Fanning honeybee exposes Nasanov's gland (white – at tip of abdomen) releasing pheromone to entice swarm into an empty hive

A pheromone (from Ancient Greek φέρω phero "to bear" and hormone, from Ancient 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. Pheromones are used from basic unicellular prokaryotes to complex multicellular eukaryotes.[2] Their use among insects has been particularly well documented. In addition, some vertebrates and plants communicate by using pheromones.


The portmanteau word "pheromone" was coined by Peter Karlson and Martin Lüscher in 1959, based on the Greek φερω pheroo ('I carry') and ὁρμων hormon ('stimulating').[3] Pheromones are also sometimes classified as ecto-hormones. They were researched earlier by various scientists, including Jean-Henri Fabre, Joseph A. Lintner, Adolf Butenandt, and ethologist Karl von Frisch who called them various names, like for instance "alarm substances". These chemical messengers are transported outside of the body and affect neurocircuits, including the autonomous nervous system with hormone or cytokine mediated physiological changes, inflammatory signaling, immune system changes and/or behavioral change in the recipient.[4] They proposed the term to describe chemical signals from conspecifics that elicit innate behaviors soon after the German biochemist Adolf Butenandt had characterized the first such chemical, bombykol, a chemically well-characterized pheromone released by the female silkworm to attract mates.[5]


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. For this reason, bacteria are too small to use pheromones as sex attractants on an individual basis. However, they do use them to determine the local population density of similar organisms and control behaviors that take more time to execute (e.g. pheromones are used in quorum sensing or to promote natural competence for transformation, i.e. sexual gene transfer). 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.[6]



Aggregation of bug nymphs

Aggregation pheromones function in mate selection, overcoming host resistance by mass attack, and defense against predators. 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; only a small percentage of sex attractants are produced by males.[7] 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.[8]


Some species release a volatile substance when attacked by a predator that can trigger flight (in aphids) or aggression (in ants, bees, termites)[9] in members of the same species. For example, Vespula squamosa use alarm pheromones to alert others to a threat.[10] In Polistes exclamans, alarm pheromones are also used as an alert to incoming predators.[11] 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.[12]


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.[13]


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.[4]


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 and identity 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'.[13]


Social insects commonly use trail pheromones. For example, ants mark their paths with pheromones consisting of 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.[14] As long as the food source remains vailable, visiting ants will continuously renew the pheromone trail. The pheromone requies continuous renewal because it evaporates quickly. When the food 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.[15] The Eciton burchellii species provides an example of using pheromones to mark and maintain foraging paths. When species of wasps such as Polybia sericea found new nests, they use pheromones to lead the rest of the colony to the new nesting site.

Gregarious caterpillars, such as the forest tent caterpillar, lay down pheromone trails that are used to achieve group movement.[16]


Main article: Sex pheromone
Male Danaus chrysippus showing the pheromone pouch and brush-like organ in Kerala, India

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, a number of bacterial species (e.g. Bacillus subtilis, Streptococcus pneumoniae, Bacillus cereus) release specific chemicals into the surrounding media to induce the "competent" state in neighboring bacteria.[17] Competence is a physiological state that allows bacterial cells to take up DNA from other cells and incorporate this DNA into their own genome, a sexual process called transformation.

Among eukaryotic microorganisms, pheromones promote sexual interaction in numerous species.[18] These species include the yeast Saccharomyces cerevisiae, the filamentous fungi Neurospora crassa and Mucor mucedo, the water mold Achlya ambisexualis, the aquatic fungus Allomyces macrogynus, the slime mold Dictyostelium discoideum, the ciliate protozoan Blepharisma japonicum and the multicellular green algae Volvox carteri. In addition, 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.[19]

