Artificial night lighting disrupts sex pheromone in a noctuid moth

1. One major, yet poorly studied, change in the environment is the increase in nocturnal light pollution. Although this strongly alters the habitat of nocturnal species, the ecological consequences are poorly known. Moths are well known to be attracted to artificial light sources, but artificial lig...

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Published inEcological entomology Vol. 40; no. 4; pp. 401 - 408
Main Authors VAN GEFFEN, KOERT G., GROOT, ASTRID T., VAN GRUNSVEN, ROY H. A., DONNERS, MAURICE, BERENDSE, FRANK, VEENENDAAL, ELMAR M.
Format Journal Article
LanguageEnglish
Published Oxford, UK Blackwell Publishing Ltd 01.08.2015
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Abstract 1. One major, yet poorly studied, change in the environment is the increase in nocturnal light pollution. Although this strongly alters the habitat of nocturnal species, the ecological consequences are poorly known. Moths are well known to be attracted to artificial light sources, but artificial light may affect them in other ways as well. 2. In this study, female Mamestra brassicae moths were subjected to various types of low‐intensity artificial night lighting with contrasting spectral compositions (green‐rich, red‐rich, warm white) or to a dark control treatment and the effects on their sex pheromone production and composition were tested. 3. Artificial night lighting reduced sex pheromone production and altered the chemical composition of the pheromone blend, irrespective of spectral composition. Specifically, amounts of the main pheromone component Z11 ‐16: Ac were reduced, while the deterring compounds Z9 ‐14: Ac , Z9 ‐16: Ac , and Z11 ‐16: OH were increased relative to Z11 ‐16: Ac when females were kept under artificial light. These changes may reduce the effectiveness of the sex pheromones, becoming less attractive for males. 4. These results show for the first time that artificial light at night affects processes that are involved in moth reproduction. The potential for mitigation through manipulation of the spectral composition of artificial light appears limited.
AbstractList 1. One major, yet poorly studied, change in the environment is the increase in nocturnal light pollution. Although this strongly alters the habitat of nocturnal species, the ecological consequences are poorly known. Moths are well known to be attracted to artificial light sources, but artificial light may affect them in other ways as well. 2. In this study, female Mamestra brassicae moths were subjected to various types of low‐intensity artificial night lighting with contrasting spectral compositions (green‐rich, red‐rich, warm white) or to a dark control treatment and the effects on their sex pheromone production and composition were tested. 3. Artificial night lighting reduced sex pheromone production and altered the chemical composition of the pheromone blend, irrespective of spectral composition. Specifically, amounts of the main pheromone component Z11‐16:Ac were reduced, while the deterring compounds Z9‐14:Ac, Z9‐16:Ac, and Z11‐16:OH were increased relative to Z11‐16:Ac when females were kept under artificial light. These changes may reduce the effectiveness of the sex pheromones, becoming less attractive for males. 4. These results show for the first time that artificial light at night affects processes that are involved in moth reproduction. The potential for mitigation through manipulation of the spectral composition of artificial light appears limited.
1. One major, yet poorly studied, change in the environment is the increase in nocturnal light pollution. Although this strongly alters the habitat of nocturnal species, the ecological consequences are poorly known. Moths are well known to be attracted to artificial light sources, but artificial light may affect them in other ways as well. 2. In this study, female Mamestra brassicae moths were subjected to various types of low‐intensity artificial night lighting with contrasting spectral compositions (green‐rich, red‐rich, warm white) or to a dark control treatment and the effects on their sex pheromone production and composition were tested. 3. Artificial night lighting reduced sex pheromone production and altered the chemical composition of the pheromone blend, irrespective of spectral composition. Specifically, amounts of the main pheromone component Z11 ‐16: Ac were reduced, while the deterring compounds Z9 ‐14: Ac , Z9 ‐16: Ac , and Z11 ‐16: OH were increased relative to Z11 ‐16: Ac when females were kept under artificial light. These changes may reduce the effectiveness of the sex pheromones, becoming less attractive for males. 4. These results show for the first time that artificial light at night affects processes that are involved in moth reproduction. The potential for mitigation through manipulation of the spectral composition of artificial light appears limited.
Author GROOT, ASTRID T.
BERENDSE, FRANK
VEENENDAAL, ELMAR M.
DONNERS, MAURICE
VAN GEFFEN, KOERT G.
VAN GRUNSVEN, ROY H. A.
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  givenname: ROY H. A.
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  organization: Nature Conservation and Plant Ecology Group, Wageningen University, Wageningen, the Netherlands
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Cinzano, P., Falchi, F. & Elvidge, C.D. (2001) The first World Atlas of the artificial night sky brightness. Monthly Notices of the Royal Astronomical Society, 328, 689-707.
Groot, A.T. (2014) Circadian rhythms of sexual activities in moths: a review. Frontiers in Ecology and Evolution, Section Chemical Ecology, 2, 1-21. DOI: 10.3389/fevo.2014.00043.
