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Telenomus podisi parasitism on Dichelops melacanthus and Podisus nigrispinus eggs at different temperatures.

Dichelops melacanthus (Dallas) (Heteroptera: Pentatomidae), the most important stink bug species feeding on maize in South America, is controlled frequently with chemical pesticides (Bueno et al. 2015). Pest outbreaks are favored by a "green bridge," i.e., by cultivating 2 crops per yr (soybean in summer, maize in fall and winter) (Bianco 2005) when an increase in the D. melachanthus population is observed during the soybean season (Chiesa et al. 2016).

The early presence of stink bugs in maize development frequently has triggered an overuse of insecticides. Current pest management adopted in the field still primarily depends on chemicals (van Lenteren & Bueno 2003). In spite of this overuse of chemical insecticides, stink bug outbreaks tend to occur earlier and with greater intensity in soybean and maize each yr (Bueno et al. 2015). Therefore, a more efficient and sustainable pest management approach is urgently needed. One of the most sustainable pest management strategies of integrated pest management, which has been applied increasingly worldwide, is augmentative biological control (van Lenteren et al. 2018).

Egg parasitoids are the most important group of biocontrol agents used in stink bug augmentative biological control management, because pests are controlled at a stage prior to plant damage (Koppel et al. 2009). Telenomus podisi Ashmead (Hymenoptera: Scelionidae) is an egg parasitoid available for field releases in augmentative biological control that acts as a biocontrol agent of different pentatomid stink bug species. However, the family Pentatomidae includes pests as well as biocontrol agents, such as the predator Podisus nigrispinus (Dallas) (Hemiptera: Pentatomidae), which also is parasitized by T. podisi (Torres et al. 1996; Medeiros et al. 1997; Pacheco & Correa-Ferreira 2000; Koppel et al. 2009; Margaria et al. 2009).

An important consideration for T podisi parasitism in the field is the possible impact of abiotic conditions, especially temperature, which directly influences development and survival of insects (Wilson & Barnett 1983), affecting sex ratio, emergence, and other biological characteristics (Canto-Silva et al. 2005). Therefore, T. podisi parasitism is directly associated with its ability to adapt to different hosts and climatic conditions. To this end, the objective of this work was to study the effects of temperature on T podisi parasitism on eggs of D. melacanthus and P. nigrispinus.

Materials and Methods


Telenomus podisi females as well as the studied hosts, D. melacanthus and P. nigrispinus, originated from insect colonies kept at Embrapa Soybean, Londrina, Parana, Brazil. Colonies were kept under controlled environmental conditions inside biochemical oxygen demand climate chambers (ELETROLab[R], model EL 212, Sao Paulo, Sao Paulo, Brazil) set at 80 [+ or -] 10% humidity, temperature of 25 [+ or -] 2 [degrees]C, and a 14:10 h (L:D) photoperiod. Hosts and parasitoids were reared according to the methodologies described by Peres and Correa-Ferreira (2004) for T. podisi, by Panizzi et al. (2000) for D. melacanthus, and by Denez et al. (2014) for P. nigrispinus, and are briefly summarized in the following paragraph.

Telenomus podisi was collected originally from soybean fields in Londrina, Parana, Brazil. The population has been maintained in the laboratory for approximately 10 yr. It is reared on eggs of Euschistus heros (Fabricius) (Hemiptera: Pentatomidae) glued to pieces of card-board (2 cm x 8 cm), and introduced into tubes together with eggs already parasitized by T. podisi close to parasitoid emergence. Small drops of honey are placed inside these tubes to provide food for the adults when they emerge. The tubes are then closed, and the eggs allowed to be parasitized for 24 h. Adults that emerge from these eggs are used for trials as well as for colony maintenance.

