Effect of Two Types of Plant Host on the Population Density of Aphis fabae, Aphis gossypii (Hemiptera: Aphididae) and their Parasitoids
Research Article
Effect of Two Types of Plant Host on the Population Density of Aphis fabae, Aphis gossypii (Hemiptera: Aphididae) and their Parasitoids
Dalal Tareq Al-Ameri1, Khalid J. Al-Hussainawy2 and Hasan Al-Khshemawee3*
1Department of Horticultural Science, College of Agriculture, University of Al- Qadisiyah, Iraq; 2Faculty of Agriculture, Al-Muthanna University, Al-Muthanna, Iraq; 3Department of Plant Protection, College of Agriculture, Wasit University, Wasit, Iraq.
Abstract | This experiment was conducted to determine the population density of Aphis gossypii and Aphis fabae on Borage (Borage officinalis: Boraginaceae) and Flora (Stachys macrosperma: Marcrosperma) plants and to know their attractive and repellent effects on both aphid species and their parasitoids. The highest density of A. gossypii on a B. officinalis plant was 74.33 adults/ang2, with a significant difference from A. fabae, which reached 22.53 adults/leave. However, the lowest density of the two aphid species was 29.66 and 1.33 adults/leave, respectively. The highest parasitism rate of A. gossypii on B. officinalis and S. macrosperma plants was recorded at 74 and 23.63%, respectively. The results showed that the highest rate of attraction on the B. officinalis was recorded at 66% for the alcoholic extract at a concentration of 25 mg/ml. In comparison, the highest rate of repellent for the cotton insect was 24% for the hot water extract. But, the highest rate of attraction to S. macrosperma plants was 22% for the hot water extract, and the highest rate of repulsion was 68% for the alcoholic extract at a concentration of 25 mg/ml on the two insects. The study also recorded three aphid parasitoids including Praon volucre (Haliday, 1833), Trioxys pallidus (Haliday, 1833), and Diaeretiella rapae.
Received | April 06, 2024; Accepted | January 13, 2025; Published | March 09, 2025
*Correspondence | Hasan Al-Khshemawee, Department of Plant Protection, College of Agriculture, Wasit University, Wasit, Iraq; Email: hasan_hadi1984@yahoo.com
Citation | Al-Ameri, D.T., K.J. Al-Hussainawy and H. Al-khshemawee. 2025. Effect of two types of plant host on the population density of Aphis fabae, Aphis gossypii (Hemiptera: Aphididae) and their parasitoids. Sarhad Journal of Agriculture, 41(1): 401-407.
DOI | https://dx.doi.org/10.17582/journal.sja/2025/41.1.401.407
Keywords | A. fabae, A. gossypii, B. officinalis, S. macrosperma, Aphid, Water extract
Copyright: 2025 by the authors. Licensee ResearchersLinks Ltd, England, UK.
This article is an open access article distributed under the terms and conditions of the Creative Commons Attribution (CC BY) license (https://creativecommons.org/licenses/by/4.0/).
Introduction
Aphids are phytophagous, belonginging to the Aphididae family, within the Hemiptera order (Rakhshani and Stay, 2021). Around 4,700 species have been identified in the world (Loxdale and Balog, 2018), of which 450 species are registered as plant pests. Approximately 100 species cause significant economic damage. In Iraq, Bandyan et al. (2021) has recorded 59 species of aphids belonging to 24 genera on different plant families. Al-Hussainawy (2012) also recorded 18 species of aphids in Basra Province on different plant families.
The aphid life cycle is complex it needs two hosts to complete the life cycle. The main host is an herbaceous or perennial plant, and the second host is an herbaceous plant (Hayder et al., 2012). Aphids were found in colonies and are characterized by a dimorphic phenomenon. They have two different forms non-winged and winged forms. It helps them search for new hosts, establish new colonies, and continuously increase density through asexual virgin reproduction (Ganassi et al., 2005). Aphids cause damage to plants by sucking nymphs and adults on the plant sap of roots, stems and leaves (Kieckhefer and Reidell, 1995). Also, some species of aphids contain enzymes in their saliva that affect the activity and inhibit the plant cell wall’s functioning, causing the plant’s yellowing and death (Riedell et al., 2003).
The aphid responds to light waves reflected from the plant during flight. The insect can be attracted to the plant as a result of the insect’s response to volatile plant materials and its recognition through the olfactory sensory centers located on the antennae (Visser et al., 1996). The insect is affected by different types of data, it is affected by the color of the plant, and by various data that it is affected by while walking on the surface of the plant, such as the structure of the plant’s wax layer and plant tissue (Powell et al., 2006). It is also affected by the information received by the antennae, as well as its discrimination of the combination of attractive odors, volatile substances produced by the plant, and repulsive substances released by the plant (Powell et al., 2000).
