Abstract
When an insect walks, it leaves chemical cues that derive from the arolium, a tarsal structure. These cues may contain important information about other species that occur in their community and can then mediate interactions of competition, predation, and information about resources with ants from their own colony. The compounds of these cues are released into the substrate in the form of chemical footprints. There are still few species studied, and little is known about the behavior of ants regarding these signals and how they use them in their interactions. Therefore, the aim of this study was to assess the behavioral strategy of different ant species when confronted with chemical footprints left by other ants, as well as identify their compounds and their relationship with the cuticular hydrocarbon profile. The experiments were performed using a Y-maze, where in one of the arms, there were chemical footprints of their own species or of other species, and the other Y arm was footprint-free. The chemical compounds of footprints and cuticle were analyzed by gas chromatography-mass spectrometry. The results show that foragers of all species detect and respond to the presence of chemical cues in the form of footprints left by other ants. Foragers of all species followed footprints of individuals of the same species both nestmates and non-nestmates; however, Neoponera villosa avoided the footprints of Cephalotes borgmeieri, and C. borgmeieri avoided the footprints of the other two species. The chemical compositions of the cuticle and footprints are related to each other and are specific to each species.
![](http://media.springernature.com/m312/springer-static/image/art%3A10.1007%2Fs00114-024-01908-6/MediaObjects/114_2024_1908_Fig1_HTML.png)
Similar content being viewed by others
References
Akino T, Yamaoka R (2005) Trail discrimination signal of Lasius japonicus (Hymenoptera: Formicidae). Chemoecology 15:21–30. https://doi.org/10.1007/s00049-005-0288-6
Arnan X, Gaucherel C, Andersen AN (2011) Dominance and species co-occurrence in highly diverse ant communities: a test of the interstitial hypothesis and discovery of a three-tiered competition cascade. Oecologia 166:783–794. https://doi.org/10.1007/s00442-011-1919-y
Baccaro FB, Feitosa RM, Fernández F, Fernandes IO, Izzo TJ, Souza JD, Solar R (2015) Guia para os gêneros de formigas do Brasil. Editora INPA, Manaus, p 388
Baroni Urbani C (1998) The number of castes in ants, where major is smaller than minor and queens wear the shield of the soldiers. Insectes Soc 45:315–333
Binz H, Foitzik S, Staab F, Menzel F (2014) The chemistry of competition: exploitation of heterospecific cues depends on the dominance rank in the community. Anim Behav 94:45–53. https://doi.org/10.1016/j.anbehav.2014.05.024
Blomquist GJ, Bagnères AG (2010) Introduction: history and overview of insect hydrocarbons. In: Insect hydrocarbons: biology, biochemistry, and chemical ecology. Cambridge University Press, pp 3–18
Carroll CR, Janzen DH (1973) Ecology of foraging by ants. Annu Rev Ecol Syst 4:231–257. https://doi.org/10.1146/annurev.es.04.110173.001311
Cerdá X, Arnan X, Retana J (2013) Is competition a significant hallmark of ant (Hymenoptera: Formicidae) ecology? Myrmecological News 18:131–147
Cerdá X, Dejean A (2011) Predation by ants on arthropods and other animals. Nation Acad of Sci (US), pp 39–78. http://hdl.handle.net/10261/58654
Cerdá X, Retana J, Cros S (1997) Thermal disruption of transitive hierarchies in Mediterranean ant communities. J Anim Ecol 66:363. https://doi.org/10.2307/5982
Cerdá X, Retana J, Manzaneda A (1998) The role of competition by dominants and temperature in the foraging of subordinate species in Mediterranean ant communities. Oecologia 117:404–412. https://doi.org/10.1007/s004420050674
Cerquera LM, Tschinkel WR (2010) The nest architecture of the ant Odontomachus brunneus. J of Insect Sci 10:64. https://doi.org/10.1673/031.010.6401
Chase ID, Seitz K (2011) Self-structuring properties of dominance hierarchies: a new perspective. In: Huber R, Bannasch DL, Brennan P (eds) Advances in genetics: aggression. Academic Press, San Diego CA, pp 51–75
Chesson P (2000) Mechanisms of maintenance of species diversity. Annu Rev Ecol Syst 31:343–366. https://doi.org/10.1146/annurev.ecolsys.31.1.343
