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Fig 5 in Publishing trends and productivity in insect taxonomy from 1946 through 2012 based on an analysis of the Zoological Record for four species-rich families

Fig 5 (continued on next page). Number of articles published by continent (Europe, North America, South America, Africa, Asia and Australia) between 1946 and 2012. A. Cicadellidae. B. Miridae. C. Pyralidae. D. Staphylinidae.

Fig 2 in Publishing trends and productivity in insect taxonomy from 1946 through 2012 based on an analysis of the Zoological Record for four species-rich families

Fig 2. Average new species described per article (Cicadellidae, Miridae, Pyralidae and Staphylinidae combined) from 1946 to 2012.

Fig 1 in Publishing trends and productivity in insect taxonomy from 1946 through 2012 based on an analysis of the Zoological Record for four species-rich families

Fig 1. Time series of newly described species for the families Cicadellidae, Miridae, Pyralidae and Staphylinidae between 1946 and 2012. A. Number of new species. B. Number of articles with new species.

Fig 4 in Publishing trends and productivity in insect taxonomy from 1946 through 2012 based on an analysis of the Zoological Record for four species-rich families

Fig 4. Total and average article length for for papers on the four families of Cicadellidae, Miridae, Pyralidae and Staphylinidae between 1946 and 2012.

Fig 3 in Publishing trends and productivity in insect taxonomy from 1946 through 2012 based on an analysis of the Zoological Record for four species-rich families

Fig 3. Average page length of new species descriptions (Cicadellidae, Miridae, Pyralidae and Staphylinidae combined) between 1946 and 2012.

Fig 5 in Publishing trends and productivity in insect taxonomy from 1946 through 2012 based on an analysis of the Zoological Record for four species-rich families

Fig 5 (continued from previous page). Number of articles published by continent (Europe, North America, South America, Africa, Asia and Australia) between 1946 and 2012. A. Cicadellidae. B. Miridae. C. Pyralidae. D. Staphylinidae.

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Figs. 1–6 in Insect galls on Bauhinia cupulata (Fabaceae): morphotypes characterization and description of a new species of Schizomyia (Cecidomyiidae, Diptera)

Figs. 1–6. Different development stages of galls induced by Schizomyia barreirensis, sp. n. (1) First stage. (2) Second stage. (3) Third stage. (4) Fourth stage. (5) Fifth stage. (6) Last stage (gall cut open to show the larval chamber).

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Figs. 19 and 20 in Insect galls on Bauhinia cupulata (Fabaceae): morphotypes characterization and description of a new species of Schizomyia (Cecidomyiidae, Diptera)

Figs. 19 and 20. Schizomyia barreirensis, sp. n. (19) Female, abdominal segments 7–8 (lateral view); (20) Ovipositor (ventral view). Scale bars in mm.

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Figs. 13–18 in Insect galls on Bauhinia cupulata (Fabaceae): morphotypes characterization and description of a new species of Schizomyia (Cecidomyiidae, Diptera)

Figs. 13–18. Schizomyia barreirensis sp. n. (13) Male, head (frontal view); (14) Male, flagellomere 3; (15) Female, flagellomere 2; (16) Tarsal claws and empodium; (17) Male, abdominal segments 3–8 (lateral view); (18) Male, terminalia (dorsal view). Scale bars in mm.

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Figure 1 in Leptoglossus occidentalis (Heteroptera: Coreidae) and Harmonia axyridis (Coleoptera: Coccinellidae), two new invasive alien species for insect fauna of Macedonia

Figure 1. The finding sites of Leptoglossus occidentalis Heidemann (triangle) and Harmonia axyridis (Pallas) (point) in Macedonia.

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Figure 2 in Leptoglossus occidentalis (Heteroptera: Coreidae) and Harmonia axyridis (Coleoptera: Coccinellidae), two new invasive alien species for insect fauna of Macedonia

Figure 2. The western conifer seed bug, Leptoglossus occidentalis Heidemann found on Pinus nigra at Prilep Lake.

