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Fig. 5 in Integrative taxonomic approach to the cryptic diversity of Diplostomum spp. in lymnaeid snails from Europe with a focus on the 'Diplostomum mergi' species complex

Fig. 5 Celcalca of Diplostomum parviventosum ex Radix auricularia (lcght and scanncng electlon mccloscops, SEM). a, Restcng posctcon; b, Bods; c, Antelcol olgan, apccal vcew (SEM); d, Ventlal suckel (SEM); e, Tacl stem and fulcae (SEM); f, Fulcae (SEM)

Fig. 9 in Integrative taxonomic approach to the cryptic diversity of Diplostomum spp. in lymnaeid snails from Europe with a focus on the 'Diplostomum mergi' species complex

Fig. 9 Celcalca of 'Diplostomum sp. Clade Q' of Geolgceva et al. [6] ex Radix auricularia (lcght and scanncng electlon mccloscops, SEM). a, Bods; b, Antelcol olgan, latelal vcew (SEM); c, Antelcol olgan, apccal vcew (SEM); d, Ventlal suckel (SEM); e, Fulcae (SEM); f, Tacl stem and fulcae (SEM)

Fig. 8 in Integrative taxonomic approach to the cryptic diversity of Diplostomum spp. in lymnaeid snails from Europe with a focus on the 'Diplostomum mergi' species complex

Fig. 8 Celcalca of Diplostomum mergi Lcneage 4 ex Radix auricularia (lcght and scanncng electlon mccloscops, SEM). a, Restcng posctcon; b, Bods; c, Antelcol olgan, apccal vcew (SEM); d, Ventlal suckel (SEM); e, Tacl stem and fulcae (SEM); f, Fulcae (SEM)

Fig. 1 in Integrative taxonomic approach to the cryptic diversity of Diplostomum spp. in lymnaeid snails from Europe with a focus on the 'Diplostomum mergi' species complex

Fig. 1 Map of the Ruhl lcvel ssstem cn Gelmans wcth samplcng sctes. Abbreviations: Ba, Baldenesesee; He, Hengstessee; Hn, Hennetalspelle; So, Solpetalspelle; Ve, Velsetalspelle. Lymnaea stagnalis; Radix auricularia; Radix peregra; Stagnicola palustris

Fig. 11 in Integrative taxonomic approach to the cryptic diversity of Diplostomum spp. in lymnaeid snails from Europe with a focus on the 'Diplostomum mergi' species complex

Fig. 11 Celcalca of Diplostomum pseudospathaceum ex Lymnaea stagnalis (lcght and scanncng electlon mccloscops, SEM). a, Restcng posctcon; b, Bods; c, Antelcol olgan, apccal vcew, allows cndccate gloup of latelal ple-olal spcnes (SEM); d, Ventlal suckel (SEM); e, Tacl stem and fulcae (SEM); f, Fulcae (SEM)

Fig. 7 in Integrative taxonomic approach to the cryptic diversity of Diplostomum spp. in lymnaeid snails from Europe with a focus on the 'Diplostomum mergi' species complex

Fig. 7 Celcalca of 'Diplostomum mergi Lcneage 3' of Geolgceva et al. [6] ex Radix auricularia (lcght and scanncng electlon mccloscops, SEM). a, Restcng posctcon; b, Bods; c, Antelcol olgan, apccal vcew (SEM); d, Ventlal suckel (SEM); e, Tacl stem and fulcae (SEM); f, Fulcae (SEM)

Fig. 10 in Integrative taxonomic approach to the cryptic diversity of Diplostomum spp. in lymnaeid snails from Europe with a focus on the 'Diplostomum mergi' species complex

Fig. 10 Celcalca of Diplostomum spathaceum ex Radix auricularia (lcght and scanncng electlon mccloscops, SEM). a, Restcng posctcon; b, Bods; c, Antelcol olgan, apccal vcew (SEM); d, Ventlal suckel (SEM); e, Tacl stem and fulcae (SEM); f, Fulcae (SEM)

