Abstract
Four types of biochars were prepared from rice husk as farm waste, sugarcane bagasse as sugar cane juice store waste, residues of Leucaena leucocephala tree as horticulture waste and chicken manure as chicken farm reduce at 700οC, then evaluated as a alternative to control Tribolium castaneum, Rhyzopertha dominica, Oryzaephlius surinamensis and Sitophilus oryzae. The character of each type has been defined using Scanning Electron Microscopy (SEM) with an Energy Dispersive X-Ray Analysis (EDX) and Fourier transform infrared spectroscopy (FTIR) were used to identify the elemental composition and functional groups distributed on biochars surface. The elemental compositions refer to the chicken manure biochar exhibited a decrease in Carbon concentration and increase Oxygen content; there is a negative correlation between C and O contents. On the other hand, the chicken manure biochar is the only tested biochar that contains Ca, P, and Cl. The chicken manure biochar has the largest number of functional groups on its surface, the mortality of insects was recorded after 10 days which showed that the chicken manure biochar was the most effective which contains more different elements and functional groups on its surface. The most affected insects were O.surinamensis and R. dominica with mortality percentages 86.66 and 73.33. Smaller particles of chicken manure biochar were more effective than larger particles against both R. dominica and O. surinamensis, the smaller particles (1.80—0.94 µm) recorded LC50 1.29 and 0.56 g/kg against R. dominica and O. surinamensis. SEM images for the affected insects showed the adhesion of biochar particles on insect’s body parts, also, the sensilla were disappeared as a result of the friction between biochar particles and insect cuticle. Our results may indicate the promising features of biochar as an alternative method to control some stored product insects with considering the source of biochar which affect its elemental and functional groups contents. Biochar had different efficacy depending upon its moisture contents, with increased moisture the toxicity of biochar decreased.
Similar content being viewed by others
Avoid common mistakes on your manuscript.
Introduction
The rust red flour beetle, Tribolium castaneum, the lesser grain borer, Rhyzopertha dominica, the saw-toothed grain beetle, Oryzaephlius surinamensis and the rice weevil, Sitophilus oryzae are classified as polyphagous, global pests in stored products throughout the world (Bell 2000). Globally, R. dominica is considered the main pest of rice, wheat and millets (Edde 2012), and it can attack a broad range of various stored products such as cereals, dried fruit, and nearly all grains and more especially wheat, barley, sorghum and rice. likewise, another cosmopolitan pest is T. castaneum, which mainly infest the products of milled grain, for example, flour and cereals, which is considered a secondary pest as it mainly attacks broken grains and grain dust (Odeyemi et al. 2005). One of the main insect pests that cause primary infestation for stored grain is the rice weevil, Sitophilus oryzae which is spread widely around the world causing massive destruction of stored products (Benzi et al. 2009). In comparison to other insect pests of stored products, the species, Oryzaephlius surinamensis does not seriously cause damage. Because it lives in the bottom layers of infected products, it is most difficult to detect (Kłys̈ and Przystupińska 2015). It primarily attacks milled grain products, and also feeds on dried fruit, sugar, yeasts, tobacco, nuts, dried meat, but the foodstuffs are the least food that attacked for this type. (Madkour et al. 2013).
To control stored product insects, it is necessary to find more safe and eco-friendly alternatives to the traditional methods as the use of inert dust (Nukenine 2010; Obeng-Ofori 2007; Obeng-Ofori and Boateng 2008). Due to its low mammalian toxicity, inert dust can provide a safe method to control stored product insects by mixing with the produce. During 1960, the activated Kaolin clay was used in the treatment of about 70% of the grain in India. Also, rock phosphate was used in Egypt as a protectant. In addition, lime, ashes and sand dust were used in the protection of grains in West Africa by some local farmers (Obeng-Ofori 2007).
The lignocellulosic materials are the main components of agricultural wastes. In Egypt, these wastes ranged annually between 22 and 26 million tons, and this large quantity of wastes could be transformed into an eco-friendly product such as biochar (Taher and Nasr 2018).
