Life table parameters of Tuta absoluta (Meyrick, 1917) (Lepidoptera: Gelechiidae) on four wild tomato species

Year 2022, , 175 - 186, 01.06.2022

Baran Aslan , Ali Kemal Birgücü , Selman Uluışık , İsmail Karaca

https://doi.org/10.16970/entoted.1016214

Cited By: 1

Abstract

Tuta absoluta (Meyrick, 1917) (Lepidoptera: Gelechiidae) is an important tomato pest that also feeds on other plants in the Solanaceae. The effects of four wild tomato species (Solanum arcanum Peralta, Solanum habrochaites S.Knapp & D.M.Spooner, Solanum peruvianum L., Solanum pimpinellifolium L.) and two accession of Solanum lycopersicum L. (LA0292 and cv. 112-432) on the life table parameters of T. absoluta were determined. Larval development time, lifespan, pupal period, fecundity, and longevity were also estimated. The study was conducted in Isparta University of Applied Sciences, Agriculture Faculty, Plant Protection Department, Isparta, Türkiye in 2020-2021. Solanum lycopersicum was the most suitable species for the development of T. absoluta. Among the wild tomato species, S. pimpinellifolium for intrinsic rate of increase, S. arcanum, and S. pimpinellifolium for net reproductive rate, S. habrochaites and S. pimpinellifolium for mean generation time and doubling time, S. pimpinellifolium and S. arcanum for finite rate of increase were higher than the others. Although the results showed significant differences between the tested wild tomato species, S. pimpinellifolium and S. arcanum were the most effective wild hosts.

Keywords

Life table, Solanum, Tuta absoluta, wild tomato species

Tuta absoluta (Meyrick, 1917) (Lepidoptera: Gelechiidae)’nın dört yabani domates türü üzerinde yaşam çizelgesi parametreleri

Abstract

Tuta absoluta (Meyrick, 1917) (Lepidoptera: Gelechiidae) önemli bir domates zararlısıdır ve Solanaceae familyasındaki diğer konukçu bitkiler ile de beslenebilmektedir. Bu çalışmada dört yabani domates türü (Solanum arcanum Peralta, Solanum habrochaites S.Knapp & D.M.Spooner, Solanum peruvianum L., Solanum pimpinellifolium L.) ve iki Solanum lycopersicum L. (LA0292 ve cv. 112-432) aksesyonunun T. absoluta'nın yaşam tablosu parametreleri üzerindeki etkileri belirlenmiştir. Ayrıca larva gelişim süresi, yaşam süresi, pupa dönemi, doğurganlık ve yaşam ömrü de hesaplanmıştır. Çalışma Isparta Uygulamalı Bilimler Üniversitesi, Ziraat Fakültesi, Bitki Koruma Bölümü (Isparta, Türkiye)’nde 2020-2021 yılları arasında yürütülmüştür. Solanum lycopersicum, T. absoluta’nın gelişmesi bakımından en uygun tür olarak belirlenmiştir. Yabani domates türlerinden, kalıtsal üreme yeteneği için S. pimpinellifolium, net üreme gücü için S. arcanum ve S. pimpinellifolium, ortalama döl süresi ve popülasyonun ikiye katlanma süresi için S. habrochaites ve S. pimpinellifolium, artış oranı sınırı için S. pimpinellifolium ve S. arcanum türleri en etkili konukçular olarak belirlenmiştir. Sonuçlar, çalışılan yabani domates türlerinde önemli farklılıklar göstermiş olmasına rağmen S. pimpinellifolium ve S. arcanum en etkili yabani konukçu türler olarak belirlenmiştir.

