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Biology and functional response of the predator, Dortus primarius (Distant) (Hemiptera: Miridae) preying on Frankliniella schultzei (Trybom) (Thysanoptera: Thripidae)



Dortus primarius (Distant) (Hemiptera: Miridae) is a general predator reported from the oriental region. This bug is naturally found in many crop ecosystems where it feeds on thrips, aphids, insect eggs and other soft-bodied insects. Although, the rearing protocol of this predatory mirid has been developed, the efficiency of this predator as a biocontrol agent is limited and needs to be investigated. The thrips, Frankliniella schultzei (Trybom) (Thysanoptera: Thripidae), is a polyphagous pest that attacks many crops in polyhouse in India. Therefore, in the present study, biology and functional response of this predator to different densities of F. schultzei larvae in the laboratory was investigated.


The mirid predator was able to develop from egg to adulthood on tomato infested plant with F. schultzei larvae in 23–24 days with 15 and 11.76% mortality of 4th and 5th instar nymphs, respectively. Both 5th instar and female adults exhibited a type III functional response. At highest prey density (40) both 5th instar and female adults consumed 21.6 and 28.6 thrips larvae per day, respectively. Functional response parameters, viz. attack rate, handling time, a/Th and T/Th showed the potency of this predator against F. schultzei.


Based on the high fecundity, predation rate and density dependent behaviour, it is predicted that D. primarius might be an efficient and potential predator. However, further research is needed to assess its release rate and other ecological studies in the field situation.


Dortus primarius (Distant) (Hemiptera: Miridae) belonging to subfamily Deraeocorinae is considered to prey upon various arthropods such as thrips, aphids, and other soft-bodied insects in okra, cauliflower, maize, brinjal and cucurbits crops (Wheeler 2001). This predator is reported from the oriental region and has not explored for its biocontrol potential yet.

The common blossom thrips or tomato thrips, Frankliniella schultzei (Trybom) (Thysanoptera: Thripidae), is a pest of various economically important vegetable crops and ornamental plants covering 55 families worldwide (Milne et al. 1996). Both larvae and adults of F. schultzei feed on flowers, fruits, pollen, tender leaves resulting in discolouration and necrotic spots, dark dotted blemishes in fruits and stunted growth of the plant. It is also a vector of several viral diseases in many crops like tomato, groundnut and tobacco (Klose et al. 1996). In India, many crops such as tomato, tobacco, cotton, grain legumes, groundnuts and lettuce are attacked and damaged by this pest (Kakkar et al. 2010).

Biological control is an ecofriendly approach which is safer to environment, non-target organisms and pollinators. Success in biological control depends on biological and behavioural studies to understand the potency and the efficiency of any predator to further exploit it for management of insect pests. The functional response determines the efficiency of the predator and describes the rate at which a predator kills its prey at different prey densities (Murdoch and Oaten 1975). This is one of the key components to assess the efficacy of biocontrol agent (Lester and Harmsen 2002) and to understand predator prey interactions. Holling (1959) defined 3 types of functional responses for insects. In type I, graph shows linear relation between the number of prey killed and the prey density, type II explains that the rate of prey consumption increases with increasing pest density and eventually reaches to the predator’s satiation point and type III exhibits a sigmoid relationship between the number of prey eaten and the number of prey offered. Functional response and developmental studies have been conducted for other mirid bugs, although this information is lacking for D. primarius and knowledge of these parameters would certainly determine the efficiency and potential of this predator against F. schultzei.

Therefore, the present study presents for the first time the life history, predation rate and functional response of D. primarius to varying densities of F. schultzei larvae. This information will provide key information to formulate and implement strategies for the biological control of F. schultzei.


Insect cultures

Individuals of F. schultzei were collected from a capsicum field, Bangalore, India, and reared in the laboratory on insecticide free bean pods. Dortus primarius was reared in laboratory on bean pods (ovipositional substrate) and provided with UV irradiated Corcyra cephalonica (Stainton) eggs as prey (Varshney et al. 2018). Both cultures were maintained at 26 ± 2 °C, 65 ± 2% relative humidity with a photoperiod of 12:12 (L:D). Larval stage of thrips was used in the experiment.

