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===Signal pheromones===
===Signal pheromones===


Signal pheromones cause short term changes; such as, the neurotransmitter release which activates a response. For instance, GnRH molecule functions as a neurotransmitter in rats to elicit lordosis, which is a behavioral effect.<ref> Kohl, J., Atzmueller, M., Fink, B. & Grammar, K. Human Pheromones: Integrative Neuroendocrinology & Ethology. NEL 22, 309-321(2001).</ref>
Signal pheromones cause short term changes; such as, the yep yep yep neurotransmitter release which activates a response. For instance, GnRH molecule functions as a neurotransmitter in rats to elicit lordosis, which is a behavioral effect.<ref> Kohl, J., Atzmueller, M., Fink, B. & Grammar, K. Human Pheromones: Integrative Neuroendocrinology & Ethology. NEL 22, 309-321(2001).</ref>


=== Primer pheromones ===
=== Primer pheromones ===

Revision as of 18:26, 23 September 2009

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 chemical signal that triggers a natural response in another member of the same species. 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.

Background

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 classified as ecto-hormones. These chemical messengers are transported outside of the body and result in a direct developmental effect on hormone levels or behavioral change.[1] They proposed the term to describe chemical signals from conspecifics which elicit innate behaviours 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).[2]

Types

Aggregation pheromones

Aggregation pheromones function in defense against predators, mate selection, and overcoming host resistance by mass attack. A group of individuals at one location are referred as aggregation, whether consisting of one sex or both sexes. Male-produced sex attractant have been called aggregation pheromones, because they usually result in the arrival of both sexes at a calling site and increase in density of conspecifics surrounding of the pheromone source. Most sex pheromones are produced by the females and small percentage of sex attractants are produced by males.[3] Aggregation pheromones have been found in members of the Coleoptera, 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 not toxic and they are effective at very low concentrations.[4]

Alarm pheromones

Some species release a volatile substance when attacked by a predator that can trigger flight (in aphids) or aggression (in ants, bees, termites)[5] 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.[6]

Epideictic pheromones

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."

Aggregation of bug nymphs

Releaser pheromones

Releaser pheromones are powerful attractant molecules that some organisms may use to attract mates from a distance of two miles or more. This type of pheromone generally elicits a rapid response but is quickly degraded. In contrast, a primer pheromone has a slower onset and a longer duration. Ex. Rabbit (mothers) release mammary pheromones that trigger immediate nursing behavior by their babies.[7]

Signal pheromones

Signal pheromones cause short term changes; such as, the yep yep yep neurotransmitter release which activates a response. For instance, GnRH molecule functions as a neurotransmitter in rats to elicit lordosis, which is a behavioral effect.[8]

Primer pheromones

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

Territorial pheromones

Laid down in the environment, territorial pheromones mark the boundaries of an organism's territory. In dogs, these hormones are present in the urine, which they deposit on landmarks serving to mark the perimeter of the claimed territory.

Trail pheromones

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.[9] As long as the food source remains, the pheromone trail will be continually renewed. The pheromone must be continually 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.[10]

Information pheromones

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.[11]

Sex pheromones

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. 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 population in orchards. At the microscopic level, a gamete pheromone may provide a trail leading the opposite sex's gametes towards it to accomplish fertilization. Pheromones are also used in the detection of oestrus in sows. Boar pheromones are sprayed into the sty, and those sows which 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.

Other pheromones

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 consisting of Oleic and Linoleic Acids helping animals identify the presence of a dead conspecifics. (Crustaceans and Hexapods)

Uses

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.

Humans

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

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).[12][13] 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.[14]

The arm pit has been hypothesized to be a source of human pheromones.

It has been suggested that women with irregular menstrual cycles became regular when exposed to male underarm extracts.[15] They hypothesized that male sweat contains pheromones, which mirror how pheromones affect other mammals.[15]

Other studies have demonstrated that the smell of androstadienone, a chemical component of male sweat, maintains higher levels of cortisol in females,[16] and that the compound is detected via the olfactory mucosa.[17] 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.[18] 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.[19][20]

Other studies have suggested that people might be using odor cues associated with the immune system to select mates who are not closely related to themselves. 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 was similar to heterosexual males.[21] According to the researchers, this research suggests a possible role for human pheromones in the biological basis of sexual orientation.[22] 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. [23]

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.[24] Orthologous receptors exist in humans providing, the authors propose, evidence for a mechanism of human pheromone detection.[25]

Some body spray advertisers claim that their products contain human sexual pheromones which act as an aphrodisiac. In the 1970s, "copulins" were patented as products which release human pheromones, based on research on rhesus monkeys.[26] Subsequently, androstenone, axillary sweat, and "vomodors" have been claimed to act as human pheromones.[27] Despite these claims, no pheromonal substance has ever been demonstrated to directly influence human behavior in a peer reviewed study.[26][27][28]