Insect parasitoids from the Aphidiidae family and Hymenoptera are among order the most important insect parasitoids on aphids. They are endoparasitoids and the parasitoid female lays eggs inside the different stages of aphids (nymphs-winged adults, Pterogota, and Apterogota) (Biondi et al., 2013). On the other hand, there are plants that are considered a bank for aphid parasitoids and are characterized by attracting them as soon as they are infected with an aphid. One of these plants is the Anchusa azurea plant, which belongs to the Aceaceae family, and it is a medicinal plant that attracts insects of parasitoids on the aphids in Dhi Qar Province.
The study aims to evaluate the effect of the host plant on the severity of aphid infestation by diagnosing and calculating the density of aphid species on two types of medicinal plants (Borage officinalis and Stachys macrosperma) that found in the Iraq. As well as, record the types of parasitoids and the rate of parasitism on aphids in the field. In addition, test the behavior of attraction and repulsion of hot, cold and alcoholic aqueous extracts of B. officinalis and S. macrosperma plants on aphids under laboratory conditions.
Materials and Methods
Plant materials
Borage (Borage officinalis: Boraginaceae) seeds obtained from local agricultural offices were planted and placed in the wooden bed belonging to the Department of Horticulture Engineering at the College of Agriculture, Al-Qadisiyah University, Al- Qadisiyah, Iraq.
The seed of the Stachys macrosperma plant were obtained from one of the local nurseries at one age, and after 40 days of germinating the seeds of the borage plant. They were transferred to plastic pots with a size of 10 kg containing the organic fertilizer and a mixture of soil at a ratio of (1:1) and planted in lines at a distance of 50 cm. The plants were left to natural infestation with insects without applying the control process (Figure 1).
Insect identification
The experiments included identifying the types of aphids that were found on both plants using taxonomic keys. The types of parasitoids present in the aphid types were also classify within the experiment.
Calculating the density of aphid species and parasitism rates
Three replicates for each plant have been used. The density was calculated by taking 10 leaves from each replicate randomly from the top, middle, and bottom of both plants. Then, the leaves were placed in polyethylene bags. It was brought to the laboratory and placed in the refrigerator for 20 mins for the purpose of killing insects. The numbers of aphids was calculated by removing the insects on both surfaces of the leaf using a soft brush on a white board. Their density and nutritional preference were determined, and the percentage of parasitism was recorded (Figure 2).
Statistical analysis
The data were analyzed by using SPSS program. The Randomized Complete Block Design (RCBD) design was used in these experiments with three replicates. The differences of means have been measured by using least significant differences (LSD) with the level of 0.05%.
Results and Discussion
The results of the phenotypic classification of the aphid species showed the found of both the cotton aphid Aphis gossypii and the bean aphid Aphis fabae on both plants. Three types of parasitoids wasps on aphid was also recorded: Praon volucre (Haliday, 1833) and Trioxys pallidus (Haliday, 1833) and Diaeretiella rapae (M’Intosh, 1885) based on classification keys.
The results of calculating the taxonomic density of aphid species on plants showed that the highest infestation rate of cotton aphids was recorded on both plants were 74.33 and 22.53, respectively. In contrast, the lowest infestation rate of bean aphids was recorded were 29.66 and 1.33, respectively, (Figure 3).
The rates of parasitism on aphids on both plants were recorded by counting the number of mummies present on the collected leaves. The highest rate of parasitism was recorded on individuals of cotton found on B. officinalis and S. macrosperma plants, which were 31.74 and 23.63%, respectively, while the rate of parasitism on aphids reached 14.66. and 20%, respectively, Figure 4.
The results showed that the effect of boiled and cold extract and alcoholic extract of B. officinalis leaves on inducing the behavior of attraction and repulsion of individuals of the aphid indicate their tendency to attract aphids. The highest rate of attraction was 66% and 64% for cotton aphids and black bean aphids, respectively. They were exposed to the alcoholic extract at a concentration of 25 mg/ml after an hour of treatment. At the same time, the highest rate of expulsion was recorded at 28% when exposing black bean aphid insects to the boiling water extract. However, the highest rate of repelling insects from cotton was 24% for the boiling water extract. The results also showed that the highest rate for the alcoholic extract on cotton was 54%, while the highest neutralization rate for the alcoholic extract on black bean sprouts was 38% (Table 1).
Table 1: Effectiveness of boiled, cold and alcoholic extract of B. officinalis leaves in attracting and repelling A. fabae and A. gossypii.
