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Acta Biológica Colombiana

Print version ISSN 0120-548X

Acta biol.Colomb. vol.26 no.1 Bogotá Jan./Apr. 2021  Epub Mar 18, 2021

https://doi.org/10.15446/abc.v26n1.83303 

Artículos

PREDATION OF Brevicoryne brassicae AND Aphis craccivora BY Eriopis connexa DEPENDING ON AVAILABILITY

Depredación de Brevicoryne brassicae y Aphis craccivora por Eriopis connexa, según disponibilidad

Djison SILVESTRE DOS SANTOS1  * 
http://orcid.org/0000-0002-4037-1733

Roseane CRISTINA PREDES TRINDADE1 
http://orcid.org/0000-0001-5714-9453

Jorge BRAZ TORRES2 
http://orcid.org/0000-0002-0717-6493

Mauricio SILVA DE LIMA2 
http://orcid.org/0000-0002-0754-7418

Lindinalva DOS SANTOS1 
http://orcid.org/0000-0002-0755-8387

Felipe COLARES BATISTA2 
http://orcid.org/0000-0002-5787-3852

1 Programa de Pós-graduação em Proteção de Plantas, Campus de Engenharias e Ciências Agrárias, Universidade Federal de Alagoas, BR 104 N, Km 85, Rio Largo, Brasil.

2 Programa de Pós-graduação em Entomologia, Departamento de Agronomia, Universidade Federal Rural de Pernambuco, Avenida Dom Manoel de Medeiros, s/no, Dois Irmãos, Recife, Brasil.


ABSTRACT

Predator species under field conditions can face different and variable densities of prey species. This work evaluated the functional response of the neotropical lady beetle Eriopis connexa (Coleoptera: Coccinellidae) subjected to different densities of the aphids Brevicoryne brassicae and Aphis craccivora (Hemiptera: Aphididae). Thus, predation rates were analyzed of fourth-instar larvae and one-day old adults of the lady beetle preying upon the aphids at constant densities of 20, 40, 50, 60, and 70 aphids with 15 repetitions per density. The aphids were offered on 5 cm leaf discs of each plant host. The handling times and attack rates were 0.03 h-1 and 0.27 h-1 for larvae and 0.03 h-1 and 0.15 h-1 for adults fed B. brassicae and 0.59 h-1 and 0.35 h-1 for larvae and 0.70 h-1 and 0.95 h-1 for adults fed A. craccivora, respectively. Both larva and adult lady beetles increased predation rate as a function of prey density offered, with an estimated maximum number of prey consumed of 30.3 and 31.6 B. brassicae and 36.3 and 34.6 of A. craccivora by larva and adult lady beetles at the highest prey density, respectively. In conclusion, larvae and adults of E. connexa exhibited a type II functional response.

Keywords: aphidofagous; Biological Control; Entomology; Insecta

RESUMEN

Las especies de depredadores en condiciones de campo pueden enfrentar densidades diferentes y variables de sus presas. Este trabajo evaluó la respuesta funcional de la mariquita neotropical Eriopis connexa (Coleoptera: Coccinellidae) sometida a diferentes densidades de los pulgones Brevicoryne brassicae y Aphis craccivora (Hemiptera: Aphididae). Se analizaron las tasas de depredación de larvas de cuarto estadio y adultos de un día de vida en las densidades constantes de 20, 40, 50, 60 y 70 pulgones con 15 repeticiones por densidad. Los pulgones se ofrecieron en discos de 5 cm de hojas de la planta huésped. Los tiempos de manejo y las tasas de ataque fueron 0.03 h-1 y 0.27 h-1 para larvas y 0.03 h-1 y 0.15 h-1 para adultos alimentados con B. brassicae y 0.59 h-1 y 0.35 h-1 para larvas y 0.70 h-1 y 0.95 h-1 para adultos alimentados con A. craccivora, respectivamente. Las larvas y las mariquitas adultas aumentaron la tasa de depredación en función de la densidad de presas ofrecidas, con un número máximo estimado de presas consumidas de 30.3 y 31.6 de B. brassicae y 36.3 y 34.6 de A. craccivora para larvas y mariquitas adultas a la mayor densidad de presas, respectivamente. En conclusión, las larvas y los adultos de E. connexa exhibieron una respuesta funcional del tipo II.

