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Sperm competition is the competitive process between spermatozoa of two or more different males to fertilize the same egg during sexual reproduction.
Competition can occur when females have multiple potential mating
partners. Greater choice and variety of mates increases a female's
chance to produce more viable offspring.
However, multiple mates for a female means each individual male has
decreased chances of producing offspring.
Sperm competition is an evolutionary pressure on males, and has led to
the development of adaptations to increase males' chance of reproductive success. Sperm competition results in a sexual conflict of interest between males and females. Males have evolved several defensive tactics including: mate-guarding, mating plugs, and releasing toxic seminal substances to reduce female re-mating tendencies to cope with sperm competition.
Offensive tactics of sperm competition involve direct interference by
one male on the reproductive success of another male, for instance by
physically removing another male's sperm prior to mating with a female. For an example, see Gryllus bimaculatus.
Sperm competition is often compared to having tickets in a raffle;
a male has a better chance of winning (i.e. fathering offspring) the
more tickets he has (i.e. the more sperm he inseminates a female with).
However, sperm are not free to produce,
and as such males are predicted to produce sperm of a size and number
that will maximize their success in sperm competition. By making many
spermatozoa, males can buy more "raffle tickets", and it is thought that
selection for numerous sperm has contributed to the evolution of anisogamy with very small sperm (because of the energy trade-off between sperm size and number). Alternatively, a male may evolve faster sperm to enable his sperm to reach and fertilize the female's ovum first. Dozens of adaptations have been documented in males that help them succeed in sperm competition.
Defensive adaptations
Mate-guarding
is a defensive behavioral trait that occurs in response to sperm
competition; males try to prevent other males from approaching the
female (and/or vice versa) thus preventing their mate from engaging in
further copulations.
Precopulatory and postcopulatory mate-guarding occurs in insects,
lizards, birds and primates. Mate-guarding also exists in the fish
species Neolamprologus pulcher,
as some males try to "sneak" matings with females in the territory of
other males. In these instances, the males guard their female by keeping
her in close enough proximity so that if an opponent male shows up in
his territory he will be able to fight off the rival male which will
prevent the female from engaging in extra-pair copulation with the rival male.
Organisms with polygynous mating systems are controlled by one
dominant male. In this type of mating system, the male is able to mate
with more than one female in a community. The dominant males will reign over the community until another suitor steps up and overthrows him.
The current dominant male will defend his title as the dominant male
and he will also be defending the females he mates with and the
offspring he sires. The elephant seal falls into this category since he
can participate in bloody violent matches in order to protect his
community and defend his title as the alpha male.
If the alpha male is somehow overthrown by the newcomer, his children
will most likely be killed and the new alpha male will start over with
the females in the group so that his lineage can be passed on.
Strategic mate-guarding occurs when the male only guards the
female during her fertile periods. This strategy can be more effective
because it may allow the male to engage in both extra-pair paternity and
within-pair paternity.
This is also because it is energetically efficient for the male to
guard his mate at this time. There is a lot of energy that is expended
when a male is guarding his mate. For instance, in polygynous
mate-guarding systems, the energetic costs of males is defending their
title as alpha male of their community.
Fighting is very costly in regards to the amount of energy used to
guard their mate. These bouts can happen more than once which takes a
toll on the physical well-being of the male. Another cost of
mate-guarding in this type of mating system is the potential increase of
the spread of disease.
If one male has an STD, he can pass that on to the females that he's
copulating with, potentially resulting in a depletion of the harem. This
would be an energetic cost towards both sexes for the reason that
instead of using the energy for reproduction, they are redirecting it
towards ridding themselves of this illness. Some females also benefit
from polygyny because extra pair copulations in females increase the
genetic diversity with the community of that species. This occurs because the male is not able to watch over all of the females and some will become promiscuous.
Eventually, the male will not have proper nutrition, which makes the male unable to produce sperm.
For instance, male amphipods will deplete their reserves of glycogen
and triglycerides only to have it replenished after the male is done
guarding that mate.
