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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

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Fig. 3 in Molecular and Morphological Snapshot Characterisation of the Protist Communities in Contrasting Alpine Glacier Forefields

Fig. 3. Rarefaction analysis derived from the clone libraries of the vegetated transects of Tiefen forefield and Wildstrubel forefield. Dashed lines correspond to 95% confidence intervals.

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Fig. 2 in Molecular and Morphological Snapshot Characterisation of the Protist Communities in Contrasting Alpine Glacier Forefields

Fig. 2. Relative abundances (in percentage) of ciliate-related sequences detected in the 18S rRNA gene clone libraries from the vegetated transects of the (a) Tiefen forefield and (b) Wildstrubel forefield. Species names are based on BLAST comparison of the sequences with the NCBI database (first similarity with a known taxonomic group).

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Fig. 1 in Molecular and Morphological Snapshot Characterisation of the Protist Communities in Contrasting Alpine Glacier Forefields

Fig. 1. Location of the two sampled forefields of the (a) Tiefen glacier and (b) Wildstrubel glacier. Dots indicate sampling spots (white: unvegetated transects; black: vegetated transects).

Fig. 55 in Rhizotrogus tedeschii, a new species from the alpine zone of the Pollino Massif, southern Italy (Coleoptera: Scarabaeidae, Melolonthinae)

Fig. 55 – Distribution of two diagnostic morphometric traits in males. BS: body length, head and pygidium excluded, ANTL/ANTW: elongation of antennomere 1.

Figs 53-54 in Rhizotrogus tedeschii, a new species from the alpine zone of the Pollino Massif, southern Italy (Coleoptera: Scarabaeidae, Melolonthinae)

Figs 53-54 – Habitat of Rhizotrogus tedeschii n. sp., main observing and sampling site near the top of Serra del Prete (39.911, 16.147), 1960 m. 53, view towards NE, where spare specimens were also observed along the crest (red circle); 54: detail of site, with extensive rocky debris, view towards SW.

Figs 15-26 in Rhizotrogus tedeschii, a new species from the alpine zone of the Pollino Massif, southern Italy (Coleoptera: Scarabaeidae, Melolonthinae)

Figs 15-26 – Variability of endophalli of Rhizotrogus cicatricosus, frontal view. 15, Spain, Fuente del Tajo; 16, Spain, Font Partegat; 17, France, Cognac; 18, France, Clermont-le-Fort; 19-20, France, Massac; 21, France, St. Gély; 22, France, Le Beausset; 23-25, Italy, Casola Valsenio; 26, Italy, Camaldoli.

Figs 35-38 in Rhizotrogus tedeschii, a new species from the alpine zone of the Pollino Massif, southern Italy (Coleoptera: Scarabaeidae, Melolonthinae)

Figs 35-38 – Endophalli, oblique view, of R. cicatricosus (35, Spain, Fuente del Tajo; 36, France, Massac; 37, Italy, Casola Valsenio) and R. tedeschii (38, topotypical paratype). Arrowhead evidencing the difference in the degree of protrusion of diverticula.

Figs 4-12 in Rhizotrogus tedeschii, a new species from the alpine zone of the Pollino Massif, southern Italy (Coleoptera: Scarabaeidae, Melolonthinae)

Figs 4-12 – Anatomical details of R. tedeschii and R. cicatricosus. 4, aedeagus in lateral view of R. tedeschii (holotype); 5, paramera in dorsal view of R. tedeschii (holotype). 6-7, comparison between male antennae of R. tedeschii n. sp. (6, specimen with 9 antennomeres) and of R. cicatricosus (7); Arrowhead evidencing antennomere 1. 8-10, variability of female antenna of R. tedeschii n sp.: 8, common condition, with original antennomeres 4 and 5 non-disjointed and forming a thicker antennomere; 9, article 4+5 similar to others; 10, non-disjonction extending to original antennomere 6, resulting in a 8-segmented antenna; 11-12, variability of female antenna of R. cicatricosus: 11, normally 10-segmented antenna; 12, 9-segmented antenna with non-disjunction of antennomeres 5-6.

Fig. 1 in Rhizotrogus tedeschii, a new species from the alpine zone of the Pollino Massif, southern Italy (Coleoptera: Scarabaeidae, Melolonthinae)

Fig. 1 – Ranges of studied species and distribution of examined specimens. Red shadowing: range of Rhizotrogus cicatricosus (from Allenspach 1970; Coca-Abia & Martin-Piera 1998; Ballerio et al. 2014; Bezdek 2016; Schaffrath 2015; Haselböck 2018). Red dots: locations of the examined specimens of R. cicatricosus from W Europe (see material and methods); blue dots: locations of the examined specimens of R. cicatricosus from Appen- nines; green dot: R. tedeschii n. sp.

Figs 39-43 in Rhizotrogus tedeschii, a new species from the alpine zone of the Pollino Massif, southern Italy (Coleoptera: Scarabaeidae, Melolonthinae)

Figs 39-43 – Female terminalia (left side, accesory glands omitted) of R. cicatricosus (39-40, Italy, Casola Valsenio; 41, France, Martinet) and R. tedeschii (42-43, paratypes). Cx: coxite, Ep: epipleurite, Ht: hemitergite, Sc: subcoxite.

Fig. 56 in Rhizotrogus tedeschii, a new species from the alpine zone of the Pollino Massif, southern Italy (Coleoptera: Scarabaeidae, Melolonthinae)

Fig. 56 – Distribution of two morphometrics traits relative to epipleural setation in males. EAL/EAD: ratio between length of setae and their distance at the subapical round; EML/EAL: ratio between the length of setae at the medial part and at the subapical round.

Figs 27-34 in Rhizotrogus tedeschii, a new species from the alpine zone of the Pollino Massif, southern Italy (Coleoptera: Scarabaeidae, Melolonthinae)

Figs 27-34 – Variability of endophalli of Rhizotrogus tedeschii n. sp., frontal view (topotypical paratypes).