Palabras clave: afidofagas; Control Biológico. Entomología; Insecta

INTRODUCTION

Predator Coccinellidae play a significant role in the biological control of pests in many agricultural crops (Biddinger et al., 2009; Obrycki, 2009; Weber and Lundgren, 2009), due to their ability to search out and consume pests (Vandenberg, 2002). The neotropical lady beetle, Eriopis connexa (Germar), consumes several types ofpreys, but prefers to attack aphids (Hagen, 1962; Oliveira et al., 2004). Eriopis connexa has been studied as potential predator against pests in horticultural crops in the Neotropical region (Sarmento et al., 2007; Duarte Gómez and Zenner de Polanía, 2009; Harterreiten-Souza etal., 2012). In Brazil, this species is also commonly associated with pests of cultivated species, including key pests (Venzon et al., 2009; Harterreiten-Souza et al., 2012; Rodrigues et al., 2013).

Predation is an important biotic factor that reduces pest insect populations in the natural environment and can reduce the use of insecticides for pest control (Wiedenmann and Smith, 1997; Sarmento et al., 2007). In biological control, the relationship between prey density and consumption rate is known as functional response (Abrams and Ginzburg, 2000; Jeschke et al., 2002). Functional response describes the behavior of the predator as a function of consumption at different densities, thus suggesting the maximum prey consumption, as well as the predator's potential in population control (Murdoch and Oaten, 1975). According to Solomon (1969), the increase in prey availability may lead the predator to increased consumption, up to a certain limit, because the opportunities to attack prey will increase over time.

Holling (1959) and Jervis and Kidd (1996) outline four fundamental types of functional response curves. Type I corresponds to the consumption of prey by the predator resulting in a linear increase. Type II occurs when the rate of predation decelerated reaching an asymptote. Type III involves a sigmoid relation also called S ascension, and Type IV establishes a dome-shaped curve. A predator that exhibits a type III functional response has greater potential to control prey population, because the proportion of prey attacked increases with increasing density (Fernandez-Arhex and Corley, 2003). However, type II functional response is most common for invertebrate predators (Van Lenteren and Bakker, 1976), because of satiation (e.g. predators) and ability to produce eggs (e.g. parasitoids), as well as restricted handling and attack time.

Thus, this study aimed to determine the functional response of the E. connexa lady beetles preying on the aphids Brevicoryne brassicae (Linnaeus, 1758) and Aphis craccivora Koch, 1854 at different densities.

MATERIAL AND METHODS

The experiments were conducted in the Entomology Laboratory from February 2017 to August 2017: Federal University of Alagoas (UFAL), Rio Largo, AL, Brazil.

Obtaining and Rearing of Predator and Preys

The lady beetles used in the experiment came from the rearing kept at the Insect Biological Control Laboratory of Universidade Federal Rural de Pernambuco -UFRPE. Adults and larvae were reared according to the methodology described in Rodrigues et al. (2013). The adults were raised in 500 mL plastic containers with lid opening covered with voile fabric to allow air circulation. Pieces ofpaper towel were placed inside the containers for oviposition substrate. The laid eggs were transferred daily to 500 mL plastic containers and held until hatching. Then, the larvae were transferred in 80 ml plastic containers at the density of two larvae per container. Inside the container, paper towel pieces of about 2 x 2 cm were placed as substrate for pupation. The insects were fed Anagasta kuehniella (Zeller) (Lepidoptera: Pyralidae) eggs, and in the adult phase were also offered a diet based on brewer's yeast and honey (1: 1).