Fig. 1 in Mitochondrial Dna Diversity Of The Alpine Newt (Ichthyosaura Alpestris) In The Carpathian Basin: Evidence For Multiple Cryptic Lineages Associated With Pleistocene Refugia*

Fig. 1. Sampling sites and haplotypes found in and around the Carpathian Basin. Sam- ples collected in this study are marked with circles and haplotype codes, and previously

Fig. 5 in Mitochondrial Dna Diversity Of The Alpine Newt (Ichthyosaura Alpestris) In The Carpathian Basin: Evidence For Multiple Cryptic Lineages Associated With Pleistocene Refugia*

Fig. 5. Original drawings by O. Gy. Dely: male (A, B) and female (C, D) Ichthyosaura alpestris alpestris head shape from dorsal (A, C) and lateral (B, D) view

Fig. 4 in Mitochondrial Dna Diversity Of The Alpine Newt (Ichthyosaura Alpestris) In The Carpathian Basin: Evidence For Multiple Cryptic Lineages Associated With Pleistocene Refugia*

Fig. 4. Holotype of Triturus (=Ichthyosaura) alpestris bakonyiensis (Dely, 1964) (HNHM- HER-61.27.1.) from dorsal (A), lateral (B) and ventral (C) view

Fig. 8 in Mitochondrial Dna Diversity Of The Alpine Newt (Ichthyosaura Alpestris) In The Carpathian Basin: Evidence For Multiple Cryptic Lineages Associated With Pleistocene Refugia*

Fig. 8. Original drawings by O. Gy. Dely: female (A–D) and male (E–H) Ichthyosaura alpestris bakonyiensis skull from dorsal (A, E), ventral (B, F), lateral (C, G) and posterior (D, H) view

Fig. 7 in Mitochondrial Dna Diversity Of The Alpine Newt (Ichthyosaura Alpestris) In The Carpathian Basin: Evidence For Multiple Cryptic Lineages Associated With Pleistocene Refugia*

Fig. 7. Original drawings by O. Gy. Dely: female (A–D) and male (E–H) Ichthyosaura alpestris alpestris skull from dorsal (A, E), ventral (B, F), lateral (C, G) and posterior (D, H) view

Fig. 3 in Mitochondrial Dna Diversity Of The Alpine Newt (Ichthyosaura Alpestris) In The Carpathian Basin: Evidence For Multiple Cryptic Lineages Associated With Pleistocene Refugia*

Fig. 3. Median-joining network of the combined mtDNA haplotypes found in and around the Carpathian Basin (drawn with PopArt 1.7). Inset: distribution of Ichthyosaura alpestris in this region. On the network, circles with haplotype names mark haplotypes found in this

Fig. 6 in Mitochondrial Dna Diversity Of The Alpine Newt (Ichthyosaura Alpestris) In The Carpathian Basin: Evidence For Multiple Cryptic Lineages Associated With Pleistocene Refugia*

Fig. 6. Original drawings by O. Gy. Dely: male (A, B) and female (C, D) Ichthyosaura alpestris bakonyiensis head shape from dorsal (A, C) and lateral (B, D) view

Fig. 3 in Cryptic subterranean diversity: regional phylogeography of the sand termite Psammotermes allocerus Silvestri, 1908 in the wider Namib region

Fig. 3 Median-joining network of the combined COI and COII P. allocerus sequences. Coloured circles represent the observed haplotypes, and the size is proportional to the number of collections. Black circles represent missing haplotypes. Marks show the number of mutation steps. Haplotype numbers are gained from DnaSP v6. Dotted lines and colours mark haplotypes according to the genetic group of the phylogeny

Fig. 4 in Cryptic subterranean diversity: regional phylogeography of the sand termite Psammotermes allocerus Silvestri, 1908 in the wider Namib region