Determination of biology

Four adult pairs of D. primarius (4 days old) were released in methacrylate cages (40 × 40 × 40 cm) with 4 tomato plants (3–4 leaf stage). They were provided either irradiated C. cephalonica eggs or larvae of F. schultzei as food ad libitum on every alternate day. Plants were checked for egg laying on each day. When egg laying was observed, plant parts bearing eggs were cut off and kept in plastic box (60 mm diameter) lined with filter paper. Once eggs are hatched, newly emerged nymphs were transferred to individual plastic box to observe developmental stages and time. Each Petri dish containing tomato leaflet and either larvae of F. schultzei or C. cephalonica eggs were offered to each nymph. Each instar of predator was provided with a constant number of eggs or thrips larvae (always higher than their daily requirement) according to the developmental stage of the predator. Developmental period (indicated by the presence of exuviae) and survival of nymph until the adult stage were recorded daily. Food and leaflets were changed daily. After adult emergence, one pair of adults was exposed to a tomato plant and provided with either larvae of F. schultzei or C. cephalonica eggs for recording the pre-oviposition period, fecundity and per cent hatching. For each prey 20 replicates were maintained. The entire experimental set up was kept at 26 ± 2 °C, 65 ± 2% RH with a photoperiod of 12:12 (L:D) in a climatic chamber.

Determination of functional response

Young female and/or 5th instar nymph of D. primarius was exposed to different densities of F. schultzei larvae. One complete generation of this predator was maintained on F. schultzei larvae to acclimatize them under laboratory conditions before initiating the experiments. Prior to the functional response study, each female adult and/or 5th instar nymph of the predator, was kept starved for 24 h. The experimental arena had a tissue paper at the base on which a tomato leaflet was kept in a small-ventilated round plastic box (13.0 cm diameter and 4.0 cm height). Based on preliminary tests, the 8 densities (1, 3,6,9,15,18, 30 and 40/leaf arena) of F. schultzei were presented to each female and nymph of mirid bug. Larvae of thrips were transferred on the leaf arena gently using a fine paint brush. The plastic boxes were held in an incubator (26 ± 2 °C, 65 ± 10% RH, 12L:12D photoperiod). The experimental units were examined after 24 h to record the number of thrips larvae survived after removing the predator. For each prey density, 6 replications were maintained. Thrips larvae consumed by the predator in each replication were not replaced during the experimental periods.

Statistical analyses

Data on biology were not normally distributed and thus analysed by performing Mann–Whitney U test. The shape of the curve was determined by polynomial logistic regression of the proportion of prey consumed as a function of the initial prey density (Trexler et al. 1988; Juliano 2001). Here, the logistic regression is appropriate because of the dichotomus nature thrips consumed or not) of dependent variable and the errors associated with such a variable are likely to be distributed binomially (Trexler and Travis 1993; Queiroz et al. 2015). To fit the data, the polynomial function from Juliano (2001) was used:

$$\frac{{N_{e} }}{{N_{o} }} = \frac{{\exp \left( {P_{0} + P_{1} N_{o} + P_{2} N_{o}^{2} + P_{3} N_{o}^{3} } \right)}}{{\left( {1 + \exp \left( {P_{0} + P_{1} N_{o} + P_{2} N_{o}^{2} + P_{3} N_{o}^{3} } \right)} \right)}}$$

where Ne is the number of preys consumed, No is the initial prey number available and P0, P1, P2 and P3 are the intercept, linear, quadratic and cubic coefficients, respectively, estimated using the method of maximum likelihood (Pervez and Omkar 2005). Linear terms (P1) if not differ significantly from zero indicate a type I response. Significant negative or positive linear coefficients (i.e. P1) from regression indicate type II or type III response, respectively (Juliano 2001).

In order to identify which functional response model better suits the data, Akaike information criterion i.e. AIC was used. The maximum likelihood approach was used to obtain parameter estimates of Holling’s type II, Roger’s random predator equation and Hassell’s type III response (Hassell 1977). Therefore, 4 different functional response models were fitted using R package frair and maximum likelihood estimate of parameters were obtained.

