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Supplementary material 2 from: Prosi R, Wiesbauer H, Müller A (2016) Distribution, biology and habitat of the rare European osmiine bee species Osmia (Melanosmia) pilicornis (Hymenoptera, Megachilidae, Osmiini). Journal of Hymenoptera Research 52: 1-36. https://doi.org/10.3897/jhr.52.10441

Female of Osmia pilicornis gnawing nesting burrow :

Supplementary material 5 from: Prosi R, Wiesbauer H, Müller A (2016) Distribution, biology and habitat of the rare European osmiine bee species Osmia (Melanosmia) pilicornis (Hymenoptera, Megachilidae, Osmiini). Journal of Hymenoptera Research 52: 1-36. https://doi.org/10.3897/jhr.52.10441

Female of Osmia pilicornis collecting pollen on Pulmonaria mollis :

Supplementary material 1 from: Prosi R, Wiesbauer H, Müller A (2016) Distribution, biology and habitat of the rare European osmiine bee species Osmia (Melanosmia) pilicornis (Hymenoptera, Megachilidae, Osmiini). Journal of Hymenoptera Research 52: 1-36. https://doi.org/10.3897/jhr.52.10441

List of distributional data of Osmia pilicornis :

Supplementary material 6 from: Prosi R, Wiesbauer H, Müller A (2016) Distribution, biology and habitat of the rare European osmiine bee species Osmia (Melanosmia) pilicornis (Hymenoptera, Megachilidae, Osmiini). Journal of Hymenoptera Research 52: 1-36. https://doi.org/10.3897/jhr.52.10441

Female of Osmia pilicornis collecting pollen on Ajuga reptans :

Supplementary material 4 from: Prosi R, Wiesbauer H, Müller A (2016) Distribution, biology and habitat of the rare European osmiine bee species Osmia (Melanosmia) pilicornis (Hymenoptera, Megachilidae, Osmiini). Journal of Hymenoptera Research 52: 1-36. https://doi.org/10.3897/jhr.52.10441

Female of Osmia pilicornis constructing nest plug :

opencc-by-4.0Feb 2017View details →

Supplementary material 1 from: Gallardo FE, Reche VA, Bertolaccini I, Zárate B, Curis C (2017) A new genus and species of Eucoilinae (Hymenoptera, Cynipoidea, Figitidae) parasitoid of Euxesta eluta Loew (Diptera, Otitidae) attacked Bt sweet corn in Argentina. Journal of Hymenoptera Research 54: 57-70. https://doi.org/10.3897/jhr.54.10096

GBIF :

Figure 5 from: Thompson AC, Bazelet CS, Naskrecki P, Samways MJ (2017) Adapting the Dragonfly Biotic Index to a katydid (Tettigoniidae) rapid assessment technique: case study of a biodiversity hotspot, the Cape Floristic Region, South Africa. Journal of Orthoptera Research 26: 63-71. https://doi.org/10.3897/jor.26.14552

Figure 5 - Map of ecosystem threat statuses and the average KBI scores (i.e. KBI/Site) of each ecosystem.

Figure 3 from: Thompson AC, Bazelet CS, Naskrecki P, Samways MJ (2017) Adapting the Dragonfly Biotic Index to a katydid (Tettigoniidae) rapid assessment technique: case study of a biodiversity hotspot, the Cape Floristic Region, South Africa. Journal of Orthoptera Research 26: 63-71. https://doi.org/10.3897/jor.26.14552

Figure 3 - Distribution of South African and Cape Floristic Region katydid species among Tettigoniidae subfamilies.

Figure 2 from: Thompson AC, Bazelet CS, Naskrecki P, Samways MJ (2017) Adapting the Dragonfly Biotic Index to a katydid (Tettigoniidae) rapid assessment technique: case study of a biodiversity hotspot, the Cape Floristic Region, South Africa. Journal of Orthoptera Research 26: 63-71. https://doi.org/10.3897/jor.26.14552

Figure 2 - Composition of South African (A, C, E) and Cape Floristic Region (B, D, F) katydid assemblages as characterised by their distribution (A, B), mobility (C, D), and trophic level (E, F) relative to their IUCN threat status.

Figure 1 from: Thompson AC, Bazelet CS, Naskrecki P, Samways MJ (2017) Adapting the Dragonfly Biotic Index to a katydid (Tettigoniidae) rapid assessment technique: case study of a biodiversity hotspot, the Cape Floristic Region, South Africa. Journal of Orthoptera Research 26: 63-71. https://doi.org/10.3897/jor.26.14552

Figure 1 - Proportion of South African (A, C, E, G) and Cape Floristic Region (B, D, F, H) katydid assemblages as characterised by the KBI assessment criteria (Threat Status, Distribution, Trophic level and Mobility).

Figure 4 from: Tan MK, Yeo H, Hwang WS (2017) Ground dwelling pygmy grasshoppers (Orthoptera: Tetrigidae) in Southeast Asian tropical freshwater swamp forest prefer wet microhabitats. Journal of Orthoptera Research 26: 73-80. https://doi.org/10.3897/jor.26.14551

Figure 4 - A canonical analysis of principal coordinates (CAP) with Euclidean distance to show association of adult assemblage with NMDS1 and NMDS2 representing microhabitat conditions. The circle represents belt transects and cross represents morpho-species.

