Population monitoring of the damselfly Mesamphiagrion gaudiimontanum (Odonata: Coenagrionidae): assessing the effects of ectoparasites, sex, age class, body size, and phenotype on survival and detectability
DOI:
https://doi.org/10.11606/1807-0205/2026.66.038Keywords:
Acari infestation, Demography, Mark-Recapture, Páramos, Sexual DimorphismAbstract
Mesamphiagrion gaudiimontanum Bota-Sierra, 2013, is an endemic and threatened damselfly species that inhabits the high mountains of the Colombian Central Cordillera. The first demographic study for the species was conducted in 2022, allowing an estimation of demographic parameters and a first test of the effects of sex, age, mite infestation, and female morphotype on survival/detectability. However, no statistical support was found for this, leaving this issue open. In this study, we monitored one population over two climatic seasons, a fundamental aspect for understanding the future of the species. We increased the sampling effort compared to the previous study and, using the capture-mark-recapture method, estimated demographic parameters for both the rainy and dry seasons, respectively: population size (951 ± 118 individuals; 2,655 ± 197 individuals); survival probability (0.90, 0.95); and life span (11.2 days, 22.7 days). We found evidence of an effect of sex, age, and mite infestation on detectability but not on survival. Regarding the female morphotype, we found no support for differences in either parameter. These findings provide valuable information for the conservation of an endemic and threatened species of the high tropical mountains.
Downloads
References
Andrés, J.A. & Cordero, A. 1998. Effects of water mites on the damselfly Ceriagrion tenellum. Ecological Entomology, 23(2): 103-109. https://doi.org/10.1046/j.1365-2311.1998.00125.x.
Anholt, B.R. 2008. Fitness landscapes, mortality schedules, and mating systems. In: Cordoba-Aguilar, A. (Ed.). Dragonflies and damselflies: model organisms for ecological and evolutionary research. Oxford, Oxford University Press. p. 167-174. https://doi.org/10.1093/acprof:oso/9780199230693.003.0013.
Anholt, B.R.; Vorburger, C. & Knaus, P. 2001. Mark-recapture estimates of daily survival rates of two damselflies (Coenagrion puella and Ischnura elegans). Canadian Journal of Zoology, 79(5): 895-899. https://doi.org/10.1139/z01-053.
Arango-Quintero, S. & Bota-Sierra, C.A. 2025. Capture histories of the damselfly Mesamphiagrion gaudiimontanum Bota-Sierra, 2013 (Odonata: Coenagrionidae). Version 1. Figshare. [dataset]. Available: https://doi.org/10.6084/m9.figshare.30117457.v1. Access: 15/09/2025.
Avendaño-Marín, J.M.; Blanco, A.H.; Flórez-V, C.; Muñoz-Quesada, F.J. & Bota-Sierra, C.A. 2024. Demography and natural history of the damselfly Mesamphiagrion gaudiimontanum (Coenagrionidae), a Páramo endemic species in the Colombian Andes. International Journal of Odonatology, 27: 151-160. https://doi.org/10.48156/1388.2024.1917283.
Bota-Sierra, C.A. & Wolff, M.I. 2013. Taxonomic revision of Mesamphiagrion Kennedy, 1920 from Colombia (Odonata: Coenagrionidae), with the description of four new species. Zootaxa, 3718: 401-440. https://doi.org/10.11646/zootaxa.3718.5.1.
Bota-Sierra, C.A.; Cordero-Rivera, A.; Novelo-Gutiérrez, R.; Sánchez-Herrera, M. & Londoño, G.A. 2024. Can high temperatures affect body size in insects? The case of rubyspot damselflies in the Colombian Western Andes. Diversity, 16(12): 1-18, 743. https://doi.org/10.3390/d16120743.
Bota‐Sierra, C.A.; García‐Robledo, C.; Escobar, F.; Novelo‐Gutiérrez, R. & Londoño, G.A. 2022. Environment, taxonomy and morphology constrain insect thermal physiology along tropical mountains. Functional Ecology, 36(8): 1924-1935. https://doi.org/10.1111/1365-2435.14083.