Biochar is a highly porous and adsorbent carbon-rich material that is produced by the heating of organic materials under low oxygen conditions (pyrolysis), it has a similar appearance to different carbon-rich materials e.g., charcoal. But it is mainly developed as a soil conditioner, almost any type of biomass feedstock can be used in the production of biochar (Aly 2016). Its production significantly benefits in the sequestration of carbon by locking it which with abundant in the biomass of the plant. The source nature, production temperature and residence time all are factors that affect the element content and the structure formation of produced biochar (Narzari et al. 2015). There is little information available on the direct effects of biochar on insect survival and or performance. The physical properties of biochar porous structure, high surface area, and abundant oxygen-containing functional groups such as hydroxyl and carboxyl on its surface) as well as the low cost of production makes it a suitable material for controlling insects (Cook and Andrade 2018; Wang et al. 2021). One of the possible alternative solutions to overcome the use of some alternative applications of conventional insecticides to control mites and insects use some alternative natural amendments like biochar that have no risk to humans and the surrounding environment (Bakhat et al. 2020; Chen et al. 2019a, b).
In this research, we did a survey of biochar prepared at 700 οC from various agricultural wastes such as rice husk collected from (Rice), Oryza sativa, sugarcane bagasse collected from (Sugar cane) Saccharin officinarum and residues of Leucaena tree (Leucaena leucocephala) tree in addition to chicken manure collected from (Egyptian domestic fowls) Gallus gallus domesticus for the control of four types of stored grain insects: R. dominica, O.surinamensis, T. castaneum, and S. oryzae. The effect of particle size on the insecticidal efficacy of the tested chicken manure biochar was also examined against both R. dominica and O. surinamensis.
Materials and methods
Tested insects
Four species of insects were used in this study: Sitophilus oryzae (Rice weevil), Tribolium castaneum (Herbst) (red flour beetle), Rhyzopertha dominica (Fabricius), (the lesser grain borer) and Oryzaephilus surinamensis (Linnaeus) (the saw toothed grain beetle) were cultured in the laboratory at 28 °C ± 1, Rh. 70 ± 10 and photoperiod L/D 12:12 h. at the Faculty of Agriculture, Alexandria University. Sitophilus oryzae were reared on whole wheat as described by (Strong et al. 1967). T. castaneum was reared on a mixture of (10:1) whole wheat: brewer’s yeast according to the methods of (Beeman et al. 2009). Rhyzopertha dominica were reared on whole wheat using the method explained by (Kavallieratos et al. 2005). Oryzaephlius surinamensis were reared on whole wheat flour, rolled oats and yeast (5:5:1) according to (Watson and Barson 1996).
Preparation of biochars
About six kilograms of four Four lignocellulosic waste materials were collected from rice husk, sugarcane bagasse, Leucaena leucocephala, and chicken manure and used as feedstock for producing biochar. chicken manure was collected from Alex university's experimental farm, rice husk was collected from the rice mill, sugarcane bagasse was collected from sugarcane juice store and L.leucocephala branches were collected from trees grown in the forestry research sector of Antoniadis botanical garden, Alexandria, Egypt. The samples were air-dried at room temperature and ground to the.
Ground samples were placed in crucibles, covered with a tightly fitting lid, and pyrolyzed under oxygen-limited conditions in two steps. First, the pyrolysis temperature was raised to 300 °C at approximately 10 °C/min and held for 60 min. Then, the biochars were allowed to cool to room temperature overnight, after that the pyrolysis temperature was raised to 700 °C at approximately 20 °C/min in a muffle furnace and held for 60 min. Then, the biochars were allowed to cool to room temperature overnight and ground to pass through a 0.051-mm sieve before further experiments.
Characterization of biochars
Elemental analysis
The elemental composition and diameter of biochars were analyzed using the technique of Scanning Electron Microscopy (SEM) with an Energy Dispersive X-Ray Analysis (EDX) and performed in a Jeol JSM- 5300 scanning electron microscope at acceleration voltage between 15 and 20 keV.