Dichelops melacanthus and P. nigrispinus were collected from soybean plants in Londrina, Parana, Brazil. Those populations were kept in the laboratory for approximately 2 yr during which new field insects were introduced each yr to maintain colony quality. Dichelops melacanthus was fed with beans (Phaseolus vulgaris L.; Fabaceae), soybeans (Glycine max L. Merr.; Fabaceae), peanuts (Arachis hypogaea L.; Fabaceae), sunflower seeds (Helianthus annuus L.; Asteraceae) and privet fruits (Ligustrum lucidum Aiton; Oleaceae). Podisus nigrispinus was fed with third to fifth instars of Anticarsia gemmatalis Hubner (Lepidoptera: Erebidae) and Spodoptera frugiperda (Smith) (Lepidoptera: Noctuidae) from the laboratory colony. Dichelops melacanthus and P. nigrispinus were kept in cages (20 cm x 20 cm sides x 24 cm tall) made of plastic screen and lined with filter paper. A Petri dish with a cotton wad soaked in distilled water (9 cm diam) was added to each cage. Three times per wk, cages were cleaned, stink bug food was replaced, and egg masses collected. After collection, some egg masses were transferred to acrylic boxes (11 cm x 11 cm x 3.5 cm) (Gerbox, Adria laboratorios Ltda., Londrina, Parana, Brazil) lined with filter paper moistened with sterile, distilled water. After eclosion, second instars were transferred to new cages identical to those previously described. Egg masses not used for stink bug colony maintenance were stored in gallon containers of liquid nitrogen at -196 [degrees]C for later use in the parasitoid experiments.


Four bioassays were independently conducted, 2 of which were used to study the biological characteristics of T. podisi developing in eggs of D. melacanthus and P. nigrispinus at different temperatures (1 trial for each host species). The other 2 bioassays were designed to study the parasitism capacity of adult T podisi on eggs of D. melacanthus and P. nigrispinus at different temperatures (1 trial for each host species).

Before beginning the experiments, T. podisi was reared for 1 generation on eggs of the respective experimental host species in order to eliminate a possible pre-imaginal conditioning by rearing them on the alternative host (E. heros). Thus, experiments were carried out with the second generation of the parasitoid reared on the host eggs.


The bioassays were conducted in a completely randomized design with 4 treatments (15, 20, 25, and 30 [+ or -] 2 [degrees]C) and 7 replicates {N = 28). Each replicate consisted of 3 individual females in plastic microtubes of 12 mm diam and 75 mm height (7 replicates x 3 females per replicate = 21 females evaluated per treatment) following the methodology used by Queiroz et al. (2017) for other species of the genus Telenomus. Rather than using a single female parasitoid, a group of females was used per replicate: female insect egg parasitoids are small and fragile, and thus vulnerable to tiny injuries during experimental manipulation, which could affect their behavior. Using a set of parasitoids for each replicate can mitigate this potential negative effect to some extent.

Telenomus podisi females (48 h old) were placed individually into glass tubes (12 mm diam x 75 mm height). A cardboard card (10 mm x 70 mm) containing 40 eggs of each host (D. melacanthus for trial 1, and P. nigrispinus for trial 2) was exposed to each female. A droplet of honey was offered to the females as food.

Parasitism was allowed for 24 h inside a biochemical oxygen demand climate chamber at 25 [+ or -] 2 [degrees]C, RH 80 [+ or -] 10%, and a 14:10 h (L:D) photoperiod. Afterwards, parasitoids were removed from the tubes and the eggs of each species were transferred to climate chambers at temperatures of 15, 20, 25, and 30 [+ or -] 2 [degrees]C, with 80 [+ or -] 10% relative humidity (RH), and a 14:10 h (L:D) photoperiod. The following biological traits were evaluated: duration of egg-to-adult period, sex ratio (sex ratio = number of females/[number of females + number of males]), and parasitoid emergence (%). The emergence of T. podisi was observed daily to determine the duration of the egg-to-adult period. Parasitoid emergence was evaluated under a stereoscope by counting the host eggs with an exit orifice that resulted from adults emerging from the egg.


The bioassays were performed in a completely randomized design with 4 treatments (15, 20, 25, and 30 [+ or -] 2 [degrees]C) and 22 replicates containing 1 T. podisi female for each host species. Eggs of both D. melacanthus and P. nigrispinus stored in liquid nitrogen were removed daily from storage to be used in the experiments.