Bota-Sierra, C.A.; Palacino, F. & Rache, L. 2016. Mesamphiagrion gaudiimontanum. The IUCN Red List of Threatened Species 2016: e.T66899676A66899678. https://doi.org/10.2305/IUCN.UK.2016-1.RLTS.T66899676A66899678.en.
Briffa, M. & Sneddon, L.U. 2007. Physiological constraints on contest behaviour. Functional Ecology, 21(4): 627-637. https://doi.org/10.1111/j.1365-2435.2006.01188.x.
Cook, L.M.; Brower, L.P. & Croze, H.J. 1967. The Accuracy of a population estimation from multiple recapture Data. Journal of Animal Ecology, 36: 57-60. https://doi.org/10.2307/3014.
Corbet, P.S. 1999. Dragonflies: behaviour and ecology of Odonata. Colchester, Harley Books.
Cordero, A.; Carbone, S.S. & Utzeri, C. 1998. Mating opportunities and mating costs are reduced in androchrome female damselflies, Ischnura elegans (Odonata). Animal Behaviour, 55(1): 185-197. https://doi.org/10.1006/anbe.1997.0603.
Cordero-Rivera, A.; Sanmartín-Villar, I.; Herrera, M.S.; Rivas-Torres, A. & Encalada, A.C. 2019. Survival and longevity in neotropical damselflies (Odonata, Polythoridae). Animal Biodiversity and Conservation, 42(2): 293-300. https://doi.org/10.32800/abc.2019.42.0293.
Cormack, R.M. 1964. Estimates of survival from the sighting of marked animals. Biometrika, 51(3/4): 429-438. https://doi.org/10.2307/2334149.
Fincke, O.M. 1994. Female colour polymorphism in damselfies: failure to reject the null hypothesis. Animal Behaviour, 47(6): 1249-1266. https://doi.org/10.1006/anbe.1994.1174.
Fincke, O.M. 1997. Conflict resolution in the Odonata: Implications for understanding female mating patterns and female choice. Biological Journal of the Linnean Society, 60(2): 201-220. https://doi.org/10.1111/j.1095-8312.1997.tb01492.x.
Fincke, O.M.; Waage, J.K. & Koenig, W.D. 1997. Natural and sexual selection components of odonate mating patterns. In: Choe, J.C. & Crespi, B.J. (Eds.). The Evolution of mating systems in insects and arachnids. Cambridge, Cambridge University Press. p. 58-74. https://doi.org/10.1017/CBO9780511721946.004.
Forbes, M.R. & Baker, R.L. 1990. Susceptibility to Parasitism: Experiments with the Damselfly Enallagma ebrium (Odonata: Coenagrionidae) and Larval Water Mites, Arrenurus spp. (Acari: Arrenuridae). Oikos, 58: 61-66. https://doi.org/10.2307/3565361.
Forbes, M.R.; Schalk, G.; Miller, J.G. & Richardson, J.M. 1997. Male-female morph interactions in the damselfly Nehalennia irene (Hagen). Canadian Journal of Zoology, 75(2): 253-260. https://doi.org/10.1139/z97-032.
Gimenez, O.; Lebreton, J.; Choquet, R. & Pradel, R. 2018. R2ucare: An R package to perform goodness‐of‐fit tests for capture-recapture models. Methods in Ecology and Evolution, 9(7): 1749-1754. https://doi.org/10.1111/2041-210X.13014.
Gómez-Llano, M.; Narasimhan, A. & Svensson, E.I. 2020. Male-Male Competition Causes Parasite-Mediated Sexual Selection for Local Adaptation. The American Naturalist, 196(3): 344-354. https://doi.org/10.1086/710039.
Gribbin, S.D. & Thompson, D.J. 1991. The effects of size and residency on territorial disputes and short-term mating success in the damselfly Pyrrhosoma nymphula (Sulzer) (Zygoptera: Coenagrionidae). Animal Behaviour, 41(4): 689-695. https://doi.org/10.1016/s0003-3472(05)80906-6.
Jolly, G.M. 1965. Explicit Estimates from Capture-Recapture Data with Both Death and Immigration-Stochastic Model. Biometrika, 52(1/2): 225-247. https://doi.org/10.2307/2333826.
