Fanning honeybee exposes Nasonov gland (white-at tip of abdomen) releasing pheromone to entice swarm into an empty hive

A pheromone (from Greek φέρω phero "to bear" + hormone from Greek ὁρμή - "impetus") is a secreted or excreted chemical factor that triggers a social response in members of the same species. Pheromones are chemicals capable of acting outside the body of the secreting individual to impact the behavior of the receiving individual.[1] There are alarm pheromones, food trail pheromones, sex pheromones, and many others that affect behavior or physiology. Their use among insects has been particularly well documented. In addition, some vertebrates and plants communicate by using pheromones.



The term "pheromone" was introduced by Peter Karlson and Martin Lüscher in 1959, based on the Greek word pherein (to transport) and hormone (to stimulate). They are also sometimes classified as ecto-hormones. They were researched earlier by various scientists, including Jean-Henri Fabre, Joseph A. Lintner, Adolph Butenandt, and the prominent ethologist Karl von Frisch who called them various names like "alarm substances." These chemical messengers are transported outside of the body and result in a direct developmental effect on hormone levels or behavioral change.[2] They proposed the term to describe chemical signals from conspecifics that elicit innate behaviors soon after the German Biochemist Adolf Butenandt characterized the first such chemical, bombykol (a chemically well-characterized pheromone released by the female silkworm to attract mates).[3]


There are physical limits on the practical size of organisms employing pheromones, because at small sizes pheromone diffuses away from the source organism faster than it can be produced, and a sensible concentration accumulates too slowly to be useful. So bacteria are too small to use pheromones as sex attractants but do use them to determine the local population density of similar organisms and control behaviors that take more time to execute (quorum sensing). In similar manner, the simple animals rotifers are, it appears, also too small for females to lay down a useful trail, but in the slightly-larger copepods the female leaves a trail that the male can follow.[4]



Aggregation of bug nymphs

Aggregation pheromones function in defense against predators, mate selection, and overcoming host resistance by mass attack. A group of individuals at one location is referred to as an aggregation, whether consisting of one sex or both sexes. Male-produced sex attractants have been called aggregation pheromones, because they usually result in the arrival of both sexes at a calling site, and increase the density of conspecifics surrounding the pheromone source. Most sex pheromones are produced by the females and small percentage of sex attractants are produced by males.[5] Aggregation pheromones have been found in members of the Coleoptera, Diptera, Hemiptera, Dictyoptera and Orthoptera. In recent decades, the importance of applying aggregation pheromones in the management of the boll weevil (Anthonomus grandis), stored product weevils (Sitophilus zeamais), Sitophilus granarius, Sitophilus oryzae, and pea and bean weevil (Sitona lineatus) has been demonstrated. Aggregation pheromones are among the most ecologically selective pest suppression methods. They are nontoxic and effective at very low concentrations.[6]


Some species release a volatile substance when attacked by a predator that can trigger flight (in aphids) or aggression (in ants, bees, termites)[7] in members of the same species. Pheromones also exist in plants: Certain plants emit alarm pheromones when grazed upon, resulting in tannin production in neighboring plants. These tannins make the plants less appetizing for the herbivore.[8]


Epideictic pheromones are different from territory pheromones, when it comes to insects. Fabre observed and noted how "females who lay their eggs in these fruits deposit these mysterious substances in the vicinity of their clutch to signal to other females of the same species they should clutch elsewhere."


Releaser pheromones are pheromones that cause an alteration in the behavior of the recipient. For example, some organisms use powerful attractant molecules to attract mates from a distance of two miles or more. In general, this type of pheromone elicits a rapid response, but is quickly degraded. In contrast, a primer pheromone has a slower onset and a longer duration. For example, rabbit (mothers) release mammary pheromones that trigger immediate nursing behavior by their babies.[9]


Signal pheromones cause short-term changes, such as the neurotransmitter release that activates a response. For instance, GnRH molecule functions as a neurotransmitter in rats to elicit lordosis behavior.[10]


Primer pheromones trigger a change of developmental events (in which they differ from all the other pheromones, which trigger a change in behavior).


Laid down in the environment, territorial pheromones mark the boundaries of an organism's territory. In cats and dogs, these hormones are present in the urine, which they deposit on landmarks serving to mark the perimeter of the claimed territory. In social seabirds, the preen gland is used to mark nests, nuptial gifts, and territory boundaries with behavior formerly described as 'displacement activity'.


Trail pheromones are common in social insects. For example, ants mark their paths with these pheromones, which are volatile hydrocarbons.

