Biology:Animal language

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Short description: Complex animal communication
Parrots (Australian ringneck)

Animal languages are forms of non-human animal communication that show similarities to human language.[1] Animals communicate through a variety of signs, such as sounds or movements. Signing among animals may be considered a form of language if the inventory of signs is large enough. The signs are relatively arbitrary, and the animals seem to produce them with a degree of volition (as opposed to relatively automatic conditioned behaviors or unconditioned instincts, usually including facial expressions). In experimental tests, animal communication may also be evidenced through the use of lexigrams by chimpanzees and bonobos.

Many researchers argue that animal communication lacks a key aspect of human language, the creation of new patterns of signs under varied circumstances. Humans, by contrast, routinely produce entirely new combinations of words. Some researchers, including the linguist Charles Hockett, argue that human language and animal communication differ so much that the underlying principles are unrelated.[2] Accordingly, linguist Thomas A. Sebeok has proposed to not use the term "language" for animal sign systems.[3] However, other linguists and biologists, including Marc Hauser, Noam Chomsky, and W. Tecumseh Fitch, assert an evolutionary continuum exists between the communication methods of animal and human language.[4]

Aspects of human language

Human and ape, in this case Claudine André with a bonobo.

Human language contains the following properties. Some experts argue these properties separate human language from animal communication:[5]

  • Arbitrariness: There is usually no rational relationship between a sound or sign and its meaning.[6] For example, there is nothing intrinsically house-like about the word "house".
  • Discreteness: Language is composed of small, separate, and repeatable parts (discrete units, e.g. morphemes) that are used in combination to create meaning.
  • Displacement: Language can be used to communicate about things that are not in the immediate vicinity either spatially or temporally.[6]
  • Duality of patterning: The smallest meaningful units (words or morphemes) consist of sequences of units without meaning (sounds or phonemes).[6] This is also referred to as double articulation.
  • Productivity: Users can understand and create an indefinitely large number of utterances.[6]
  • Semanticity: Specific signals have specific meanings.[6]

Research with apes, like that of Francine Patterson with Koko[7] (gorilla) or Allen and Beatrix Gardner with Washoe[8][9] (chimpanzee), suggested that apes are capable of using language that meets some of these requirements, including arbitrariness, discreteness, and productivity.[10]

In the wild, chimpanzees have been seen "talking" to each other when warning about approaching danger. For example, if one chimpanzee sees a snake, he makes a low, rumbling noise, signaling for all the other chimps to climb into nearby trees.[11] In this case, the chimpanzees' communication does not indicate displacement, as it is entirely contained to an observable event.

Arbitrariness has been noted in meerkat calls; bee dances demonstrate elements of spatial displacement; and cultural transmission has possibly occurred through language between the bonobos named Kanzi and Panbanisha.[12]

Human language may also not be completely "arbitrary." Research has shown that almost all humans naturally demonstrate limited crossmodal perception (e.g. synesthesia) and multisensory integration, as illustrated by the Kiki and Bouba study.[13][14] Other recent research has tried to explain how the structure of human language emerged, comparing two different aspects of hierarchical structure present in animal communication and proposing that human language arose out of these two separate systems.[15]

Claims that animals have language skills akin to humans however, are extremely controversial. In his book The Language Instinct,[16] Steven Pinker illustrates that claims of chimpanzees acquiring language are exaggerated and rest on very limited or specious evidence.[16]

The American linguist Charles Hockett theorized that there are sixteen features of human language that distinguish human communication from that of animals. He called these the design features of language. The features mentioned below have so far been found in all spoken human languages, and at least one is missing from any other animal communication system.