Based on AIC value the analysis to type III response was restricted. For modelling of type III functional response with prey depletion following equation suggested by Hassell (1978); Juliano (2001) was used.

$$N_{e} = \frac{{{\text{N}}_{{\text{o}}} \left\{ {1 - \exp [(d + bN_{o} )(T_{h} N_{e} - T)]} \right\}}}{{\left( {1 + cN_{o} } \right)}}$$

where T is the total time available for search (24 h), Ne is the number of preys consumed, No is the initial prey number available, Th is the prey-handling time and b, c and d are constants to be estimated for type III response. The number of preys eaten (Ne) follow the same relationship defined for the Roger’s Type-II response, however the attack rate (a) is assumed to vary with initial prey density in the following hyperbolic relationship:

$$a = \frac{{d + bN_{o} }}{{1 + cN_{o} }}$$
$$a = \frac{{bN_{o} }}{{1 + cN_{o} }}$$

where ‘d’ is non-significantly different from 0, so it was removed. Predator’s attack rate per handling time (a/Th) (indicates the effectiveness of predation) and the maximum predation rate (T/Th) were also calculated (Rahman et al. 2012).


Biology of D. primarius

In the biology trials, D. primarius adults could successfully complete its life cycle on both C. cephalonica eggs and F. schultzei nymphs. Nymphs of D. primarius hatched 7.9 days after oviposition. Nymphal duration was significantly lower on C. cephalonica eggs (15.2 ± 0.26 days) than on F. schultzei larvae (16.4 ± 0.23) (Mann-Whitney U test: U = 96.0; P = 0.004) (Table 1). Male longevity (15.95 ± 0.64 days) (Mann-Whitney U test: U = 112.0; P = 0.017), female longevity (21.6 ± 0.47 days) (Mann-Whitney U test: U = 96.0; P = 0.004) and per cent adult emergence (77.7 ± 1.22) (Mann-Whitney U test: U = 112.0; P = 0.017) were significantly higher on F. schultzei larvae than on C. cephalonica eggs (Table 1). During nymphal development, 5 and 10.52% mortality rate was observed in 3rd and 5th instar nymphs of D. primarius, respectively, when reared on C. cephalonica eggs. Similarly, when reared on F. schultzei larvae, 15 and 11.76% mortality rate was observed in 4th and 5th instar nymph of the predator.

Table 1 Biology of Dortus primarius on tomato plant fed with Corcyra cephalonica eggs and Frankliniella schultzei larvae. In row means with different letters are significantly different with each other (Mann- Whitney U test; P < 0.05)

Functional response

The four functional response model fits were compared and Hassell’s type III model exhibited lower AIC value for both 5th instar and adult (Table 2). Significantly positive linear terms and negative quadratic terms detected from logistic regression analyses for both 5th instar and female predator revealed type III functional response, which is positively density dependent (Fig. 1a, b; Table 3). In the present study, predation increased after density value 6, with upper processing limit of 21.3 thrips per 24 h in 5th instar nymph and with a maximum limit of 28.6 thrips per 24 h in case of a female predator.

Table 2 Functional response: Akaike Information Criterion (AIC) of four functional response models fitted for 5th-instar nymph and adult female of Dortus primarius when fed on Frankliniella schultzei larvae
Fig. 1
figure 1

a Functional response of fifth instar of Dortus primarius at different prey density of Frankliniella schultzei larvae during a 24 h period. b Functional response of adult female of Dortus primarius at different prey density of Frankliniella schultzei larvae during a 24 h period

Table 3 Maximum likelihood estimates for parameters of the logistic model fit to proportion of F. schultzei larvae consumed by D. primarius versus initial prey density at 26 ± 2 °C

The functional response parameters of 5th instar and adult over a 24 h period were estimated using Eq. (2). The handling time (Th) as estimated by Eq. (2) for 5th instar was lower than adult, although there was non-significant difference in handling time between these two stages (Table 4). Attack rate for both stages was also determined using a reduced model (Eq. (4)) and nonlinear least square regression indicated non-significance of ‘d’ parameter; therefore, it was removed from the model. The estimated attack rates of 5th instar varied from 0.14 to 1.33. Similarly, for adult, attack rate varied from 0.21 to 2.73, at prey density from 1 to 40. The value of a/Th for 5th instar was 8.54, 21.8, 35.9, 45.6, 58.2, 62.5, 73.5 and 78.6, and was 9.75, 26.4, 45.9, 61.0, 82.8, 90.9, 112.9 and 124.3 for female at density varied from 1 to 40. Maximum theoretical predation rate was higher in 5th instar than in adult (Table 4).

