  50. ^ a b Tanurdzic M, Banks JA (2004). "Sex-determining mechanisms in land plants". The Plant Cell. 16 (Suppl): S61–S71. doi:10.1105/tpc.016667. PMC 2643385. PMID 15084718.
  51. ^ Warner DA, Shine R (January 2008). "The adaptive significance of temperature-dependent sex determination in a reptile". Nature. 451 (7178): 566–568. Bibcode:2008Natur.451..566W. doi:10.1038/nature06519. PMID 18204437. S2CID 967516.
  52. ^ Beukeboom LW, Perrin N (2014). The Evolution of Sex Determination. Oxford University Press. p. 16. ISBN 978-0-19-965714-8.
  53. ^ Wallis MC, Waters PD, Graves JA (October 2008). "Sex determination in mammals – before and after the evolution of SRY". Cellular and Molecular Life Sciences. 65 (20): 3182–95. doi:10.1007/s00018-008-8109-z. PMC 11131626. PMID 18581056. S2CID 31675679.
  54. ^ Pierce BA (2012). Genetics: a conceptual approach (4th ed.). New York: W.H. Freeman. pp. 73–74. ISBN 978-1-4292-3250-0. OCLC 703739906.
  55. ^ Kaiser VB, Bachtrog D (2010). "Evolution of sex chromosomes in insects". Annual Review of Genetics. 44: 91–112. doi:10.1146/annurev-genet-102209-163600. PMC 4105922. PMID 21047257.
  56. ^ Dellaporta SL, Calderon-Urrea A (October 1993). "Sex determination in flowering plants". The Plant Cell. 5 (10): 1241–1251. doi:10.1105/tpc.5.10.1241. JSTOR 3869777. PMC 160357. PMID 8281039.
  57. ^ Fusco G, Minelli A (2019). The Biology of Reproduction. Cambridge University Press. pp. 306–308. ISBN 978-1-108-49985-9.
  58. ^ Smith CA, Katz M, Sinclair AH (February 2003). "DMRT1 is upregulated in the gonads during female-to-male sex reversal in ZW chicken embryos". Biology of Reproduction. 68 (2): 560–570. doi:10.1095/biolreprod.102.007294. PMID 12533420.
  59. ^ Majerus ME (2003). Sex Wars: Genes, Bacteria, and Biased Sex Ratios. Princeton University Press. p. 59. ISBN 978-0-691-00981-0.
  60. ^ Bull JJ (1983). Evolution of sex determining mechanisms. Benjamin/Cummings Publishing Company, Advanced Book Program. p. 17. ISBN 0-8053-0400-2.
  61. ^ Thiriot-Quiévreux C (2003). "Advances in chromosomal studies of gastropod molluscs". Journal of Molluscan Studies. 69 (3): 187–202. doi:10.1093/mollus/69.3.187.
  62. ^ Yoshimura A (2005). "Karyotypes of two American field crickets: Gryllus rubens and Gryllus sp. (Orthoptera: Gryllidae)". Entomological Science. 8 (3): 219–222. doi:10.1111/j.1479-8298.2005.00118.x. S2CID 84908090.
  63. ^ Meyer BJ (1997). "Sex Determination and X Chromosome Dosage Compensation: Sexual Dimorphism". In Riddle DL, Blumenthal T, Meyer BJ, Priess JR (eds.). C. elegans II. Cold Spring Harbor Laboratory Press. ISBN 978-0-87969-532-3. Archived from the original on 6 May 2021. Retrieved 17 April 2021.
  64. ^ De Prins J, Saithoh K (2003). "Karyology and Sex Determination". In Kristensen N (ed.). Handbuch Der Zoologie / Handbook of Zoology. Vol. Arthropoda: Insecta: Lepidoptera, Moths and Butterflies. Walter de Gruyter. pp. 449–468. doi:10.1515/9783110893724.449. ISBN 978-3-11-016210-3. Retrieved 29 September 2020 – via Google Books.
