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Fig. 1 in Biology of the Bee Canephorula apiformis and Its Cleptoparasite Melectoides bellus: Nesting Habits, Floral Preferences, and Mature Larvae (Hymenoptera, Apidae)

Fig. 1. Position (arrows) of Valley of ZondaUllum and Valley of Iglesia, San Juan Province, Argentina.

Fig. 12 in Biology of the Bee Canephorula apiformis and Its Cleptoparasite Melectoides bellus: Nesting Habits, Floral Preferences, and Mature Larvae (Hymenoptera, Apidae)

Fig. 12. (Above) SEM micrograph of part of the domelike closure end of cocoon of Melectoides bellus, showing coarse silk fibers on external surface. Periphery of closure end toward bottom of micrograph.

Fig. 10 in Biology of the Bee Canephorula apiformis and Its Cleptoparasite Melectoides bellus: Nesting Habits, Floral Preferences, and Mature Larvae (Hymenoptera, Apidae)

Fig. 10. (Above) SEM micrograph of filter of the cocoon of Canephorula apiformis, as seen from inside the cocoon. Upper part of filter cut away.

Figs. 6–9 in Biology of the Bee Canephorula apiformis and Its Cleptoparasite Melectoides bellus: Nesting Habits, Floral Preferences, and Mature Larvae (Hymenoptera, Apidae)

Figs. 6–9. Diagrams of cocoon of Canephorula apiformis. 6. Entire cocoon showing external shape, side view, with upper right side cut away to show internal structure. 7. Cross section of the upper end enlarged, showing inner structure, and greatly enlarged section of cocoon wall demonstrating layers of silk and feces. 8. Upper end with outer silk layer removed to show radiating ridges of leathery layer. 9. Diagram of cocoon of Melectoides bellus, side view, showing external shape, upper right side cut away. Scale (= 5.0 mm) refers to figs. 6, 8, and 9.

Fig. 17 in Biology of the Bee Canephorula apiformis and Its Cleptoparasite Melectoides bellus: Nesting Habits, Floral Preferences, and Mature Larvae (Hymenoptera, Apidae)

Fig. 17. Frequency of individuals of Canephorula apiformis and Melectoides bellus on flowers during the months of activity in the Valley of ZondaUllum, San Juan Province, Argentina.

Figs. 29–34 in Biology of the Bee Canephorula apiformis and Its Cleptoparasite Melectoides bellus: Nesting Habits, Floral Preferences, and Mature Larvae (Hymenoptera, Apidae)

Figs. 29–34. Postdefecating larva of Melectoides bellus. 29. Entire larva, lateral view. 30. Head, lateral view. 31. Head, frontal view, pigmentation on left, sensilla and spicules on right. 32, 33. Right mandible, dorsal and inner views. 34. Spiracle, side view. Scale (= 1.0 mm) refers to fig. 29.

Figs. 22–28 in Biology of the Bee Canephorula apiformis and Its Cleptoparasite Melectoides bellus: Nesting Habits, Floral Preferences, and Mature Larvae (Hymenoptera, Apidae)

Figs. 22–28. Postdefecating larva of Canephorula apiformis. 22. Entire larva, lateral view. 23. Head, lateral view. 24. Head, frontal view, pigmentation on left, sensilla and spicules on right. 25–27. Right mandible, dorsal, inner, and ventral views. 28. Spiracle, side view. Scale (= 1.0 mm) refers to fig. 22.

Figs. 2, 3 in Biology of the Bee Canephorula apiformis and Its Cleptoparasite Melectoides bellus: Nesting Habits, Floral Preferences, and Mature Larvae (Hymenoptera, Apidae)

Figs. 2, 3. Nest sites of Canephorula apiformis in the Valley of ZondaUllum, San Juan Province, Argentina. 2. (Above) nests located in left side of picture. 3. (Below) nests at the margin of the road (arrows).

Fig. 16 in Biology of the Bee Canephorula apiformis and Its Cleptoparasite Melectoides bellus: Nesting Habits, Floral Preferences, and Mature Larvae (Hymenoptera, Apidae)

Fig. 16. (Below) SEM micrograph of front end of cocoon of Isepeolus viperinus, showing coarse outer silk layer, finer intermediate silk layers, and very fine innermost silk layer with fenestrations at closure.

Figs. 18, 19. 18 in Biology of the Bee Canephorula apiformis and Its Cleptoparasite Melectoides bellus: Nesting Habits, Floral Preferences, and Mature Larvae (Hymenoptera, Apidae)

Figs. 18, 19. 18. Above, blooming periods of plant species visited by Canephorula apiformis and Melectoides bellus, years 1993–1994 and 1996–1997, in the Valley of ZondaUllum, San Juan Province, Argentina. Below, frequency of C. apiformis collected on different floral species during the months of activity. 19. Frequency of individuals of Melectoides bellus collected on different floral species identified in fig. 18 during the months of activity.

