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Figure 5 in Composition of meiobenthonic Platyhelminthes from brackish environments of the Galician and Cantabrian coasts of Spain with the description of a new species of Djeziraia (Polycystididae, Kalyptorhynchia)

Figure 5. Percentage of turbellarians in relation to the substrate type. M, muddy; S, sandy; SG, sandy-gravel; SM, sandy-muddy; SST, sandy-stony; ST, stony.

Figure 4 in Composition of meiobenthonic Platyhelminthes from brackish environments of the Galician and Cantabrian coasts of Spain with the description of a new species of Djeziraia (Polycystididae, Kalyptorhynchia)

Figure 4. Number of turbellarians found in relation to the water temperature (black bars) and to the concentration of dissolved oxygen in the samples (grey bars) (the samples without dissolved oxygen and temperature data were not considered).

Figure 1 in Composition of meiobenthonic Platyhelminthes from brackish environments of the Galician and Cantabrian coasts of Spain with the description of a new species of Djeziraia (Polycystididae, Kalyptorhynchia)

Figure 1. Location of the sample sites, with turbellarians (black points) and without turbellarians (white circles). The locality numbers correspond to those given in Tables I–III.

Figure 3 in Composition of meiobenthonic Platyhelminthes from brackish environments of the Galician and Cantabrian coasts of Spain with the description of a new species of Djeziraia (Polycystididae, Kalyptorhynchia)

Figure 3. Number of turbellarians found in relation to the conductivity and to the salinity (conductivity data of the brackish localities were not considered, because they were punctual measurements).

Figure 2 in Composition of meiobenthonic Platyhelminthes from brackish environments of the Galician and Cantabrian coasts of Spain with the description of a new species of Djeziraia (Polycystididae, Kalyptorhynchia)

Figure 2. Djeziraia longistyla sp. nov. (A) General organization in dorsal view (from the living animal); (B) atrial organs; (C) stylet (photograph from the living animal). b, bursa; cg, caudal glands; cod, common oviduct; fd-I, female duct type I; fd-II, female duct type II; ga, common genital atrium; gd, genital duct; gp, gonopore; ov, ovary; ovd, oviduct; p, proboscis; pg, prostatic glands; ph, pharynx; pv, prostatic vesicle; rs, receptaculum seminis; st, stylet; te, testis; u, uterus; vi, vitellaria; vs, vesicula seminalis; vd, vitelloduct.

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Figs. 11−18 in Species inventory, preys and host plants of Anthocoridae sensu lato (Hemiptera: Heteroptera) in Shiraz and its environs (Iran, Fars province)

Figs. 11−18. Parameres of Anthocoridae. 11 − Temnostethus reduvinus parilis (Horváth, 1891), 12 − Anthocoris minki pistaciae Wagner, 1957, 13 − Orius albidipennis (Reuter, 1884), 14 − O. niger (Wolff, 1811), 15 − O. laevigatus laevigatus (Fieber, 1860), 16 − O. laticollis discolor (Reuter, 1884), 17 − O. horvathi (Reuter, 1884), 18 − O. vicinus (Ribaut, 1923). Abbreviations: cn − cone, dt − denticule, fg − flagellum. Scale bars = 0.05 mm.

Fig. 35 in Psychodidae (Diptera) of the Jeseníky Protected Landscape Area and its environs with descriptions of two new Berdeniella species from the Czech Republic

Fig. 35. Vysoký vodopád waterfall near Velký Jezerník Mt. – Marchantiopsida and moss in the spray zone, suitable for development of immature stages of several genera of psychodine moth flies. Photo Michal Ulrych.

Fig. 34 in Psychodidae (Diptera) of the Jeseníky Protected Landscape Area and its environs with descriptions of two new Berdeniella species from the Czech Republic

Fig. 34. Velká kotlina basin (upper part, avalanche scars) with snow fields in June – locality of Berdeniella kocii sp. nov. Photo Michal Ulrych.

Fig. 32 in Psychodidae (Diptera) of the Jeseníky Protected Landscape Area and its environs with descriptions of two new Berdeniella species from the Czech Republic

Fig. 32. Filipovické louky meadows near Horní Domašov, swamps and brooks – locality of Berdeniella kocii sp. nov. Photo Lenka Niklová.

Fig. 33 in Psychodidae (Diptera) of the Jeseníky Protected Landscape Area and its environs with descriptions of two new Berdeniella species from the Czech Republic

Fig. 33. Mezikotlí (woodlands between Malá and Velká kotlina basins) – characteristic scenery of Jeseníky PLA. Photo Michal Ulrych.

Figs. 25-31 in Psychodidae (Diptera) of the Jeseníky Protected Landscape Area and its environs with descriptions of two new Berdeniella species from the Czech Republic

Figs. 25-31. Berdeniella kocii sp. nov., J. 25 – basal antennomeres; 26 – wing; 27 – dorsal view of fore claw; 28 – lateral view of gonocoxite and gonostyle; 29 – dorsal view of epandrium and surstyli; 30 – dorsal view of aedeagal complex and gonopode; 31 – dorsal view of apodemal cavity (variability). Scales = 0.1 mm (Figs. 25, 27-31); 1 mm (Fig. 26).