Many if not all insect species, such as the ant Leptothorax acervorum, the moth Helicoverpa zea, the bee Xylocopa varipuncta and the butterfly Edith's checkerspot release sex pheromones to attract a mate, and many lepidopterans (moths and butterflies) can detect a potential mate from as far away as 10 km (6.2 mi).[20] Traps containing pheromones are used by farmers to detect and monitor insect populations in orchards. In addition, Colias eurytheme butterflies release pheromones, an olfactory cue important for mate selection.[21]

The effect of Hz-2V virus infection on the reproductive physiology and behavior of female Helicoverpa zea moths is that in the absence of males they exhibited calling behavior and called as often but for shorter periods on average than control females. Even after these contacts virus-infected females made many frequent contacts with males and continued to call; they were found to produce five to seven times more pheromone and attracted twice as many males as did control females in flight tunnel experiments.[22]

Pheromones are also utilized by bee and wasp species. Some pheromones can also be used to suppress the sexual behavior of other individuals allowing for a reproductive monopoly – the wasp R. marginata uses this.[23] With regard to the Bombus hyperboreus species, males, otherwise known as drones, patrol circuits of scent marks (pheromones) to find queens.[24] In paraticular, pheromones for the Bombus hyperboreus, include octadecenol, 2,3-dihydro-6-transfarnesol, citronellol, and geranylcitronellol.[25]

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.


Processing chemosignals like pheromones has evolved in all animal phyla and thus is the oldest phylogenetic receptive system shared by all organisms including bacteria. It has been suggested that it serves survival by generating appropriate behavioral responses to the signals of threat, sex and dominance status among members of the same species.[27]

Furthermore, it has been suggested that in the evolution of unicellular prokaryotes to multicellular eukaryotes, primordial pheromone signaling between individuals may have evolved to paracrine and endocrine signaling within individual organisms.[28]

Some authors assume that approach-avoidance reactions in animals, elicited by chemical cues, form the phylogenetic basis for the experience of emotions in humans.[29]

The vomeronasal organ

In reptiles, amphibia and non-primate mammals pheromones are detected by regular olfactory membranes, and also by the vomeronasal organ (VNO), or Jacobson's organ, which lies at the base of the nasal septum between the nose and mouth and is the first stage of the accessory olfactory system.[30] While the VNO is present in most amphibia, reptiles, and non-primate mammals, it is absent in birds, adult catarrhine monkeys (downward facing nostrils, as opposed to sideways), and apes.[31] An active role for the human VNO in the detection of pheromones is disputed; while it is clearly present in the fetus it appears to be atrophied, shrunk or completely absent in adults. Three distinct families of vomeronasal receptors, putatively pheromone sensing, have been identified in the vomeronasal organ named 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.[30]


Non-human animals

Pheromone trapping

Main article: Pheromone trap

Pheromones of certain pest insect species, such as the Japanese beetle, acrobat ant, and the gypsy moth, can be used to trap the respective insect for monitoring purposes, to control the population by creating confusion, to disrupt mating, and to prevent further egg laying.

Avoidance of inbreeding

Mice can distinguish close relatives from more distantly related individuals on the basis of scent signals,[32] which enables them to avoid mating with close relatives and minimizes deleterious inbreeding.[33] Jiménez et al. showed that inbred mice had significantly reduced survival when they were reintroduced into a natural habitat.[33] In addition to mice, two species of bumblebee, in particular Bombus bifarius and Bombus frigidus, have been observed to use pheromones as a means of kin recognition to avoid inbreeding.[34] For example, B. bifarius males display “patrolling” behavior in which they mark specific paths outside their nests with pheromones and subsequently “patrol” these paths.[34] Unrelated reproductive females are attracted to the pheromones deposited by males on these paths, and males that encounter these females while patrolling can mate with them.[34] Interestingly, other bees of the Bombus species are found to emit pheromones as precopulatory signals, such as Bombus lapidarius.[35]


See also: Body odor

While humans are highly dependent upon visual cues, when in close proximity smells also play a role in sociosexual behaviors. An inherent difficulty in studying human pheromones is the need for cleanliness and odorlessness in human participants.[36] Experiments have focused on three classes of putative human pheromones: axillary steroids, vaginal aliphatic acids, and stimulators of the vomeronasal organ.