Forty-eight-h-old females were individually placed into Duran tubes (1.5 mL) (Dovil Ltda., Sao Paulo, Sao Paulo, Brazil) containing cardboard cards (0.8 cm x 5 cm) with approximately 40 eggs of D. melacanthus (trial 3) or P. nigrispinus (trial 4). A droplet of honey was placed on the wall of the tube for feeding, and tubes were then sealed with plastic film.

The tubes were kept inside biochemical oxygen demand climate chambers set to the respective treatment temperature, 80 [+ or -] 10% RH, and a 14:10 h (L:D) photoperiod. The eggs were exposed to parasitism for 24 h, and the cards were replaced daily until the females died. The cards containing parasitized eggs were stored in plastic bags (4 cm x 23 cm) and kept inside a biochemical oxygen demand climate chamber at 25 [+ or -] 2 [degrees]C, 80 [+ or -] 10% RH, and a 14:10 h (L:D) photoperiod until emergence and death of adults. The parameters evaluated were daily parasitism, cumulative percentage of parasitism, total number of eggs parasitized per female, and longevity of parental females.


The results obtained in the experiments were submitted to exploratory analysis to evaluate the normality assumptions of the residuals (Shapiro & Wilk 1965), homogeneity of variance of treatments, and additivity of the model to allow the application of ANOVA (Burr & Foster 1972). Egg to adult period (trial 1) and longevity of parental females (trial 3) were square-root transformed. Emergence of T. podisi from P. nigrispinus eggs (trial 2) was transformed into arcsine [mathematical expression not reproducible]. Sex ratio of T. podisi emerged from P. nigrispinus eggs (trials 2 & 4) were transformed into to perform ANOVA. Then, averages were compared by the Tukey test at a 5% error probability, with the statistical analysis program SAS (SAS Institute 2009).



Egg to adult periods of T. podisi in eggs of D. melacanthus (trial 1) and P. nigrispinus (trial 2) were inversely related to an increase in temperature (10.8 and 10.9 d at 30 [degrees]C, and 58.8 and 67.2 d at 15 [degrees]C, respectively). Thus, an increase in temperature from 15 to 30 [degrees]C caused a reduction of the egg to adult period of T. podisi in eggs of D. melacanthus by 48.0 d, and in eggs of P. nigrispinus by 56.3 d (Table 1).

The emergence (%) of T. podisi offspring from D. melacanthus and P. nigrispinus eggs was influenced by temperature, with the highest parasitoid emergence from D. melacanthus eggs at 20 [degrees]C, and from P. nigrispinus eggs at 25 and 30 [degrees]C (Table 1). Emergence from eggs of D. melacanthus was > 80% at 20 and 25 [degrees]C (97.4 and 80.5%, respectively), but much lower at 15 [degrees]C(27.5%). Emergence (%) from eggs of the predator P. nigrispinus was > 80% at temperatures of 20, 25, and 30 [degrees]C (87.7, 98.4, and 97.7%, respectively), and also lower at 15 [degrees]C (3.8%) (Table 1).

Temperature influenced sex ratio (sex ratio = number of females/[number of males + number of females]), which decreased with increasing temperature in both hosts (D. melacanthus and P. nigrispinus) (Table 1). However, sex ratio was always above 0.5 at all evaluated temperatures, both in pest and predator eggs (Table 1). The highest sex ratio was found when parasitoids were exposed to 15 [degrees]C on both host species. The lowest value was recorded at 25 [degrees]C in D. melacanthus eggs and at 30 [degrees]C in P. nigrispinus eggs (Table 1).


Parasitism capacity of T. podisi was affected by temperature in both hosts (Figs. 1 & 2). The number of parasitized eggs per d varied depending on temperature and host, with the highest parasitism always observed on the first d of each experiment. Cumulative parasitism (%) of D. melacanthus eggs reached 80% on the 24th, 20th, 14th, and 8th d of adult lifespan at 15, 20, 25, and 30 [degrees]C, respectively (Fig. 1). Similarly, cumulative parasitism (%) of P. nigrispinus eggs reached 80% on the 18th, 17th, 14th, and 12th d of adult lifespan at 15, 20, 25, and 30 [degrees]C, respectively (Fig. 2).