The Aphis craccivora colony originated from lima beans (Phaseolus lunatus L.) (Fabaceae) grown in an experimental field of UFAL, in Rio Largo, AL, Brazil. These aphids were reared in cowpea plants (Vigna unguiculata (L.) Walp.) (Fabaceae), cultivar (Vita 7), susceptible to black aphid (Valente et al., 2014). Cowpea plants were cultivated in 500 ml plastic cups containing soil and substrate in the ratio of 1:1 in cages protected with anti-aphid mesh (4.0 cm x 4.0 cm x 0.4 cm), kept in a greenhouse. Then, 15 days after planting, the plants were infested by apterous females placed with tweezers. At five-day intervals, the insects were transferred to new plants. This procedure was performed routinely to maintain breeding stock and use in studies.

The Brevicoryne brassicae colony was collected in cabbage plants of cv. Georgia, Brassica oleracea var. acephala D.C. (Brassicaceae), naturally infested in the field, in the UFAL Olericulture Sector, in Rio Largo, AL. These insects were transported to the laboratory and screened to remove parasitized individuals. They were then transferred to potted kale plants and kept in cages with anti-aphid mesh (1.0 m x 1.0 m x 0.5 m) in a greenhouse.

Functional Response of Eriopis connexa on the aphids Brevicoryne brassicae and Aphis craccivora

The predation rate of the lady beetle E. connexa on the aphids B. brassicae and A. craccivora was determined at different prey densities. This bioassay used fourth instar larvae and one-day-old adults of E. connexa and apterous adult aphids of B. brassicae and A. craccivora. Larvae and adult lady beetles used in the study were deprived of food for 24 hours to regulate the level of satiety. Six aphid densities were tested (20, 40, 50, 60, and 70) for both species with 15 replicates per density. The densities were established from the average rate of daily consumption obtained in preliminary tests.

The aphids were offered on 5.0 cm diameter leaf discs. The aphid B. brassicae was offered on cassava leaf discs, while the aphid A. craccivora was offered on cowpea leaf discs. Beforehand, the leaves were washed with water, neutral detergent, and 0.5 % sodium hypochlorite. When dry, the leaf discs were placed in 6.5 cm diameter Petri dishes lined with filter paper lightly moistened with distilled water and subsequently infested with the prey at respective densities. The transfer of prey was carried out with the aid of tweezers. After transfering the aphids to the plates, they were closed with PVC plastic film for 24 hours for the insects to settle. Fourth instar larvae along with adult lady beetles were individually transferred to Petri dishes according to the corresponding treatment, where they remained for 24 h. After that period, we recorded the number of live aphids remaining in each replicate and control without the presence of the predator, as well as the number of live lady beetle in each treatment.

In the first analysis step, the shape of the functional response curve was determined by logistic regression for the proportion of prey consumed as a function of the original prey densities per predator using Proc CATMOD in the SAS program, following the protocol described in Juliano (1993). Initially, the cubic model was tested because of its ability to capture all possible variations of the functional response curves. Then, the terms of the equation were reduced until their significance was obtained. The sign of the linear term of the equation generated from the proportion of prey consumed/killed by prey density was used to determine the type of functional response. When not significant, it indicates Type I functional response; a negative indicates Type II functional response; and a positive functional response indicates Type III. The parameters determined in the second step were handling time (Ht) and attack rate (a') of the functional response. These parameters were estimated by non-linear regression using the least squares method (PROC NLIN of the SAS) according to the methodology described by Juliano (1993) and compared by 95 % confidence interval.

