Main Article Content

Authors

The Guatemalan potato moth Tecia solanivora is considered one of the most serious pests of the potato crop in Colombia. Currently, most efforts for controlling populations of the insect are focused in the development  of methodologies to disrupt its reproduction. Therefore, it is necessary to understand the behavior and factors affecting the reproductive potential of T. solanivora. In this study the mating frequency of T. solanivora and its effect on  adult reproductive potential was determined. To determine the mating frequency of females, two experiments were conducted in which males and females of T. solanivora were confined in different proportions. To establish the mating frequency of males, two experiments were carried out. In the first, one virgin female was offered daily to each male confined individually. In the second, different numbers of females were offered to an individual male. Most females mate just once, and those females that mate more than once do not obtain a significant benefit in their reproductive potential or in their longevity. Males mate an average of five times depending on the number of females available. A significant decline in male reproductive potential with increasing number of copulations was observed, although they seem to have the capacity to dose their ejaculation depending on the number of females available. The viability of the implementation of methodologies based on the mass capture of males for the control of T. solanivora is discussed.

RINCÓN, D. F., & GARCÍA-G., J. (2007). Mating frequency of the Guatemalan potato moth Tecia solanivora (Lepidoptera: Gelechiidae). Revista Colombiana De Entomología, 33(2), 133–140. https://doi.org/10.25100/socolen.v33i2.9332

ARIAS, J. 1996. Evaluación de la incidencia y severidad de daño de la polilla gigante de la papa Tecia solanivora (Lepidoptera: Gelechiidae) en Antioquia. En: Seminario experiencias y avances en el manejo de la polilla guatemalteca de la papa (1997, Bogotá D. C.) Memorias de Seminario. Sociedad Colombiana de Entomología (Socolen), Bogotá D.C.

ARNQVIST, G.; NILSSON, T. 2000. The evolution of polyandry: multiple mating and female fitness in insects. Animal Behaviour 60: 145-154.

BAKER, R.; DENNIFF, M.; FUTERMAN, P.; FOWLER, K.; POMIANKOWSKI, A.; CHAPMAN, T. 2003. Accessory gland size influences time to sexual maturity and mating frequency in the stalk-eyed fly, Cyrtodiopsis dalmanni. Behavioral Ecology 14: 607-611.

BARAH, A.; SENGUPTA, A. 1991. Correlation and regression studies between pupal weight and fecundity of muga silkworm Antheraea assama Westwood (Lepidoptera: Saturniidae) on four different foodplants. Acta Physiologica Hungarica 78 (3): 261264.

BOGGS, C. 1986. Reproductive strategies of female butterflies: variation in and constraints on fecundity. Ecological Entomology 11 (1): 7-15.

BOGGS, C.; GILBERT, L. 1979. Male contribution to egg production in butterflies: evidence for transfer of nutrients at mating. Science 206: 83-84.

BOSA, C.; COTES, A.; FUKUMOTO, T.; BENGTSSON, M.; WITZGALL, P. 2005. Pheromone-mediated communication disruption in Guatemalan potato moth, Tecia solanivora. Entomologia Experimentalis et Applicata 114: 137-142.

BROWN, W.; BJORK, A.; SCHNEIDER, K.; PITNICK, S. 2004. No evidence that polyandry benefits females in Drosophila melanogaster. Evolution 58 (6): 1242-1250.

CALVO, D.; MOLINA, M. 2005. Fecundity–body size relationship and other reproductive aspects of Streblote panda (Lepidoptera: Lasiocampidae). Annals of the Entomological Society of America 98 (2): 191-196.

CHAPMAN, R. 2004. The Insects: Structure and Function. 4th Edition. Cambridge University Press. Cambridge (UK).

DEWSBURY, D. 1982. Ejaculate cost and male choice. American Naturalist 119: 601-610.

ESPINAL, C.; MARTÍNEZ, H.; PINZÓN, N.; BARRIOS, C. 2005. La cadena de la papa en Colombia una mirada global de su estructura y dinámica 1991-2005. Ministerio de Agricultura y Desarrollo Rural. Observatorio de Agrocadenas, Bogotá D.C. Colombia.

FENEMORE, P. 1977. Oviposition of potato tuber moth, Phthorimaea operculella Zell. (Lepidoptera: Gelechiidae); fecundity in relation to mated state, age, and pupal weight. New Zealand Journal of Zoology 4: 187-191.

GAGE, M. 1991. Risk of sperm competition directly affects ejaculate size in the Mediterranean fruit fly. Animal Behaviour 42: 10361037.

GAGE, M. 1995. Continuous variation in reproductive strategy as an adaptive response to population density in the moth Plodia interpunctella. Proceedings of the Royal Society of London, Series B 261: 25-30.

GARCÍA, J.; OJEDA, D.; LÓPEZ-ÁVILA, A. 2003. Determinación de hábitos reproductivos de la polilla guatemalteca de la papa Tecia solanivora (Povolny, 1973) (Lepidoptera: Gelechiidae), pp. 158 -163. En: Tecia solanivora II Taller Nacional. Abril 24 – 25. Memorias.

HELIÖVAARA, K.; VÄISÄNEN, R.; VARAMA, M. 1990. Fecundity and egg viability in relation to female body size in Neodiprion sertifer (Hymenoptera: Diprionidae). Holarctic Ecology 13 (2): 166-172.

HERRERA, F. 1998. La polilla guatemalteca de la papa. Biología, comportamiento y prácticas de manejo integrado. Ministerio de Agricultura y Desarrollo Rural. Corporación Colombiana de Investigación Agropecuaria (Corpoica). Bogotá D.C. (Colombia), 15 p.

