African Journal of
Agricultural Research

  • Abbreviation: Afr. J. Agric. Res.
  • Language: English
  • ISSN: 1991-637X
  • DOI: 10.5897/AJAR
  • Start Year: 2006
  • Published Articles: 6855

Full Length Research Paper

Management of Dinoderus porcellus L. (Coleoptera: Bostrichidae) infesting yam chips using varietal resistance and botanical powders of three medicinal plants

Loko Yeyinou Laura Estelle
  • Loko Yeyinou Laura Estelle
  • Laboratory of Applied Entomology, Faculty of Sciences and Technology of Dassa (FAST-Dassa), National University of Sciences Technologies Engineering and Mathematics of Abomey (UNSTIM), BP 14 Dassa, Benin.
  • Google Scholar
Gnaho Annick Christelle
  • Gnaho Annick Christelle
  • Laboratory of Applied Entomology, Faculty of Sciences and Technology of Dassa (FAST-Dassa), National University of Sciences Technologies Engineering and Mathematics of Abomey (UNSTIM), BP 14 Dassa, Benin.
  • Google Scholar
Toffa Joelle
  • Toffa Joelle
  • Laboratory of Applied Entomology, Faculty of Sciences and Technology of Dassa (FAST-Dassa), National University of Sciences Technologies Engineering and Mathematics of Abomey (UNSTIM), BP 14 Dassa, Benin.
  • Google Scholar
Orobiyi Azize
  • Orobiyi Azize
  • Laboratory of Applied Entomology, Faculty of Sciences and Technology of Dassa (FAST-Dassa), National University of Sciences Technologies Engineering and Mathematics of Abomey (UNSTIM), BP 14 Dassa, Benin.
  • Google Scholar
Dansi Alexandre
  • Dansi Alexandre
  • Laboratory of Biotechnology, Genetic Resources and Plant and Animal Breeding (BIORAVE), FAST-Dassa, UNSTIM, BP 14 Dassa, Benin.
  • Google Scholar
Tamo Manuele
  • Tamo Manuele
  • International Institute of Tropical Agriculture, 08 BP 0932, Cotonou, Benin.
  • Google Scholar


  •  Received: 26 July 2018
  •  Accepted: 13 September 2018
  •  Published: 04 October 2018

 ABSTRACT

In Benin, stored yam chips are severely attacked by Dinoderus porcellus Lesne which causes important losses. The use of medicinal plants combined with the insect-resistant yam chips can be an efficient alternative of chemical insecticides for yam chips protection. This study aims to evaluate an integrated pest management of D. porcellus using combined effects of resistant yam chips (Boniwouré, Gaboubaba, Wonmangou, and Yakanougo landraces) and leaves powder of Bridelia ferruginea Benth, Blighia sapida Juss and Khaya senegalensis Cronquist. For that, repellence, weight loss, mortality and progeny production were evaluated with Antouka commercial insecticide as positive control and untreated yam chips as negative control. The results revealed that all treatments are strongly repellent and showed important reproductive inhibition rate and remarkable inhibition of emergency of D. porcellus progeny. The weight loss due of yam chips treated with the three medicinal plants was not significantly different from those treated with Antouka, but significantly different from untreated yam chips. Only K. senegalensis at 2% (w/w) combined with Wonmangou landrace was able to achieve 66.2% of mortality after 21 days of experimentation. Hence, combination of resistant yam chips with leaves powder of these three medicinal plants could be promoted for integrated management of D. porcellus.

Key words: Dinoderus porcellus, integrated pest management, medicinal plants, resistance varietal, storage, yam chips.

 


 INTRODUCTION

Yam  (Dioscorea   spp.)    is    an    important    crop   that contributes to food security and  poverty reduction in sub-Saharan Africa. Generally, it is cultivated for underground starchy tubers consumption and are mainly produced in West Africa. That production represents 96.3% of the world production (FAO, 2016). Yam tubers are good sources of carbohydrates, dietetary fibers, proteins, vitamin C, and minerals (Opara, 1999; Tortoe et al., 2017) and are eaten on diverse forms: boiled, roasted, fried, pounded, and dough of yam flour (Ayodeji et al., 2012). With an estimated annual production of 3,041,245 tonnes in 2016, Benin ranks fourth behind Nigeria, Ghana and Côte d'Ivoire in yam consumption, with 425 kcal per capital per day (FAO, 2016). Yam production is now entirely part of customs and traditions of populations to the point that we can speak of yam civilization (Baco et al., 2004).

Despite its economic, food and socio-cultural functions, yam production remains hampered by numerous biotic (pests and diseases, etc.) and abiotic (poor soils, climate change, etc.) factors. Also, the difficulty of fresh tubers conservation causes important post-harvest losses (65-85% of the weight of tubers) and an irregularity of its availability throughout the year (Babajide et al., 2008). To overcome the highly perishable nature of tubers, yams are transformed into chips which are traditionally dried under the sun (Hounhouigan et al., 2003), thus enhancing food security (Babajide et al. 2008). Unfortunately, dried yam chips in traditional storage systems are severely attacked by Dinoderus porcellus Lesne (Coleoptera: Bostrichidae), which easily destroys stocks in few days (Ategbo et al., 1998, Vernier et al., 2005) and can cause losses of up to 50% of stocks (Loko et al., 2013). This pest, also found in dried cassava chips (Schäfer et al., 2000) causes’ visual damage by penetrating the chips thus depreciating their market value and negatively influence the quality of reconstituted yam paste (Babarinde et al., 2013). To protect yam chips against insects attack, farmers use chemical insecticides of cotton (Loko et al., 2013), but that leads to several cases of food poisoning and deaths of entire families (Adedoyin et al., 2008; Adeleke, 2009). Due to this deplorable situation, it urges to find out alternative methods that will take into account populations’ environment and health protection, and which will be less expensive and available for all. Botanical control meet these criteria and can act as repellents, feeding deterrents, toxicants, growth retardants, and chemosterilants (Hikal et al., 2017). Similarly, genetical control by the use of resistant varieties have enormous potential to reduce storage insect pest populations, and it is an environment-friendly management option (Keneni et al., 2011). Therefore, the use of botanical pesticides and insect-resistant yam chips to control D. porcellus appear as a promising alternative.