RESULTS AND DISCUSSION

The mean prey consumption by fourth instar larvae and adults of E. connexa at different densities of adult B. brassicae and A. craccivora tended to stabilize at higher densities, resulting in a type II functional response curve. The estimated attack rate and handling time were, respectively, 0.026 and 0.0.34 h-1 for larvae and 0.029 h-1 and 0.60 h-1 for adults preying on B. brassicae; and 0.59 and 0.35 h-1 for larvae and 0.70 and 0.95 h-1 adults preying on A. craccivora (Tables 1 and 2). Both larvae and adult E. connexa increased the number of aphids preyed on with increased prey density until reaching asymptote. They consumed a maximum mean of 30.3 and 31.6 of B. brassicae and 36.3 and 34.6 of A. craccivora, of larvae and adults, respectively.

Table 1 Holling disc equation and functional response type of Eriopis connexa larvae and adults preying on the aphids Brevicoryne brassicae and Aphis craccivora. 1 Intercept. 2 Linear coefficient. 3 Quadratic coefficient- 4 Functional response 

Table 2 Handling time and attack rate of Eriopis connexa larvae and adults fed with the aphids Brevicoryne brassicae and Aphis craccivora. 

The Holling disc equation fit the results for the different stages of the E. connexa lady beetle on the different densities of both aphids (Table 1). When the proportion of prey consumed decreased for both larvae and adults of E. connexa, for both species of aphids, the number of preys consumed increased (Fig. 1 and 2). Pervez and Omkar (2005), studying the predation behavior ofthree lady beetle species Cheilomenes sexmaculata (Fabr.), Propylea dissecta (Mulsant) and Coccinella transversalis (Fabr.) (Coleoptera: Coccinellidae) on aphids A. craccivora and Myzus persicae (Sulzer), observed that all the lady beetles presented type II functional response for both preys. However, the handling time was quite varied among lady beetle species. The predators used in the Pervez and Omkar (2005) had longer handling time than the one found in this study. This demonstrates that each predator exhibits different predatory behavior with increased availability of prey; some are more voracious, especially those exhibiting shorter handling time and higher attack rates. (Mills, 1982; Ofuya and Akinbohungbe, 1988; Pervez, 2004). Handling time is an important variable of a predator's effectiveness and consumption rate, since it reflects the time that they take to kill, consume, and digest the prey (Veeravel and Baskaran, 1997).

Figure 1 (a) Functional response of fourth instar larvae and (b) adults of Eriopis connexa in different densities of the aphid Brevicoryne brassicae. (c) Functional response of fourth instar larvae and (d) adults of Eriopis connexa at different densities of aphid Aphis craccivora. 

This was clear in the present study, in which the attack and handling time were varied between the two aphid species offered. Both larvae and adults of E. connexa exhibited a less handling time and a lower attack rate praying on B. brassicae, than on A. craccivora (Table 1), which resulted in a higher predation on the latter species. This result was somewhat expected due to their different size, as well as other characteristics related to quality of prey, reflected in the prey species, as well as the age of the predator. Vieira et al., (1997) found that fourth instar larvae of Scymnus (Pullus) argentinicus (Weise, 1906) (Coleoptera: Coccinellidae) used less handling time and preyed on older instars of Schizaphis graminum (Rond.) (Hemiptera: Aphididae). This response of the predator can be attributed to the opportunity to encounter prey, which are greater depending on availability, time, and size. An increase in the availability of prey may lead to an increase in consumption, because prey is encountered more frequently, resulting in the consumption of an additional number of prey, even though the predator is already satiated (Garcia, 1990).

Type II functional response found for larvae and adults (Fig. 1) of E. connexa for both species of aphids, involves deceleration of the number of aphids consumed, due to the increase in their availability, and is the most common type of predation response among coccinellids (Atlihan and Ózgókce, 2002; Pervez and Omkar, 2005; Britto et al., 2009; Saleh et al., 2010; Atlihan et al., 2010). These results are also consistent with those obtained by Ofuya and Akingbohungbe (1988), in which the predator Cheilomenes luneta (Fabr.), feeding on the aphid A. craccivora presented a Type II functional response. Bortoli et al. (2014), evaluating the functional response of larvae and adults of lady beetle Cryptolaemus montrouzieri (Mulsant, 1850) on the cochineal Planococcus citri, also obtained type II functional response, for both phases.