Also, if the amount of energy intake does not equal the energy
expended, then this could be potentially fatal to the male. Males may
even have to travel long distances during the breeding season in order
to find a female which absolutely drain their energy supply. Studies
were conducted to compare the cost of foraging of fish that migrate and
animals that are residential. The studies concluded that fish that were
residential had fuller stomachs containing higher quality of prey
compared to their migrant counterparts.
With all of these energy costs that go along with guarding a mate,
timing is crucial so that the male can use the minimal amount of energy.
This is why it is more efficient for males to choose a mate during
their fertile periods. Also, males will be more likely to guard their mate when there is a high density of males in the proximity.
Sometimes, organisms put in all this time and planning into courting a
mate in order to copulate and she may not even be interested. There is a
risk of cuckoldry of some sort, since a rival male can successfully
court the female that the male originally courting her could not do.
However, there are benefits that are associated with
mate-guarding. In a mating- guarding system, both parties, male and
female, are able to directly and indirectly benefit from this. For
instance, females can indirectly benefit from being protected by a mate.
The females can appreciate a decrease in predation and harassment from
other males while being able to observe her male counterpart.
This will allow her to recognize particular traits that she finds
ideal so that she'll be able to find another male that emulates those
qualities. In polygynous relationships, the dominant male of the
community benefits because he has the best fertilization success.
Communities can include 30 up to 100 females and, compared to the other
males, will greatly increase his chances of mating success.
Males who have successfully courted a potential mate will attempt
to keep them out of sight of other males before copulation. One way
organisms accomplish this is to move the female to a new location.
Certain butterflies, after enticing the female, will pick her up and fly
her away from the vicinity of potential males.
In other insects, the males will release a pheromone in order to make
their mate unattractive to other males or the pheromone masks her scent
completely. Certain crickets will participate in a loud courtship until the female accepts his gesture and then it suddenly becomes silent.
Some insects, prior to mating, will assume tandem positions to their
mate or position themselves in a way to prevent other males from
attempting to mate with that female.
The male checkerspot butterfly has developed a clever method in order
to attract and guard a mate. He will situate himself near an area that
possesses valuable resources that the female needs. He will then drive
away any males that come near and this will greatly increase his chances
of copulation with any female that comes to that area.
In post-copulatory mate-guarding males are trying to prevent
other males from mating with the female that they have mated with
already. For example, male millipedes in Costa Rica will ride on the
back of their mate letting the other males know that she's taken. Japanese beetles will assume a tandem position to the female after copulation.
This can last up to several hours allowing him to ward off any rival
males giving his sperm a high chance to fertilize that female's egg.
These, and other, types of methods have the male playing defense by
protecting his mate. Elephant seals are known to engage in bloody
battles in order to retain their title as dominant male so that they are
able to mate with all the females in their community.
Copulatory plugs are frequently observed in insects, reptiles, some mammals, and spiders.
Copulatory plugs are inserted immediately after a male copulates with a
female, which reduce the possibility of fertilization by subsequent
copulations from another male, by physically blocking the transfer of
sperm. Bumblebee mating plugs, in addition to providing a physical barrier to further copulations, contain linoleic acid, which reduces re-mating tendencies of females. A species of Sonoran desert Drosophila, Drosophila mettleri,
uses copulatory plugs to enable males to control the sperm reserve
space females have available. This behavior ensures males with higher
mating success at the expense of female control of sperm (sperm
selection).
Similarly, Drosophila melanogaster males release toxic seminal fluids, known as ACPs (accessory gland proteins), from their accessory glands to impede the female from participating in future copulations.
These substances act as an anti-aphrodisiac causing a dejection of
subsequent copulations, and also stimulate ovulation and oogenesis. Seminal proteins can have a strong influence on reproduction, sufficient to manipulate female behavior and physiology.
Another strategy, known as sperm partitioning, occurs when males
conserve their limited supply of sperm by reducing the quantity of sperm
ejected. In Drosophila,
ejaculation amount during sequential copulations is reduced; this
results in half filled female sperm reserves following a single
copulatory event, but allows the male to mate with a larger number of
females without exhausting his supply of sperm. To facilitate sperm partitioning, some males have developed complex ways to store and deliver their sperm. In the blue headed wrasse, Thalassoma bifasciatum,
the sperm duct is sectioned into several small chambers that are
surrounded by a muscle that allows the male to regulate how much sperm
is released in one copulatory event.
