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Insecticidal effects of an encapsulated formulation of lambda-cyhalothrin on the southern green stinkbug Nezara viridula (L.) and one of its predators, Podisus maculiventris (Say), were investigated in the laboratory. Both pentatomids were exposed to the insecticide via contaminated drinking water and by residual contact. Nymphs and adults of N. viridula were more susceptible to the insecticide than nymphs of P. maculiventris, both by ingestion and contact exposure. For the respective ways of exposure, LC50 values calculated for P. maculiventrisfourth instars were 30-190 times and 3-13 times higher than those of N. viridulafourth instars. Insecticidal activity of the pyrethroid by ingestion was 6-10 times greater against nymphs of N. viridula than against adults of the pest. In both the ingestion and residual contact experiments, nymphs of P. maculiventris recovered from initial knockdown. LC50 values for predator nymphs increased 1.7- to 2.7-fold between 24 and 48 h after the start of the experiment. Recovery from knockdown was not observed in N. viridula. The data from the current laboratory study suggest that encapsulated lambda-cyhalothrin may be effective for controlling the southern green stinkbug with little adverse effects on the predator P. maculiventris, but field experiments are needed to confirm this. Possible reasons for the differential toxicity of the insecticide to both pentatomids are discussed.

The southern green stinkbug, Nezara viridula (L.), is a highly polyphagous pest that is widely distributed in the tropical and subtropical regions of the world (Todd 1989; Panizzi et al. 2000). This pentatomid causes important economic damage to various field crops, including soybean, beans, rice, corn, cotton and tobacco. In Europe, it has been found increasingly in greenhouses, where it attacks vegetable crops like tomato, sweet pepper, and eggplant. Control of this pest is based largely on the intensive use of chemical pesticides, including carbamates, organophosphates and some pyrethroids (Jackai et al. 1990; Ballanger & Jouffret 1997; Panizzi et al. 2000). For instance, in Brazil it was estimated that in the mid 1990s over 4 million liters of insecticides were used annually to control stinkbugs in soybean (Corrêa-Ferreira & Moscardi 1996). Such massive use of insecticides not only increases production cost, it may also affect populations of beneficial insects and trigger pest resurgence problems.

In several regions, efforts have been made to develop integrated pest management (IPM) programs against N. viridula (Panizzi et al. 2000). Biological control of the pest has focused mainly on the potential of parasitoids (Jones 1988). Releases of the scelionid egg parasitoid Trissolcus basalis (Wollaston) have successfully suppressed outbreaks of the southern green stinkbug in soybean (Corrêa-Ferreira & Moscardi 1996). Several arthropod predators also have an important impact on N. viridula populations. De Clercq et al. (2002) reported high predation rates by nymphs and adults of the predatory pentatomid Podisus maculiventris (Say) on the different life stages of the southern green stinkbug. This generalist predator is native to North America where it is commonly found in a variety of natural and agricultural ecosystems (De Clercq 2000). Although it appears to have a preference for larvae of lepidopterous and coleopterous insects, the predator frequently has been found in association with N. viridula in the southern United States (Drake 1920; Ragsdale et al. 1981; Stam et al. 1987). Podisus maculiventrishas been used in European greenhouses since 1997 for augmentative biological control of caterpillar outbreaks, and predation on N. viridula may be an additional asset here for this beneficial insect (De Clercq et al. 2002).

In France, Ballanger & Jouffret (1997) reported effective control of N. viridula in soybean with foliar sprays of lambda-cyhalothrin. This contact and stomach insecticide belonging to the pyrethroid group has been used against a broad spectrum of pests in a variety of crops (Anonymous 2000). In 1999, a micro-encapsulated formulation (Zeon Technology™) of this pyrethroid was commercialised, offering reduced health hazards and an improved environmental profile (Ham 1999; Anonymous 2000). In the current study, insecticidal activity of an encapsulated formulation of lambda-cyhalothrin to N. viridula and its predator P. maculiventris was assessed in the laboratory. Both pentatomids were exposed to the insecticide via ingestion and residual contact. The implications of our findings for the control of the southern green stinkbug and the use of the predator P. maculiventrisin IPM programs targeted against this and other agricultural pests are discussed.