The number of eggs laid per d by parasitoid females (daily parasitism) decreased constantly in both host species over the adult parasitoid lifespan (Figs. 1 & 2). In D. melacanthus eggs, parasitism was highest within the first 24 h at all tested temperatures, when average numbers of parasitized eggs were 4.1, 10.6, 10.9, and 12.3 at 15, 20, 25, and 30 [degrees]C, respectively (Fig. 1). In P. nigrispinus eggs, parasitism was highest during the first 24 h only at 20 and 25 [degrees]C, whereas at 15 [degrees]C (Fig. 2A) and 30 [degrees]C (Fig. 2D), maximum parasitism was observed on the second and fourth d, with 0.5, 8.2, 9.7, and 10.8 eggs parasitized at temperatures of 15, 20, 25, and 30 [degrees]C, respectively (Fig. 2).

Longevity of parental females of T. podisi was inversely proportional to the increase in temperature on both hosts (Table 2). Reared on D. melacanthus eggs, the maximum longevity of T. podisi parental females was 89.0 d at 15 [degrees]C, and decreased to 41.7, 30.8, and 13.9 d at temperatures of 20, 25, and 30 [degrees]C, respectively. Reared on P. nigrispinus eggs, the maximum longevity of T. podisi was 133.5 d at 15 [degrees]C followed by 59.7, 42.5, and 31.8 d at temperatures of 20, 25, and 30 [degrees]C, respectively (Table 2).

The total number of eggs parasitized per female throughout development varied with temperature and host species. Reared on D. melacanthus eggs, the number of parasitized eggs did not differ between 20 and 25 [degrees]C, with a mean of 101.5 and 100.0 eggs, respectively. At temperatures of 15 and 30 [degrees]C, the mean number of parasitized eggs was 40.8 and 67.5, respectively. In eggs of P. nigrispinus, the total number of parasitized eggs differed between all tested temperatures (15,20,25, and 30 [degrees]C, with 13.6, 61.6,100.9, and 82.6 parasitized eggs, respectively) (Table 2).


Telenomus podisi parasitism was highly influenced by both temperature and host species, indicating a possible effect of these parameters on the success of a biocontrol program with this egg parasitoid. Our results are of theoretical and practical interest and can contribute significantly to a successful T. podisi release for the management of D. melacanthus.

The inverse relationship between increasing temperatures and shorter egg to adult periods is one of the consequences of a higher parasitoid metabolic activity at higher temperatures (Hernandez & Diaz 1996; Bueno et al. 2009). Higher metabolic activity implies a higher parasitoid population growth rate, which can be an advantage for biological control as new adults will emerge earlier. Although faster population growth is favorable, an increase in temperature also can have negative effects on T. podisi parasitism. At extremely high temperatures, optimal development time is impaired and mortality increases (Bueno et al. 2008). We observed a similar relationship when rearing T. podisi on D. melacanthus eggs at 30 [degrees]C. However, increased larval mortality was not observed in T. podisi on P. nigrispinus eggs. This might be associated with size differences between D. melacanthus (smaller) and P. nigrispinus (larger) eggs, as previously observed for other parasitoids (Smith 1996). Host egg size may affect host suitability for a parasitoid. Besides size, other differences between host eggs include egg surface and chorion structure, which might directly impact loss of water and nutrients at 30 [degrees]C. The impact of host egg characteristics on parasitoid survival and development has been pointed out already by Consoli et al. (1999).

Temperature impacts larval development and survival, as well as several adult biological traits. At 30 [degrees]C, parental female longevity was reduced, thus shortening the period of parasitism. It contributed to lowering the total number of parasitized eggs, which is an undesirable effect in biological control. The impact of temperature on the longevity of T. podisi adults may be due to an incapability for lipogenesis, as observed for most parasitoid species (Visser & Ellers 2008). However, as an ectothermic insect, the metabolic rate and lipid consumption of T. podisi (Huey & Berrigan 2001) will depend on temperature. Thus, allocation of lipids acquired during the larval stage will determine the adult lifespan and fecundity of T. podisi (Visser & Ellers 2008) and, therefore, its lifetime reproductive success (Huey & Berrigan 2001).