Fourier transform infrared (FT-IR)
The spectroscopic characterization of biochar was conducted using the FT-IR technique to identify the functional groups that was distributed on the biochar surface. Burker tensor 37 spectrometers were used in this identification in the range of 400–4000 cm−1 using the technique of KBr pellet as 1.0 mg of samples was added to 100 mg KBr pressed, then exposed to infrared radiation (Wu et al. 2012; Guo and Chen 2014).
Data analysis
Analyses of variance (ANOVA) p < 0.05 were conducted with Co-Stat 6.400 program software, and then the homogeneous means were grouped using Tukey's HSD test.
Insecticidal activity of biochars
Four types of biochar were ground and pass through a sieve (0.125–0.56 mm) and applied at 5 g/kg with 20 g sterilized wheat in a 250 ml glass jar and lids were fitted. Jars were tilled up and down (10x) and rotated by hand for 2 min., with a brief period of shaking at 120 s. The jars were kept closed for 15 min after shaking to allow any free dust to settle. Twenty adults of each insect were separately placed in each treated jar. Each treatment was replicated three times. All of the procedures of the experiment were carried out under the same conditions as the rearing. Mortality percentages were recorded after 10 days of exposure for the four types of biochar.
The three different particle sizes of chicken manure biochar were ground to pass through three different sieves, largest size (0.500–0.250 mm), medium size (0.250–0.125 mm), smallest size (0.125–0.56 mm) before assay. Insecticidal activity of three different particle sizes of chicken manure biochar was assessed against adults of R. dominica and O. surinamensis. Average particle size distribution between (3.96–5.40, 4.02–4.23, 1.80–0.94 µm) was measured by Scanning electron microscope (SEM) (Fig. 1). Samples of wheat were mixed with different doses of biochar each at 0.5, 1, 3 and 5 g/kg. The biochars were applied as described in the previous experiment. Mortality percentage (M%) was determined after 10 days. The LC50 values, and their upper and lower confidence interval limits, as well as intercept, were estimated by probit analysis were calculated according to (Finney 1971) using LdP line software (Ehab Soft, Cairo, Egypt). Non-overlapping, 95% fiducially limits were used to determine significant differences among treatments (P < 0.05).
Insects scanning electron microscopy
The most affected adults were R. dominica and O. surinamensis treated with chicken manure biochar after 10 days of exposure to biochar as compared with unexposed insects. The samples were fixed by immersing them immediately in 4F1G (Fixative, phosphate buffer solution) PH = 7.4 at 4 ◦C for 3 h according to the methods of (Tahmasebi et al. 2015). Specimens were then postfixed in 2% OsO4 in the same buffer at 4◦ C for 2 h. Samples were washed in the buffer and dehydrated at 4◦C through a graded series of ethanol. Insects were dried using a critical point method, mounted using carbon paste on an AL- stub and coated with gold up to a thickness of 400 A in a sputter–coating unit (JFC-1100 E). Observations of R. dominica and O. surinamensis morphology in the coded specimens were performed in a Jeol JSM- 5300 scanning electron microscope operated between 15 and 20 keV.
Role of biochar moisture content on its toxicity
the performance of two more effective tested biochar chicken manure and L. leucocephala against the most susceptible tested insect O. surinamensis was examined, mixing 5 g/g biochar with different concentrations of distilled water 0, 25, 50, 100, 150 (w/w) and applied on 20 gm wheat grain in a 250 ml glass jar in the same way mentioned above. Twenty adults of O. surinamensis were added into each jar. Mortality were recorded after 10 days.