Table 4 Coefficient of attack rate (a) and handling time (Th) and other derived parameters for 5th instar and female of D. primarius


It seems, this is the first study to investigate the biological parameters and functional response of D. primarius on F. schultzei. In this study, a detailed analysis of various biological parameters of D. primarius preying upon thrips larvae and of the factitious prey C. cephalonica eggs on tomato plants was explored. In present study, nymphal development period of D. primarius preying on C. cephalonica eggs (15.2 days) was more than 2 days longer than that reported for Nesidiocoris tenuis (Reuter) (12.9 days) (Sanchez et al. 2009) and for Macrolophus pygmaeus (Rambur) (13.68 days) (Perdikis and Lykouressis 2000). However, obtained results corroborate with the findings of Molla´et al. (2014) who reported 15.36 days nymphal development period of M. pygmaeus when fed on Ephestia kuehniella (Zeller) eggs. In the present study, nymphal development period was shorter on C. cephalonica eggs than on F. schultzei larvae. There are many reports on predatory mirids where, rapid development was observed when fed on E. kuehniella eggs compared to natural preys such as Myzus persicae (Sulzer), Trialeurodes vaporariorum Westwood and Tetranychus urticae Koch; (Tedeschi et al., 1999). It may be due to high nutritional quality of Lepidoptera eggs. Similarly, Kiman & Yeargan (1985) found that Orius insidiosus (Say) had a shorter developmental period (13.4 days) when fed on Heliothis virescens (Fabricius) eggs than when fed on Neohydatothrips variabilis (Beach) (= Sericothrips variabilis (Beach)) (15.8 days). Male and female longevity of D. primarius were higher on F. schultzei larvae than on C. cephalonica eggs. The nutrition quality of host plant of prey may indirectly influences the survival, fitness and predation of the predators on these preys (Kumari et al., 2021). Studies revealed that anthocorid bugs, Orius laevigatus (Fieber) and O. majusculus (Reuter) fed on Frankliniella occidentalis (Pergande), nymphs lived longer (45.1 and 46.1, respectively) (Riudavets, 1995).

The overall number of F. schultzei larvae consumed by the nymphal instars of D. primarius was 196–210. Obtained findings indicate that D. primarius can complete its life cycle and reproduce when fed on F. schultzei larvae.

It is evident from the functional response study that D. primarius can consume 22–28 thrips /day. Functional response parameters (attack rate and handling time) indicated the voracity of both stages of this predator. In the present study, 5th instar and adult female exhibited type III functional response with a density dependant predation at low and medium densities. Type III response was also observed in M. caliginosus at varying density of T. vaporariorum (Hamdan 2006); Nesidiocoris tenuis against Bemisia tabaci (Gennadius) pupae at 35 °C (Madbouni et al. 2017); Macrolophus basicornis (Stal) and Engytatus varians (Distant) at varying density of Tuta absoluta (Meyrick) eggs (Van Lenteren, et al. 2016). Type III response is associated with learning behaviour and earlier it was considered to be characteristic of vertebrate predators (Holling 1959). Later, Van Lenteren and Bakker (1978) reported this behaviour in invertebrate predators and parasitoids. Several studies indicated a type II response for most of the mirid bug (Montserrat et al. 2000; Fantinou et al. 2008, 2009; Alvarado et al. 1997; Maselou et al. 2014, 2015; Madbouni et al. 2017; Ingegno et al. 2019). Natural enemies exhibiting type III response could be considered as an efficient biocontrol agent to manage the prey population (Fernández-Arhex and Corley 2003). Types of response depend on various factors, viz. prey species, size (Streams 1994), predator’s hunger level, size, stage (Varshney et al. 2018), temperature and other abiotic factors (Madbouni et al. 2017), experimental arena (Hemerik and Yano 2011); types of analysis used for assessment of functional response (Van Lenteren et al. 2016). In the present study, lower handling time (Th) and higher theoretical predation rate (T/Th) were observed for 5th instar larvae. This could be attributed to their greater requirements for food and energy to grow and attain the adulthood (Hodek and Honek, 1996). The estimation of the predation effectiveness (a/Th) can be useful for determining the possibility of the optimal ratio between predator and target pest for inoculative release (Wang et al. 2019).