Considering that the shortened egg to adult period observed at 30 [degrees]C may have reduced the amount of lipids acquired during the T. podisi larval development, it probably led to reduced adult longevity and a smaller number of parasitized eggs. Parasitoid foraging decisions are commonly affected by the availability of lipid reserves, and the number of mature eggs (Godfray 1994) in females. Lipids carried over from the larval stage can be allocated to either egg production or to adult lipid reserves, leading to a constant trade-off between reproduction and lifespan (Pexton & Mayhew 2002).

Not only extremely high temperatures, but extremely low temperatures also can impair T. podisi parasitism. The low T. podisi emergence observed at 15 [degrees]C from D. melacanthus eggs (27.5%) and P. nigrispinus eggs (3.8%) may be related to the proximity of this value to the lower lethal temperature of T. podisi. Previous reports support this hypothesis. Yeargan (1980) observed low emergence of T. podisi on eggs of Podisus maculiventris (Say) (Hemiptera: Pentatomidae) at 15.5 [degrees]C, and also Nakama & Foerster (2001) and Torres et al. (1997) who reported a viability of less than 50% when T. podisi was exposed to 15 [degrees]C. However, it is important to consider that extremely low or high temperatures usually do not occur over long periods in the field and, therefore, field trials which help to understand the real effects of extreme weather conditions on T. podisi still need to be conducted.

Another important trait to be considered in biological control is sex ratio (number of females/[number of females + number of males]), since only females parasitize and, in consequence, control the target host in the field. Thus, it is desirable to increase the production of females (Bueno et al. 2009). In general, an increase in temperature was related to a decrease in sex ratio. While parasitism occurred at 25 [degrees]C, and subsequent larval development took place at several temperatures (trials 1 and 2), the higher number of females emerging at 15 [degrees]C suggests their higher cold tolerance compared with males. This might be due to larger size or larger fat body of females, a hypothesis supported by Yeargan (1980), who reported that at 15.5 [degrees]C only females emerge. Likewise, Doetzer & Foerster (2007) reported a higher occurrence of females under natural conditions during the coldest months in the off-season of soybean in southern Parana, Brazil.

It is also important to analyze the distribution of T. podisi lifetime parasitism because the active time of parasitoid females might vary related to temperature (Reznik & Vaghina 2006), hosts (Reznik et al. 2001), and parasitoid species (Pratissoli & Parra 2000), and may directly influence parasitoid use in the field. For example, whether parasitoid activity is higher in the first d of life or is evenly distributed throughout adulthood is important when choosing the best parasitoid release strategy (Bueno et al. 2010) for various reasons.

The sooner the parasitoid reaches 80% of its lifetime parasitism, the better, because parasitoids would be less exposed to mortality factors under field conditions. In practice, those factors could be pesticide spraying necessary for crop management, or an abrupt change in weather conditions that may kill the egg parasitoid (Carmo et al. 2010; Denis et al. 2011). On the other hand, one of the factors that can reduce field efficiency of egg parasitoids is the lack of synchronization between the occurrence of the most susceptible stage of the target host with the period of greater adult parasitism activity (Cingolani et al. 2014). Thus, a longer T. podisi lifetime parasitism distribution would be preferable.

Taking into account that synchronization between parasitoid and host is an important challenge in augmentative biological control, T. podisi exhibited favorable traits for a prospective successful biocontrol agent. As opposed to other parasitoids such as Trichogramma pretiosum Riley (Hymenoptera: Trichogrammatidae), which reached over 80% lifetime parasitism (cumulative parasitism) already on the 12th, 10th, 5th, and 7th d of adulthood when exposed to 18, 20, 25, and 30 [degrees]C, respectively (Bueno et al. 2012). Telenomus podisi reached this parasitism level only at the 24th, 20th, 14th, and 8th d of parasitoid adulthood at 15, 20, 25, and 30 [degrees]C on D. melacanthus eggs, respectively. Similarly, T. podisi reached 80% lifetime parasitism on the 18th, 17th, 14th, and 12th d of parasitoid adulthood at 15, 20, 25, and 30 [degrees]C on P. nigrispinus eggs, respectively. Therefore, a much longer period is available for synchronization of the parasitoid with its target pest, reducing the chance for release failures in the field.