A strategy common among insects is for males to participate in
prolonged copulations. By engaging in prolonged copulations, a male has
an increased opportunity to place more sperm within the female's
reproductive tract and prevent the female from copulating with other
males.
It has been found that some male mollies (Poecilia)
have developed deceptive social cues to combat sperm competition.
Focal males will direct sexual attention toward typically non-preferred
females when an audience of other males is present. This encourages the
males that are watching to attempt to mate with the non-preferred
female. This is done in an attempt to decrease mating attempts with
the female that the focal male prefers, hence decreasing sperm
competition.
Offensive adaptations
Offensive
adaptation behavior differs from defensive behavior because it involves
an attempt to ruin the chances of another male's opportunity in
succeeding in copulation by engaging in an act that tries to terminate
the fertilization success of the previous male. This offensive behavior is facilitated by the presence of certain traits, which are called armaments. An example of an armament are antlers. Further, the presence of an offensive trait sometimes serves as a status signal. The mere display of an armament can suffice to drive away the competition without engaging in a fight, hence saving energy.
A male on the offensive side of mate-guarding may terminate the guarding
male's chances at a successful insemination by brawling with the
guarding male to gain access to the female. In Drosophila,
males release seminal fluids that contain additional toxins like
pheromones and modified enzymes that are secreted by their accessory
glands intended to destroy the sperm that have already made their way
into the female's reproductive tract from a recent copulation. However, this proved to be wrong because Drosophila melanogaster seminal fluid can actually protect the sperm of other males. Based on the "last male precedence"
idea, some males can remove sperm from previous males by ejaculating
new sperm into the female; hindering successful insemination
opportunities of the previous male.
Mate choice
The "good sperm hypothesis" is very common in polyandrous mating systems.
The "good sperm hypothesis" suggests that a male's genetic makeup will
determine the level of his competitiveness in sperm competition. When a male has "good sperm" he is able to father more viable offspring than males that do not have the "good sperm" genes.
Females may select males that have these superior "good sperm" genes
because it means that their offspring will be more viable and will
inherit the "good sperm" genes which will increase their fitness levels
when their sperm competes.
Studies show that there is more to determining the
competitiveness of the sperm in sperm competition in addition to a
male's genetic makeup. A male's dietary intake will also affect sperm
competition. An adequate diet consisting of increased amounts of diet
and sometimes more specific ratio in certain species will optimize sperm
number and fertility. Amounts of protein and carbohydrate intake were
tested for its effects on sperm production and quality in adult fruit
flies (Diptera: Tephritidae). Studies showed these flies need to
constantly ingest carbohydrates and water to survive, but protein is
also required to attain sexual maturity.
In addition, The Mediterranean fruit fly, male diet has been shown to
affect male mating success, copula duration, sperm transfer, and male
participation in leks.
These all require a good diet with nutrients for proper gamete
production as well as energy for activities, which includes
participation in leks.
In addition, protein and carbohydrate amounts were shown to have
an effect on sperm production and fertility in the speckled cockroach.
Holidic diets were used which allowed for specific protein and
carbohydrate measurements to be taken, giving it credibility. A direct
correlation was seen in sperm number and overall of food intake. More
specifically, optimal sperm production was measured at a 1:2 protein to
carbohydrate ratio. Sperm fertility was best at a similar protein to
carbohydrate ratio of 1:2. This close alignment largely factors in
determining male fertility in Nauphoeta cinerea.
Surprisingly, sperm viability was not affected by any change in diet or
diet ratios. It's hypothesized that sperm viability is more affected by
the genetic makeup, like in the "good sperm hypothesis". These ratios
and results are not consistent with many other species and even conflict
with some. It seems there can't be any conclusions on what type of diet
is needed to positively influence sperm competition but rather
understand that different diets do play a role in determining sperm
competition in mate choice.