LEWIS, S. 2004. Multiple mating and repeated copulations: effects on male reproductive success in red flour beetles. Animal Behaviour 67: 799-804.

LÓPEZ-ÁVILA, A. 2000. Insectos plaga del cultivo de la papa en Colombia y su manejo. Papas Colombianas 2000, con el mejor entorno ambiental. 25 años Fedepapa. Ventana al Campo Andino 3 (1-2): 152-159.

LÓPEZ-ÁVILA, A.; ESPITIA-MALAGÓN, E. 2000. Plagas y benéficos en el cultivo de la papa en Colombia. Boletín técnico divulgativo. Programa Nacional de Manejo Integrado de Plagas. Corpoica-Pronatta. Editorial Produmedios. Bogotá D.C., Colombia. 35 p.

MARSHALL, L.; McNEIL J. 1989. Spermatophore mass as an estimate of male nutrient investment: a closer look in Pseudaletia unipuncta Haworth (Lepidoptera: Noctuidae). Functional Ecology 3: 605-612.

MARTIN, O.; HOSKEN, D. 2002. Strategic ejaculation in the common dung flies Sepsis cynipsea. Animal Behaviour 63: 541546.

OKUNAGA, Y.; OCHOA, R. 1987. Estudio de la dinámica reproductiva de la palomilla de papa Scrobipalpopsis solanivora y relación natalidad-mortalidad para S. solanivora y Phthorimaea operculella. En: XII Reunión ANAP. Panamá, 9 al 13 de marzo, p. 402-418.

PARKER, G. 1998. Sperm competition and the evolution of ejaculates: towards a theory base. En: Birkhead, T; Moller, A. (eds.). Sperm competition and sexual selection. Academia Press, London, pp. 3-54.

PYLE, D.; GROMKO, M. 1981. Genetic basis for repeated mating in Drosophila melanogaster. American Naturalist 117: 133-146. R, DEVELOPMENT CORE TEAM. 2007. R: A language and environment for statistical computing. R Foundation for Statistical Computing, Vienna, Austria. URL http://www.R-project.org.

SÁNCHEZ, M. 1999. Efecto de la trampa de feromona sexual en el Monitoreo de poblaciones de la polilla guatemalteca de la papa Tecia solanivora (Povolny). Trabajo de grado para optar al titulo de Biólogo. Pontificia Universidad Javeriana. Facultad de Ciencias Básicas, Departamento de Biología. Bogotá D.C., Colombia. 143 p.

SIMMONS, L. 2001. Sperm competition and its evolutionary consequences in the insects. Monographs in behavior and ecology. Princeton University Press. Oxford (UK). 434 p.

SIMMONS, L.; PARKER G. 1989. Nuptial feeding in insects: mating effort versus parental investment. Ethology 81: 332-343.

SIMMONS, L.; TOMKINS, J.; ALCOCK, J. 2000. Can minor males of Dawson’s burrowing bee, Amegilla dawsoni (Hymenoptera: Anthophorini) compensate for reduced access to virgin females through sperm competition? Behavioral Ecology 11: 319-325.

SOLYMAR, B.; CADE, W. 1990. Heritable variation for female mating frequency in field crickets, Gryllus integer. Behavioral Ecology and Sociobiology 26: 73-76.

THORNHILL, R.; ALCOCK, J. 2001. The evolution of insect mating systems. Harvard University Press, Cambridge (United Kingdom).

TORRES, F.; NOTZ, A.; VALENCIA, L. 1997. Ciclo de vida y otros aspectos reproductivos de la polilla de la papa Tecia solanivora (Povolny) (Lepidoptera: Gelechiidae) en el estado Táchira, Venezuela. Boletín Entomología Venezolana 12 (1): 81-94.

TORRES-VILA, L.; JENNIONS, M. 2005. Male mating history and female fecundity in the Lepidoptera: do male virgins make better partners? Behavioral Ecology and Sociobiology 57: 318-326.

TORRES-VILA, L.; RODRÍGUEZ-MOLINA, C. 2004. Polyandry and fecundity in Lepidoptera: can methodological and conceptual approaches bias outcome? Behavioral Ecology and Sociobiology 55: 315-324.

TRIVERS, L. 1972. Parental investment and sexual selection, pp. 136-179. En: Campbell, B. (ed.) Sexual selection and the descent of man, 1871-1971. Aldine, Chicago.

VARGAS, B.; RUBIO, S.; LÓPEZ-ÁVILA, A. 2004. Estudios de hábitos y comportamiento de la polilla guatemalteca de la papa Tecia solanivora (Lepidoptera: Gelechiidae) en papa almacenada. Revista Colombiana de Entomología 30 (2): 211217.

WARD, P.; SIMMONS, L. 1991. Copula duration and testes size in the yellow dung fly, Scathophaga stercoraria (L.): The effects of diet, body size, and the mating history. Behavioral Ecology and Sociobiology 29: 77-85.

WEDELL, N. 2005a. Sperm competition in butterflies and moths, pp. 49-81. En: Insect Evolutionary Ecology. M. Fellowes y G. Holloway (eds.). Royal Entomological Society. CABI Publishing, CAB International. Wallingford (Reino Unido).

WEDELL, N. 2005b. Female receptivity in butterflies and moths. The Journal of Experimental Biology 208: 3433-3440.

WEDELL, N.; WIKLUND, C.; COOK, P. 2002. Monoandry and polyandry as alternative lifestyles in a butterfly. Behavioral Ecology 13 (4): 450-455.

YAMANE, T.; MIYATAKE, T. 2005. Intra-specific variation in strategic ejaculation according to level of polyandry in Callosobruchus chinensis. Journal of Insect Physiology 51: 1240-1243.