You smell different! Temperature interferes with intracolonial recognition in Odontomachus brunneus

Authors

  • Luiz Carlos Santos Junior Universidade Estadual de Mato Grosso do Sul
  • Kamylla Balbuena Michelutti Universidade Estadual de Mato Grosso do Sul
  • Rafaella Caroline Bernardi Universidade Estadual de Mato Grosso do Sul
  • Emerson Pereira Silva Universidade Federal da Grande Dourados
  • Claudia Andrea Lima Cardoso Universidade Estadual de Mato Grosso do Sul
  • William Fernando Antonialli - Junior Universidade Estadual de Mato Grosso do Sul

DOI:

https://doi.org/10.13102/sociobiology.v69i1.6235

Keywords:

Cuticular Hydrocarbons, Temperature, Chain length, Intraspecific recognition

Abstract

Intracolonial recognition among social insects is performed mainly by means of cuticular hydrocarbons (CHCs) that provide chemical communication, although their primary function is the avoidance of desiccation. Therefore, the ability to adjust to climatic variation may be related to the composition of CHCs. The hypothesis adopted in this work was that workers of the ant Odontomachus brunneus, when exposed to higher or lower average temperatures, change the CHCs composition, as a readjustment to the new conditions, and that this, in turn, leads to a change in intraspecific recognition capacity. To test this hypothesis, colonies of O. brunneus reared in the laboratory were subdivided into four groups. Two groups were kept at the same temperature, in order to assess the effect of isolation itself, while one group was kept at high temperature and another was kept at low temperature. Two groups were maintained at 25 °C, with no further conditions imposed. Subsequently, encounters were induced between individuals from these groups and from the high and low temperature groups, followed by the extraction of CHCs from each individual. The results indicated significant differences in recognition time and CHC composition between the high/low temperature groups and those kept at 25 °C. Antennation time during nestmate encounters was significantly longer for the groups submitted to temperature treatments (high and low), compared to those kept at 25 °C, suggesting recognition difficulty. In order to adjust to changing temperature conditions, O. brunneus undergoes changes in the composition of CHCs and in intraspecific recognition capacity.

Downloads

Download data is not yet available.

Author Biographies

Luiz Carlos Santos Junior, Universidade Estadual de Mato Grosso do Sul

Ecology Laboratory, Center for Integrated Environmental Monitoring and Analysis

Kamylla Balbuena Michelutti, Universidade Estadual de Mato Grosso do Sul

Ecology Laboratory, Center for Integrated Environmental Monitoring and Analysis

Rafaella Caroline Bernardi, Universidade Estadual de Mato Grosso do Sul

Ecology Laboratory, Center for Integrated Environmental Monitoring and Analysis

Emerson Pereira Silva, Universidade Federal da Grande Dourados

Ecology Laboratory, Center for Integrated Environmental Monitoring and Analysis

Claudia Andrea Lima Cardoso, Universidade Estadual de Mato Grosso do Sul

Ecology Laboratory, Center for Integrated Environmental Monitoring and Analysis

William Fernando Antonialli - Junior, Universidade Estadual de Mato Grosso do Sul

Ecology Laboratory, Center for Integrated Environmental Monitoring and Analysis

References

Antonialli-Junior WF, Lima SM, Andrade LHC, Súarez YR (2007). Comparative study of the cuticular hydrocarbon in queens, workers and males of Ectatomma vizottoi (Hymenoptera, Formicidae) by Fourier transform infrared photoacoustic spectroscopy. Genetics and Molecular Research, 6: 492-499.

