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International Journal of Tropical Insect Science https://doi.org/10.1007/s42690-020-00370-x MINI-REVIEW Phyto-derivatives: an efficient eco-friendly way to manage Trogoderma granarium (Everts) (Coleoptera: Dermestidae) Waqar Islam 1 & Ali Noman 2 & Komivi Senyo Akutse 3 & Muhammad Qasim 4 & Habib Ali 5 & Ijaz Haider 6 & Mohamed Hashem 7,8 & Saad Alamri 7,9 & Omar Mahmoud al Zoubi 10 & Khalid Ali Khan 7,11,12 Received: 26 August 2020 / Accepted: 6 November 2020 # African Association of Insect Scientists 2020 Abstract Worldwide, stored products are attacked by a large number of pests resulting in significant economic losses. Among these stored grain pests, khapra beetle, Trogoderma granarium (Everts) (Coleoptera: Dermestidae) is one of the top ranked pests that has ability to survive under diverse climate conditions. The management of this pest is mainly done by using synthetic chemicals which have side effects on consumers, ecosystem and non-target organisms. However, phyto-derivatives were found to be the effective environment friendly alternatives against T. granarium. Therefore, in this review, success of phyto-derivatives against khapra beetle from conventional means to modern research has been critically analyzed, summarized and discussed. In context, the different life stages of the insect starting from egg laying to adult development have been briefly explained. The review focuses upon recent research conducted on the evaluation of dozens of phyto-derivatives. In addition, the article has also highlighted some limitations of plant derived compounds and concludes via hoping that the future formulated pesticides will be safer, economical, least toxic to human and our planet ecosystem. Keywords Botanicals . Phyto-chemicals . Food security . Extracts . Stored products Introduction Agricultural and animal stored products are attacked by more than 20,000 field insects including six hundred species of beetles, more than 70 moth species and around 355 species of mites, resulting in quantitative and qualitative losses * Waqar Islam waqarislam@m.fafu.edu.cn; ddoapsial@yahoo.com 1 2 Institute of Geography, Fujian Normal University, Fuzhou 350007, China Department of Botany, Government College University, Faisalabad, Pakistan 3 International Centre of Insect Physiology and Ecology, P.O. Box 30772-00100, Nairobi, Kenya 4 Key Laboratory of Molecular Biology of Crop Pathogens and Insects, Institute of Insect Sciences, College of Agriculture & Biotechnology, Ministry of Agricultural and Rural Affairs, Zhejiang University, Hangzhou 310058, People’s Republic of China 5 Department of Agriculture Engineering, Khawaja Fareed University, Rahim Yar Khan, Pakistan worldwide (Nagpal and Kumar 2012; Rajendran 2005). These losses are more associated with developing countries because of poor sanitary conditions during commodity procurement, processing, non-hygienic transportation, conventional storage techniques and technically and poorly maintained storage units (Dubey et al. 2008; Hubert et al. 2004). 6 Entomological Institute, Ayub Agriculture Research Institute, Faisalabad, Pakistan 7 Department of Biology, College of Science, King Khalid University, 61413 Abha, Saudi Arabia 8 Botany and Microbiology Department, Faculty of Science, Assiut University, 71516 Assiut, Egypt 9 Prince Sultan Bin Abdulaziz Center for Environmental and Tourism Research and Studies, King Khalid University, Abha 61413, Saudi Arabia 10 Department of Biology, Facility of science in Yanbu, Taibah University, Medina, Kingdom of Saudi Arabia 11 Research Center for Advanced Materials Science (RCAMS), King Khalid University, P.O. Box 9004, 61413 Abha, Saudi Arabia 12 Unit of Bee Research and Honey Production, Faculty of Science, King Khalid University, P.O. Box 9004, Abha 61413, Saudi Arabia Int J Trop Insect Sci Stored grain insect infestation exhibits 10–20% grain losses worldwide (Pedigo and Rice 2014; Rajendran and Sriranjini 2008). The damages in terms of quality and quantity due to stored pests infestation are very high, which not only results in human health hazards (malnutrition), but also causes millions of dollars loss to national exchequer annually (Nagpal and Kumar 2012). The khapra beetle, Trogoderma granarium (Everts) (Coleoptera: Dermestidae) is a key stored product insect pest that has been categorized as an A2 quarantine organism by European and Mediterranean Plant Protection Organization (EPPO 2011). The pest is considered as one of the hundred “world’s worst” invaders (Lowe et al. 2000). The khapra beetle presence is observed in stored grain commodities throughout the year worldwide, indicating that the pest have developed a survival ability in worst conditions, and have become a global threat to food security (Dwivedi and Shekhawat 2004). Infestations are difficult to control because of the insect’s ability to survive without food for long periods, its preference for dry conditions and low-moisture food, and its resistance to many insecticides (Derbalah 2012; Islam 2017a). Khapra beetle infested grains harbor the insect residues leading to severe adverse effects upon human being digestive system and reduction of the nutritional values of the grains (Arain et al. 2006). Management of the pest is very important for quality assurance and food safety of the cereal stored grain commodities. According to quarantine laws, it is pre-requisite to ensure the pest free grains before export to other countries, which highly limit exportation of infested grains and consequently subjected to rejections of export orders. Although conventional and non-conventional chemical management of the khapra beetle minimize the pest pressure, however, it was observed that repeated use of these techniques year after year has resulted in development of resistance in the pest against the chemicals and the scenario has become challenging for entomology researchers (Ahmedani et al. 2007). Also, chemicals pose adverse effects on human health and surrounding ecosystem (Damalas and Eleftherohorinos 2011; Islam and Ahmed 2016; Islam et al. 2016a). Therefore, the importance of phyto-derivatives as an alternative to manage the khapra beetle increases ten folds more as they are environmentally safe, cheaper, locally available and pest did not acquire resistance against them as well (Islam 2017b; Islam et al. 2016b). In this review, we highlighted the importance