Variable patterns of predation behavior are also a feature of E. connexa, which has various strategies when preying on different organisms. The lady beetle C. sanguinea (Linnaeus, 1763) presents type II response when preying on Tetranychus evansi (Thomas, 1878) (Acari: Tetranychidae). However, when the prey was the aphid Macrosiphum euphorbiae (Baker and Pritchard, 1960) (Hemiptera: Aphididae), it showed a type III functional response (Sarmento et al., 2007), which characterizes a predation behavior change according to the type of available prey.

These results are relevant because the potential consumption of the studied aphid species by the lady beetle E. connexa is not known, although this lady beetle has been observed associated with infestations of these aphids (Rodrigues et al., 2013; Costa et al., 2018). Future research should focus on the biological performance of this lady beetle species feeding on these preys, as well as other pests common in bean and brassica crops. The susceptibility of E. connexa to insecticides recommended for use in these crops should be tested to conserve this lady beetle populations in crops. This species of lady beetle has shown high resistance to pyrethroid insecticides, which do not or minimally control aphids (Torres et al., 2015; Costa et al., 2018), but are commonly used to control leafhoppers in host cultures of these aphids. Therefore, maintaining E. connexa in these agroecosystems is important for apply integrated pest management. This could validate the predation of B. brassicae by this lady beetle in the field, since they are commonly associated with brassica crops.

CONCLUSION

Larvae and adults of E. connexa exhibit type II functional response when confined with different densities of aphids B. brassicae and A. craccivora.

ACKNOWLEDGMENTS

The authors thank Guillermo González (Santiago, Chile) for the critical review of the manuscript.

REFERENCES

Abrams PA, Ginzburg LR. The nature of predation: prey dependent, ratio dependent, or neither. Trends Ecol Evol. 2000;15(8):337-341. Doi: https://doi.org/10.1016/s0169-5347(00)01908-xLinks ]

Atlihan R, Özgökçe MS. Development, fecundity and prey consumption of Exochomus nigromaculatus feeding on Hyalopterus pruni. Phytoparasitica 2002;30(5):443-450. Doi: http://doi.org/10.1007/BF0297974Links ]

Biddinger DJ, Weber DC, Hull LA. Coccinellidae as predators of mites: Stethorini in biological control. Biol Control. 2009;51(2):268-283. Doi: https://doi.org/10.1016/j.biocontrol.2009.05.014Links ]

Bortoli AS, Gravena AR, Vacari AM, Laurentis VL, Bortoli CP. Resposta funcional da joaninha Cryptolaemus predando cochonilha branca em diferentes temperaturas e substratos vegetais. Caatinga. 2014;27(3):63-71. [ Links ]

Britto EPJ, Gondim Jr MGC, Torres JB, Fiaboe KKM, Moraes GJ, Knapp M. Predation and reproductive output of the ladybird beetle Stethorus tridens preying on tomato red spider mite Tetranychus evansi. Biol Control. 2009;54(3): 363-368. Doi: http://doi.org/10.1007/s10526-008-9178-5Links ]

Costa PMG, Torres JB, Rondelli VM, Lira R. Field-evolved resistance to A-cyhalothrin in the lady beetle Eriopis connexa. Bull Entomol Res. 2018;108(3):380-387. Doi: http://doi.org/10.1017/S0007485317000888Links ]

Duarte Gómez W, Zenner de Polanía I. Tabla de vida del cucarrón depredador Eriopis connexa (Germar). Rev Actual Div Cien. 2009(2);12:147-155. [ Links ]

Fernandez-Arhex V, Corley JC. The functional response of parasitoids and its implications for biological control. Biocontrol Sci Techno 2003;13(4): 403-413. Doi: https://doi.org/10.1080/0958315031000104523Links ]

