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Figures 118-123 from: Gonzalez VH, Griswold T, Simões M (2017) On the identity of the adventive species of Eufriesea Cockerell in the USA: systematics and potential distribution of the coerulescens species group (Hymenoptera, Apidae). Journal of Hymenoptera Research 55: 55-102. https://doi.org/10.3897/jhr.55.12209

Figures 118-123 - Male terminalia of E. micheneri (paratype. Mexico: Jalisco, Talpa, KUNHM-ENT 1121712). 118 Seventh metasomal sternum in ventral view 119, 120 Eighth metasomal sternum in ventral and lateral views 121–123 Genital capsule in dorsal, ventral, and lateral views.

Figures 34-39 from: Gonzalez VH, Griswold T, Simões M (2017) On the identity of the adventive species of Eufriesea Cockerell in the USA: systematics and potential distribution of the coerulescens species group (Hymenoptera, Apidae). Journal of Hymenoptera Research 55: 55-102. https://doi.org/10.3897/jhr.55.12209

Figures 34-39 - Male lectotype of E. coerulescens. 34 Facial view 35 Detail of clypeus with arrows indicating weak sublateral ridges that form a median longitudinal depression 36 Dorsal habitus 37 Lateral habitus 38 right and left forewings 39 Dorsal view of mesoscutellum.

Figures 40-45 from: Gonzalez VH, Griswold T, Simões M (2017) On the identity of the adventive species of Eufriesea Cockerell in the USA: systematics and potential distribution of the coerulescens species group (Hymenoptera, Apidae). Journal of Hymenoptera Research 55: 55-102. https://doi.org/10.3897/jhr.55.12209

Figures 40-45 - Male terminalia of E. coerulescens (Mexico: Nuevo León, ECO-TAP-E-104040). 40 Seventh metasomal sternum in ventral view 41, 42 Eighth metasomal sternum in ventral and lateral views 43–45 Genital capsule in dorsal, ventral, and lateral views.

Figures 46-50 from: Gonzalez VH, Griswold T, Simões M (2017) On the identity of the adventive species of Eufriesea Cockerell in the USA: systematics and potential distribution of the coerulescens species group (Hymenoptera, Apidae). Journal of Hymenoptera Research 55: 55-102. https://doi.org/10.3897/jhr.55.12209

Figures 46-50 - Female of E. coerulescens (Mexico: San Luis Potosí, ECO-TAP-E-104161; Querétaro, ECO-TAP-E-104753 [Fig. 46]). 46 Facial view 47 Dorsal habitus 48 Lateral habitus 49 Dorsal view of mesoscutellum 50 Second metasomal tergum.

Figure 129 from: Gonzalez VH, Griswold T, Simões M (2017) On the identity of the adventive species of Eufriesea Cockerell in the USA: systematics and potential distribution of the coerulescens species group (Hymenoptera, Apidae). Journal of Hymenoptera Research 55: 55-102. https://doi.org/10.3897/jhr.55.12209

Figure 129 - Potential distribution for all species of Eufriesea of the coerulescens group combined (top map) and for E. coerulescens alone (bottom map) with collection localities.

Figures 14-19 from: Gonzalez VH, Griswold T, Simões M (2017) On the identity of the adventive species of Eufriesea Cockerell in the USA: systematics and potential distribution of the coerulescens species group (Hymenoptera, Apidae). Journal of Hymenoptera Research 55: 55-102. https://doi.org/10.3897/jhr.55.12209

Figures 14-19 - Detail of the subapical projection (indicated by an arrow) above the spurs of the male metatibia in anterior (14, 16, 18) and lateral views (15, 17, 19). 14, 15 E. barthelli (paratype. Mexico: Jalisco, Ajijic, KUNHM-ENT 0504535); 16, 17 E. engeli (paratype, KUNHM-ENT 0504531) 18, 19 E. micheneri (paratype. Mexico: Jalisco, Talpa, KUNHM-ENT 1121712).

Figure 5 from: Watts C, Thornburrow D, Stringer I, Cave V (2017) Population expansion by Cook Strait giant wētā, Deinacrida rugosa (Orthoptera: Anostostomatidae), following translocation to Matiu/Somes Island, New Zealand, and subsequent changes in abundance. Journal of Orthoptera Research 26: 171-180. https://doi.org/10.3897/jor.26.21712

Figure 5 - Distribution of geckos and skinks as detected using tracking tunnels on Matiu/Somes Island. Data are combined presence-absence of footprints on cards from tracking tunnels baited with peanut butter during three nights in 2008 and four nights in both 2013 and 2015. 2008 data from Watts et al. (2009, 2011).

