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Animal communication is the transfer of information from one or a group of animals (sender or senders) to one or more other animals (receiver or receivers) that affects the current or future behavior of the receivers. Information may be sent intentionally, as in a courtship display, or unintentionally, as in the transfer of scent from the predator to prey with kairomones. Information may be transferred to an "audience" of several receivers. Animal communication is a rapidly growing area of study in disciplines including animal behavior, sociology, neurology, and animal cognition. Many aspects of animal behavior, such as symbolic name use, emotional expression, learning, and sexual behavior, are being understood in new ways.

When the information from the sender changes the behavior of a receiver, the information is referred to as a "signal". Signalling theory predicts that for a signal to be maintained in the population, both the sender and receiver should usually receive some benefit from the interaction. Signal production by senders and the perception and subsequent response of receivers are thought to coevolve. Signals often involve multiple mechanisms, e.g., both visual and auditory, and for a signal to be understood, the coordinated behavior of both sender and receiver requires careful study.

Animal languages

The sounds animals make are important because they communicate the animals' state. Some animals species have been taught simple versions of human languages. Animals can use, for example, electrolocation and echolocation to communicate about prey and location.

Modes

Visual

Gestures

Most animals understand communication through a visual display of distinctive body parts or bodily movements. Animals will reveal or accentuate a body part to relay certain information. The parent herring gull displays its bright yellow bill on the ground next over its chick when it has returned to the nest with food. The chicks exhibit a begging response by tapping the red spot on the lower mandible of the parent herring gull's bill. This signal stimulates the parent to regurgitate food and completes the feeding signal. The distinctive morphological feature accentuated in this communication is the parent's red-spotted bill, while the tapping towards the ground makes the red spot visible to the chick, demonstrating a distinctive movement. Frans de Waal studied bonobos and chimps to understand if language was somehow evolved by gestures. He found that both apes and humans only use intentional gestures to communicate.

Facial expression

Another important signal of emotion in animal communication are facial gestures. Blue and Yellow Macaws were studied to understand how they reacted to interactions with a familiar animal caretaker. Studies show that Blue and Yellow Macaws demonstrated a significant amount of blushing frequently during mutual interactions with a caretaker. In another experiment, Jeffrey Mogil studied facial expression in mice in response to increments of increasing pain. He found that mice exhibited five recognizable facial expressions: orbital tightening, nose and cheek bulge, and changes in ear and whisker carriage.

Gaze-following

Social animals use gaze-following as a form of communication through monitoring head and eye orientation in other mammals. Studies have been conducted on apes, monkeys, dogs, birds, wolves, and tortoises, and have focused on two different tasks: "follow another's gaze into distant space" and "follow another's gaze geometrically around a visual barrier, e.g., by repositioning themselves to follow a gaze cue when faced with a barrier blocking their view". A broad range of animals have been proven to exhibit the latter, however, only apes, dogs, wolves, and corvids (ravens) have been able to follow another's gaze into distant space. Marmosets and ibis were unable to demonstrate "geometric gaze following". Researchers do not yet have a clear picture of the cognitive basis of gaze following, but developmental evidence indicates that "simple" gaze following and "geometric" gaze following probably rely on different cognitive mechanisms.

Colour change

Colour change can be separated into changes that occur during growth and development, and those triggered by mood, social context, or abiotic factors such as temperature. The latter are seen in many taxa. Some cephalopods, such as the octopus and the cuttlefish, have specialized skin cells (chromatophores) that can change the apparent colour, opacity, and reflectiveness of their skin. In addition to their use for camouflage, rapid changes in skin colour are used while hunting and in courtship rituals. Cuttlefish may display two entirely different signals simultaneously from opposite sides of their body. When a male cuttlefish courts a female in the presence of other males, he displays a male pattern facing the female and a female pattern facing away, to deceive other males. Some colour signals occur in cycles. For example, when a female olive baboon begins to ovulate, her anogenital area swells and turns a bright red/pink. This signals to males that she is ready to mate. Humboldt squid are bioluminescent and thus capable of communicating visually in dark ocean environments.

Bioluminescent communication

Communication by the production of light occurs commonly in vertebrates and invertebrates in the oceans, particularly at depths (e.g., angler fish). Two well-known forms of land bioluminescence occur in fireflies and glow worms. Other insects, insect larvae, annelids, arachnids, and even species of fungi possess bioluminescent abilities. Some bioluminescent animals produce the light themselves, whereas others have a symbiotic relationship with bioluminescent bacteria. Animals exhibit bioluminescent light to lure in prey, attract a mate, or protect themselves from potential predators. (See also: List of bioluminescent organisms)

Signaling

There are many different types of signals that animals use to differentiate their position of direction, location, and distance. Practitioners study the issues of animal position by geometric viewings. Environmental and social influences are indicators of geometric viewings. Animals rely on signals called electrolocating and echolocating; they use sensory senses in order to navigate and find prey. Signals are used as a form of commutation through the environment. Active signals or other types of signals influence receivers behavior and signals move quicker in distance to reach receivers.

Auditory

Many animals communicate through vocalization. Vocal communication serves many purposes, including mating rituals, warning calls, conveying location of food sources, and social learning. In a number of species, males perform calls during mating rituals as a form of competition against other males and to signal to females. Examples include frogs, hammer-headed bats, red deer, humpback whales, elephant seals, and songbirds. Other instances of vocal communication include the alarm calls of the Campbell monkey, the territorial calls of gibbons, and the use of frequency in greater spear-nosed bats to distinguish between groups. The vervet monkey gives a distinct alarm call for each of its four different predators, and the reactions of other monkeys vary appropriately according to the call. For example, if an alarm call signals a python, the monkeys climb into the trees, whereas the "eagle" alarm causes monkeys to seek a hiding place on the ground. Prairie dogs also use complex calls that signal predator differences. According to Con Slobodchikoff and others, prairie dog calls communicate the type, size, and speed of an approaching predator.  Whale vocalizations have been found to have different dialects based on social learning. Mammalian acoustic culture was first discovered in southern resident orcas in 1978.

Not all animals use vocalization as a means of auditory communication. Many arthropods rub specialized body parts together to produce sound. This is known as stridulation. Crickets and grasshoppers are well known for this, but many others use stridulation as well, including crustaceans, spiders, scorpions, wasps, ants, beetles, butterflies, moths, millipedes, and centipedes. Another means of auditory communication is the vibration of swim bladders in bony fish. The structure of swim bladders and the attached sonic muscles varies greatly across bony fish families, resulting in a wide variety of sounds. Striking body parts together can also produce auditory signals. A well-known example of this is the tail tip vibration of rattlesnakes as a warning signal. Other examples include bill clacking in birds, wing clapping in manakin courtship displays, and chest beating in gorillas.

Burrowing animal species are known to whistle to communicate threats, and sometimes mood. Species such as the marmot species, including the groundhog (woodchuck), and the alpine marmot show this trait. Whistling is used by animals such as prairie dogs to communicate threats, with prairie dogs having one of the most complex communication systems in the animal kingdom. Prairie dogs are able to communicate an animal's speed, shape, size, species, and for humans specific attire and if the human is carrying a gun. This method of communication is usually done by having a sentry stand on two feet and surveying for potential threats while the rest of the pack finds food. Once a threat has been identified the sentry sounds a whistle alarm, (sometimes describing the threat) at which point the pack retreats to their burrows. The intensity of the threat is usually determined by how long the sentry whistles. The sentry continues to whistle the alarm until the entirety of the pack has gone to safety, at which point the sentry returns to the burrow.