Keywords

Yaşam çizelgesi, Solanum, Tuta absoluta, yabani domates türleri

References

• Aksoy, E. & O. B. Kovancı, 2016. Mass trapping low-density populations of Tuta absoluta with various types of traps in field-grown tomatoes. Journal of Plant Diseases and Protection, 123 (2): 51-57.
• Al-Jboory, I. J., A. Katbeh-Bader & S. Al-Zaidi, 2012. First observation and identification of some natural enemies collected from heavily infested tomato by Tuta absoluta (Meyrick) (Lepidoptera: Gelechiidae) in Jordan. Middle-East Journal of Scientific Research, 11 (6): 787-790.
• Biondi, A. & N. Desneux, 2019. Special issue on Tuta absoluta: recent advances in management methods against the background of an ongoing worldwide invasion. Journal of Pest Science, 92 (4): 1313-1315.
• Biondi, A., R. N. C. Guedes, F. H. Wan & N. Desneux, 2018. Ecology, worldwide spread, and management of the invasive South American tomato pinworm, Tuta absoluta: past, present, and future. Annual Review of Entomology, 63 (1): 239-258.
• Birch, L. C., 1948. The intrinsic rate of natural increase of an insect population. Journal of Animal Ecology, 17 (1): 15-26.
• Campos, M. R., A. Biondi, A. Adiga, R. N. C. Guedes & N. Desneux, 2017. From the western Palaearctic region to beyond: Tuta absoluta ten years after invading Europe. Journal of Pest Science, 90 (3): 787-796.
• Caparros Megido, R., E. Haubruge & F. J. Verheggen, 2013. Pheromone-based management strategies to control the tomato leafminer, Tuta absoluta (Lepidoptera: Gelechiidae). Biotechnology, Agronomy and Society and Environment, 17 (3): 475-82.
• Çekin, D. & B. Yaşar, 2015. The life table of Tuta absoluta (Meyrick, 1917) (Lepidoptera: Gelechiidae) on different tomato varieties. Journal of Agricultural Sciences, 21 (2): 199-206 (in Turkish with abstract in English).
• Chi, H., 1988. Life table analysis incorporating both sexes and variable development rates among individuals. Environmental Entomology, 17 (1): 26-34.
• Chi, H. & H. Liu, 1985. Two new methods for the study of insect population ecology. Bulletin of the Institute of Zoology, Academia Sinica. 24 (2): 225-240.
• Chi, H., M. You, R. Atlıhan, C. L. Smith, A. Kavousi, M. S. Özgökçe, A. Güncan, S. J. Tuan, J. W. Fu, Y. Y. Xu, F. Q. Zheng, B. H. Ye, D. Chu, Y. Yu, G. Gharekhani, P. Saska, T. Gotoh, M. I. Schneider, P. Bussaman, A. Gökçe & T. X. Liu, 2020. Age-stage, two-sex life table: An introduction to theory, data analysis, and application. Entomologia Generalis, 40 (2): 103-124.
• Chunwongse, J., C. Chunwongse, L. Black & P. Hanson, 2002. Molecular mapping of the Ph‐3 gene for late blight resistance in tomato. The Journal of Horticultural Science and Biotechnology, 77 (3): 281-286.
• Cocco, A., S. Deliperi & G. Delrio, 2013. Control of Tuta absoluta (Meyrick) (Lepidoptera: Gelechiidae) in greenhouse tomato crops using the mating disruption technique. Journal of Applied Entomology, 137 (1): 16-28.
• Deevey, E. S., 1947. Life Tables for natural populations of animals. The Quarterly Review of Biology, 22 (4): 283-314.
• Desneux, N., M. G. Luna, T. Guillemaud & A. Urbaneja, 2011. The invasive South American tomato pinworm, Tuta absoluta, continues to spread in Afro-Eurasia and beyond: the new threat to tomato world production. Journal of Pest Science, 84 (4): 403-408.