Axillary steroids

Axillary steroids are produced by the testes, ovaries, apocrine glands, and adrenal glands.[37] These chemicals are not biologically active until puberty when sex steroids influence their activity.[38] The change in activity during puberty suggest that humans may communicate through odors.[37] Several axillary steroids have been described as potential human pheromones: androstadienol, androstadienone, androstenol, androstenone, and androsterone.

Further evidence of a role for pheromones in sociosexual behavior comes from two double blind, placebo-controlled experiments. The first from 1998, by Cutler, had 38 male volunteers apply either a "male pheromone" or control odor and record six different sociosexual behaviors over two weeks.[46] This study found an increase in sexual behavior in the pheromone users compared to the control group.[46] The study 2002 by McCoy and Pitino was similar, except that participants were women, not men. Females treated with "female pheromone" reported significant increases in many of the behaviors including "sexual intercourse", "sleeping next to a partner", "formal dates", and "petting/affection/kissing".[47] The researchers believed that pheromones had a positive sexual attractant effect.[47] The third study was performed on 44 postmenopausal women and was published in 2004 by Rako and Friebely in the Journal of Sex Research. The study confirmed the previous results (McCoy & Pitino, 2002) for reproductive-aged women for the two subjective behaviors studied; weekly averages of informal dating and male approaches were not significantly increased for pheromone users.[48] The study found among postmenopausal women, a significantly greater proportion of those using pheromone than those using placebo showed an increase over their own baseline in intimate sociosexual behaviors.[48]

Vaginal aliphatic acids

A class of aliphatic acids (volatile fatty acids as a kind of carboxylic acid) was found in female rhesus monkeys that produced six types in the vaginal fluids.[49] The combination of these acids is referred to as "copulins". One of the acids, acetic acid, was found in all of the sampled female’s vaginal fluid.[49] Even in humans one-third have all six types of copulins, which increase in quantity prior to ovulation.[49] Copulins are used to signal ovulation; however, as human ovulation is concealed it is thought that they may be used for reasons other than sexual communication.[37]

Stimulators of the vomeronasal organ

The human vomeronasal organ has epithelia that may be able to serve as a chemical sensory organ; however, the genes that encode the VNO receptors are nonfunctional pseudogenes in humans.[36] Also, while there are sensory neurons in the human VNO there seem to be no connections between the VNO and the central nervous system. The associated olfactory bulb is present in the fetus, but regresses and vanishes in the adult brain. There have been some reports that the human VNO does function, but only responds to hormones in a "sex-specific manner". There also have been pheromone receptor genes found in olfactory mucosa.[36] Unfortunately, there have been no experiments that compare people lacking the VNO, and people that have it. It is disputed on whether the chemicals are reaching the brain through the VNO or other tissues.[37]

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.[50] Orthologous receptors exist in humans providing, the authors propose, evidence for a mechanism of human pheromone detection.[51]

Even though there are disputes about the mechanisms by which pheromones function there is evidence that pheromones do affect humans.[52] Even with all of this evidence, nothing is conclusive on whether or not humans have functional pheromones. Even if there are experiments that suggest that certain pheromones have a positive effect on human, there are just as many that state the opposite or that they have no effect whatsoever.[37]

A possible theory being studied now is that these axillary odors are being used to provide information about the immune system. Milinski and colleagues found that the artificial odors that people chose are determined in part by their major histocompatibility complexes (MHC) combination.[53] Information about an individual’s immune system could be used as a way of "sexual selection" so that the female could obtain good genes for her offspring.[36] Wedekind and colleagues found that both men and women prefer the axillary odors of people whose MHC is different from their own.[54]