In predatory/zoophytophagous, mirid bug most of the studies are restricted to dicyphine bugs. This study improves the insight into the biology, predation rate and ability of D. primarius to reduce thrips population. Functional response studies are important to understand predator prey interaction and efficiency of new predator to reduce prey population at different density. For 5th instar and adult, the percentage prey killed increased up to density of 18 and then over this range the response was stabilized. Thus, it can be inferred that these two stages of predator are efficient to bring down the thrips population in a prey density range of upto 18 thrips /leaflet. Thus, there is a necessity to explore and develop suitable control strategies either through augmentation or conservation of this predator to manage F. schultzei.

This study was conducted in the laboratory and limited to a small arena unlike natural conditions where many factors may influence functional response parameters like characteristics of host plants (De Clercq et al. 2000), light intensity, spatial complexity (Zamani et al. 2006) and intraguild predation (Finke and Denno 2005).


The study dealt with biology and the potential of D. primarius as biocontrol agent of F. schultzei. However, this predator has not been extensively explored. Hence, further studies are warranted to evaluate its establishment, survival, prey switching behaviour, prey preference and interaction with other predators in a natural ecosystem to understand their ecology and to incorporate this predator in a biocontrol program. In natural ecosystems, predators have overlapping niches and thus predator-predator interaction also needs to be studied along with the functional response. Abundance and scarcity of prey influence conspecific and heterospecific interactions of predator and may hinder biocontrol program.

Availability of data and materials

The datasets used and/or analysed during the current study are available from the corresponding author on reasonable request.


N e :

The number of preys consumed

N o :

The initial prey number available

T :

Total time available for search (24 h)

T h :

Prey-handling time

a :

Attack rate

a/Th :

Predator’s attack rate per handling time

T/T h :

Maximum predation rate


  • Alvarado P, Baltà O, Alomar O (1997) Efficiency of four Heteroptera as predators of Aphis gossypii and Macrosiphum euphorbiae (Hom.: Aphididae). Entomophaga 42:215–226.

    Article  Google Scholar 

  • De Clercq P, Mohaghegh J, Tirry L (2000) Effect of host plant on the functional response of the predator Podisus nigrispinus (Heteroptera Pentatomidae). Biol Cont 18:65–70

    Article  Google Scholar 

  • Fantinou AA, Perdikis DC, Maselou DA, Lambropoulos PD (2008) Prey killing without consumption: does Macrolophus pygmaeus show adaptive foraging behavior? Biol. Cont 47:187–193

    Google Scholar 

  • Fantinou AA, Perdikis DC, Maselou DA, Lambropoulos PD (2009) Preference and consumption of Macrolophus pygmaeus preying on mixed instar assemblages of Myzus persicae. Biol Cont 51:76–80

    Article  Google Scholar 

  • Fernández-Arhex V, Corley JC (2003) The functional response of parasitoids and its implications for biological control. Biocontrol Sci Technol 13:403–413.

    Article  Google Scholar 

  • Finke DL, Denno RF (2005) Predator diversity and the functioning of ecosystems: the role of intraguild predation in dampening trophic cascades. Ecol Lett 8:1299–1306

    Article  Google Scholar 

  • Hamdan A-JS (2006) Functional and numerical responses of the predatory bug Macrolophus caliginosus Wagner fed on different densities of eggs of the greenhouse whitefly, Trialeurodes vaporariorum (Westwood). J Biol Res 6:147–154

    Google Scholar 

  • Hassell MP (1978) The dynamics of arthropod predator prey systems. Princeton University Press, Princeton

    Google Scholar 

  • Hassell M, Lawton J, Beddington J (1977) Sigmoid functional responses by invertebrate predators and parasitoids. J Anim Ecol 46:249–262

    Article  Google Scholar 

  • Hemerik L, Yano E (2011) Scaling up from individual behaviour of Orius sauteri foraging on Thrips palmi to its daily functional response. Popul Ecol 53:563–572

    Article  Google Scholar 

  • Hodek I, Honek A (1996) Ecology of Coccinellidae. Kluwer Academic Publishers, Dordrecht, Boston, London, p 464

    Book  Google Scholar 

  • Holling CS (1959) Some characteristics of simple types of predation and parasitism. Can Entomol 91:385–398

    Article  Google Scholar 

  • Ingegno BL, Messelink GJ, Bodino N, Iliadou A, Driss L, Woelke JB, Leman A, Tavella L (2019) Functional response of the mirid predators Dicyphus bolivari and Dicyphus errans and their efficacy as biological control agents of Tuta absoluta on tomato. J Pest Sci 92:1457–1466.