B. officinalis extract |
A. fabae |
A. gossypii |
||||
Attracting % |
Repelling % |
Balance % |
Attracting % |
Repelling % |
Balance % |
|
Cold water |
58 |
22 |
36 |
65 |
16 |
49 |
Boiled water |
54 |
28 |
26 |
52 |
24 |
24 |
Alcoholic |
64 |
26 |
38 |
66 |
12 |
54 |
LSD (0.05) for the attraction ratio = 4.454; LSD (0.05) for expulsion ratio = 3.616
Table 2: Effectiveness of boiled, cold and alcoholic extract of S. macrosperma leaves in attracting and repelling A. fabae and A. gossypii.
S. macrosperma extract |
A. fabae |
A. gossypii |
||||
Attracting % |
Repelling % |
Balance % |
Attracting % |
Repelling % |
Balance % |
|
Cold water |
24 |
48 |
-24 |
32 |
60 |
-28 |
Boiled water |
22 |
42 |
-20 |
36 |
60 |
24- |
Alcoholic |
28 |
68 |
-40 |
32 |
64 |
-32 |
LSD (0.05) for the attraction ratio = 3.517; LSD (0.05) for expulsion ratio = 4.638
Table 2 also shows that the boiled and cold aqueous extract and 96% ethyl alcohol of the S. macrosperma plant tended to repel aphids. The highest expulsion rate was 68% and 64% for black beans and cotton, respectively, when exposed to the alcoholic extract at a concentration of 25 mg/ after an hour of treatment. However, the highest rate of attraction was 22% when exposing black bean insects to the boiling water extract. In comparison, the highest rate of attraction to cotton insects was 36% to the boiling water extract. Table 2 also showed that the highest balance percentage for the alcoholic extract on black bean was -40%, while the highest balance percentage for the alcoholic extract on cotton seeds was -32%.
Aphids have a wide family range and have the ability to adapt in the absence of the main host to migrate to secondary hosts. The rate of aphid infestation on plants may vary depending on the difference in the preference of aphids for those families. It is linked to several phenotypic factors such as the thickness and area of the plant leaf, the density and length of the hairs, and the color of the plant. In addition, to the chemical factors represented by the secondary compounds produced by the plant, which include flavonoids, the chemical factors represented by the secondary compounds produced by the plant, include flavonoids, phenols, terpenes, and tannins. All of them play a role in the difference in the aphid’s preference for the host and thus the rates of insect infection (Dai et al., 2018).
The B. officinalis plant belongs to the Aceaceae family, is considered an insect-attracting plant (Dogimont et al., 2010). This may explain the preference of aphid species compared to the low numerical density of aphid species on the tangerine plant, which is characterized by containing compounds that are unpalatable or repellent to aphids.
This was indicated by Davis et al. (2017), who studied the effective components of the oil extract of the leaves of the Stachys rieder plant. It tested its effect on the adults of both the corn weevil Sitophilus zeamais and the booklice Liposcelis bostrychophila. They found that there are 40 components in the essential oil, representing 96.01% of oil components, five of which have a killing effect on insects namely acetanisole, anisole, 1, 8-cineole, eugenol, and geraniol, indicating their effectiveness in causing killing through fumigation and contact.
For the presence of parasitoids and the difference in parasitism rates, the highest parasitism rate was recorded on the types of aphids found on the B. officinalis plant, which is due to the fact that the plant is known to be attractive to aphid parasitoids (Fujinuma et al., 2010). The parasitism exploits volatile compounds from the plant infected with aphids as a guide to determine the location of the infestation. It is known as herbivore induced plant volatiles (HIPVs).
Fujinuma et al. (2010) have investigated whether the B. officinalis plant is an attractive plant for aphid parasitoids by testing the susceptibility of females of the parasitoid Aphidius colemani to being attracted to the odors emanating from plants (Borage, Japanese radish, and barley infested with aphids, Myzus persicae, and Rhopalosiphum padi) and mechanically damaged by 4-arm olfactometer device. It has recorded the highest rate of attraction for parasitic adults to the B. officinalis plant. The variation in the percentage of attraction and repulsion may be due to variation in the chemical components of these plants (Asadi et al., 2018).
Therefore, these extracts may affect the behavioral reactions of the insect of feeding, including orientation. Thus, they are effective stimulants or inhibitors to feeding. Sometimes the insect is attracted to a substance that is not desirable to it because the influential substances within the components of the food may not be perceived by the insect because the concentration of its vapor may not be sufficient. It affects the olfactory response (Jankowska, 2010). The repulsive feature is useful in keeping insects away from the places where they are protected from infection. The attracting feature is useful in attracting insects and catching them to where the toxic substance is located, killing them (Suleiman et al., 2012).
