Animal sexual behaviour


Animal sexual behaviour takes many different forms, including within the same species. Common mating or reproductively motivated systems include monogamy, polygyny, polyandry, polygamy and promiscuity. Other sexual behaviour may be reproductively motivated or non-reproductively motivated.
When animal sexual behaviour is reproductively motivated, it is often termed mating or copulation; for most non-human mammals, mating and copulation occur at oestrus, which increases the chances of successful impregnation. Some animal sexual behaviour involves competition, sometimes fighting, between multiple males. Females often select males for mating only if they appear strong and able to protect themselves. The male that wins a fight may also have the chance to mate with a larger number of females and will therefore pass on his genes to their offspring.
Historically, it was believed that only humans and a small number of other species performed sexual acts other than for reproduction, and that animals' sexuality was instinctive and a simple "stimulus–response" behaviour. However, in addition to homosexual behaviours, a range of species masturbate and may use objects as tools to help them do so. Sexual behaviour may be tied more strongly to the establishment and maintenance of complex social bonds across a population which support its success in non-reproductive ways. Both reproductive and non-reproductive behaviours can be related to expressions of dominance over another animal or survival within a stressful situation.

Mating systems

In sociobiology and behavioural ecology, the term "mating system" is used to describe the ways in which animal societies are structured in relation to sexual behaviour. The mating system specifies which males mate with which females, and under what circumstances. There are four basic systems:

Monogamy

occurs when one male and one female mate exclusively with each other. A monogamous mating system is one in which individuals form long-lasting pairs and cooperate in raising offspring. These pairs may last for a lifetime, such as in pigeons, or it may occasionally change from one mating season to another, such as in emperor penguins. In contrast with tournament species, these pair-bonding species have lower levels of male aggression, competition and little sexual dimorphism. Zoologists and biologists now have evidence that monogamous pairs of animals are not always sexually exclusive. Many animals that form pairs to mate and raise offspring regularly engage in sexual activities with extra-pair partners. This includes previous examples, such as swans. Sometimes, these extra-pair sexual activities lead to offspring. Genetic tests frequently show that some of the offspring raised by a monogamous pair come from the female mating with an extra-pair male partner. These discoveries have led biologists to adopt new ways of talking about monogamy. According to Ulrich Reichard :
Whatever makes a pair of animals socially monogamous does not necessarily make them sexually or genetically monogamous. Social monogamy, sexual monogamy, and genetic monogamy can occur in different combinations.
Social monogamy is relatively rare in the animal kingdom. The actual incidence of social monogamy varies greatly across different branches of the evolutionary tree. Over 90% of avian species are socially monogamous. This stands in contrast to mammals. Only 3% of mammalian species are socially monogamous, although up to 15% of primate species are. Social monogamy has also been observed in reptiles, fish, and insects.
Sexual monogamy is also rare among animals. Many socially monogamous species engage in extra-pair copulations, making them sexually non-monogamous. For example, while over 90% of birds are socially monogamous, "on average, 30% or more of the baby birds in any nest sired by someone other than the resident male." Patricia Adair Gowaty has estimated that, out of 180 different species of socially monogamous songbirds, only 10% are sexually monogamous.
The incidence of genetic monogamy, determined by DNA fingerprinting, varies widely across species. For a few rare species, the incidence of genetic monogamy is 100%, with all offspring genetically related to the socially monogamous pair. But genetic monogamy is strikingly low in other species. Barash and Lipton note:
Such low levels of genetic monogamy have surprised biologists and zoologists, forcing them to rethink the role of social monogamy in evolution. They can no longer assume social monogamy determines how genes are distributed in a species. The lower the rates of genetic monogamy among socially monogamous pairs, the less of a role social monogamy plays in determining how genes are distributed among offspring.

Polygamy

The term polygamy is an umbrella term used to refer generally to non-monogamous matings. As such, polygamous relationships can be polygynous, polyandrous or polygynandrous. In a small number of species, individuals can display either polygamous or monogamous behaviour depending on environmental conditions. An example is the social wasp Apoica flavissima. In some species, polygyny and polyandry is displayed by both sexes in the population. Polygamy in both sexes has been observed in red flour beetle. Polygamy is also seen in many Lepidoptera species including Mythimna unipuncta.
A tournament species is one in which "mating tends to be highly polygamous and involves high levels of male-male aggression and competition." Tournament behaviour often correlates with high levels of sexual dimorphism, examples of species including chimpanzees and baboons. Most polygamous species present high levels of tournament behaviour, with a notable exception being bonobos.