Results
The elemental composition
To identify the elemental composition and diameter of the four biochar types, the technique of electron dispersive X-ray analysis (EDX) was used. The results for each type of biochar were presented in (Fig. 2a−d), respectively. To compare the four types. The results were summarized in (Table 1) as presented by the mass percent and atomic percent. The most abundant elements were carbon and oxygen with the difference in their ratio. In the first three types L. leucocephala, sugarcane bagasse and rice husk the carbon percentages were higher than that of oxygen with a mass % of 89.48 ± 0.52, 83.24 ± 0.57and 48.36 ± 0.77, the least carbon with percentage was noticed is for rice husk biochar. The second element in its percentage in these three types is oxygen with mass % of 9.04 ± 0.64, 14.16 ± 0.82 and 35.26 ± 1.01, respectively. potassium is common in all types with different percentages, and it is the last element found in L. leucocephala type with a mass % of 1.48 ± 0.12 while its mass% in the types of sugarcane bagasse and rice husk were 1.94 ± 0.15 and 1.15 ± 0.12 with the presence of silicon in both types but with a higher percentage in rice husk (15.23 ± 0.37) compared with that of sugarcane bagasse (0.67 ± 0.09). Many other elements were found in the fourth type, chicken manure rather than carbon, oxygen and potassium which were common in the first three types. These elements were Ca, P, and Cl with mass% of 16.80 ± 0.33, 0.62 ± 0.06 and 0.40 ± 0.05 respectively. Another difference, that the percentage of oxygen was higher than that of carbon, the mass% of both 35.51 ± 0.36 and 45.24 ± 0.96 for C and O respectively. Finally, the potassium was present in mass percentage closer to that of the first three types which were 1.44 ± 0.10.
Fourier transforms infrared (FT-IR) analysis
The FTIR spectra of all types, (a) Leucaena leucocephala, (b) chicken manure, (c) rice husk and (d) sugarcane bagasse respectively in the region of 4000–500 cm-1 were shown in (Fig. 3), and summarized in (Table 2). The results of FTIR analysis shows that the four types are relatively different in their functional groups also the chicken manure biochar shows the largest number of functional group on its surface.
Insecticidal activity of biochars
The toxicity of the four biochars to the target insect species was represented in (Table 3). The obtained results showed that the chicken manure biochar exhibited the highest effectiveness. The obtained results showed that the chicken manure biochar exhibited the highest effectiveness against both O.surinamensis and R. dominica with mortality percentages 86.66 and 73.33% followed by Leucaena leucocephala biochar 50.00 and 30.00%, respectively at tested concentration 5 g/kg. Nevertheless, rice husk and sugarcane bagasse bochair presented lower toxicity on O.surinamensis and R. dominica. Moreover, there was no toxicity effect for all of the tested biochars against S. oryzae and T. castaneum.
Effect of different particle size chicken manure biochar
Different particle size chicken manure biochar was tested for contact toxicity against adults of R. dominica and O. surinamensis and their LC50 values are shown in (Table 4; Fig. 2). The different particle size of chicken manure biochar showed significant toxic activity and it was clear that with a decrease in the particle size, the toxicity activity also increases. It was observed that chicken manure biochar was more toxic to O. surinamensis adults than to R. dominica adults. The lowest particle size (1.80–0.94 µm) of the biochar resulted in strong activity against R. dominica and O. surinamensis adults with LC50 values of 1.29 and 0.56 g/kg, respectively. Whereas in the case of particle size (4.02–4.23 µm) the LC50 value was 11.25 and 12.33 g/kg respectively. But the largest particle size (3.96 -5.40 µm) showed the lowest toxicity. These results also revealed that an increase in mortality with decreased biochar particular size to (1.80–0.94 µm) was observed in both tested insects.
Insects scanning electron microscopy
Scanning electron micrographs of O. surinamensis and R. dominica (most affected by biochar) shows the adhesion of biochar particles on insect’s body parts compared with untreated ones. (Fig. 4) shows no scarification of adult’s cuticle was observed after exposure. Biochar particles were seen heavily clustered on the whole body of O.surinamensis more than R. dominica. The sensilla were not seen in different body parts which may result from the friction between biochar particles and cuticles during the insect’s movement.
