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Fig. 4 in Biogeography, ecology, acoustics and chromosomes of East African Eurycorypha Stål species (Orthoptera, Phaneropterinae) with the description of new species

Fig. 4 Oscillograms of calling songs of Eurycorypha species, overview (one echeme in E. punctipennis and E. varia, sequence of two echemes in E. combretoides and E. resonans). In the male–female duet

Fig. 2 in Biogeography, ecology, acoustics and chromosomes of East African Eurycorypha Stål species (Orthoptera, Phaneropterinae) with the description of new species

Fig. 2 Oscillograms presenting details of syllable structure in Eurycorypha resonans n. sp. (a part of syllable of disyllabic echeme; b one complete syllable from the polysyllabic echeme) and E. varia Brunner von Wattenwyl (c part of syllable)

Fig. 11 in Biogeography, ecology, acoustics and chromosomes of East African Eurycorypha Stål species (Orthoptera, Phaneropterinae) with the description of new species

Fig. 11 Female abdominal apices of Eurycorypha species. a, b Eurycorypha punctipennis Chopard, lateral view on ovipositor (a), ventral view on subgenital plate (b). c, d Eurycorypha resonans n. sp., lateral view on ovipositor (c), ventral view on subgenital plate (d). e, f Eurycorypha conclusa n. sp, lateral view on ovipositor (e), ventral view on subgenital plate (f)

Fig. 13 East African Eurycorypha species. a–c in Biogeography, ecology, acoustics and chromosomes of East African Eurycorypha Stål species (Orthoptera, Phaneropterinae) with the description of new species

Fig. 13 East African Eurycorypha species. a–c Eurycorypha meruensis Sjöstedt, southern slopes of Mount Kilimanjaro, Tanzania, 1430 m, banana–coffee plantation, male (a) and female (b), male nymph, fifth instar (c). d–f E. varia Brunner von Wattenwyl, southern slopes of Mount Kilimanjaro, Tanzania, 1710 m, lower border of montane forest, male (d), female (e), female nymph, fifth instar (f)

Fig. 12 in Biogeography, ecology, acoustics and chromosomes of East African Eurycorypha Stål species (Orthoptera, Phaneropterinae) with the description of new species

Fig. 12 Nymphs of Eurycorypha species. a Ant-like stage of cf. E. combretoides n. sp. (third instar), savanna bushland, East Kilimanjaro. b Nymph of E. varia Brunner von Wattenwyl (probably fourth instar), southern slopes of Kilimanjaro, forest edge above Kidia, 1700 m

Fig. 9 East African Eurycorypha species. a in Biogeography, ecology, acoustics and chromosomes of East African Eurycorypha Stål species (Orthoptera, Phaneropterinae) with the description of new species

Fig. 9 East African Eurycorypha species. a Eurycorypha punctipennis Chopard, male, Msaranga valley, southern slopes of Mount Kilimanjaro. b Eurycorypha punctipennis Chopard, female, same locality as male. c Eurycorypha resonans n. sp., male, banana–coffee plantation, village Mahoma, southern slopes of Mount Kilimanjaro. d Eurycorypha resonans n. sp., female, same locality as male. e Eurycorypha combretoides n. sp., male, Chala area, savanna, East Kilimanjaro. f Ant- mimiking male nymph of E. combretoides n. sp. (fourth instar), collected on a bush of Maytenus senegalensis at eastern savanna area of Mount Kilimanjaro and reared to adult

Figures 8 in REVIEW Diplura in caves: diversity, ecology, evolution and biogeography

Figures 8. Distribution of cave-adapted diplurans: A, worldwide; B, Euro-Mediterranean region. In yellow: karst areas (source: Chen et al., 2017). In orange: deserts (source: Olson & Dinerstein, 2002). In blue: ice cover during the Last Glacial Maximum (source: Ehlers et al., 2011). In black: hypogenic karst areas (source: Klimchouk, 2007).

Figure 1 in REVIEW Diplura in caves: diversity, ecology, evolution and biogeography

Figure 1. Maximum likelihood (ML) trees of Diplura. A, ML tree obtained from 18S rDNA data available in Genbank. B, ML tree obtained from COI data. Only bootstrap support values above 70 are shown.

Figure 7 in REVIEW Diplura in caves: diversity, ecology, evolution and biogeography

Figure 7. Pretarsal adaptations in cave-adapted campodeid species: A, Lepidocampa beltrani from Caverna Batu, La Reúnion Island, France; B, Turkmenocampa mirabilis from Kaptarhana cave, Koytendog District, Lebap, Turkmenistan; C, Anisuracampa sp. from Win Twin Cave, Ywangan, Shan State, Myanmar; D, Patrizicampa sardoa from Grotta di Mesu'e Monte, Baunei, Sardinia, Italy.