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Fig. 1 in Identification of predatory and parasitoid insect species associated with Melanaphis sacchari (Hemiptera: Aphididae), a sorghum pest in Nuevo León, Mexico

Fig. 1. Melanaphis sacchari predators and parasitoids found in Nuevo León, Mexico. (A) Allograpta sp. in adult status, (B) Chilocorus cacti (lef), and Chilocorus stigma (right), (C) Olla v-nigrum, (D) Chrysoperla sp., (E) Allograpta sp. (lef) in larval status, and Cycloneda sanguinea (right), (F) Hippodamia convergens, (G) Ocyptamus dimidiatus, (H) Scymnus sp., (I) Pachyneuron sp., (J) Aphidius sp., (K) Melanaphis sacchari mummies.

Fig. 4 in Forecasting the impact of an invasive macrophyte species in the littoral zone through aquatic insect species composition

Fig. 4. Comparison among Bray-Curtis dissimilarity indices of aquatic insect assemblages associated with white ginger lily banks and native vegetation profile in the littoral zone of a tropical reservoir in the Brazilian Savanna (Group 1, white ginger lily; Group 2, invaded forest; Group 3, native macrophyte; Group 4, riparian vegetation).

Fig. 2 in Forecasting the impact of an invasive macrophyte species in the littoral zone through aquatic insect species composition

Fig. 2. Comparison between ecological variables of aquatic insect assemblages associated with invasive white ginger lily bank and other native vegetation banks in the littoral zone of a tropical reservoir in the Brazilian Savanna (A, abundance; B, richness; C, Simpson diversity; IM, invasive macrophyte; IF, invaded forest; NM, native macrophyte; RV, riparian vegetation).

Fig. 1 in Forecasting the impact of an invasive macrophyte species in the littoral zone through aquatic insect species composition

Fig. 1. Location and characterization of vegetation profile banks of the Fazzari reservoir in the Brazilian Savanna (Cerrado Biome, Brazil).

Fig. 3 in Forecasting the impact of an invasive macrophyte species in the littoral zone through aquatic insect species composition

Fig. 3. Analyses of non-metric MDS of aquatic insect assemblages associated with white ginger lilY banks and native vegetation profiles in the littoral zone of a tropical reservoir in the Brazilian Savanna (●, white ginger lilY; ○, invaded forest; ∆, native macrohYte; ▲, riparian vegetation).

Fig. 10 in The stick insect genus Medauroidea Zompro, 2000: Taxonomic note and extension to Laos and Cambodia with one new species, M. romantica sp. nov. (Phasmida: Phasmatidae: Clitumninae)

Fig. 10. Medauroidea romantica sp. nov. (photographs by J. Constant). A–D, specimens in nature in type location. E, typical habitat of the species.

Fig. 7 in The stick insect genus Medauroidea Zompro, 2000: Taxonomic note and extension to Laos and Cambodia with one new species, M. romantica sp. nov. (Phasmida: Phasmatidae: Clitumninae)

Fig. 7. Medauroidea romantica sp. nov., eggs. A, dorsal view. B, lateral view. C, anterodorsal view. D, colour variation, lateral and dorsal view.

Fig. 6 in The stick insect genus Medauroidea Zompro, 2000: Taxonomic note and extension to Laos and Cambodia with one new species, M. romantica sp. nov. (Phasmida: Phasmatidae: Clitumninae)

Fig. 6. Medauroidea romantica sp. nov., paratype ♀. A, habitus, dorsal view. B. habitus, lateral view. C, habitus, ventral view. D, head and thorax, dorsal view. E, terminalia, dorsal view. F, terminalia ventral view. G, terminalia, lateral view. H, head and thorax, lateral view.

Fig. 9 in The stick insect genus Medauroidea Zompro, 2000: Taxonomic note and extension to Laos and Cambodia with one new species, M. romantica sp. nov. (Phasmida: Phasmatidae: Clitumninae)

Fig. 9. Medauroidea romantica sp. nov., nymphs (photographs by X. Vermeersch). A–C, newborn first instar nymph. A–B, habitus. C, detail of head. D, fully grown first instar nymph, habitus. E, second instar nymph (top) and fully grown first instar nymph (bottom).