Hostname: page-component-586b7cd67f-2brh9 Total loading time: 0 Render date: 2024-11-23T15:39:35.881Z Has data issue: false hasContentIssue false

Do floral resources affect fitness of adult Cydia pomonella (Linnaeus 1758) (Lepidoptera: Tortricidae)?

Published online by Cambridge University Press:  22 June 2021

Silvia Mátray
Affiliation:
Julius Kühn Institute (JKI) – Federal Research Centre for Cultivated Plants, Institute for Biological Control, Heinrichstr. 243, Darmstadt, D-64287, Germany
Annette Herz*
Affiliation:
Julius Kühn Institute (JKI) – Federal Research Centre for Cultivated Plants, Institute for Biological Control, Heinrichstr. 243, Darmstadt, D-64287, Germany
*
Author for correspondence: Annette Herz, E-mail: [email protected]

Abstract

The introduction of flowering plants into orchards can increase functional biodiversity in pome fruit cultivation. Plants provide nectar, pollen and prey resources supporting pollinators and natural enemies. However, pests may also benefit from floral diets and a careful selection of plants is necessary to reduce any risk of pest proliferation. The codling moth Cydia pomonella is a major pest in apple growing worldwide and adults are known to consume sugars. The impact of floral diets (parsnip, wild carrot, coriander, red clover) on longevity, fecundity and fertility of adult codling moth was examined under laboratory conditions. In general, male moths lived longer than females, regardless of dietary treatments. Moths survived longest when supplied with parsnip flowers as a floral diet. Contrary to carrot, coriander resulted in higher longevity of adult C. pomonella compared to moths provided with red clover as a negative control. Adult nutrition on floral diets did not affect fecundity substantially. As expected, the majority of eggs were laid within the first week. Prolongation of moths’ lifespan by floral diets did not significantly increase the total number of eggs laid in contrast to a diet with 25% sucrose solution. According to these results, the risk of inadvertently promoting codling moth when growing selected flowering plants in the orchard will be rather low, because the fitness of the moths and especially the reproduction of the females will not be substantially enhanced.

Type
Research Paper
Copyright
Copyright © The Author(s), 2021. Published by Cambridge University Press

Access options

Get access to the full version of this content by using one of the access options below. (Log in options will check for institutional or personal access. Content may require purchase if you do not have access.)