Olfactory

Despite being the oldest method of communication, chemical communication is one of the least understood forms due in part to the sheer abundance of chemicals in our environment and the difficulty of detecting and measuring all the chemicals in a sample. The ability to detect chemicals in the environment serves many functions, a crucial one being the detection of food, a function that first arose in single-celled organisms (bacteria) living in the oceans during the early days of life on Earth. As this function evolved, organisms began to differentiate between chemical compounds emanating from resources, conspecifics (same species; i.e., mates and kin), and heterospecifics (different species; i.e., competitors and predators).

For instance, a small minnow species may do well to avoid habitat with a detectable concentration of chemical cues associated with a predator species such as a northern pike. Minnows with the ability to perceive the presence of predators before they are close enough to be seen and then respond with adaptive behavior (such as hiding) are more likely to survive and reproduce. Atlantic salmon go a step further than detecting a predator's cue: when an individual is damaged by a predator, it releases a chemical cue to its conspecifics. As has also been observed in other species, acidification and changes in pH physically disrupt these chemical cues, which has various implications for animal behavior.

Scent marking and scent rubbing are common forms of olfactory communication in mammals. An example of scent rubbing by an animal can be seen from bears, bears do this as a way to mark territory or let others know they are there and to stay away. Wolves scent-mark frequently during the breeding season.

Electric

Electrocommunication is a rare form of communication in animals. It is seen primarily in aquatic animals, though some land mammals, notably the platypus and echidnas, sense electric fields that might be used for communication.

Weakly electric fishes provide an example of electrocommunication, together with electrolocation. These fish use an electric organ to generate an electric field, which is detected by electroreceptors. Differences in the waveform and frequency of changes in the field convey information on species, sex, and identity. These electric signals can be generated in response to hormones, circadian rhythms, and interactions with other fish. They can also serve to mediate social hierarchy amongst species that have a social order. Some predators, such as sharks and rays, are able to eavesdrop on these electrogenic fish through passive electroreception.

Touch

For more on the mechanism for touch, see Somatosensory system and Mechanoreceptors

Touch is a key factor in many social interactions. Examples include:

Fighting

In a fight, touch may be used to challenge an opponent and to coordinate movements during the fight. It may also be used by the loser to indicate submission.

Mating

Mammals often initiate mating by grooming, stroking or rubbing against each other. This provides the opportunity to apply chemical signals and to assess those excreted by the potential mate. Touch may also announce the intention of the male to mount the female, as when a male kangaroo grabs the tail of a female. During mating, touch stimuli are important for pair positioning, coordination and genital stimulation.

Social integration

Touch is widely used for social integration, a use that is typified by the social grooming of one animal by another. Social grooming has several functions; it removes parasites and debris from the groomed animal, it reaffirms the social bond or hierarchical relationship between the animals, and it gives the groomer an opportunity to examine olfactory cues on the groomed individual, perhaps adding additional ones. This behaviour has been observed in social insects, birds and mammals.

Foraging

Some ant species recruit fellow workers to new food finds by first tapping them with their antennae and forelegs, then leading them to the food source while keeping physical contact. "Patrollers" leave the nest to check for danger nearby and return to recruit "foragers" by making physical contact. Another example of this is the waggle dance of honey bees.

Huddling

Prolonged physical contact or huddling also serves social integration. Huddling promotes heat exchange, together with the transfer of olfactory or tactile information. Some organisms live in constant contact in a colony, for example colonial corals. When individuals are linked tightly in this way an entire colony can react on the aversive or alarm movements made by only a few individuals. In several herbivorous insect nymphs and larvae, aggregations where there is prolonged contact play a major role in group coordination. These aggregations may take the form of a procession or a rosette.

Seismic

Seismic communication is the exchange of information using self-generated vibrational signals transmitted via a substrate such as the soil, water, spider webs, plant stems, or a blade of grass. This form of communication has several advantages, for example it can be sent regardless of light and noise levels, and it usually has a short range and short persistence, which may reduce the danger of detection by predators. The use of seismic communication is found in many taxa, including frogs, kangaroo rats, mole rats, bees, nematode worms, and others. Tetrapods usually make seismic waves by drumming on the ground with a body part, a signal that is sensed by the sacculus of the receiver. The sacculus is an organ in the inner ear containing a membranous sac that is used for balance, but can also detect seismic waves in animals that use this form of communication. Vibrations may be combined with other sorts of communication.

Thermal

A number of different snakes have the ability to sense infrared (IR) thermal radiation, which allows these reptiles to derive thermal images from the radiant heat emitted by predators or prey at wavelengths between 5 and 30 μm. The accuracy of this sense is such that a blind rattlesnake can target its strike to the vulnerable body parts of a prey animal. It was previously thought that the pit organs evolved primarily as prey detectors, but it is now believed that they may also be used to control body temperature.

The facial pits enabling thermoregulation underwent parallel evolution in pitvipers and some boas and pythons, having evolved once in pitvipers and multiple times in boas and pythons. The electrophysiology of the structure is similar between lineages, but it differs in gross structure anatomy. Most superficially, pitvipers possess one large pit organ on either side of the head, between the eye and the nostril (loreal pit), while boas and pythons have three or more comparatively smaller pits lining the upper and sometimes the lower lip, in or between the scales. Those of the pitvipers are the more advanced, having a suspended sensory membrane as opposed to a simple pit structure. Within the family Viperidae, the pit organ is seen only in the subfamily Crotalinae: the pitvipers. Despite the detection of IR radiation, the pits' IR mechanism is dissimilar to photoreceptors; while photoreceptors detect light via photochemical reactions, the protein in the facial pits of snakes is a temperature sensitive ion channel. It senses infrared signals through a mechanism involving warming of the pit organ, rather than chemical reaction to light. This is consistent with the thin pit membrane, which allows incoming IR radiation to quickly and precisely warm a given ion channel and trigger a nerve impulse, as well as vascularize the pit membrane to rapidly cool the ion channel back to its original "resting" or "inactive" temperature.

Common vampire bats (Desmodus rotundus) have specialized IR sensors in their nose-leaf. Vampire bats are the only mammals that feed exclusively on blood. The IR sense enables Desmodus to localize homeothermic animals such as cattle and horses within a range of about 10 to 15 cm. This infrared perception may be used in detecting regions of maximal blood flow on targeted prey.

Autocommunication

Autocommunication is a type of communication in which the sender and receiver are the same individual. The sender emits a signal that is altered by the environment and eventually is received by the same individual. The altered signal provides information that can indicate food, predators or conspecifics. Because the sender and receiver are the same animal, selection pressure maximizes signal efficacy, i.e. the degree to which an emitted signal is correctly identified by a receiver despite propagation distortion and noise. There are some species, such as the pacific herring, which have evolved to intercept these messages from their predators. They are able to use it as an early warning sign and respond defensively. There are two types of autocommunication. The first is active electrolocation, where the organism emits an electrical pulse through its electric organ and senses the projected geometrical property of the object. This is found in the electric fish Gymnotiformes (knifefishes) and Mormyridae(elephantfish). The second type of autocommunication is echolocation, found in bats and toothed whales. Echolocation involves emitting sounds and interpreting the vibrations that return from objects. In bats, echolocation also serves the purpose of mapping their environment. They are capable of recognizing a space they have been in before without any visible light because they can memorize patterns in the feedback they get from echolocation.