Figure 4 from: Watts C, Thornburrow D, Stringer I, Cave V (2017) Population expansion by Cook Strait giant wētā, Deinacrida rugosa (Orthoptera: Anostostomatidae), following translocation to Matiu/Somes Island, New Zealand, and subsequent changes in abundance. Journal of Orthoptera Research 26: 171-180. https://doi.org/10.3897/jor.26.21712

Figure 4 - Distribution of adult Deinacrida rugosa presence as evidenced by combining detection with tracking tunnels baited with peanut butter and finding them by searching at night. Searches extended 15 m from each tracking tunnel. Results are presence-absence derived from three searches over three nights in 2008, and four searches over four nights in both 2013 and 2015. Areas searched (tracking tunnel transects) are indicated as white lines. 2008 data from Watts et al. (2009, 2011).

Figure 1 from: Watts C, Thornburrow D, Stringer I, Cave V (2017) Population expansion by Cook Strait giant wētā, Deinacrida rugosa (Orthoptera: Anostostomatidae), following translocation to Matiu/Somes Island, New Zealand, and subsequent changes in abundance. Journal of Orthoptera Research 26: 171-180. https://doi.org/10.3897/jor.26.21712

Figure 1 - Arrangement of tracking tunnel transects (shown in white) along the footpaths on Matiu-Somes Island. Each circle indicates the location of a tracking tunnel. The dark hatched area indicates where Deinacrida rugosa were released in 1996. The light hatched area shows where 186 adult D. rugosa were taken for translocation in 2007 and 2008. Note that no wētā were removed from the North transect.

Figures 100-101 from: Massa B (2017) Revision of the tropical African genus Tetraconcha (Orthoptera: Tettigoniidae: Phaneropterinae) with the description of ten new species. Journal of Orthoptera Research 26: 211-232. https://doi.org/10.3897/jor.26.21469

Figures 100-101 - 100. Specimen of T. annoyeri sp. n. photographed in the field on the litter of the Dzanga-N'Doki National Park. 101. Canopy of the forest of the Dzanga-N'Doki National Park, where some Tetraconcha were collected in 2008-2012 (Photo by P. Annoyer).

Figures 67-78 from: Massa B (2017) Revision of the tropical African genus Tetraconcha (Orthoptera: Tettigoniidae: Phaneropterinae) with the description of ten new species. Journal of Orthoptera Research 26: 211-232. https://doi.org/10.3897/jor.26.21469

Figures 67-78 - Habitus in lateral view of males of: 67. Tetraconcha banzyvilliana; 68. T. stichyrata; 69. T. fenestrata; 70. T. smaragdina; 71. T. ruzzieri sp. n.; 72. T. morettoi sp. n.; 73. T. perezi sp. n.; 74. T. loubesi sp. n.; 75. T. danflousi sp. n.; 76. Drepanophyllum marmoratum; 77. Stenamblyphyllum dilutum; 78. Debrona cervina.

Figures 11-22 from: Massa B (2017) Revision of the tropical African genus Tetraconcha (Orthoptera: Tettigoniidae: Phaneropterinae) with the description of ten new species. Journal of Orthoptera Research 26: 211-232. https://doi.org/10.3897/jor.26.21469

Figures 11-22 - Tetraconcha ruzzieri sp. n. paratype male (Ivory Coast, Taï Nat. Park): 11. Stridulatory area; 12. Stridulatory file below the left tegmen; 13. Subgenital plate in ventral view; 14. Cerci in dorsal view. Tetraconcha fenestrata holotype male (Cameroon): 15. Stridulatory area of the left tegmen; 16. Stridulatory file below the left tegmen. Tetraconcha fenestrata male (Cameroon, Mukonje Farm): 17. Subgenital plate in ventral view; 18. Cerci in dorsal view. Tetraconcha danflousi sp. n. holotype male (Ivory Coast, Taï Nat. Park): 19. Stridulatory area; 20. Stridulatory file below the left tegmen and "window" of the left tegmen; 21. Subgenital plate and cerci in ventral view; 22. Cerci in dorsal view. Figs 15 and 16 after Orthoptera Species File.

Figures 32-48 from: Massa B (2017) Revision of the tropical African genus Tetraconcha (Orthoptera: Tettigoniidae: Phaneropterinae) with the description of ten new species. Journal of Orthoptera Research 26: 211-232. https://doi.org/10.3897/jor.26.21469

Figures 32-48 - Tetraconcha smaragdina male (Central African Republic, N'Doki): 32. Stridulatory area (the arrow shows the distance between the base of left tegmen and the maximum width of cubital areas); 33. Stridulatory area of the holotype (Cameroon); 34. Stridulatory file below the left tegmen; 35. Cerci in dorsal view; 36. Subgenital plate in ventral view of the holotype. Tetraconcha loubesi sp. n. holotype male (Central African Republic, N'Doki): 37. Stridulatory area; 38. Stridulatory file below the left tegmen; 39. Cerci in dorsal view; 40. Subgenital plate in ventral view). Tetraconcha morettoi sp. n. holotype male (Central African Republic, N'Doki): 41. Stridulatory area; 42. Stridulatory file below the left tegmen; 43. Subgenital plate in ventral view; 44. Cerci in dorsal view. Tetraconcha ndokiensis sp. n. holotype male (Central African Republic, N'Doki): 45. Stridulatory area; 46. Stridulatory file below the left tegmen; 47. Subgenital plate and cerci in dorsal view; 48. Subgenital plate and cerci in ventral view.