Garcia MA. Ecologia nutricional de parasitóides e predadores terrestres. In: Panizzi AR, Parra JRP, editors. Ecologia nutricional de insetos e suas implicações no manejo de pragas. São Paulo: Manole;1990. p.289-311. [ Links ]

Hagen KS. Biology and ecology of predaceous Coccinellidae. 1962. Ann Rev Entomol. 7: 289-326. Doi: https://doi.org/10.1146/annurev.en.07.010162.001445Links ]

Harterreiten-Souza ES, Togni PHB, Milane PVGN, Cavalcante KR, Medeiros MA, DE Pires CSS, Sujii ER. Seasonal Fluctuation in the population of Harmonia axyridis (Pallas, 1773) (Coleoptera: Coccinellídae) and co-occurrence with other coccinellids in the Federal District of Brasil. Pap Avulsos de Zool. 2012;52(11):133-139. Doi: http://dx.doi.org/10.1590/S0031-10492012001100001Links ]

Holling CS. Some characteristics of simple types of predation and parasitism. Can Entomol. 1959;91(7):385-398. Doi: https://doi.org/10.4039/Ent91385-7Links ]

Jervis MA, Kidd NA. Insect Natural Enemies: Practical Approaches to their Study and Evaluation. Oxford, Great Britain: Chapman and Hall;1996.p. 504. [ Links ]

Jeschke JM, Kopp M, Tollrian R. Predator functional responses: discriminating between handling and digesting prey. Ecol Monogr. 2002;72(1):95-112. Doi: https://doi.org/10.1890/0012-96150720095Links ]

Juliano SA. Non-linear curve fitting: predation and functional response curves. Scheiner SM, Gurevitch J, editors. Design and Analysis of Ecological Experiments. New York: Chapman & Hall, 1993.p. 158-183. [ Links ]

Mills NJ. Satiation and the functional response: A test of a new model. Ecol Entomol. 1982;7(3):305-315. Doi: https://doi.org/10.1111/j.1365-2311.1982.tb00671.xLinks ]

Murdoch WW, Oaten A. Predation and population stability. Adv Ecol Res. 1975;9:1-131. Doi: https://doi.org/10.1016/S0065-2504(08)60288-3Links ]

ObryckI JJ, Harwooda JD, Kringb TJ, O'Neil RJ. Aphidophagy by Coccinellidae: application of biological control in agroecosystems. Biol Control. 2009;51(2):244-254. Doi: https://doi.org/10.1016/j.biocontrol.2009.05.009Links ]

Ofuya TI, Akingbohungbe AE. Functional and numerical responses of Cheilomenes lunata (Fabricius) (Coleoptera: Coccinellidae) feeding on the cowpea aphid, Aphis craccivora Koch (Homoptera: Aphididae). Insect Sci Appl. 1998;9: 543-546. Doi: https://doi.org/10.1017/S1742758400011127Links ]

Pervez A. Functional and numerical responses of Propylea dissecta (Mulsant) (Col., Coccinellidae). J Appl Entomol. 2004;128(2):140-146. Doi: http://doi:10.1111/j.1439-0418.2004.00824.xLinks ]

Pervez A, Omkar. Functional responses ofcoccinellid predators: an illustration of logistic approach. J Insect Sci. 2005;5:1-6. Doi: https://dx.doi.org/10.1093%2Fjis%2F5.1.5Links ]

Rodrigues ARS, Spindola AF, Torres JB, Siqueira HAA, Colares F. Response of different populations of seven lady beetle species to lambda-cyhalothrin with record of resistance. Ecotoxicol Environ Saf. 2013;96:53-60. Doi: http://doi:10.1016/j.ecoenv.2013.06.014Links ]

Saleh A, Ghabeish I, Al-Zyoud F, Ateyyat M, Swais M. Functional response of the predator Hippodamia variegata (Goeze) (Coleoptera: Coccinellidae) feeding on the aphid Brachycaudus helichrysi (Kaltenbach) infesting chrysanthemum in the laboratory. Jordan J Biol Sci. 2010;3(1):17-20. [ Links ]