The impact of biochar moisture content on its toxic efficiency
We examined the efficacy of the two most effective biochar chicken manure and L. leucocephala with moisture content 0, 25, 50, 100, 150% against O.surinamensis after an exposure period 10 days (Table 5). Types of biochar had different efficacy. Depending upon its moisture contents, with increased moisture the toxicity of biochar decreased. Dry biochar caused significant highest toxicity effect 93.33 ± 6.66 and 43.33 ± 8.81, toxicity decreased gradually upon 36.66 ± 6.66 and 6.66 ± 3.33 at 150% moisture content (w/w) with chicken manure and L. leucocephala biochar. Moreover, chicken manure biochar remained more toxic than L.leucocephala biochar with all examined moisture content.
Discussion
In this research, we examined the toxicity of four types biochar rice husk, sugarcane bagasse, L. leucocephala, and chicken manure of biochar against Tribolium castaneum, Rhyzopertha dominica, Oryzaephlius surinamensis and Sitophilus oryzae. we found that chicken manure biochar was the most effective one biochar against R. dominica and O. surinamensis. Other studies have found that biochar was an effective material that can be used to control insects. (Chen et al. 2019b) examined the effect of three types of biochar (derived from the straw of corn, wheat, or rice) on the reproduction of English grain aphid Sitobion avenae. On wheat, biochar caused decreased in aphid lifetime fertility and population growth. Also, biochar application to paddy fields may play a role in suppressing the Cnaphalocrocis medinalis population (Chen et al. 2019a). To explain the mechanism for the chicken manure biochar effect on insects. Following characterization, a notable difference between rice husk, sugarcane bagasse, L. leucocephala, and chicken manure biochar. Elemental compositions refer to the chicken manure biochar exhibited a decrease in Carbon concentration and increase Oxygen content; there was a negative correlation between C and O contents. Moreover, the chicken manure biochar is the only tested biochar that contains Ca, P, and Cl (Ahmad et al. 2014; Pan et al. 2019). The results of FTIR analysis showed that the chicken manure biochar has the largest number of a functional group on its surface compated with other tested biochars, which were -OH group stretching (3000–3700 cm -1), C-H methyl (2800-3000 cm-1), C-H methylene (2512 cm-1), C = O /HCOO (1600-1800 cm-1), C-H asymmetric (1420-1450 cm-1), C-O (1000-1260 cm-1), C-H aromatic (700-900 cm-1) and inorganic matter stretching (400-700 cm-1). Insect cuticle is a layered, fibrous composite of chitin, water, protein, catechol, lipid and occasionally metal and mineral. Chitin (N-acetylglucosamines) has many C-H, N–H, and O–H groups (Chapman 1998; Vincent and Wegst 2004). So that, biochars may be adhered on the insect’s surface functional groups causing death.
The skeletal structure of biochar that looks like a carbon sponge, and its ability to retain H2O, material may be abrasive to an insect’s cuticle leading to an increased potential for dehydration (Cook and de Andrade 2018), while the mineral stricture is hardly biodegradable, the re-condensed vapor that can be joined in the biochar pores and its surfaces or less aromatic and more biodegradable and con be considered organic phase, the biochar to be more toxic than other which does not enough mineral groups (Wilson 2014).