Polygyny

occurs when one male gets exclusive mating rights with multiple females. In some species, notably those with harem-like structures, only one of a few males in a group of females will mate. Technically, polygyny in sociobiology and zoology is defined as a system in which a male has a relationship with more than one female, but the females are predominantly bonded to a single male. Should the active male be driven out, killed, or otherwise removed from the group, in a number of species the new male will ensure that breeding resources are not wasted on another male's young. The new male may achieve this in many different ways, including:
  • competitive infanticide: in lions, hippopotamuses, and some monkeys, the new male will kill the offspring of the previous alpha male to cause their mothers to become receptive to his sexual advances since they are no longer nursing. To prevent this, many female primates exhibit ovulation cues among all males, and show situation-dependent receptivity.
  • harassment to miscarriage: amongst wild horses and baboons, the male will continually attack pregnant females until they miscarry.
  • Pheromone-based spontaneous abortion
  • in some rodents such as mice, a new male with a different scent will cause females who are pregnant to spontaneously fail to implant recently fertilised eggs. This does not require contact; it is mediated by scent alone. It is known as the Bruce effect.
Von Haartman specifically described the mating behaviour of the European pied flycatcher as successive polygyny. Within this system, the males leave their home territory once their primary female lays her first egg. Males then create a second territory, presumably in order to attract a secondary female to breed. Even when they succeed at acquiring a second mate, the males typically return to the first female to exclusively provide for her and her offspring.
Polygynous mating structures are estimated to occur in up to 90% of mammal species. As polygyny is the most common form of polygamy among vertebrates, it has been studied far more extensively than polyandry or polygynandry.

Polyandry

occurs when one female gets exclusive mating rights with multiple males. In some species, such as redlip blennies, both polygyny and polyandry are observed.
The males in some deep sea anglerfishes are much smaller than the females. When they find a female they bite into her skin, releasing an enzyme that digests the skin of their mouths and her body and fusing the pair down to the blood-vessel level. The male then slowly atrophies, losing first his digestive organs, then his brain, heart, and eyes, ending as nothing more than a pair of gonads, which release sperm in response to hormones in the female's bloodstream indicating egg release. This extreme sexual dimorphism ensures that, when the female is ready to spawn, she has a mate immediately available. A single anglerfish female can "mate" with many males in this manner.

Polygynandry

occurs when multiple males mate indiscriminately with multiple females. The numbers of males and females need not be equal, and in vertebrate species studied so far, there are usually fewer males. Two examples of systems in primates are promiscuous mating chimpanzees and bonobos. These species live in social groups consisting of several males and several females. Each female copulates with many males, and vice versa. In bonobos, the amount of promiscuity is particularly striking because bonobos use sex to alleviate social conflict as well as to reproduce. This mutual promiscuity is the approach most commonly used by spawning animals, and is perhaps the "original fish mating system." Common examples are forage fish, such as herrings, which form huge mating shoals in shallow water. The water becomes milky with sperm and the bottom is draped with millions of fertilised eggs.

Parental investment and reproductive success

Female and male sexual behaviour differ in many species. Often, males are more active in initiating mating, and bear the more conspicuous sexual ornamentation like antlers and colourful plumage. This is a result of anisogamy, where sperm are smaller and much less costly to produce than eggs. This difference in physiological cost means that males are more limited by the number of mates they can secure, while females are limited by the quality of genes of her mates, a phenomenon known as Bateman's principle. Many females also have extra reproductive burdens in that parental care often falls mainly, or exclusively, on them. Thus, females are more limited in their potential reproductive success. In species where males take on more of the reproductive costs, such as sea horses and jacanas, the role is reversed, and the females are larger, more aggressive and more brightly coloured than the males.
In hermaphroditic animals, the costs of parental care can be evenly distributed between the sexes, e.g. earthworms. In some species of planarians, sexual behaviour takes the form of penis fencing. In this form of copulation, the individual that first penetrates the other with the penis, forces the other to be female, thus carrying the majority of the cost of reproduction. Post mating, banana slugs will some times gnaw off their partners penis as an act of sperm competition called apophallation. This is costly as they must heal, and spend more energy courting conspecifics that can act as male and female. A hypothesis suggests these slugs may be able to compensate the loss of the male function by directing energy that would have been put towards it to the female function. In the grey slug, the sharing of cost leads to a spectacular display, where the mates suspend themselves high above the ground from a slime thread, ensuring none of them can refrain from taking on the cost of egg-bearer.