• Duarte, L., M. D. A. Martinez & V. H. P. Bueno, 2015. Biology and population parameters of Tuta absoluta (Meyrick) under laboratory conditions. Revista Protección Vegetal, 30 (1): 19-29.
• Erdoğan, P. & N. Babaroğlu, 2014. Life table of the tomato leaf miner, Tuta abosluta (Meyrick) (Lepidoptera: Gelechiidae). Journal of Agricultural Faculty of Gaziosmanpaşa University, 2014 (2): 80-89.
• Firdaus, S., A. W. van Heusden, N. Hidayati, E. D. J. Supena, R. G. F. Visser & B. Vosman, 2012. Resistance to Bemisia tabaci in tomato wild relatives. Euphytica, 187 (1): 31-45.
• Gervassio, N. G. S., D. Aquion, C. Vallina, A. Biondi & M. G. Luna, 2019. A re‑examination of Tuta absoluta parasitoids in South America for optimized biological control. Journal of Pest Science, 92 (4): 1343-1357.
• Gharekhani, G. H. & H. Salek-Ebrahimi, 2014. Life table parameters of Tuta absoluta (Lepidoptera: Gelechiidae) on different varieties of tomato. Journal of Economical Entomology, 107 (5): 1765-1770.
• Giorgini, M., E. Guerrieri, P. Cascone & L. Guntuo, 2019. Current strategies and future outlook for managing the neotropical tomato pest Tuta absoluta (Meyrick) in the Mediterranean Basin. Neotropical Entomology, 48 (1): 1-17.
• Gontijo, P. C., M. C. Picanço, E. J. G. Pereira, J. C. Martins, M. Chediak & R. N. C. Guedes, 2013. Spatial and temporal variation in the control failure likelihood of the tomato leaf miner, Tuta absoluta. Annals of Applied Biology, 162 (1): 50-59.
• Guedes, R. N. C., E. Roditakis, M. R. Campos, K. Haddi, P. Bielza, H. A. A. Siqueira, A. Tsagkarakou, J. Vontas & R. Nauen, 2019. Insecticide resistance in the tomato pinworm Tuta absoluta: patterns, spread, mechanisms, management and outlook. Journal of Pest Science, 92 (4): 1329-1342.
• Han, P., Y. Bayram, L. Shaltiel-Harpaz, F. Sohrabi, A. Saji, U. P. T. Esenali, A. Jalilov, A. Ali, P. R. Shashank, K. Ismoilov, Z. Lu, S. Wang, G. Zhang, F. Wan, A. Biondi & N. Desneux, 2019. Tuta absoluta continues to disperse in Asia: damage, ongoing management and future challenges. Journal of Pest Science, 92 (4): 1317-1327.
• Huang, Y. B. & H. Chi, 2012. Assessing the application of the jackknife and bootstrap techniques to the estimation of the variability of the net reproductive rate and gross reproductive rate: a case study in Bactrocera cucurbitae (Coquillett) (Diptera: Tephritidae). Journal of Agriculture and Forestry, 61 (1): 37-45.
• Kairo, M. T. K. & S. T. Murphy, 1995. The life history of Rodolia iceryae Janson (Coleoptera:Coccinellidae) and the potential for use in innoculative releases against Icerya pattersoni Newstead (Homoptera: Margarodidae) on coffee. Journal of Applied Entomology, 119 (4): 487-491.
• Kılıç, T., 2010. First record of Tuta absoluta in Turkey. Phytoparasitica, 38 (3): 243-244.
• Lanfermeijer, F. C., J. Warmink & J. Hille, 2005. The products of the broken Tm‐2 and the durable Tm‐22 resistance genes from tomato differ in four amino acids. Journal of Experimental Botany, 56 (421): 2925-2933.
• Lawo, J. P. & N. C. Lawo, 2011. Misconceptions about the comparison of intrinsic rates of natural increase. Journal of Applied Entomology, 135 (10): 715-725.
• Maluf, W., V. Fátima Silva, M. Graças Cardoso, L. Gomes, Á. Neto, G. Maciel & D. Nízio, 2010. Resistance to the South American tomato pinworm Tuta absoluta in high acylsugar and/or high zingiberene tomato genotypes. Euphytica, 176 (1): 113-123.