It is important to point out that even though temperature is considered one of the most important factors in augmentative biological control success, it is not the only factor responsible for changes in development and survival of egg parasitoids. Other biotic and abiotic factors, such as photoperiod, relative humidity, interspecific and intraspecific competition, may interfere with biological control (Bueno et al. 2012). However, T. podisi generally was influenced by temperature in eggs of both D. melacanthus and P. nigrispinus. The extreme temperatures of 15 and 30 [degrees]C were unfavorable for T. podisi parasitism (although it still occurred) because traits were impaired at those temperatures, especially parasitism and adult longevity. In regions where those extreme temperatures may occur commonly, additional studies are necessary to investigate the possible need for increased parasitoid numbers during field releases. Even though the release of T. podisi in the field may negatively impact the predator P. nigrispinus, it is probably still safer than the use of chemical insecticides, which would be the alternative measure to T. podisi in the control of stink bugs.


The authors thank "Empresa Brasileira de Pesquisa Agropecuaria" (Embrapa Soybean); "Coordenacao de Aperfeicoamento de Pessoal de Nivel Superior" (CAPES); "Conselho Nacional de Desenvolvimento Cientffico e Tecnologico" (CNPq) (grants 303779/2015-2 and 402797/2016); and "Universidade Federal do Parana" (UFPR) for funding that supported this research.

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Yeargan KV 1980. Effects of temperature on development rate of Telenomus podisi (Hymenoptera: Scelionidae). Annals of the Entomological Society of America 73: 339-342.

Erica Ayumi Taguti (1), Jaciara Gongalves (1), Adeney de Freitas Bueno (2,*), and Suelhen Thais Marchioro (3)

(1) Programs de Pos-Graduacao em Entomologia, Departamento de Zoologia, Setor de Ciencias Biologicas, Universidade Federal do Parana, Curitiba, Parana , Brazil; E-mail: (E. A. T.), (J. G.)

(2) Embrapa Soja, Rodovia Carlos Joao Strass, s/n, Caixa postal 231 - Distrito de Warta, 86001-970 Londrina, Parana, Brazil; E-mail: (A. D. F. B.)

(3) Universidade Federal da Fronteira Sul, Campus Laranjeiras do Sul, Rodovia BR 158 - km 405, 85301-970 Laranjeiras do Sul, Parana, Brazil; E-mail: (S. T. M.)

(*) Corresponding author; E-mail:

Caption: Fig. 1. Distribution of lifetime parasitism of Telenomus podisi Ashmead (Hymenoptera: Scelionidae) in Dichelops melacanthus eggs (Dallas) (Hemiptera: Pentatomidae) at different temperatures. (A) 15 [degrees]C, (B) 20 [degrees]C, (C) 25 [degrees]C, (D) 30 [degrees]C at 80 [+ or -] 10% RH and a 14:10 h (L:D) photoperiod. Arrows indicate parasitism of 80%.

Caption: Fig. 2. Distribution of lifetime parasitism Telenomus podisi Ashmead (Hymenoptera: Scelionidae) in Podisus nigrispinus eggs (Dallas) (Hemiptera: Pentatomidae) at different temperatures. (A) 15 [degrees]C, (B) 20 [degrees]C, (C) 25 [degrees]C, (D) 30 [degrees]C at 80 [+ or -] 10% RH and a 14:10 h (L:D) photoperiod. Arrows indicate parasitism of 80%.
Table 1. Biological trait values of Telenomus podisi Ashmead
(Hymenoptera: Scelionidae) on eggs of Dichelops meloconthus (Dallas)
(Hemiptera: Pentatomidae) and Podisus nigrispinus (Dallas) (Hemiptera:
Pentatomidae) at 80 [+ or -] 10% RH and a 14:10 h (L:D) photoperiod.

