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Supplementary material 5 from: Bennett AMR, Cardinal S, Gauld ID, Wahl DB (2019) Phylogeny of the subfamilies of Ichneumonidae (Hymenoptera). Journal of Hymenoptera Research 71: 1-156. https://doi.org/10.3897/jhr.71.32375

: Data type: Phylogenetic trees (Winclada format)

Supplementary material 6 from: Bennett AMR, Cardinal S, Gauld ID, Wahl DB (2019) Phylogeny of the subfamilies of Ichneumonidae (Hymenoptera). Journal of Hymenoptera Research 71: 1-156. https://doi.org/10.3897/jhr.71.32375

: Data type: Phylogenetic trees (Winclada format)

Supplementary material 4 from: Bennett AMR, Cardinal S, Gauld ID, Wahl DB (2019) Phylogeny of the subfamilies of Ichneumonidae (Hymenoptera). Journal of Hymenoptera Research 71: 1-156. https://doi.org/10.3897/jhr.71.32375

: Data type: phylogenetic data (Hennig86 format)

Supplementary material 2 from: Bennett AMR, Cardinal S, Gauld ID, Wahl DB (2019) Phylogeny of the subfamilies of Ichneumonidae (Hymenoptera). Journal of Hymenoptera Research 71: 1-156. https://doi.org/10.3897/jhr.71.32375

: Data type: phylogenetic data (Hennig86 format)

Supplementary material 3 from: Bennett AMR, Cardinal S, Gauld ID, Wahl DB (2019) Phylogeny of the subfamilies of Ichneumonidae (Hymenoptera). Journal of Hymenoptera Research 71: 1-156. https://doi.org/10.3897/jhr.71.32375

: Data type: phylogenetic data (nexus format)

Supplementary material 1 from: Bennett AMR, Cardinal S, Gauld ID, Wahl DB (2019) Phylogeny of the subfamilies of Ichneumonidae (Hymenoptera). Journal of Hymenoptera Research 71: 1-156. https://doi.org/10.3897/jhr.71.32375

: Data type: phylogenetic data (nexus format)

Fig 6 from: Tanaka S, Kotaki T, Nishide Y, Ben-Hamouda A, Abdellaoui K, Ebbe MAB, Ely SO (2019) Effects of water extracts of feces from three locust species and various plants on oviposition and embryonic development in the desert locust Schistocerca gregaria. Journal of Orthoptera Research 28(2): 195-204. https://doi.org/10.3897/jor.28.34665

Fig 6 Effects of water extracts of frass produced by desert locusts (Sg), migratory locusts (Lm), and Bombay locusts (Ns) fed with rescue grass leaves on the number of A. Egg pods and B. Holes dug by adult desert locusts presented with extracts mixed with sand. Three cups containing frass extracts of the three locust species were simultaneously presented to locusts in each of two locust cages (light and dark histograms) for seven days. Numbers in parentheses indicate the total numbers of days observed. Bars on histograms indicate one standard deviation. Different letters in each comparison (light or dark histograms) in (A) indicate significant differences at the 5% level with Tukey's multiple comparison test. n.s. indicates no significant differences in each comparison with ANOVA (light or dark histograms).

Fig 3 from: Kenyeres Z, Takács G, Bauer N (2019) Response of orthopterans to macroclimate changes: A 15-year case study in Central European humid grasslands. Journal of Orthoptera Research 28(2): 187-193. https://doi.org/10.3897/jor.28.34102

Fig 3 Significant decreasing and increasing trends in the relative abundance of some characteristic Orthoptera species in the studied grasslands (2002–2017). Temporal trends were evaluated by the Mann-Kendall trend test.

Fig 2 from: Strauß J (2019) What determines the number of auditory sensilla in the tympanal hearing organs of Tettigoniidae? Perspectives from comparative neuroanatomy and evolutionary forces. Journal of Orthoptera Research 28(2): 205-219. https://doi.org/10.3897/jor.28.33586

Fig 2 Standardized effects of call patterns in Neoconocephalus on the number of CA sensilla and CA length for a. Pulse rate; b. Structure of continuous or discontinuous calls; and c. Pulse pattern. The evolutionary derived call characters are a slow pulse rate, discontinuous calls, and double pulses. Significance levels: * 0.05 > p > 0.01; ** 0.01 > p > 0.001. Adapted from Strauß et al. 2017, with permission from John Wiley and Sons.

Fig 5 from: Tanaka S, Kotaki T, Nishide Y, Ben-Hamouda A, Abdellaoui K, Ebbe MAB, Ely SO (2019) Effects of water extracts of feces from three locust species and various plants on oviposition and embryonic development in the desert locust Schistocerca gregaria. Journal of Orthoptera Research 28(2): 195-204. https://doi.org/10.3897/jor.28.34665

Fig 5 Effects of water extracts of frass produced by A, B. Bombay locusts and C, D. Migratory locusts fed with rescue grass leaves on the numbers of egg pods laid (A, C) and holes dug (B, D) by adult female desert locusts presented with extracts mixed with sand. Two cups containing frass extract (treated) and water (control) were simultaneously presented to locusts in each of two locust cages, and the data were combined. Numbers in parentheses indicate the total numbers of days observed. Bars on histograms indicate one standard deviation. Asterisks indicate significant differences at the 5% level with a t-test. n.s. indicates no significant difference.