of phytoderivatives by underlining the conventional approach of plant extracts and their success stories. Furthermore, we reviewed the recent research focusing on the application of phytoextracts against T. granarium in 21st century. The biology of the pest was also discussed through its life stages for better understanding of the insect behavior and consequently pointed out some limitations in phyto-derivatives control strategies. The review aims to increase awareness among the readers and community, and guide stakeholders on the new means of successful eco-friendly management approaches against khapra beetle. An overview on khapra beetle To understand and improve the management of the pest, it is important to have knowledge about the pest identification, biology and its ecological distribution so that adequate and effective control measures could be developed and adopted against this insect pest. Identification Oblong to oval shaped adult beetles are about 1.6-3.0 mm in length and 0.9–1.7 mm wide. Male beetles are brown-black in color having reddish brown marks, while females exhibit lighter color in contrast. Females are larger than males. The antennae of the insect are mounted upon a small deflexed head and it bears eleven segments fitting into a groove like structure. Female could lay approximately 125 eggs during its life span. These eggs are cylindrical, round ended at one side (0.7 by 0.25 mm), and are initially milky white containing spiny projections, but later, after several hours, eggs turn into pale yellowish. At hatching point, the larvae are yellowish white and have brownish hairs ranging between 1.6 and 1.8 mm in length constituting a hairy tail. The larval color changes to reddish or golden with increasing age gradually shortening towards the tail. At maturity, they occupy 6 mm length and 1.5 mm width (Hadaway 1956). The khapra beetle’s physiology and development are significantly impacted by its diet. Biology Although the adults bear wings, they do not use them for flying. Adults carry out mating process for reproduction and fertilized females can live up to seven days, but non-fertilized ones can survive up to a month, while males’ life span is about two weeks. Five days after emergence, the reproductive mating is initiated, leading to egg laying (25 eggs on an average per female per day) at higher temperature regimes such as 40 °C, but the oviposition stops at lower temperature, i.e., 20 °C. Egg hatching occurs after approximately 10–14 days, while completion of life cycle from egg to adult can vary from 26 to 220 days depending on the temperature and diet. However, eggs hatch better under the optimum temperature of 35 °C, while lower temperatures lead the eggs to diapauses condition, where they can survive for years (Anonymous 1981) (Fig. 1). Distribution As many countries now rely upon quarantine measures to control entry of invasive insect pests and diseases, the distribution maps or data of particular insect globally is very Int J Trop Insect Sci Fig. 1 Life cycle of khapra Beetle, Trogoderma granarium (http:// khaprabeetleathreat2australia. weebly.com/life-cycle.html) important (Banks 1977). Khapra beetle is distributed worldwide (Szito 2006) and exhibits resistance against many conventional synthetic chemicals. Mass eradication campaigns were launched in several countries such as USA in 1960s to reduce the pest infestations. However, complete eradication of the insect species was not achieved in USA because 67% of the country climate is favorable for the pest survival (French and Venette 2005). Why phyto-derivatives? In the 19th century, extensive use of chemicals as fumigants and insecticides was coined. These chemicals are still effective against some life stages of khapra beetle (Nayak et al. 2013; Pimentel et al. 2007). The practice of using fumigants is still favorite in developing countries (Rehman et al. 2013; Wasala et al. 2016). The continuous use of chemicals has allowed khapra beetle to acquire resistance against them (Donahaye 2000). This resistance is alarming in south Asia, USA and Australia which may lead to big disaster toward the control of the pest in future (Leelaja et al. 2007; Rajashekar et al. 2006). Chemicals are the major cause of destruction to human health and global ecosystem (Dubey et al. 2007; Islam et al. 2017b). For example, ozone depletion is caused by extensive use of methyl bromide globally, and was consequently banned from the international markets (WMO 1995). Contact insecticides have been found to have more detrimental effects upon human specifically during handling and utilization. More than 500 insect species and mites are resistant to the synthetic contact poisons such as deltamethrin, cypermathrin, chloropyrifos and malathion (Subramanyam and Hagstrum 1995). Furthermore, Champ (1985) reported that the stored grain insects including khapra beetle have developed resistance at some stage of their life against the synthetic chemicals. This resistance in the pests is leading gradually towards the emergence of immune strains (Sharma and Meshram 2006), and consequently led to the banning of a lot of chemicals. Due to the concerns of public about the effects of chemical residues accumulation into stored food grains, efforts have been made to search for alternatives methods that are safer, cheaper and environment friendly (Isman 2006; Kéı̈ ta et al. 2000). The phyto-derivatives were therefore found very useful to tackle the issue. Conventional success stories of phyto-derivatives led to explore the botanicals Consumers concerns toward the critical effects of chemicals, led researchers to focus pest control strategy on newer, cheaper, nontoxic and safer insecticides (Dayan et al. 2009). The ultimate actions converged to the conventional means where plants were used as toxicants with anti-insecticidal activity and other different purposes in daily life (Talukder 2006). Plant derived products are bio degradable, least hazardous to ecosystem and mammals, and efforts to exploit plant derived compounds for their insecticidal potential become important (Dubey et al. 2008; Yao et al. 2008). Anciently, ashes approach was famous in Indian subcontinent and in Egyptian zones to manage stored commodities (Varma and Dubey 1999). Similarly, the false hellebore scientifically known as Veratrum album and pyrethrum were also used by Romans and Chinese as rodenticide (Ahmed and Grainge 1986). In Indian