RESUMO

The increase of agricultural areas with glyphosate-resistant (GR) crops, and use of this herbicide in Brazil, makes necessary to assess its impacts on non-target organisms. The objective was to evaluate the development, reproduction and life table parameters of Podisus nigrispinus (Heteroptera: Pentatomidae) reared on GR-soybean plants treated with glyphosate formulations (Zapp-Qi, Roundup-Transorb-R and Roundup-Original) at the recommended field dose (720g acid equivalent ha-1). Glyphosate formulations had no affect on nymph and adult weight of this predator. Fourth instar stage was shortest with Zapp Qi. Egg-adult period was similar between treatments (26 days) with a survival over 90%. Zapp-Qi and Roundup-Transorb-R (potassium-salt: K-salt) reduced the egg, posture and nymph number per female, and the longevity and oviposition periods of this predator. Podisus nigrispinus net reproductive rate was highest in GR-soybean plants treated with Roundup-Original (isopropylamine-salt: IPA-salt). However, the duration of one generation, intrinsic and finite increase rates, and time to duplicate the population, were similar between treatments. Glyphosate toxicity on P. nigrispinus depends of the glyphosate salt type. IPA-salt was least harmless to this predator. Formulations based on K-salt altered its reproductive parameters, however, the development and population dynamic were not affect. Therefore, these glyphosate formulations are compatible with the predator P. nigrispinus with GR-soybean crop.

Assuntos

Glicina/análogos & derivados , Herbicidas/toxicidade , Heterópteros/efeitos dos fármacos , Animais , Brasil , Monitoramento Ambiental , Feminino , Glicina/toxicidade , Heterópteros/crescimento & desenvolvimento , Ninfa/efeitos dos fármacos , Ninfa/crescimento & desenvolvimento , Reprodução/efeitos dos fármacos , Glifosato

RESUMO

In eusocial bees, workers and queens are diploid (2n), whereas males are haploid (n). However, in some species, including the stingless bee Melipona quadrifasciata anthidioides Lepeletier, 1836, 2n males arise from fertilized eggs resulting from the crossing between a queen and her brother. In the present study, we provide a comparative analysis of the digestive and regenerative cells in n and 2n pupae and adult males of M. quadrifasciata anthidioides. In n and 2n pupae and adult males, the number of regenerative cells/nest was similar. In n and 2n pupae, the mean number of digestive cells/midgut area was 2076 ± 0.60, whereas in adults it was 1234 ± 1.42 digestive cells/midgut area. The nuclear area of the digestive cells was also similar in both n and 2n adult males (~154 µm²) and smaller in pupae (~91 µm²); this variation might be a result of DNA amplification in digestive cells during bee development. The results from our current study provide further understanding of the morphological and physiological aspects of the digestive tract of bees and show that the ploidy difference between n and 2n male stages does not affect the number of digestive and regenerative cells in the midgut of M. quadrifasciata anthidioides.

RESUMO

In eusocial bees, workers and queens are diploid (2n), whereas males are haploid (n). However, in some species, including the stingless bee Melipona quadrifasciata anthidioides Lepeletier, 1836, 2n males arise from fertilized eggs resulting from the crossing between a queen and her brother. In the present study, we provide a comparative analysis of the digestive and regenerative cells in n and 2n pupae and adult males of M. quadrifasciata anthidioides. In n and 2n pupae and adult males, the number of regenerative cells/nest was similar. In n and 2n pupae, the mean number of digestive cells/midgut area was 2076 ± 0.60, whereas in adults it was 1234 ± 1.42 digestive cells/midgut area. The nuclear area of the digestive cells was also similar in both n and 2n adult males (~154 µm²) and smaller in pupae (~91 µm²); this variation might be a result of DNA amplification in digestive cells during bee development. The results from our current study provide further understanding of the morphological and physiological aspects of the digestive tract of bees and show that the ploidy difference between n and 2n male stages does not affect the number of digestive and regenerative cells in the midgut of M. quadrifasciata anthidioides.

