Journals / International Journal of Secondary Metabolite / 2019 / Cilt: 6 - Sayı: 2

The Effect of Nutrient-Allelochemicals Interaction on Food Consumption and Growth Performance of Alder Leaf Beetle, Agelastica alni L. (Coleoptera: Chrysomelidae)

Pages
196–204
Publication Date
2022-10-19
DOI
—
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AI Summary & Key Takeaways

AI Insight
⚡ TL;DR(Too Long; Didn't Read)

According to the results, the amount of gallic acid consumed did not affect the food consumption and the amount of pupa lipids.

📌 3 Key Takeaways

🎯
Objective & Hypothesis:In this study, the effects of secondary metabolites on the feeding preference and growth of generalist caterpillars, Agelastica alni L., were investigated.
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Key Findings & Data:Feeding experiment has been applied with a total of 11 diet; 6 of which were prepared by adding different concentrations of gallic acid (1, 3, 5 %) and quinine (0.125, 0.25, 0.5 %) to the control diet, 3 diet of which prepared by adding different concentrations of gallic acid and quinine.
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Conclusion & Impact:According to the results, the amount of gallic acid consumed did not affect the food consumption and the amount of pupa lipids.
🔬Design:Research Article
📍Scope:Comprehensive Sample
⚙️Variables:Secondary metabolite · Gallotannin · quinine

Abstract

In this study, the effects of secondary metabolites on the feeding preference and growth of generalist caterpillars, Agelastica alni L., were investigated. Feeding experiment has been applied with a total of 11 diet; 6 of which were prepared by adding different concentrations of gallic acid (1, 3, 5 %) and quinine (0.125, 0.25, 0.5 %) to the control diet, 3 diet of which prepared by adding different concentrations of gallic acid and quinine. According to the results, the amount of gallic acid consumed did not affect the food consumption and the amount of pupa lipids. However, the amount of gallic acid consumed positively affects the pupal mass and the pupal crude protein. In addition, the amount of quinine consumed negatively affected the developmental performance of larvae except for the food consumption. As the count of secondary metabolites in the diet increases, the pupal mass and the pupal crude protein decrease. Overall, during the co-evolution processs, A. alni larvae may be able to adapt to gallotannins. However, quinine, an alkaloid, is a feeding deterrence and growth suppressor for larvae.

Özet

In this study, the effects of secondary metabolites on the feeding preference and growth of generalist caterpillars, Agelastica alni L., were investigated. Feeding experiment has been applied with a total of 11 diet; 6 of which were prepared by adding different concentrations of gallic acid (1, 3, 5 %) and quinine (0.125, 0.25, 0.5 %) to the control diet, 3 diet of which prepared by adding different concentrations of gallic acid and quinine. According to the results, the amount of gallic acid consumed did not affect the food consumption and the amount of pupa lipids. However, the amount of gallic acid consumed positively affects the pupal mass and the pupal crude protein. In addition, the amount of quinine consumed negatively affected the developmental performance of larvae except for the food consumption. As the count of secondary metabolites in the diet increases, the pupal mass and the pupal crude protein decrease. Overall, during the co-evolution processs, A. alni larvae may be able to adapt to gallotannins. However, quinine, an alkaloid, is a feeding deterrence and growth suppressor for larvae.

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Cite This Article

ALTUN, N., YILDIZ, D., BİLGENER, M. (2022). The Effect of Nutrient-Allelochemicals Interaction on Food Consumption and Growth Performance of Alder Leaf Beetle, Agelastica alni L. (Coleoptera: Chrysomelidae). International Journal of Secondary Metabolite, Cilt: 6 - Sayı: 2, 196–204. https://ajindex.com/articles/541673

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References (4)

  1. Ryan, M. F. (2002). Insect Chemoreception Fundamental and Applied, 1st ed.; Kluwer Academic Publishers:
  2. Dordrecht, USA, 2002; pp. 28; 1-4020-0270-X. [2] Heflin, L.E., Raubenheimer, D., Simpson, S.J., Watts, S.A. (2016). Balancing macronutrient intake in cultured Lytechinus variegatus. Aquaculture, 450, 295-300.[3] Gall, M.L., Behmer, S.T. (2014). Effects of protein and carbohydrate on an insect herbivore: The vista from a fitness landscape. Integr. Comp. Biol., 54, 942-954. [4] Mattson, W. J. (1980). Herbivory in Relation to Plant Nitrogen Content. Annu. Rev. Ecol. Evol. Syst., 11, 119-161.[5] Hasheminia, S. M., Sendi, J.J., Jahromi, K.T., Moharramipour, S. (2013).
  3. Effect of milk thistle, Silybium marianum, extract on toxicity, development, nutrition, and enzyme activities of the small white butterfly, Pieris rapae. J Insect Sci., 13, 146. [6] El-Keredy, A. (2014). Genetic and behavioral influences of quinine and monosodium glutamate on Drosophila melanogaster. Egypt J. Genet. Cytol., 43, 377-391. [7] Bilgener, M. (1988). Chemical Components of Howler Monkeys (Alouatta palliata) Food Choice and Kinetics of Tannin Binding with Natural Polymers. Doctoral Thesis, Boston University, USA, 1988. [8] Hagerman, A.E., Robbins, C.T., Weerasuriya, Y., Wilson, T. C., McArthur, C. (1992). Tannin chemistry in relation to digestion. J. Range Manage, 45, 57-62. [9] He, Q., Shi, B., Yao, K. (2006). Interactions of gallotannins with proteins, amino acids, phospholipids and sugars. Food Chem, 95, 250-254. [10] Kessler, S., Gonzales, J., Vlimant, M., Glauser, G., Guerin, P.M. (2014). Quinine and artesunate inhibit feeding in the African malaria mosquito Anopheles gambiae: the role of gustatory organs within the mouthparts. Physiol. Entomol, 39, 172-182.[11] Swain, T. (1976). Angiosperm reptile co-evolution. In: Bellairs d'A Cox CB (eds). — Morphology and Biology of Reptiles. A. Linnean Society Symposium Series (3). [12] Levinson, H. Z. (1976). The defensive role of alkaloids in insects and plants. Experientia, 32, 408-411. [13] Tischler, W. (1977).
  4. Continuity, Of the biosystems Alder (Alnus) Alder (Agelastica alni). Zeitschrift fuer Angewandte Zoologia, 64, 69-92. [in Germany]. [14] Glendinning, J.I. (2007). How do predators cope with chemically defended foods? Biol. Bull., 213, 252–266.[15] Yamamoto, I. V. (1969). Mass rearing of tobacco hornworm. II. Larval rearing and pupation. J. Ecol. Entomol., 62, 1427-1431. [16] Lee, K.P., Behmer, S. T., Simpson, S. J., Raubenheimer