• Mata-Nicolás, E., J. Montero-Pau, E. Gimeno-Paez, A. García-Pérez, P. Ziarsolo, J. Blanca, E. van der Knaap, M. J. Díez & J. Cañizares, 2021. Discovery of a major QTL controlling trichome IV density in tomato using K-seq genotyping. Genes, 12 (243):1-18.
• Maxted, N., B. J. M. Brehm & S. Kell, 2013. Resource Book for Preparation of National Conservation Plans for Crop Wild Relatives and Landraces. Food and Agriculture Organization of the United Nations Commission on Genetic Resources for Food and Agriculture, Rome, Italy, 456 pp.
• Meyer, J. S., C. G. Ingersoll, L. L. McDonald & M. S. Boyce, 1986. Estimating uncertainty in population growth rates: jackknife vs. bootstrap techniques. Ecology, 67 (5): 1156-1166.
• Miller, J. C. & S. D. Tanksley, 1990. RFLP analysis of phylogenetic relationships and genetic variation in the genus Lycopersicon. Theoretical and Applied Genetics, 80 (4): 437-448.
• Mukwa, L. F. T., J. Mukendi, F. G. Adakate, D. M. Bugeme, A. Kalonji-Mbuyi & S. Ghimire, 2021. First report of the South American tomato pinworm Tuta absoluta (Meyrick) (Lepidoptera: Gelechiidae) and its damage in the Democratic Republic of Congo. BioInvasions Records, 10 (1): 33-44.
• Özgökçe, M. S. & R. Atlıhan, 2005. Biological features and life table parameters of the mealy plum aphid Hyalopterus pruni on different apricot cultivars. Phytoparasitica, 33 (1): 7-14.
• Parniske, M., B. B. H. Wulff, G. Bonnema, C. M. Thomas, D. A. Jones & J. D. G. Jones, 1999. Homologues of the Cf‐9 disease resistance gene (Hcr9s) are present at multiple loci on the short arm of tomato chromosome 1. Molecular Plant- Microbe Interactions, 12 (2): 93-102.
• Pereyra, P. C. & N. E. Sánchez, 2006. Effect of two solanaceous plants on developmental and population parameters of the tomato leaf miner, Tuta absoluta (Meyrick) (Lepidoptera:Gelechiidae). Neotropical Entomology, 35 (5): 671-676.
• Pinder, J. E., J. G. Wiener & M. H. Smith, 1978. The Weibull distribution: a new method of summarizing survivorship data. Ecology, 59 (1): 175-179.
• Prasanna, H. C., D. P. Sinha, G. K. Rai, R. Krishna, S. P. Kashyap, N. K. Singh & V. G. Malathi, 2015. Pyramiding Ty‐2 and Ty‐3 genes for resistance to monopartite and bipartite tomato leaf curl viruses of India. Plant Pathology, 64 (2): 256-264.
• Rostami, E., H. Madadi, H. Abbasipour, H. Allahyari & A. G. S. Cutbertson, 2017. Life table parameters of the tomato leaf miner Tuta absoluta (Lepidoptera: Gelechiidae) on different tomato cultivars. Journal of Applied Entomology, 141 (1): 88-96.
• Seah, S., J. Yaghoobi, M. Rossi, C. A. Gleason & V. M. Williamson, 2004. The nematode‐resistance gene, Mi‐1, is associated with an inverted chromosomal segment in susceptible compared to resistant tomato. Theoretical and Applied Genetics, 108 (8): 1635-1642.
• Silva, G. A., E. A. Queiroz, L. P. Arcanjo, M. C. Lopes, T. A. Araújo, T. S. V. Galdino, R. I. Samuels, N. Rodrigues-Silva & M. C. Picanço, 2021. Biological performance and oviposition preference of tomato pinworm Tuta absoluta when offered a range of Solanaceous host plants. Scientific Reports, 11 (1153): 1-10.
• Sohrabi, F., H. Nooryazdan, B. Gharati & Z. Saeidi, 2016. Evaluation of ten tomato cultivars for resistance against tomato leaf miner, Tuta absoluta (Meyrick) (Lepidoptera: Gelechiidae) under field infestation conditions. Entomologia Generalis, 36 (2): 163-175.