                          Temperature   Egg to adult
Host                      ([degrees]C)  (d) (1)

D. melacanthus (trial 1)  15               58.8 [+ or -] 0.8 a (2)
                          20               22.1 [+ or -] 0.1 b
                          25               12.6 [+ or -] 0.2 c
                          30               10.8 [+ or -] 0.3 d
                          CV (%)            2.12
                          P               < 0.0001
                          df error         24
                          F             2,727.13
P. nigrispinus (trial 2)  15               67.2 [+ or -] 0.5 a (2)
                          20               21.1 [+ or -] 0.1 b
                          25               14.1 [+ or -] 0.1 c
                          30               10.9 [+ or -] 0.2 d
                          CV (%)            1.31
                          P               < 0.0001
                          df error         22
                          F             6,962.25

Host                      (%) (1)

D. melacanthus (trial 1)   27.5 [+ or -] 3.2 c (3)
                           97.4 [+ or -] 1.2 a
                           80.5 [+ or -] 6.6 b
                           69.7 [+ or -] 6.8 b
                          < 0.0001
P. nigrispinus (trial 2)    3.8 [+ or -] 1 c (3)
                           87.7 [+ or -] 1.4 b
                           98.4 [+ or -] 0.4 a
                           97.7 [+ or -] 0.8 a
                          < 0.0001

Host                      rato (1)

D. melacanthus (trial 1)    0.90 [+ or -] 0.05 a
                            0.71 [+ or -] 0.06 ab
                            0.50 [+ or -] 0.05 b
                            0.57 [+ or -] 0.05 b
P. nigrispinus (trial 2)    1.00 [+ or -] 0.00 a (4)
                            0.92 [+ or -] 0.01 b
                            0.89 [+ or -] 0.03 b
                            0.60 [+ or -] 0.01 c
                          < 0.0001

(1) Means [+ or -] SE followed by the same letter (separately for each
host) did not differ significantly (Tukey's test, P > 0.05).
(2) Original means followed by statistics performed on
[mathematical expression not reproducible] transformed data.
(3) Original means followed by statistics performed on arcsine
[mathematical expression not reproducible] transformed data.
(4) Original means followed by statistics performed on
[mathematical expression not reproducible] transformed data.

Table 2. Parasitism capacity of Telenomus podisi Ashmead (Hymenoptera:
Scelionidae) on eggs of Dichelops melacanthus (Dallas) (Hemiptera:
Pentatomidae) and Podisus nigrispinus (Dallas) (Hemiptera:
Pentatomidae) at 80 [+ or -] 10% RH and a 14:10 h (L:D) photoperiod.

Host                      Temperature ([degrees]C)

D. melacanthus (trial 3)  15
                          CV (%)
                          df error
P. nigrispinus (trial 4)  15
                          CV (%)
                          df error

Host                      Longevity of parental females (d) (1)

D. melacanthus (trial 3)   89.0 [+ or -] 6.3 a (2)
                           41.7 [+ or -] 2.4 b
                           30.8 [+ or -] 2.5 c
                           13.9 [+ or -] 0.9 d
                          < 0.0001
P. nigrispinus (trial 4)  133.5 [+ or -] 5.6 a (2)
                           59.7 [+ or -] 3.2 b
                           42.5 [+ or -] 2.2 c
                           31.8 [+ or -] 1.5 d
                          < 0.0001

Host                      Total number of parasitzed eggs per female (1)

D. melacanthus (trial 3)   40.80 [+ or -] 2.17 c (2)
                          101.58 [+ or -] 3.96 a
                          100.00 [+ or -] 3.98 a
                           67.50 [+ or -] 4.14 b
                          < 0.0001
P. nigrispinus (trial 4)   13.68 [+ or -] 1.96 d (3)
                           61.65 [+ or -] 4.05 c
                          100.94 [+ or -] 3.57 a
                           82.65 [+ or -] 4.95 b
                          < 0.0001

(1) Means [+ or -] SE followed by the same letter (separately for each
host) did not differ statistically (Tukey's test, P > 0.05).
(2) Original means followed by statistics performed on
[mathematical expression not reproducible] transformed data.
(3) Original means followed by statistics performed on
[mathematical expression not reproducible] transformed data.

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Article Details
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Author:Taguti, Erica Ayumi; Gongalves, Jaciara; Bueno, Adeney de Freitas; Marchioro, Suelhen Thais
Publication:Florida Entomologist
Geographic Code:30SOU
Date:Sep 1, 2019
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