Certain ants lay down an initial trail of pheromones as they return to the nest with food. This trail attracts other ants and serves as a guide.[11] As long as the food source remains, the pheromone trail will be continuously renewed. The pheromone must be continuously renewed because it evaporates quickly. When the supply begins to dwindle, the trail making ceases. In at least one species of ant, trails that no longer lead to food are also marked with a repellent pheromone.[12]


Information pheromones are indicative of an animal's identity or territory. For example, dogs and cats deposit chemicals in and around their territory, which then serve as an indicator for other members of the species about the presence of the occupant in that territory.[9]


In animals, sex pheromones indicate the availability of the female for breeding. Male animals may also emit pheromones that convey information about their species and genotype.

At the microscopic level, male copepods can follow a three-dimensional pheromone trail left by a swimming female, and male gametes of many animals use a pheromone to help find a female gamete, for fertilization.[13]

Many insect species release sex pheromones to attract a mate, and many lepidopterans (moths and butterflies) can detect a potential mate from as far away as 10 kilometers (6.25 mi). Traps containing pheromones are used by farmers to detect and monitor insect populations in orchards.

Pheromones are also used in the detection of oestrus in sows. Boar pheromones are sprayed into the sty, and those sows that exhibit sexual arousal are known to be currently available for breeding. Sea urchins release pheromones into the surrounding water, sending a chemical message that triggers other urchins in the colony to eject their sex cells simultaneously.


This classification, based on the effects on behavior, remains artificial. Pheromones fill many additional functions.

  • Nasonov pheromones (worker bees)
  • Royal pheromones (bees)
  • Calming (appeasement) pheromones (mammals)
  • Necromones, given off by a deceased and decomposing organism; consisting of oleic and linoleic acids, they allow crustaceans and hexapods to identify the presence of dead conspecifics.[14]


Pheromones have evolved in all animal phyla, to signal sex and dominance status, and are responsible for stereotypical social and sexual behaviour among members of the same species. In mammals, these chemical signals are believed to be detected primarily by the vomeronasal organ (VNO), a chemosensory organ located at the base of the nasal septum.[15] The VNO is present in most amphibia, reptiles, and non-primate mammals but is absent in birds, adult catarrhine monkeys, and apes.[16] An active role for the human VNO in the detection of pheromones is disputed; the VNO is clearly present in the foetus but appears to be atrophied or absent in adults. Three distinct families of putative pheromone receptors have been identified in the vomeronasal organ (V1Rs, V2Rs, and V3Rs). All are G protein-coupled receptors but are only distantly related to the receptors of the main olfactory system, highlighting their different role.[15]


Non-human animals

Pheromones of pest insect species, such as the Japanese beetle and the gypsy moth, can be used to induce many behaviors. As a result, a pheromone trap can be used to trap pests for monitoring purposes, to control the population by creating confusion, to disrupt mating, as well as to prevent further egg laying.

In mammals and reptiles, pheromones may be detected by the vomeronasal organ (VNO), or Jacobson's organ, which lies between the nose and mouth and is the first stage of the accessory olfactory system. Some pheromones in these animals are detected by regular olfactory membranes.


The German physician and hygienist Gustav Jäger (1832–1917) was, it is presumed[by whom?], the first to formalize the concept of human pheromones, which he named "anthropines" (from the Greek anthropos, meaning man). He correctly identified them as lipophilic compounds that are associated with skin and follicles that determine the individual signature of human odors.[17]

Few well-controlled scientific studies have ever been published suggesting the possibility of pheromones in humans.[citation needed]

The best-known case involves the synchronization of menstrual cycles among women based on unconscious odor cues (the McClintock effect, named after the primary investigator, Martha McClintock, of the University of Chicago).[18][19] This study exposed a group of women to a whiff of perspiration from other women. It was found that it caused their menstrual cycles to speed up or slow down depending on the time in the month the sweat was collected: before, during, or after ovulation. Therefore, this study proposed that there are two types of pheromone involved: "One, produced prior to ovulation, shortens the ovarian cycle; and the second, produced just at ovulation, lengthens the cycle". However, recent studies and reviews of the McClintock methodology have called into question the validity of her results.[20] A newspaper report[21] suggested that women with irregular menstrual cycles became regular when exposed to male underarm extracts, and hypothesized that male sweat contains pheromones, which mirror how pheromones affect other mammals.[21]

The male armpit has been hypothesized to be a source of human pheromones.

