Independent site, not affiliated with the journal Reproduction, its publishers or the Society for Reproduction and Fertility. About this site

Home › Research topics

Research topic

Comparative reproductive biology

Comparing how different animals reproduce shows which mechanisms are shared and which are local inventions. This overview introduces the main questions of comparative reproductive biology and where the evidence stands.

By the reproduction-online.org editorial team · Published 28 October 2026 · 4 min read

Comparative reproductive biology looks across species, from fish and birds to rodents, ruminants and primates, to understand which features of reproduction are ancient and widely shared and which have evolved separately in particular groups. The approach serves two purposes. It reveals general principles, such as the central role of the brain hormone GnRH, and it warns against assuming that results from one laboratory species apply automatically to others, including humans.

Many ways to make males and females

Because humans and many familiar animals have X and Y chromosomes, it is tempting to think that sex is determined the same way everywhere. In fact the mechanisms are remarkably diverse and can change quickly over evolutionary time. Almost all mammals and many flies have XY systems, in which males carry two different sex chromosomes; birds, snakes, butterflies and some fish have ZW systems, in which females do. In all crocodiles, most turtles and some fish, the temperature at which eggs develop decides sex. In ants, bees and wasps, males develop from unfertilised eggs, a system found in about 12 percent of animal species. Hermaphrodites, individuals with both male and female organs, are the rule in most flowering plants but make up only around 5 percent of animal species.

Despite this variety at the top of the cascade, some of the genes acting further down, which direct the developing gonad towards testis or ovary, are shared across distant groups. Why sex determination systems turn over so often is still debated; conflicts between the interests of different parts of the genome, or of the two sexes, are among the leading explanations, but few systems have been studied in enough depth to test them.

Two ways to trigger ovulation

GnRH controls reproduction in all vertebrates, but mammals use it in two distinct ways to trigger ovulation. In spontaneous ovulators, including rats, mice, guinea pigs, sheep, monkeys and women, rising oestrogen from maturing follicles provokes the surge of luteinising hormone that releases the egg. In induced ovulators, such as rabbits, ferrets, cats and camels, the surge is triggered by nerve signals generated during mating, which activate noradrenaline-producing neurons in the brainstem that in turn stimulate GnRH release. In these species, oestrogen acts in the brain to promote sexual behaviour, while its ability to trigger the surge on its own appears reduced or absent. The boundary is not absolute: mating-induced surges occasionally occur in spontaneous ovulators. Because most research on GnRH has used spontaneous ovulators, induced ovulators remain comparatively under-studied, and comparisons between the two groups are still refining models of how ovulation is controlled.

Model organisms and their limits

Comparative work also depends on choosing the right model. The zebrafish, a small tropical fish with almost transparent embryos, has become a popular species for studying vertebrate gene function. When its genome was sequenced, roughly 70 percent of human genes were found to have at least one obvious zebrafish counterpart, and the analysis also identified chromosome regions that influence sex determination in the fish. Such overlap makes fish useful for studying gonad development and fertility, but the remaining differences are a reminder that findings must be tested in other species before being generalised. Rodents, rabbits, ruminants and birds, all well represented in the archive, fill similar roles for other questions.

Stress and reproduction across species

Stress responses offer another example of a shared system with species-specific details. When an animal faces a challenge, its adrenal glands release glucocorticoid hormones such as cortisol or corticosterone. Elevated glucocorticoids can inhibit reproduction at several levels: they can reduce GnRH release from the hypothalamus, suppress the release of the pituitary hormones that drive the gonads, and act directly on the testis or ovary. Balanced glucocorticoid levels are needed for normal gonadal function, and exposure to stress or high glucocorticoid levels before birth can have lasting effects on the offspring’s own stress system. How these effects differ between species and between males and females remains an active comparative question.

Can mothers influence the sex of their offspring?

A long-running debate in evolutionary biology concerns whether mammalian mothers can bias the sex ratio of their offspring. A 1973 theory, known as the Trivers–Willard hypothesis, proposed that when mothers are in good condition, natural selection should favour producing sons, who can gain more from extra investment, and that mothers in poor condition should favour daughters. The original paper cited mammal data consistent with this idea.