Some body spray advertisers claim that their products contain human sexual pheromones that act as an aphrodisiac. Despite these claims, no pheromonal substance has ever been demonstrated to directly influence human behavior in a peer reviewed study.[37][55] Thus, the role of pheromones in human behavior remains speculative and controversial.[56]

See also


  1. "Definition of pheromone". MedicineNet Inc. 19 March 2012.
  2. Kleerebezem, M; Quadri, LE (October 2001). "Peptide pheromone-dependent regulation of antimicrobial peptide production in Gram-positive bacteria: a case of multicellular behavior.". Peptides. 22 (10): 1579–96. doi:10.1016/S0196-9781(01)00493-4. PMID 11587786.
  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. 1 2 Kohl JV, Atzmueller M, Fink B, Grammer K (October 2001). "Human pheromones: integrating neuroendocrinology and ethology". Neuro Endocrinol. Lett. 22 (5): 309–21. PMID 11600881.
  5. Butenandt, A.; Beckamnn, R.; Hecker, E. (1961). "Über den Sexuallockstoff des Seidenspinners .1. Der biologische Test und die Isolierung des reinen Sexuallockstoffes Bombykol". Hoppe-Seylers Zeitschrift für Physiologische Chemie. 324: 71–83. doi:10.1515/bchm2.1961.324.1.71.
  6. Dusenbery, David B. (2009). Living at Micro Scale, Chapter 19. Harvard University Press, Cambridge, Mass. ISBN 978-0-674-03116-6.
  8. Landolt, J.P. (1997). "Sex attractant and aggregation pheromones of male phytophagous insects". American Entomologist. 43 (1): 12–22.
  9. 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.
  10. Landoldt, P. J., Reed, H. C., and Heath, R. R. "An Alarm Pheromone from Heads of Worker Vespula squamosa (Hymenoptera: Vespidae)", "Florida Entomologist", June 1999.
  11. Post, Downing and Jeanne (1984). "Alarm response to venom by social wasps Polistes exclamans and P. fuscatus". Journal of Chemical Ecology 10 (10): 1425–1433. doi:10.1007/BF00990313.
  12. J. du P. Bothma (2002). Game Ranch Management (4th ed.). Van Schaik. ISBN 978-0-627-02471-9.
  13. 1 2 Kimball, J.W. Pheromones. Kimball's Biology Pages. Sep 2008
  14. "Excited ants follow pheromone trail of same chemical they will use to paralyze their prey". Retrieved 2006-03-14.
  15. "Study: Ants Use Scents Like Road Signs". Retrieved 2006-03-14.
  16. Fitzgerald, T. D. (July 2008). "Use of pheromone mimic to cause the disintegration and collapse of colonies of tent caterpillars ( Malacosoma spp.).". Journal of Applied Entomology. 132 (6): 451–460. doi:10.1111/j.1439-0418.2008.01286.x.
  17. Bernstein C, Bernstein H (September 1997). "Sexual communication". J. Theor. Biol. 188 (1): 69–78. doi:10.1006/jtbi.1997.0459. PMID 9299310.
  18. Danton H. O’Day, Paul A. Horgen (1981) Sexual Interactions in Eukaryotic Microbes Academic Press, New York. ISBN 0125241607 ISBN 978-0125241601
  19. Dusenbery, David B. (2009). Living at Micro Scale, Chapters 19 & 20. Harvard University Press, Cambridge, Mass. ISBN 978-0-674-03116-6.
  20. Raina, AK; Klun, JA. (1984). "Brain factor control of sex pheromone production in the female corn earworm moth". Science. 225 (4661): 531–3. doi:10.1126/science.225.4661.531.