Antonialli-Junior WF, Súarez YR, Izida T, Andrade LHC, Lima SM (2008). Intra- and interspecific variation of cuticular hydrocarbon composition in two Ectatomma species (Hymenoptera: Formicidae) based on Fourier transform infrared photoacoustic spectroscopy. Genetics and Molecular Research, 7: 559-566. doi: 10.4238/vol7-2gmr454

Bernier UR, Carlson DA, Geden CJ (1998). Gas chromatography/mass spectrometry analysis of the cuticular hydrocarbons from parasitic wasps of the genus Muscidifurax. Journal of the American Society for Mass Spectrometry, 9: 320-332. doi: 10.1016/s1044-0305(97)00288-2

Blomquist GJ, Bagnères AG (2010). Introduction: history and overview of insect hydrocarbons. In: (eds Blomquist GJ, Bagnères A-G), Insect hydrocarbons: biology, biochemistry, and chemical ecology, Cambridge, UK: Cambridge University Press, pp 3-18.

Boulay, R., V. Soroker, E.J. Godzinska, A. Hefetz & A. Lenoir (2000a). Octopamine reverses the isolation-induced increase in trophallaxis in the carpenter ant Camponotus fellah. Journal of Experimental Biology, 203: 513-520

Boulay, R., A. Hefetz, V. Soroker and A. Lenoir (2000b). Individuality in hydrocarbon production obliges Camponotus fellah workers frequent exchanges for colony integration. Animal Behaviour, 59: 1127-1133.

Boulay R, Aron S, Cerdá X, Doums C, Graham P, Hefetz A, Monnin T (2017). Social life in arid environments: the case study of Cataglyphis Ants. Annual Review of Entomology, 62: 305-321. doi: 10.1146/annurev-ento-031616-034941

Buczkowski G, Kumar R, Suib SL, Silverman J (2005). Dietrelated modification of cuticular hydrocarbon profiles of the argentine ant, Linepithema humile, diminishes intercolony Aggression. Journal of Chemical Ecology, 31: 829-843. doi: 10.1007/s10886-005-3547-7

Chown SL, Sørensen JG, Terblanche JS (2011). Water loss in insects: An environmental change perspective. Journal of Insect Physiology, 57: 1070-1084. doi: 10.1016/j.jinsphys. 2011.05.004

Chung H, Carroll SB (2015). Wax, sex and the origin of species: Dual roles of insect cuticular hydrocarbons in adaptation and mating. BioEssays, 37: 822-830. doi: 10.1002/bies.201500014

Cuvillier-Hot V, Cobb M, Malosse C, Peeters C (2001). Sex, age and ovarian activity affect cuticular hydrocarbons in Diacamma ceylonense, a queenless Ant. Journal of Insect Physiology, 47: 485-493. doi: 10.1016/S0022-1910(00)00137-2

Dahbi, A. and A. Lenoir (1998b). Nest separation and the dynamics of the gestalt odor in the polydomous ant Cataglyphis iberica (Hymenoptera, Formicidae). Behavioral Ecology and Sociobiology, 42: 349-355.

Duarte BF, Michelutti KB, Antonialli-Junior WF, Cardoso CAL (2019). Effect of temperature on survival and cuticular composition of three different ant species. Journal of Thermal Biology, 80: 178-189. doi: 10.1016/j.jtherbio.2019.02.005

Gibbs A, Pomonis JG (1995). Physical properties of insect cuticular hydrocarbons: The effects of chain length, methylbranching and unsaturation. Comparative Biochemistry and Physiology Part B: Biochemistry and Molecular Biology, 112: 243-249. doi: 10.1016/0305-0491 (95)00081-x

Gibbs AG (1998). Water-proofing properties of cuticular lipids. American Zoologist, 38: 471-482.

Gibbs AG, Chippindale AK, Rose MR (1997). Physiological mechanisms of evolved desiccation resistance in Drosophila melanogaster. Journal of Experimental Biology, 200: 1821-1832.

Gibbs AG (2007). Waterproof cockroaches: the early work of Ramsay JA. Journal of Experimental Biology, 210: 921-922. doi: 10.1242/jeb.000661

Hefetz A (2007). The evolution of hydrocarbon pheromone parsimony in ants (Hymenoptera: Formicidae): interplay of colony odor uniformity and odor idiosyncrasy. Myrmecological News, 10: 59-68.