• Son, D., S. Bonzi, I. Somda, T. Bawin, S. Boukraa, F. Verheggen, F. Francis, A. Legrève & B. Schiffers, 2017. First record of Tuta absoluta (Meyrick, 1917) (Lepidoptera: Gelechiidae) in Burkina Faso. African Entomology, 25 (1): 259-263.
• Sylla, S., T. Brévault, A. B. Bal, A. Chailleux, M. Diatte, N. Desneux & K. Diarra, 2017. Rapid spread of the tomato leafminer, Tuta absoluta (Lepidoptera, Gelechiidae), an invasive pest in sub-Saharan Africa. Entomologia Generalis, 36 (3): 269-283.
• Tingle, C. C. D. & M. J. W. Copland, 1989. Progeny production and adult longevity of the mealybug parasitoids Anagyrus pseudococci, Leptomastix dactylopii and Leptomastidea abnormis (Hymenoptera: Encyrtidae) in relation to temperature. Entomophaga, 34 (1): 111-120.
• Tukey, J. W., 1949. Comparing individual means in the analyses of variance. Biometrics, 5 (2): 99-114.
• Uchoa-Fernandes, M., L. T. Della & E. Vilela, 1995. Mating, oviposition and pupation of Scrobipalpuloides absoluta (Meyr.) (Lepidoptera: Gelechiidae). Anais da Sociedade Entomológica do Brasil, 24(1): 159-164.
• Wang, X., L. Gao, J. C. Jiao, S. Stravoravdis, P. S. Hosmani, S. Saha, J. Zhang, S. Mainiero, S. R. Strickler, C. Catala, G. B. Martin, L. A. Mueller, J. Vrebalov, J. J. Giovannoni, S. Wu & Z. Fei, 2020. Genome of Solanum pimpinellifolium provides insights into structural variants during tomato breeding. Nature Communications, 11 (5817): 1-11.
• Wang, J. J., J. H. Tsai, Z. M. Zhao & L. S. Li, 2000. Development and reproduction of the psocid Liposcelis bostrychophila (Psocoptera: Liposcelididae) as a function of temperature. Annals of the Entomological Society of America, 93 (2): 261-270.
• Yu, L. Y., Z. Z. Chen, F. Q. Zheng, A. J. Shi, T. T. Guo, B. H. Yeh, H. Chi & Y. Y. Xu, 2013a. Demographic analysis, a comparison of the jackknife and bootstrap methods, and predation projection: A Case Study of Chrysopa pallens (Neuroptera: Chrysopidae). Journal of Economical Entomology, 106 (1): 1-9.
• Yu, J. Z., H. Chi & B. H. Chen, 2013b. Comparison of the life tables and predation rates of Harmonia dimidiata (F.) (Coleoptera: Coccinellidae) fed on Aphis gossypii Glover (Hemiptera: Aphididae) at different temperatures. Biological Control, 64 (1): 1-9.
• Zamir D., I. Eksteinmichelson, Y. Zakay, N. Navot, M. Zeidan, M. Sarfatti & H. Czosnek, 1994. Mapping and introgression of a Tomato yellow leaf curl virus tolerance gene, Ty‐1. Theoretical and Applied Genetics, 88 (2): 141-146.
• Zappalà, L., A. Biondi, A. Alma, I. J. Al-Jboory, J. Arno, A. Bayram, A. Chailleux, D. El-Arnaouty, Y. Gerling & Y. Guenaoui, 2013. Natural enemies of the South American moth, Tuta absoluta, in Europe, North Africa and Middle East, and their potential use in pest control strategies. Journal of Pest Science, 86 (4): 635-647.
• Zhang, H., C. Li, E. L. Davis, J. Wang, J. D. Griffin, J. Kofsky & B. H. Song, 2016. Genome‐wide association study of resistance to soybean cyst nematode (Heterodera glycines) HG Type 2.5.7 in wild soybean (Glycine soja). Frontiers in Plant Science, 7 (1214): 1-11.
• Zuriaga, E., J. M. Blanca, L. Cordera, A. Sifres, W. G. Blas-Cerdán, R. Morales & F. Nuez, 2009. Genetic and bioclimatic variation in Solanum pimpinellifolium. Genetic Resources and Crop Evolution, 56 (1): 39-51.