Iglesias, F., Jacquin-Joly, E., Marco, M.-P., Camps, F. & Fabrias, G. (1999) Temporal distribution of PBAN-like immunoreactivity in the hemalymph of Mamestra brassciae females in relation to sex pheromone production and calling behavior. Archives of Insect Biochemistry and Physiology, 40, 80-87.
Rafaeli, A. (1994) Pheromonotropic stimulation of moth pheromone gland cultures in-vitro. Archives of Insect Biochemistry and Physiology, 25, 287-299.
Agee, H.R. (1973) Spectral sensitivity of the compound eyes of field-collected adult bollworms and tobacco budworms. Annals of the Entomological Society of America, 66, 613-615.
Gemeno, C., Sans, A., Lopez, C., Albajes, R. & Eizaguirre, M. (2006) Pheromone antagonism in the European corn borer moth Ostrinia nubilalis. Journal of Chemical Ecology, 32, 1071-1084.
Löfstedt, C., Herrebout, W.M. & Menken, S.B.J. (1991) Sex pheromones and their potential role in the evolution of reproductive isolation in small ermine moths (Yponomeutidae). Chemoecology, 2, 20-28.
Subchev, M.A., Stanimovora, L.S. & Milkova, T.S. (1987) The effect of compounds related to cis-ll-hexadecenyl acetate on its attractiveness to the males of Mamestra brassicae L. (Lepidoptera: Noctuidae) and some other noctuid species. Folia Biologica, 35, 143-150.
Den Otter, C.J. & Van der Haagen, M.M. (1989) Sex pheromone attractants and inhibitors in the cabbage armyworm Mamestra brassicae L. (Lep.: Noctuidae): electrophysiological discrimination. Insect Science and Application, 10, 235-242.
Eliyahu, D., Nagalakshmi, V., Applebaum, S.W., Kubli, E., Choffat, Y. & Rafaeli, A. (2003) Inhibition of pheromone biosynthesis in Helicoverpa armigera by pheromonostatic peptides. Journal of Insect Physiology, 49, 569-574.
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Pawson, S.M. & Bader, M.K.F. (2014) LED lighting increases the ecological impact of light pollution irrespective of color temperature. Ecological Applications, 24, 1561-1568.
Renou, M. & Lucas, P. (1994) Sex pheromone reception in Mamestra brassicae L. (Lepidoptera): responses of olfactory receptor neurones to minor components of the pheromone blend. Journal of Insect Physiology, 40, 75-85.
Groenendijk, D. & Ellis, W.N. (2011) The state of the Dutch larger moth fauna. Journal of Insect Conservation, 15, 95-101.
Stone, E.L., Jones, G. & Harris, S. (2012) Conserving energy at a cost of biodiversity? Impacts of LED lighting on bats. Global Change Biology, 18, 2458-2465.
Groot, A.T., Blanco, C.A., Classen, A., Inglis, O., Santangelo, R.G., Lopez, J.D. et al. (2010a) Variation in sexual communication of the tobacco budworm, Heliothis virescens. Southwestern Entomologist, 35, 367-372.
Groot, A.T., Inglis, O., Bowdridge, S., Santangelo, R.G., Blanco, C., López, J.D. Jr. et al. (2009) Geographic and temporal variation in moth chemical communication. Evolution, 63, 1987-2003.
Van de Veire, M. & Dirinck, P. (1986) Sex pheromone components of the cabbage armyworm Mamestra brassicae. Isolation, identification and field experiments. Entomologia Experimentalis et Applicata, 41, 153-155.
Van Geffen, K.G., Van Eck, E., De Boer, R.H.A., Van Grunsven, R.H.A., Salis, L., Berendse, F. et al. (2015) Artificial light at night inhibits mating in a Geometrid moth. Insect Conservation and Diversity, . DOI: 10.1111/icad.12116..
Poot, H., Ens, B.J., de Vries, H., Donners, M.A.H., Wernand, M.R. & Marquenie, J.M. (2008) Green light for nocturnally migrating birds. Ecology and Society, 13, 47.
Struble, D.L., Arn, H., Buser, H.R., Städler, E. & Freuler, J. (1980) Identificantion of 4 sex pheromone components isolated from calling fermales of Mamestra brassicae. Zeitschrift für Naturvorschung B - A Journal of Chemical Science, 35, 45-48.
Descoins, C., Priesner, E., Gallois, M., Am, H. & Martin, G. (1978) Sur la secretion pheromonale des femelles vierges de Mamestra br
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Snippet 1. One major, yet poorly studied, change in the environment is the increase in nocturnal light pollution. Although this strongly alters the habitat of...
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SubjectTerms chemical composition
Disruption
Ecological effects
Environmental changes
Exterior lighting
Females
habitats
Light
Light pollution
Light sources
Lighting
males
Mamestra brassicae
moths
Pheromones
pollution
reproduction
sex pheromone composition
sex pheromones
sexual communication
Spectral composition
Title Artificial night lighting disrupts sex pheromone in a noctuid moth
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Volume 40
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