  65. ^ Janzen FJ, Phillips PC (November 2006). "Exploring the evolution of environmental sex determination, especially in reptiles". Journal of Evolutionary Biology. 19 (6): 1775–1784. doi:10.1111/j.1420-9101.2006.01138.x. PMID 17040374.
  66. ^ Fusco G, Minelli A (2019). The Biology of Reproduction. Cambridge University Press. p. 124. ISBN 978-1-108-49985-9.
  67. ^ Todd EV, Liu H, Muncaster S, Gemmell NJ (2016). "Bending Genders: The Biology of Natural Sex Change in Fish". Sexual Development. 10 (5–6): 223–2241. doi:10.1159/000449297. hdl:10536/DRO/DU:30153787. PMID 27820936. S2CID 41652893.
  68. ^ González EJ, Martínez-López M, Morales-Garduza MA, García-Morales R, Charruau P, Gallardo-Cruz JA (September 2019). "The sex-determination pattern in crocodilians: A systematic review of three decades of research". The Journal of Animal Ecology. 88 (9): 1417–1427. Bibcode:2019JAnEc..88.1417G. doi:10.1111/1365-2656.13037. PMID 31286510.
  69. ^ Gilbert SF (2000). "Environmental Sex Determination". Developmental Biology. 6th Edition. Archived from the original on 12 June 2021. Retrieved 19 May 2021.
  70. ^ Charlesworth B (August 2003). "Sex determination in the honeybee". Cell. 114 (4): 397–398. doi:10.1016/S0092-8674(03)00610-X. PMID 12941267.
  71. ^ de la Filia A, Bain S, Ross L (June 2015). "Haplodiploidy and the reproductive ecology of Arthropods" (PDF). Current Opinion in Insect Science. 9: 36–43. Bibcode:2015COIS....9...36D. doi:10.1016/j.cois.2015.04.018. hdl:20.500.11820/b540f12f-846d-4a5a-9120-7b2c45615be6. PMID 32846706. S2CID 83988416. Archived (PDF) from the original on 25 June 2021. Retrieved 25 June 2021.
  72. ^ Fisher RA (1930). The Genetical Theory of Natural Selection. Oxford: Clarendon Press. pp. 141–143 – via Internet Archive.
  73. ^ Hamilton WD (April 1967). "Extraordinary sex ratios. A sex-ratio theory for sex linkage and inbreeding has new implications in cytogenetics and entomology". Science. 156 (3774): 477–488. Bibcode:1967Sci...156..477H. doi:10.1126/science.156.3774.477. JSTOR 1721222. PMID 6021675.
  74. ^ Schwander T, Oldroyd BP (28 September 2008). "Androgenesis: where males hijack eggs to clone themselves".
  75. ^ Kobayashi K, Hasegawa E, Yamamoto Y, Kawatsu K, Vargo EL, Yoshimura J, et al. (2013). "Sex ratio biases in termites provide evidence for kin selection". Nature Communications. 4: 2048. Bibcode:2013NatCo...4.2048K. doi:10.1038/ncomms3048. hdl:2123/11211. PMID 23807025.
  76. ^ "Trend Analysis of the sex Ratio at Birth in the United States" (PDF). U.S. Department of Health and Human Services, National Center for Health Statistics.
  77. ^ Davis DL, Gottlieb MB, Stampnitzky JR (April 1998). "Reduced ratio of male to female births in several industrial countries: a sentinel health indicator?". JAMA. 279 (13): 1018–1023. doi:10.1001/jama.279.13.1018. PMID 9533502.
  78. ^ a b "Field Listing—Sex ratio". CIA Factbook. The Central Intelligence Agency of the United States. Retrieved 18 April 2024. (2023 estimates)
  79. ^ Whitfield J (June 2004). "Everything you always wanted to know about sexes". PLOS Biology. 2 (6): e183. doi:10.1371/journal.pbio.0020183. PMC 423151. PMID 15208728. One thing biologists do agree on is that males and females count as different sexes. And they also agree that the main difference between the two is gamete size: males make lots of small gametes—sperm in animals, pollen in plants—and females produce a few big eggs.