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Fig 1. A parasitoid wasp and 1 in Predatory behavior of long-legged flies (Diptera: Dolichopodidae) and their potential negative effects on the parasitoid biological control agent of the Asian citrus psyllid (Hemiptera: Liviidae)

Fig 1. A parasitoid wasp and 1 of 7 species of predaceous long-legged flies collected in this study. The photograph is insufficient for identification. Although predation events could not be duplicated in captivity, the parasitoid wasp ap- pears to be within a size range that the long-legged fly would attack (e.g., Barrentine 2011). Scale bar = 2 mm.

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Fig. 1 in New data on the biology and distribution of Leptoglossus occidentalis Heidemann, 1910 (Hemiptera: Heteroptera: Coreidae: Coreinae: Anisoscelini).

Fig. 1.- Leptoglossus occidentalis Heidemann, 1910, Rabat, Morocco, 11.02.2019. (Photograph: Samantha Zaza).

Fig. 5 in Biology of the blind geobiont scarab beetle genus Chaetonyx Schaum, 1862 (Scarabaeidae: Orphninae) with new distribution records of Ch. robustus Schaum, 1862 from Bulgaria

Fig. 5. Life cycle of Chaetonyx robustus. Diagram is constructed based on the investigation of the local population in riverside habitat at the Zemen Gorge, SW Bulgaria, in April 2012 to November 2014.

Fig. 4 in Biology of the blind geobiont scarab beetle genus Chaetonyx Schaum, 1862 (Scarabaeidae: Orphninae) with new distribution records of Ch. robustus Schaum, 1862 from Bulgaria

Fig. 4. Different stages of Chaetonyx robustus. A, B: Eggs and first instar larvae (laboratory rearing, eggs collected on 03–VIII–2014); C: Pupae, collected on 07–VII–2013 (in vivo imaging); D: Adult, pupa, larvae from the three instars and eggs (in vivo imaging, material was collected on 07–VII–2013). Scale bars: A: 1 mm; B: 0.5 mm; C, D: 2.5 mm.

Fig. 3 in Biology of the blind geobiont scarab beetle genus Chaetonyx Schaum, 1862 (Scarabaeidae: Orphninae) with new distribution records of Ch. robustus Schaum, 1862 from Bulgaria

Fig. 3. Adults of Chaetonyx robustus, excavated from the site near town of Zemen (in situ imaging). A: sampling on 04–VIII–2012; B: sampling on 02–IX–2012.

Fig. 2 in Biology of the blind geobiont scarab beetle genus Chaetonyx Schaum, 1862 (Scarabaeidae: Orphninae) with new distribution records of Ch. robustus Schaum, 1862 from Bulgaria

Fig. 2. Adults of Chaetonyx robustus with different degrees of sclerotization, collected on 04– VIII–2012 from the sampling site. A: Slightly sclerotized, just emerged from the pupae; B: Moderate sclerotization; C: Fully sclerotized, adult from previous generation. Scale bar: 2.5 mm.

Fig. 3 in Biology and life history of Atanycolus cappaerti (Hymenoptera: Braconidae), a North American larval parasitoid attacking the invasive emerald ash borer (Coleoptera: Buprestidae)

Fig. 3. Immature stages of Atanycolus cappaerti. (A) Egg on Agrilus planipennis larva at 3× magnification; (B) 1st instar at 3× magnification; (C) 2nd instar at 3× magnification; (D) 3rd instar at 3× magnification; (E) 4th instar at 3× magnification; (F) 5th instar at 1.8× magnification; (G) 6th instar at 1.8× magnification; (H) pupal cocoon at 1.8× magnification; (I) eclosed adult.

Fig. 4 in Field and laboratory biological observations on the uncommon Cyrtocoris egeris (Heteroptera: Pentatomidae: Cyrtocorinae)

Fig. 4. Feeding damage of Cyrtocoris egeris on a stem of the Brazilian orchid tree, Bauhinia forficata (note thickening of the stem, outer bark cracked with a rugose appearance and accompanied by hatched eggs).

Fig. 3 in Field and laboratory biological observations on the uncommon Cyrtocoris egeris (Heteroptera: Pentatomidae: Cyrtocorinae)

Fig. 3. Mimetic behavior of Cyrtocoris egeris on a stem of the Brazilian orchid tree, Bauhinia forficata (note the similarity of the bug scutellar process with the plant spine).

Fig. 2 in Field and laboratory biological observations on the uncommon Cyrtocoris egeris (Heteroptera: Pentatomidae: Cyrtocorinae)

Fig. 2. (A) Egg masses, composed of hatched and unhatched eggs, of Cyrtocoris egeris on a stem of the Brazilian orchid tree, Bauhinia forficata, found in the field; (B) nymphs around the egg shells (chorions) and unhatched eggs (pinkish) shown in the upper part and hatched eggs in the lower part.