In the main yam chips production areas of Benin, three medicinal plants (Bridelia ferruginea Benth, Blighia sapida Juss and Khaya senegalensis Cronquist) were recorded   as   used  by  farmers  to  protect  their  stocks against storage insect pests (Loko et al., 2013). Studies carried out by Loko et al. (2017a) revealed the insect repellency and insecticidal properties of the leaves of these three medicinal plants. Moreover, a study led by Loko et al. (2017b) has allowed to identify four yam landraces (Gaboubaba, Boniwouré, Yakanougo and Wonmangou) which   chips are resistant to D. porcellus attacks. Therefore, to contribute to the strengthening of food security in Benin through the identification of an integrated pest management strategy of D. porcellus this study aims evaluate the interactions of resistant yam chips from the four landraces with leaves powder of B. sapida, K. senegalensis and B. ferruginea.

 


 MATERIALS AND METHODS

Yam landraces source

Tubers of four yam landraces of Dioscorea cayenensis Lam. – Dioscorea rotundata Poir. complex, belonging to varietal group of "Kokoro" were collected from farmers across the Northen and the Central  region of the republic of Benin. Gaboubaba and Yakanougo were collected from Koko village, Boniwouré from Kataban village, and Wonmangou from Fôbouko village. These 4 landraces were selected according to their resistance to D. porcellus (Loko et al., 2017b) and their good agronomic (productivity, number of tubers), culinary (quality of pounded and boiled yam) and technological (quality of yam chips, ease of pounding) characteristics (Loko et al., 2015).

Collection and preparation of medicinal plant powders

Leaves of B. sapida, K. senegalensis and B. ferruginea were collected from the town of Dassa-Zoumé (latitude: 7° 41′ 33″ North, and longitude: 2° 13′ 25″ East). Their identity was confirmed by the National Herbarium of the University of Abomey-Calavi. The collected leaves were washed and dried at ambient temperature for 20 days in the shade in order to prevent the degradation of bioactive compounds by sunlight. After drying, the leaves were transformed into powder using an electrical blender and sieved to obtain the finest particles using a 300 µm sieve (Loko et al., 2017a). The fine powder obtained from each plant species put in black polyethylene bags in dark cool and dry place until use. The compilation of physico-chemical composition of leaves powder of these three medicinal plants on the basis of literature was presented in Table 1.

 

 

Processing of yam chips

Yam chips were obtained from processing of tubers of the 4 yam landraces following the method described by Babajide et al. (2006). For that, yam tubers were washed with water to remove sand and other unwanted elements, and peeled with a knife. The tubers were cut into slices of 2 to 3 cm. The yam slices obtained were pre-cooked in water at 50°C for 2 h. They were also macerated in this pre-cooking water for 24 h in order to soften them. The slices were strained and dried in the autoclave at 60°C for at least 3 days in order to have 12 to 14% of final moisture. The dried chips obtained were put in polythene bags and stored in the laboratory at ambient temperature. The chips samples were sterilized at 105°C for 2 h in order to kill the hidden insects and their eggs. The samples were then exposed to ambient temperature for 1 h.

Rearing of D. porcellus

D. porcellus was collected from infested yam chips purchased from Dassa  market  and  maintained on healthy yam chips in the laboratory using the method described by Onzo et al. (2015). The experimental plan was composed of cylindrical plastic boxes opened at one extremity. The opened extremity  is  covered by a muslin cloth allowing an adequate aeration and preventing insects from running out. Dried yam chips (500 g) were infested in the plastic boxes with 50 adults (3-5 days old) of D. porcellus. The plastic boxes were  kept  on  shelves  in  the laboratory at ambient temperature (Oni and Omoniyi, 2012). After two weeks, adult beetles were removed from the breeding boxes in order to obtain a F1 generation that was used for all experiments (Isha et al., 2009).

Repellence test

The experimental device consisting of a flat circular plastic tray (36 cm in diameter by 2 cm in height) with a cardboard divided into twelve equal compartments and delimited in the centre by a circle having 5 cm of radius glued at the bottom (Babadjide et al., 2008; Loko et al. 2017b), which was used to assess repellency in D. porcellus due to yam chips combined with leaves powder of the three medicinal plants. Ten grams of healthy chips of each resistant landrace mixed with a concentration of leaves powder (1, 3, 5, 7 and 10% w/w) were placed in each compartment of tray equidistantly from the centre (Chebet et al., 2013). Similarly, the Antouka commercial insecticide (Permethrin 3 g/kg + pyrimiphos 16 g/kg; Dustable powder) recommended for the protection of stored food from insect pests was applied on 10 g of untreated yam chips of each landraces at 0.05% (w/w) as recommended by the manufacturer, and put in compartments as positive control (Loko et al. 2017b). While untreated yam chips of the four landraces were used as a negative control. For each treatment, 25 adults of D. porcellus (3-7 days old) starved for 24 h were released in the center of the tray, which was immediately covered with a transparent muslin cloth, to prevent the insects from escaping (Isah et al., 2009). The experiments were replicated at 3 different times (15, 30, and 45 days) with 4 replications (a total of 12 repetitions) for each leaves powder concentration. The total number of insects found in untreated yam chips (P) and treated yam chips (G) was recorded after 1, 12, and 24 h of infestation (Loko et al., 2017a). According to Dutra et al. (2016), repellent effect of plants was estimated by calculating the percent repellency (PR) and repellency index (IR). Repulsion percentage (PR) was calculated using the following formula of McDonald et al. (1970):

PR = [(Nc - Nt) / (Nc + Nt)] × 100

Where Nc = number of insects present in untreated yam chips; Nt = number of insects present in treated yam chips. The mean repellency value of each treatment was calculated and assigned to the repellent classes from 0 to V: class 0 (PR ≤ 0.1%), class I (PR = 0.1 - 20%), class II (PR = 20.1 - 40%), Class III (40.1 - 60%), Class IV (60.1 - 80%) and Class V (80.1 - 100%).