Other studies have demonstrated that the smell of androstadienone, a chemical component of male sweat, maintains higher levels of cortisol in females,[22] and that the compound is detected via the olfactory mucosa.[23] The scientists suggest that the ability of this compound to influence the endocrine balance of the opposite sex makes it a human pheromonal chemosignal. In 2002, a study showed an unnamed synthetic chemical in women's perfume appeared to increase intimate contact with men. The authors hypothesize, but do not demonstrate, that the observed behavioural differences are olfactorily mediated.[24] This and a previous study by the same authors with the still undisclosed "pheromone" preparation has been heavily criticized for having methodological flaws and that upon re-analyzing there was no effect seen.[25][26]

Pheromone action in humans should not be confused with major histocompatibility complex interaction. Using a brain imaging technique, Swedish researchers have shown that homosexual and heterosexual males' brains respond differently to two odors that may be involved in sexual arousal, and that the homosexual men respond in the same way as heterosexual women, though it could not be determined whether this was cause or effect.[citation needed] The study was expanded to include homosexual women; the results were consistent with previous findings meaning that homosexual women were not as responsive to male-identified odors, while their response to female cues were similar to that of heterosexual males.[27] According to the researchers, this research suggests a possible role for human pheromones in the biological basis of sexual orientation.[28] In 2008, it was found using functional magnetic resonance imaging that the right orbitofrontal cortex, right fusiform cortex, and right hypothalamus respond to airborne natural human sexual sweat.[29]

In 2006, it was shown that a second mouse receptor sub-class is found in the olfactory epithelium. Called the trace amine-associated receptors (TAAR), some are activated by volatile amines found in mouse urine, including one putative mouse pheromone.[30] Orthologous receptors exist in humans providing, the authors propose, evidence for a mechanism of human pheromone detection.[31]

Some body spray advertisers claim that their products contain human sexual pheromones that act as an aphrodisiac. In the 1970s, "copulins" were patented as products that release human pheromones, based on research on rhesus monkeys.[32] Subsequent to this, androstenone, axillary sweat, and "vomodors" have been claimed to act as human pheromones.[33] Despite these claims, no pheromonal substance has ever been demonstrated to directly influence human behavior in a peer reviewed study.[32][33][34]

