First Report of the Fall Armyworm, Spodoptera Frugiperda (Lepidoptera: Noctuidae), Natural Enemies from Africa

First Report of the Fall Armyworm, Spodoptera Frugiperda (Lepidoptera: Noctuidae), Natural Enemies from Africa

See discussions, stats, and author profiles for this publication at: https://www.researchgate.net/publication/325760323 First report of the fall armyworm, Spodoptera frugiperda (Lepidoptera: Noctuidae), natural enemies from Africa Article in Journal of Applied Entomology · June 2018 DOI: 10.1111/jen.12534 CITATIONS READS 2 443 9 authors, including: Paddy Likhayo Esayas Mendesil Kenya Agricultural and Livestock Research Organization Jimma University 12 PUBLICATIONS 228 CITATIONS 27 PUBLICATIONS 142 CITATIONS SEE PROFILE SEE PROFILE Mulatu Wakgari Gashawbeza Ayalew Haramaya University Ethiopian Institute of Agricultural Research 11 PUBLICATIONS 4 CITATIONS 16 PUBLICATIONS 103 CITATIONS SEE PROFILE SEE PROFILE Some of the authors of this publication are also working on these related projects: Species Diversity and Management of Termites using Entomopathogenic Nematodes in Groundnut (Arachis hypogaea L.) in Ethiopia View project Integrated cereal management View project All content following this page was uploaded by Paddy Likhayo on 28 January 2019. The user has requested enhancement of the downloaded file. Received: 17 April 2018 | Accepted: 17 May 2018 DOI: 10.1111/jen.12534 SHORT COMMUNICATION First report of the fall armyworm, Spodoptera frugiperda (Lepidoptera: Noctuidae), natural enemies from Africa Birhanu Sisay1,2,3 | Josephine Simiyu4 | Peter Malusi4 | Paddy Likhayo4 | Esayas Mendesil1 | Nsami Elibariki5 | Mulatu Wakgari2 | Gashawbeza Ayalew3 | Tadele Tefera1 1International Center of Insect Physiology & Ecology (icipe), Addis Ababa, Ethiopia Abstract 2Haramaya University, Dire Dawa, Ethiopia The fall armyworm (FAW), Spodoptera frugiperda, is a major pest of maize in North 3Melkasa Agricultural Research Center, and South America. It was first reported from Africa in 2016 and currently estab- Adama, Ethiopia lished as a major invasive pest of maize. A survey was conducted to explore for natu- 4International Center of Insect Physiology & Ecology (icipe), Nairobi, Kenya ral enemies of the fall armyworm in Ethiopia, Kenya and Tanzania in 2017. Smallholder 5National Biolgical Control Program, Kibaha, maize farms were randomly selected and surveyed in the three countries. Five differ- Tanzania ent species of parasitoids were recovered from fall armyworm eggs and larvae, in- Correspondence cluding four within the Hymenoptera and one Dipteran. These species are new Tadele Tefera, International Center of Insect associations with FAW and were never reported before from Africa, North and South Physiology & Ecology (icipe), PO Box 5689, Addis Ababa, Ethiopia. America. In Ethiopia, Cotesia icipe was the dominant larval parasitoid with parasitism Email: [email protected] ranging from 33.8% to 45.3%, while in Kenya, the tachinid fly, Palexorista zonata, was Funding information the primary parasitoid with 12.5% parasitism. Charops ater and Coccygidium luteum United States Agency for International were the most common parasitoids in Kenya and Tanzania with parasitism ranging Development, Grant/Award Number: AID-OAA-L-15-00001; Feed the Future from 6 to 12%, and 4 to 8.3%, respectively. Although fall armyworm has rapidly Collaborative Research on Integrated spread throughout these three countries, we were encouraged to see a reasonable Pest Management Innovation Lab of the US Agency for International level of biological control in place. This study is of paramount importance in designing Development, Grant/Award Number: AID- a biological control program for fall armyworm, either through conservation of native OAA-L-15-00001 natural enemies or augmentative release. KEYWORDS diptera, hymenoptera, insect parasitism, maize, Spodoptera frugiperda 1 | INTRODUCTION 2017, the pest invaded Sub- Saharan Africa. Recent reports con- firmed the occurrence of fall armyworm in 28 countries in Africa Maize is the most important staple food crop in Africa, where it is (Cock, Beseh, Buddie, Cafa, & Crozier, 2017; Day et al., 2017) indicat- grown predominantly by smallholder farmers (FAOSTAT, 2017). ing the rapid spread of the pest in the African continent, threatening Currently, however, the production of maize is threatened by the the food security of millions of people. Recent studies conducted fall armyworm, Spodoptera frugiperda (J.E.Smith) (Lepidoptera: by Centre for Agriculture and Biosciences International in 12 maize- Noctuidae). The pest, which is indigenous in the Americas, is highly producing countries showed that, without control, fall armyworm polyphagous, causing economic damage in various crops such as can cause maize yield losses ranging from 8.3 m to 20.6 m tonnes maize, sorghum, beans and cotton (Abrahams et al., 2017; Day et al., per year (Day et al., 2017). 2017). This invasive pest was first reported in West Africa in late In North and South American countries where fall armyworm 2016 (Goergen, Kumar, Sankung, Togola, & Tamo, 2016); by early is a major problem, chemical insecticide use is a common practice. J Appl Entomol. 