The repellency index (IR) was calculated according to the following formula:

IR = 2G / G + P

Where G = percentage of insects attracted by treated yam chips, and P = percentage of insects attracted by untreated yam chips. The IR values ​​are between 0 and 2 (Gusmão et al., 2013) with, IR = 1 indicates a similar repellency between treated and untreated yam chips (neutral treatment), IR> 1 indicates a lower repellency of treated yam chips compared to untreated yam chips (attractive treatment) and IR <1 correspond to a greater repulsion of treated yam chips compared to untreated yam chips (repellent treatment) (Padín et al., 2013).

Feeding deterrence test

Feeding deterrence test was based on the method used by Isah et al. (2012), and Onzo et al. (2015). For that, 50 g of disinfected yam chips from each resistant landraces mixed with different concentrations of leaves powder of each medicinal plants (1, 3, 5, 7, and 10 % w/w), and Antouka commercial insecticide (Permethrin 3 g/kg + pyrimiphos 16 g/kg, Dustable powder) at 0.05% (w/w) as  a positive control were put in experimental boxes (6 cm in height and 8 cm in diameter). In the experiment, the untreated yam chips were used as negative control. In each box, yam chips of each landrace were infested with 20 adults of D. porcellus (3-7 days old) starved for 24 h. These boxes were covered by a muslin cloth to prevent the escape of insects and serves as aeration medium. Each treatment was repeated 4 times. The boxes were placed in the laboratory in a completely randomized block for 30, 60 and 90 days (Isah et al., 2012). At the end of each experimental period, the damage due to D. porcellus attacks was evaluated on the basis of proportion of yam chips consumed by the pests. This proportion was estimated according to the formula (Chijindu and Boateng, 2008):

Mortality test

Mortality test was conducted according to the methodology used by Chebet et al. (2013) with some modifications. Leaves powder of each of the three medicinal plants were mixed with 100 g of disinfected yam chips of each landrace in plastic boxes (10 cm of high and 13 cm in diameter) at different concentrations (0, 2, 4, 6, 8, 10% w/w). Yam chips impregnated with Antouka synthetic insecticide (Permethrin 3 g/kg + pyrimiphos 16 g/kg, DP) (0.05% weight/weight) were used as a positive control. Ten pairs of unsexed adult insects were introduced into treated and untreated yam chips. Each box was covered with a transparent muslin cloth, to prevent the insects from escaping.  Treatments were arranged in a completely randomised design with 4 replicates. The dead adults were counted after 1, 3, 5, 7, 14 and 21 days of infestation (Othira et al., 2009). The adult mortality rate was calculated according to the formula of Asawalam et al. (2006) and corrected with Abbott's formula (Abbott, 1925) to eliminate the natural mortality of control:

Where T = treated yam chips and C = untreated yam chips.

Reproductive inhibition test

Twenty grams of yam chips from the four resistant yam landraces were introduced into the experimental boxes (height: 6 cm and diameter: 8 cm) and mixed with different concentrations of powders of each medicinal plant (1, 3, 5, 7, and 10% w/w) (Chebet et al., 2003), and Antouka commercial insecticide (Permethrin 3 g/kg + pyrimiphos 16 g/kg; DP) at 0.05% (w/w) as a positive control. The untreated yam chips were used as negative control. Twenty newly emerged adults (3-7 days old) of D. porcellus (10 males and 10 females) were introduced into the centre of each experimental box. They were allowed to lay eggs for one week after which they were removed (Chijindu et al., 2008). The treatments were arranged in a completely randomised design with 4 replicates. The emerged adults of F1 progeny were counted 35 days after the begining of experiment. For that, experimental boxes were prospected and emerged adults were collected every 2 days until there is no emerged adult. The percent reduction in adult emergence or reproductive inhibition rate (IR %) was calculated according to Tapondjou et al. (2002) using the formula:

Where, NU = number of newly emerged adult insects in untreated yam chips, NT = number of newly emerged adult insects in treated yam chips.

Statistical analysis

Data on percentage mortality, repellency, weight loss, and reproductive inhibition were arcsine-transformed (arscine√x), while data on the number of emerged F1 progeny were log-transformed (log(x + 1)) in order to homogenize their variance. The transformed data were then subjected to general linear model (GLM) using IBM SPSS Statistics 25 software package. Significant differences among the means were separated using Student Newman keuls statistic at the 5% level of probability. The original data are presented in tables and figures. Principal component analysis (ACP) was also carried out with Minitab software version 18 in order to examine the contribution of each combination of resistant yam chips treated with leaves powder of medicinal plants on D. porcellus control. For that, the different combinations of resistant yam chips and leaves powder of medicinal plants were considered as individuals and corresponding mean values of repellency, mortality, reproductive inhibition, and weight loss were as variables.