subcontinent, neem leaves were popular for management of stored grain pests (Ahmed and Koppel 1985). Clay or mud granaries are still famous in developing areas where a Int J Trop Insect Sci mixture of ash and cowpeas are added in granaries for their sterilization (Wolfson et al. 1991). Leaves of Ocimum suave and Eugenia aromatica are traditionally used for protecting granaries in Africa (Okwute 2012). For storage of beans in Rwanda, Ocimum canum leaves are used for their anti-toxic properties against insects (Mishra et al. 2012). Mixing the turmeric powder in wheat and rice granaries was a traditional practice for controlling stored insect pests in south Asia (Saxena et al. 1988). Many more approaches underline the use of phyto-derivatives such as Citronella, Derris, Pyrethrum and Necotiana as insecticides for centuries (Park et al. 2003; Sim et al. 2006). Plant products have been successfully exploited as insecticides, insect repellents and insect anti-feedants in the 20th century (Hedin and Hollingworth 1997; Mordue and Blackwell 1993). A large number of primary and secondary metabolites have been extracted from the tropical plants to utilize against stored product insect pests (Hiiesaar et al. 2001). Scientists in previous century exploited plant derived products and concluded that plant-derivatives are least harmful to environment because of their novel and specific mode of action Berger 1994; Klepzig and Schlyter 1999; Lindgren et al. 1996; Schmutterer 1990). Phyto-derivatives as a shield against khapra beetle Ancient practices have proven the success of phyto-chemicals, but these practices actually need to be carried out in different physiological ways that may clearly explore the anti-feedant, toxic, repellency, attractant and detergency or growth retarding effects (Ng 2006). However, whatever way the plant derived compounds should be used, the main purpose is always to manage the stored insects like khapra beetle (Fig. 2). Nowadays, Rynia, Azadirachta, Nicotina, Rotenone, Sabadilla and Pyrethrin are commercially available and are considered successful against the infestation of khapra beetle. Active ingredient extracted from roots and woody parts of Ryania speciosa has lower toxic and residual effects. There is specific botanical ingredient (ryanodine) that affects khapra beetle muscles by enhancing rapid calcium flow into cells leading to death of the beetle (Dayan et al. 2009; Dimetry 2012). Azadirachta indica is the most popular plant in Asia and African regions that is categorized as contact poison against khapra beetle (Isman 2006). It also bears systemic properties, deterrent potential and growth inhibitory or oval inhibition properties against khapra beetle (Isman 2006; Morgan 2009). Another popular and anciently known toxic agent is Nicotine, which is basically derived from Nicotiana tobacum, have direct effects on the nervous systems of khapra beetle. The poison occupies the nerve junctions leading to the insect death (Isman 2006). Root extracts derived from Lonchocarpus and Derris plant species, commercially known as Rotenone, are popular in India and China as a slow poison that neutralizes almost all the stored grain pests including khapra beetle. Rotenone shows broad spectrum action by blocking the respiratory system of khapra beetle. Derivatives from Schoenocaulon officinale seeds are known as stomach poison for the khapra beetle and also effectively occupies the nervous system of the insect leading to its paralysis and death (Copping and Duke 2007). Multiple seed derivatives of Chrysanthemum cinerariaefolium play a significant role of conventional household insecticide that shows degradable activity against the target insect and can be immediately used when the commodity is stored (Copping and Duke 2007; Isman 2006). Researchers actively started documenting the successful effects of phyto-derivatives against khapra beetle in late 20th century, when increased doses of palm, groundnut and coconut oils were found to significantly minimize the adult emergence, as well as enhancing larval and adult mortality of khapra beetle (Odeyemi 1991). In addition, increased level of oils exhibited reduction in seed damage and weight loss in groundnut seeds. Jood et al. (1996) exploited the efficiency of citrus, garlic, podina powders and neem oil against khapra beetle larvae that infested sorghum grains for six months, and found that both neem kernel powder and neem oil highly minimized the grain damage by khapra beetle larvae. Further observations about other treatments (citrus, garlic, podina powders) revealed that after initial three months, grain damage started becoming visible and become more prominent after six months. However, the damage level was least in neem based treatments compared to citrus, garlic and podina. After the six months of storage, the color of the grains remained the same but their aroma, texture, taste and overall conditions become adverse in all the treatments. Dwivedi and Kumar (1999) investigated twelve acetone compounds and ether based plant extracts for their oviposition deterrent properties against khapra beetle and reported that leaves and seed extracts of Cassia occidentalis and Withania somnifera were effective in deterring oviposition of the pest. Reports of Sharma (1999) explained that 4% neem seed kernel powder and 5% neem leaf powder protected maize seeds for five months against Rhyzopertha dominica and T. granarium infestation. At the beginning of 20th century, attempts of using phytoextracts entered a desperate research phase, when several scientists evaluated a large number of plant-derivatives against khapra beetle. Some authors also evaluated Citrus reticulate, Acacia nilotica, Lantana camara, Tegetus indica, Cassia fistula, Anethum sowa, Emblica officinalis, Ziziphus jujube against khapra beetle and reported the success of their different parts, decoctions and derived essential oils (Dwivedi et al. 2003; Dwivedi and Shekhawat 2004; Sagheer et al. 2013). Following the importance of A. indica for management of various agricultural pests, many researchers also tried to explore its potential against the various growth stages of khapra beetle, and reported its inhibitory effects on the beetle (Hanif et al. 2015; Haq et al. 2014; Hasan et al. 2012; Howard et al. Int J Trop Insect Sci Fig. 2 Various types of phyto-dertivatives that can be used against khapra beetle 2009). Additionally, various