Functions

There are many functions of animal communication. However, some have been studied in more detail than others. This includes:

Communication during contests

Animal communication plays a vital role in determining the winner of contest over a resource. Many species have distinct signals that signal aggression or willingness to attack or signals to convey retreat during competitions over food, territories, or mates.

Mating rituals

Animals produce signals to attract the attention of a possible mate or to solidify pair bonds. These signals frequently involve the display of body parts or postures. For example, a gazelle will assume characteristic poses to initiate mating. Mating signals can also include the use of olfactory signals or mating calls unique to a species. Animals that form lasting pair bonds often have symmetrical displays that they make to each other. Famous examples are the mutual presentation of reeds by great crested grebes studied by Julian Huxley, the triumph displays shown by many species of geese and penguins on their nest sites, and the spectacular courtship displays by birds of paradise. "Copulation calls" in mammals can indicate a female's breeding status or attract other mates.

Ownership/territorial

Signals used to claim or defend a territory, food, or a mate. Polygynous lizards (Anolis carolinensis) will show greater signs of aggression from farther distances between males than between females when defending a territory or mate. It is believed that males have evolved to remain distant from each other due to higher reproductive consequences as opposed to females.

Redirected aggression

Some animals who are fearful of stimuli will attack anyone near them.

Food-related signals

Many animals make "food calls" to attract a mate, offspring, or other members of a social group to a food source. Perhaps the most elaborate food-related signal is the Waggle dance of honeybees studied by Karl von Frisch. One well-known example of begging of offspring in a clutch or litter is altricial songbirds. Young ravens will signal to older ravens when they encounter new or untested food.  Rhesus macaques will send food calls to inform other monkeys of a food source to avoid punishment.  Pheromones are released by many social insects to lead the other members of the society to the food source. For example, ants leave a pheromone trail on the ground that can be followed by other ants to lead them to the food source.

Alarm calls

Alarm calls communicate the threat of a predator. This allows all members of a social group (and sometimes other species) to respond accordingly. This may include running for cover, becoming immobile, or gathering into a group to reduce the risk of attack. Alarm signals are not always vocalizations. Crushed ants will release an alarm pheromone to attract more ants and send them into an attack state.

Meta-communication

Signals that will modify the meaning of subsequent signals. One example is the 'play face' in dogs which signals that a subsequent aggressive signal is part of a play fight rather than a serious aggressive episode.

Interpretation of animal behaviour

As described above, many animal gestures, postures, and sounds, convey meaning to nearby animals. These signals are often easier to describe than to interpret. It is tempting, especially with domesticated animals and apes, to anthropomorphize, that is, to interpret animal actions in human terms, but this can be quite misleading; for example, an ape's "smile" is often a sign of aggression. Also, the same gesture may have different meanings depending on context within which it occurs. For example, a domestic dog's tail wag and posture may be used in different ways to convey many meanings as illustrated in Charles Darwin's The Expression of the Emotions in Man and Animals published in 1872. Some of Darwin's illustrations are reproduced here.

• Examples of tail position indicating different emotions in dogs
• "Small dog watching a cat on a table"
• "Dog approaching another dog with hostile intentions"
• "Dog in a humble and affectionate frame of mind"
• "Half-bred shepherd dog"
• "Dog caressing his master"

Interspecific communication

Much animal communication is intraspecific, that is, it occurs between members of the same species. As for interspecific communication, that between predator and prey is of particular interest.

Prey to predator

If a prey animal moves, makes a noise or vibrations, or emits a smell in such a way that a predator can detect it, it is communicating with its predator. This is consistent with the definition of "communication" given above. This type of communication is known as interceptive eavesdropping if a predator intercepts a message intended for conspecifics.

There are however, some actions of prey species are clearly directed to actual or potential predators. A good example is warning coloration: species such as wasps that are capable of harming potential predators are often brightly coloured, and this modifies the behavior of the predator, who either instinctively or as the result of experience will avoid attacking such an animal. Some forms of mimicry fall in the same category: for example hoverflies are coloured in the same way as wasps, and although they are unable to sting, the strong avoidance of wasps by predators gives the hoverfly some protection. There are also behavioural changes that act in a similar way to warning colouration. For example, canines such as wolves and coyotes may adopt an aggressive posture, such as growling with their teeth bared, to indicate they will fight if necessary, and rattlesnakes use their well-known rattle to warn potential predators of their venomous bite. Sometimes, a behavioural change and warning colouration will be combined, as in certain species of amphibians which have most of their body coloured to blend with their surroundings, except for a brightly coloured belly. When confronted with a potential threat, they show their belly, indicating that they are poisonous in some way.

Another example of prey to predator communication is the pursuit-deterrent signal. Pursuit-deterrent signals occur when prey indicates to a predator that pursuit would be unprofitable because the signaler is prepared to escape. Pursuit-deterrent signals provide a benefit to both the signaler and receiver; they prevent the sender from wasting time and energy fleeing, and they prevent the receiver from investing in a costly pursuit that is unlikely to result in capture. Such signals can advertise prey's ability to escape, and reflect phenotypic condition (quality advertisement), or can advertise that the prey has detected the predator (perception advertisement). Pursuit-deterrent signals have been reported for a wide variety of taxa, including fish (Godin and Davis, 1995), lizards (Cooper etc. al., 2004), ungulates (Caro, 1995), rabbits (Holley 1993), primates (Zuberbuhler et al. 1997), rodents (Shelley and Blumstein 2005, Clark, 2005), and birds (Alvarez, 1993, Murphy, 2006, 2007). A familiar example of quality advertisement pursuit-deterrent signal is stotting (sometimes called pronking), a pronounced combination of stiff-legged running while simultaneously jumping shown by some antelopes such as Thomson's gazelle in the presence of a predator. At least 11 hypotheses for stotting have been proposed. A leading theory today is that it alerts predators that the element of surprise has been lost. Predators like cheetahs rely on surprise attacks, proven by the fact that chases are rarely successful when antelope stot. Predators do not waste energy on a chase that will likely be unsuccessful (optimal foraging behavior). Quality advertisement can be communicated by modes other than visual. The banner-tailed kangaroo rat produces several complex foot-drumming patterns in a number of different contexts, one of which is when it encounters a snake. The foot-drumming may alert nearby offspring but most likely conveys vibrations through the ground that the rat is too alert for a successful attack, thus preventing the snake's predatory pursuit.

Predator to prey

Typically, predators attempt to reduce communication to prey as this will generally reduce the effectiveness of their hunting. However, some forms of predator to prey communication occur in ways that change the behavior of the prey and make their capture easier, i.e. deception by the predator. A well-known example is the angler fish, an ambush predator which waits for its prey to come to it. It has a fleshy bioluminescent growth protruding from its forehead which it dangles in front of its jaws. Smaller fish attempt to take the lure, placing themselves in a better position for the angler fish to catch them. Another example of deceptive communication is observed in the genus of jumping spiders (Myrmarachne). These spiders are commonly referred to as "antmimicking spiders" because of the way they wave their front legs in the air to simulate antennae.

Human/animal

Various ways in which humans interpret the behavior of animals, or give commands to them, are consistent with the definition of interspecies communication. Skillful interpretation of animal communications may be critical to the welfare of animals that are being cared for or trained by humans.

Non-human animal species may interpret the signals of humans differently than humans themselves. For instance, a pointing command refers to a location rather than an object in dogs.