Materials and Methods

Insect Cultures

A laboratory colony of N. viridula was established in 1999 with insects originating from field collections in France, Spain and Italy. Stinkbugs were fed on green bean pods (Phaseolus vulgaris L.) and sunflower seeds (Helianthus annuus L.). A culture of P. maculiventris was started in 1999 with specimens originating from a field collection in 1996 near Beltsville, Maryland, USA. The predators were fed mainly larvae of the greater wax moth, Galleria mellonella L. Colonies of all insects were maintained in growth chambers at 23 ± 1°C, 75 ± 5% RH and a 16:8 h light:dark photoperiod.


A commercial formulation of micro-encapsulated lambda-cyhalothrin (Karate Zeon®, 100 g/l) was obtained from Syngenta, Ruisbroek, Belgium.

Toxicity Bioassays

Exposure via ingestion.In these experiments, nymphs and adults of N. viridulaand nymphs of P. maculiventris were exposed to insecticide through treated drinking water. Both pentatomids take up moisture in the absence of food and are regularly seen drinking even when food is available. Moisture can be supplied via plant materials, like green beans, but can also be provided as free water. Using gravimetric methods, we estimated that unfed newly molted fourth instars of P. maculiventrisand N. viridula take up about 2 and 4.5 μl of free water, respectively, during a 24-h period.

Newly molted fourth instars and reproductively active adult female N. viridula were randomly collected from stock cultures and transferred to plastic petri dishes (9 cm diam) lined with absorbent paper. A replicate consisted of four insects in a dish for N. viridulanymphs, whereas adults were placed singly in dishes. Newly molted fourth instars of P. maculiventriswere placed in petri dishes (9 cm diam) in groups of three. Each dish was supplied with a moisture source, consisting of a paper plug fitted into a plastic dish (2.5 cm diam). The paper plug was saturated with 2 ml of the insecticide in tap water. Control groups were supplied with tap water alone. At least 20 nymphs or 10 adults were tested with each of at least 10 concentrations. Choice of concentrations was based on preliminary range-finding tests. Test concentrations ranged from 0 to 200 mg a.i./l (11 concentrations) and from 0 to 100 mg a.i./l (10 concentrations) for N. viridulanymphs and adults, respectively, and from 0 to 800 mg a.i./l (13 concentrations) for P. maculiventrisnymphs. Both pentatomids were exposed to the contaminated moisture source during a 1-wk period. To stimulate drinking behavior, the insects were not provided with food during the first 24 h. From the second day on, nymphs and adults of N. viridula were supplied with sunflower seeds as needed; predator nymphs were fed greater wax moth larvae ad libitum.

In range-finding tests, the ability of P. maculiventrisin particular to recover from initial poisoning became apparent. Therefore, mortality counts were performed 1, 2, and 7 d after the initial treatment. Mortality percentages included dead and affected individuals. Insects were scored as affected when they were incapable of coordinated movement upon prodding with a fine brush.

Residual exposure.To evaluate residual contact activity of lambda-cyhalothrin, fourth instars of both pentatomids were exposed by tarsal contact to dry residues on filter paper. Whatman No. 41 filter papers were fitted into petri dishes (9 cm diam) and the dishes were sprayed in a Cornelis spray chamber (Van Laecke & Degheele 1993). Each dish was sprayed with 2 ml of insecticide suspension in water, yielding a homogeneous spray deposit on the filter paper of approximately 5 mg/cm2. For the controls, dishes were sprayed with 2 ml of water. The plates were left to dry for about 1 h before introducing the insects. A replicate consisted of a petri dish containing three P. maculiventris or four N. viridula nymphs. Twenty to 40 insects were tested per concentration, with a minimum of 10 concentrations. Concentrations were chosen on the basis of range-finding tests and ranged from 0 to 200 mg a.i./l (12 concentrations) for N. viridulanymphs and from 0 to 400 mg a.i./l (10 concentrations) for P. maculiventrisnymphs. To stimulate food searching by the nymphs and maximize contact with the treated surface, no food or moisture were provided during the first 24 h. From the second day on, the insects were supplied with water and food. Water was supplied via a soaked paper plug in a 2-cm-diam cup. Nymphs of P. maculiventris were given freshly killed wax moth larvae and those of N. viridulawere offered sunflower seeds. Mortality counts were made after 1, 2, and 7 d, allowing for the assessment of recovery after initial knockdown.