Sarmento RA, Pallini A, Venzon M, Souza OFF, Molina-Rugama AJ, Oliveira CL. Functional response of the predator Eriopis connexa (Coleoptera: Coccinellidae) to different prey types. Braz Arch Biol Technol. 2007;50(1):121-126. Doi: http://dx.doi.org/10.1590/S1516-89132007000100014Links ]

Solomon ME. Population dynamics. Londres: Edward Arnold Study; 1969. p. 18-59. [ Links ]

Torres JB, Rodrigues ARS, Barros EM, Santos DS. Lambda-Cyhalothrin Resistance in the Lady Beetle Eriopis connexa (Coleoptera: Coccinellidae) Confers Tolerance to Other Pyrethroids. J Econ Entomol. 2015;108(1):60-68. Doi: https://doi.org/10.1093/jee/tou035Links ]

Valente ECN, Trindade RCP, Broglio SMF, Duarte AG, Rodrigues VMR, Lima HMA, et al. Aspectos Biológicos de Aphis craccivora Koch (Hemiptera: Aphididae) em cultivares de feijão-caupi Vigna unguiculata (L.) WALP. Ciên Agr. 2014;12(1):17-20. Doi: http://dx.doi.org/10.28998/rca.v12i1.1072Links ]

Van Lenteren JC, Bakker K. Functional responses in invertebrates. Neth J Zool. 1976;26(2):567-572. [ Links ]

Vandenberg NJ. Coccinellidae latreille 1807. In: Arnett Junior RH, Thomas MC, Skelley PE, Frank JH, editors. American beetles, Polyphaga: Scarabaeoidea through Curculionoidea. Boca Raton: CRC Press; 2002. p. 371-389. [ Links ]

Veeravel R, Baskaran P. Functional and numerical responses of Coccinella transversalis and Cheilomenes sexmaculata Fabr. feeding on the melon aphid, Aphisgossypii Glover. Insect Sci Appl. 1997;17:335-339. [ Links ]

Venzon M, Lemos F, Sarmento RA, Rosado MC, Pallini A. Predação por coccinelídeos e crisopídeo influenciada pela teia de Tetranychus evansi. Pesq Agropec Bras. 2009;44(1):1086-1091. Doi: http://dx.doi.org/10.1590/S0100-204X2009000900003Links ]

Vieira GF, Bueno VHP, Auad AM. Resposta funcional de Scymnus (Pullus) argentinicus (Weise) (Coleoptera: Coccinellidae) a diferentes densidades do pulgão verde Schizaphis graminum (Rond.) (Homoptera: Aphididae). An Soc Entomol Bras. 1997;26(3):495-502. Doi: http://dx.doi.org/10.1590/S0301-80591997000300012Links ]

Weber DC, Lundgren JG. Assessing the trophic ecology of the Coccinellidae: their roles as predators and as prey. Biol Control. 2009;51:199-214. Doi: https://doi.org/10.1016/j.biocontrol.2009.05.013Links ]

Wiedenmann RN, Smith JW. Attributes of the natural enemies in ephemeral crop habitats. Biol Control. 1997;10(1):16-22. Doi: https://doi.org/10.1006/bcon.1997.0544Links ]

Associate Editor: Patricio Ponce.

Citation/Citar este artículo como: Santos DS, Trindade RCP, Torres JB, Lima MS, Santos LD, Batista FC. Predation of Brevicoryne brassicae and Aphis craccivora by Eriopis connexa depending on availability. Acta Biol Colomb. 2021;26(1):99-104. Doi: http://dx.doi.org/10.15446/abc.v26n1.83303

CONFLICT OF INTEREST The authors declare that there is no conflict of interest.

Received: November 01, 2019; Revised: March 09, 2020; Accepted: July 27, 2020

* For correspondence: djisonsilvestre@yahoo.com.br

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