  • Vocal-auditory channel: Sounds are emitted from the mouth and perceived by the auditory system.[6] While this applies to many animal communication systems, there are many exceptions, such as those relying on visual communication. One example is cobras extending the ribs behind their heads to send the message of intimidation or of feeling threatened.[17] In humans, sign languages provide many examples of fully formed languages that use a visual channel.
  • Broadcast transmission and directional reception:[6] This requires that the recipient can tell the direction that the signal comes from and thus the originator of the signal.
  • Rapid fading (transitory nature): The signal lasts a short time.[6] This is true of all systems involving sound. It does not take into account audio recording technology and is also not true for written language. It tends not to apply to animal signals involving chemicals and smells which often fade slowly. For example, a skunk's smell, produced in its glands, lingers to deter a predator from attacking.[18]
  • Interchangeability: All utterances that are understood can be produced.[6] This is different from some communication systems where, for example, males produce one set of behaviors and females another and they are unable to interchange these messages so that males use the female signal and vice versa. For example, Heliothine moths have differentiated communication: females are able to send a chemical to indicate preparedness to mate, while males cannot send the chemical.[19]
  • Total feedback: The sender of a message is aware of the message being sent.[6]
  • Specialization: The signal produced is intended for communication and is not due to another behavior.[6] For example, dog panting is a natural reaction to being overheated, but is not produced to specifically relay a particular message.
  • Semanticity: There is some fixed relationship between a signal and a meaning.[6]

Primates

Humans are able to distinguish real words from fake words based on the phonological order of the word itself. In a 2013 study, baboons were shown to have this skill as well. The discovery has led researchers to believe that reading is not as advanced a skill as previously believed, but instead based on the ability to recognize and distinguish letters from one another. The experimental setup consisted of six young adult baboons, and results were measured by allowing the animals to use a touch screen and select whether or not the displayed word was a real word, or a non-word such as "dran" or "telk". The study lasted for six weeks, with approximately 50,000 tests completed in that time. The researchers minimized common bigrams, or combinations of two letters, in non-words, and maximized them in real words. Further studies will attempt to teach baboons how to use an artificial alphabet.[20]

In a 2016 study, a team of biologists from several universities concluded that macaques possess vocal tracts physically capable of speech, "but lack a speech-ready brain to control it".[21][22]

Non-primates

Among the most studied examples of non-primate languages are:

Birds

  • Bird songs: Songbirds can be highly articulate. Grey parrots along with macaws are well known for their ability to mimic human language, and at least one specimen, Alex, appeared able to answer a number of simple questions about objects he was presented with, such as answering simple mathematical equations and identifying colors. Parrots, hummingbirds and songbirds display vocal learning patterns.[citation needed]

Insects

  • Bee dancing: Used to communicate direction and distance of food source in many species of bees. In 2023 James C. Nieh, Associate Dean and Professor of Biology with the University of California, San Diego performed an experiment to determine if the dances of bees were innate skills that bees possessed or developed through observation of older bees within their hive.[23] The research group determined that the dance bees performed was to some degree innate, but the consistency and accuracy of the dance was a skill passed down by older bees. Although the experimental hive that contained only workers of the same age developed better accuracy when conveying angle and direction as they got older, their ability to communicate distance never reached the level of the control beehives.[23]

Mammals

  • African forest elephants: Cornell University's Elephant Listening Project[24] began in 1999 when Katy Payne began studying the calls of African forest elephants in Dzanga National Park in the Central African Republic. Andrea Turkalo has continued Payne's work in Dzanga National Park by observing elephant communication.[24] For nearly 20 years, Turkalo has spent the majority of her time using a spectrogram to record the noises that the elephants make. After extensive observation and research, she has been able to recognize elephants by their voices. Researchers hope to translate these voices into an elephant dictionary, but this will likely not occur for many years.[why?] Because elephant calls are often made at very low frequencies, the spectrogram is designed to detect lower frequencies than humans can perceive, allowing Turkalo to better understand the elephants' noisemaking. Cornell's research on African forest elephants has challenged the idea that humans are considerably better at using language than animals, and that animals only have a small set of information they can convey to others. As Turkalo explained, "many of their calls are in some ways similar to human speech."[25]
  • Mustached bats: Since these animals spend most of their lives in the dark, they rely heavily on their auditory system to communicate, including via echolocation and using calls to locate each other. Studies have shown that mustached bats use a wide variety of calls to communicate with one another. These calls include 33 different sounds, or "syllables", that the bats either use alone or combine in various ways to form composite syllables.[26]
  • Prairie dogs: Con Slobodchikoff studied prairie dog communication and discovered that they use different alarm calls and escape behaviors for different species of predators. Their calls transmit semantic information, which was demonstrated when playbacks of alarm calls in the absence of predators led to escape behavior appropriate for the types of predators associated with the calls. The alarm calls also contain descriptive information about the general size, color, and speed of the predator.[27]