Other aspects

Evolution

The importance of communication is evident from the highly elaborate morphology, behaviour and physiology that some animals have evolved to facilitate this. These include some of the most striking structures in the animal kingdom, such as the peacock's tail, the antlers of a stag and the frill of the frill-necked lizard, but also include even the modest red spot on a European herring gull's bill. Highly elaborate behaviours have evolved for communication such as the dancing of cranes, the pattern changes of cuttlefish, and the gathering and arranging of materials by bowerbirds. Other evidence for the importance of communication in animals is the prioritisation of physiological features to this function. For example, birdsong appears to have brain structures entirely devoted to its production. All these adaptations require evolutionary explanation.

There are two aspects to the required explanation:

• identifying a route by which an animal that lacked the relevant feature or behaviour could acquire it;
• identifying the selective pressure that makes it adaptive for animals to develop structures that facilitate communication, emit communications, and respond to them.

Significant contributions to the first of these problems were made by Konrad Lorenz and other early ethologists. By comparing related species within groups, they showed that movements and body parts that in the primitive forms had no communicative function could be "captured" in a context where communication would be functional for one or both partners, and could evolve into a more elaborate, specialised form. For example, Desmond Morris showed in a study of grass finches that a beak-wiping response occurred in a range of species, serving a preening function, but that in some species this had been elaborated into a courtship signal.

The second problem has been more controversial. The early ethologists assumed that communication occurred for the good of the species as a whole, but this would require a process of group selection which is believed to be mathematically impossible in the evolution of sexually reproducing animals. Altruism towards an unrelated group is not widely accepted in the scientific community, but rather can be seen as reciprocal altruism, expecting the same behaviour from others, a benefit of living in a group. Sociobiologists argued that behaviours that benefited a whole group of animals might emerge as a result of selection pressures acting solely on the individual. A gene-centered view of evolution proposes that behaviours that enabled a gene to become wider established within a population would become positively selected for, even if their effect on individuals or the species as a whole was detrimental;

In the case of communication, an important discussion by John Krebs and Richard Dawkins established hypotheses for the evolution of such apparently altruistic or mutualistic communications as alarm calls and courtship signals to emerge under individual selection. This led to the realization that communication might not always be "honest" (indeed, there are some obvious examples where it is not, as in mimicry). The possibility of evolutionarily stable dishonest communication has been the subject of much controversy, with Amotz Zahavi in particular arguing that it cannot exist in the long term. Sociobiologists have also been concerned with the evolution of apparently excessive signaling structures such as the peacock's tail; it is widely thought that these can only emerge as a result of sexual selection, which can create a positive feedback process that leads to the rapid exaggeration of a characteristic that confers an advantage in a competitive mate-selection situation.

One theory to explain the evolution of traits like a peacock's tail is 'runaway selection'. This requires two traits—a trait that exists, like the bright tail, and a preexisting bias in the female to select for that trait. Females prefer the more elaborate tails, and thus those males are able to mate successfully. Exploiting the psychology of the female, a positive feedback loop is enacted and the tail becomes bigger and brighter. Eventually, the evolution will level off because the survival costs to the male do not allow for the trait to be elaborated any further. Two theories exist to explain runaway selection. The first is the good genes hypothesis. This theory states that an elaborate display is an honest signal of fitness and truly is a better mate. The second is the handicap hypothesis. This explains that the peacock's tail is a handicap, requiring energy to keep and makes it more visible to predators. Thus, the signal is costly to maintain, and remains an honest indicator of the signaler's condition. Another assumption is that the signal is more costly for low quality males to produce than for higher quality males to produce. This is simply because the higher quality males have more energy reserves available to allocate to costly signaling.

Cognitive aspects

Ethologists and sociobiologists have characteristically analysed animal communication in terms of more or less automatic responses to stimuli, without raising the question of whether the animals concerned understand the meaning of the signals they emit and receive. That is a key question in animal cognition. There are some signalling systems that seem to demand a more advanced understanding. A much discussed example is the use of alarm calls by vervet monkeys. Robert Seyfarth and Dorothy Cheney showed that these animals emit different alarm calls in the presence of different predators (leopards, eagles, and snakes), and the monkeys that hear the calls respond appropriately—but that this ability develops over time, and also takes into account the experience of the individual emitting the call. Metacommunication, discussed above, also seems to require a more sophisticated cognitive process.

Signature whistles

It has been reported that bottlenose dolphins can recognize identity information from signature whistles even when otherwise stripped of the characteristics of the whistle; making bottlenose dolphins the only animals other than humans that have been shown to transmit identity information independent of the caller's voice or location. The paper concludes that:

The fact that signature whistle shape carries identity information independent from voice features presents the possibility to use these whistles as referential signals, either addressing individuals or referring to them, similar to the use of names in humans. Given the cognitive abilities of bottlenose dolphins, their vocal learning and copying skills, and their fission–fusion social structure, this possibility is an intriguing one that demands further investigation.

— V. M. Janik, et al.

The same researchers later found that common bottlenose dolphin (Tursiops truncatus) mothers inflect their signature whistle when their dependent calf is present. Signature whistles, which are in a higher frequency range than humans can hear, have an important role in facilitating mother–calf contact. In the Sarasota Dolphin Research Program's library of recordings were 19 female common bottlenose dolphins producing signature whistles both with and without the presence of their calf. In all 19 cases, the mother dolphin inflected the signature whistle when their calf was present, by reaching a higher frequency, or using a wider frequency range. Similarly, humans use higher fundamental frequencies and a wider pitch range to inflect child–directed speech (CDS). This has rarely been discovered in other species. The researchers stated that CDS benefits for humans are cueing the child to pay attention, long-term bonding, and promoting the development of lifelong vocal learning, with parallels in these bottlenose dolphins in an example of convergent evolution.

Human behaviour

Another controversial issue is the extent to which human behaviours resemble animal communication, or whether all such communication has disappeared as a result of our linguistic capacity. Some of our bodily features—eyebrows, beards and moustaches, deep adult male voices, perhaps female breasts—strongly resemble adaptations to producing signals. Ethologists such as Irenäus Eibl-Eibesfeldt have argued that facial gestures such as smiling, grimacing, and the eyebrow flash on greeting are universal human communicative signals that can be related to corresponding signals in other primates. Given how recently spoken language has emerged, it is very likely that human body language does include some more or less involuntary responses that have a similar origin to the communication we have.

Humans also often seek to mimic animals' communicative signals in order to interact with them. For example, cats have a mild affiliative response of slowly closing their eyes; humans often mimic this signal towards a pet cat to establish a tolerant relationship. Stroking, petting and rubbing pet animals are all actions that probably work through their natural patterns of interspecific communication.

Dogs have shown an ability to understand human communication. In object choice tasks, dogs utilize human communicative gestures such as pointing and direction of gaze in order to locate hidden food and toys. However, in contrast to humans pointing has a different meaning for dogs as it refers to a direction or location. It has also been shown that dogs exhibit a left gaze bias when looking at human faces, indicating that they are capable of reading human emotions. Dogs do not make use of direction of gaze or exhibit left gaze bias with other dogs.

A new approach in the 21st century in the field of animal communication uses applied behavioural analysis, specifically functional communication training. This form of training previously has been used in schools and clinics with humans with special needs, such as children with autism, to help them develop language. Sean Senechal at the AnimalSign Center has been using an approach similar to functional communication training with domesticated animals, such as dogs since 2004 and horses since 2000, with encouraging results and benefits to the animals and people. Functional communication training for animals, Senechal calls "Animal Sign Language". This includes teaching communication through gestures (like simplified American sign language), Picture Exchange Communication System, tapping, and vocalisation. The process for animals includes simplified and modified techniques.