    Article  Google Scholar 

  • Juliano SA (2001) Non-linear curve fitting: predation and functional response curves. In: Scheiner SM, Gurevitch J (eds) Design and analysis of ecological Experiments, 2nd edn. Chapman and Hall, New York, USA, pp 178–196

    Google Scholar 

  • Kakkar G, Seal DR, Kumar V (2010) Common blossom thrips scientific name: Frankliniella schultzei Trybom (Insecta: Thysanoptera: Thripidae), Accessed on 20 Oct 2021)

  • Kiman ZB, Yeargan KV (1985) Development and reproduction of the predator Orius insidiosus (Hemiptera, Anthocoridae) reared on diets of selected plant material and arthropod prey. Ann Entomol Soc Am 78(4):464–467

    Article  Google Scholar 

  • Klose MJ, Sdoodee R, Teakle DS, Milne JR, Walter GRS, GH, (1996) Transmission of three strains of Tobacco streak ilar virus by different thrips species using virus-infected pollen. J Phytopathol 144:281–284

    Article  Google Scholar 

  • Kumari D, Verma SC, Sharma PL, Gaikwad MB (2021) Biology, predatory potential and functional response of Mallada desjardinsi (Navas) on melon aphid, Aphis gossypii glover. Int J Trop Insect Sci 41:495–501

    Article  Google Scholar 

  • Lester PJ, Harmsen S (2002) Functional and numerical responses do not always indicate the most effective predator for biological control: an analysis of two predators in a two-prey system. J Appl Ecol 39:455–468

    Article  Google Scholar 

  • Madbouni MAZ, Samih MA, Namvar P, Biondi A (2017) Temperature-dependent functional response of Nesidiocoris tenuis (Hemiptera: Miridae) to different densities of pupae of cotton whitefly, Bemisia tabaci (Hemiptera: Aleyrodidae). Eur J Entomol 114:325–331.

    Article  Google Scholar 

  • Maselou DA, Perdikis DC, Fantinou A (2015) Effect of hunger level on prey consumption and functional response of the predator Macrolophus pygmaeus. Bull Insectol 68:211–218

    Google Scholar 

  • Maselou DA, Perdikis DC, Sabelis MW, Fantinou AA (2014) Use of plant resources by an omnivorous predator and the consequences, for effective predation. Biol Control 79:92–100.

    Article  Google Scholar 

  • Milne JR, Jhumlekhasing M, Walter GH (1996) Understanding host plant relationships of polyphagous flower thrips, a case study of Frankliniella schultzei (Trybom), In: Goodwin S, Gillespie P (eds) Proceedings of the 1995 Australia and New Zealand Thrips Workshop: methods, biology, ecology and management, NSW Agriculture, Gosford, Australia, pp 8–14

  • Molla´ O, Biondi A, Alonso-Valiente M, Urbaneja A, (2014) A comparative life history study of two mirid bugs preying on Tuta absoluta and Ephestia kuehniella eggs on tomato crops: implications for biological control. Biocontrol 59:175–183

    Article  Google Scholar 

  • Montserrat M, Albajes R, Castane C (2000) Functional response of four heteropteran predators preying on greenhouse whitefly (Homoptera: Aleyrodidae) and western flower thrips (Thysanoptera: Thripidae). Environ Entomol 29:1075–1082

    Article  Google Scholar 

  • Murdoch WW, Oaten A (1975) Predation and population stability. Adv Ecol Res 9:2–131

    Google Scholar 

  • Perdikis D, Lykouressis DP (2000) Effects of various items, host plants and temperatures on the development and survival of Macrolophus pygmaeus Rambur (Hemiptera: Miridae). Biol Control 17:55–60

    Article  Google Scholar 

  • Pervez A, Omkar, (2005) Functional responses of coccinellid predators: an illustration of a logistic approach. J Insect Sci 5:319–325