References

Altieri, MA and Schmidt, LL (1985) Cover crop manipulation in northern California orchards and vineyards: effects on arthropod communities. Biological Agriculture & Horticulture 3, 124.CrossRefGoogle Scholar
Ambrosino, MD, Luna, JM, Jepson, PC and Wratten, SD (2006) Relative frequencies of visits to selected insectary plants by predatory hoverflies (Diptera: Syrphidae), other beneficial insects, and herbivores. Environmental Entomology 35, 394400.CrossRefGoogle Scholar
Atanassov, A and Shearer, PW (2005) Peach extrafloral nectar impacts life span and reproduction of adult Grapholita molesta (Busck) (Lepidoptera: Tortricidae). Journal of Agricultural and Urban Entomology 22, 4147.Google Scholar
Baggen, LR and Gurr, GM (1998) The influence of food on Copidosoma koehleri (Hymenoptera: Encyrtidae), and the use of flowering plants as a habitat management tool to enhance biological control of potato moth, Phthorimaea operculella (Lepidoptera: Gelechiidae). Biological Control 11, 917.CrossRefGoogle Scholar
Baker, HG and Baker, I (1983) Floral nectar sugar constituents in relation to pollinator type. In Jones, CE and Little, RJ (eds), Handbook of Experimental Pollination Biology. New York: Van Nostrand Reinhold, pp. 117141.Google Scholar
Balzan, MV and Wäckers, FL (2013) Flowers to selectively enhance the fitness of a host-feeding parasitoid: adult feeding by Tuta absoluta and its parasitoid Necremnus artynes. Biological Control 67, 2131.CrossRefGoogle Scholar
Barnes, MM (1991) Codling moth occurrence, host race formation, and damage. In van der Geest, LPS and Evenhuis, HH (eds), World Crop Pests – Tortricid Pests: Their Biology, Natural Enemies and Control, vol. 5. Amsterdam: Elsevier Science Publishers, pp. 313327.Google Scholar
Bathon, H (1981) Zur Zucht des Apfelwicklers, Laspeyresia pomonella (L.)(Lep., Tortricidae), auf einem künstlichen Nährmedium. Mittteilungen der deutschen Gesellschaft für allgemeine und angewandte Entomologie 2, 136140.Google Scholar
Beers, EH and Brunner, JF (1992) Implementation of the codling moth phenology model on apples in Washington State. Acta Phytopathologica et Entomologica Hungarica 27, 97102.Google Scholar
Benz, G (1991) Physiology, reproduction and ecology. In van der Geest, LPS and Evenhuis, HH (eds), World Crop Pests – Tortricid Pests: Their Biology, Natural Enemies and Control, vol. 5. Amsterdam: Elsevier Science Publishers, pp. 89147.Google Scholar
Blomefield, TL and Giliomee, JH (2012) Fecundity and mortality of codling moth, Cydia pomonella (L.)(Lepidoptera: Tortricidae), under field conditions in South Africa. African Entomology 20, 316324.CrossRefGoogle Scholar
Boggs, CL (1987) Ecology of nectar and pollen feeding in Lepidoptera. In Slansky, F and Rodriguez, JG (eds), Nutritional Ecology of Insects, Mites, and Spiders. New York: Wiley and Sons, pp. 369391.Google Scholar
Boggs, CL (1997) Reproductive allocation from reserves and income in butterfly species with differing adult diets. Ecology 78, 181191.CrossRefGoogle Scholar
Brown, MW (2001) Flowering ground cover plants for pest management in peach and apple orchards. IOBC wprs Bulletin 24, 379382.Google Scholar
Cahenzli, F and Erhardt, A (2012) Enhancing offspring quality or quantity? Different ways for using nectar amino acids in female butterflies. Oecologia 169, 10051014.CrossRefGoogle ScholarPubMed
Cahenzli, F, Sigsgaard, L, Daniel, C, Herz, A, Jamar, L, Kelderer, M, Kramer Jacobsen, S, Kruczyńska, D, Matray, S, Porcel, M, Sekrecka, M, Świergiel, W, Tasin, M, Telfser, J and Pfiffner, L (2019) Perennial flower strips for pest control in organic apple orchards-A pan-European study. Agriculture, Ecosystems & Environment 278, 4353.CrossRefGoogle Scholar