Linguistics

External videos
Do animals have language? - Michele Bishop, TED Ed, 4:54, September 10, 2015

For linguistics, the interest of animal communication systems lies in their similarities to and differences from human language:

1. Human languages are characterized for having a double articulation (in the characterization of French linguist André Martinet). It means that complex linguistic expressions can be broken down in meaningful elements (such as morphemes and words), which in turn are composed of smallest phonetic elements that affect meaning, called phonemes. Animal signals, however, do not exhibit this dual structure.
2. In general, animal utterances are responses to external stimuli, and do not refer to matters removed in time and space. Matters of relevance at a distance, such as distant food sources, tend to be indicated to other individuals by body language instead, for example wolf activity before a hunt, or the information conveyed in honeybee dance language. It is therefore unclear to what extent utterances are automatic responses and to what extent deliberate intent plays a part.
3. In contrast to human language, animal communication systems are usually not able to express conceptual generalizations. (Cetaceans and some primates may be notable exceptions).
4. Human languages combine elements to produce new messages (a property known as creativity). One factor in this is that much human language growth is based upon conceptual ideas and hypothetical structures, both being far greater capabilities in humans than animals. This appears far less common in animal communication systems, although current research into animal culture is still an ongoing process with many new discoveries. In 2009 it was reported that affixation may play a role in the call meanings of Campbell's mona monkey.

Errors in communication

There becomes possibility for error within communication between animals when certain circumstances apply. These circumstances could include distance between the two communicating subjects, as well as the complexity of the signal that is being communicated to the "listener" of the situation. It may not always be clear to the "listener" where the location of the communication is coming from, as the "singer" can sometimes deceive them and create more error.

See also

• Animal consciousness
• Anthrozoology (human–animal studies)
• Biocommunication
• Biosemiotics
• Body language
• Dear enemy effect and Nasty neighbour effect
• Deception in animals
• Degeneracy (biology)
• Emotion in animals
• Forms of activity and interpersonal relations
• Human–animal communication
• International Society for Biosemiotic Studies
• Origin of language
• Origin of speech
• Sir Philip Sidney game
• Talking animal
• Zoomusicology
• Zoosemiotics