 

 


 RESULTS

Repellent effect of resistant yam chips combined with leaves powder on D. porcellus

The synthetic insecticide Antouka and resistant yam chips combined with leaves powder of B. sapida, K. senegalensis and B. ferruginea at all concentrations had a strong repellent effect on D. porcellus (Table 2). However, no significant interaction between resistant yam chips and leaves powder of the three medicinal plants on D. porcellus repellency were observed (p ≥ 0.05). Moreover, the interaction between resistant yam chips, medicinal plants and leaves powder concentration on repellence of D. porcellus was not significant (p ≥ 0.05) for all treatments. The results showed that percent repellency of D. porcellus adults by resistant yam chips treated with different concentration of leaves powder of the three medicinal plants had not varied significantly than commercial insecticide Antouka after 1 h of experiment (p ≥ 0.05). However, yam chips of Yakanougo landrace combined with leaves powder of B. sapida respectively at 7 and 3% were more repellent than Antouka insecticide after 12 h (p ≤ 0.05) and 24 h (p ≤ 0.05) of experiment. The results also showed that leaves powder of B. sapida, K. senegalensis and B. ferruginea had repellent classes ranging from II to IV with a repellency index varying from 0.33 to 0.65 (Table 2). Similarly to Antouka insecticide, leaves powder of B. sapida combined with yam chips of Wonmangou landrace at 5 and 7%, Yakanougo landrace at 3, 5 and 7%, and Boniouré landrace at 5 and 7% exhibited a class IV of repellence (Table 1). Similar trend was observed with yam chips of Boniwouré landrace combined with leaves powder of K. senegalensis at 5%.

 

 

Effect of resistant yam chips combined with leaves powder on D. porcellus damages

There was a statistically significant interaction of resistant yam chips combined with leaves powder of the three medicinal plants on reduction of D. porcellus damages after 30 (p ≤ 0.05), and 60 (p ≤ 0.05) days of experiments. After 90 days of experimentation this interaction was not significant (p ≥ 0.05). However, no concentration-dependent reduction of weight loss was observed with leaves powder of different medicinal plants (p ≥ 0.05). After 30 days of experiment, only leaves powder of B. sapida combined with yam chips of Gaboubaba at 3%, and Wonmangou at 1 and 5% exhibed a significant reduction of weight loss (p ≤ 0.01) than untreated yam chips. The combination of yam chips of resistant landraces with different concentrations of leaves powders of B. sapida, K. senegalensis and B. ferruginea caused a significant reduction of weight loss than untreated yam chips at 60 (p ≤ 0.001), and 90 days (p ≤ 0.001) of experiments. No significant difference was observed between weight loss of yam chips protected with synthethic insecticide Antouka and those protected with leaves powder of the three medicinal plants during all the experimental periods (Table 3).

 

 

Effect of resistant yam chips combined with leaves powder on D. porcellus mortality

The combination of resistant yam chips with different concentration of leaves powder of the three medicinal plants increased the mortality of D. porcellus during all experimental period than untreated yam chips (Figure 1). A significant interaction (p ≤ 0.05) of resistant yam chips treated with different leaves powder concentrations of K. senegalensis on D. porcellus mortality (Figure 1b) was observed after 1, and 3 days of experiment. However, after 5 days of experiment, no significant interaction (p ≥ 0.05) between resistant yam chips, medicinal plants and leaves powder concentration on D. porcellus mortality was recorded. The results showed that mortality was concentration-dependent increasing with increasing dosage of leaves powder of medicinal plants after 21 days of experiment (p ≤ 0.05). The highest mortality was recorded with the synthetic insecticide Antouka with a mean mortality rate of 84.8% (Figure 1). While, the lowest mortality rates were observed on untreated yam chips with a mean mortality rate of 10.5% after 21 days of experiment. The combination of leaves powder of K. senegalensis with yam chips of the four resistant landraces  at 8%, of leaves powder of B. sapida with yam chips of Yakanougo and Boniouré landraces at 6%, and of leaves powder of B. ferruginea with yam chips of Gabouba landrace at 6% caused a mortality of more than 50% of the D. porcellus population.

 

 

Effect of resistant yam chips combined with leaves powder on D. porcellus reproduction

A mean number of D. porcellus adults emerged from  resistant   yam  chips  treated  with  different concentrations of leaves powder of B. sapida, K. senegalensis and B. ferruginea was significantly different from those of untreated yam chips after 35 (p ≤ 0.001) and 37 days (p ≤ 0.001) of experimentation (Table 4). However, no significant difference was noted between resistant yam chips treated with leaves powder of the three medicinal plants and insecticide Antouka during experimentations. Significant concentration-dependent  reproductive  inhibition  was  observed after 35 days of experimentation (p ≤ 0.05). Signicant interaction between medicinal plants and concentrations of leaves powder on reproductive inhibition rate was observed (p ≤ 0.001)  after  35   days   of   experimentation.  The resistant yam chips of the four landraces combined with leaves powder of K. senegalensis significantly inhibited D. porcellus reproduction (p ≤ 0.001) after 35 days of experimentation. While, in    37   days   of   experimentation,   reproductive inhibition rate of all treatments weren’t significatively different from what we noticed with synthetic insecticide Antouka, except yakanougo and Boniouré landraces combined respectively with leaves powder of B. sapida at 10% and B. ferruginae at 5% (Table 4).

 

 

Contribution of each combination of resistant yam chips with leaves powder on D. porcellus control

Principal component analysis showed that the first three axes represent about 81.5% of total variability. The first axis was positively correlated with weight loss and repellency while the second axis was correlated with mortality and reproductive inhibition of D. porcellus. Furthermore, observing  the  loading  plot  and  the  score plot obtained from principal component analysis, the 12 combinations of resistant yam chips treated with leaves powder have been grouped in 4 groups (Figure 2). The first group composed of yam chips of Yakanougo, Wonmangou and Gaboubaba landraces combined with leaves powder of K. senegalensis are characterised by their high reproductive inhibition rate of D. porcellus. The second group characterised by a strong repellency effect on D. porcellus contains yam chips of Boniouré landrace treated with leaves powder of B. sapida and K. senegalensis, and yam chips of Gaboubaba landrace combined with leaves powder of B. sapida. The integration of Gaboubaba with leaves powder of K. senegalensis which composed the third group was characterised by a low weight loss. The fourth group was composed of the five remaining  combinations  which  are characterised by a high mortality of D. porcellus.