Data Analysis

Mortality of the test insects after 1, 2, and 7 d was corrected for control mortality by Abbott’s formula (Abbott 1925). Lethal concentration values and their 95% confidence limits were calculated from probit-regressions with POLO PC (LeOra Software 1987). All concentrations tested were used for LC-calculations; numbers (n) given in the footnotes of Table 1 and Table 2 thus reflect actual numbers of insects tested and used in probit-regressions.


In our laboratory setup, there was no indication of a repellent or antifeedant effect for encapsulated lambda-cyhalothrin. In ingestion assays, both P. maculiventrisand N. viridula were regularly observed to suck on moisture sources contaminated with varying concentrations of the compound. In the residual contact experiment, nymphs of both pentatomids were usually on the treated surfaces (filter paper, petri dish walls) and only occasionally on the untreated lid.

Nymphs and adults of N. viridula were more susceptible to the insecticide than nymphs of their predator P. maculiventris, both by ingestion (Table 1) and contact exposure (Table 2). For the respective routes of exposure, LC50 values calculated for P. maculiventrisfourth instars were 30-190 times and 3-13 times higher than those of N. viridulafourth instars. Further, insecticidal activity of the pyrethroid by ingestion was 6-10 times greater against nymphs of N. viridula than against adults of the pest. Lethal concentration values calculated for N. viridulanymphs were lower for ingestion exposure than for contact exposure, suggesting that lambda-cyhalothrin was more active by ingestion than by tarsal contact with dry residues. However, some of the nymphs in the ingestion bioassays were partially or fully in tarsal contact with the moist plug when drinking, so these insects may have been exposed to the insecticide both via ingestion and via contact with wet residues. Differences in biological activity due to exposure routes were less apparent in the predatory pentatomid P. maculiventris.

In both the ingestion and residual contact experiments, nymphs of P. maculiventris recovered from initial knockdown. LC50 values for predator nymphs increased 1.7- to 2.7-fold between 24 and 48 h after the start of the experiment. Recovered predators were able to attack prey and feed normally. Comparisons of the LC50 values for P. maculiventris fourth instars after 2 and 7 d, however, show that some of the individuals that appeared to have recovered after 2 d died before reaching the fifth stadium when they were continuously exposed to contaminated drinking water or filter paper during a 7 d period. At 23°C, optimally fed fourth instars of both pentatomids usually reach the next stadium in 4-5 d (De Clercq & Degheele 1992). There was little or no recovery from knockdown in N. viridula. Here, LC50 values after 1 and 2 d were generally similar and further decreased with exposure time. Likewise, slopes were equal after 1 and 2 d (χ2, P > 0.05), but were significantly increased after 7 d of exposure. Only in the ingestion study with adults, LC90 values suggest there may have been some recovery at the upper end.


In our experiment, both nymphs and adults of N. viridula were susceptible to encapsulated lambda-cyhalothrin. However, nymphs suffered about 5 times greater mortality when exposed by ingestion than by residual contact. For the control of N. viridula, the practical significance of ingestion exposure may be limited given that pyrethroids have no systemic properties. It is unlikely that the insect would ingest the compound in the field, except when it would drink from fresh spray deposits. Although lambda-cyhalothrin is widely recommended for the control of a broad range of insect pests, including stinkbugs, there are few studies reporting on the insecticidal effects of this pyrethroid on the southern green stinkbug. According to Ballanger & Jouffret (1997) and Gouge et al. (1999), the pest can be adequately controlled in soybean with non-encapsulated lambda-cyhalothrin at 20-30 g a.i./ha. In topical application experiments on third instars of N. viridula, Baptista et al. (1995) reported LD50 values of 0.82-0.25 μg/g for a technical grade formulation of lambda-cyhalothrin 3-24 h after treatment; the pyrethroid was 20-40 times more active against the pest than monocrotophos.