References

1. "Animal communication". Encyclopedia Britannica. Retrieved 2020-10-31.
2. Shah, Sonia (20 September 2023). "The Animals Are Talking. What Does It Mean? - Language was long understood as a human-only affair. New research suggests that isn't so. + comment". The New York Times. Archived from the original on 21 September 2023. Retrieved 21 September 2023.{{cite news}}: CS1 maint: bot: original URL status unknown (link)
3. Seyfarth, Robert M.; Cheney, Dorothy L. (2003-02-01). "Signalers and Receivers in Animal Communication". Annual Review of Psychology. 54 (1): 145–173. doi:10.1146/annurev.psych.54.101601.145121. ISSN 0066-4308. PMID 12359915.
4. ^ Maynard-Smith and Harper, 2003
5. Warren, Michael (2018). "Animal Languages in the Middle Ages: Representations of Interspecies Communication ed. by Alison Langdon". Studies in the Age of Chaucer. 40 (1): 491–495. doi:10.1353/sac.2018.0028. ISSN 1949-0755. S2CID 165256417.
6. Beecher, Michael D. (2021). "Why Are No Animal Communication Systems Simple Languages?". Frontiers in Psychology. 12. doi:10.3389/fpsyg.2021.602635. ISSN 1664-1078. PMC 8018278. PMID 33815200.
7. Jones, Te K.; Allen, Kathryne M.; Moss, Cynthia F. (2021-11-09). "Communication with self, friends and foes in active-sensing animals". Journal of Experimental Biology. 224 (22). Bibcode:2021JExpB.224B2637J. doi:10.1242/jeb.242637. ISSN 0022-0949. PMID 34752625. S2CID 243940410.
8. Tinbergen, N.; Perdeck, A. C. (1951-01-01). "On the Stimulus Situation Releasing the Begging Response in the Newly Hatched Herring Gull Chick (Larus Argentatus Argentatus Pont.)". Behaviour. 3 (1): 1–39. doi:10.1163/156853951X00197. ISSN 0005-7959.
9. Pollick, Amy S.; Waal, Frans B. M. de (2007-05-08). "Ape gestures and language evolution". Proceedings of the National Academy of Sciences. 104 (19): 8184–8189. Bibcode:2007PNAS..104.8184P. doi:10.1073/pnas.0702624104. ISSN 0027-8424. PMC 1876592. PMID 17470779.
10. Bertin, Aline; Beraud, Arielle; Lansade, Léa; et al. (22 August 2018). "Facial display and blushing: Means of visual communication in blue-and-yellow macaws (Ara Ararauna)?". PLOS ONE. 13 (8): e0201762. Bibcode:2018PLoSO..1301762B. doi:10.1371/journal.pone.0201762. PMC 6104955. PMID 30133471. ProQuest 2091762411.
11. Mogil, Jeffrey S. (April 2009). "Animal models of pain: progress and challenges". Nature Reviews Neuroscience. 10 (4): 283–294. doi:10.1038/nrn2606. ISSN 1471-003X. PMID 19259101. S2CID 205504814.
12. ^ Shepherd, Stephen V. (2010-03-19). "Following Gaze: Gaze-Following Behavior as a Window into Social Cognition". Frontiers in Integrative Neuroscience. 4: 5. doi:10.3389/fnint.2010.00005. ISSN 1662-5145. PMC 2859805. PMID 20428494.
13. Range, Friederike; Virányi, Zsófia (2011-02-23). Wylie, Doug (ed.). "Development of Gaze Following Abilities in Wolves (Canis Lupus)". PLOS ONE. 6 (2): e16888. Bibcode:2011PLoSO...616888R. doi:10.1371/journal.pone.0016888. ISSN 1932-6203. PMC 3044139. PMID 21373192.
14. Cloney, R.A.; Florey, E. (1968). "Ultrastructure of cephalopod chromatophore organs". Z. Zellforsch. Mikrosk. Anat. 89 (2): 250–280. doi:10.1007/bf00347297. PMID 5700268. S2CID 26566732.
15. Hanlon, R.T.; Messenger, J.B. (1996). Cephalopod Behaviour. Cambridge University Press. p. 121. ISBN 978-0-521-64583-6.
16. Williams, Sarah (2012). "Two-faced fish tricks competitors". Science Now. Archived from the original on March 8, 2013. Retrieved March 16, 2013.
17. Motluk, Alison (2001). "Big Bottom". New Scientist. 19 (7).
18. Deep Sea Squid May Communicate Through Glowing Pigmentation, Researchers Find
19. Mason, Julia (July 18, 2018). "Glowing in the Deep". The Dish on Science. Archived from the original on May 6, 2021. Retrieved October 31, 2020.
20. "Bioluminescence | Smithsonian Ocean". ocean.si.edu. 30 April 2018. Retrieved 2020-10-25.
21. Echeverri, Sebastian A; Miller, Audrey E; Chen, Jason; McQueen, Eden W; Plakke, Melissa; Spicer, Michelle; Hoke, Kim L; Stoddard, Mary Caswell; Morehouse, Nathan I (2021-05-21). "How Signaling Geometry Shapes the Efficacy and Evolution of Animal Communication Systems". Integrative and Comparative Biology. 61 (3): 787–813. doi:10.1093/icb/icab090. ISSN 1540-7063. PMID 34021338.
22. Jones, Te K.; Allen, Kathryne M.; Moss, Cynthia F. (December 9, 2021). "Communication with self, friends and foes in active-sensing animals". Journal of Experimental Biology. 224 (22). Bibcode:2021JExpB.224B2637J. doi:10.1242/jeb.242637. ISSN 0022-0949. PMID 34752625. S2CID 243940410.
23. Reichert, Michael S; Enriquez, Maya S; Carlson, Nora V (2021-03-21). "New Dimensions for Animal Communication Networks:Space and Time". Integrative and Comparative Biology. 61 (3): 814–824. doi:10.1093/icb/icab013. ISSN 1540-7063. PMID 33744960.
24. Ehrlich, Paul R.; David S. Dobkin & Darryl Wheye. ""Bird Voices" and "Vocal Development" from Birds of Stanford essays". Retrieved 9 Sep 2008.
25. Schwartzkopff, J (January 1977). "Auditory Communication in Lower Animals: Role of Auditory Physiology". Annual Review of Psychology. 28 (1): 61–84. doi:10.1146/annurev.ps.28.020177.000425. ISSN 0066-4308. PMID 324382.
26. Slabbekoorn, Hans; Smith, Thomas B (2002-04-29). "Bird song, ecology and speciation". Philosophical Transactions of the Royal Society B: Biological Sciences. 357 (1420): 493–503. doi:10.1098/rstb.2001.1056. ISSN 0962-8436. PMC 1692962. PMID 12028787.
27. Mikula, P.; Valcu, M.; Brumm, H.; Bulla, M.; Forstmeier, W.; Petrusková, T.; Kempenaers, B. & Albrecht, T. (2021). "A global analysis of song frequency in passerines provides no support for the acoustic adaptation hypothesis but suggests a role for sexual selection". Ecology Letters. 24 (3): 477–486. Bibcode:2021EcolL..24..477M. doi:10.1111/ele.13662. PMID 33314573.
28. Zuberbühler, Klaus (2001). "Predator-specific alarm calls in Campbell's monkeys, Cercopithecus campbelli" (PDF). Behavioral Ecology and Sociobiology. 50 (5): 414–422. Bibcode:2001BEcoS..50..414Z. doi:10.1007/s002650100383.
29. Boughman, J W (1998-02-07). "Vocal learning by greater spear-nosed bats". Proceedings of the Royal Society B: Biological Sciences. 265 (1392): 227–233. doi:10.1098/rspb.1998.0286. ISSN 0962-8452. PMC 1688873. PMID 9493408.
30. Price, Tabitha; Wadewitz, Philip; Cheney, Dorothy; Seyfarth, Robert; Hammerschmidt, Kurt; Fischer, Julia (2015-08-19). "Vervets revisited: A quantitative analysis of alarm call structure and context specificity". Scientific Reports. 5 (1): 13220. Bibcode:2015NatSR...513220P. doi:10.1038/srep13220. ISSN 2045-2322. PMC 4541072. PMID 26286236.
31. Jabr, Ferris (2017-05-12). "Can Prairie Dogs Talk? (Published 2017)". The New York Times. ISSN 0362-4331. Retrieved 2020-10-25.
32. "New Language Discovered: Prairiedogese". NPR.org. Retrieved 2020-10-25.
33. "YIPS, BARKS AND CHIRPS: THE LANGUAGE OF PRAIRIE DOGS". 2016-10-27. Archived from the original on 2016-10-27. Retrieved 2020-10-25.
34. "Prairie dogs' language decoded by scientists | CBC News". CBC. Retrieved 2020-10-25.
35. January 2006, Bjorn Carey 03 (3 January 2006). "Whales Found to Speak in Dialects". livescience.com. Retrieved 2020-10-25.{{cite web}}: CS1 maint: numeric names: authors list (link)
36. Weilgart, Linda; Whitehead, H. (1997-05-01). "Group-specific dialects and geographical variation in coda repertoire in South Pacific sperm whales". Behavioral Ecology and Sociobiology. 40 (5): 277–285. Bibcode:1997BEcoS..40..277W. doi:10.1007/s002650050343. ISSN 1432-0762. S2CID 11845118.