Kemp, D.J. & Alcock, J. 2003. Lifetime resource utilization, flight physiology, and the evolution of contest competition in territorial insects. The American Naturalist, 162(3): 290-301. https://doi.org/10.1086/376890.
Kirkton, S.D. & Schultz, T.D. 2001. Age-specific behavior and habitat selection of adult male damselflies, Calopteryx maculata (Odonata: Calopterygidae). Journal of Insect Behavior, 14(4): 545-556. https://doi.org/10.1023/A:1011180207852.
Laake, J.L. 2013. RMark: An R Interface for Analysis of Capture-Recapture Data with MARK.
Laake, J.L.; Johnson, D.S. & Conn, P.B. 2013. marked: An R package for maximum likelihood and Markov Chain Monte Carlo analysis of capture-recapture data. Methods in Ecology and Evolution, 4(9): 885-890. https://doi.org/10.1111/2041-210X.12065.
Marden, J.H. & Waage, J.K. 1990. Escalated damselfly territorial contests are energetic wars of attrition. Animal Behaviour, 39(5): 954-959. https://doi.org/10.1016/S0003-3472(05)80960-1.
Matsubara, K. & Hironaka, N.M. 2005. Postcopulatory guarding behaviour in a territorial damselfly, Pseudagrion p. pilidorsum (Brauer), for submerged ovipositing females (Zygoptera: Coenagrionidae). Odonatologica, 34(4): 387-396.
Matsubara, K.; Tojo, S. & Suzuki, N. 2005. Age-related changes in flight muscle mass, lipid reserves and flight capacity during adult maturation in males of the territorial damselfly Calopteryx atrata (Odonata: Calopterygidae). Zoological Science, 22(5): 587-592. https://doi.org/10.2108/zsj.22.587.
McPeek, M.A. 2008. Ecological factors limiting the distributions and abundances of Odonata. In: Cordoba-Aguilar, A. (Ed.). Dragonflies and damselflies: model organisms for ecological and evolutionary research. Oxford, Oxford University Press. p. 51-61. https://doi.org/10.1093/acprof:oso/9780199230693.003.0005.
Palacino-Rodríguez, F.; Palacino, D.A.; Munguia-Steyer, R. & Juen, L. 2020. Effects of seasonality and environmental change on an Andean damselfly Mesamphiagrion laterale (Odonata: Coenagrionidae). Journal of Insect Conservation, 24(3): 499-511. https://doi.org/10.1007/s10841-020-00237-z.
R: A Language and Environment for Statistical Computing (R Core Team). 2025. R: A language and environment for statistical computing. R Foundation for Statistical Computing. https://www.r-project.org.
Raihani, G.; Serrano‐Meneses, M.A. & Córdoba Aguilar, A. 2008. Male mating tactics in the American rubyspot damselfly: territoriality, nonterritoriality and switching behaviour. Animal Behaviour, 75(6): 1851-1860. https://doi.org/10.1016/j.anbehav.2007.11.002.
Reinhardt, K. 1996. Negative effects of Arrenurus water mites on the flight distances of the damselfly Nehalennia speciosa (Odonata: Coenagrionidae). Aquatic Insects, 18(4): 233-240. https://doi.org/10.1080/01650429609361626.
Richards, S.A. 2005. Testing ecological theory using the information‐theoretic approach: examples and cautionary results. Ecology, 86(10): 2805-2814. https://doi.org/10.1890/05-0074.
Richards, S.A. 2008. Dealing with overdispersed count data in applied ecology. Journal of Applied Ecology, 45(1): 218-227. https://doi.org/10.1111/j.1365-2664.2007.01377.x.
Robertson, H.M. 1985. Female dimorphism and mating behaviour in a damselfly, Ischnura ramburi: Females mimicking males. Animal Behaviour, 33(3): 805-809. https://doi.org/10.1016/S0003-3472(85)80013-0.
Sanmartín-Villar, I. & Cordero-Rivera, A. 2022. Odonata survival: Insights from mark-recapture experiments. In: Cordoba-Aguilar, A. (Ed.). Dragonflies and damselflies: model organisms for ecological and evolutionary Research (Second). Oxford, Oxford University Press, p. 129-140. https://doi.org/10.1093/oso/9780192898623.001.0001.
