Chemical communication in insects

Pheromones can be used instead of insecticides in orchards. Pest insects are attracted by sex pheromones, allowing farmers to evaluate pest levels, and if need be to provide sufficient pheromone to disrupt mating.

Chemical communication in insects is social signalling between insects of the same or different species, using chemicals. These chemicals may be volatile, to be detected at a distance by other insects' sense of smell, or non-volatile, to be detected on an insect's cuticle by other insects' sense of taste. Many of these chemicals are pheromones, acting like hormones outside the body.

Among the many functions of chemical communication are attracting mates, aggregating conspecific individuals of both sexes, deterring other individuals from approaching, announcing a new food source, marking a trail, recognizing nest-mates, marking territory and triggering aggression.

Chemical communication within a species can be usurped by other species in chemical mimicry. The mimic produces allomones or pheromones to influence the behaviour of another insect, the dupe, to the mimic's advantage. The process is important in ant mimicry where species that do not look like ants are accepted into the ant colony.

History of research

In 1960, Dethier, Brown, and Smith categorised chemical signals into six groups.[1]

Chemical signals by the behaviour they induce (Dethier, Brown, and Smith 1960)[1]
Category Resulting behaviour
Locomotory stimulant Makes insects disperse, such as by speeding up their movements or slowing down their turning rate
Arrestant Makes insects aggregate by contact, such as by slowing their movements or speeding up their turning rate
Attractant Makes insects move towards the source
Repellent Makes insects move away from the source
Feeding, mating, or ovipositional stimulant Encourages feeding, mating, or oviposition
Deterrent Inhibits feeding or oviposition

In 1965, the entomologist Edward O. Wilson published a paper on chemical communication in the social insects, arguing that their societies were principally organised by "complex systems of chemical signals".[2] By 1990, Mahmoud Ali and David Morgan noted that the field had grown too large to review comprehensively.[1]

Semiochemicals

In addition to the use of means such as making sounds, generating light, and touch for communication, a wide range of insects have evolved chemical signals, semiochemicals. Types of semiochemicals include pheromones and kairomones. Chemoreception is the physiological response of a sense organ to a chemical stimulus where the chemicals act as signals to regulate the state or activity of a cell.[1][3]

Semiochemicals are often derived from plant metabolites.[3] They can be grouped by which individuals they act upon:

  • Pheromones serve communication between insects of the same species.[3]
  • Allomones benefit their producer by the effect they have upon the receiver.[3]
  • Kairomones benefit their receiver instead of their producer.[3]
  • Synomones benefit the producer and the receiver.[3]

While some chemicals are targeted at individuals of the same species, others are used for communication across species. The use of scents is especially well-developed in social insects.[3] Cuticular hydrocarbons are nonstructural materials produced and secreted to the cuticle surface to fight desiccation and pathogens. They are important, too, as pheromones, especially in social insects.[4]

Pheromones

A fanning honeybee exposes Nasonov's gland (white stripe at tip of abdomen) releasing pheromone to entice swarm into an empty hive

Pheromones are of two main kinds: primer pheromones, which generate a long-duration change in the insect that receives them, or releaser pheromones, which cause an immediate change in behaviour.[1] Primers include the queen pheromones essential to maintain the caste structure of social Hymenopteran colonies; they tend to be non-volatile and are dispersed by workers across the colony.[5] In some ants and wasps, the queen pheromones are cuticular hydrocarbons.[6]

Releaser pheromones[1]
Type Function Notes
Sex Bring sexes together for mating Well-studied in Lepidoptera
Invitation Stimulate feeding or oviposition at a site
Aggregation Bring individuals together Temporarily in sub-social insects; permanently in social insects
Dispersal or spacing Reduce intraspecific competition for a scarce resource
Alarm Signal attack or alarm Mostly in colonial insects
Trail Mark a line on a surface as a path to be followed Mainly in Hymenoptera (e.g. ants) and Isoptera (termites); a few Lepidoptera (e.g. processionary moths)
Territorial and home range Mark a territory or range
Surface and funeral Dead ants stimulate their removal from the nest. Possibly assist in recognition of colony or species
Pheromonal glands (UPPER CASE) in social insects

Eusocial insects including ants, termites, bees, and social wasps produce pheromones from several types of exocrine gland. These include mandibular glands in the head, and Dufour's, tergal, and other glands in the abdomen.[5]