Susceptibility of the spined soldier bug, P. maculiventris, to classical and novel insecticides has been studied to some extent (see De Clercq 2000 for a review). Besides direct and residual contact, predatory pentatomids can be poisoned by drinking contaminated free water or plant sap (in case of systemic compounds) or by feeding on contaminated prey (De Clercq et al. 1995). In the current study, P. maculiventris was less vulnerable to lambda-cyhalothrin than N. viridula, both in the ingestion and contact exposure bioassays. Based on lethal concentration values, nymphs of the predator were somewhat more susceptible to the compound by residual contact than by ingestion. The LC50 value for fourth instars of P. maculiventrisexposed to lambda-cyhalothrin via ingestion was similar to that found in an earlier study for nymphs treated similarly with deltamethrin (158 mg a.i./l, Mohaghegh et al. 2000). In a number of studies, P. maculiventris and related asopines have demonstrated a better tolerance to pyrethroids than their lepidopterous prey (Yu 1988; Zanuncio et al. 1993; Picanço et al. 1996). Yu (1988) hypothesized that thickness and lipid content of the cuticle may affect the penetration rate of the lipophilic pyrethroids and may thus be responsible for differences in toxicity to the heavily sclerotized pentatomid predators and their soft-bodied caterpillar prey. The finding of Baptista et al. (1995) that lambda-cyhalothrin was 5-9 times more toxic to the velvetbean caterpillar, Anticarsia gemmatalis(Hübner) than to N. viridula supports this hypothesis. It may, however, not explain the differences found in our study because P. maculiventrisand N. viridula are both pentatomids with a similarly sclerotized cuticle. Different drinking rates explain only in part the observed differences in toxicity of lambda-cyhalothrin to the studied pentatomids by ingestion. Preliminary gravimetric tests indicated that unfed fourth instars of N. viridula ingested twice as much free water during a 24-h period than did those of P. maculiventris, despite similar body weights (approximately 12.5 mg). Alternatively, higher detoxification or excretion rates may be responsible for the lower susceptibility of P. maculiventris to lambda-cyhalothrin as compared to N. viridula. Pyrethroids are known to be metabolised in insects mainly by esterases and microsomal oxidases (Shono et al. 1979). Yu (1987, 1988) found, however, that these enzyme activities were generally lower in the spined soldier bug than in its caterpillar prey. Likewise, first tests have shown about 8-fold higher esterase activities in the phytophagous pentatomid N. viridula than in the predatory pentatomid P. maculiventris (unpublished data). Recently, it has been shown that glutathione S-tranferases also may play a significant role in detoxifying pyrethroids (e.g., Kostaropoulos et al. 2001). In this context, it is worth noting that Yu (1987) reported about 2-fold higher glutathione transferase activity toward CDNB in the spined soldier bug than in its lepidopterous prey. Further studies on the pharmacokinetics of lambda-cyhalothrin are warranted to explain the difference in toxicity of the compound to the studied pentatomids.

A number of field studies have demonstrated adverse effects of lambda-cyhalothrin on various beneficial arthropods, including predatory heteropterans, although in some cases negative effects on field populations of natural enemies were transient (Pilling & Kedwards 1996; Cole et al. 1997; van den Berg et al. 1998; Al-Deeb et al. 2001; Stewart et al. 2001). Encapsulation of broad-spectrum insecticides, including pyrethroids, is aimed at improving their selectivity and suitability for IPM programs (Scher et al. 1998; Ham 1999). However, several studies comparing encapsulated and non-encapsulated formulations of various insecticides have shown highly variable results with a range of beneficial arthropods (see Pogoda et al. 2001 for references). Pogoda et al. (2001) reported that a micro-encapsulated formulation of lambda-cyhalothrin was as toxic as an emulsifiable-concentrate formulation of the compound to the oriental fruit moth, Grapholita molesta (Busck). These workers also found that the encapsulated formulation of lambda-cyhalothrin was less toxic than the emulsifiable concentrate to a pyrethroid-resistant population of the phytoseiid mite Typhlodromus pyri Scheuten but more toxic to a pyrethroid-susceptible population of the predator.

The current laboratory trials indicate that encapsulated lambda-cyhalothrin has a good insecticidal activity against the southern green stinkbug and is relatively safe to the predatory stinkbug P. maculiventris. However, field studies are in place to test further the selectivity of this insecticide toward P. maculiventris. Further research also is needed to determine if the studied encapsulated formulation of lambda-cyhalothrin is more selective toward P. maculiventris and other natural enemies compared with other formulations of the compound.


The authors thank Thomas Van Leeuwen for his helpful suggestions and Bea Roos for excellent technical assistance.