Datura species were proved toxic and shown repellent effects against khapra beetle (Ali et al. 2012; Mahfuz and Khanam 2007; Omar et al. 2012; Saleem et al. 2014). Another relevant aspect in application of phytoproducts is the effective required dose against the khapra beetle. Many scientists reported that relatively higher doses of the phyto-derivatives were proved lethal against the target insect. For example, 100% larval mortality was observed at 75% concentration of citrus decoctions (Dwivedi and Bajaj 2001) (Table 1). Similarly, Al- Moajel (2004) reported that 73% concentration of Capsicum frutescens, Lawsania inermis and Allium ascalonicum resulted 62–85% mortality of khapra beetle, seven days post-application. Similarly, leaf extract of Rhazya stricta (Alvi et al. 2018) as well as Myrtus communis and Ruta graveolens (Othman 2018) caused higher mortality of T. granarium (Table 1). In addition, Mesua ferrea and Raphanus sativus caused approximately 82% mortality, however, the mortality was reduced to 62%, when application dose of dried leaf powders was reduced (Al-Moajel 2004) (Table 1). Int J Trop Insect Sci Table 1 Recent research findings illustrating about the successful utilization of phyto-extracts for management of khapra beetle Plant species Types of plant extract Successful results at Applied dose References Citrus reticulata Seed extracts Acacia nilotica, Lantana camara, Tegetus indica, Cassia fistula Rhazya stricta, A. indica, Helitropium bacciferumm Acetone based leaf extracts 100% larval mortality at 75% concentration level 75.21%-88.66% ovicidal activity at 80% concentration level (Dwivedi and Bajaj 2001) (Dwivedi and Bajaj 2001) (El Nadi et al. 2001) A. indica Seed oil Anethum sowa Leaf extracts Emblica officinalis, Ziziphus jujube Capsicum frutescens, Lawsania inermis, Allium ascalonicum, Mesua ferrea, Raphanus sativus Amaranthus vitidis, Salsola baryosma Annona squamosa Acetone based leaf extracts Aqueous extracts of R. stricta at 1000 ppm concentration with six days exposure recorded 80% adult mortality followed by A. indica (73.3%) and H. bacciferumm (70%. Acetonic extracts of R. stricta at 1000 ppm concentration with six days exposure recorded 86.7% adult mortality followed by A. indica (80%) and H. bacciferumm (73.3%. Similarly, methanolic extracts of R. stricta at 1000 ppm concentration with six days exposure recorded 90% adult mortality followed by A. indica (86.7%) and H. bacciferumm (80%. 100% adult mortality at 50–200 µl doze and No egg hatching at 100–200 µl doze Reduced insect feeding by recording 13.61% seed weight loss as compared to control (53.40%) at 8 ppm concentration. 100% repellency at 85% concentration level 62–85% larval mortality at 6% concentration level Aqueous, acetonic and methanolic extracts Powders of different dried leaves and roots Leaf extracts Hexane, methanolic and ethyl acetate extracts Haloxylon recurvum Leaf extracts Acorus calamus Rhizome extracts Hyptis suaveolens Poit. Schinus molle Methanol based seed and leaf extracts Fruit and leaf essential oils Limonium echioides, Tamarix boveana, Suaeda fruticosa Ethyl acetate and methanolic extracts Nicotiana tabacum, Cardaria draba, Sinapis arvensis Aqueous extracts of vegetative parts 19.58% and 22.08% larval mortality at 1.5% concentration Ethyl extract resulted in 55.73% antifeedent activity at 7 days old larvae followed by 53.45% by hexane and 38.65% for methanolic extract 17% insect mortality at 1.5% concentration level with the exposure of 168 h. Insect showed 11.10, 22.59 and 44.70% morality at exposure time of 3, 5 and 7 days, respectively, whereas 22.18, 24.44 and 27.77% mortality was observed with 30, 50 and 70 uL of oil respectively. Seed extracts provided 24.9% more mortality than leaf extracts 80.43% insecticidal activity was resulted by fruit oils followed by 74.84% activity by leaf oils. At 50 µg/ 20 mg, both extracts from L. echioides recorded moderate anti-feeding activity followed by Tamarix boveana and Suaeda fruticosa. Similarly, L. echioides extracts showed 93% and 70% larval mortality after 28 and 18 days, respectively. Mean larval mortality by 6% concentration of tobacco extract was 1.54% at 96 h (Arivudainambi and Singh 2003) (Dwivedi et al. 2003) (Dwivedi and Shekhawat 2004) (Al-Moajel 2004) (Hassan et al. 2005) (Rao et al. 2005) (Hasan et al. 2006) (Musa et al. 2009) (Abdel-Sattar et al. 2010) (Saidana et al. 2010) (Sarmamy et al. 2011) Int J Trop Insect Sci Table 1 (continued) Plant species Types of plant extract Datura alba Leaf extracts D. stramonium, Solanum nigrum, Quercus infectoria, Xanthium strumarium Ethanolic fruit extracts P. nigrum, N. sativa, A. indica, C. longa Leaf extracts Curcuma longa, Zingiber officinale, A. sativum, Ficus exasperate, Garcinia kola A. indica, D. stramonium Seed, bulb, rhizomes and leaf powders D. stramonium, Eucalyptus camaldulensis, Moringa oleifera, Nigella sativa Essential oils A. indica, Calotropis procera, Solenostemma argel, Aristolochia bracteolate Ethanolic extracts of leaves, shoots and seeds Syzygium aromaticum, E. camaldulensis, Elettaria cardamomum, Foeniculum vulgare, A. cepa, Carum carvi Melia azadarach, D. stramonium, A. indica Essential oils Leaves and peel extracts Essential oils Eruca sativa, Piper nigrum, Withania somnifera Leaf and seed extracts A. indica, D. stramonium, Eruca sativa R. stricta Myrtus communis, Ruta graveolens, Rosemarinus officanalsi, Ocimum basilicum, Mentha piperita Seed and leaf extracts Seed and leaf extracts Leaf extracts D. alba, Calotropis procera Essential oils Successful results at Applied dose exposure time while C. draba exhibited 1.96% and S. arvensis shown 1.21%. 2.5% concentration exhibited 33.5% and 45% mortality after 30 and 60 days exposure periods. 100% adult mortality at 2 and 4% concentration of D. stramonium and X. strumarium fruit extracts. 100% and 97.43% larval mortality at 1% concentration and 8 days exposure time by D. stramonium and S. nigrum respectively. Similarly 91.87% and 91.45% repellent action was recorded by D. stramonium and S. nigrum respectively at 4% concentration after 24 h of treatment. Mortality rate was 14.36% and 6.78% by A. indica and P. nigram after an exposure of one month. Adult mortality between 80-96.2% at 49 days of exposure by A. sativum as compared to control (10.6%). 