There were substantial variations in the effectiveness of various particle sizes of measured chicken manure biochar and their fractions, the smallest particles (1.80 to 0.94 μm) were shown to be extremely effective in controlling all tested insects, indicating that particle size was a biochar property that can influence its toxicity. According to the current findings, inert dust particles with diameters ranging from (1.80 to 0.94 μm) showed greater insecticidal effects than bigger particles. Also, substantiate was a considerably favorable association between the effectiveness of the tested biochars and its particles size. Biochar small particles have a greater surface area than the other biochar containing larger particles. Hence, the larger was the surface it covers and the greater the toxicity it produces, as the contact area between the insect’s body and the particles increases. Our studies were in agreement with those optioned by (Cook and de Andrade 2018) who found the ants in contact with biochar particles (< 150 mm) had the lowest mean survival, followed by the survival of ants exposed to the coarse material (> 1.0 mm). The particles of inert dust with sizes of < 45 μm were strongly influencing the insecticidal action than larger particles against R. dominica, S. oryzae and C. ferruginous (Vayias et al. 2009; Baliota and Athanassiou 2020).Our results showed that the mortality of Oryzaephlius surinamensis decreased from 80% at 25% to 36.66 at 150% chicken manure biochar moisture content. This means that biochar becomes ineffective when saturated with water. Some of the findings were similar to those of previous studies. this is one of the disadvantages of using biochar to control stored material insects. There are numerous examples of inert dust's effectiveness being affected by increasing moisture content the lower the moisture content, the greater the mortality increase. Moreover, the increased grain moisture content causes a decrease in the toxicity of diatomaceous earth against S. oryzae and R. dominica. grain moisture content 11.8% moisture content caused 95 and 72% mortality but grain moisture content 15.0% caused 53 and 17% mortality of S. oryzae and R. dominica, respectively. (Fields and Korunic 2000).The possible mechanism of action of biochar can be explained by different suppositions such as (1) biochar particles known to degrade hydrocarbons in nature so they therefore possibly degrade alkanes which present in insect cuticles (Ahmad et al. 2014). (2) The degradation of the peritrophic membrane was further accelerated by the biochar which is known for its capability to degrade hydrocarbons and aromatic structures in nature (Ahmad et al. 2014). (3) Reduced efficiency in converting consumed food into a growth and energy source associated with possible energy diversion from growth to the detoxification process (Wang et al. 2021). (4)The SEM of treated insects indicted that biochar is material that may be abrasive to an insect’s cuticle leading to an increased potential for dehydration (Cook and de Andrade 2018). The SEM of treated insects indicted that biochar is material that may be abrasive to an insect’s cuticle leading to an increased potential for dehydration (Cook and de Andrade 2018). May be entering on insect’s spiracles and effect or interfering on respiration process.
Conclusion
Our results refer to the insecticidal activity of biochar may be chemical or physical effect. As shown by SEM image, the physical effect observed by desiccation that happened to the insect also the inverse relationship between the moisture content of biochar and its toxicity which may reflect the mechanism of moisture absorption from the insect body. On the other hand, the chemical effect observed by the FTIR analysis that shows the large number of active groups that distributed on the surface of manure type that gave the higher insecticidal activity. Finally, more studies are needed to explain the mode of insecticidal activity of biochar.
References
Ahmad M, Rajapaksha AU, Lim JE, Zhang M, Bolan N, Mohan D, Vithanage M, Lee SS, Ok YS (2014) Biochar as a sorbent for contaminant management in soil and water: a review. Chemosphere 99:19–33. https://doi.org/10.1016/j.chemosphere.2013.10.071
Aly HM (2016) Short communication: Biochar and its importance in adsorption of antibiotic and heavy metals from aqueous solutions. Ecol Quest 24:75–78. https://doi.org/10.12775/EQ.2016.014
Bakhat HF, Bibi N, Fahad S, Hammad HM, Abbas S, Shah GM, Zakir A, Murtaza B, Ashraf MR (2020) Rice husk bio-char improves brinjal growth, decreases insect infestation by enhancing silicon uptake. SILICON 23:1–10. https://doi.org/10.1007/s12633-020-00719-4
Baliota GV, Athanassiou CG (2020) Evaluation of a greek diatomaceous earth for stored product insect control and techniques that maximize its insecticidal efficacy. Appl Sci 10(18):6441. https://doi.org/10.3390/app10186441
Beeman RW, Haas S, Friesen K (2009) Beetle Beetle Wrangling Tips. (An Introduction tothe Care and Handling of Tribolium castaneum). http://bru.gmprc.ksu.edu/proj/tribolium/wrangle.asp. (Last modified on 31.03.09.)