Fig 2 from: Tanaka S, Kotaki T, Nishide Y, Ben-Hamouda A, Abdellaoui K, Ebbe MAB, Ely SO (2019) Effects of water extracts of feces from three locust species and various plants on oviposition and embryonic development in the desert locust Schistocerca gregaria. Journal of Orthoptera Research 28(2): 195-204. https://doi.org/10.3897/jor.28.34665

Fig 2 Effects of water extracts of frass obtained from lab-reared desert locust fed with romaine lettuce in Tunisia on the number of A. Egg pods laid and B. Holes dug by adult female desert locusts presented with sand mixed with frass extracts. Two cups containing frass extracts (treated) and water (control) were simultaneously presented to locusts in each of two locust cages for seven or eight days, and the data were combined. Numbers in parentheses indicate the total numbers of days observed. Asterisks indicate a significant difference at the 5% level with a t-test. n.s. indicates no significant difference.

Fig 9 from: Tanaka S, Kotaki T, Nishide Y, Ben-Hamouda A, Abdellaoui K, Ebbe MAB, Ely SO (2019) Effects of water extracts of feces from three locust species and various plants on oviposition and embryonic development in the desert locust Schistocerca gregaria. Journal of Orthoptera Research 28(2): 195-204. https://doi.org/10.3897/jor.28.34665

Fig 9 Effects of water extracts of rescue grass-fed desert locust frass on A. Egg widths (mean ± SD; n = 10) and B. Antennal lengths of embryos (mean ± SD; n = 6–11). Eggs were incubated in sand wetted with the frass extract (treated) or water (control) on day three after oviposition at 30°C. C–F. Photographs show embryos observed on days 5 and 9. Triangles in (A) and (B) indicate the time when the treatment started. Vertical bars in C–F indicate 1 mm. White arrows indicate an embryonic antenna in C–E.

Fig 2 from: Kenyeres Z, Takács G, Bauer N (2019) Response of orthopterans to macroclimate changes: A 15-year case study in Central European humid grasslands. Journal of Orthoptera Research 28(2): 187-193. https://doi.org/10.3897/jor.28.34102

Fig 2 Decreasing and increasing trends in the relative abundance of some orthopteran parameters (2002–2017). Temporal trends were evaluated by the Mann-Kendall trend test.

Fig 1 from: Strauß J (2019) What determines the number of auditory sensilla in the tympanal hearing organs of Tettigoniidae? Perspectives from comparative neuroanatomy and evolutionary forces. Journal of Orthoptera Research 28(2): 205-219. https://doi.org/10.3897/jor.28.33586

Fig 1 The auditory system of bushcrickets. a. Schematic of the acoustic trachea (at) from the acoustic spiracle (as) in the thorax into the foreleg with tympanal membranes (ty) in the proximal tibia; b. Transverse section of the tibia at the level of the tympana and crista acustica in Gampsocleis gratiosa; in Gampsocleis gratiosa; c. The sensory organs in the proximal tibia of the male Tettigonia viridissima. The dorsal cuticle has been removed after axonal tracing of the tympanal nerve with cobalt solution to stain sensory neurons of the subgenual organ (SGO), intermediate organ (IO) and crista acustica. The crista acustica is placed between the anterior tympanum (aty) and posterior tympanum (pty). The tympanal flaps (tf) cover the tympanal membranes. Arrows indicate the tectorial membrane; d. Morphological differences of sensory neurons along the crista acustica from G. gratiosa, showing the (di) third-most proximal, (dii) middle, and (diii) third-most distal sensillum. Abbreviations: at, anterior trachea; aty, anterior tympanum; cc, cap cell; de, dendrite; dow, dorsal tracheal wall; hc, haemolymph channel; IO, intermediate organ; nmc, nerve muscle channel; nsc, nucleus of scolopale cell; pn, perikarya of sensory neurons; pt, posterior trachea; pty, posterior tympanum; s, septum; sb, supporting band; scol, scolopale cap and rods; SGO, subgenual organ; sli, slit; sn, sensory neuron; tf, tympanal flap; tm, tectorial membrane. Scales: 500 µm (B), 100 µm (C), 50 µm (D). Figure a. reprinted from Strauß et al. 2014, with permission from John Wiley and Sons. b., d. redrawn from Lin et al. 1994, with permission from John Wiley and Sons.