Aquatic mammals

  • Bottlenose dolphins: Dolphins can hear one another up to 6 miles apart underwater.[28] Researchers observed a mother dolphin successfully communicating with her baby using a telephone. It appeared that both dolphins knew who they were speaking with and what they were speaking about. Not only do dolphins communicate via nonverbal cues, they also seem to chatter and respond to other dolphins' vocalizations.[29]
Spectrogram of humpback whale vocalizations. Detail is shown for the first 24 seconds of the 37 second humpback whale "song" recording. The whale songs and echolocation "clicks" are visible as horizontal striations and vertical sweeps respectively.
  • Whales: Two groups of whales, the humpback whale and a subspecies of blue whale found in the Indian Ocean, are known to produce repeated sounds at varying frequencies, known as whale songs. Male humpback whales perform these vocalizations only during the mating season, and so it is surmised the purpose of songs is to aid sexual selection. Humpbacks also make a sound called a feeding call, which is five to ten seconds in length at a nearly constant frequency. Humpbacks generally feed cooperatively by gathering in groups, swimming underneath shoals of fish and lunging up vertically through the fish and out of the water together. Prior to these lunges, whales make their feeding call. The exact purpose of the call is not known, but research suggests that fish react to it. When the sound was played back to them, a group of herring responded to the sound by moving away from the call, even though no whale was present.[citation needed]
  • Sea lions: Since 1971, Ronald J. Schusterman and his research associates have studied sea lions' cognitive ability. They have discovered that sea lions are able to recognize relationships between stimuli based on similar functions or connections made with their peers, rather than only the stimuli's common features. This is called equivalence classification. This ability to recognize equivalence may be a precursor to language.[30] Research is currently being conducted at the Pinniped Cognition & Sensory Systems Laboratory to determine how sea lions form these equivalence relations. Sea lions have also been proven to understand simple syntax and commands when taught an artificial sign language similar to one used with primates.[31] The sea lions studied were able to learn and use a number of syntactic relations between the signs they were taught, such as how the signs should be arranged in relation to each other. However, the sea lions rarely used the signs semantically or logically.[32] In the wild it is thought that sea lions use reasoning skills associated with equivalence relations in order to make important decisions that can affect their survival, e.g. recognizing friends and relatives or avoiding enemies and predators.[30] Sea lions use various postural positions and a range of barks, chirps, clicks, moans, growls and squeaks to communicate.[33] It has yet to be proven that sea lions use echolocation as a means of communication.[34]

The effects of learning on auditory signaling in these animals is of interest to researchers. Several investigators have pointed out that some marine mammals appear to have the capacity to alter both the contextual and structural features of their vocalizations as a result of experience. Janik and Slater have stated that learning can modify vocalizations in one of two ways, by influencing the context in which a particular call is used, or by altering the acoustic structure of the call itself.[35] Male California sea lions can learn to inhibit their barking in the presence of any male dominant to them, but vocalize normally when dominant males are absent.[36] The different call types of gray seals can be selectively conditioned and controlled by different cues,[37] and the use of food reinforcement can also modify vocal emissions. A captive male harbor seal named Hoover demonstrated a case of vocal mimicry, but similar observations have not been reported since. Still shows that under the right circumstances pinnipeds may use auditory experience in addition to environmental consequences such as food reinforcement and social feedback to modify their vocal emissions.[citation needed]

In a 1992 study, Robert Gisiner and Schusterman conducted experiments in which they attempted to teach syntax to a female California sea lion named Rocky.[32] Rocky was taught signed words, then she was asked to perform various tasks dependent on word order after viewing a signed instruction. It was found that Rocky was able to determine relations between signs and words, and form basic syntax.[32] A 1993 study by Schusterman and David Kastak found that the California sea lion was capable of understanding abstract concepts such as symmetry, sameness and transitivity. This suggests that equivalence relations can form without language.