  80. ^ Pierce BA (2012). Genetics: A Conceptual Approach. W.H. Freeman. p. 74. ISBN 978-1-4292-3252-4.
  81. ^ Dawkins R (2016). The Selfish Gene. Oxford University Press. pp. 183–184. ISBN 978-0-19-878860-7. However, there is one fundamental feature of the sexes which can be used to label males as males, and females as females, throughout animals and plants. This is that the sex cells or 'gametes' of males are much smaller and more numerous than the gametes of females. This is true whether we are dealing with animals or plants. One group of individuals has large sex cells, and it is convenient to use the word female for them. The other group, which it is convenient to call male, has small sex cells. The difference is especially pronounced in reptiles and in birds, where a single egg cell is big enough and nutritious enough to feed a developing baby for. Even in humans, where the egg is microscopic, it is still many times larger than the sperm. As we shall see, it is possible to interpret all the other differences between the sexes as stemming from this one basic difference.
  82. ^ Robin VV, Sinha A, Ramakrishnan U (2011). "Determining the sex of a monomorphic threatened, endemic passerine in the sky islands of southern India using molecular and morphometric methods". Current Science. 101 (5): 676–679. ISSN 0011-3891. JSTOR 24078632. Many species of birds are, however, monomorphic and difficult to sex visually, particularly in the field and some even in hand. Some examples are the Hill Mynah, Gracula religiosa and the Black-capped Chickadee, Parus atricapillus.
  83. ^ a b c Choe J (2019). "Body Size and Sexual Dimorphism". In Cox R (ed.). Encyclopedia of Animal Behavior. Vol. 2. Academic Press. pp. 7–11. ISBN 978-0-12-813252-4.
  84. ^ a b Mori E, Mazza G, Lovari S (2017). "Sexual Dimorphism". In Vonk J, Shackelford T (eds.). Encyclopedia of Animal Cognition and Behavior. Cham: Springer International Publishing. pp. 1–7. doi:10.1007/978-3-319-47829-6_433-1. ISBN 978-3-319-47829-6. Retrieved 5 June 2021.
  85. ^ Wilkinson GS, Reillo PR (22 January 1994). "Female choice response to artificial selection on an exaggerated male trait in a stalk-eyed fly" (PDF). Proceedings of the Royal Society B. 225 (1342): 1–6. Bibcode:1994RSPSB.255....1W. CiteSeerX 10.1.1.574.2822. doi:10.1098/rspb.1994.0001. S2CID 5769457. Archived from the original (PDF) on 10 September 2006.
  86. ^ Drees BM, Jackman J (1999). "Southern black widow spider". Field Guide to Texas Insects. Houston, Texas: Gulf Publishing Company. Archived from the original on 31 August 2003. Retrieved 8 August 2012 – via Extension Entomology, Insects.tamu.edu, Texas A&M University.
  87. ^ Stuart-Smith J, Swain R, Stuart-Smith R, Wapstra E (2007). "Is fecundity the ultimate cause of female-biased size dimorphism in a dragon lizard?". Journal of Zoology. 273 (3): 266–272. doi:10.1111/j.1469-7998.2007.00324.x.
  88. ^ Shaw AJ (2000). "Population ecology, population genetics, and microevolution". In Shaw AJ, Goffinet B (eds.). Bryophyte Biology. Cambridge: Cambridge University Press. pp. 379–380. ISBN 978-0-521-66097-6.
  89. ^ a b Schuster RM (1984). "Comparative Anatomy and Morphology of the Hepaticae". New Manual of Bryology. Vol. 2. Nichinan, Miyazaki, Japan: The Hattori botanical Laboratory. p. 891.
  90. ^ Crum HA, Anderson LE (1980). Mosses of Eastern North America. Vol. 1. New York: Columbia University Press. p. 196. ISBN 978-0-231-04516-2.