References Cited


W. S. Abbott 1925. A method of computing the effectiveness of an insecticide. J. Econ. Entomol 18:265–267. Google Scholar


M. A. Al-Deeb, G. E. Wilde, and K. Y. Zhu . 2001. Effects of insecticides used in corn, sorghum, and alfalfa on the predator Orius insidiosus (Hemiptera: Anthocoridae). J. Econ. Entomol 94:1353–1360. Google Scholar


Anonymous 2000. Karate with Zeon technology. Technical bulletin. Syngenta, Basel, Switzerland. 25 pp. Google Scholar


Y. Ballanger and P. Jouffret . 1997. La punaise verte et le soja. Phytoma 50:32–34. Google Scholar


G. C de Baptista, J. R P. Parra, and Mde L. Haddad . 1995. Toxicidade comparativa de lambda-cyhalothrin à lagarta-da-soja, Anticarsia gemmatalisHueb., 1818 (Lepidoptera, Noctuidae) e ao percevejo verde, Nezara viridula (L., 1758) (Hemiptera, Pentatomidae). Sci. Agric. Piracicaba 52:183–188. Google Scholar


J. H F. Cole, E. D. Pilling, R. Boykin, and J. R. Ruberson . 1997. Effects of Karate® insecticide on beneficial arthropods in Bollgard® cotton. pp. 1118-1120. InProceedings 1997 Beltwide Cotton Conferences, New Orleans. Nat. Cotton Counc. Amer., Memphis, TN. Google Scholar


B. S. Corrêa-Ferreira and F. Moscardi . 1996. Biological control of soybean stink bugs by inoculative releases of Trissolcus basalis. Entomol. Exp. Appl 79:1–7. Google Scholar


P. De Clercq 2000. Chapter 32: Predaceous Stinkbugs (Pentatomidae: Asopinae). pp. 737-789. In C. W. Schaefer, and A. R. Panizzi [eds.], Heteroptera of Economic Importance. CRC Press, Boca Raton, FL. 828 pp. Google Scholar


P. De Clercq, A. De Cock, L. Tirry, E. Vinuela, and D. Degheele . 1995. Toxicity of diflubenzuron and pyriproxyfen to the predatory bug Podisus maculiventris. Entomol. Exp. Appl 74:17–22. Google Scholar


P. De Clercq and D. Degheele . 1992. Development and survival of Podisus maculiventris (Say) and Podisus sagitta (Fab.) (Heteroptera: Pentatomidae) at various constant temperatures. Canadian Entomol 124:125–133. Google Scholar


P. De Clercq, K. Wyckhuys, H. N de Oliveira, and J. Klapwijk . 2002. Predation by Podisus maculiventris on different life stages of Nezara viridula. Florida Entomol 85:197–202. Google Scholar


C. J. Drake 1920. The southern green stink-bug in Florida. Florida State Plant Board Q. Bull 4:41. 94. Google Scholar


D. H. Gouge, M. O. Way, A. Knutson, G. Cronholm, and C. Patrick . 1999. Managing soybean insects. Texas Agricultural Extension Service, B-1501, 36 pp. Google Scholar


D. Ham 1999. New technology brings improved insect control. Australian Cottongrower 20:102–103. Google Scholar


L. E N. Jackai, A. R. Panizzi, G. G. Kundu, and K. P. Srivastava . 1990. Insect pests of soybean in the tropics. pp. 91-156 In S. R. Singh [ed.], Insect Pests of Tropical Food Legumes. John Wiley & Sons, Chichester, U.K. 451 pp. Google Scholar


W. A. Jones 1988. World review of the parasitoids of the southern green stink bug, Nezara viridula (L.) (Heteroptera: Pentatomidae). Ann. Entomol. Soc. Amer. 81:262–273. Google Scholar


I. Kostaropoulos, A. I. Papadopoulos, A. Metaxakis, E. Boukouvala, and E. Papadopoulou-Mourkidou . 2001. Gluthatione S-transferase in the defence against pyrethroids in insects. Insect Biochem. Molec. Biol 31:313–319. Google Scholar


LeOra Software 1987. Polo-PC: a user’s guide to probit or logit analysis. LeOra Software, Berkeley, CA. Google Scholar


J. Mohaghegh, P. De Clercq, and L. Tirry . 2000. Toxicity of selected insecticides to the spined soldier bug, Podisus maculiventris (Heteroptera: Pentatomidae). Biocontr. Sci. Technol. 10:33–40. Google Scholar