The distinctive sounds of sea lions are produced both above and below water. To mark territory, sea lions "bark", with non-alpha males making more noise than alphas. Although females also bark, they do so less frequently and most often in connection with birthing pups or caring for their young. Females produce a highly directional bawling vocalization, the pup attraction call, which helps mothers and pups locate one another. As noted in Animal Behavior, their amphibious lifestyle has made them need acoustic communication for social organization while on land.

Sea lions can hear frequencies between 100 Hz and 40,000 Hz, and vocalize from 100 to 10,000 Hz.[38]

Mollusks

  • Caribbean reef squid have been shown to communicate using a variety of color, shape, and texture changes. Squid are capable of rapid changes in skin color and pattern through nervous system control of chromatophores.[39] In addition to camouflage and appearing larger in the face of a threat, squid use color, patterns, and flashing to communicate with one another in various courtship rituals. Caribbean reef squid can send one message via color patterns to a squid on their right, while they send another message to a squid on their left.[40][41]

Fish

  • Freshwater Elephant Fish have been observed to have their own language[42][43]
  • Mexican Tetra have been observed communicating with a series of clicks, and have also been observed to have regional accents[44]

Comparison of "animal language" and "animal communication"

It is worth distinguishing "animal language" from "animal communication", although there is some comparative interchange in certain cases (e.g. Cheney & Seyfarth's vervet monkey call studies).[45] Animal language typically does not include bee dancing, bird song, whale song, dolphin signature whistles, prairie dogs, nor the communicative systems found in most social mammals.[citation needed] The features of language as listed above are a dated formulation by Hockett in 1960. Through this formulation Hockett made one of the earliest attempts to break down features of human language for the purpose of applying Darwinian gradualism. Although an influence on early animal language efforts (see below), it is no longer considered the key architecture at the core of animal language research.[citation needed]

Clever Hans, an Orlov Trotter horse that was claimed to have been able to perform arithmetic and other intellectual tasks

Animal language results are controversial for several reasons (for a related controversy, see also Clever Hans). In the 1970s, John C. Lilly was attempting to "break the code": to fully communicate ideas and concepts with wild populations of dolphins so that he could share human and dolphin culture, history, and more. This effort failed. Early chimpanzee work was with chimpanzee infants raised as if they were human; a test of the nature vs. nurture hypothesis.[citation needed] Chimpanzees have a laryngeal structure very different from that of humans, and it has been suggested that chimpanzees are not capable of voluntary control of their breathing, although better studies are needed to accurately confirm this. This combination is thought to make it very difficult for the chimpanzees to reproduce the vocal intonations required for human language. Researchers eventually moved towards a gestural (sign language) modality, as well as keyboard devices laden with buttons adorned with symbols (known as "lexigrams") that the animals could press to produce artificial language. Other chimpanzees learned by observing human subjects performing the task.[citation needed] This latter group of researchers studying chimpanzee communication through symbol recognition (keyboard) as well as through the use of sign language (gestural), are on the forefront of communicative breakthroughs in the study of animal language, and they are familiar with their subjects on a first name basis: Sarah, Lana, Kanzi, Koko, Sherman, Austin and Chantek.[citation needed]

Perhaps the best known critic of animal language is Herbert Terrace. Terrace's 1979 criticism using his own research with the chimpanzee Nim Chimpsky[46][47] was scathing and basically spelled the end of animal language research in that era, most of which emphasized the production of language by animals. In short, he accused researchers of over-interpreting their results, especially as it is rarely parsimonious to ascribe true intentional "language production" when other simpler explanations for the behaviors (gestural hand signs) could be put forth. Also, his animals failed to show generalization of the concept of reference between the modalities of comprehension and production; this generalization is one of many fundamental ones that are trivial for human language use. The simpler explanation according to Terrace was that the animals had learned a sophisticated series of context-based behavioral strategies to obtain either primary (food) or social reinforcement, behaviors that could be over-interpreted as language use.