15% of A. indica and D. stramonium gave 32.10 and 27% larval mortality after 9 d. D. stramonium, E. camaldulensis, N. sativa and M. oleifera gave 25.0, 20.2, 16.1 and 12.8% mortality after 168 h. A. indica seed extract 95% larval mortality 10% concentration 30 days. C. procera and S. argel leaf extract 37.5% and 32.5% mortality, respectively. A. bracteolate shoot extract 17.5% larval mortality. Clove oil showed 60% repellency (highest) while funnel oil was categorized having least repellent effects as 20%. Furthermore clove oil gave 91.67% adult mortality at 4% after 48 h. D. stramonium, A. indica and M. azadarach 15% and 300 ppm phosphine 72 h exposure, gave 86.47, 83.03 and 76.24%, respectively. 8% of P. nigrum, W. somnifera and E. sativa gave 26.30, 15.39 and 10.84% larval mortality, respectively. 12% concentration of D. stramonium gave the most mortality (39.3%) followed by A. indica giving 32.2% and E. sativa (19.9%. After 120 h, the leaf extract caused 72.11% mortality, while seed extract caused 69.50% mortality 7% and 9% concentrations of M. communis and the concentration 9% of R. graveolens caused 100% mortality of T. granarium. 20% concentration of C. procera showed a maximum mortality of 55.96% while 20% concentration of D. alba caused mean References (Ali et al. 2012) (Omar et al. 2012) (Hasan et al. 2012) (Asawalam and Onu 2014) (Haq et al. 2014) (Saleem et al. 2014) (Mahmoud et al. 2015) (Gharsan 2015) (Hanif et al. 2015) (Javed et al. 2016) (Islam et al. 2017a) (Alvi et al. 2018) (Othman 2018) (Khan et al. 2019) Int J Trop Insect Sci Table 1 (continued) Plant species Types of plant extract Successful results at Applied dose References Mentha piperita, Thymus vulgaris, Rosmarinus officinalis, Melissa officinalis Lantana camara, Ruta chalepensis, Rhazya stricta Leaf extracts mortality of 57.44% 96 h of exposure to R. officinalis extracts resulted in 78.67% mean mortality (Panezai et al. 2019) aqueous, ethanolic and acetonic extracts The extraction solvents of the phyto-derived extracts also play a significant role in their activity. The popular extraction agents can be water, hexane, acetone or methanol. For example, acetonic extract of Cassia fistula caused 88.66% larvicidal activity on the pest (Dwivedi and Bajaj 2001). Similarly, acetonic extraction of R. stricta, A. indica and Helitropium bacciferumm caused 1.4 folds more mortality of T. granarium larvae than methanolic and aqueous extracts (El Nadi et al. 2001) (Table 1). Rao et al. (2005) reported significant mortality (35.68%-55.58%) of seven days old T. granarium larvae by hexane, acetone and methanolic based Annona squamosa extracts. Selection of different plant parts (leaves, roots, stem and seed) in the extraction of the valuable toxic products against khapra beetle is also related to the plant species. For instance, Musa et al. (2009) evaluated methanolic extracts of Hyptis suaveolens leaves and seeds against T. granarium in stored groundnut and observed 75–80% mortality as compared to control. Correspondingly, Javed et al. (2016) reported the toxic activity of leaves and root extracts of Eruca sativa, Piper nigrum and Withania somnifera against the target insect (Table 1). All the efforts in the current era exhibit positive intend from the researchers to identify the safe approaches of managing khapra beetle. We have tried to summarize the recent research findings related to utilization of phyto-derivatives against khapra beetle in Table 1. Limitations of phyto-derivatives against khapra beetle Although the phyto-chemicals or plant-derived extracts have been proven successful as an alternative control strategy against khapra beetle, there are still some obstacles or limitations. For example, when we talk about the plant extracts, our immediate intention goes towards making traditionally the plant products which sometimes could be hazardous because of lack of extraction The ethanolic and acetonic extracts of L. camara was the most effective, where caused mortality rates of 73.3 and 83% at 400 ppm after 2 d, respectively, and 86.7 and 90% mortalities after 6 d, respectively (Asiry and Zaitoun 2020) experience and technical knowledge. Technically safe and highly careful routes are taken in the extraction of phyto-derivatives, which should be strictly followed to meet the quality of the phyto-derived products. Similarly, the high variation in the genetics of the plants, species diversity, and their seasonal availability sometimes reduce their application anytime. Furthermore, no mechanized means of collection, storage, processing and packaging of these plant products are common or well documented, which leads to the deterioration of these products faster than other synthetic chemicals (Islam et al. 2018a, b; Rajashekar et al. 2012). Although the criteria for commercialization of plant extracts for organic agriculture farming was introduced by International Federation of Organic Agriculture Movements (IFOAM 2012) (Fig. 3) but still proper commercialization has not been done regarding phyto-derivatives. This lack of proper commercialization is an indication that we do not have any credited laboratories to test the quality, purity and efficacy of commercially available plant extracts in the market (Kühne 2008). Some ethical and religious aspects also consider the use of some plant products as harmful for human beings, since they think that residual effects of these plant extracts may act as spermicides (Obeng-Ofori 2010). In addition to the lack of technical knowledge, the assessment of the toxicity of phyto-derivatives extracts to mammalians and other non-target organisms of the food chain remained negligible and needs adequate attention. For example, rotenone derived from various plants genera such as Derris, Lonchocarpus and Terphrosia was found toxic to mammals, fish and human beings as their lethal dose (LD 50 ) ranged between 132 and 1500 mg.kg − 1 (Rajashekar et al. 2012) thus making these plant genera more suspected to be one of the cause of Parkinson disease (Zehnder et al. 2007). Furthermore, the awareness and lack of knowledge on the application these phytoderivatives represent a major factor that reduces their use against the khapra beetle. Int J Trop Insect Sci Conclusions and future prospects The research efforts documented in this review clearly illustrate the available possibilities in manufacturing the phyto extracts, curtailing the economic population growth of khapra beetle. The phyto-products are less hazardous to environment, Fig. 3 Standard procedure for preparation of plant