Campbell, A, Wilby, A, Sutton, P and Wäckers, F (2017) Getting more power from your flowers: multi-functional flower strips enhance pollinators and pest control agents in apple orchards. Insects 8, 101.CrossRefGoogle ScholarPubMed
Cisneros, FH and Barnes, MM (1974) Contribution to the biological and ecological characterization of apple and walnut host races of codling moth, Laspeyresia pomonella (L.): moth longevity and oviposition capacity. Environmental Entomology 3, 402406.CrossRefGoogle Scholar
Corbet, SA (2003) Nectar sugar content: estimating standing crop and secretion rate in the field. Apidologie 34, 110.CrossRefGoogle Scholar
Daniel, C, Matray, S, Stoeckli, S and Niggli, U (2018) Pest management in organic apple, pear and stone fruit. In Vacante, V and Kreiter, S (eds), Handbook of Pest Management in Organic Farming. Wallingford: CAB International, pp. 130150.CrossRefGoogle Scholar
Deseö, KV (1971) Study of factors influencing the fecundity and fertility of codling moth (Laspeyresia pomonella L., Lepidoptera, Tortricidae). Acta Phytopathologica 6, 243252.Google Scholar
Foti, MC, Peri, E, Wajnberg, E, Colazza, S and Rostás, M (2019) Contrasting olfactory responses of two egg parasitoids to buckwheat floral scent are reflected in field parasitism rates. Journal of Pest Science 92, 747756.CrossRefGoogle Scholar
Geier, PW (1963) The life history of codling moth, Cydia pomonella (L) (Lepidoptera: Tortricidae), in the Australian Capital Territory. Australian Journal of Zoology 11, 323367.CrossRefGoogle Scholar
Geier, PW and Briese, DT (1978) The demographic performance of a laboratory strain of codling moth, Cydia pomonella (Lepidoptera: Tortricidae). Journal of Applied Ecology 15, 679696.CrossRefGoogle Scholar
Géneau, CE, Wäckers, FL, Luka, H, Daniel, C and Balmer, O (2012) Selective flowers to enhance biological control of cabbage pests by parasitoids. Basic and Applied Ecology 13, 8593.CrossRefGoogle Scholar
Gu, H, Hughes, J and Dorn, S (2006) Trade-off between mobility and fitness in Cydia pomonella L. (Lepidoptera: Tortricidae). Ecological Entomology 31, 6874.CrossRefGoogle Scholar
Gurr, GM, Wratten, SD, Landis, DA and You, M (2017) Habitat management to suppress pest populations: progress and prospects. Annual Review of Entomology 62, 91109.CrossRefGoogle ScholarPubMed
Hagley, EA (1972) Observations on codling moth longevity and egg hatchability. Environmental Entomology 1, 123125.CrossRefGoogle Scholar
Herz, A, Cahenzli, F, Penvern, S, Pfiffner, L, Tasin, M and Sigsgaard, L (2019) Managing floral resources in apple orchards for pest control: ideas, experiences and future directions. Insects 10, 247.CrossRefGoogle ScholarPubMed
Howell, JF (1981) Codling moth: the effect of adult diet on longevity, fecundity, fertility, and mating. Journal of Economic Entomology 74, 1318.CrossRefGoogle Scholar
Irvin, NA, Scarratt, SL, Wratten, SD, Frampton, CM, Chapman, RB and Tylianakis, JM (2006) The effects of floral understoreys on parasitism of leafrollers (Lepidoptera: Tortricidae) on apples in New Zealand. Agricultural and Forest Entomology 8, 2534.CrossRefGoogle Scholar
Jado, RH, Araj, SE, Abu-Irmaileh, B, Shields, MW and Wratten, SD (2019) Floral resources to enhance the potential of the parasitoid Aphidius colemani for biological control of the aphid Myzus persicae. Journal of Applied Entomology 143, 3442.CrossRefGoogle Scholar
Kaplan, EL and Meier, P (1958) Nonparametric estimation from in complete observations. Journal of the American Statistical Association 53, 457481.CrossRefGoogle Scholar
Klotz, S, Kühn, I, Durka, W and Briemle, G (2002) BIOLFLOR-Eine Datenbank zu biologisch-ökologischen Merkmalen der Gefäßpflanzen in Deutschland. Schriftenreihe für Vegetationskunde 38, 334pp. Retrieved 14 April 2020, from http://www.ufz.de/biolflor/index.jsp.Google Scholar