RESUMO

In eusocial bees, workers and queens are diploid (2n), whereas males are haploid (n). However, in some species, including the stingless bee Melipona quadrifasciata anthidioides Lepeletier, 1836, 2n males arise from fertilized eggs resulting from the crossing between a queen and her brother. In the present study, we provide a comparative analysis of the digestive and regenerative cells in n and 2n pupae and adult males of M. quadrifasciata anthidioides. In n and 2n pupae and adult males, the number of regenerative cells/nest was similar. In n and 2n pupae, the mean number of digestive cells/midgut area was 2076 ± 0.60, whereas in adults it was 1234 ± 1.42 digestive cells/midgut area. The nuclear area of the digestive cells was also similar in both n and 2n adult males (~154 µm²) and smaller in pupae (~91 µm²); this variation might be a result of DNA amplification in digestive cells during bee development. The results from our current study provide further understanding of the morphological and physiological aspects of the digestive tract of bees and show that the ploidy difference between n and 2n male stages does not affect the number of digestive and regenerative cells in the midgut of M. quadrifasciata anthidioides.

RESUMO

Mass rearing of parasitoids depends on choosing appropriate alternative hosts. The objective of this study was to select alternative hosts to rear the parasitoid Palmistichus elaeisis Delvare & LaSalle, 1993 (Hymenoptera: Eulophidae). Pupae of the lepidopterans Anticarsia gemmatalis Hübner, 1818 (Lepidoptera: Noctuidae), Bombyx mori Linnaeus, 1758 (Lepidoptera: Bombycidae) and Thyrinteina arnobia (Stoll, 1782) (Lepidoptera: Geometridae) were exposed to parasitism by females of P. elaeisis. The duration of the life cycle of P. elaeisis was 21.60 ± 0.16 and 24.15 ± 0.65 days on pupae of A. gemmatalis and B. mori, respectively, with 100.0% parasitism of the pupae and 71.4 and 100.0% emergence of parasitoids from the first and second hosts, respectively. The offspring number of P. elaeisis was 511.00 ± 49.70 and 110.20 ± 19.37 individuals per pupa of B. mori and A. gemmatalis, respectively. The reproduction of P. elaeisis from pupae of T. arnobia after six generations was similar to the other hosts.

RESUMO

Mass rearing of parasitoids depends on choosing appropriate alternative hosts. The objective of this study was to select alternative hosts to rear the parasitoid Palmistichus elaeisis Delvare & LaSalle, 1993 (Hymenoptera: Eulophidae). Pupae of the lepidopterans Anticarsia gemmatalis Hübner, 1818 (Lepidoptera: Noctuidae), Bombyx mori Linnaeus, 1758 (Lepidoptera: Bombycidae) and Thyrinteina arnobia (Stoll, 1782) (Lepidoptera: Geometridae) were exposed to parasitism by females of P. elaeisis. The duration of the life cycle of P. elaeisis was 21.60 ± 0.16 and 24.15 ± 0.65 days on pupae of A. gemmatalis and B. mori, respectively, with 100.0% parasitism of the pupae and 71.4 and 100.0% emergence of parasitoids from the first and second hosts, respectively. The offspring number of P. elaeisis was 511.00 ± 49.70 and 110.20 ± 19.37 individuals per pupa of B. mori and A. gemmatalis, respectively. The reproduction of P. elaeisis from pupae of T. arnobia after six generations was similar to the other hosts.

RESUMO

Mass rearing of parasitoids depends on choosing appropriate alternative hosts. The objective of this study was to select alternative hosts to rear the parasitoid Palmistichus elaeisis Delvare & LaSalle, 1993 (Hymenoptera: Eulophidae). Pupae of the lepidopterans Anticarsia gemmatalis Hübner, 1818 (Lepidoptera: Noctuidae), Bombyx mori Linnaeus, 1758 (Lepidoptera: Bombycidae) and Thyrinteina arnobia (Stoll, 1782) (Lepidoptera: Geometridae) were exposed to parasitism by females of P. elaeisis. The duration of the life cycle of P. elaeisis was 21.60 ± 0.16 and 24.15 ± 0.65 days on pupae of A. gemmatalis and B. mori, respectively, with 100.0% parasitism of the pupae and 71.4 and 100.0% emergence of parasitoids from the first and second hosts, respectively. The offspring number of P. elaeisis was 511.00 ± 49.70 and 110.20 ± 19.37 individuals per pupa of B. mori and A. gemmatalis, respectively. The reproduction of P. elaeisis from pupae of T. arnobia after six generations was similar to the other hosts.