extracts human beings, easy to use, cheaper in context, biodegradable and locally available. There is therefore a strong need to conduct more research on the phyto-toxic plants against khapra beetle commercialization of these phyto-products should be focused. This would not only make them available for small scale farmers, but also at low prices so that people may Int J Trop Insect Sci identify a clear difference between both synthetic and botanical products. Awareness campaigns about the khapra beetle damage, biology, ecology, and importance of plant extracts should also be run within farmer communities and other stake-holders so that our ecosystem may be saved from harmful chemicals application against target insects. Acknowledgements The authors would like to acknowledge the support of Research Center for Advanced Materials Sciences (RCAMS) at King Khalid University, Abha, Saudi Arabia through a grant RCAMS/ KKU/08–20. Compliance with ethical standards Conflict of interest The authors have no conflicts of interest. References Abdel-Sattar E, Zaitoun AA, Farag MA, Gayed SHE, Harraz FMH (2010) Chemical composition, insecticidal and insect repellent activity of Schinus molle L. leaf and fruit essential oils against Trogoderma granarium and Tribolium castaneum. Nat Prod Res 24:226–235 Ahmed S, Grainge M (1986) Potential of the neem tree (Azadirachta indica) for pest control and rural development. Econ Bot 40:201– 209 Ahmed S, Koppel B (1985) Plant extracts for pest control: village level processing and use by limited resource farmers. Proc American Assoc Advan Sci, Annual Meeting, Los Angeles, California, USA, May 26–31 Ahmedani MS, Khaliq A, Tariq M, Anwar M, Naz S (2007) Khapra beetle (Trogoderma granarium Everts): A serious threat to food security and safety. Pak J Agric Sci 44:481–493 Ali A, Ahmad F, Biondi A, Wang Y, Desneux N (2012) Potential for using Datura alba leaf extracts against two major stored grain pests, the khapra beetle Trogoderma granarium and the rice weevil Sitophillus oryzae. J Pest Sci 85:359–366 Al-Moajel NH (2004) Testing some various botanical powders for protection of wheat grain against Trogoderma granarium Evert. J Biol Sci 4:592–597 Alvi AM, Iqbal N, Bashir MA, Rehmani MIA, Ullah Z, Latif A, Saeed Q (2018) Efficacy of Rhazya stricta leaf and seed extracts against Rhyzopertha dominica and Trogoderma granarium. Kuwait J Sci 45:64–71 Anonymous (1981) Data sheets on quarantine organisms Trogoderma granarium (Everts) European and Mediterranean. Plant Protec Org Bull 11:1–6 Arain MA, Ahmad T, Afzal M (2006) Preliminary studies on Khapra beetle Trogoderma granarium Everts. infestation in wheat under Lab. conditions. Pak Entomol 28:27–29 Arivudainambi NM, Singh RP (2003) Fumigant toxicity of Neem (Azadirachta indica A. Juss.) seed oil volatiles against khapra beetle, Trogoderma granarium. Ann Plant Prot Sci 11:207–211 Asawalam EF, Onu L (2014) Evaluation of some plant powders against Khapra beetle (Trogoderma granarium Everts)(Coleoptera: Dermestidae) on stored groundnut. Adv Med Plant Res 2:27–33 Asiry KA, Zaitoun AA (2020) Evaluation of the toxicity of three plant extracts against the Khapra beetle Trogoderma granarium Everts (Coleoptera: Dermestidae) under laboratory conditions. Rev Soci Entomol Argent 79:5–12 Banks HJ (1977) Distribution and establishment of Trogoderma granarium Everts (Coleoptera: Dermestidae): climatic and other influences. J Stored Prod Res 13:183–202 Berger A (1994) Using natural pesticides: current and future perspectives. A report for the Plant Protection Improvement Programme in Botswana, Zambia and Tanzania. Rapport-Sveriges Lantbruksuniversitet, Institutionen foer Vaextskyddsvetenskap, Alnarp Champ BR (1985) Occurrence of resistance to pesticides in grain storage pests. Pesticides and humid tropical grain storage systems (Ed. B R Champ, E Highly). Austral Centre Int Agric Res Proc 14:229–255 Copping LG, Duke SO (2007) Natural products that have been used commercially as crop protection agents. Pest Manag Sci 63:524–554 Damalas CA, Eleftherohorinos IG (2011) Pesticide exposure, safety issues, and risk assessment indicators. Int J Environ Res Pub Health 8: 1402–1419 Dayan FE, Cantrell CL, Duke SO (2009) Natural products in crop protection. Bioorgan Med Chem 17:4022–4034 Derbalah AS (2012) Efficacy of some botanical extracts against Trogoderma granarium in wheat grains with toxicity evaluation. Sci World J 2012:639854 Dimetry NZ (2012) Prospects of botanical pesticides for the future in integrated pest management programme (IPM) with special reference to neem uses in Egypt. Arch Phytopathol Plant Protec 45: 1138–1161 Donahaye EJ (2000) Current status of non-residual control methods against stored product pests. Crop Protec 19:571–576 Dubey SC, Suresh M, Singh B (2007) Evaluation of Trichoderma species against Fusarium oxysporum f. sp. ciceris for integrated management of chickpea wilt. Biol Cont 40:118–127 Dubey NK, Srivastava B, Kumar A (2008) Current status of plant products as botanical pesticides in storage pest management. J Biopestic 1:182–186 Dwivedi SC, Kumar RR (1999) Screening of some plant extracts for their oviposition deterrent properties against the Khapra beetle, Trogoderma granarium. E J Adv Zool 20:6–9 Dwivedi SC, Bajaj M (2001) Efficacy of botanicals as ovicide against Trogoderma granarium. J Adv Zool 22:5–7 Dwivedi SC, Shekhawat NB (2004) Repellent effect of some indigenous plant extracts against Trogoderma granarium (Everts). Asian J Exp Sci 18:47–51 Dwivedi SC, Sharma Y, Sharma T (2003) Evaluation of Anethum sowa as seed protectant against larvae of Trogoderma granarium (Everts). Baltic J Coleopterol 3:57–61 El Nadi AH, Elhag EA, Zaitoon AA, Al-Doghairi MA (2001) Toxicity of three plants extracts to Trogoderma granarium Everts (Coleoptera: Dermestidae). Pak J Biol Sci 4:1503–1505 EPPO (2011) Normes OEPP/EPPO Standards Data sheets on pests recommended for regulation Fiches informatives sur les organismesrecommandés pour réglementation. EPPO Bulletin 41: 407–408. https://doi.org/10.1111/j.1365-2338.2011.02509.x French S, Venette RC (2005) Mini risk assessment, Khapra Beetle, Trogoderma granarium (Everts) (Coleoptera: Dermestidae). USDA–APHIS–PPQ–Cooperative Agriculture Pest Survey–Pest Risk Assessment (PRA), p 22 Gharsan FN (2015) Evaluation of some plant oils against larvae of Khapra beetle (Trogoderma granarium E) (Coleoptera: Dermestidae). Int J Life Sci Res 4:109–114 