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Interspecies communication

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Interspecies communication is communication between different species of animals, plants, or microorganisms. Although researchers have explored the topic for many years, only recently has interspecies communication been recognized as an established field of inquiry.[1]

Mutualism

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Nonverbal communication between dog and human

Cooperative interspecies communication implies sharing and understanding information between two or more species that work towards the benefit of both species (mutualism).[citation needed]

Since the 1970s, primatologist Sue Savage-Rumbaugh has been working with primates at Georgia State University's Language Research Center (LRC), and more recently, the Iowa Primate Learning Sanctuary. In 1985, using lexigram symbols, a keyboard and monitor, and other computer technology, Savage-Rumbaugh began her groundbreaking work with Kanzi, a male bonobo (P. paniscus). Her research has made significant contributions to a growing body of work in sociobiology studying language learning in non-human primates and exploring the role of language and communication as an evolutionary mechanism.[citation needed]

Koko, a lowland gorilla, began learning a modified American Sign Language as an infant, when Francine "Penny" Patterson, PhD, started working with her in 1975. Penny and Koko worked together at the Gorilla Foundation in one of the longest interspecies communication studies ever conducted until Koko's death in 2018. It was claimed that Koko had a vocabulary of over 1000 signs, and understood a greater amount of spoken English.[2] However, scientific consensus is that Koko did not demonstrate a true understanding of language, due to a lack of regard for syntax or grammar.

In April 1998, Koko gave an AOL live chat. Sign language was used to relay to Koko questions from the online audience of 7,811 AOL members.[citation needed] The following is an excerpt from the live chat.[2]

AOL: MInyKitty asks Koko are you going to have a baby in the future?
PENNY: OK, is that for Koko? Koko are you going to have a baby in the future?
KOKO: Koko-love eat ... sip.
AOL: Me too!
PENNY: What about a baby? You going to have baby? She's just thinking...her hands are together...
KOKO: Unattention.
PENNY: Oh poor sweetheart. She said 'unattention.' She covered her face with her hands..which means it's not happening, basically, or it hasn't happened yet. . . I don't see it.
AOL: That's sad!
PENNY: It is responding to the question. In other words, she hasn't had one yet, and she doesn't see a future here. The way the situation is actually with Koko & Ndume, she has 2 males to 1 female which is the reverse of what she needs. I think that is why she said that, because in our current situation, it isn't possible for her to have a baby. She needs several females and one male to have a family.

Research observing cooperative communication has largely focused on primates, and predatory animals. Red-fronted lemurs and sifakas recognize one another's alarm calls.[3] The same has been found in West African Diana monkey and Campbell's monkeys.[4] When one species elicits an alarm signal specific to a certain predator, the other species react in the same pattern as the species that called. For example, leopards hunt both species by capitalizing the elements of stealth and surprise. If the monkeys detect the leopard before it attacks (usually resulting in mobbing), the leopard will typically not attack. Therefore, when a leopard alarm call is given, both species respond by positioning near the leopard signaling that it has been found out. It also seems that the monkeys are able to distinguish a leopard alarm call from, for example, a raptor alarm call. When a raptor alarm call is given, the monkeys respond by moving towards the forest floor and away from aerial attack. It is not simply that the monkeys act upon hearing the alarm calls but rather they are able to actually extract particular information from a call. Responses to heterospecific alarm calls are not confined to simian species but have also been found in ground squirrels, specifically the yellow-bellied marmot and the golden-mantled ground squirrel.[5] Researchers have determined that bird species are able to understand, or at least respond, to alarms calls by species of mammals and vice versa; red squirrels' acoustic response to raptors is near-identical to that of birds, making the latter also aware to a potential predatory threat, while eastern chipmunks are keen to mobbing calls by eastern tufted titmice.[6] Whether heterospecific understanding is a learned behavior or not is unclear. In 2000 it was found that age and interspecies experience were important factors in the ability for bonnet macaques to recognize heterospecific calls.[7] Macaques who were exposed longer to other species' alarm calls were more likely to correctly respond to heterospecific alarm calls. Key to this early learning was the reinforcement of a predatory threat, when an alarm call was given a corresponding threat had to be presented in order to make the association. Interspecies communication may not be an innate ability but rather a sort of imprinting coupled with an intense emotion (fear) early in life.