In 1984 Louis Herman published an account of artificial language in the bottlenosed dolphin in the journal Cognition.[48] A major difference between Herman's work and previous research was his emphasis on a method of studying language comprehension only (rather than language comprehension and production by the animal(s)), which enabled rigorous controls and statistical tests, largely because he was limiting his researchers to evaluating the animals' physical behaviors (in response to sentences) with blinded observers, rather than attempting to interpret possible language utterances or productions. The dolphins' names here were Akeakamai and Phoenix.[48] Irene Pepperberg used the vocal modality for language production and comprehension in a grey parrot named Alex in the verbal mode,[49][50][51][52] and Sue Savage-Rumbaugh continues to study bonobos[53][54] such as Kanzi and Panbanisha. R. Schusterman duplicated many of the dolphin results in his California sea lions ("Rocky"), and came from a more behaviorist tradition than Herman's cognitive approach. Schusterman's emphasis is on the importance on a learning structure known as equivalence classes.[55][56]

However, overall, there has not been any meaningful dialog between the linguistics and animal language spheres, despite capturing the public's imagination in the popular press. Also, the growing field of language evolution is another source of future interchange between these disciplines. Most primate researchers tend to show a bias toward a shared pre-linguistic ability between humans and chimpanzees, dating back to a common ancestor, while dolphin and parrot researchers stress the general cognitive principles underlying these abilities. More recent related controversies regarding animal abilities include the closely linked areas of theory of mind, Imitation (e.g. Nehaniv & Dautenhahn, 2002),[57] Animal Culture (e.g. Rendell & Whitehead, 2001),[58] and Language Evolution (e.g. Christiansen & Kirby, 2003).[59]

There has been a recent emergence in animal language research which has contested the idea that animal communication is less sophisticated than human communication. Denise Herzing has done research on dolphins in the Bahamas whereby she created a two-way conversation via a submerged keyboard.[60] The keyboard allows divers to communicate with wild dolphins. By using sounds and symbols on each key the dolphins could either press the key with their nose or mimic the whistling sound emitted in order to ask humans for a specific prop. This ongoing experiment has shown that in non-linguistic creatures sophisticated and rapid thinking does occur despite our previous conceptions of animal communication. Further research done with Kanzi using lexigrams has strengthened the idea that animal communication is much more complex than once thought.[61]

See also

Researchers

Animals

References

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  60. ↑ Herzing, Denise L.; Delfour, Fabienne; Pack, Adam A. (2012). "Responses of human-habituated wild Atlantic Spotted Dolphins to play behaviours using a two-way human/dolphin interface". International Journal of Comparative Psychology 25 (2): 137–165. doi:10.46867/IJCP.2012.25.02.02. http://www.wilddolphinproject.org/wp-content/uploads/2011/11/Herzing_etal-copy-2.pdf. 
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Further reading