Hadaway AB (1956) The biology of the Dermestid beetles, Trogoderma granarium Everts and Trogoderma versicolor (Creutz.). Bull Entomol Res 46:781–796 Hanif CMS, Hasan M-U, Sagheer M, Saleem S, Ali K, Akhtar S (2015) Omparative insecticidal effectiveness of essential oils of three Int J Trop Insect Sci locally grown plants phosphine gas against Trogoderma granarium. Pak J Agric Sci 52:709–715 Haq MZU, Khan MA, Abubakar AA, Irfanullah RM, Khan MAM, Kamran M (2014) Impact of Phytopesticides on Trogoderma granarium (Everts) (Coleoptera: Dermestidae) in Stored Wheat. World Appl Sci J 31:1722–1733 Hasan M-U, Sagheer M, Ullah E, Ahmad F, Wakil W (2006) Insecticidal activity of different doses of Acorus calamus oil against Trogoderma granarium (Everts). Pak J Agric Sci 43:1–2 Hasan M-U, Sagheer M, Ali Q, Iqbal J, Shahbaz M (2012) Growth regulatory effect of extracts of Azadirachta indica, Curcuma longa, Nigella sativa and Piper nigrum on developmental stages of Trogoderma granarium (Everts)(Coleoptera: Dermestidae). Pak Entomol 34:111–115 Hassan M-U, Siddique MA, Sagheer M, Aleem M (2005) Comparative efficacy of ethanol leaf extracts of Amaranthus viridis L. and Salsola baryosma (Schultes) and Cypermethrin against Trogoderma granarium (Everts). Pak J Agric Sci 42:61–63 Hedin PA, Hollingworth RM (1997) New applications for phytochemical pest-control agents. Phytochem Pest Cont American Chem Soci, Washington, pp 1–13 Hiiesaar K, Metspalu L, Kuusik A (2001) An estimation of influences evoked by some natural insecticides on greenhouse pest insects and mites. Practice oriented results on the use of plant extracts and pheromones in pest control. In: Proc Int Workshop, Tartu, Inst Plant Protec, p 17–27 Howard AFV, Adongo EA, Hassanali A, Omlin FX, Wanjoya A, Zhou G, Vulule J (2009) Laboratory evaluation of the aqueous extract of Azadirachta indica (neem) wood chippings on Anopheles gambiae s.s. (Diptera: Culicidae) mosquitoes. J Med Entomol 46:107–114 Hubert J, Stejskal V, Munzbergova Z, Kubatova A, Váňová M, Žd’árková E (2004) Mites and fungi in heavily infested stores in the Czech Republic. J Econ Entomol 97:2144–2153 IFOAM (2012) Definition of organic agriculture. International Federation of Organic Agriculture Movements. Retrieved from IFOAM, http:// www.ifoam.org/growing_organic/definitions/doa/index.html. Accessed 5 April 2012 Islam W (2017) Eco-friendly approaches for the management of red flour beetle: Tribolium castaneum (Herbst). Sci Lett 5:105–114 Islam W (2017b) Management of plant virus diseases; farmer’s knowledge and our suggestions. Hosts Viruses 4:28–33 Islam W, Ahmed M (2016) Inhibitory effects of organic extracts against Aspergilus flavus and their comparative efficacy upon germination of infested rice seeds. PSM Microbiol 1:79–84 Islam W, Awais M, Noman A, Wu Z (2016) Success of bio products against bacterial leaf blight disease of rice caused by Xanthomonas oryzae pv. oryzae. PSM Microbiol 1:50–55 Islam W, Rasool A, Wu Z (2016b) Inhibitory effects of medicinal plant extracts against Tribolium castaneum (Herbst.)(Coleoptera: Tenebrionidae). MAYFEB J Agric Sci 3:15–20 Islam W, Nazir I, Noman A, Zaynab M, Wu Z (2017a) Inhibitory effect of different plant extracts on Trogoderma granarium (Everts)(Coleoptera: Dermestidae). Int J Agric Environ Res 3:121– 130 Islam W, Zaynab M, Qasim M, Wu Z (2017b) Plant-virus interactions: Disease resistance in focus. Hosts Viruses 4:5–20 Islam W, Adnan M, Tayyab M, Hussain M, Islam SU (2018a) Phytometabolites; an impregnable shield against plant viruses. Nat Prod Commun 13:105–112 Islam W, Qasim M, Noman A, Tayyab M, Chen S, Wang L (2018) Management of tobacco mosaic virus through natural metabolites. Rec Nat Prod 12:403–415 Isman MB (2006) Botanical insecticides, deterrents, and repellents in modern agriculture and an increasingly regulated world. Ann Rev Entomol 51:45–66 Javed M, Majeed ZM, Arshad M, Hannan AA, Ghafoor AH (2016) Insecticidal potentiality of Eruca sativa (Mill.), Piper nigrum (L.) and Withania somnifera (L.) extracts against Trogoderma granarium (Everts)(Coleoptera: Dermestidae). Int J Fauna Biol Stud 3:18–20 Jood S, Kapoor AC, Singh R (1996) Evaluation of some plant products against Trogoderma granarium everts in sorghum and their effects on nutritional composition and organoleptic characteristics. J Stored Prod Res 32:345–352 Kéı̈ ta SM, Vincent C, Schmit J-P, Ramaswamy S, Bélanger A (2000) Effect of various essential oils on Callosobruchus maculatus (F.)(Coleoptera: Bruchidae). J Stored Prod Res 36:355–364 Khan SA, Ranjha MH, Khan AA, Sagheer M, Abbas A, Hassan Z (2019) Insecticidal efficacy of wild medicinal plants, Dhatura alba and Calotropis procera, against Trogoderma granarium (Everts) in wheat store grains. Pak J Zool 51:289–294 Klepzig KD, Schlyter F (1999) Laboratory evaluation of plant-derived antifeedants against the pine weevil Hylobius abietis (Coleoptera: Curculionidae). J Econ Entomol 92:644–650 Kühne S (2008) Prospects and limits of botanical insecticides in organic farming. Agron Glasnik 70:377–382 Leelaja BC, Rajashekar Y, Reddy PV, Begum K, Rajendran S (2007) Enhanced fumigant toxicity of allyl acetate to stored-product beetles in the presence of carbon dioxide. J Stored Prod Res 43:45–48 Lindgren BS, Nordlander G, Birgersson G (1996) Feeding deterrence of verbenone to the pine weevil, Hylobius abietis (L.)(Col., Curculionidae). J Appl Entomol 120:397–403 Lowe S, Browne M, Boudjelas S, De Poorter M (2000) 100 of the world’s worst invasive alien species: a selection from the global invasive species database. Invasive Species Specialist Group, Auckland, p 12. https://www.iucn.org/content/100-worlds-worst-invasive-alienspecies-a-selection-global-invasive-species-database Mahfuz I, Khanam LAM (2007) Toxicity of some indigenous plant extracts against Tribolium confusum Duval. J Bio Sci 15:133–138 Mahmoud AK, Bedawi SM, Satti AA (2015) Efficacy of some botanical extracts in the control of khapra beetle (Trogoderma granarium). J Sci 5:213–217 Mishra BB, Tripathi SP, Tripathi CPM (2012) Repellent effect of leaves essential oils from Eucalyptus globulus (Mirtaceae) and Ocimum basilicum (Lamiaceae) against two major stored grain insect pests of Coleopterons. Nat Sci 10:50–54 Mordue AJ, Blackwell A (1993) Azadirachtin: an update. J Insect Physiol 39:903–924 Morgan ED (2009) Azadirachtin, a scientific gold mine. Bioorgan Med Chem 17:4096–4105 Musa AK, Dike MC, Onu I (2009) Evaluation of nitta (Hyptis suaveolens Poit) seed and leaf extracts and seed powder for the control of Trogoderma granarium Everts (Coleoptera: Dermestidae) in stored groundnut. Am Eurasian J Agron 2:176–179 Nagpal M, Kumar A (2012) Grain losses in India and government policies. Qual Assur Saf Crops Foods 4:143–143 Nayak MK, Holloway JC, Emery RN, Pavic H, Bartlet J, Collins PJ (2013) Strong resistance to phosphine in the rusty grain beetle, Cryptolestes ferrugineus (Stephens)(Coleoptera: Laemophloeidae): its characterisation, a rapid assay for diagnosis and its distribution in Australia. Pest Manag Sci 69:48–53 Ng TB (2006) Naturally occurring anti-insect proteins: current status and future aspects. Adv Phytomed Nat Occurring Bioactive Comp 3: 405–422 Obeng-Ofori D (2010) Residual insecticides, inert dusts and botanicals for the protection of durable stored products against pest infestation in developing countries. 