2018;1–5. wileyonlinelibrary.com/journal/jen © 2018 Blackwell Verlag GmbH | 1 2 | SISAY ET AL. For example, in Brazil, an average of five insecticide sprays per 2017. In Tanzania, the survey was conducted from July to November maize cycle may be required (Ribeiro et al., 2014). Invasion of fall 2017. Geographical data such as latitude, altitude and longitude armyworm in Africa alarmed governments of different countries in were taken in each location. Damaged maize plants were assessed Africa to apply different insecticides in maize fields as an emergency for fall armyworm egg masses, larvae, pupae and parasitoid cocoons, response to fall armyworm invasion (Kumela et al., 2018). Most respectively. The egg masses were collected and placed in plastic smallholder farmers in Africa, however, cannot afford repeated in- cups with 5 grams of natural diet (fresh maize leaf). The larvae and secticide sprayings. Furthermore, dependence on chemical insecti- pupae were collected and they were placed in rectangular plastic cides results in the development of resistance to major classes of containers (4 cm height × 15 cm width × 21 cm length), covered on insecticide (e.g., Yu, Nguyen, & Abo- Elghar, 2003), increased risk to top with fine screen from which the parasitoids could not go through human health due to lack of appropriate safety precautions (Day the mesh. The larvae were fed with pieces of fresh maize leaves, et al., 2017), effects on nontarget organisms and risks for the envi- about 60 g, which were replaced every 48 hr until pupation. The ronment. This highlights the need for the development of integrated eggs, larvae and pupae were kept in the laboratory at room tem- pest management (IPM) strategies that are suitable to African small- perature of 24–26°C, 50%–70% RH and a photoperiod of 12:12 (L:D) holder farmers. Given the fact that fall armyworm is a new invasive h until parasitoids emerged. No parasitoid emerged from pupae. The pest in Africa, apart from reports on its occurrence, natural enemies parasitoids that emerged from the eggs and larvae were recorded associated with FAW are not documented for Africa. For IPM devel- every 24 hr. For dead eggs or larvae where nothing emerged, no opment for FAW, therefore, it is imperative to determine recruitment dissections were made to examine for dead parasitoids. Parasitoids of local natural enemies. The objective of this study was, therefore, were preserved in 70% ethanol and sent for identification to the to assess association of new local parasitoids with the fall armyworm Natural History Museum, UK. We did not find multiple parasitism in in Ethiopia, Kenya and Tanzania. This study reports for the first- time this study. Per cent of parasitism was calculated by dividing number parasitoids associated with the fall armyworm in Africa. of larvae parasitized by total number of larvae collected multiplied by 100 (Pair, Raulston, Sparks, & Martin, 1986). 2 | MATERIALS AND METHODS 2.3 | Statistical analysis 2.1 | Study area description Per cent parasitism of natural enemies were summarized and de- Survey of fall armyworm natural parasitoids was conducted in scriptive statistics (means and percentages) were calculated using major maize growing areas affected with the fall armyworms in MINITAB 16 statistical software. Ethiopia, Kenya and Tanzania. The sites in Ethiopia were Hawassa (7º00.89′N 38º23.256E – 7º1.154′N 38º22.568′E), Jimma (7º27.855′N 36º25.32′E – 7º40.137′N 36º47.349′E) and Awash- 3 | RESULTS Melkassa (8º24.842′N 39º19.355′E – 8º25.222′N 39º19.237′E). The study was conducted in five sites in Kenya: Taita Taveta In Ethiopia from the total sample of fall armyworm collected, three (03°13.336′S 037°44.551′E – 03°81.853′S 037°44.017′E), Kwale species of larval parasitoids emerged, that is, Cotesia icipe Fernandez- (01°30.133′ S 036°53.966′E– 01°35.636′S 036°55.082′E), Homabay Triana & Fiobe, Palexorista zonata (Curran) and Coccygidium luteum (04°19.612′S039°22.450′E–04°20.0101′S039°22.442′E), (Brullé) (Table 1). Cotesia icipe was the most common parasitoid that Machakos (01°07.593′S037º26.396′E–01°13.835′S037°27.363′E) emerged from all surveyed areas of Ethiopia with parasitism rang- and Transzoia (01°45.711′S037°28.840′E– 01°46.126′S 037°37. ing from 33.8% in Awash-Melkasa to 45.3% in Jimma. On the other 761′E). In Tanzania, the sites were Morogoro (S06º26.958′ E037º hand, parasitism by a tachinid fly P. zonata and C. luteum was rela- 31.916′– S07°07.533′ E037°30.765′), Tanga (S05°08.100′ E038°55. tively lower (<6.4%). Different species of egg and larval parasitoids 776′– S 05°44.765′ E038°15.285′) and Pwani (S06°26.666′ E038° emerged from fall armyworm egg and larvae collected in Kenya, 20.191′). among which the parasitic wasp Charops ater Szépligeti and P. zo- nata caused about 12% parasitism, while Chelonus curvimaculatus Cameron and C. icipe showed low levels of parasitism (<6%). Egg par- 2.2 | Assessment of natural enemies of the asitism by C. curvimaculatus was quite low (4.8%). In Tanzania, C.

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