Lavandero, B, Wratten, SD, Didham, RK and Gurr, G (2006) Increasing floral diversity for selective enhancement of biological control agents: a double-edged sward? Basic and Applied Ecology 7, 236243.CrossRefGoogle Scholar
May, PG (1985) Nectar uptake rates and optimal nectar concentrations of two butterfly species. Oecologia 66, 381386.CrossRefGoogle ScholarPubMed
Mills, N (2005) Selecting effective parasitoids for biological control introductions: codling moth as a case study. Biological Control 34, 274282.CrossRefGoogle Scholar
Penvern, S, Fernique, S, Cardona, A, Herz, A, Ahrenfeldt, E, Dufils, A, Jamar, L, Korsgaard, M, Kruczyńska, D, Matray, S, Ozolina-Pole, L, Porcel, M, Ralle, B, Steinemann, B, Świergiel, W, Tasin, M, Telfser, J, Warlop, F and Sigsgaard, L (2019) Farmers’ management of functional biodiversity goes beyond pest management in organic European apple orchards. Agriculture, Ecosystems & Environment 284, 111.CrossRefGoogle Scholar
Pfiffner, L and Wyss, E (2004) Use of sown wildflower strips to enhance natural enemies of agricultural pests. In Gurr, GM, Wratten, SD and Altieri, MA (eds), Ecological Engineering for Pest Management: Advances in Habitat Manipulation for Arthropods. Wallingford: CABI-Publishing, pp. 167188.Google Scholar
Pfiffner, L, Cahenzli, F, Steinemann, B, Jamar, L, Chor Bjørnc, M, Porcel, M, Tasin, M, Telfser, J, Kelderer, M, Lisek, J and Sigsgaard, L (2019) Design, implementation and management of perennial flower strips to promote functional agrobiodiversity in organic apple orchards: a pan-European study. Agriculture, Ecosystems & Environment 278, 6171.CrossRefGoogle Scholar
R Core Team (2018) R: A Language and Environment for Statistical Computing. Vienna, Austria: R Foundation for Statistical Computing. Available at https://www.R-project.org/.Google Scholar
Savopoulou-Soultani, M, Milonas, PG and Stavridis, DG (1998) Role of availability of food to the adult Lobesia botrana (Lepidoptera: Tortricidae) in its reproductive performance. Journal of Economic Entomology 91, 13411348.CrossRefGoogle Scholar
Schumacher, P, Weyeneth, A, Weber, DC and Dorn, S (1997) Long flights in Cydia pomonella L. (Lepidoptera: Tortricidae) measured by a flight mill: influence of sex, mated status and age. Physiological Entomology 22, 149160.CrossRefGoogle Scholar
Sigsgaard, L, Betzer, C, Naulin, C, Eilenberg, J, Enkegaard, A, Kristensen, K and Michaud, JP (2013) The effect of floral resources on parasitoid and host longevity: prospects for conservation biological control in strawberries. Journal of Insect Science 13, 104.CrossRefGoogle ScholarPubMed
Simon, S, Bouvier, JC, Debras, JF and Sauphanor, B (2010) Biodiversity and pest management in orchard systems: a review. Agronomy for Sustainable Development 30, 139152.CrossRefGoogle Scholar
Stephens, MJ, France, CM, Wratten, SD and Frampton, C (1998) Enhancing biological control of leafrollers (Lepidoptera: Tortricidae) by sowing buckwheat (Fagopyrum esculentum) in an orchard. Biocontrol Science and Technology 8, 547558.CrossRefGoogle Scholar
Stevens, P, Froud, K and Jamieson, L (2002) Effects of adult feeding on longevity and fecundity of Ctenopseustis obliquana (Lepidoptera: Tortricidae). New Zealand Journal of Crop and Horticultural Science 30, 229234.CrossRefGoogle Scholar
Tschumi, M, Albrecht, M, Entling, MH and Jacot, K (2015) High effectiveness of tailored flower strips in reducing pests and crop plant damage. Proceedings of the Royal Society B: Biological Sciences 282, 18.Google ScholarPubMed