It is unusual for interspecies communication to be observed in an older animal taking care of a younger animal of a different species. For example, Owen and Mzee, the odd couple of an orphaned baby hippopotamus and a 130-year-old Aldabran tortoise, display this relationship rarely seen in the animal world. Dr. Kahumbu of the sanctuary that holds the two believes that the two vocalize to one another in neither a stereotypical tortoise nor a hippopotamus fashion.[8] Owen does not respond to hippopotamus calls. It is likely that when Owen was first introduced to Mzee he was still young enough to be imprinted.[citation needed]

Parasitism and eavesdropping

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Unlike cooperative communication, parasitic communication involves an unequal sharing of information (parasitism). In terms of alarm calls, this means that the warnings are not bi-directional. It may be that the other species has simply not been able to decipher the calls of the first species. Much of the research done on this type of communication has been in bird species, including the nuthatch and the great tit. Nuthatches are able to discriminate between subtle differences in chickadee alarm calls, which broadcast the location and size of a predator.[9] Since chickadees and nuthatches typically occupy the same habitat, mobbing predators together acts as a deterrent that benefits both species. Nuthatches screen chickadee alarm calls in order to determine whether it is cost-efficient, in terms of energy consumption, to mob a particular predator, because not all predators pose the same risk to nuthatches as to chickadees. Screening may be most important in the winter when energy demands are the highest.

Song of a Great Tit.

Work by Gorissen, Gorissen, and Eens (2006) has focused on blue tit song matching (or, "song imitation") by great tits.[10] Blue and great tits compete for resources such as food and nesting cavities and their coexistence has important fitness consequences for both species. These fitness costs might promote interspecific aggression because resources need to be defended against heterospecifics as well. So, the use of efficient vocal strategies such as matching might prove to be effective in interspecific communication. Hence, heterospecific matching could be a way of phrasing a threat in the language of the heterospecfic intruder. It could equally be well argued that these imitations of blue tit sounds have no function at all and are merely the result of learning mistakes in the sensitive period of great tits because blue and great tits form mixed foraging flocks together. While the authors agree with the first hypothesis, it is plausible that the latter also being true given the data on age and experience in primates.

Eavesdropping has been found in tungara frogs and their sympatric heterospecifics.[11] The scientists posit that mixed-species choruses may reduce their risk of predation without increasing mate competition.

Predator–prey

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Chemical signals in wolf urine are avoided by their prey[12]

Much of the communication between predators and prey can be defined as signaling. In some animals, the best way to avoid being preyed upon is an advertisement of danger or unpalatability, or aposematism. Given the effectiveness of this, it is no surprise that many animals employ styles of mimicry to ward off predators. Some predators also use aggressive mimicry as a hunting technique. For example, Photuris fireflies mimic female Photinus fireflies by scent and glow patterns in order to lure interested male Photinus fireflies, which they then kill and eat. Lophiiformes, or anglerfish, are also famous for their use of escas as bait for small unsuspecting fish.[13]

Two examples of predator–prey signaling were found in caterpillars and ground squirrels. When physically disturbed, Lepidoptera larvae produce a clicking noise with their mandibles followed by an unpalatable oral secretion.[14] Scientists believe this to be “acoustic aposematism” which has only been previously found in a controlled study with bats and tiger moths.[15] While the defense mechanisms of ground squirrels to predatory rattlesnakes have been well studied (i.e. tail flagging), only recently have scientists discovered that these squirrels also employ a type of infrared heat signaling.[16] By using robotic models of squirrels, the researchers found that when infrared radiation was added to tail flagging, rattlesnakes shifted from predatory to defensive behavior and were less likely to attack than when no radiation component was added.


Allomones

[edit]
This section is an excerpt from Allomone.[edit]
Dasyscolia ciliata on the flowers of Ophrys speculum

An allomone (from Ancient Greek ἄλλος allos "other" and pheromone) is a type of semiochemical produced and released by an individual of one species that affects the behaviour of a member of another species to the benefit of the originator but not the receiver.[17] Production of allomones is a common form of defense against predators, particularly by plant species against insect herbivores. In addition to defense, allomones are also used by organisms to obtain their prey or to hinder any surrounding competitors.[18]

Many insects have developed ways to defend against these plant defenses (in an evolutionary arms race). One method of adapting to allomones is to develop a positive reaction to them; the allomone then becomes a kairomone. Others alter the allomones to form pheromones or other hormones, and yet others adopt them into their own defensive strategies, for example by regurgitating them when attacked by an insectivorous insect.