The difference in the ability to attract and repel the extract of B. officinalis and S. macrosperma plants for aphid species may be due to the chemicals, minerals and nutrients present in both plants and even the odors emanating from them. Griffiths-Lee et al. (2020) have indicated the effectiveness of the B. officinalis plant in attracting many insects when grown in greenhouses with strawberry plants. It was observed that pollinating insects such as bees, bumblebees, butterflies, beetles, and many insects are attracted.
Asnaashari et al. (2010) showed the effectiveness of the methylated extract of the plant Stachys byzantina at concentrations of 5, 10, and 20 mg/ml as an insecticide to kill adults of Oryzaephilus mercator insect. It recorded a kill rate of 13.3, 26.6, and 33.3, respectively, after 48 hrs of treatment, indicating that the plant contains anti-insect compounds, which identified as three types of phenylethanoids, namely 2’-O-arabinosyl verbascoside, verbascoside, and aeschynanthoside C, and three flavinoid compounds, which are 7-O-glucoside, 7-O-(6-p-coumaroyl)-glucoside, and apigenin.
Conclusions and Recommendations
The study concludes that the population density of A. gossypii is higher than the density of A. fabae on borage plants. The B. officinalis extract has an attractive effect on aphids, while the S. macrosperma plant has a repellent effect. The study has recorded three parasitoids Praon volucre (Haliday, 1833), Trioxys pallidus (Haliday, 1833), and Diaeretiella rapae on A. gossypii and A. fabae.
Acknowledgements
The authors are grateful to the Iraqi Government and the respective universities (University of Al-Qadisiyah, Iraq, Al-Muthanna University, Al-Muthanna, Iraq and Wasit University, Wasit, Iraq) for their support and provision of the equipment.
Novelty Statement
The study is first of its kind to evaluate the effect of the host plant on the severity of aphid infestation by diagnosing and calculating the density of aphid species on two types of medicinal plants (Borage officinalis and Stachys macrosperma) that are found in the Iraq.
Author’s Contribution
Dalal Tareq Al-Ameri: Conceptualization
Hasan Al-Khshemawee: Methodology and writing-original draft preparation
Khalid J. Al-Hussainawy: Software, data curation investigation, writing-review and editing, and supervision
Conflict of interest
The authors have declared no conflict of interest.
References
Al-Hussainawy, K.J., 2012. A taxonomical and ecological study of some species of Aphids (Hemiptera: Aphididae) and estimate perdition efficiency for two ladybird on them in Basrah. MCS thesis, College of Agriculture, Basrah Univ., pp. 125.
Al-Hussainawy, K.J., A.S. Jabbar and A.A.Z.A. Jassani. 2019. A taxonomical study of Aphid parasitoids (Hymenoptera: Aphidiidae) and their host aphid associations in Dhi Qar province.
Asadi, M., G. Nouri-Ganbalani, H. Rafiee-Dastjerdi, M. Hassanpour and B. Naseri. 2018. The effects of Rosmarinus officinalis L. and Salvia officinalis L. (Lamiaceae) essential oils on demographic parameters of Habrobracon hebetor Say (Hym.: Braconidae) on Ephestia kuehniella Zeller (Lep.: Pyralidae) larvae. J. Essential Oil Bearing Plants, 21(3): 713-731. https://doi.org/10.1080/0972060X.2018.1491331
Asnaashari, S., A. Delazar, S.S. Alipour, L. Nahar, A.S. Williams, A. Pasdaran, M. Mojarab, F.F. Azad and S.D. Sarker. 2010. Chemical composition, free-radical-scavenging and insecticidal activities of the aerial parts of Stachys byzantina. Arch. Biol. Sci., 62(3): 653-662. https://doi.org/10.2298/ABS1003653A
Bandyan, S.K., R.S. Peters, N.B. Kadir, M. Ferrer-Suay and W.H. Kirchner. 2021. A survey of aphid parasitoids and hyperparasitoids (Hymenoptera) on six crops in the Kurdistan Region of Iraq. J. Hymenoptera Res., 81: 9-21. https://doi.org/10.3897/jhr.81.59784
Biondi, A., L. Zappalà, J.D. Stark and N. Desneux. 2013. Do biopesticides affect the demographic traits of a parasitoid wasp and its biocontrol services through sublethal effects. PLoS One, 8(9): e76548. https://doi.org/10.1371/journal.pone.0076548