 

 

 

 

 

 


 DISCUSSION

The  results   of   this   study    showed    that   the combination of yam chips from resistant landraces with leaves powder of B. ferruginea, B. sapida and K. senegalensis has a repellent effect similar to synthetic insecticide Antouka on D. porcellus. These results were not surprising because in previous studies  leaves  powder  of B. ferruginea, B. sapida and K. senegalensis (Loko et al., 2017a) as well as yam chips from yam landraces (Loko et al., 2017b) were repellent to D. porcellus. Although the interaction between resistant yam chips and medicinal plants has not been significant,  the  high  repellence  observed  on  D. porcellus could be due, on one hand to the effect of physicochemical compounds in yam chips and in the other hand to the presence of repulsive volatile substances in the leaves of each of the three medicinal plants (Table 1). Indeed, the color, smell and texture of yam chips could play a determining role in the repulsion of D. porcellus (Onzo et al., 2015). In addition, the triterpenoid, tannins and saponoside contained in the leaves powder of B. ferruginea (Addae-Mensah and Achenbach, 1985), B. sapida (Ubulom et al., 2012) and K. senegalensis (Makut et al., 2008) are known repulsive for phytophagous insects because of vapor acting on their olfactory receptors (Moore and Lenglet, 2004). The fact that some associations of resistant landraces and powders of medicinal plants have given a high repulsion values which is ​​above 60% (class IV), revealed the importance of their use in the long-term conservation of yam chips against D. porcellus; because stocks can  effectively be  protected against this pest, thereby tendency for infestation will be reduced.

The weight losses caused by D. porcellus on yam chips treated at different concentrations of B. sapida, K. senegalensis and B. ferruginea leaves powder were lower than the one caused on the negative control. According to a previous research, the  losses  caused  by storage insects on the chips depend on some factors such as chips texture (Campbell and Runnion, 2003), partial starch gelatinization after the pre-cooking (which causes the curing of the chips) (Rajamma et al., 1996), biochemical composition of chips (which could encourageor discourage the survival and multiplication of pests) (Wong and Lee, 2011), and environmental conditions (temperature, humidity, etc.) (Chukwulobe and Echezona, 2014). In addition, the combined effect of anti-nutritional factors such as tannins, saponins and phytic acid contained in yam chips (Djeri et al., 2015) and leaves powder of the three medicinal plants tested (B. sapida, K. senegalensis and B. ferruginea) could explain the low weight losses caused by D. porcellus. All these factors put together influence the development of D. porcellus and therefore reduce the consumption rate of yam chips by this main pest.

The results also showed that the mortality of D. porcellus induced by treated yam chips with different concentrations of leaves powder of B. sapida, K. senegalensis and B. ferruginea. This could be explained by the synergistic effect of antinutritional compounds present in yam chips (Djeri et al., 2015) and the chemical compounds present in leaves powder of medicinal plants (Chebet et al., 2013). Indeed, leaves powder of medicinal plants caused an asphyxiation of insects by penetrating into the internal organs of the insect through its respiratory systems (Fernando and Karunaratne, 2012; Kedia et al., 2015). According to Sousa et al. (2005) vegetables powder involve the dehydration of insects by erosion of cuticle layer which causes the death of the insect. The fact that some combinations of resistant yam chips with leaves powder of medicinal plants at some given concentrations caused mortality rates higher than 50% of D. porcellus is promising for the adoption and the use of this integrated method for the management of this pest by farmers. These results are similar to those of Maina and Lale (2004), Babarinde et al. (2008), and Lale and Mustapha (2000), who showed the potential that the integration of insect repellent/insecticidal plant extracts with varietal resistance in the protection of stored products against harmful insects. Thus, the combination of the yam chips of four landraces with leaves powder of B. ferruginea, B. sapida and K. senegalensis must be promoted for the integrated management of D. porcellus.

The combination of B. ferruginea, B. sapida and K. senegalensis leaves powder with resistant yam chips caused an inhibition in the reproduction of D. porcellus and also affected the mean number of D. porcellus adult emerged (F1 progeny). Based on previous studies, the reproductive inhibition of D. porcellus may be caused by physiological and behavioral changes in adult insects due to their contact with plant products. This contact could affect their egg-laying ability (Kedia et al., 2015). However, the reduction in the emergence of insects by different plant products is largely related to the ovicidal properties, which prevents the hatching of eggs (Jadhav and Jadhav, 1984) and/or linked to the larvicidal activity, which prevents the larval maturity into adults. Similar studies reported by Mukanga et al. (2010) showed that the powders of five botanical species (eucalyptus, guava, neem, tephrosia and water hyacinth) reduced weight loss and the emergence of Prostephanus truncatus populations in dried cassava chips. Nevertheless, exhaustive studies are necessary to identify the active compounds in each of the three medicinal plants and in the yam chips of the four landraces as well as their syntheses for an effective scientific formulation in the control of D. porcellus.

 


 CONCLUSION

Our results showed that the combined use of resistant yam chips and leaves powder of B. ferruginea, B. sapida and K. senegalensis at all concentrations have a great potential for the management of D. porcellus. However, further studies will be necessary to identify the active components contained both in the yam chips and in the leaves powder of the three medicinal plants responsible for the repellent and insecticidal effect on D. porcellus. Biological activities of leaves powder of these three medicinal plants and resistant landraces  associated  with their availabilities in Beninese agriculture, make them less expensive than synthetic pesticides for poor-resources farmers. Moreover, combination of resistant yam chips with repellent and insecticidal plants such as B. ferruginea, B. sapida and K. senegalensis for integrated management of D. porcellus is an environmental friendly alternative method adapted for small farm holder of the republic of Benin. Because of their strong repellent effect on D. porcellus, we recommend for yam chips short term conservation (3-6 months) the use of Boniouré or Gaboubaba landraces treated with leaves powder of B. sapida. While for yam chips long term conservation we recommend the use of Yakanougo, Wonmangou or Gaboubaba landraces combined with leaves powder of K. senegalensis because of their high reproductive inhibition rate of D. porcellus.

 


 CONFLICT OF INTERESTS

The authors have not declared any conflict of interests.