Chivers DP, Wisenden BD, Smith RJF (1996) Damselfly larvae learn to recognize predators from chemical cues in the predator’s diet. Anim Behav 52:315–320. https://doi.org/10.1006/anbe.1996.0177
Cisterne A, Vanderduys EP, Pike DA, Schwarzkopf L (2014) Wary invaders and clever natives: sympatric house geckos show disparate responses to predator scent. Behav Ecol 25:604–611. https://doi.org/10.1093/beheco/aru031
D’Ettorre P, Kellner K, Delabie JHC, Heinze J (2005) Number of queens in founding associations of the ponerine ant Pachycondyla villosa. Insectes Soc 52:327–332. https://doi.org/10.1007/s00040-005-0815-z
Dejean A, Corbara B (1990) Predatory behavior of a neotropical arboricolous ant - Pachycondyla villosa (Formicidae, Ponerinae). Sociobiology 17:271–286
Dejean A, Corbara B (1998) Study of different foraging paths of the predatory neotropical ponerine ant Pachycondyla ( = Neoponera) villosa (Hymenoptera, Formicidae). Sociobiology 32:409–426
Delabie JH, Feitosa RM, Serrão JE, Mariano CDSF, Majer JD (2015) As formigas Poneromorfas do Brasil. SciELO-Editus-Editora da UESC
Devigne C, Detrain C (2002) Collective exploration and area marking in the ant Lasius niger. Insectes Soc 49:357–362. https://doi.org/10.1007/PL00012659
Devigne C, Detrain C (2006) How does food distance influence foraging in the ant Lasius niger: the importance of home-range marking. Insectes Soc 53:46–55. https://doi.org/10.1007/s00040-005-0834-9
Devigne C, Renon AJ, Detrain C (2004) Out of sight but not out of mind: modulation of recruitment according to home range marking in ants. Anim Behav 67:1023–1029. https://doi.org/10.1016/j.anbehav.2003.09.012
Drechsler P, Federle W (2006) Biomechanics of smooth adhesive pads in insects: influence of tarsal secretion on attachment performance. J Comp Physiol A 192:1213–1222. https://doi.org/10.1007/s00359-006-0150-5
Eltz T (2006) Tracing pollinator footprints on natural flowers. J Chem Ecol 32:907–915. https://doi.org/10.1007/s10886-006-9055-6
Federle W, Riehle M, Curtis ASG, Full RJ (2002) An integrative study of insect adhesion: mechanics and wet adhesion of pretarsal pads in ants. Integr Comp Biol 42:1100–1106. https://doi.org/10.1093/icb/42.6.1100
Ferrero DM, Lemon JK, Fluegge D et al (2011) Detection and avoidance of a carnivore odor by prey. Proc Natl Acad Sci U S A 108:11235–11240. https://doi.org/10.1073/pnas.1103317108
Flynn AM, Smee DL (2010) Behavioral plasticity of the soft-shell clam, Mya arenaria (L.), in the presence of predators increases survival in the field. J Exp Mar Bio Ecol 383:32–38. https://doi.org/10.1016/j.jembe.2009.10.017
Futuyma DJ, Moreno G (1988) The evolution of ecological specialization. Annu Rev Ecol Syst 19:207–233. https://doi.org/10.1146/annurev.es.19.110188.001231
Geiselhardt SF, Geiselhardt S, Peschke K (2011) Congruence of epicuticular hydrocarbons and tarsal secretions as a principle in beetles. Chemoecology 21:181–186. https://doi.org/10.1007/s00049-011-0077-3
Geiselhardt SF, Lamm S, Gack C, Peschke K (2010) Interaction of liquid epicuticular hydrocarbons and tarsal adhesive secretion in Leptinotarsa decemlineata Say (Coleoptera: Chrysomelidae). J Comp Physiol A 196:369–378. https://doi.org/10.1007/s00359-010-0522-8
Hammer Ø, Harper DAT, Ryan PD (2001) PAST: Paleontological Statistics Software Package for education and data analysis. Palaeontol Electronica 4:9. 178kb. http://palaeo-electronica.org/2001_1/past/issue1_01.htm
Hölldobler B, Wilson EO (1990) The ants. Harvard University Press
Holway DA (1998) Loss of intraspecific aggression in the success of a widespread invasive social insect. Science 80(282):949–952. https://doi.org/10.1126/science.282.5390.949
Human KG, Gordon DM (1996) Exploitation and interference competition between the invasive Argentine ant, Linepithema humile, and native ant species. Oecologia 105:405–412. https://doi.org/10.1007/BF00328744
Jackson DE, Ratnieks FL (2006) Communication in Ants Curr Biol 16:R570–R574. https://doi.org/10.1016/j.cub.2006.07.015
Jaffe K, Deneubourg JL (1992) On foraging, recruitment systems and optimum number of scouts in eusocial colonies. Insectes Soc 39:201–213. https://doi.org/10.1007/BF01249295
Jutsum AR, Saunders TS, Cherrett JM (1979) Intraspecific aggression is the leaf-cutting ant Acromyrmex octospinosus. Anim Behav 27:839–844. https://doi.org/10.1016/0003-3472(79)90021-6