Howard RW, Blomquist GJ (2005). Ecological, behavioral, and biochemical aspects of insect hydrocarbons. Annual Review of Entomology, 50: 371-393. doi: 10.1146/annurev.ento.50.071803.130359

Howard RW, Pérez-Lachaud G, Lachaud JP (2001). Cuticular hydrocarbons of Kapala sulcifacies (Hymenoptera: Eucharitidae and its host, the Ponerine Ant Ectatomma ruidum (Hymenoptera: Formicidae). Annals of the Entomological Society of America, 94: 707-716. doi: 10.1603/0013-8746(2001)094[0707:choksh]2.0.co;2

Jaffe K, Marcuse M (1983). Nestmate recognition and territorial behaviour in the ant Odontomachus bauri emery (Formicidae: Ponerinae). Insectes Sociaux, 30: 466-481. doi: 10.1007/bf022 23978

Lenoir A, Hefetz A, Simon T, Soroker V (2001). Comparative dynamics of gestalt odour formation in two ant species Camponotus fellahand Aphaenogaster senilis (Hymenoptera: Formicidae). Physiological Entomology, 26: 275-283. doi: 10.1046/j.0307-6962.2001.00244.x

Menzel F, Blaimer BB, Schmitt T (2017). How do cuticular hydrocarbons evolve? Physiological constraints and climatic and biotic selection pressures act on a complex functional trait. Proceedings of the Royal Society B: Biological Sciences, 284: 1-10. doi: 10.1098/rspb.2016.1727

Menzel F, Zumbusch M, Feldmeyer B (2018). How ants acclimate: impact of climatic conditions on the cuticular hydrocarbon profile. Functional Ecology, 32: 657-666. doi: 10.11 11/1365-2435.13008

Mercier J, Lenoir A, Dejean A (1997). Ritualised versus aggressive behaviours displayed by Polyrhachis laboriosa (F. Smith) during intraspecific competition. Behavioural Processes, 41: 39-50. doi: 10.1016/s0376-6357(97)00026-0

Michelutti KB, Soares ERP, Sguarizi-Antonio D, Piva RC, Súarez YR, Cardoso CAL, Antonialli-Junior WF (2018). Influence of temperature on survival and cuticular chemical profile of social wasps. Journal of Thermal Biology, 71: 221-231. doi: 10.1016/j.jtherbio.2017.11.019

Monnin T (1999). Dominance hierarchy and reproductive conflicts among subordinates in a monogynous queenless ant. Behavioral Ecology, 10: 323-332. doi: 10.1093/beheco/10.3.323

Moore HE, Adam CD, Drijfhout FP (2014). Identifying 1st instar larvae for three forensically important blowfly species using “fingerprint” cuticular hydrocarbon analysis. Forensic Science International, 240: 48-53. doi: 10.1016/j.forsciint.2014.04.002

Nielsen, J., J.J. Boomsma, N.J. Oldham, H.C. Petersen & E.D. Morgan (1999). Colony-level and season-specific variation in cuticular hydrocarbon profiles of individual workers in the ant Formica truncorum. Insectes Sociaux, 46: 58-65.

Oliveira PS, Hölldobler B (1989). Orientation and communication in the neotropical ant Odontomachus bauri Emery (Hymenoptera, Formicidae, Ponerinae). Ethology, 83: 154-166. doi: 10.1111/j.1439-0310.1989.tb00525.x

Provost, E., G. Rivière, M. Roux, E.D. Morgan and A.-G. Bagnères (1993). Change in the chemical signature of the ant Leptothorax lichtensteini Bondroit with time. Insect Biochemistry and Molecular Biology, 23: 945-957.

Sainz-Borgo C, Cabrera A, Hernández JV (2011). Nestmate recognition in the ant Odontomachus bauri (Hymenoptera: Formicidae). Sociobiology, 58: 1-18.