A third class of allelochemical (chemical used in interspecific communication), synomones, benefit both the sender and receiver.[17]

"Allomone was proposed by Brown and Eisner (Brown, 1968) to denote those substances which convey an advantage upon the emitter. Because Brown and Eisner did not specify whether or not the receiver would benefit, the original definition of allomone includes both substances that benefit the receiver and the emitter, and substances that only benefit the emitter. An example of the first relationship would be a mutualistic relationship, and the latter would be a repellent secretion."[19]

Kairomones

[edit]
This section is an excerpt from Kairomone.[edit]
A kairomone is a semiochemical released by an organism that mediates interspecific interactions in a way that benefits a different species at the expense of the emitter.[20] Derived from the Greek καιρός, meaning "opportune moment"[21][22][23], it serves as a form of "eavesdropping", enabling the receiver to gain an advantage, such as locating food or evading predators, even if it poses a risk to the emitter. Unlike allomones, which benefit the producer at the receiver's cost, or synomones, which are mutually beneficial, kairomones favor only the recipient. Primarily studied in entomology, kairomones can play key roles in predator-prey dynamics, mate attraction, and even applications in pest control.[20][24]

Synomones

[edit]
This section is an excerpt from Semiochemical § Synomone.[edit]

A synomone is an interspecific semiochemical that is beneficial to both interacting organisms, the emitter and receiver, e.g. floral synomone of certain Bulbophyllum species (Orchidaceae) attracts fruit fly males (Tephritidae: Diptera) as pollinators, so can be classed as an attractant. In this true mutualistic inter-relationship, both organisms gain benefits in their respective sexual reproductive systems – i.e. orchid flowers are pollinated and the Dacini fruit fly males are rewarded with a sex pheromone precursor or booster. The floral synomone, also acts as a reward to pollinators, is either in the form of a phenylpropanoid (e.g. methyl eugenol[25][26][27]) or a phenylbutanoid (e.g. raspberry ketone[28] and zingerone[29][30]).

Another example of a synomone is trans-2-hexenal, emitted by trees in the Mimosa / Acacia clade of the Fabaceae. These trees form distinctive hollow structures in which ants nest. When a leaf is disrupted by an herbivore, the damaged cells emit trans-2-hexenal (among other volatiles), which is detected by the ants. The ants swarm to the herbivore, biting and stinging to defend their host plant. The tree repays them in turn by providing sugary nectar and fat- and protein-rich Beltian bodies to feed the ant colony.

Criticism

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Social scientists and others have historically criticized research in interspecies communication, characterizing it as anthropomorphizing. This perspective has become less common in recent years. A 2013 TED Talk featured a proposal to construct an Interspecies Internet by presenters musician Peter Gabriel, Internet protocol co-inventor Vint Cerf, cognitive psychologist Diana Reiss, and director of MIT's Center for Bits and Atoms Neil Gershenfeld.[31][32] A follow-up workshop to review progress and plan future activities occurred in 2019 and was co-hosted by MIT's Center for Bits and Atoms, Google, and the Jeremy Coller Foundation.[33] The ongoing efforts coalesced into a think-tank to accelerate understanding of interspecies communication. Workshops and public conferences were held in 2020 and 2021.[34][35][36]

See also

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  • Alien language – Hypothetical non-Earth language
  • Animal communication – Transfer of information from animal to animal
  • Anna Breytenbach – South African interspecies communicator
  • Clever Hans – Horse who performed math tricks (born c. 1895)
  • Great ape language – Efforts to teach nonhuman primates to communicate with humans
  • Human–animal communication – Verbal and non-verbal interspecies communication
  • Jim Nollman – American composer
  • John C. Lilly – American physician, scientist, psychonaut, and philosopher
  • Quorum-sensing – Biological ability to detect and respond to cell population density
  • Symbiosis – Close, long-term biological interaction between distinct organisms (usually species)

Further reading

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  • McKenney David; Brown Kathryn; Allison David (1995). "Influence of Pseudomonas aeruginosa Exoproducts on Virulence Factor Production in Burkholderia cepacia: Evidence of Interspecies Communication". Journal of Bacteriology. 177 (23): 6989–6991. doi:10.1128/jb.177.23.6989-6992.1995. PMC 177571. PMID 7592496. P. aeruginosa exoproducts help B. cepacia to attach to different surfaces.
  • The New Scientist: Lab chimp speaks his own language 2 January 2003, Anil Ananthaswamy
  • Doctor Dolittle's Delusion, Subtitle: Animals and the Uniqueness of Human Language. 2004 Yale University Press by Anderson