Kaliszewicz A, Uchmański J (2009) A cross-phyla response to Daphnia chemical alarm substances by an aquatic oligochaete. Ecol Res 24:461–466. https://doi.org/10.1007/s11284-008-0522-0
Knaden M, Wehner R (2003) Nest defense and conspecific enemy recognition in the desert ant Cataglyphis fortis. J Insect Behav 16:717–730. https://doi.org/10.1023/B:JOIR.0000007706.38674.73
Larabee FJ, Suarez AV (2015) Mandible-powered escape jumps in trap-jaw ants increase survival rates during predator-prey encounters. PLoS ONE 10:1–10. https://doi.org/10.1371/journal.pone.0124871
Large S, Smee D, Trussell G (2011) Environmental conditions influence the frequency of prey responses to predation risk. Mar Ecol Prog Ser 422:41–49. https://doi.org/10.3354/meps08930
Lenoir A, Depickère S, Devers S et al (2009) Hydrocarbons in the ant Lasius niger: from the cuticle to the nest and home range marking. J Chem Ecol 35:913–921. https://doi.org/10.1007/s10886-009-9669-6
Li D, Jackson RR (2005) Influence of diet-related chemical cues from predators on the hatching of egg-carrying spiders. J Chem Ecol 31:333–342. https://doi.org/10.1007/s10886-005-1344-y
Lima LD, Antonialli-Junior WF (2013) Foraging strategies of the ant Ectatomma vizottoi (Hymenoptera, Formicidae). Rev Bras Entomol 57:392–396. https://doi.org/10.1590/S0085-56262013005000038
Martin S, Drijfhout F (2009) A review of ant cuticular hydrocarbons. J Chem Ecol 35:1151–1161. https://doi.org/10.1007/s10886-009-9695-4
Menzel F, Woywod M, Blüthgen N, Schmitt T (2010) Behavioural and chemical mechanisms behind a Mediterranean ant-ant association. Ecol Entomol 35:711–720. https://doi.org/10.1111/j.1365-2311.2010.01231.x
Nicolis SC, Deneubourg JL (1999) Emerging patterns and food recruitment in ants: an analytical study. J Theor Biol 198:575–592. https://doi.org/10.1006/jtbi.1999.0934
Nielsen J, Boomsma JJ, Oldham NJ et al (1999) Colony-level and season-specific variation in cuticular hydrocarbon profiles of individual workers in the ant Formica truncorum. Insectes Soc 46:58–65. https://doi.org/10.1007/s000400050113
Orivel J, Dejean A (2001) Comparative effect of the venoms of ants of the genus Pachycondyla (Hymenoptera: Ponerinae). Toxicon 39:195–201. https://doi.org/10.1016/S0041-0101(00)00113-6
Poulin RX, Lavoie S, Siegel K et al (2018) Chemical encoding of risk perception and predator detection among estuarine invertebrates. Proc Natl Acad Sci U S A 115:662–667. https://doi.org/10.1073/pnas.1713901115
R CORE TEAM (2021) R: a language and environment for statistical computing. R Foundation for Statistical Computing, Vienna. http://www.R-project.org
Rodrigues CAP, Lima JCS, Almeida RPS, Oliveira FC, Antonialli-Junior WF (2023) The influence of abiotic factors on the foraging activity of Cephalotes borgmeieri (Kempf, 1951). Sociobiology 70:e9085–e9085. https://doi.org/10.13102/sociobiology.v70i1.9085
Santos PGD, Santos EGD, Guimarães IDC, Michelutti KB, Cardoso CAL, Antonialli-Junior WF (2022) Deciphering the chemical phenotype in Atta laevigata (Smith, 1858)(Hymenoptera: Formicidae): a relationship between polymorphism and cuticular hydrocarbons. Pap Avulsos de Zool 62:e202262009. https://doi.org/10.11606/1807-0205/2022.62.009
Sanz-Veiga PA, Jorge LR, Benitez-Vieyra S, Amorim FW (2017) Pericarpial nectary-visiting ants do not provide fruit protection against pre-dispersal seed predators regardless of ant species composition and resource availability. PLoS ONE 12:e0188445. https://doi.org/10.1371/journal.pone.0188445
Savolainen R, Vepsäläinen K, Vepsalainen K (1988) A competition hierarchy among boreal ants: impact on resource partitioning and community structure. Oikos 51:135. https://doi.org/10.2307/3565636
Shaffery HM, Relyea RA (2015) Predator-induced defenses in five species of larval Ambystoma. Copeia 103:552–562. https://doi.org/10.1643/ce-14-043
Smee DL, Weissburg MJ (2006) Hard clams (Mercenaria mercenaria) evaluate predation risk using chemical signals from predators and injured conspecifics. J Chem Ecol 32:605–619. https://doi.org/10.1007/s10886-005-9021-8
Smith AA, Millar JG, Hanks LM, Suarez AV (2012) Experimental evidence that workers recognize reproductives through cuticular hydrocarbons in the ant Odontomachus brunneus. Behav Ecol Sociobiol 66:1267–1276. https://doi.org/10.1007/s00265-012-1380-x