Evolutionary consequences
One evolutionary response to sperm competition is the variety in penis morphology of many species. For example, the shape of the human penis may have been selectively shaped by sperm competition. The human penis may have been selected to displace seminal fluids implanted in the female reproductive tract by a rival male. Specifically, the shape of the coronal ridge may promote displacement of seminal fluid from a previous matinga thrusting action during sexual intercourse. A 2003 study by Gordon G. Gallup
and colleagues concluded that one evolutionary purpose of the thrusting
motion characteristic of intense intercourse is for the penis to
“upsuck” another man's semen before depositing its own.
Evolution to increase ejaculate volume in the presence of sperm competition has a consequence on testis size. Large testes
can produce more sperm required for larger ejaculates, and can be found
across the animal kingdom when sperm competition occurs.
Males with larger testes have been documented to achieve higher
reproductive success rates than males with smaller testes in male yellow pine chipmunks.
In chichlid fish, it has been found that increased sperm competition
can lead to evolved larger sperm numbers, sperm cell sizes, and sperm
swimming speeds.
In some insects and spiders, for instance Nephila fenestrate,
the male copulatory organ breaks off or tears off at the end of
copulation and remains within the female to serve as a copulatory plug. This broken genitalia is believed to be an evolutionary response to sperm competition. This damage to the male genitalia means that these males can only mate once.
Female choice for males with competitive sperm
Female factors can influence the result of sperm competition through a process known as "sperm choice".
Proteins present in the female reproductive tract or on the surface of
the ovum may influence which sperm succeeds in fertilizing the egg.
During sperm choice, females are able to discriminate and
differentially use the sperm from different males. One instance where
this is known to occur is inbreeding; females will preferentially use
the sperm from a more distantly related male than a close relative.
Post-copulatory inbreeding avoidance
Inbreeding ordinarily has negative fitness consequences (inbreeding depression),
and as a result species have evolved mechanisms to avoid inbreeding.
Inbreeding depression is considered to be due largely to the expression
of homozygous deleterious recessive mutations. Outcrossing between unrelated individuals ordinarily leads to the masking of deleterious recessive mutations in progeny.
Numerous inbreeding avoidance
mechanisms operating prior to mating have been described. However,
inbreeding avoidance mechanisms that operate subsequent to copulation
are less well known. In guppies,
a post-copulatory mechanism of inbreeding avoidance occurs based on
competition between sperm of rival males for achieving fertilization.
In competitions between sperm from an unrelated male and from a full
sibling male, a significant bias in paternity towards the unrelated male
was observed.
In vitro fertilization experiments in the mouse, provided evidence of sperm selection at the gametic level.
When sperm of sibling and non-sibling males were mixed, a
fertilization bias towards the sperm of the non-sibling males was
observed. The results were interpreted as egg-driven sperm selection
against related sperm.
Female fruit flies (Drosophila melanogaster) were mated with males of four different degrees of genetic relatedness in competition experiments. Sperm competitive ability was negatively correlated with relatedness.
Female crickets (Teleogryllus oceanicus)
appear to use post-copulatory mechanisms to avoid producing inbred
offspring. When mated to both a sibling and an unrelated male, females
bias paternity towards the unrelated male.
Empirical support
It has been found that because of female choice (see sexual selection), morphology of sperm in many species occurs in many variations to accommodate or combat (see sexual conflict) the morphology and physiology of the female reproductive tract.
However, it is difficult to understand the interplay between female
and male reproductive shape and structure that occurs within the female
reproductive tract after mating that allows for the competition of sperm. Polyandrous females mate with many male partners. Females of many species of arthropod, mollusk and other phyla have a specialized sperm-storage organ called the spermatheca in which the sperm of different males sometimes compete for increased reproductive success. Species of crickets, specifically Gryllus bimaculatus,
are known to exhibit polyandrous sexual selection. Males will invest
more in ejaculation when competitors are in the immediate environment of
the female.