 


 ACKNOWLEDGEMENT

This study was supported by L’Oréal-UNESCO for Women in Science in Sub Saharan Africa through the 2014 postdoctoral fellowship won by the first author.

 



 REFERENCES

Abalaka ME, Adeyemo SO, Daniyan SY (2011). Evaluation of the antimicrobial potentials of leaf extracts of Khaya senegalensis. Journal of Pharmaceutical Research and Opinion 1(2):48-51.

 

Abbott WS (1925). A method for computing the effectiveness of an insecticide. Journal of Economic Entomology 18:265-267.
Crossref

 

Abubakar L, Bagna EA, Dogarai BBS (2017). Effects of column fractions of the leaves extract of Bridelia ferruginea on bacteria. Bayero Journal of Pure and Applied Sciences 10(1):137-141.
Crossref

 

Addae-Mensah I, Achenbach H (1985). Terpenoids and flavonoids of Bridelia ferruginea. Phytochemistry 24(8):1817-1819.
Crossref

 

Adebayo EA, Ishola OR (2009). Phytochemical and antimicrobial screening of the crude extracts from the root, stem bark and leaves of Bridelia ferruginea. African Journal of Biotechnology 8(4):650-653.

 

Adedoyin OT, Ojuawo A, Adesiyun OO, Mark F, Anigilage EA (2008). Poisoning due to the yam flour consumption in five families in Ilorin, Central Nigeria. West African Journal of Medicine 27(1):41-43.

 

Adeiza AA, Mohammed A, Mamman M (2010). Comparative in vivo evaluation of the trypanocidal activities of aqueous leaf, stem-bark and root extracts of Khaya senegalensis on Trypanosoma evansi. Journal of Medicinal Plants Research 4(17):1770-1777.

 

Adeleke SI (2009). Food poisoning due to yam flour consumption in Kano (Northwest) Nigeria. The Online Journal of Health and Allied Sciences 8(2):10.

 

Aka LO, Obidike RI (2010). Time Profile Antidiabetic Activity of the Aqueous Leaf Extracts of Bridelia ferruginea in Albino Rats. Nigerian Journal of Experimental and Applied Biology 11(1):7-11.

 

Ameyaw Y, Barku VYA, Ayivor J, Forson A (2012). Phytochemical screening of some indigenous medicinal plant species used in the management of diabetes mellitus in Ghana. Journal of Medicinal Plants Research 6(30):4573-4581.
Crossref

 

Asawalam EF, Emosairue SO, Hassanali A (2006). Bioactivity of Xylopia aetiopica (Dunal) a rich essential oil constituent on maize weevil Sitophilus zeamais Motch (Coleoptera: Curculionidae). Electronic Journal of Environmental, Agricultural and Food Chemistry 5:1195-1204.

 

Ategbo E, Bricas N, Hounhouigan J, Mitchikpe E, Nkpenu KE, Orkwor G, Vernier P (1998). Le développement de la filière cossettes d'igname pour l'approvisionnement des villes au Nigeria, au Bénin et au Togo In Berthaud, J, Bricas, N, Marchand, J-L (Eds) L'igname, plante séculaire et culture d'avenir : actes du séminaire international, Cirad, Inra, Orstom, Coraf, Cirad, Inra, Orstom, Coraf, Coll Colloques pp. 339-341.

 

Babajide JM, Atanda OO, Ibrahim TA, Majolagbe HO, Akinbayode SA (2008). Quantitative effect of 'abafe' (Piliostigma thionnigii) and 'agehu' (Khaya ivorensis) leaves on the microbial load of dry-yam 'gbodo'. African Journal of Microbiology Research 2:292-298.

 

Babajide JM, Oyewole OB, Henshaw FO, Babajide SO, Olasantan FO (2006). Effect of local preservatives on quality of traditional dry-yam slices "gbodo" and its products. World Journal of Agricultural Science 2(3):267-273.

 

Babarinde SA, Adebayo MA, Oduyemi K (2008). Integrating varietal resistance with Xylopia aethiopica (Dunal) A Richard seed extract for the management of Sitophilus zeamais Motschulsky in stored maize. African Journal of Biotechnology 7(8):1187-1191.

 

Babarinde SA, Babarinde GO, Odewole AF, Alagbe OO (2013). Effect of the prevalent insect species of yam chips on consumers' acceptability of yam paste. Journal of Agricultural Extension and Rural Development 46(3):97-101.

 

Baco MN, Tostain S, Mongbo RL, Dainou O, Agbangla C (2004). Gestion dynamique de la diversité variétale des ignames cultivées (Dioscorea cayenensis-D rotundata) dans la commune de Sinendé au nord Bénin. Plant Genetic Resources Newsletter 139:18-24.

 

Campbell JF, Runnion C (2003). Patch exploitation by female red flour beetles, Tribolium castaneum. Journal of Insect Science 3:20-27.

 

Chebet F, Deng AL, Ogendo JO, Kamau AW, Bett PK (2013). Bioactivity of selected plant powders against Prostephanus truncatus (Coleoptera: Bostrichidae) in stored maize grains. Plant Protection Science 49(1):34-43.
Crossref

 

Chijindu EN, Boateng BA (2008). Effect of Nutritional Content of Processed Cassava Chips on Development of Prostephanus truncatus (Horn). World Journal of Agricultural Science 4(3):404-408.

 

Chijindu EN, Boateng BA, Ayertey JN, Cudjoe AR, Okonkwo NJ (2008). The effect of processing method of cassava chips on the development of Prostephanus truncatus (Horn) (Coleoptera: Bostrichidae). African Journal of Agricultural Research 3(8):537-541.

 

Chukwulobe MN, Echezona BC (2014). Relative susceptibility of dried root/tuber and Musa chips to red flour beetle Tribolium casteneum (Herbst) (Coleoptera: Tenebrionidae) Infestation. International Journal of Plant and Soil Science 3:1398-1414. 