A. R. Panizzi, J. E. McPherson, D. G. James, M. Javahery, and R. M. McPherson . 2000. Chapter 13: Stink bugs (Pentatomidae). pp. 421-474 In C. W. Schaefer, and A. R. Panizzi [eds.], Heteroptera of Economic Importance. CRC Press, Boca Raton, FL. 828 pp. Google Scholar


M. C. Picanço, R. N C. Guedes, V. C. Batalha, and R. P. Campos . 1996. Toxicity of insecticides to Dione juno juno (Lepidoptera: Heliconidae) and selectivity to two of its predaceous bugs. Trop. Sci 36:51–53. Google Scholar


E. D. Pilling and T. J. Kedwards . 1996. Effects of lambda-cyhalothrin on natural enemies of rice insect pests. pp. 361-366. InProceedings 1996 Brighton Crop Protection Conference: Pests & Diseases, Brighton, UK. British Crop Prot. Counc., Farnham, UK. Google Scholar


M. K. Pogoda, D. J. Pree, and D. B. Marshall . 2001. Effects of encapsulation on the toxicity of insecticides to the Oriental fruit moth (Lepidoptera: Tortricidae) and the predator Typhlodromus pyri (Acari: Phytoseiidae). Canadian Entomol 133:819–826. Google Scholar


D. W. Ragsdale, A. D. Larson, and L. D. Newsom . 1981. Quantitative assessment of the predators of Nezara viridula eggs and nymphs within a soybean agroecosystem using an ELISA. Environ. Entomol 10:402–405. Google Scholar


H. B. Scher, M. Rodson, and K-S. Lee . 1998. Microencapsulation of pesticides by interfacial polymerization utilizing isocyanate or aminoplast chemistry. Pestic. Sci 54:394–400. Google Scholar


T. Shono, K. Ohasawa, and J. E. Casida . 1979. Metabolism of trans- and cis-permethrin, trans- and cis-cypermethrin, and decamethrin by microsomal enzymes. J. Agric. Food Chem 27:316–325. Google Scholar


P. A. Stam, L. D. Newsom, and E. N. Lambremont . 1987. Predation and food as factors affecting survival of Nezara viridula (L.) (Hemiptera: Pentatomidae) in a soybean ecosystem. Environ. Entomol 16:1211–1216. Google Scholar


S. D. Stewart, L. C. Graham, M. J. Gaylor, and L. A. Vanderberg . 2001. Combining exclusion techniques and larval death-rate analyses to evaluate mortality factors of Spodoptera exigua (Lepidoptera: Noctuidae) in cotton. Florida Entomol 84:7–22. Google Scholar


J. W. Todd 1989. Ecology and behavior of Nezara viridula. Annu. Rev. Entomol 34:273–292. Google Scholar


H. van den Berg, K. Hassan, and M. Marzuki . 1998. Evaluation of pesticide effects on arthropod predator populations in soya bean in farmers’ fields. Biocontr. Sci. Technol 8:125–137. Google Scholar


K. Van Laecke and D. Degheele . 1993. Effect of insecticide synergist combinations on the survival of Spodoptera exigua. Pestic. Sci 37:283–288. Google Scholar


S. J. Yu 1987. Biochemical defense capacity in the spined soldier bug (Podisus maculiventris) and its lepidopterous prey. Pestic. Biochem. Physiol 28:216–223. Google Scholar


S. J. Yu 1988. Selectivity of insecticides to the spined soldier bug (Heteroptera: Pentatomidae) and its lepidopterous prey. J. Econ. Entomol 81:119–122. Google Scholar


J. C. Zanuncio, R. N C. Guedes, J. F. Garcia, and L. A. Rodrigues . 1993. Impact of two formulations of deltamethrin in aerial application against Eucalyptus caterpillar pests and their predaceous bugs. Meded. Fac. Landbouww. Univ. Gent 58:477–481. Google Scholar


Table 1.

Toxicity of an encapsulated formulation of lambda-cyhalothrin to N. viridulaand P. maculiventris by ingestion after 1, 2, and 7 days.


Table 2.

Toxicity of an encapsulated formulation of lambda-cyhalothrin to N. viridulaand P. maculiventris by residual contact after 1, 2, and 7 days.

Published: 1 June 2004

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