  • Bickerton, D. (2005). Language evolution: a brief guide for linguists. link
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  • Fitch, W.T.; Hauser, M.D. (2004). "Computational constraints on syntactic processing in a nonhuman primate". Science 303 (5656): 377–380. doi:10.1126/science.1089401. PMID 14726592. Bibcode: 2004Sci...303..377F. http://eamusic.dartmouth.edu/~larry/music1052008/grad_student_readings/sievers/Primate_Constraints.pdf. 
  • Fouts, R. S. (1973). "Acquisition and testing of gestural signs in four young chimpanzees". Science 180 (4089): 978–80. doi:10.1126/science.180.4089.978. PMID 17735931. Bibcode: 1973Sci...180..978F. 
  • "Overlooked evidence for semantic compositionality and signal reduction in wild chimpanzees (Pan troglodytes)". Animal Cognition 25 (3): 631–643. 2022. doi:10.1007/s10071-021-01584-3. PMID 34822011. 
  • Gardner R. Allen and Gardner Beatrice T. (1980) Comparative psychology and language acquisition. In Thomas A. Sebok and Jean-Umiker-Sebok (eds.): Speaking of Apes: A Critical Anthology of Two-Way Communication with Man. New York: Plenum Press, pp. 287–329.
  • Gomez, R.L; Gerken, L. (2000). "Infant artificial language learning and language acquisition". Trends in Cognitive Sciences 4 (5): 178–186. doi:10.1016/S1364-6613(00)01467-4. PMID 10782103. 
  • Goodall, J. (1964). "Tool Using and Aimed Throwing in a Community of Free-Living Chimpanzees". Nature 201 (4926): 1264–1266. doi:10.1038/2011264a0. PMID 14151401. Bibcode: 1964Natur.201.1264G. 
  • Hauser, M.D.; Chomsky, N.; Fitch, W.T. (2002). "The faculty of language: what is it, who has it, and how did it evolve?". Science 298 (5598): 1569–1579. doi:10.1126/science.298.5598.1569. PMID 12446899. 
  • Hayes, C. (1951). The Ape in Our House. New York: Harper & Row.
  • Herman, L. M.; Forestell, P. H. (1985). "Reporting presence or absence of named objects by a language-trained dolphin". Neuroscience and Biobehavioral Reviews 9 (4): 667–691. doi:10.1016/0149-7634(85)90013-2. PMID 4080284. 
  • Herman, L. M. Kuczaj; Holder, M. D.; Holder, Mark D. (1993). "Responses to anomalous gestural sequences by a language-trained dolphin: Evidence for processing of semantic relations and syntactic information". Journal of Experimental Psychology: General 122 (2): 184–194. doi:10.1037/0096-3445.122.2.184. PMID 8315399. 
  • Hockett, C. (1960). "The origin of speech". Scientific American 203 (3): 88–96. doi:10.1038/scientificamerican0960-88. PMID 14402211. Bibcode: 1960SciAm.203c..88H. 
  • Holder, M. D., Herman, L. M. & Kuczaj, S. III (1993). A bottlenosed dolphin's responses to anomalous gestural sequences expressed within an artificial gestural language. In H. R. Roitblat, L. M. Herman & P.E. Nachtigall (Eds): Language and Communication: Comparative Perspectives, 299–308. Hillsdale, NJ: Lawrence Erlbaum.
  • Hurford J.R., Studdert-Kennedy, M., & Knight, C. (Eds.) (1998) Approaches to the evolution of language: Social and cognitive bases. Cambridge: Cambridge University Press.
  • Huxley, Julian & Ludwig Koch (photographs by Ylla) 1938. Animal language. Text by Julian Huxley, long-playing record of animal language by Ludwig Koch. London, Country Life. Reprinted and republished by Grosset & Dunlap, New York 1964. Record in the 1964 reissue is by Columbia Special Products, 33 1/3 rpm, small format, ZVT 88894. Side 1 contains Sounds at the Zoo (presumably Zoological Society of London) and African sounds; side 2 African sounds continued.
  • Kako, E. (1999). "Elements of syntax in the systems of three language-trained animals". Animal Learning & Behavior 27: 1–14. doi:10.3758/BF03199424. 