10th Int Working Conf Stored Prod Protec, 774–788 Odeyemi OO (1991) Control of khapra beetle, Trogoderma granarium Everts. in decorticated groundnut with vegetable oils. Appl Entomol Phytopathol 58:31–38 Int J Trop Insect Sci Okwute SK (2012) Plants as potential sources of pesticidal agents: a review. In: Soundararajan RP (ed) Pesticides - Advances in Chemical and BotanicalPesticides. IntechOpen, London, pp 207– 232. https://doi.org/10.5772/46225 Omar K, Faraj NM, Malik SAA, Al-Farhani IM (2012) Effect of some medicinal plants extracts and cypermthrin against Khapra Beetle (Trogoderma granarium Everts). Emirates J Food Agric 24:120– 127 Othman NS (2018) A Study of the effects of some water [lant extracts on the killing rates of the two insects Trogoderma granarium Everts Dermestidae: Coleoptera and Oryzaephilus surinamensis (L.) Silvanidae: Coleoptera. J Kerbala Agric Sci 5:304–310 Panezai GM, Javaid M, Shahid S, Noor W, Bibi Z, Ejaz A (2019) Effect of four plant extracts against Trogoderma granarium and Tribolium castaneum. Pak J Bot 51:1149–1153 Park C, Kim S-I, Ahn Y-J (2003) Insecticidal activity of asarones identified in Acorus gramineus rhizome against three coleopteran storedproduct insects. J Stored Prod Res 39:333–342 Pedigo LP, Rice ME (2014) Entomology and pest management. Waveland Press, Long Grove Pimentel MAG, Faroni LRDA, Tótola MR, Guedes RNC (2007) Phosphine resistance, respiration rate and fitness consequences in stored-product insects. Pest Manag Sci 63:876–881 Rajashekar Y, Reddy P, Begum K, Leelaja B, Rajendran S (2006) Studies on aluminium phosphide tablet formulation. Pestol 30:41–45 Rajashekar Y, Bakthavatsalam N, Shivanandappa T (2012) Botanicals as grain protectants. Psyche: J Entomol 2012, Article ID 646740 Rajendran S (2005) Detection of insect infestation in stored foods. Adv Food Nutri Res 49:163–232 Rajendran S, Sriranjini V (2008) Plant products as fumigants for storedproduct insect control. J Stored Prod Res 44:126–135 Rao NS, Sharma K, Sharma RK (2005) Anti-feedant and growth inhibitory effects of seed extracts of custard apple, Annona squamosa against Khapra Beetle, Trogoderma granarium. J Agric Technol 1:43–54 Rehman A, Mehboob S, Islam W, Khan NA (2013) Reaction of gram (Cicer arietinum L.) varieties against gram blight disease (Didymella rabiei (Kovatsch.) Arx) and its management through foliar fungicides in rain fed areas of Pakistan. Pak J Phytopathol 25:07–14 Sagheer M, Hasan M, Ali Z, Yasir M, Ali Q, Ali K, Majid A, Khan FZA (2013) Evaluation of essential oils of different citrus species against Trogoderma granarium (Everts)(Coleoptera: Dermestidae) collected from Vehari and Faisalabad districts of Punjab, Pakistan. Pak Entomol 35:37–41 Saidana D, Halima-Kamel MB, Boussaada O, Mighri Z, Helal AN (2010) Potential bioinsecticide activities of some Tunisian halophytic species against Trogoderma granarium. Tunisian J Plant Protec 5:51– 62 Saleem S, Hasan M-U, Sagheer M, Sahi ST (2014) Insecticidal activity of essential oils of four medicinal plants against different stored grain insect pests. Pak J Zool 46:1407–1414 Sarmamy AG, Hashim H, Sulayman A (2011) Insecticidal effects of some aqueous plant extracts on the control of Khapra Trogoderma granarium Evert. In: Int Conf Chem Biol Environ Sci (ICCEBS2011), pp. 55–70 Saxena RC, Jilani G, Kareem AA (1988) Effects of neem on stored grain insects. Focus Phytochem Pestic 1:97–111 Schmutterer H (1990) Properties and potential of natural pesticides from neem tree, Azadirachta indica. Ann Rev Entomol 35:271–297 Sharma RK (1999) Efficacy of neem products against storage pests in maize. Ann Agric Res 20:198–201 Sharma K, Meshram NM (2006) Bioactivity of essential oils from Acorus calamus Linn. and Syzygium aromaticum Linn. against Sitophilus oryzae Linn. in stored wheat. Biopestic Int 2:144–152 Sim M-J, Choi D-R, Ahn Y-J (2006) Vapor phase toxicity of plant essential oils to Cadra cautella (Lepidoptera: Pyralidae). J Econ Entomol 99:593–598 Subramanyam B, Hagstrum DW (1995) Resistance measurement and management. Integ Manag Insects Sored Prod 11:331–397 Szito A (2006) Trogoderma granarium (insect). Global Invasive Species Database. http://www.issg.org/database/species/ecology.asp?si= 142&fr=1&sts=. Accssed 1 April 2015 Talukder FA (2006) Plant products as potential stored-product insect management agents-A mini review. Emirates J Agric Sci 18:17–32 Varma J, Dubey NK (1999) Prospectives of botanical and microbial products as pesticides of tomorrow. Curr Sci 76:172–179 Wasala WMCB, Dissanayake CAK, Gunawardhane CR, Wijewardhane RMNA, Gunathilake DMCC, Thilakarathne BMKS (2016) Efficacy of insecticide incorporated bags against major insect pests of stored paddy in Sri Lanka. Proced Food Sci 6:164–169 WMO (1995) Scientific Assessment of Ozone Depletion, 1994: Global Ozone Research and Monitoring Project 37, Genoa, Italy. World Meteorol Org, Geneva Wolfson JL, Shade RE, Mentzer PE, Murdock LL (1991) Efficacy of ash for controlling infestations of Callosobruchus maculatus (F.)(Coleoptera: Bruchidae) in stored cowpeas. J Stored Prod Res 27:239–243 Yao Y, Cai W, Yang C, Xue D, Huang Y (2008) Isolation and characterization of insecticidal activity of (Z)-asarone from Acorus calamus L. Insect Sci 15:229–236 Zehnder G, Gurr GM, Kühne S, Wade MR, Wratten SD, Wyss E (2007) Arthropod pest management in organic crops. Ann Rev Entomol 52: 57–80 Publisher’s note Springer Nature remains neutral with regard to jurisdictional claims in published maps and institutional affiliations.