See also


  1. ^
  2. ^ Kohl, J., Atzmueller, M., Fink, B. & Grammar, K. Human Pheromones: Integrative Neuroendocrinology & Ethology. NEL 22, 309-321.(2001)
  3. ^ Karlson P., Lüscher M. (1959). "Pheromones: a new term for a class of biologically active substances". Nature 183 (4653): 55–56. doi:10.1038/183055a0. PMID 13622694. 
  4. ^ Dusenbery, David B. (2009). Living at Micro Scale, Chapter 19. Harvard University Press, Cambridge, Mass. ISBN 978-0-674-03116-6.
  5. ^
  6. ^ Landolt, J. P. 1997. Sex attractant and aggregation pheromones of male phytophagous insects. In American Entomologist Vol. 43- 1
  7. ^ Šobotník, J., Hanus, R., Kalinová, B., Piskorski, R., Cvačka, J., Bourguignon, T., Roisin, Y. (April 2008). "(E,E)-α-Farnesene, an Alarm Pheromone of the Termite Prorhinotermes canalifrons". Journal of Chemical Ecology 34 (4): 478–486. doi:10.1007/s10886-008-9450-2. PMID 18386097. 
  8. ^ J.du P. Bothma, Game ranch management, fourth edition, Van Schaik publishers, 2002
  9. ^ a b Kimball, J.W. Pheromones. Kimball's Biology Pages. Sep 2008
  10. ^ Kohl, J., Atzmueller, M., Fink, B. & Grammar, K. Human Pheromones: Integrative Neuroendocrinology & Ethology. NEL 22, 309-321(2001).
  11. ^ "Excited ants follow pheromone trail of same chemical they will use to paralyze their prey". Retrieved 2006-03-14. 
  12. ^ "Study: Ants Use Scents Like Road Signs". Retrieved 2006-03-14. 
  13. ^ Dusenbery, David B. (2009). Living at Micro Scale, Chapters 19 & 20. Harvard University Press, Cambridge, Mass. ISBN 978-0-674-03116-6.
  14. ^ Yao, M.; Rosenfeld, J.; Attridge, S.; Sidhu, S.; Aksenov, V.; Rollo, C.D.. "The Ancient Chemistry of Avoiding Risks of Predation and Disease". Evolutionary biology (Springer, Heidelberg, ALLEMAGNE) 36 (3): 267–281. doi:10.1007/s11692-009-9069-4. ISSN 00713260. Retrieved July 22, 2011. 
  15. ^ a b Pantages E, Dulac C (2000). "A novel family of candidate pheromone receptors in mammals". Neuron 28 (3): 835–845. doi:10.1016/S0896-6273(00)00157-4. PMID 11163270. 
  16. ^ Keverne EB (1999). "The vomeronasal organ". Science 286 (5440): 716–720. doi:10.1126/science.286.5440.716. PMID 10531049. 
  17. ^ Jäger, Gustav. Die Entdeckung der Seele. Republished as CD-ROM by Grönbeck Verlag, 2007. ISBN 3980842029
  18. ^ McClintock MK (January 1971). "Menstrual synchorony and suppression.". Nature 229 (5282): 244–5. doi:10.1038/229244a0. PMID 4994256. 
  19. ^ Stern K, McClintock MK (1998). "Regulation of ovulation by human pheromones". Nature 392 (6672): 177-9. doi:10.1038/32408. PMID 9515961.
  20. ^ Yang, Zhengwei; Jeffrey C. Schank (2006). "Women Do Not Synchronize Their Menstrual Cycles". Human Nature 17 (4): 434–447. doi:10.1007/s12110-006-1005-z. Retrieved 2007-06-25. 
  21. ^ a b Looking for love potion number nine, Cathryn M. Delude, Boston Globe, September 2, 2003.
  22. ^ Wyart C, Webster WW, Chen JH, Wilson SR, McClary A, Khan RM, Sobel N (February 2007). "Smelling a single component of male sweat alters levels of cortisol in women". Journal of Neuroscience 27 (6): 1261–5. doi:10.1523/JNEUROSCI.4430-06.2007. PMID 17287500. 
  23. ^ Savic I, Hedén-Blomqvist E, Berglund H. (2009). Pheromone signal transduction in humans: What can be learned from olfactory loss. Hum Brain Mapp. 30(9):3057-3065. PMID 19235878 doi:10.1002/hbm.20727
  24. ^ "San Francisco State University study shows that synthetic pheromones in women's perfume increase intimate contact with men". San Francisco State University Office of Public Affairs. March 20 2002. 
  25. ^ Anders Winman (2004). "Do perfume additives termed human pheromones warrant being termed pheromones?". Physiology & Behavior 82 (4): 697–701. doi:10.1016/j.physbeh.2004.06.006. PMID 15327919. 
  26. ^ Charles J. Wysocki, George Preti (1998). "Pheromonal Influences". Archives of Sexual Behavior 27 (6): 627–641. doi:10.1023/A:1018729302720. PMID 9883309. 
  27. ^ Berglund H, Lindström P, Savic I (May 2006). "Brain response to putative pheromones in lesbian women". Proc. Natl. Acad. Sci. U.S.A. 103 (21): 8269–74. doi:10.1073/pnas.0600331103. PMC 1570103. PMID 16705035. 
  28. ^ Wade, N. "Gay Men are found to have Different Scent of Attraction." NY Times, May 9, 2005
  29. ^ [|Zhou, Wen]; Denise Chen (March 20 2008). "Encoding human sexual chemosensory cues in the orbitofrontal and fusiform cortices.". J Neurosci 25 (53): 14416–21. doi:10.1523/JNEUROSCI.3148-08.2008. PMC 2667117. PMID 19118174. 
  30. ^ Liberles SD, Buck LB (2006). "A second class of chemosensory receptors in the olfactory epithelium". Nature 442 (7103): 645–50. doi:10.1038/nature05066. PMID 16878137. 
  31. ^ Pearson H (2006). "Mouse data hint at human pheromones". Nature 442 (7102): 495. doi:10.1038/442495a. PMID 16885951. 
  32. ^ a b Wyatt, Tristram D. (2003). Pheromones and Animal Behaviour: Communication by Smell and Taste. Cambridge: Cambridge University Press. ISBN 0-521-48526-6. p. 298 Quoting Preti & Weski (1999) "No peer reviewed data supporting the presences of...human...pheromones that cause rapid behavioral changes, such as attraction and/or copulation have been documented."
  33. ^ a b Hays, Warren S. T., Human pheromones: have they been demonstrated? Behavioral Ecology and Sociobiology, 2003, 54:89-97
  34. ^ Bear, Mark F.; Barry W. Connors, Michael A. Paradiso (2006). Neuroscience: Exploring the Brain. Lippincott Williams & Wilkins. ISBN 0781760038.  p. 264 ...there has not yet been any hard evidence for human pheromones that might [change] sexual attraction (for members of either sex) [naturally]

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  • Pheromone —   [Kurzbildung zu griechisch phérein »tragen« und Hormon], Singular Pheromon das, s, Ekto|hormone, von Tieren produzierte, leicht flüchtige Substanzen, die nach außen abgegeben, Stoffwechsel und Verhalten anderer Individuen der gleichen Art… …   Universal-Lexikon

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  • pheromone — ► NOUN ▪ a chemical substance released by an animal and causing a response in others of its species. ORIGIN from Greek pherein convey + HORMONE(Cf. ↑hormone) …   English terms dictionary

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