37. Ford, John Kenneth Baker (1984). Call Traditions and Dialects of Killer Whales (Orcinus Orca) in British Columbia. Retrospective Theses and Dissertations, 1919-2007 (Thesis). University of British Columbia. p. 284. doi:10.14288/1.0096602.
38. Souhaut M; Shields MW (2021). "Stereotyped whistles in southern resident killer whales". Aquatic Biology. 9. PeerJ: e12085. doi:10.7717/peerj.12085. PMC 8404572. PMID 34532160.
39. Ladich, Friedrich (2001). "Sound-generating and -detecting motor system in catfish: Design of swimbladder muscles in doradids and pimelodids". The Anatomical Record. 263 (3): 297–306. doi:10.1002/ar.1105. ISSN 1097-0185. PMID 11455539. S2CID 24896586.
40. ^ Searcy, William A. (March 2013). "Principles of Animal Communication. Second Edition. By Jack W. Bradbury and Sandra L. Vehrencamp. Sunderland (Massachusetts): Sinauer Associates. $99.95. xiv + 697 p.; ill. + C-1–C-6 (credits) + I-1–I-47 (index). ISBN: 978-0-87893-045-6. 2011". The Quarterly Review of Biology. 88 (1): 48. doi:10.1086/669301. ISSN 0033-5770.
41. "Prairie dog alarm calls encode labels about predator colors. By: N. Slobodchiko V · Andrea Paseka · Jennifer L. Verdolin. Published 31 December 2008 via Springer-Verlag" (PDF). Archived from the original (PDF) on 2 June 2021. Retrieved 3 June 2021.
42. Alarm calling in yellow-bellied marmots: I. The meaning of situationally variable alarm calls by Daneil T. Blumstein & Kenneth B. Armitage Department of Systematics and Ecology, University of Kansas. Published by Animal Behavior, via UCLA Life Sciences
43. Brown, Grant E.; Chivers, Douglas P.; Smith, R. Jan F. (1995-02-01). "Localized defecation by pike: a response to labelling by cyprinid alarm pheromone?". Behavioral Ecology and Sociobiology. 36 (2): 105–110. Bibcode:1995BEcoS..36..105B. doi:10.1007/BF00170715. ISSN 1432-0762. S2CID 31875357.
44. Brown, Grant; Adrian, James; Patton, Todd; Chivers, Douglas (Dec 2001). "Fathead minnows learn to recognize predator odor when exposed to concentrations of artificial alarm pheromone below their behavioral-response threshold". Canadian Journal of Zoology. 79 (12): 2239–2245. Bibcode:2001CaJZ...79.2239B. doi:10.1139/z01-194. ProQuest 220512135 – via ProQuest.
45. ^ "Acid Rain Is Totally So Last Century, Right? Not Exactly: A Canadian scientist explains how acid rain is still making its mark – IISD Experimental Lakes Area". 16 May 2018. Retrieved 2020-10-26.
46. du P. Bothma, J.; le Richet, E. A. N. (1995-04-01). "Evidence of the use of rubbing, scent-marking andscratching-posts by Kalahari leopards". Journal of Arid Environments. 29 (4): 511–517. Bibcode:1995JArEn..29..511D. doi:10.1016/S0140-1963(95)80023-9. ISSN 0140-1963.
47. Gosling, L. Morris; Roberts, S. Craig (2001). "Scent-marking by male mammals: cheat-proof signals to competitors and mates" (PDF). Advances in the Study of Behavior. 30: 169–217. doi:10.1016/S0065-3454(01)80007-3. ISBN 9780120045303.
48. du P. Bothma, J.; Richet, E.A.N. le (1995). "Evidence of the use of rubbing, scent-marking andscratching-posts by Kalahari leopards". Journal of Arid Environments. 29 (4): 511–517. Bibcode:1995JArEn..29..511D. doi:10.1016/s0140-1963(95)80023-9.
49. Clapham, Melanie. Chemical signalling in brown bears, ursus arctos : an assessment of scent marking strategies and social function. OCLC 1065010384.
50. Mech, L. David; Boitani, Luigi (2010-10-01). Wolves: Behavior, Ecology, and Conservation. University of Chicago Press. ISBN 978-0-226-51698-1.
51. "Electrocommunication". archive.fo. 2012-05-29. Archived from the original on 2012-05-29. Retrieved 2020-10-26.
52. Worm, Martin; Kirschbaum, Frank; von der Emde, Gerhard (2017-09-13). "Social interactions between live and artificial weakly electric fish: Electrocommunication and locomotor behavior of Mormyrus rume proboscirostris towards a mobile dummy fish". PLOS ONE. 12 (9): e0184622. Bibcode:2017PLoSO..1284622W. doi:10.1371/journal.pone.0184622. PMC 5597219. PMID 28902915.
53. Donati, Elisa; Worm, Martin; Mintchev, Stefano; van der Wiel, Marleen; Benelli, Giovanni; von der Emde, Gerhard; Stefanini, Cesare (2016-12-01). "Investigation of Collective Behaviour and Electrocommunication in the Weakly Electric Fish, Mormyrus rume, through a biomimetic Robotic Dummy Fish". Bioinspiration & Biomimetics. 11 (6): 066009. Bibcode:2016BiBi...11f6009D. doi:10.1088/1748-3190/11/6/066009. ISSN 1748-3190. PMID 27906686. S2CID 26047199.
54. Breed, Michael D.; Moore, Janice (2015-05-16). Animal Behavior. Academic Press. ISBN 978-0-12-801683-1.
55. Kuo, Zing (Jan 1, 1960). "Studies on the basic factors in animal fighting: VI. Inter-species coexistence in birds". The Journal of Genetic Psychology. 97: 15. ProQuest 1297122533 – via ProQuest.
56. Yamamoto, Maria Emilia; Araujo, Arrilton; Arruda, Maria de Fatima; Lima, Ana Karinne Moreira; Siqueira, Jose de Oliveira; Hattori, Wallisen Tadashi (2014-11-01). "Male and female breeding strategies in a cooperative primate". Behavioural Processes. Neotropical Behaviour. 109: 27–33. doi:10.1016/j.beproc.2014.06.009. ISSN 0376-6357. PMID 25010563. S2CID 205979349.
57. Dunbar, R. I. M. (2010-02-01). "The social role of touch in humans and primates: Behavioural function and neurobiological mechanisms". Neuroscience & Biobehavioral Reviews. Touch, Temperature, Pain/Itch and Pleasure. 34 (2): 260–268. doi:10.1016/j.neubiorev.2008.07.001. ISSN 0149-7634. PMID 18662717. S2CID 30450770.
58. "Ants' body odor, physical contact get worker ants working, study finds". news.stanford.edu. Retrieved 2020-10-26.
59. Sukhchuluun, Gansukh; Zhang, Xue-Ying; Chi, Qing-Sheng; Wang, De-Hua (2018-05-18). "Huddling Conserves Energy, Decreases Core Body Temperature, but Increases Activity in Brandt's Voles (Lasiopodomys brandtii)". Frontiers in Physiology. 9: 563. doi:10.3389/fphys.2018.00563. ISSN 1664-042X. PMC 5968109. PMID 29867585.
60. "Coral Reef Protection: What Are Coral Reefs? | Habitat Protection | US EPA". archive.epa.gov. Retrieved 2020-10-26.
61. Cocroft, Reginald (October 2001). "Vibrational Communication and the Ecology of Group-Living, Herbivorous Insects". Integrative and Comparative Biology. 41: 1215–1221 – via Oxford Academic.
62. Hill, Peggy (October 2001). "Vibration and Animal Communication: A Review". Integrative and Comparative Biology. 41: 1135–1142 – via Oxford Academic.
63. Narins, Peter (April 1990). "Seismic Communication in Anuran Amphibians". BioScience. 40 (4): 268–274. doi:10.2307/1311263. JSTOR 1311263 – via Oxford Academic.
64. Kardong, Kenneth V.; Mackessy, Stephen P. (1991). "The Strike Behavior of a Congenitally Blind Rattlesnake". Journal of Herpetology. 25 (2): 208–211. doi:10.2307/1564650. ISSN 0022-1511. JSTOR 1564650.
65. Bakken, George S.; Krochmal, Aaron R. (2007-08-15). "The imaging properties and sensitivity of the facial pits of pitvipers as determined by optical and heat-transfer analysis". Journal of Experimental Biology. 210 (16): 2801–2810. Bibcode:2007JExpB.210.2801B. doi:10.1242/jeb.006965. ISSN 0022-0949. PMID 17690227. S2CID 25037159.
66. Pough, F.; Andrews, Robin; Cadle, John; Crump, Martha; Savitzky, Alan; Wells, Kentwood (2003-01-01). Herpetology (Third ed.). New York: Prentice Hall. p. 726.
67. ^ Gracheva, Elena O.; Ingolia, Nicholas T.; Kelly, Yvonne M.; Cordero-Morales, Julio F.; Hollopeter, Gunther; Chesler, Alexander T.; Sánchez, Elda E.; Perez, John C.; Weissman, Jonathan S.; Julius, David (April 2010). "Molecular basis of infrared detection by snakes". Nature. 464 (7291): 1006–1011. Bibcode:2010Natur.464.1006G. doi:10.1038/nature08943. ISSN 1476-4687. PMC 2855400. PMID 20228791.