Figure 3 from: Tan MK, Yeo H, Hwang WS (2017) Ground dwelling pygmy grasshoppers (Orthoptera: Tetrigidae) in Southeast Asian tropical freshwater swamp forest prefer wet microhabitats. Journal of Orthoptera Research 26: 73-80. https://doi.org/10.3897/jor.26.14551

Figure 3 - Correlation between total abundance of pygmy grasshoppers and dry dicot leaf litter. The model was fitted using generalized linear mixed-effects model using Poisson error structure.

Figure 4 from: Thompson AC, Bazelet CS, Naskrecki P, Samways MJ (2017) Adapting the Dragonfly Biotic Index to a katydid (Tettigoniidae) rapid assessment technique: case study of a biodiversity hotspot, the Cape Floristic Region, South Africa. Journal of Orthoptera Research 26: 63-71. https://doi.org/10.3897/jor.26.14552

Figure 4 - Distribution of Katydid Biotic Index (KBI) among ecosystem threat statuses (mean ± s.e.).

Figure 2 from: Tan MK, Yeo H, Hwang WS (2017) Ground dwelling pygmy grasshoppers (Orthoptera: Tetrigidae) in Southeast Asian tropical freshwater swamp forest prefer wet microhabitats. Journal of Orthoptera Research 26: 73-80. https://doi.org/10.3897/jor.26.14551

Figure 2 - A non-metric multidimensional scaling (NMDS) using Bray-Curtis distance to summarize microhabitat condition data, showing two hulls representing belt transects (1, circle) close to and (2, triangular) far from the main stream. Stress value for first two axes = 0.17.

Figure 1 from: Olivero P, Robillard T (2017) Same-sex sexual behavior in Xenogryllus marmoratus (Haan, 1844) (Grylloidea: Gryllidae: Eneopterinae): Observation in the wild from YouTube. Journal of Orthoptera Research 26: 1-5. https://doi.org/10.3897/jor.26.14569

Figure 1 - Screenshots of the video showing same-sex sexual behavior between males of Xenogryllus marmoratus (Haan, 1844). For details, see the results section.

Figure 1 from: Tan MK, Yeo H, Hwang WS (2017) Ground dwelling pygmy grasshoppers (Orthoptera: Tetrigidae) in Southeast Asian tropical freshwater swamp forest prefer wet microhabitats. Journal of Orthoptera Research 26: 73-80. https://doi.org/10.3897/jor.26.14551

Figure 1 - A non-metric multidimensional scaling (NMDS) using Bray-Curtis distance to summarize microhabitat condition data, indicating the different microhabitat conditions. Stress value for first two axes = 0.17.

Figure 3 from: Peralta-Rincon JR, Escudero G, Edelaar P (2017) Phenotypic plasticity in color without molt in adult grasshoppers of the genus Sphingonotus (Acrididae: Oedipodinae). Journal of Orthoptera Research 26: 21-27. https://doi.org/10.3897/jor.26.14550

Figure 3 - Individual changes in color in the final surviving azure sand grasshoppers when kept on bluish-gray stones (blue lines, N = 2) or reddish-brown soil (red lines, N = 3). The comparison is between the same individuals at the beginning of the experiment and once frozen and cleaned at the end. Color is expressed in the three independent dimensions of the CIE-L*a*b* space (see text).

Figure 2 from: Peralta-Rincon JR, Escudero G, Edelaar P (2017) Phenotypic plasticity in color without molt in adult grasshoppers of the genus Sphingonotus (Acrididae: Oedipodinae). Journal of Orthoptera Research 26: 21-27. https://doi.org/10.3897/jor.26.14550

Figure 2 - Average changes in color over time (days since the start of each treatment) for adult azure sand grasshoppers kept on bluish-gray stones (blue symbols and lines) or reddish-brown soil (red symbols and lines). Color is expressed in the three independent dimensions of the CIE-L*a*b* space (see text). Lines show the predicted values for each CIE-L*a*b dimension according to a fitted model containing Time, Substrate, Sex, Time:Substrate and sqTime; we excluded the subject random effect for better visualization. Continuous lines and circles are for females while dashed lines and triangles are for males. The "Red Earth" treatment had to be restarted using grasshoppers from the same field location but captured later in time. As a result, the timing of data collection is out of phase between treatments, and L is initially slightly lower for "Red Earth" individuals (since the species gets darker with age).

Figure 1 from: Peralta-Rincon JR, Escudero G, Edelaar P (2017) Phenotypic plasticity in color without molt in adult grasshoppers of the genus Sphingonotus (Acrididae: Oedipodinae). Journal of Orthoptera Research 26: 21-27. https://doi.org/10.3897/jor.26.14550

Figure 1 - Example of an image taken for color measurement. The individual was held in place by the transparent plastic lid of the Petri dish to obtain a correct position. Brightness and hue were measured in the red diamond-shaped part of the thorax. The color of a small area of the background paper was also measured (red circle) as a reference gray standard to correct for lighting variation among images.

Figure 6 from: Kenyeres Z, Szentirmai I (2017) Effects of different mowing regimes on orthopterans of Central-European mesic hay meadows. Journal of Orthoptera Research 26: 29-37. https://doi.org/10.3897/jor.26.14549

Figure 6 - PCA based on the orthopteran samples of four study sites (sites I–IV) (black circle: mowing once a year in May; black square: mowing twice a year in May and September; empty circle: mowing once a year in September; black triangle: abandoned).