Testing it has proved difficult. A 2023 analysis of five decades of records from wild baboons in Kenya, covering 1,372 offspring, found no support for adaptive biasing of offspring sex, and its authors noted that evidence for such hypotheses in mammals, especially primates, has been mixed. Whether and how mothers could adjust offspring sex around the time of conception is still an open question.

What is established and what is still debated

  • Established: sex determination mechanisms are diverse but share some downstream genes; mammals ovulate either spontaneously or in response to mating; stress hormones can suppress the reproductive axis; zebrafish share many genes with humans.
  • Still debated: why sex determination systems change so often; how induced ovulation is controlled at the molecular level; how far stress effects differ between species and sexes; and whether mammals adaptively adjust offspring sex ratios.

The archive collected under this topic is unusually broad. Alongside research on cell adhesion molecules, signalling pathways and the effects of plant extracts on fertility in rats, it includes society proceedings and obituaries of pioneers of reproductive endocrinology published in the 1960s, a reminder that the comparative approach has been part of the discipline since its early days. For a conservation perspective on the same diversity, see the wildlife reproduction and conservation page.

Sources

  1. Bachtrog D et al., PLoS Biology, 2014 — Sex determination: why so many ways of doing it?
  2. Bakker J, Baum MJ, Frontiers in Neuroendocrinology, 2000 — Neuroendocrine regulation of GnRH release in induced ovulators
  3. Howe K et al., Nature, 2013 — The zebrafish reference genome sequence and its relationship to the human genome
  4. Whirledge S, Cidlowski JA, Minerva Endocrinologica, 2010 — Glucocorticoids, stress, and fertility
  5. Trivers RL, Willard DE, Science, 1973 — Natural selection of parental ability to vary the sex ratio of offspring
  6. Zipple MN et al., The American Naturalist, 2023 — Five decades of data yield no support for adaptive biasing of offspring sex ratio in wild baboons (Papio cynocephalus)

References from the journal archive

These articles were published in Reproduction, the Journal of Reproduction and Fertility or Reviews of Reproduction and are still cited at their old addresses on this domain. Each link leads to the publisher’s version through its DOI.