  21. Papke, Randi S.; Kemp, Darell J.; Rutowski, Ronald L. (2007). "Multimodal Signalling: Structural Ultraviolet Reflectance Predicts Male Mating Success Better than Pheromones in the Butterfly Colias eurytheme L. (Pieridae)". Animal Behavior. 73: 47–54. doi:10.1016/j.anbehav.2006.07.004.
  22. Burand JP, Tan W, Kim W, Nojima S, Roelofs W. Infection with the insect virus Hz-2v alters mating behavior and pheromone production in female Helicoverpa zea moths. J Insect Sci. 2005;5:6.
  23. Sen, Ruchira; Gadagkar, Raghavendra (2010). "Natural history and behaviour of the primitively eusocial wasp (Hymenoptera: Vespidae): a comparison of the two sexes". Journal of Natural of History.
  24. "Alpinobombus". Natural History Museum. Retrieved 26 September 2015
  25. Svensson, Bo. G; Bergstrom, Gunnar (1979). "MARKING PHEROMONES OF Alpinobornbus MALES". Journal of Chemical Ecology. 5 (4).
  26. Yao, M.; Rosenfeld, J.; Attridge, S.; Sidhu, S.; Aksenov, V.; Rollo, C.D. (2009). "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 0071-3260. Retrieved July 22, 2011.
  27. Hildebrand, J. G. (1995). "Analysis of chemical signals by nervous systems". Proc. Natl. Acad. Sci. U.S.A. 92 (1): 67–74. doi:10.1073/pnas.92.1.67.
  28. Stoka, AM (June 1999). "Phylogeny and evolution of chemical communication: an endocrine approach" (PDF). Journal of molecular endocrinology. 22 (3): 207–25. doi:10.1677/jme.0.0220207. PMID 10343281.
  29. R.S. Herz, T. Engen, Odor memory: review and analysis, Psychon. Bull. Rev. 3 (1996) 300–313.
  30. 1 2 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.
  31. Keverne EB (1999). "The vomeronasal organ". Science. 286 (5440): 716–720. doi:10.1126/science.286.5440.716. PMID 10531049.
  32. Sherborne AL, Thom MD, Paterson S, et al. (December 2007). "The genetic basis of inbreeding avoidance in house mice". Curr. Biol. 17 (23): 2061–6. doi:10.1016/j.cub.2007.10.041. PMC 2148465Freely accessible. PMID 17997307.
  33. 1 2 Jiménez JA, Hughes KA, Alaks G, Graham L, Lacy RC (1994). ") "An experimental study of inbreeding depression in a natural habitat". Science. 266 (5183): 271–3. doi:10.1126/science.7939661. PMID 7939661.
  34. 1 2 3 Foster, Robert L. (1992). "Nestmate Recognition as an Inbreeding Avoidance Mechanism in Bumble Bees (Hymenoptera: Apidae)". Journal of the Kansas Entomological Society. Kansas (Central States) Entomological Society. 65 (3): 238–243. JSTOR 25085362.
  35. Martin, Stephen. "Host Specific Social Parasites (Psithyrus) Indicate Chemical Recognition System in Bumblebees". Journal of Chemical Ecology. 36 (8): 855–863. doi:10.1007/s10886-010-9805-3.
  36. 1 2 3 4 5 Karl Grammer; Fink, Bernhard; Neave, Nick (2005). "Human pheromones and sexual attraction". European Journal of Obstetrics and Gynecology and Reproductive Biology. 118 (2): 135–142. doi:10.1016/j.ejogrb.2004.08.010. PMID 15653193.
  37. 1 2 3 4 5 6 7 Warren S. T. Hays (2003). "Human pheromones: have they been demonstrated?". Behavioral Ecology and Sociobiology. 54 (2): 98–97. doi:10.1007/s00265-003-0613-4.
  38. 1 2 3 Taymour Mostafa; Khouly, Ghada El; Hassan, Ashraf (2012). "Pheromones in sex and reproduction: Do they have a role in humans?". Journal of Advanced Research. 3 (1): 1–9. doi:10.1016/j.jare.2011.03.003.
  39. 1 2 Kirk-Smith, Michael (1978). "Human social attitudes affected by androstenol". Research Communications in Psychology, Psychiatry & Behavior. 3 (4): 379–384. ISSN 0362-2428.