Mimicry

Chemical communication within a species can be usurped by other species in chemical mimicry. The mimic produces allomones or pheromones to influence the behaviour of another insect, the dupe, to the mimic's advantage.[7] The type of mimicry can be Batesian, in which the mimic gains protection by resembling a harmful insect;[8] it can also be Müllerian, in which different well-defended insects resemble each other, in this case chemically, to minimise losses to predators;[9] aggressive, enabling a predatory mimic to approach its prey;[10] or reproductive, as in Pouyannian mimicry, when an orchid chemically (and visually) resembles a pollinator such as a bee or wasp, which tries to copulate with the flower, transferring pollen in the process.[11] It occurs, too, in ant mimicry, where a mimic such as a butterfly larva is enabled to live within a colony of ants, that would otherwise kill it, by producing antlike semiochemicals.[12]

Human uses of pheromones

Human uses of pheromones include their application instead of insecticides in orchards. Pest insects such as fruit moths are attracted by sex pheromones, allowing farmers to evaluate pest levels, and if need be to provide sufficient pheromone to disrupt mating.[13]

References

  1. ^ a b c d e f Ali, Mahmoud Fadl; Morgan, E. David (1990). "Chemical communication in insect communities: a guide to insect pheromones with special emphasis on social insects". Biological Reviews. 65 (3): 227–247. doi:10.1111/j.1469-185X.1990.tb01425.x. S2CID 86609942.
  2. ^ Wilson, Edward O. (3 September 1965). "Chemical Communication in the Social Insects". Science. 149 (3688). American Association for the Advancement of Science (AAAS): 1064–1071. Bibcode:1965Sci...149.1064W. doi:10.1126/science.149.3688.1064. PMID 17737837.
  3. ^ a b c d e f g Gullan, P. J.; Cranston, P. S. (2005). The Insects: An Outline of Entomology (3rd ed.). Oxford: Blackwell Publishing. ISBN 978-1-4051-1113-3.
  4. ^ Yan, Hua; Liebig, Jürgen (1 April 2021). "Genetic basis of chemical communication in eusocial insects". Genes & Development. 35 (7–8). Cold Spring Harbor Laboratory Press & The Genetics Society: 470–482. doi:10.1101/gad.346965.120. PMC 8015721. PMID 33861721.
  5. ^ a b Hefetz, Abraham (28 March 2019). "The critical role of primer pheromones in maintaining insect sociality". Zeitschrift für Naturforschung C. 74 (9–10): 221–231. doi:10.1515/znc-2018-0224. PMID 30920959.
  6. ^ Yan, Hua; Liebig, Jürgen (1 April 2021). "Genetic basis of chemical communication in eusocial insects". Genes & Development. 35 (7–8): 470–482. doi:10.1101/gad.346965.120. PMC 8015721. PMID 33861721.
  7. ^ von Beeren, Christoph; Pohl, Sebastian; Witte, Volker (2012). "On the Use of Adaptive Resemblance Terms in Chemical Ecology". Psyche: A Journal of Entomology. 2012: 1–7. doi:10.1155/2012/635761. hdl:2123/11217.
  8. ^ Augner, Magnus; Bernays, Elizabeth A. (1998). "Plant defence signals and Batesian mimicry". Evolutionary Ecology. 12 (6): 667–679. Bibcode:1998EvEco..12..667A. doi:10.1023/a:1006581415114. S2CID 24632371.
  9. ^ Dettner, K.; Liepert, C. (1994). "Chemical Mimicry and Camouflage". Annual Review of Entomology. 39 (1): 129–154. doi:10.1146/annurev.en.39.010194.001021.
  10. ^ Eberhard, William G. (1977-12-16). "Aggressive Chemical Mimicry by a Bolas Spider". Science. 198 (4322): 1173–1175. Bibcode:1977Sci...198.1173E. doi:10.1126/science.198.4322.1173. PMID 17818935. S2CID 35215325.
  11. ^ Vereecken, N. J.; McNeil, J. N. (2010). "Cheaters and liars: chemical mimicry at its finest" (PDF). Canadian Journal of Zoology. 88 (7): 725–752. doi:10.1139/z10-040. ISSN 0008-4301. S2CID 82791533.
  12. ^ Akino, T.; Knapp, J. J.; Thomas, J. A.; Elmes, G. W. (1999). "Chemical mimicry and host specificity in the butterfly Maculinea rebeli, a social parasite of Myrmica ant colonies". Proceedings of the Royal Society of London B: Biological Sciences. 266 (1427): 1419–1426. doi:10.1098/rspb.1999.0796. PMC 1690087.
  13. ^ "Using Pheromones Instead of Insecticides". CSIRO. Retrieved 29 June 2022.

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