 

Djeri B, Tchobo PF, Adjrah Y, Karou DS, Ameyapoh Y, Soumanou MM, Souza C (2015). Nutritional potential of yam chips (Dioscorea cayenensis-Dioscorea rotundata Poir) obtained using two methods of production in Togo. African Journal of Food Science 9(5):278-284.
Crossref

 

Dutra KA, d'Oliveira JV, Navarro DMAF, Barbosa DRS, Santos JPO (2016). Control of Callosobruchus maculatus (FABR) (Coleoptera: Chrysomelidae: Bruchinae) in Vigna unguiculata (L) WALP with essential oils from four Citrus spp Plants. Journal of Stored Products Research 68:25-32.
Crossref

 

Food and Agriculture Organization (FAO) (2016). FAOSTAT Database Food and Agriculture Organization, Roma, Italy. 

View

 

Fernando HS, Karunaratne MM (2012). Ethnobotanicals for storage insect pest management: Effect of powdered leaves of Olax zeylanica in suppressing infestations of rice weevil Sitophilus oryzae (L) (Coleoptera: Curculionidae). Journal of Tropical Forestry and Environment 2(1):20-25.
Crossref

 

Gusmão NMS, d'Oliveira JV, Navarro DMAF, Dutra KA, da Silva WA, Wanderley MJA (2013). Contact and fumigant toxicity and repellency of Eucalyptus citriodora Hook, Eucalyptus staigeriana F, Cymbopogon winterianus Jowitt and Foeniculum vulgare Mill essential oils in the management of Callosobruchus maculatus (Fabr) (Coleoptera: Chrysomelidae, Bruchinae). Journal of Stored Products Research 54:41-47.
Crossref

 

Hikal WM, Baeshen RS, Said-Al Ahl HAH, Ujházy K (2017). Botanical insecticide as simple extractives for pest control. Cogent Biology 3:1.
Crossref

 

Houndjo CF, Agbodjogbe W, Assogba FM, Kohoude JM, Ayedoun MA, Dansou PH, Moudachirou M, Gbénou JD (2017). Comparative study of Antihyperglycemic activity of aqueous extracts from the leaves of Bridelia ferruginea, Lophira lanceolata and Oxytenanthera abyssinica, with their mixture. International Journal of Current Research in Chemistry and Pharmaceutical Sciences 4(11):22-33.
Crossref

 

Hounhouigan JD, Kayodé APP, Bricas N, Nago MC (2003). Les caractéristiques culinaires et organoleptiques des ignames recherchées en milieu urbain au Bénin. Annales des Sciences Agronomiques du Bénin 4:143-160.

 

Isah MD, Ayertey JN, Boateng BA (2009). Suitability of dried chips of plantain, cocoyam, yam and cassava for the development of the larger grain borer Prostephanus truncatus (Horn) (Coleoptera: Bostrichidae). International Journal of Applied Sciences 3(4):12-20.

 

Isah MD, Ayertey JN, Ukeh DA, Umoetok SBA (2012). Damage and weight loss to dried chips of cassava, cocoyam, yam and plantain exposed to Prostephanus truncatus (horn) (Coleoptera: Bostrichidae) over three different time durations. Entomology Journal 9(3):137-145.
Crossref

 

Jadhav KD, Jadhav LD (1984). Use of vegetable oils, plant extracts and synthetic Products as protectants from pulse beetle Callosobruchus maculatus in stored grain. Journal of Food Science and Technology 14:100-113.

 

Kawo AH, Suleiman ZA, Yusha'u M (2011). Studies on the antibacterial activity and chemical constituents of Khaya senegalensis and Ximenia americana leaf extracts. African Journal of Microbiology Research 5(26):4562-4568.

 

Kazeem MI, Raimi OG, Balogun RM, Ogundajo AL (2013). Comparative study on the α-amylase and α-glucosidase inhibitory potential of different extracts of Blighia sapida Koenig. American Journal of Research Communication 1(7):178-192.

 

Kedia A, Prakash B, Mishra PK, Singh P, Dubey NK (2015). Botanicals as ecofriendly biorational alternatives of synthetic pesticides against Callosobruchus spp (Coleoptera: Bruchidae)-a review. Journal of Food Science and Technology 52(3):1239-1257.
Crossref

 

Keneni G, Bekele E, Getu E, Imtiaz M, Damte T, Mulatu B, Dagne K (2011). Breeding food legumes for resistance to storage insect pests: potential and limitations. Sustainability 3:1399-1415.
Crossref

 

Kubmarawa D, Khan ME, Punah AM, Hassan M (2008). Phytochemical screening and antimicrobial efficacy of extracts from Khaya senegalensis against human pathogenic bacteria. African Journal of Biotechnology 7(24):4563-4566.

 

Lale NES, Mustapha A (2000). Potential of combining neem (Azadirachta indica A Juss) seed oil with varietal resistance for the management of the cowpea bruchid, Callosobruchus maculatus (F). Journal of Stored Products Research 36:215-222.
Crossref

 

Loko YL, Adjatin A, Dansi A, Vodouhè R, Sanni A (2015). Participatory evaluation of Guinea yam (Dioscorea cayenensis Lam– D rotundata Poir complex) landraces from Benin and agro-morphological characterization of cultivars tolerant to drought, high soil moisture and chips storage insects. Genetic Resources and Crop Evolution 62(8):1181-1192.
Crossref

 

Loko YL, Alagbe O, Dannon EA, Datinon B, Orobiyi A, Thomas-Odjo A, Dansi A, Tamò M (2017a). Repellent effect and insecticidal activities of Bridelia ferruginea, Blighia sapida, and Khaya senegalensis leaves powders and extracts against Dinoderus porcellus in infested dried yam chips. Psyche Article ID 5468202, 18

 

Loko YL, Dansi A, Tamo M, Bokonon-Ganta AH, Assogba P, Dansi M, Sanni A (2013). Storage insects on yam chips and their traditional management in Northern Benin. ScientificWorldJournal, Article ID 484536. 
Crossref

 

Loko YL, Gnaho AC, Orobiyi A, Agre P, Dansi A, Tamo M (2017b). Resistance of dried chips of yam (Dioscorea cayenensis-D rotundata complex) landraces to Dinoderus porcellus Lesne (Coleoptera: Bostrichidae). Cogent Food and Agriculture 3(1):1411180.
Crossref

 

Maina YT, Lale NES (2004). Integrated Management of Callosobruchus maculatus (F) Infesting Cowpea Seeds in Storage Using Varietal Resistance, Application of Neem (Azadirachta indica A Juss) Seed Oil and Solar Heat. International Journal of Agriculture and Biology 6(3):440-446.