  40. McClintock MK (January 1971). "Menstrual synchrony and suppression". Nature. 229 (5282): 244–5. doi:10.1038/229244a0. PMID 4994256.
  41. Stern K, McClintock MK (March 1998). "Regulation of ovulation by human pheromones". Nature. 392 (6672): 177–9. doi:10.1038/32408. PMID 9515961..
  42. 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.
  43. Strassmann BI (March 1999). "Menstrual synchrony pheromones: cause for doubt". Hum. Reprod. 14 (3): 579–80. doi:10.1093/humrep/14.3.579. PMID 10221677.
  44. C. Van Toller; Kirk-Smith, M.; Wood, N.; Lombard, J.; Dodd, G.H. (1983). "Skin conductance and subjective assessments associated with the odour of 5-α-androstand-3-one". Biological Psychology. 16 (1–2): 85–107. doi:10.1016/0301-0511(83)90056-X. PMID 6682682.
  45. 1 2 3 Tom A. Hummer (2009). "Putative human pheromone androstadienone attunes the mind specifically to emotional information". Hormones and Behavior. 44 (4): 548–559. doi:10.16/j.yhbeh.2009.01.002.
  46. 1 2 Winnifred B. Cutler; Friedmann, Erika; McCoy, Norma L. (1998). "Pheromonal Influences on Sociosexual Behavior in Men". Archives of Sexual Behavior. 27 (1): 1–13. doi:10.1023/A:1018637907321. PMID 9494686.
  47. 1 2 Norma L McCoy; Pitino, L (2002). "Pheromonal influences on sociosexual behavior in young women". Physiology & Behavoir. 75 (3): 367–375. doi:10.1016/S0031-9384(01)00675-8.
  48. 1 2 "Pheromonal influences on sociosexual behavior in postmenopausal women". The Journal of Sex Research. 41 (4): 372–380. November 2004. doi:10.1080/00224490409552244. PMID 15765277.
  49. 1 2 3 Richard P. Michael; Bonsall, R.W.; Kutner, M. (1975). "Volatile fatty acids, "copulins", in human vaginal secretions". Psychoneuroendocrinoloy. 1 (2): 153–163. doi:10.1016/0306-4530(75)90007-4.
  50. 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.
  51. Pearson H (2006). "Mouse data hint at human pheromones". Nature. 442 (7102): 495. doi:10.1038/442495a. PMID 16885951.
  52. Charles J. Wysocki; Preti, George (2004). "Facts, fallacies, fears, and frustrations with human pheromones". The Anatomical Record. 281A (1): 1201–11. doi:10.1002/ar.a.20125. PMID 15470677.
  53. Milinski, Manfred (2001). "Evidence for MHC-correlated perfume preferences in humans". Behavioral Ecology. 12 (2): 140–9. doi:10.1093/beheco/12.2.140.
  54. Claus Wedekind; Seebeck, T.; Bettens, F.; Paepke, A. J. (1995). "MHC-Dependent Mate Preferences in Humans". Proceedings: Biological Sciences. 260 (1359): 245–9. doi:10.1098/rspb.1995.0087. PMID 7630893.
  55. Bear, Mark F.; Barry W. Connors; Michael A. Paradiso (2006). Neuroscience: Exploring the Brain. Lippincott Williams & Wilkins. ISBN 0-7817-6003-8. p. 264 ...there has not yet been any hard evidence for human pheromones that might [change] sexual attraction (for members of either sex) [naturally]
  56. Dale Purves; et al. (2008). Principles of Cognitive Neuroscience. Sinauer. ISBN 978-0-87893-694-6.

Further reading

External links

This article is issued from Wikipedia - version of the 10/17/2016. The text is available under the Creative Commons Attribution/Share Alike but additional terms may apply for the media files.