Figs. 16-24 in Psychodidae (Diptera) of the Jeseníky Protected Landscape Area and its environs with descriptions of two new Berdeniella species from the Czech Republic

Figs. 16-24. Berdeniella kocii sp. nov., J. 16 – head; 17 – facets; 18 – apical antennomeres; 19 – dorsal view of terminal lobe of labium; 20 – maxilla and maxillary palpus; 21 – lateral view of thoracic sclerites; 22 – lateral view of epandrium and surstylus; 23 – dorsal view of apodemal cavity (variability); 24 – lateral view of aedeagal complex. Scales = 0.1 mm.

Figs. 8-15 in Psychodidae (Diptera) of the Jeseníky Protected Landscape Area and its environs with descriptions of two new Berdeniella species from the Czech Republic

Figs. 8-15. Berdeniella desnensis sp. nov., J. 8 – facets; 9 – apical antennomeres; 10 – dorsal view of terminal lobe of labium; 11 – dorsal view of fore claw; 12 – dorsal view of epandrium and surstyli; 13 – same, lateral view; 14 – dorsal view of aedeagal complex and gonopode; 15 – dorso-caudal view of aedeagal complex. Scales = 0.1 mm (Figs. 8-10, 12-15); 0.05 mm (Fig. 11).

Figs. 1-7 in Psychodidae (Diptera) of the Jeseníky Protected Landscape Area and its environs with descriptions of two new Berdeniella species from the Czech Republic

Figs. 1-7. Berdeniella desnensis sp. nov., J. 1 – head; 2 – basal antennomeres; 3 – maxilla and maxillary palpus; 4 – lateral view of thoracic sclerites; 5 – wing; 6 – lateral view of gonocoxite and gonostyle; 7 – lateral view of aedeagal complex. Scales = 0.1 mm (Figs. 1-4, 6-7); 1 mm (Fig. 5).

FIG. 8. A in Mortality in a predator-free insular environment: the dwarf deer of Crete

FIG. 8. A, Examples of catastrophic (left) and attritional (right) age profiles for sika deer (Cervus nippon), adapted from Kubo et al. (2011). The catastrophic profile is based on randomly harvested deer from eastern Hokkaido, while the attritional profile is based on field-collected carcasses from Kinkazan Island, Honshu. B, Examples of survivorship curves for sika deer from Nara Park (left) and Kinkazan Island (right), adapted from Koike and Ohtaishi (1987). Both curves represent populations that are not hunted. Note that the scale in B is arithmetic.

FIG. 7 in Mortality in a predator-free insular environment: the dwarf deer of Crete

FIG. 7. Survivorship curves (lx) and mortality rates (qx) (top and bottom, respectively) for Candiacervus ropalophorus (Gerani 4) and Candiacervus sp. II (Liko).

FIG. 6 in Mortality in a predator-free insular environment: the dwarf deer of Crete

FIG. 6. Mortality profiles (dx) for Candiacervus ropalophorus from Gerani 4 (top left, actual numbers for all ages; bottom left, juveniles only) and Candiacervus sp. II from Liko (top right, all ages). Bottom right, reconstruction of Can. ropalophorus by Alexis Vlachos.

FIG. 5 in Mortality in a predator-free insular environment: the dwarf deer of Crete

FIG. 5. Long bone elements of Late Pleistocene Cretan deer (Candiacervus) are remarkably variable in both size and shape. A, Six metapodial size classes as determined by de Vos (1979, 1984); size class 2 includes three different antler types, resulting in a total of at least eight groupings (whether these are considered species or ecomorphs). B, Composite mount representing size class 2 (Candiacervus sp. II) from Liko Cave. Shoulder height and withers height in life would be about 55 and 58 cm respectively.

FIG. 4 in Mortality in a predator-free insular environment: the dwarf deer of Crete

FIG. 4. Mortality profiles (dx) for Candiacervus ropalophorus from Gerani 4 (left) and Candiacervus sp. II from Liko (right), based on age estimations inferred from wear stages of all molars (top histograms) or of m1, m2, or m3 considered singly (other histograms). Although some differences can be observed between the profiles, patterns are essentially the same.

FIG. 3 in Mortality in a predator-free insular environment: the dwarf deer of Crete

FIG. 3. Three dental wear patterns found in Candiacervus mandibles (Gerani 4), with a graphical comparison of ages estimated per molar locus vs. average age based on all molars (A and B directly above, C and D on opposite page). A, Mandible in which all molars show a degree of abrasion that is closely correlated with their position in the eruption sequence, resulting in compatible age estimates. B, Mandible in which m2 shows greater wear than either m1 or m3, resulting in potential overestimation of age relative to the other molars. C, Mandible in which m3 shows greater wear than either m1 or m2, thus greatly overestimating age relative to m1. D, Comparison of ages estimated per m1, m2, and m3 tooth loci (symbols) and averages of separate m1, m2, and m3 ages (lines), for a sample of 88 mandibles.