68. Kürten, L.; Schmidt, U.; Schäfer, K. (1984-06-01). "Warm and cold receptors in the nose of the vampire bat Desmodus rotundas". Naturwissenschaften. 71 (6): 327–328. Bibcode:1984NW.....71..327K. doi:10.1007/BF00396621. ISSN 1432-1904. PMID 6472483. S2CID 31899356.
69. Wilson, Ben; Dill, Lawrence M. (March 2002). "Pacific herring respond to stimulated odontocete echolocation sounds". Canadian Journal of Fisheries and Aquatic Sciences. 59 (3): 542. Bibcode:2002CJFAS..59..542W. doi:10.1139/f02-029.
70. Haldar, Vivekananda; Chakraborty, Niladri (2017-07-01). "A novel evolutionary technique based on electrolocation principle of elephant nose fish and shark: fish electrolocation optimization". Soft Computing. 21 (14): 3827–3848. doi:10.1007/s00500-016-2033-1. ISSN 1433-7479. S2CID 207013387.
71. Jones, Gareth (2005-07-12). "Echolocation". Current Biology. 15 (13): R484 – R488. Bibcode:2005CBio...15.R484J. doi:10.1016/j.cub.2005.06.051. ISSN 0960-9822. PMID 16005275. S2CID 235311777.
72. Vanderelst, Dieter; Steckel, Jan; Boen, Andre; Peremans, Herbert; Holderied, Marc W (2016-08-02). Eichenbaum, Howard (ed.). "Place recognition using batlike sonar". eLife. 5: e14188. doi:10.7554/eLife.14188. ISSN 2050-084X. PMC 4970868. PMID 27481189.
73. Stritih, Natasa; Kosi, Alenka (Nov 2017). "Olfactory signaling of aggressive intent in male-male contests of cave crickets (Tropglophilus neglectus; Orthoptera: Rhaphidophoridae)". PLOS ONE. 12 (11): e0187512. Bibcode:2017PLoSO..1287512S. doi:10.1371/journal.pone.0187512. PMC 5675388. PMID 29112984. ProQuest 1961423777.
74. Clutton-Brock, Tim (2016-05-31). Mammal Societies. John Wiley & Sons. ISBN 978-1-119-09532-3.
75. Jenssen, Thomas A.; Orrell, Kimberly S.; Lovern, Matthew B. (2000). "Sexual Dimorphisms in Aggressive Signal Structure and Use by a Polygynous Lizard, Anolis carolinensis". Copeia. 2000 (1): 140–149. doi:10.1643/0045-8511(2000)2000[0140:SDIASS]2.0.CO;2. ISSN 0045-8511. JSTOR 1448245. S2CID 9813895.
76. Bowen, Jon; Heath, Sarah (2005). Behaviour problems in small animals : practical advice for the veterinary team. Edinburgh: Elsevier Saunders. p. 127. ISBN 978-0702027673. Retrieved 16 June 2022.
77. Cäsar, Cristiane; Byrne, Richard W.; Hoppitt, William; Young, Robert J.; Zuberbühler, Klaus (2012-08-01). "Evidence for semantic communication in titi monkey alarm calls". Animal Behaviour. 84 (2): 405–411. doi:10.1016/j.anbehav.2012.05.010. ISSN 0003-3472. S2CID 45749417.
78. Sasaki, Takao; Hölldobler, Bert; Millar, Jocelyn G.; Pratt, Stephen C. (2014-09-15). "A context-dependent alarm signal in the ant Temnothorax rugatulus". Journal of Experimental Biology. 217 (18): 3229–3236. doi:10.1242/jeb.106849. hdl:2286/R.I.28102. ISSN 0022-0949. PMID 25013103. S2CID 2102542.
79. ^ Hasson, O. (October 1991). "Pursuit-deterrent signals: communication between prey and predator". Trends in Ecology & Evolution. 6 (10): 325–329. Bibcode:1991TEcoE...6..325H. doi:10.1016/0169-5347(91)90040-5. ISSN 0169-5347. PMID 21232498.
80. "Map of Life | Vibrational communication in animals". Archived from the original on 2020-11-29. Retrieved 2020-10-28.
81. Tauzin, Tibor; Csík, Andor; Kis, Anna; Topál, József (2015). "What or where? The meaning of referential human pointing for dogs (Canis familiaris)" (PDF). Journal of Comparative Psychology. 129 (4): 334–338. doi:10.1037/a0039462. ISSN 1939-2087. PMID 26147704.
82. Morris, Desmond (1958). "The Comparative Ethology of Grassfinches (erythrurae) and Mannikins (amadinae)". Proceedings of the Zoological Society of London. 131 (3): 389–439. doi:10.1111/j.1096-3642.1958.tb00695.x. ISSN 1469-7998.
83. discussed at length by Richard Dawkins under the subject of his book The Selfish Gene
84. Chandler, Christopher H.; Ofria, Charles; Dworkin, Ian (2013). "Runaway Sexual Selection Leads to Good Genes". Evolution. 67 (1): 110–119. doi:10.1111/j.1558-5646.2012.01750.x. ISSN 0014-3820. JSTOR 23327705. PMID 23289565. S2CID 15929198.
85. ^ V. M. Janik, L. S. Sayigh, and R. S. Wells: "Signature whistle shape conveys identity information to bottlenose dolphins", Proceedings of the National Academy of Sciences, vol. 103 no 21, May 23, 2006
86. ^ Null (September 25, 2023). "Motherese in bottlenose dolphins". Proceedings of the National Academy of Sciences of the United States of America. Retrieved December 26, 2023.
87. ^ Sayigh, Laela S.; El Haddad, Nicole; Tyack, Peter L.; Janik, Vincent M.; Wells, Randall S.; Jensen, Frants H. (4 July 2023). "Bottlenose dolphin mothers modify signature whistles in the presence of their own calves". Proceedings of the National Academy of Sciences. 120 (27). National Academy of Sciences: e2300262120. Bibcode:2023PNAS..12000262S. doi:10.1073/pnas.2300262120. hdl:10023/27844. PMC 10318978. PMID 37364108.
88. Gleason, Jean Berko., and Nan Bernstein Ratner. "The Development of Language", 8th ed. Pearson, 2013.
89. Smith, Eric Alden (2017-09-29). Evolutionary Ecology and Human Behavior. Routledge. ISBN 978-1-351-52132-1.
90. Hare, Brian; Call, Josep; Tomasello, Michael (1998-01-01). "Communication of Food Location Between Human and Dog (Canis Familiaris)". Evolution of Communication. 2 (1): 137–159. doi:10.1075/eoc.2.1.06har. ISSN 1387-5337.
91. Tauzin, Tibor; Csík, Andor; Kis, Anna; Topál, József (November 2015). "What or where? The meaning of referential human pointing for dogs (Canis familiaris)". Journal of Comparative Psychology. 129 (4): 334–338. doi:10.1037/a0039462. ISSN 1939-2087. PMID 26147704.
92. Guo, Kun; Meints, Kerstin; Hall, Charlotte; Hall, Sophie; Mills, Daniel (2009-05-01). "Left gaze bias in humans, rhesus monkeys and domestic dogs". Animal Cognition. 12 (3): 409–418. doi:10.1007/s10071-008-0199-3. ISSN 1435-9456. PMID 18925420. S2CID 5661394.
93. "Do animals have language? - Michele Bishop". TED Ed. 10 September 2015. Retrieved 11 September 2015.
94. Thompson, Roger K. R.; Oden, David L. (2000). "Categorical Perception and Conceptual Judgments by Nonhuman Primates: The Paleological Monkey and the Analogical Ape". Cognitive Science. 24 (3): 363–396. doi:10.1207/s15516709cog2403_2. ISSN 1551-6709.
95. "Rudiments of Language Discovered in Monkeys". Wired. ISSN 1059-1028. Retrieved 2020-10-31.
96. Real, Leslie A. (1994-12-15). Behavioral Mechanisms in Evolutionary Ecology. University of Chicago Press. ISBN 978-0-226-70595-8.
97. Gergely, Anna; Compton, Anna; Newberry, Ruth; Miklósi, Ádám (Apr 2016). "Social Interaction with an "Unidentified Moving Object" Elicits A-Not_B Error in Domestic Dogs". PLOS ONE. 11 (4): e0151600. Bibcode:2016PLoSO..1151600G. doi:10.1371/journal.pone.0151600. PMC 4830451. PMID 27073867. S2CID 16369609.

External links

• Animal Communicator – Documentary
• Zoosemiotics: animal communication on the web Archived 2005-10-25 at the Wayback Machine
• The Animal Communication Project
• International Bioacoustics Council research on animal language.
• Max Planck Institute of Animal Behavior research on animal vocalizations.
• Animal Sounds different animal sounds to listen and download.
• The British Library Sound Archive Archived 2010-07-22 at the Wayback Machine contains over 150,000 recordings of animal sounds and natural atmospheres from all over the world.

• Animal communication
• Communication
• Zoosemiotics
• Interspecies communication