Fig 9 from: Tanaka S (2017) Locusta migratoria (Orthoptera: Acrididae) embryos monitor neighboring eggs for hatching synchrony. Journal of Orthoptera Research 26: 103-115. https://doi.org/10.3897/jor.26.20935

Fig 9 - The effect of the time of clumping of Locusta migratoria separated eggs on the hatching time. The differences in mean hatching times between eggs clumped and those kept with distance from one another (controls) are plotted against the time of egg clumping gauged based on the mean hatching time for the control eggs (A). SDs of the mean hatching times for the clumped eggs (closed circles) and control eggs (open circles) are similarly plotted in (B). Each datum point is based on 17–20 eggs.

Figures 1-10 from: Massa B (2017) Revision of the tropical African genus Tetraconcha (Orthoptera: Tettigoniidae: Phaneropterinae) with the description of ten new species. Journal of Orthoptera Research 26: 211-232. https://doi.org/10.3897/jor.26.21469

Figures 1-10 - Debrona cervina male (Kenya, Arabuko Sokoke Forest): 1. Stridulatory area; 2. Stridulatory file below the left tegmen; 3. Cerci and subgenital plate in lateral view; 4. Habitus in dorsal view; 5. Subgenital plate in dorsal view; 6. Subgenital plate in ventral view. Debrona cervina female (same locality): 7. Ovipositor in lateral view. Drepanophyllum marmoratum female (Central African Republic, N'Doki): 8. Ovipositor in lateral view. Tetraconcha sp. (probably smaragdina) female (Cameroon, Mukonje Farm): 9. Ovipositor in lateral view. Stenamblyphyllum dilutum lectotype female (Cameroon, Victoria): 10. Ovipositor in lateral view.

Fig 8 from: Tanaka S (2017) Locusta migratoria (Orthoptera: Acrididae) embryos monitor neighboring eggs for hatching synchrony. Journal of Orthoptera Research 26: 103-115. https://doi.org/10.3897/jor.26.20935

Fig 8 - The effect of the time of separation of paired Locusta migratoria eggs on the hatching time. The differences in mean hatching times between eggs separated and those kept in contact with each other (controls) are plotted against the time of egg separation gauged based on the mean hatching time for the control eggs (A). Comparison of SDs of the mean hatching times (B) and the intervals of hatching in each pair (C) for the eggs separated (open circles) and the control eggs (closed circles). Each datum point is based on 14–24 eggs.

Fig 5 from: Tanaka S (2017) Locusta migratoria (Orthoptera: Acrididae) embryos monitor neighboring eggs for hatching synchrony. Journal of Orthoptera Research 26: 103-115. https://doi.org/10.3897/jor.26.20935

Fig 5 - The intervals from the beginning to end of hatching periods for Locusta migratoria eggs incubated in different mass sizes from day 10 onward. The data are based on the experiment described in Fig. 4. No significant difference was observed in the means among the treatments (p > 0.05; Steel-Dwass test).

Fig 6 from: Tanaka S (2017) Locusta migratoria (Orthoptera: Acrididae) embryos monitor neighboring eggs for hatching synchrony. Journal of Orthoptera Research 26: 103-115. https://doi.org/10.3897/jor.26.20935

Fig 6 - The hatching times for Locusta migratoria eggs incubated in different mass sizes. In each pair of comparisons, the mean time of hatching for the eggs in the larger mass was designated as 0 h (A–D). The numbers in parentheses indicate the number of hatched eggs. Bars indicate one SD. Asterisks indicate a significant difference between the two treatments (p < 0.05; t-test). Differences in hatching time in different masses are shown in (E) by designating the mean hatching time for singly kept eggs as 0 h. Horizontal bars indicate one SD.

Fig 4 from: Tanaka S (2017) Locusta migratoria (Orthoptera: Acrididae) embryos monitor neighboring eggs for hatching synchrony. Journal of Orthoptera Research 26: 103-115. https://doi.org/10.3897/jor.26.20935

Fig 4 - The effect of egg mass sizes on the ranges of hatching times of Locusta migratoria eggs. The frequency distributions of hatching times plotted as deviations from the mean (designated as 0 h) for each egg pod tested. The data for the egg pods are the same as those given in Fig. 1B. SDs are shown. The numbers in parentheses indicate the numbers of hatched eggs and pods used.

Fig 3 from: Tanaka S (2017) Locusta migratoria (Orthoptera: Acrididae) embryos monitor neighboring eggs for hatching synchrony. Journal of Orthoptera Research 26: 103-115. https://doi.org/10.3897/jor.26.20935

Fig 3 - The effect of egg separation on embryogenesis in Locusta migratoria at 30°C. The times (mean ± SD) required to hatch for Locusta migratoria eggs kept as a mass (closed bars) or as separated eggs (open bars) at 30°C. Asterisks indicate a significant difference between the 2 treatments at the 5% level with a t-test. Error bars indicate SD. n = 13–20 each.