Bell CH (2000) Fumigation in the 21st century. Crop Prot 19:563–569. https://doi.org/10.1016/S0261-2194(00)00073-9
Benzi V, Stefanazzi N, Ferrero AA (2009) Biological activity of essential oils from leaves and fruits of pepper tree (Schinus molle L.) to control rice weevil (Sitophilus oryzae L.). Chil J Agric Res 69:154–159. https://doi.org/10.4067/S0718-58392009000200004
Chapman RF (1998) The insects. Structure and function. Cambridge University Press 1998 Published in the United States of America by Cambridge University Press, NewYork
ChenY, Shen Y, Li B, Meng L (2019a) The effect of biochar amendment to soils on Cnaphalocrocis medinalis Guenee (Lepidoptera: Pyralidae) on rice. Crop Prot 104842.https://doi.org/10.1016/j.cropro.2019.06.002
Chen Y, Shen Y, Meng L, Li B (2019b) The effect of biochar with different feedstock materials on the English grain aphid Sitobion avenae Fab. (Hemiptera: Aphididae). Crop Prot 124:104859. https://doi.org/10.1016/j.cropro.2019.104859
Cook SP, de Andrade NR (2018) Laboratory evaluation of the direct impact of biochar on adult survival of four forest insect species. Northwest Sci 92:1–8. https://doi.org/10.3955/046.092.0102
Edde P (2012) A review of the biology and control of Rhyzopertha dominica (F.) the lesser grain borer. J Stored Prod Res 48:1–18. https://doi.org/10.1016/j.jspr.2011.08.007
Fields P, Korunic Z (2000) The effect of grain moisture content and temperature on the efficacy of diatomaceous earths from different geographical locations against stored-product beetles. J Stored Prod Res 36(1):1–13. https://doi.org/10.1016/S0022-474X(99)00021-1
Finney DJ (1971) Probit Analysis, 2nd edn. Cambridge University Press
Guo J, Chen B (2014) Insights on the molecular mechanism for the recalcitrance of biochars: interactive effects of carbon and silicon components. Environ Sci Technol 48:9103–9112. https://doi.org/10.1021/es405647e
Kavallieratos NG, Athanassiou CG, Pashalidou FG, Andris NS, Tomanović Ž (2005) Influence of grain type on the insecticidal efficacy of two diatomaceous earth formulations against Rhyzopertha dominica (F)(Coleoptera: Bostrychidae). Pest Manag Sci Former Pestic Sci 61:660–666. https://doi.org/10.1002/ps.1034|
Kłys̈ M, Przystupińska A (2015) The mortality of Oryzaephilus surinamensis Linnaeus, 1758 (Coleoptera: Silvanidae) induced by powdered plants. J Plant Prot Res 55:110–116. https://doi.org/10.1515/jppr-2015-0014
Madkour MH, Zaitoun AA, Singer FA (2013) Repellent and toxicity of crude plant extracts on saw-toothed grain beetle (Oryzaephilus surinamensis L.). J Food Agric Environ 11:381–384
Narzari R, Bordoloi N, Chutia RS, Borkotoki B (2015) Biochar: an overview on its production, properties and potential benefits. Biol Biotechnol Sustain Dev, pp 13–40. https://doi.org/10.13140/RG.2.1.3966.2560
Nukenine EN (2010) Stored product protection in Africa: Past, present and future. In: Proceedings of the 10th International Working Conference on Stored Product Protection, Julius-Kuhn-Archiv, pp 26–41. https://doi.org/10.5073/jka.2010.425.177
Obeng-Ofori D (2007) The use of botanicals by resource poor farmers in Africa and Asia for the protection of stored agricultural products. Stewart Postharvest Rev 3:1–8. https://doi.org/10.2212/spr.2007.6.10
Obeng-Ofori D, Boateng BA (2008) Global Popu-lation Growth, Crop Losses and Postharvest Technology. In: Cornelius EW, Obeng-Ofori D (eds) Smartline Publishers Accra, Ghana. Smartline Publish-ing Limited, Accra, pp 1–46
Odeyemi, OO, Oyedare BM, Ashamo MO (2005) Resistance of seven biscuit types to infestation by Tribolium castaneum (Herbst)(Coleoptera: Tenebrionidae). Zool Res 26:300–304. https://www.bioline.org.br/abstract?id=zr05012