    Article  Google Scholar 

  • Queiroz OS, Ramos RS, Gontijo LM, Picanco MC (2015) Functional response of three species of predatory pirate bugs attacking eggs of Tuta absoluta (Lepidoptera: Gelechiidae). Environ Entomol 44:246–251

    Article  Google Scholar 

  • Rahman VJ, Babu A, Roobakkumar A, Perumalsamy K (2012) Functional and numerical responses of the predatory mite, Neoseiulus longispinosus, to the red spider mite, Oligonychus coffeae, infesting tea. J Insect Sci 12:125

    Article  Google Scholar 

  • Riudavets J (1995) Predators of Frankliniella occidentalis (Perg.) and Thrips tabaci Lind.: a review. Wageningen Agric Univ Papers 95(1):43–87

    Google Scholar 

  • Sanchez JA, Lacasa A, Arno J, Castan˜e C, Alomar O, (2009) Life history parameters for Nesidiocoris tenuis (Reuter) (Het., Miridae) under different temperature regimes. J Appl Entomol 133:125–132

    Article  Google Scholar 

  • Streams F (1994) Effect of prey size on attack components of the functional response by Notonecta undulata. Oecologia 98:57–63

    CAS  Article  Google Scholar 

  • Tedeschi R, De Clercq P, Van de Veire M, Tirry L (1999) Development and predation of Macrolophus caliginosus (Heteroptera: Miridae) on different prey. Med Fac Landbouw Univ Gent 64:235–240

    Google Scholar 

  • Trexler JC, Travis J (1993) Nontraditional regression analysis. Ecology 74:1629–1637

    Article  Google Scholar 

  • Trexler JC, McCulloch CE, Travis J (1988) How can the functional response best be determined? Oecologia 76:206–214

    Article  Google Scholar 

  • Van Lenteren JH, Hemerik L, Lins JC Jr, Bueno VHP (2016) Functional responses of three neotropical mirid predators to eggs of Tuta absoluta on tomato. Insects 7:34.

    Article  PubMed Central  Google Scholar 

  • Van Lenteren JC, Bakker K (1978) Behavioral aspects of the functional response of a parasite (Pseudeucoila bochei Weld) to its host (Drosophila melanogaster). Neth J Zool 28:213–233

    Article  Google Scholar 

  • Varshney R, Budhlakoti N, Ballal CR (2018) Functional response of Geocoris ochropterus Fieber (Hemiptera: Geocoridae) to different egg densities of Helicoverpa armigera (Hübner). Phytoparasitica 46:451–458

    CAS  Article  Google Scholar 

  • Wang S, Di N, Chen Xu, Zhang F, Biondi A, Desneuz N, Wang Su (2019) Life history and functional response to prey density of the flower bug Orius sauteri attacking the fungivorous sciarid fly Lycoriella pleuroti. J Pest Sci 92:715–722.

    Article  Google Scholar 

  • Wheeler AG (2001) Biology of the plant bugs (Hemiptera: Miridae): pests, predators, opportunists. Cornell University Press, New York

    Google Scholar 

  • Zamani AA, Talebi AA, Fathipour Y, Baniameri V (2006) Temperature-dependent functional response of two aphid parasitoids, Aphidius colemani and Aphidius matricariae (Hymenoptera: Aphidiidae), on the cotton aphid. J Pest Sci 79:183–188

    Article  Google Scholar 

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The authors are grateful to Indian Council of Agricultural Research, New Delhi, India, and Director, ICAR−NBAIR Bengaluru, India, for providing research facilities and encouragement. We are also thankful to Mrs. Usha Ravikumar for technical assistance.


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RV conceived the study. RV performed experiments and analysed the biology data. NB conducted functional response analysis. RV wrote the manuscript. Both the authors read and approved the manuscript.

Corresponding author

Correspondence to Richa Varshney.

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Varshney, R., Budhlakoti, N. Biology and functional response of the predator, Dortus primarius (Distant) (Hemiptera: Miridae) preying on Frankliniella schultzei (Trybom) (Thysanoptera: Thripidae). Egypt J Biol Pest Control 32, 31 (2022).

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  • Dortus primarius
  • Frankliniella schultzei
  • Functional response
  • Developmental period