Evidence exists that illustrates the ability of genetically
similar spermatozoa to cooperate so as to ensure the survival of their
counterparts thereby ensuring the implementation of their genotypes
towards fertilization. Cooperation confers a competitive advantage by
several means, some of these include incapacitation of other competing
sperm and aggregation of genetically similar spermatozoa into structures
that promote effective navigation of the female reproductive tract and
hence improve fertilization ability. Such characteristics lead to
morphological adaptations that suit the purposes of cooperative methods
during competition. For example, spermatozoa possessed by the wood mouse (Apodemus sylvaticus)
possess an apical hook which is used to attach to other spermatozoa to
form mobile trains that enhance motility through the female reproductive
tract.
Spermatozoa that fail to incorporate themselves into mobile trains are
less likely to engage in fertilization. Other evidence suggests no
link between sperm competition and sperm hook morphology.
Selection to produce more sperm can also select for the evolution of larger testes.
Relationships across species between the frequency of multiple mating
by females and male testis size are well documented across many groups
of animals. For example, among primates, female gorillas are relatively
monogamous, so gorillas have smaller testes than humans, which in turn have smaller testes than the highly promiscuous bonobos.
Male chimpanzees that live in a structured multi-male, multi-female
community, have large testicles to produce more sperm, therefore giving
him better odds to fertilize the female. Whereas the community of
gorillas consist of one alpha male and two or three females, when the
female gorillas are ready to mate, normally only the alpha male is their
partner.
Regarding sexual dimorphism
among primates, humans falls into an intermediate group with moderate
sex differences in body size but relatively large testes. This is a
typical pattern of primates where several males and females live
together in a group and the male faces an intermediate number of
challenges from other males compared to exclusive polygyny and monogamy but frequent sperm competition.
Other means of sperm competition could include improving the sperm itself or its packaging materials (spermatophore).
The male black-winged damselfly
provides a striking example of an adaptation to sperm competition.
Female black-winged damselflies are known to mate with several males
over the span of only a few hours and therefore possess a receptacle
known as a spermatheca
which stores the sperm. During the process of mating the male
damselfly will pump his abdomen up and down using his specially adapted
penis which acts as a scrub brush to remove the sperm of another male.
This method proves quite successful and the male damselfly has been
known to remove 90-100 percent of the competing sperm.
Male dunnocks (
Prunella modularis) peck at the female's cloaca, removing sperm of previous mates.
A similar strategy has been observed in the dunnock, a small bird. Before mating with the polyandrous female, the male dunnock pecks at the female's cloaca in order to peck out the sperm of the previous male suitor.
In the fly Dryomyza anilis, females mate with multiple males. It benefits the male to attempt to be the last one to mate with a given female.
This is because there seems to be a cumulative percentage increase in
fertilization for the final male, such that the eggs laid in the last
oviposition bout are the most successful.
A notion emerged in 1996 that in some species, including humans, a
significant fraction of sperm specialize in a manner such that they
cannot fertilize the egg but instead have the primary effect of stopping
the sperm from other males from reaching the egg, e.g. by killing them
with enzymes or by blocking their access. This type of sperm
specialization became known popularly as "kamikaze sperm" or "killer
sperm", but most follow-up studies to this popularized notion have
failed to confirm the initial papers on the matter. While there is also currently little evidence of killer sperm in any non-human animals certain snails have an infertile sperm morph ("parasperm") that contains lysozymes, leading to speculation that they might be able to degrade a rivals' sperm.
The parasitoid wasp Nasonia vitripennis,
mated females can choose whether or not to lay a fertilized egg (which
develops into a daughter) or an unfertilized egg (which develops into a
son), therefore females suffer a cost from mating, as repeated matings
constrain their ability to allocate sex in their offspring. The
behaviour of these kamikaze-sperm is referred to in academic literature as "sperm-blocking", using basketball as a metaphor.
Sperm competition has led to other adaptations such as larger ejaculates, prolonged copulation, deposition of a copulatory plug
to prevent the female re-mating, or the application of pheromones that
reduce the female's attractiveness.
The adaptation of sperm traits, such as length, viability and velocity
might be constrained by the influence of cytoplasmic DNA (e.g. mitochondrial DNA);
mitochondrial DNA is inherited from the mother only and it is thought
that this could represent a constraint in the evolution of sperm.