Pan J, Ma J, Liu X, Zhai L, Ouyang X, Liu H (2019) Effects of different types of biochar on the anaerobic digestion of chicken manure. Bioresour Technol 275:258–265
Strong RG, Sbur DE, Partida GJ (1967) Rearing stored-product insects for laboratory studies: lesser grain borer, granary weevil, rice weevil, Sitophilus zeamais, and Angoumois grain moth. J Econ Entomol 60:1078–1082. https://doi.org/10.1093/jee/60.4.1078
Taher S, Nasr M (2018) Agricultural wastes-to-green energy in Egypt. Adv Biotechnol Microbiol 8. https://doi.org/10.19080/AIBM.2018.08.555750
Tahmasebi P, Javadpour F, Sahimi M (2015) Three-dimensional stochastic characterization of shale SEM images. Transp Porous Media 110:521–531. https://doi.org/10.1007/s11242-015-0570-1
Vayias BJ, Athanassiou CG, Korunic Z, Rozman V (2009) Evaluation of natural diatomaceous earth deposits from south-eastern Europe for stored-grain protection: the effect of particle size. Pest Manag Sci 65:1118–1123. https://doi.org/10.1002/ps.1801
Vincent JFV, Wegst U (2004) Design and mechanical properties of insect cuticle. Arthropod Struct Dev 33:187–199
Wang X, Xu J, Sun T, Ali S (2021) Synthesis of Cordyceps fumosorosea-biochar nanoparticles and their effects on growth and survival of Bemisia tabaci (Gennadius). Front Microbiol 12:630220. https://doi.org/10.3389/fmicb.2021.630220
Watson E, Barson G (1996) A laboratory assessment of the behavioural responses of three strains of Oryzaephilus surinamensis (L.)(Coleoptera: Silvanidae) to three insecticides and the insect repellent N, N-Diethyl-m-Toluamide. J Stored Prod Res 32:59–67. https://doi.org/10.1016/0022-474X(95)00033-4
Wilson K (2014) How biochar works in soil. Biochar J 32:25–33. http://www.biochar-journal.org/en/ct/32
Wu W, Yang M, Feng Q, McGrouther K, Wang H, Lu H, Chen Y (2012) Chemical characterization of rice straw-derived biochar for soil amendment. Biomass Bioenerg 47:268–276. https://doi.org/10.1016/j.biombioe.2012.09.034
Acknowledgements
The authors thank the Egyptian Academy of Science Research and Technology for financial support for the bilateral proposal with the Czech Academy of Science
Funding
Open access funding provided by The Science, Technology & Innovation Funding Authority (STDF) in cooperation with The Egyptian Knowledge Bank (EKB).
Author information
Authors and Affiliations
Corresponding author
Ethics declarations
Conflict of interest
The authors declare that they have no conflict of interest.
Additional information
Publisher's Note
Springer Nature remains neutral with regard to jurisdictional claims in published maps and institutional affiliations.
Rights and permissions
Open Access This article is licensed under a Creative Commons Attribution 4.0 International License, which permits use, sharing, adaptation, distribution and reproduction in any medium or format, as long as you give appropriate credit to the original author(s) and the source, provide a link to the Creative Commons licence, and indicate if changes were made. The images or other third party material in this article are included in the article's Creative Commons licence, unless indicated otherwise in a credit line to the material. If material is not included in the article's Creative Commons licence and your intended use is not permitted by statutory regulation or exceeds the permitted use, you will need to obtain permission directly from the copyright holder. To view a copy of this licence, visit http://creativecommons.org/licenses/by/4.0/.
About this article
Cite this article
Hassan, N.A., Aly, H.M., Wahba, T.F. et al. Laboratory evaluation of four types of biochar to manage some stored product insects. Int J Trop Insect Sci 42, 2959–2968 (2022). https://doi.org/10.1007/s42690-022-00824-4
Received:
Accepted:
Published:
Issue Date:
DOI: https://doi.org/10.1007/s42690-022-00824-4