See also

References

  1. ^ Kohl, J., Atzmueller, M., Fink, B. & Grammar, K. Human Pheromones: Integrative Neuroendocrinology & Ethology. NEL 22, 309-321.(2001)
  2. ^ Karlson, P., Lüscher, M. (1959). Pheromones: a new term for a class of biologically active substances. Nature 183, 55-56. PMID 13622694
  3. ^ https://www.msu.edu/user/miller20/carmona.htm
  4. ^ Landolt, J. P. 1997. Sex attractant and aggregation pheromones of male phytophagous insects. In American Entomologist Vol. 43- 1
  5. ^ 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: 478–486, doi:10.1007/s10886-008-9450-2 {{citation}}: External link in |title= (help)CS1 maint: multiple names: authors list (link)
  6. ^ J.du P. Bothma, Game ranch management, fourth edition, Van Schaik publishers, 2002
  7. ^ Kimball, J.W. Pheromones. Kimball's Biology Pages. Sep 2008. [1]
  8. ^ Kohl, J., Atzmueller, M., Fink, B. & Grammar, K. Human Pheromones: Integrative Neuroendocrinology & Ethology. NEL 22, 309-321(2001).
  9. ^ "Excited ants follow pheromone trail of same chemical they will use to paralyze their prey". Retrieved 2006-03-14.
  10. ^ "Study: Ants Use Scents Like Road Signs". Retrieved 2006-03-14.
  11. ^ Kimball, J.W. Pheromones. Kimball's Biology Pages. Sep 2008. [2]
  12. ^ McClintock MK (1971). "Menstrual synchrony and suppression". Nature 229 (5282): 244-5. PMID 4994256
  13. ^ Stern K, McClintock MK (1998). "Regulation of ovulation by human pheromones". Nature 392 (6672): 177-9. doi:10.1038/32408. PMID 9515961.
  14. ^ Yang, Zhengwei (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. {{cite journal}}: Unknown parameter |coauthors= ignored (|author= suggested) (help)
  15. ^ a b Looking for love potion number nine, Cathryn M. Delude, Boston Globe, September 2, 2003.
  16. ^ Wyart C, Webster WW, Chen JH, Wilson SR, McClary A, Khan RM, Sobel N (2007). "Smelling a single component of male sweat alters levels of cortisol in women". The Journal of Neuroscience : the Official Journal of the Society for Neuroscience. 27 (6): 1261–5. doi:10.1523/JNEUROSCI.4430-06.2007. PMID 17287500. {{cite journal}}: Unknown parameter |month= ignored (help)CS1 maint: multiple names: authors list (link)
  17. ^ 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
  18. ^ "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. 2002. {{cite journal}}: Cite has empty unknown parameter: |coauthors= (help); Unknown parameter |month= ignored (help)
  19. ^ Anders Winman (2004). "Do perfume additives termed human pheromones warrant being termed pheromones?". Physiology & Behavior Volume , Issue 4, 30 September , Pages. 82 (4): 697–701. doi:10.1016/j.physbeh.2004.06.006. PMID 15327919. {{cite journal}}: line feed character in |journal= at position 22 (help)
  20. ^ Charles J. Wysocki, George Preti (1998). "Pheromonal Influences". Archives of Sexual Behavior. 27 (6): 627–641. doi:10.1023/A:1018729302720. PMID 9883309.
  21. ^ Berglund H, Lindström P, Savic I (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. {{cite journal}}: Unknown parameter |month= ignored (help)CS1 maint: multiple names: authors list (link)
  22. ^ Wade, N. "Gay Men are found to have Different Scent of Attraction." NY Times, May 9, 2005
  23. ^ Zhou, Wen (2008). "Encoding human sexual chemosensory cues in the orbitofrontal and fusiform cortices". J Neurosci. 25 (53): 14416–21. {{cite journal}}: Check |authorlink= value (help); External link in |authorlink= (help); Unknown parameter |coauthors= ignored (|author= suggested) (help); Unknown parameter |month= ignored (help)
  24. ^ Liberles SD, Buck LB. 2006. A second class of chemosensory receptors in the olfactory epithelium. Nature. 442(7103):645-50. PMID 16878137
  25. ^ Pearson H. 2006. Mouse data hint at human pheromones. Nature. 442(7102):495. PMID 16885951
  26. ^ 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."
  27. ^ a b Hays, Warren S. T., Human pheromones: have they been demonstrated? Behavioral Ecology and Sociobiology, 2003, 54:89-97
  28. ^ Bear, Mark F. (2006). Neuroscience: Exploring the Brain. Lippincott Williams & Wilkins. ISBN 0781760038. {{cite book}}: Unknown parameter |coauthors= ignored (|author= suggested) (help) p. 264 ...there has not yet been any hard evidence for human pheromones that might [change] sexual attraction (for members of either sex) [naturally]

Further reading

  • Kohl, JV., Atzmueller, M., Fink, B. & Grammer, K. (2001). Human Pheromones: Integrating Neuroendocrinology and Ethology. Neuroendocrinology Letters, 22(5), 319-331. Full text
  • Wilson, E. O., Bossert, W. H. (1963). Chemical communication among animals. Recent Progress in Hormone Research, 19, 673-716.
  • Wyatt, Tristram D. (2003). Pheromones and Animal Behaviour: Communication by Smell and Taste. Cambridge: Cambridge University Press. ISBN 0-521-48526-6.

External links

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