  1. EFFECT OF m -XYLOHYDROQUINONE ON THE GENITAL ORGANS AND FERTILITY OF MALE RATS Journal of Reproduction and Fertility, 1963 · DOI 10.1530/jrf.0.0050077
  2. POL BOUIN 1870-1962 Journal of Reproduction and Fertility, 1963 · DOI 10.1530/jrf.0.0050301
  3. J. B. COLLIP 1893-1965 Journal of Reproduction and Fertility, 1966 · DOI 10.1530/jrf.0.0110167
  4. SELMAR ASCHHEIM 1878-1965 Journal of Reproduction and Fertility, 1966 · DOI 10.1530/jrf.0.0110165
  5. EFFECT OF CLOMIPHENE ON FERTILITY IN MALE RATS Journal of Reproduction and Fertility, 1967 · DOI 10.1530/jrf.0.0140039
  6. PROCEEDINGS OF THE INDIAN SOCIETY FOR THE STUDY OF REPRODUCTION Journal of Reproduction and Fertility, 1967 · DOI 10.1530/jrf.0.0140523
  7. ENDOCRINE STUDIES AT HIGH ALTITUDE Journal of Reproduction and Fertility, 1968 · DOI 10.1530/jrf.0.0160055
  8. THE REPRODUCTIVE ORGANS OF THE FEMALE PLAINS VISCACHA, LAGOSTOMUS MAXIMUS Journal of Reproduction and Fertility, 1971 · DOI 10.1530/jrf.0.0250365
  9. EFFECT OF CHROMATOGRAPHIC FRACTIONS OF DAUCUS CAROTA LINN. (SEEDS) ON FERTILITY IN FEMALE ALBINO RATS Journal of Reproduction and Fertility, 1972 · DOI 10.1530/jrf.0.0310143
  10. EFFECT OF CHROMATOGRAPHIC FRACTIONS OF POLYGONUM HYDROPIPER LINN. (ROOTS) ON FERTILITY IN FEMALE ALBINO RATS Journal of Reproduction and Fertility, 1972 · DOI 10.1530/jrf.0.0290421
  11. OBSERVATIONS ON REPRODUCTION IN THE MONGOLIAN GERBIL, MERIONES UNGUICULATUS Journal of Reproduction and Fertility, 1973 · DOI 10.1530/jrf.0.0330185
  12. ADAPTATIONS FOR URINARY MARKING IN RODENTS: PREPUCE LENGTH AND MORPHOLOGY Journal of Reproduction and Fertility, 1975 · DOI 10.1530/jrf.0.0440567
  13. EFFECT OF CHROMATOGRAPHIC FRACTIONS OF THE PLANT ACHYRANTHES ASPERA LINN. ON FERTILITY IN FEMALE ALBINO MICE Journal of Reproduction and Fertility, 1975 · DOI 10.1530/jrf.0.0430127
  14. The effects of ingested petroleum on oviposition and some aspects of reproduction in experimental colonies of mallard ducks (Anas platyrhynchos) Journal of Reproduction and Fertility, 1978 · DOI 10.1530/jrf.0.0540335
  15. The effect of the removal of the various accessory sex glands on the fertility of male rats Journal of Reproduction and Fertility, 1981 · DOI 10.1530/jrf.0.0620423
  16. The fertility of hypothyroid male mice Journal of Reproduction and Fertility, 1988 · DOI 10.1530/jrf.0.0830819
  17. Mating behaviour and insemination in the hopping mouse ( Notomys alexis ) Journal of Reproduction and Fertility, 1991 · DOI 10.1530/jrf.0.0930187
  18. Tdy -negative XY, XXY and XYY female mice: breeding data and synaptonemal complex analysis Journal of Reproduction and Fertility, 1993 · DOI 10.1530/jrf.0.0970151
  19. Sir Alan Parkes, CBE, ScD, FRS 1900–1990 Journal of Reproduction and Fertility, 1994 · DOI 10.1530/jrf.0.1000001
  20. Neoteny and the thyroid in ratites Reviews of Reproduction, 1996 · DOI 10.1530/ror.0.0010078
  21. Sodefrin: a novel sex pheromone in a newt Reviews of Reproduction, 1999 · DOI 10.1530/ror.0.0040001
  22. Cadherins: crucial regulators of structure and function in reproductive tissues Reviews of Reproduction, 2000 · DOI 10.1530/ror.0.0050053
  23. Effects of stress on reproduction in non-rodent mammals: the role of glucocorticoids and sex differences Reviews of Reproduction, 2000 · DOI 10.1530/ror.0.0050105
  24. Evolution of reproductive proteins from animals and plants Reproduction, 2006 · DOI 10.1530/rep.1.00357
  25. The effect of glycosaminoglycans on rat gametes in vitro and the associated signal pathway Reproduction, 2008 · DOI 10.1530/rep-07-0267
  26. Can mammalian mothers influence the sex of their offspring peri-conceptually? Reproduction, 2010 · DOI 10.1530/rep-10-0137
  27. Increase of fecundity by probiotic administration in zebrafish ( Danio rerio ) Reproduction, 2010 · DOI 10.1530/rep-10-0145
  28. The SLIT–ROBO pathway: a regulator of cell function with implications for the reproductive system Reproduction, 2010 · DOI 10.1530/rep-10-0017
  29. Apoptosis in the germ line Reproduction, 2011 · DOI 10.1530/rep-10-0232
  30. Many routes to the same destination: lessons from skeletal muscle development Reproduction, 2011 · DOI 10.1530/rep-10-0394
  31. Mixtures of endocrine-disrupting contaminants induce adverse developmental effects in preweaning rats Reproduction, 2014 · DOI 10.1530/rep-13-0447
  32. Role of pigment epithelium-derived factor in the reproductive system Reproduction, 2014 · DOI 10.1530/rep-14-0251
  33. Adverse effects of perinatal nicotine exposure on reproductive outcomes Reproduction, 2015 · DOI 10.1530/rep-15-0295
  34. Oncofertility: a grand collaboration between reproductive medicine and oncology Reproduction, 2015 · DOI 10.1530/rep-15-0163
  35. The role of non-coding RNAs in male sex determination and differentiation Reproduction, 2015 · DOI 10.1530/rep-15-0106