 

Makut MD, Gyar SD, Pennap GRI, Anthony P (2008). Phytochemical screening and antimicrobial activity of the ethanolic and methanolic extracts of the leaf and bark of Khaya senegalensis. African Journal of Biotechnology 7(9):1216-1219.

 

McDonald LL, Guy RH, Speirs RD (1970). Preliminary evaluation of new candidate materials as toxicants, repellents and attractants against stored product insects. Marketing Res Report No 882, Agricultural Research Service United States Department of Agriculture, Washington, DC 8.

 

Moore SJ, Lenglet AD (2004). An overview of plants used as insect repellents In: Willcox M, Bodeker G, Rasoanaivo P (eds): Traditional Medicinal Plants and Malaria Vol 4 Traditional Herbal Medicine for Modern Times Series CRC Press, Boca Raton.

 

Mukanga M, Deedat Y, Mwangala FS (2010). Toxic effects of five plant extracts against the larger grain borer, Prostephanus truncates. African Journal of Agricultural Research 5(24):3369-3378.

 

Olmo LRV, da Silva MFGF, Fo ER, Vieira PC, Fernandes JB, Pinheiro AL, Vilela EF (1997). Limonoids from leaves of Khaya senegalensis Phytochemistry 44(6):1157-1161.
Crossref

 

Oni MO, Omoniyi AO (2012). Studies on Temperature Influence on Oviposition and Development of Immature Stages of the Yam Beetle Dinoderus Porcellus Lesne Coleoptera: Bostrichidae on Dried Yam Species. The Journal of Agricultural Science 4(2):213-218.

 

Onzo A, Biaou JT, Loko LY, Tamo M, Dansi A (2015). Vulnérabilité des cossettes issues de quelques cultivars d'igname à l'attaque de Dinoderus porcellus Lesne (Coleoptera: Bostrichidae) en conditions de laboratoire. International Journal of Biological and Chemical Sciences 8(6):2494-2507.
Crossref

 

Opara LU (1999). Yam storage In: Bakker-Arkema (ed); Handbook of Agricultural Engineering, The American Society of Agricultural Engineers 4:182-214.

 

Oreagba IA, Ishola IO, Oremule BO (2016). Gastroprotective and antisecretory properties of the hydroethanolic leaf extract of Blighia Sapida (Sapindaceae) in rats. International Journal of Medical and Dental Science Invention 1(2):38-47.

 

Othira JO, Onek LA, Deng LA, Omolo EO (2009). Insecticidal potency of Hyptis spicigera preparations against Sitophilus zeamais (l) and Tribolium castaneum (herbst) on stored maize grains. African Journal of Agricultural Research 4(3):187-192.

 

Padín SB, Fusé C, Urrutia MI, Dal Bello GM (2013). Toxicity and repellency of nine medicinal plants against Tribolium castaneum in stored wheat. Bulletin of Insectology 66(1):45-49.

 

Rajamma P, Premkumar T, Kurup GT, Palaniswami MS, Potty VP, Padmaja G (1996). Influence of varieties and method of processing on insect infestation in dry cassava chips tropical tuber crops: Problem Prospects and Future Strategies pp. 321-328.

 

Schäfer K, Goergen G, Borgemeister C (2000). An illustrated identification key to four different species of adult Dinoderus (Coleoptera: Bostrichidae), commonly attacking dried cassava chips in West Africa. Journal of Stored Products Research 36(3):245-252.
Crossref

 

Sousa AH, Maracaja PB, Silva RM, Moura MN, Andrade WG (2005). Bioactivity of vegetal powders against Callosobruchus maculatus (Coleoptera: Bruchidae) in Caupi bean and seed physiological analysis. Revista de Biolo E Ciencias Da Terr 5:19-23.

 

Tapondjou LA, Adler C, Bouda H, Fontem DA (2002). Efficacy of powder and essential oil from Chenopodium ambrosioides leaves as post-harvest grain protectants against six-stored product beetles. Journal of Stored Products Research 38:395-402.
Crossref

 

Tortoe C, Johnson PNT, Abbey L, Baidoo E, Anang D, Acquaah SG, Saka E (2012). Sensory properties of pre-treated blast-chilled yam (Dioscorea rotundata) as a convenience food product. African Journal of Food Science and Technology 3(2):59-65.

 

Ubulom PME, Imandeh GN, Ettebong EO, Udobi CE (2012). Potential Larvicidal Properties of Blighia sapida leaf extracts against larvae of An gambiae, Cu quinquefasciatus and Ae aegypti. British Journal of Pharmaceutical Research 2(4):259-268.
Crossref

 

Vernier P, Goergen G, Dossou RA, Letourmy P, Chaume J (2005). Utilization of biological insecticides for the protection of stored yam chips. Outlook on Agriculture 34(3):173-179
Crossref

 

Wong L, Lee C (2011). Relationship between population growth of the red flour beetle Tribolium castaneum and protein and carbohydrate content in flour and starch. Journal of Economic Entomology 104:2087-2094.
Crossref

 

yodeji SP, Olabanji OM, Adeyeri MK (2012). Design of a process plant for the production of poundo yam. International Journal of Engineering 6:10-24.

 




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