  • Kanwal, J.S.; Matsumura, S.; Ohlemiller, K.; Suga, N. (1994). "Analysis of acoustic elements and syntax in communication sounds emitted by mustached bats". Journal of the Acoustical Society of America 94 (3): 1229–1254. doi:10.1121/1.410273. PMID 7962992. Bibcode: 1994ASAJ...96.1229K. 
  • Kellogg, W.N., & Kellogg, L.A. (1933). The ape and the child. New York: Whittlesey House (McGraw-Hill).
  • Knight, C., Studdert-Kennedy, M., Hurford, J.R. (Eds.) (2000). The evolutionary emergence of language: Social function and the origins of linguistic form. Cambridge: Cambridge University Press.
  • Kohts. N. (1935). Infant ape and human child. Museum Darwinianum, Moscow.
  • Ladygina-Kohts, N.N, & de Waal, F.B.M. (2002). Infant Chimpanzee and Human Child: A Classic 1935 Comparative Study of Ape Emotions and Intelligence (Tr: B. Vekker). New York: Oxford University Press.
  • Lenneberg, E.H. (1971). "Of language, knowledge, apes, and brains". Journal of Psycholinguistic Research 1 (1): 1–29. doi:10.1007/BF01066934. PMID 24197536. 
  • Miles, H.L. (1990) "The cognitive foundations for reference in a signing orangutan" in S.T. Parker and K.R. Gibson (eds.) "Language" and intelligence in monkeys and apes: Comparative Developmental Perspectives. Cambridge Univ. Press.
  • Pinker, S. (1984). Language Learnability and Language Development. Cambridge, MA: Harvard University Press. Reprinted in 1996 with additional commentary.
  • Pinker, S.; Bloom, P. (1990). "Natural language and natural selection". Behavioral and Brain Sciences 13 (4): 707–784. doi:10.1017/S0140525X00081061. 
  • Plooij, F.X. (1978). "Some basic traits of language in wild chimpanzees?" in A. Lock (ed.) Action, Gesture and Symbol. New York: Academic Press.
  • Premack, D. (1971). "Language in a chimpanzee?". Science 172 (3985): 808–822. doi:10.1126/science.172.3985.808. PMID 5572906. Bibcode: 1971Sci...172..808P. 
  • Roitblat, H.R., Herman, L.M. & Nachtigall, P.E. (Eds.)(1993). Language and Communication: Comparative Perspectives, 299–308. Hillsdale, NJ: Lawrence Erlbaum.
  • Rumbaugh Duane M. (1980) Language behavior of apes. In Thomas A. Sebok and Jean-Umiker-Sebok(eds.): Speaking of Apes: A Critical Anthology of Two- Way Communication with Man. New York: Plenum Press, pp. 231–259.
  • Savage-Rumbaugh, E.S.; McDonald, K.; Sevcik, R.A.; Hopkins, W.D.; Rupert, E (1986). "Spontaneous symbol acquisition and communicative use by pygmy chimpanzees (Pan paniscus)". Journal of Experimental Psychology: General 115 (3): 211–235. doi:10.1037/0096-3445.115.3.211. PMID 2428917. 
  • Sayigh, L.S., Tyack, P.L., Wells, R.S. & Scott, M.D. (1990). Signature whistles of free-ranging bottlenose dolphins (Tursiops truncatus): stability and mother-offspring comparisons. Behavioral Ecology and Sociobiology, 247–260.
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  • Schusterman, R. J.; Kastak, D. (1993). "A California Sea-Lion (Zalaphos californianus) is capable of forming equivalence relations". The Psychological Record 43 (4): 823–839. doi:10.1007/BF03395915. 
  • Schusterman, R. J.; Krieger, K. (1984). "California sea lions are capable of semantic comprehension". The Psychological Record 38 (3): 311–348. doi:10.1007/BF03395027. 
  • Skinner, B.F. (1957). Verbal behavior. Englewood Cliffs, NJ: Prentice-Hall.
  • Wilkie, R.; McKinnon, A. (2013). "George Herbert Mead on Humans and Other Animals: Social Relations after Human-Animal Studies". Sociological Research Online 18 (4): 19. doi:10.5153/sro.3191. http://www.socresonline.org.uk/18/4/19.html. 
  • Wittmann, Henri (1991). "Classification linguistique des langues signées non vocalement". Revue Québécoise de Linguistique Théorique et Appliquée 10 (1): 215–88. http://www.nou-la.org/ling/1991a-class.pdf. 

External links



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