Uyttenbroeck, R, Hatt, S, Paul, A, Boeraeve, F, Piqueray, J, Francis, F, Danthine, S, Frederich, M, Dufrene, M, Bodson, B and Monty, A (2016) Pros and cons of flowers strips for farmers. A review. Biotechnologie Agronomie Societe et Environnement 20, 225235.Google Scholar
van Rijn, PC and Wäckers, FL (2016) Nectar accessibility determines fitness, flower choice and abundance of hoverflies that provide natural pest control. Journal of Applied Ecology 53, 925933.CrossRefGoogle Scholar
Vattala, HD, Wratten, SD, Phillips, CB and Wäckers, FL (2006) The influence of flower morphology and nectar quality on the longevity of a parasitoid biological control agent. Biological Control 39, 179185.CrossRefGoogle Scholar
Villa, M, Marrão, R, Mexia, A, Bento, A and Pereira, JA (2017) Are wild flowers and insect honeydews potential food resources for adults of the olive moth, Prays oleae? Journal of Pest Science 90, 185194.CrossRefGoogle Scholar
Voudouris, CC, Sauphanor, B, Franck, P, Reyes, M, Mamuris, Z, Tsitsipis, JA, Vontas, J and Margaritopoulos, JT (2011) Insecticide resistance status of the codling moth Cydia pomonella (Lepidoptera: Tortricidae) from Greece. Pesticide Biochemistry and Physiology 100, 229238.CrossRefGoogle Scholar
Wäckers, FL (2004) Assessing the suitability of flowering herbs as parasitoid food sources: flower attractiveness and nectar accessibility. Biological Control 29, 307314.CrossRefGoogle Scholar
Wäckers, FL and van Rijn, PCJ (2005) Food for protection: an introduction. In Wäckers, FL, van Rijn, PCJ and Bruin, J (eds), Plant-Provided Food for Carnivorous Insects: A Protective Mutualism and its Applications. Cambridge: Cambridge University Press, pp. 114.CrossRefGoogle Scholar
Wäckers, FL, Björnsen, A and Dorn, S (1996) A comparison of flowering herbs with respect to their nectar accessibility for the parasitoid Pimpla turionellae. Proceedings of the Section Experimental and Applied Entomology of The Netherlands Entomological Society 7, 177182.Google Scholar
Wäckers, FL, Romeis, J and van Rijn, P (2007) Nectar and pollen feeding by insect herbivores and implications for multitrophic interactions. Annual Review of Entomology 52, 301323.CrossRefGoogle ScholarPubMed
Wade, MR and Wratten, SD (2007) Excised or intact inflorescences? Methodological effects on parasitoid wasp longevity. Biological Control 40, 347354.CrossRefGoogle Scholar
Wenninger, EJ and Landolt, PJ (2011) Apple and sugar feeding in adult codling moths, Cydia pomonella: effects on longevity, fecundity, and egg fertility. Journal of Insect Science 11, 161.CrossRefGoogle ScholarPubMed
Wiesmann, R (1935) Untersuchungen über den weiblichen Genitalapparat, das Ei und die Embryonalentwicklung des Apfelwicklers Carpocapsa (Cydia) pomonella. Mitteilungen der Schweizerischen Entomologischen Gesellschaft 16, 370377.Google Scholar
Winkler, K, Wäckers, FL, Kaufman, LV, Larraz, V and van Lenteren, JC (2009 a) Nectar exploitation by herbivores and their parasitoids is a function of flower species and relative humidity. Biological Control 50, 299306.CrossRefGoogle Scholar
Winkler, K, Wäckers, F and Pinto, DM (2009 b) Nectar-providing plants enhance the energetic state of herbivores as well as their parasitoids under field conditions. Ecological Entomology 34, 221227.CrossRefGoogle Scholar
Winkler, K, Wäckers, FL, Termorshuizen, AJ and van Lenteren, JC (2010) Assessing risks and benefits of floral supplements in conservation biological control. BioControl 55, 719727.CrossRefGoogle Scholar
Witzgall, P, Stelinski, L, Gut, L and Thomson, D (2008) Codling moth management and chemical ecology. Annual Review of Entomology 53, 503522.CrossRefGoogle ScholarPubMed
Wyss, E (1995) The effects of weed strips on aphids and aphidophagous predators in an apple orchard. Entomologia Experimentalis et Applicata 75, 4349.CrossRefGoogle Scholar