Seber, G.A. 1965. A Note on the Multiple-Recapture Census. Biometrika, 52(1/2): 249-259. https://doi.org/10.2307/2333827.
Serrano‐Meneses, M.A.; Cordoba‐Aguilar, A.; Azpilicueta‐Amorín, M.; González‐Soriano, E. & Szekely, T. 2008. Sexual selection, sexual size dimorphism and Rensch’s rule in Odonata. Journal of Evolutionary Biology, 21(5): 1259-1273. https://doi.org/10.1111/j.1420-9101.2008.01567.x.
Serrano‐Meneses, M.A.; López-García, K. & Carrillo-Muñoz, A.I. 2018. Assortative mating by size in the American rubyspot damselfly (Hetaerina americana). Journal of Insect Behavior, 31(6): 585-598. https://doi.org/10.1007/s10905-018-9701-1.
Sherratt, T.N.; Hassall, C.; Laird, R.A.; Thompson, D.J. & Cordero‐Rivera, A. 2011. A comparative analysis of senescence in adult damselflies and dragonflies (Odonata). Journal of Evolutionary Biology, 24(4): 810-822. https://doi.org/10.1111/j.1420-9101.2010.02222.x.
Siva‐Jothy, M.T. 2000. A mechanistic link between parasite resistance and expression of a sexually selected trait in a damselfly. Proceedings of the Royal Society of London. Series B: Biological Sciences, 267(1461): 2523-2527. https://doi.org/10.1098/rspb.2000.1315.
Siva‐Jothy, M.T. & Plaistow, S.J. 1999. A fitness cost of eugregarine parasitism in a damselfly. Ecological Entomology, 24(4): 465-470. https://doi.org/10.1046/j.1365-2311.1999.00222.x.
Suhonen, J.; Rantala, M.J. & Honkavaara, J. 2008. Territoriality in odonates. In: A. Cordoba-Aguilar, A. (Ed.). Dragonflies and damselflies: model organisms for ecological and evolutionary research. Oxford, Oxford University Press, p. 203-217. https://doi.org/10.1093/acprof:oso/9780199230693.003.0016.
Van Gossum, H.; Dumont, H. & Stoks, R. 2004. Sex- and morph-specific predation risk: Colour or behaviour dependency? European Journal of Entomology, 101(3): 373-378. https://doi.org/10.14411/eje.2004.052.
Van Gossum, H.; Sherratt, T.N.; Cordero-Rivera, A. & Córdoba-Aguilar, A. 2008. The evolution of sex-limited colour polymorphism. In: Cordoba-Aguilar, A. (Ed.). Dragonflies and damselflies: model organisms for ecological and evolutionary research. Oxford, Oxford University Press. p. 219-231. https://doi.org/10.1093/acprof:oso/9780199230693.003.0017.
Van Gossum, H.; Stoks, R. & De Bruyn, L. 2001. Frequency-dependent male mate harassment and intra-specific variation in its avoidance by females of the damselfly Ischnura elegans. Behavioral Ecology and Sociobiology, 51(1): 69-75. https://doi.org/10.1007/s002650100418.
Waller, J.T. & Svensson, E.I. 2017. Body size evolution in an old insect order: No evidence for Cope’s Rule in spite of fitness benefits of large size. Evolution, 71(9): 2178-2193. https://doi.org/10.1111/evo.13302.
Willink, B. & Svensson, E.I. 2017. Intra-and intersexual differences in parasite resistance and female fitness tolerance in a polymorphic insect. Proceedings of the Royal Society B: Biological Sciences, 284(1847): 1-8, 20162407: https://doi.org/10.1098/rspb.2016.2407.
Downloads
Published
Issue
Section
License
Copyright (c) 2026 Sebastian Arango-Quintero, Cornelio Andrés Bota-Sierra

This work is licensed under a Creative Commons Attribution 4.0 International License.
Responsibility: The scientific content and the opinions expressed in the manuscript are the sole responsibility of the author(s).
Copyrights: The Authors. The journal is licensed under a Creative Commons attribution-type CC-BY.
How to Cite
Funding data
-
Fondation Segré
Grant numbers 2023C-21