Dai, Y., M.F. Wang, S.L. Jiang, Y.F. Zhang, M.N. Parajulee and F.J. Chen. 2018. Host-selection behavior and physiological mechanisms of the cotton aphid, Aphis gossypii, in response to rising atmospheric carbon dioxide levels. J. Insect Physiol., 109: 149-156. https://doi.org/10.1016/j.jinsphys.2018.05.011
Davis, T.S., Y. Wu and S.D. Eigenbrode. 2017. The effects of bean leafroll virus on life history traits and host selection behavior of specialized pea aphid (Acyrthosiphon pisum, Hemiptera: Aphididae) genotypes. Environ. Entomol., 46(1): 68-74. https://doi.org/10.1093/ee/nvw150
Dogimont, C., A. Bendahmane, V. Chovelon and N. Boissot. 2010. Host plant resistance to aphids in cultivated crops: Genetic and molecular bases, and interactions with aphid populations. Compt. Rendus. Biol., 333(6-7): 566-573. https://doi.org/10.1016/j.crvi.2010.04.003
Fujinuma, M., Y. Kainoh and H. Nemoto. 2010. Borago officinalis attracts the aphid parasitoid Aphidius colemani (Hymenoptera: Braconidae). Appl. Ent. Zool., 45(4): 615-620. https://doi.org/10.1303/aez.2010.615
Ganassi, S., P. Grazioso, A. Moretti and M.A. Sabatini. 2010. Effects of the fungus Lecanicillium lecanii on survival and reproduction of the aphid Schizaphis graminum. Biocontrol, 55: 299-312. https://doi.org/10.1007/s10526-009-9250-9
Griffiths‐Lee, J., E. Nicholls and D. Goulson. 2020. Companion planting to attract pollinators increases the yield and quality of strawberry fruit in gardens and allotments. Ecol. Entomol., 45(5): 1025-1034. https://doi.org/10.1111/een.12880
Hayder, B., B.K. Agarwala and I.K. Kaddou. 2012. New records of aphids of the Subfamily Aphidinae (Homoptera: Aphididae) infested herbaceous plants and shrubs for Iraqi aphid fauna. Adv. Biores., 3(4): 66-75.
Jankowska, B., 2010. Effect of intercropping white cabbage with french marigold (Tagetes patula nana) and pot marigold (Calendula officinalis) on diamondback moth (Plutella xylostella l.) population density and it’s parasitoid complex. Vegetable Crops Res. Bull., 73: 107. https://doi.org/10.2478/v10032-010-0023-x
Kieckhefer, R.W., J.L. Gellner and W.E. Riedell. 1995. Evaluation of the aphid‐day standard as a predictor of yield loss caused by cereal aphids. Agron. J., 87(5): 785-788. https://doi.org/10.2134/agronj1995.00021962008700050001x
Loxdale, H.D. and Balog, A., 2018. Aphid specialism as an example of ecological–evolutionary divergence. Biol. Rev., 93(1): 642-657. https://doi.org/10.1111/brv.12361
Powell, G., C.R. Tosh and J. Hardie. 2006. Host plant selection by aphids: Behavioral, evolutionary, and applied perspectives. Ann. Rev. Entomol., 51(1): 309-330. https://doi.org/10.1146/annurev.ento.51.110104.151107
Powell, G.L.E.N. and J.I.M. Hardie. 2000. Host‐selection behaviour by genetically identical aphids with different plant preferences. Physiol. Ent., 25(1): 54-62. https://doi.org/10.1046/j.1365-3032.2000.00164.x
Rakhshani, E. and P. Starý. 2021. Aphid Parasitoids: Aphidiinae (Hym., Braconidae). In biological control of insect and mite pests in Iran: A review from fundamental and applied aspects. pp. 333-399. https://doi.org/10.1007/978-3-030-63990-7_9
Riedell, W.E., R.W. Kieckhefer, M.A. Langham and L.S. Hesler. 2003. Root and shoot responses to bird cherry‐oat aphids and barley yellow dwarf virus in spring wheat. Crop Sci., 43(4): 1380-1386. https://doi.org/10.2135/cropsci2003.1380
Suleiman, M., N.D. Ibrahim and Q. Majeed. 2012. Control of Sitophilus zeamais (Motsch) (Coleoptera: Curculionidae) on Sorghum using some plant powders. Int. J. Agric. For., 2(1): 53-57. https://doi.org/10.5923/j.ijaf.20120201.09
Visser, J.H., P.G.M. Piron and J. Hardie. 1996. The aphids peripheral perception of plant volatiles. In: Proceedings of the 9th International Symposium on Insect-Plant Relationships. pp. 35-38. https://doi.org/10.1007/978-94-009-1720-0_8
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