Figure 3. Cave-adapted dipluran species described from 1871 in REVIEW Diplura in caves: diversity, ecology, evolution and biogeography

Figure 3. Cave-adapted dipluran species described from 1871 to 2020; photographs of the authors arranged from right to left and from top to bottom: Alpheus Spring Packard, Armand Viré, Filippo Silvestri, Jean Robert Denis, Petr Wygodzinsky, Boris Pimenovitch Chevrizov, Bruno Condé, Jean Pagés and Mark Alan Muegge. Courtesy of Bernd Hauser, Sergei Golovatch and Ernest C. Bernard.

Figures 4 in REVIEW Diplura in caves: diversity, ecology, evolution and biogeography

Figures 4. Two cave-adapted Diplura: A, Plusiocampa hoffmanni Sendra & Paragamian, 2020 from Spilaio Sfento Trypa Cave, Crete, Greece (author: Kaloust Paragamian); B, Gollumjapyx smeagol from Avenc d'En Serenge, Cabanes, Castellón, Spain. Courtesy of José María Azkárraga.

Figure 6 in REVIEW Diplura in caves: diversity, ecology, evolution and biogeography

Figure 6. Olfactory chemoreceptor of the last antennomere in soil-adapted species: A, Campodea (Paurocampa) suensoni Tuxen, 1930 from Dos Aguas, Valencia, Spain; and cave-adapted species: B, Cycladiacampa irakleiae Sendra, 2020 from Spilaio Ioanni Cave, Irakleia Island, Greece; C, Pacificampa daidarabotchi Sendra, 2018 from Mejito-do Cave, Kyushu Island, Japan; D, undescribed Plusiocampinae from Huitième Ciel Cave. Banqiao, Hubei, China; E, Turkmenocampa mirabilis Sendra & Stoev, 2017 from Kaptarhana Cave, Koytendog District, Lebap, Turkmenistan; F, Remycampa herbanica from Montaña Blanca Cave, Fuerteventura Island, Spain.

Figure 5 in REVIEW Diplura in caves: diversity, ecology, evolution and biogeography

Figure 5. Bar chart showing the relative number of soil (orange) and cave-adapted (blue) dipluran species per family, subfamily and genus.

FIGURE 12 in The Crotonia fauna of New Zealand revisited (Acari: Oribatida): taxonomy, phylogeny, ecological distribution and biogeography

FIGURE 12. Environmental dissimilarity index of distribution records of the three major species groups of New Zealand Crotonia.

FIGURE 11 in The Crotonia fauna of New Zealand revisited (Acari: Oribatida): taxonomy, phylogeny, ecological distribution and biogeography

FIGURE 11. Relationship between annual water deficit and vapour pressure deficit for all locality records of New Zealand Crotonia in relation to the main types of vegetation community.

FIGURE 10 in The Crotonia fauna of New Zealand revisited (Acari: Oribatida): taxonomy, phylogeny, ecological distribution and biogeography

FIGURE 10. Environmental envelopes of all records of New Zealand Crotonia (a–c) and its major species groups (d–f). Note range of values on axes differs between (a–c) and (d–f).

FIGURE 9 in The Crotonia fauna of New Zealand revisited (Acari: Oribatida): taxonomy, phylogeny, ecological distribution and biogeography

FIGURE 9. Distribution of Crotonia spp. in New Zealand, based on records in Appendix 1. Crotonia obtecta and C. ramsayi sp. nov. are represented by single records and not mapped, nor is C. brevicornuta, recorded only from Campbell Island. Dashed line = Alpine Fault.

FIGURE 7 in The Crotonia fauna of New Zealand revisited (Acari: Oribatida): taxonomy, phylogeny, ecological distribution and biogeography

FIGURE 7. Details of bothridia of a) Crotonia ramsayi sp. nov.; b) Crotonia unguifera (Michael, 1908); c) Crotonia caudalis (Hammer, 1966); d) Crotonia brachyrostrum (Hammer, 1966); e) Crotonia cophinaria (Michael, 1908). Scale bars = 20 µm.

FIGURE 2 in The Crotonia fauna of New Zealand revisited (Acari: Oribatida): taxonomy, phylogeny, ecological distribution and biogeography

FIGURE 2. Lateral views of caudal clusters: a) Crotonia ramsayi sp. nov. paratype female; b) C. unguifera, female. Scale bar = 50 µm.