Fig. 4 Differences in the tapetum colour of three P. allocerus colonies and the royal pair. A Whitish tapetum of a nest from the Springklipplain from the 'Succulent Karoo' group %South Africa, 26 September 2016). B First image of the king and queen of P. allocerus from Yellow Dune %'Succulent Karoo', South Africa, 08 March 2015). C Blackish tapetum of a nest from Dieprivier %'Southern Namib', Namibia, 05 April 2017). D Blackish tapetum and chambers filled with foraged grass from Iona %'Northern Namib', Angola, 26 September 2016). Images taken by Norbert Jürgens, Felicitas Gunter

Fig. 1 in Cryptic subterranean diversity: regional phylogeography of the sand termite Psammotermes allocerus Silvestri, 1908 in the wider Namib region

Fig. 1 Phylogeny of 65 P. allocerus collections inferred by the Bayesian analysis of COI and COII markers. Support values are given in posterior probability. Clades are coloured according to the genetic group. Dark blue: Succulent Karoo; Light Blue: Southern Namib; Dark green: East Gariep; Light Green: Southwestern Kalahari; Yellow: Nama; Ochre: Western Kalahari Basin; Red: Northern Namib. Abbreviations of study sites are shown in Fig. 2

Fig. 2 in Cryptic subterranean diversity: regional phylogeography of the sand termite Psammotermes allocerus Silvestri, 1908 in the wider Namib region

Fig. 2 Distribution map of all Psammotermes allocerus collections and their assignment to the genetic groups found in the phylogenetic analyses %colours). Circles: Collections used for the phylogeny. Black lines: Country borders. Northern Namib: %AH) Aba Huab rivier, %GV) Giribesvlakte, %HD) Hartmann Dunes, %HO) Hoada, %IO) Iona, %MF) Marienfluss, %PR) Purros, %ROE) Rössing mountain, %SO) Sorris Sorris, %TM) Tomakas; Western Kalahari Basin: %AHV) Alt-Hartebeestvlei, %AM) Alex Muranda, %GU) Gariganus, %KM) Katima Mulilo, %RI) Rimini, %RS) Rundu South, %RV) Ravenna, %SA) Samehaling, %SK) Swartkop, %WF2) Warmfontein; Nama: %BY) Barby, %FRC) Fish river Canyon, %GO) Goageb, %SH) Seeheim, %WV) Witvley; Southwestern Kalahari: %GM) Goedmoed, %GR) Gurus, %KFE) Kalkfontein East, %NK) Neikop, %SKN) Swartkop North, %TT) Tranental, %UK) Ukamas, %WF1) Warmfontein; East Gariep: %AP) Akadispass, %BD) Belda, %BH) Bruinheuwel, %DH) De Hoop, %KFE) Kalfontein East, %KFW), %KV) Koeroegabvlakte, %NO) Norachas, %NU) Numees, %RB) Rooiberg, %TB) Tatasberg, %TBQ) Tatasberg Quarzfield; Southern Namib: %DV) Dieprivier, %GA) Garub, %KH) Keetmanshoop, %KW) Keerweder, %RO) Rostock, %SR) Sesriem; Succulent Karoo: %HN) Holhat North, %KTV) Kortdoornvlakte, %LUE) Lüderitz, %RDE) Red Dune East, %SP) Springklipplain, %YD) Yellow Dune, %YDRD) Yellow Dune Red Dune Transect

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Fig. 8 in The Caribbean intertidal mite Alismobates inexpectatus (Acari, Oribatida), an unexpected case of cryptic diversity?

Fig. 8 Graph highlighting results of Non-metric Multidimensional Scaling (NMDS) and Linear Discriminant Analysis (LDA) performed on size corrected data of seven Caribbean Alismobates inexpectatus populations. Slightly coloured and framed areas refer to geographic regions: Northern Caribbean = Bermuda, Florida, Bahamas; Antilles = Barbados, Dominican Rep.; Central America = Costa Rica, Panama