Smith AA, Millar JG, Suarez AV (2016) Comparative analysis of fertility signals and sex-specific cuticular chemical profiles of Odontomachus trap-jaw ants. J Exp Biol 219:419–430. https://doi.org/10.1242/jeb.128850
TIBCO Software Inc (2020) Data Science Workbench, version 14. http://tibco.com
Thygesen UH, Farnsworth KD, Andersen KH, Beyer JE (2005) How optimal life history changes with the community size-spectrum. Proc R Soc B Biol Sci 272:1323–1331. https://doi.org/10.1098/rspb.2005.3094
Traniello J (1989) Foraging strategies of ants. Annu Rev Entomol 34:191–210. https://doi.org/10.1146/annurev.ento.34.1.191
Trunzer B, Heinze J, Hölldobler B (1998) Cooperative colony founding and experimental primary polygyny in the ponerine ant Pachycondyla villosa. Insectes Soc 45:267–276. https://doi.org/10.1007/s000400050087
Valadares L, Nascimento FS, do, (2016) Chemical cuticular signature of leafcutter ant Atta sexdens (Hymenoptera, Formicidae) worker subcastes. Rev Bras Entomol 60:308–311. https://doi.org/10.1016/j.rbe.2016.06.008
Van den Dool HAND, Kratz PD (1963) A generalization of the retention index system including linear temperature programmed gas-liquid partition chromatography. J Chromatogr
Weissburg M, Smee DL, Ferner MC (2014) The sensory ecology of nonconsumptive predator effects. Am Nat 184:141–157. https://doi.org/10.1086/676644
Wilms J, Eltz T (2008) Foraging scent marks of bumblebees: footprint cues rather than pheromone signals. Naturwissenschaften 95:149–153. https://doi.org/10.1007/s00114-007-0298-z
Wisenden BD (2000) Olfactory assessment of predation risk in the aquatic environment. Philos Trans R Soc B Biol Sci 355:1205–1208. https://doi.org/10.1098/rstb.2000.0668
Wüst M, Menzel F (2017) I smell where you walked - how chemical cues influence movement decisions in ants. Oikos 126:149–160. https://doi.org/10.1111/oik.03332
Zöttl M, Lienert R, Clutton-Brock T et al (2013) The effects of recruitment to direct predator cues on predator responses in meerkats. Behav Ecol 24:198–204. https://doi.org/10.1093/beheco/ars154
Acknowledgements
The authors thank Rodrigo S.M. Feitosa, PhD, and Aline M. Oliveira, PhD, for the species identification.
Funding
This study was financed in part by the Coordenação de Aperfeiçoamento de Pessoal de Nível Superior (CAPES) (concession numbers 88882.457261/2019–01 and 88887.704043/2022–00 to PGS), in addition to Fundação de Apoio ao Desenvolvimento do Ensino, Ciência e Tecnologia do Estado de Mato Grosso do Sul (FUNDECT), and Conselho Nacional de Desenvolvimento Científico e Tecnológico (CNPq) (concession number 312671/2021–0 to CALC).
Author information
Authors and Affiliations
Contributions
All authors contributed to the study conception and design. Material preparation, data collection, and analysis were performed by PGS, EGS, ICG, CALC, SELJ, and WFAJ. The first draft of the manuscript was written by PGS, and all authors commented on the previous versions of the manuscript. All authors read and approved the final manuscript. All authors have given consent to submit this manuscript and have contributed sufficiently to the scientific work.
Corresponding author
Ethics declarations
Competing interests
The authors declare no competing interests.
Additional information
Communicated by: John A. Byers
This manuscript is all original work and has not been published previously (partially or in full).
Publisher's Note
Springer Nature remains neutral with regard to jurisdictional claims in published maps and institutional affiliations.
Rights and permissions
Springer Nature or its licensor (e.g. a society or other partner) holds exclusive rights to this article under a publishing agreement with the author(s) or other rightsholder(s); author self-archiving of the accepted manuscript version of this article is solely governed by the terms of such publishing agreement and applicable law.
About this article
Cite this article
dos Santos, P.G., dos Santos, E.G., de Carvalho Guimarães, I. et al. Hydrocarbons in Formicidae: influence of chemical footprints on ant behavioral strategies. Sci Nat 111, 24 (2024). https://doi.org/10.1007/s00114-024-01908-6
Received:
Revised:
Accepted:
Published:
DOI: https://doi.org/10.1007/s00114-024-01908-6