Smith AA, Millar JG, Hanks LM, Suarez AV (2012). Experimental evidence that workers recognize reproductive through cuticular hydrocarbons in the ant Odontomachus brunneus. Behavioral Ecology and Sociobiology, 66: 1267-1276. doi: 10.1007/ s00265-012-1380-x

Starks PT, Watson RE, Dipaola MJ, Dipaola CP (1998). The effect of queen number on nestmate discrimination in the facultatively polygynous ant Pseudomyrmex pallidus (Hymenoptera: Formicidae). Ethology, v. 104, p. 573-584.

Soares ERP, Batista NR, Souza RS, Torres VO, Cardoso CAL, Nascimento FS, Antonialli-Junior WF (2017). Variation of cuticular chemical compounds in three species of Mischocyttarus (Hymenoptera: Vespidae) eusocial wasps. Revista Brasileira de Entomologia, 61: 224-231. doi: 10.1016/j.rbe.2017.05.001

Soroker, V., D. Fresneau and A. Hefetz (1998). Formation of colony odor in ponerine ant Pachycondyla apicalis. Journal of Chemical Ecology, 24: 1077-1090.

Soroker V, Lucas C, Simon T, Hefetz A, Fresneau D, Durand JL (2003). Hydrocarbon distribution and colony odour homogenisation in Pachycondyla apicalis. Insectes Sociaux, 50: 212-217. doi: 10.1007/s00040-003-0669-1

Sorvari J, Theodora P, Turillazzi S, Hakkarainen H, Sundström L (2008). Food resources, chemical signaling, and nest mate recognition in the ant Formica aquilonia. Behavioral Ecology, 19: 441-447. doi: 10.1093/beheco/arm160

Sprenger PP, Burkert LH, Abou B, Federle W, Menzel F (2018). Coping with the climate: Cuticular hydrocarbon acclimation of ants under constant and fluctuating conditions. Journal of Experimental Biology, 221: jeb-171488. doi: 10.1242/jeb.171488

Suarez AV, Tsutsui ND, Holway DA, Case TJ (1999). Behavioral and genetic differentiation between native and introduced populations of the argentine ant. Biological Invasions, 1: 43-53. doi: 10.1023/a:1010038413690

Thomas ML, Tsutsui ND, Holway DA (2004). Intraspecific competition influences the symmetry and intensity of aggression in the argentine ant. Behavioral Ecology, 16: 472-481. doi: 10.1093/beheco/ari014

Vander Meer, R.K., D. Saliwanchik and B. Lavine, 1989. Temporal changes in colony cuticular hydrocarbon patterns of Solenopsis invicta: Implications for nestmate recognition. Journal of Chemical Ecology, 15: 2115-2125.

Vander-Meer RK, Morel L. (1998). Pheromone communication in social insects: ants, wasps, bees, and termites. Colorado, CO: Westview Press.

Wagner D, Tissot M, Gordon D (20001). Task-related environment alters the cuticular hydrocarbon composition of harvester ants. Journal of Chemical Ecology, 27: 1805-1819. doi: 10.10 23/a:1010408725464

Weiss K, Parzefall C, Herzner G (2014). Multifaceted defense against antagonistic microbes in developing offspring of the parasitoid wasp Ampulex compressa (Hymenoptera, Ampulicidae). PLoS ONE, 9: 1-14. doi: 10.1371/journal.pone.0098784

Zavatini JA (1992). Dinâmica atmosférica no Mato Grosso do Sul. Geografia (Rio Claro). Ageteo, 17: 65-91.

Downloads

Published

2022-02-08

How to Cite

Santos Junior, L. C., Michelutti, K. B., Bernardi, R. C., Silva, E. P., Cardoso, C. A. L., & Antonialli - Junior, W. F. (2022). You smell different! Temperature interferes with intracolonial recognition in Odontomachus brunneus. Sociobiology, 69(1), e6235. https://doi.org/10.13102/sociobiology.v69i1.6235

Issue

Section

Research Article - Ants

Most read articles by the same author(s)