References

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  1. ^ Steingo, Gavin (2024). Interspecies Communication: Sound and Music beyond Humanity. Chicago: University of Chicago Press. ISBN 978-0-226-83136-7.
  2. ^ a b "Koko's First Interspecies Web Chat: Transcript". Archived from the original on 6 February 2007.
  3. ^ Fichtel, C. (2004) Reciprocal recognition of sifaka (Propithecus verreauxi verreauxi) and redfronted lemur (Eulemur fulvus rufus) alarm calls. Animal Cognition 7:45–52.
  4. ^ Zuberbuhler, K. (2000) Interspecies semantic communication in two forest primates. Proc R Soc Lond Ser B Biol Sci 267:713–718.
  5. ^ Shriner, W.M.K.E.E. (1998). "Yellow-bellied marmot and golden-mantled ground squirrel responses to heterospecific alarm calls". Animal Behaviour. 55 (3): 529–536. doi:10.1006/anbe.1997.0623. PMID 9514669. S2CID 45982940.
  6. ^ Solomon, Christopher (18 May 2015). "When Birds Squawk, Other Species Seem to Listen". The New York Times. ISSN 0362-4331. Retrieved 21 May 2015.
  7. ^ Ramakrishnan, U.; Coss, R. G. (2000). "Recognition of Heterospecific Alarm Vocalization by Bonnet Macaques (Macaca radiata)". Journal of Comparative Psychology. 114 (1): 3–12. doi:10.1037/0735-7036.114.1.3. PMID 10739307. S2CID 25651463.
  8. ^ Owen & Mzee
  9. ^ Templeton, C.N.; Greene, E. (2007). "Nuthatches eavesdrop on variations in heterospecific chickadee mobbing alarm calls". PNAS. 104 (13): 5479–5482. Bibcode:2007PNAS..104.5479T. doi:10.1073/pnas.0605183104. PMC 1838489. PMID 17372225.
  10. ^ Gorissen, L.; Gorissen, M.; Eens, M. (2006). "Heterospecific song matching in two closely related songbirds (Parus major and P. caeruleus): Great tits match blue tits but not vice versa". Behavioral Ecology and Sociobiology. 60 (2): 260–269. Bibcode:2006BEcoS..60..260G. doi:10.1007/s00265-006-0164-6. S2CID 19530765.
  11. ^ Phelps, S.M.; Rand, A.S.; Ryan, M.J. (2007) The mixed-species chorus as public information: túngara frogs eavesdrop on a heterospecific. Behav. Ecol. 18:108–114.
  12. ^ Osada, Kazumi; Kurihara, Kenzo; Izumi, Hiroshi; Kashiwayanagi, Makoto (24 April 2013). Bolhuis, Johan J. (ed.). "Pyrazine Analogues Are Active Components of Wolf Urine That Induce Avoidance and Freezing Behaviours in Mice". PLOS ONE. 8 (4): e61753. Bibcode:2013PLoSO...861753O. doi:10.1371/journal.pone.0061753. ISSN 1932-6203. PMC 3634846. PMID 23637901.
  13. ^ Smith, William John (2009). The Behavior of Communicating: an ethological approach. Harvard University Press. p. 381. ISBN 978-0-674-04379-4. Others rely on the technique adopted by a wolf in sheep's clothing—they mimic a harmless species. ... Other predators even mimic their prey's prey: angler fish (Lophiiformes) and alligator snapping turtles Macroclemys temmincki can wriggle fleshy outgrowths of their fins or tongues and attract small predatory fish close to their mouths.
  14. ^ Brown, S.G.; Boettner, G.H.; Yack, J.E. (2007) Clicking caterpillars: acoustic aposematism in Antheraea polyphemus and other Bombycoidea. J Exp Biol 210:993–1005.
  15. ^ Hristov, N. I.; Conner, W. E. (2005). "Sound strategy: acoustic aposematism in the bat–tiger moth arms race". Naturwissenschaften. 92 (4): 164–169. Bibcode:2005NW.....92..164H. doi:10.1007/s00114-005-0611-7. PMID 15772807. S2CID 18306198.
  16. ^ Rundus, A.S.; Owings, D.H.; Joshi, S.S.; Chinn, E; Giannini, N. Ground squirrels use an infrared signal to deter rattlesnake predation. Proceedings of the National Academy of Sciences 104:14372-14376.
  17. ^ a b Grasswitz, T.R. and G.R. Jones (2002). "Chemical Ecology". Encyclopedia of Life Sciences. John Wiley & Sons, Ltd. doi:10.1038/npg.els.0001716.