Fig 1 from: Tanaka S, Kotaki T, Nishide Y, Ben-Hamouda A, Abdellaoui K, Ebbe MAB, Ely SO (2019) Effects of water extracts of feces from three locust species and various plants on oviposition and embryonic development in the desert locust Schistocerca gregaria. Journal of Orthoptera Research 28(2): 195-204. https://doi.org/10.3897/jor.28.34665

Fig 1 Effects of water extracts of desert locust frass collected under umbrella thorn trees in the Mauritanian desert on the number of A., B. Egg pods laid, and C., D. Holes dug by adult female desert locusts presented with extracts mixed with sand. Frass were collected at sites #1 and #2 in 2016 and 2017, respectively. Two cups containing frass extracts (treated) and water (control) were simultaneously presented to locusts in each of two locust cages for seven or five days, and the data were combined. Numbers in parentheses indicate the total numbers of days observed. Bars on histograms indicate one standard deviation. Asterisks indicate a significant difference at the 5% level with a t-test. n.s. indicates no significant difference.

Fig 8 from: Tanaka S, Kotaki T, Nishide Y, Ben-Hamouda A, Abdellaoui K, Ebbe MAB, Ely SO (2019) Effects of water extracts of feces from three locust species and various plants on oviposition and embryonic development in the desert locust Schistocerca gregaria. Journal of Orthoptera Research 28(2): 195-204. https://doi.org/10.3897/jor.28.34665

Fig 8 Effects of water extracts of rescue grass-fed Bombay locust (Ns) and migratory locust (Lm) frass on desert locust egg hatching rates. Five groups of 20 eggs were buried in sand wetted with each extract and water alone (control, C) within three days after oviposition and were observed for hatching at 30°C. Asterisks indicate significant differences at the 5% level with GLMM.

Fig 7 from: Tanaka S, Kotaki T, Nishide Y, Ben-Hamouda A, Abdellaoui K, Ebbe MAB, Ely SO (2019) Effects of water extracts of feces from three locust species and various plants on oviposition and embryonic development in the desert locust Schistocerca gregaria. Journal of Orthoptera Research 28(2): 195-204. https://doi.org/10.3897/jor.28.34665

Fig 7 Effects of hot and cool water extracts of rescue grass-fed desert locust frass on the number of A. Egg pods laid and B. Holes dug by adult female desert locusts. Frass were extracted with boiling and cool water and the extracts were mixed with sand. Sand cups containing these extracts and water as a control were presented to locusts in the same cage for 4 days. Numbers in parentheses indicate the total numbers of days observed. Bars on histograms indicate one standard deviation. Different letters in (A) indicate significant differences at the 5% level with Tukey's multiple comparison test. n.s. in (B) indicates no significant difference with ANOVA at the 5% level.

Fig 5 from: Kenyeres Z, Takács G, Bauer N (2019) Response of orthopterans to macroclimate changes: A 15-year case study in Central European humid grasslands. Journal of Orthoptera Research 28(2): 187-193. https://doi.org/10.3897/jor.28.34102

Fig 5 CCA ordination based on Orthoptera parameters and environmental parameters (Confus: Conocephalus fuscus; Eucdec: Euchorthippus declivus; gra: graminicole species; mo-ata: mean of the monthly active thermic amount (10°C); mo-eta: mean of the monthly effective thermic amount (10°C); m-ther&ther: moderately-thermophilic and thermophilic species; pra: pratinicole species; rain-spr: rainfall in spring; Roeroe: Roeseliana roeselii; s-r: species richness; tem-m: annual mean temperature; tem-min: annual minimum temperature; tem-sum: mean temperature in summer; the: thermophilic species).

Fig 4 from: Kenyeres Z, Takács G, Bauer N (2019) Response of orthopterans to macroclimate changes: A 15-year case study in Central European humid grasslands. Journal of Orthoptera Research 28(2): 187-193. https://doi.org/10.3897/jor.28.34102

Fig 4 Trends in macroclimate parameters on the studied area (2002–2017). Temporal trends were evaluated by the Mann-Kendall trend test.

Fig 3 from: Tanaka S, Kotaki T, Nishide Y, Ben-Hamouda A, Abdellaoui K, Ebbe MAB, Ely SO (2019) Effects of water extracts of feces from three locust species and various plants on oviposition and embryonic development in the desert locust Schistocerca gregaria. Journal of Orthoptera Research 28(2): 195-204. https://doi.org/10.3897/jor.28.34665

Fig 3 Effects of water extracts of leaves of various plants and desert locust frass collected after locusts fed on these plants on the numbers of egg pods laid by adult female desert locusts presented with sand mixed with extracts. Sand wetted with water was also presented as a control. Three cups containing leaf, frass extract, and water (control) were simultaneously presented to locusts in one (A, C, D) or two locust cages (B, E, F) for three to five days, and the data were combined in (B), (E), and (F). Numbers in parentheses indicate the total numbers of days observed. Bars on histograms indicate one standard deviation. Different letters in each panel indicate significant differences at the 5% level with Tukey's multiple comparison test. DG, Dactylis glomerata (orchard grass); BO, Brassica oleracea var. capitata (cabbage); SB, Sorghum bicolor (sorghum); LS, Lactuca sativa var. longifolia (romaine lettuce); BR, Brassica rapa var. perviridis (Japanese mustard spinach); MS, Miscanthus sinensis (silver grass).