  91. ^ Briggs DA (1965). "Experimental taxonomy of some British species of genus Dicranum". New Phytologist. 64 (3): 366–386. doi:10.1111/j.1469-8137.1965.tb07546.x.
  92. ^ Zahavi A, Zahavi A (1997). The handicap principle: a missing piece of Darwin's puzzle. Oxford University Press. ISBN 978-0-19-510035-8.
  93. ^ Kliman R (2016). Herridge EJ, Murray RL, Gwynne DT, Bussiere L (eds.). Encyclopedia of Evolutionary Biology. Vol. 2. Academic Press. pp. 453–454. ISBN 978-0-12-800426-5.
  94. ^ Henshaw JM, Fromhage L, Jones AG (August 2019). "Sex roles and the evolution of parental care specialization". Proceedings. Biological Sciences. 286 (1909): 20191312. doi:10.1098/rspb.2019.1312. PMC 6732396. PMID 31455191.
  95. ^ Brennan P (2010). "Sexual Selection | Learn Science at Scitable". Nature Education Knowledge. 3 (10): 79. Archived from the original on 9 October 2021. Retrieved 25 July 2021.
  96. ^ Macedo RH, Manica LT (2019). "Sexual Selection and Mating Systems: Contributions from a Neotropical Passerine Model". In Reboreda JC, Fiorini VD, Tuero DT (eds.). Behavioral Ecology of Neotropical Birds. Springer. p. 75. ISBN 978-3-030-14280-3.
  97. ^ Udry JR (November 1994). "The Nature of Gender" (PDF). Demography. 31 (4): 561–573. doi:10.2307/2061790. JSTOR 2061790. PMID 7890091. Archived (PDF) from the original on 11 December 2016.
  98. ^ Haig D (April 2004). "The Inexorable Rise of Gender and the Decline of Sex: Social Change in Academic Titles, 1945–2001" (PDF). Archives of Sexual Behavior. 33 (2): 87–96. CiteSeerX 10.1.1.359.9143. doi:10.1023/B:ASEB.0000014323.56281.0d. PMID 15146141. S2CID 7005542. Archived from the original (PDF) on 25 May 2011.
  99. ^ Prince, Virginia. 2005. "Sex vs. Gender." International Journal of Transgenderism. 8(4).
  100. ^ Neil R., Carlson (2010). Psychology: The science of behavior. Fourth Canadian edition. Pearson. pp. 140–141. ISBN 978-0205702862.
  101. ^ "Gender and Genetics". WHO. Archived from the original on 11 November 2012. Retrieved 31 July 2020.
  102. ^ "Sex & Gender". Office of Research on Women's Health. Archived from the original on 23 July 2020. Retrieved 31 July 2020.
  103. ^ Kimmel MS (2017). The gendered society (Sixth ed.). New York: Oxford University Press. p. 3. ISBN 978-0-19-026031-6. OCLC 949553050.
  104. ^ "GENDER". Social Science Dictionary. Archived from the original on 2 February 2011. Retrieved 20 March 2015.
  105. ^ Lindsey, Linda L. (2010). "Ch. 1. The Sociology of gender" (PDF). Gender Roles: A Sociological Perspective. Pearson. ISBN 978-0-13-244830-7. Archived from the original (PDF) on 5 April 2015.
  106. ^ Kimmel 2017, p. 3.
  107. ^ Paludi MA (2008). The Psychology of Women at Work: Challenges and Solutions for Our Female Workforce. ABC-CLIO. p. 153. ISBN 978-0-275-99677-2. Archived from the original on 20 October 2021. Retrieved 6 September 2021.
  108. ^ O'Halloran K (2020). Sexual Orientation, Gender Identity and International Human Rights Law: Common Law Perspectives. London: Routledge, Taylor & Francis Group. pp. 22–28, 328–329. ISBN 978-0-429-44265-0. OCLC 1110674742.
  109. ^ "Gender: definitions". WHO/Europe. Archived from the original on 25 September 2021. Retrieved 22 August 2021.


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