  18. ^ Brown, William L. Jr.; Eisner, Thomas; Whittaker, Robert H. (1 January 1970). "Allomones and Kairomones: Transspecific Chemical Messengers". BioScience. 20 (1): 21. doi:10.2307/1294753. ISSN 0006-3568. JSTOR 1294753.
  19. ^ Weldon, Paul J. Journal of Chemical Ecology. p. 719. doi:10.1007/BF00987681. S2CID 33065758.
  20. ^ a b Grasswitz, T.R.; G.R. Jones (2002). "Chemical Ecology". Encyclopedia of Life Sciences. John Wiley & Sons, Ltd. doi:10.1038/npg.els.0001716. ISBN 978-0-470-01617-6.
  21. ^ Brown, W L Jr.; Eisner, T; Whittaker, R H (1970). "Allomones and kairomones: Transpecific chemical messengers". BioScience. 20 (1): 21–22. doi:10.2307/1294753. JSTOR 1294753.
  22. ^ "kairomone, n.". OED Online. September 2012. Oxford University Press. http://www.oed.com/view/Entry/241005?redirectedFrom=kairomone (accessed 3 October 2012).
  23. ^ Wood William F. (1983). "Chemical Ecology: Chemical Communication in Nature". Journal of Chemical Education. 60 (7): 1531–539. Bibcode:1983JChEd..60..531W. doi:10.1021/ed060p531.
  24. ^ Wyatt, Tristram D. (2003). Pheromones and Animal Behaviour. Cambridge: Cambridge University Press. pp. 2, 230–31. ISBN 978-0-521-48526-5.
  25. ^ Tan, K.H., R. Nishida and Y.C. Toong (2002). "Bulbophyllum cheiri's floral synomone lures fruit flies to perform pollination". Journal of Chemical Ecology. 28 (6): 1161–1172. doi:10.1023/A:1016277500007. PMID 12184394. S2CID 36621985.{{cite journal}}: CS1 maint: multiple names: authors list (link)
  26. ^ Nishida, R., K.H. Tan, S.L. Wee, A.K.W. Hee and Toong, Y. C. (2004). "Phenylpropanoids in the fragrance of the fruit fly orchid, Bulbophyllum cheiri, and their relationship to the pollinator, Bactrocera papayae". Biochemical Systematics and Ecology. 32 (3): 245–252. Bibcode:2004BioSE..32..245N. doi:10.1016/S0305-1978(03)00179-0.{{cite journal}}: CS1 maint: multiple names: authors list (link)
  27. ^ Tan, K.H., L.T. Tan, and R. Nishida (2006). "Floral phenylpropanoid cocktail and architecture of Bulbophyllum vinaceum orchid in attracting fruit flies for pollination". Journal of Chemical Ecology. 32 (11): 2429–2441. Bibcode:2006JCEco..32.2429T. doi:10.1007/s10886-006-9154-4. PMID 17082990. S2CID 15812115.{{cite journal}}: CS1 maint: multiple names: authors list (link)
  28. ^ Tan, K.H.; Nishida, R. (2005). "Synomone or Kairomone? - Bulbophyllum apertum (Orchidaceae) flower releases raspberry ketone to attract Bactrocera fruit flies". Journal of Chemical Ecology. 31 (3): 509–519. doi:10.1007/s10886-005-2023-8. PMID 15898497. S2CID 39173699.
  29. ^ Tan, K.H. and R. Nishida (2000). "Mutual reproductive benefits between a wild orchid, Bulbophyllum patens, and Bactrocera fruit flies via a floral synomone". Journal of Chemical Ecology. 26 (2): 533–546. Bibcode:2000JCEco..26..533T. doi:10.1023/A:1005477926244. S2CID 24971928.
  30. ^ Tan, K.H. and R. Nishida (2007). "Zingerone in the floral synomone of Bulbophyllum baileyi (Orchidaceae) attracts Bactrocera fruit flies during pollination". Biochemical Systematics and Ecology. 35 (6): 334–341. Bibcode:2007BioSE..35..334T. doi:10.1016/j.bse.2007.01.013.
  31. ^ Dolgin, Elie (17 July 2019). "The Internet Is Coming to the Rest of the Animal Kingdom". IEEE Spectrum. Retrieved 15 August 2021.
  32. ^ Cerf, Diana Reiss, Peter Gabriel, Neil Gershenfeld and Vint (2013), "The interspecies internet? An idea in progress", TED, retrieved 15 August 2021{{citation}}: CS1 maint: multiple names: authors list (link)
  33. ^ "Interspecies Internet Workshop". cba.mit.edu. Retrieved 15 August 2021.
  34. ^ "Conversations 2020 Public Conference". Interspecies Internet. Retrieved 15 August 2021.
  35. ^ "Conversations 2021". Interspecies Internet. Retrieved 15 August 2021.
  36. ^ "Interspecies Internet". Interspecies Internet. Retrieved 15 August 2021.
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