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Fig. 4. A plan and a in On the diversity of subterranean beetles of the Dinarides: new leiodid taxa (Coleoptera: Leiodidae) from Serbia

Fig. 4. A plan and a longitudinal section of the Simina Jama Pit, village of Gornje Košlje, Debelo Brdo saddle, Mt Povlen, near the town of Ljubovija, western Serbia (modified after Anđelić et al. 2011). The red circles indicate the places where specimens of Bozidaria serbooccidentalis Ćurčić & Pavićević gen. et sp. nov. were found.

Fig. 10 in On the diversity of subterranean beetles of the Dinarides: new leiodid taxa (Coleoptera: Leiodidae) from Serbia

Fig. 10. Illustrations of morphological characters presented in the Key to the taxa of the genus Proleonhardella Jeannel, 1910 (after Jeannel 1924; Ćurčić et al. 2008a). A. Short elytra, less than twice as long as pronotum. B. Long elytra, more than twice as long as pronotum. C. Globular antennomere VIII in males. D. Slightly elongate antennomere VIII in males. E. Elytra parallel in basal half. F. Elytra narrowed in basal half.

Fig. 7. Pit 4-1-3-27 in On the diversity of subterranean beetles of the Dinarides: new leiodid taxa (Coleoptera: Leiodidae) from Serbia

Fig. 7. Pit 4-1-3-27, village of Kaluđerske Bare, Mt Tara, near the town of Bajina Bašta, western Serbia (modified after Bosco 2016). A. Entrance. B. A chamber in which one type specimen of Proleonhardella (Proleonhardella) tarensis Ćurčić & Pavićević sp. nov. was collected. C. A 3D view. D. A plan and a longitudinal section. The red circles indicate the places where specimens of P. (P.) tarensis Ćurčić & Pavićević sp. nov. were found.

Fig. 6 in On the diversity of subterranean beetles of the Dinarides: new leiodid taxa (Coleoptera: Leiodidae) from Serbia

Fig. 6. Proleonhardella (Proleonhardella) tarensis Ćurčić & Pavićević sp. nov. from Pit 4-1-3-27, village of Kaluđerske Bare, Mt Tara, near the town of Bajina Bašta, western Serbia. Holotype male (IZFB-21/27), aedeagus. A. Dorsal view. B. Lateral view. Scale bar = 200 μm.

Fig. 1 in On the diversity of subterranean beetles of the Dinarides: new leiodid taxa (Coleoptera: Leiodidae) from Serbia

Fig. 1. Illustrations of morphological characters presented in the Key to the leptodirine leiodid genera of the phyletic series of "Leonhardella" (after Jeannel 1911, 1924; Ćurčić et al. 2008a). A. Absence of mesosternal carina. B. Presence of mesosternal carina. C. Absence of a concavity on mesosternal carina. D. Presence of a deep concavity on mesosternal carina. E. Presence of elliptical body shape. F. Presence of pholeuonoid body shape. G. Presence of dilated protarsi in males. H. Presence of undilated protarsi in males. I. Presence of a short rounded basal projection on basal bulbus. J. Presence of a long subtriangular basal projection on basal bulbus. K. Presence of subglobular antennomere VIII. L. Presence of elongate antennomere VIII. M. Presence of paramerae with two setae. N. Presence of paramerae with three setae.

opencc-by-4.0Dec 2021View details →

Fig. 1 in Distribution Pattern, Nest-Tree Features And Breeding Performance Of Population Of The Black Stork, Ciconia Nigra (Ciconiiformes, Ciconiidae), In Northwestern Serbia

Fig. 1. The proportion of tree species picked for nest placement by the Black Stork (Ciconia nigra) in Northwestern Serbia (n = 44).

Fig. 7 in The taxonomic status of recently described Isophya taxa from Serbia (Tettigoniidae, Phaneropterinae)

Fig. 7. Distribution of Isophya modestior Brunner von Wattenwyl, 1882 based on unpublished and literature data (see Supp. file 9). Dashed line represents distribution by Hochkirch et al. (2016).

Fig. 6 in The taxonomic status of recently described Isophya taxa from Serbia (Tettigoniidae, Phaneropterinae)

Fig. 6. Syllables of Isophya modestior Brunner von Wattenwyl, 1882 showing different characteristics compared to the typical song. A. Tumane 25°C. B. Vajuga 24°C (the line under oscillogram indicates 100 ms).

Fig. 5 in The taxonomic status of recently described Isophya taxa from Serbia (Tettigoniidae, Phaneropterinae)

Fig. 5. Comparative measurements of male calling song characters in recently described taxa of Isophya Brunner von Wattenwyl, 1878 and Isophya modestior modestior Brunner von Wattenwyl, 1882. A. Main syllable length (ms). B. Number of pulses in main syllable. C. Oscillograms of male calling songs of the species of Isophya (the line under oscillogram indicates 100 ms).

Fig. 4 in The taxonomic status of recently described Isophya taxa from Serbia (Tettigoniidae, Phaneropterinae)

Fig. 4. General appearance of Isophya modestior Brunner von Wattenwyl, 1882. A–B. Green form (A: male, B: female). C–D. Melanistic form (C: male, D: female). Photos: A–B: Ionuț Ștefan Iorgu; C: Dragiša Savić; D: Laslo Horvat.

Fig. 3 in The taxonomic status of recently described Isophya taxa from Serbia (Tettigoniidae, Phaneropterinae)

Fig. 3. Species tree generated with BEAST analyzing four sequenced loci (H3, ITS2, COI, 12S) simultaneously.

Fig. 2 in The taxonomic status of recently described Isophya taxa from Serbia (Tettigoniidae, Phaneropterinae)

Fig. 2. Specimens of Isophya modestior Brunner von Wattenwyl, 1882 collected by Carl Brunner von Wattenwyl and deposited in the Natural History Museum Vienna. A. Syntype. B. Lectotype.

Fig. 1. A in The taxonomic status of recently described Isophya taxa from Serbia (Tettigoniidae, Phaneropterinae)

Fig. 1. A. Comparative measurements of recently described taxa of Isophya Brunner von Wattenwyl, 1878 and Isophya modestior modestior Brunner von Wattenwyl, 1882. Measurements presented in bar graph are used from original descriptions of type material. B. Map with localities of newly described Isophya taxa and I. modestior modestior.

opencc-by-4.0Oct 2015View details →

Fig. 1 in Colias caucasica balcanica (Pieridae) rediscovered in Montenegro, with additional new records for Serbia

Fig. 1. Antheraea yamamai (Guérin-Méneville, 1861) male, Montenegro, Pivska planina Mt., Polje Crkvičko village, Rudine, 07.08.2015, in coll. NMNHS. Photo: Stoyan Beshkov.

opencc-zeroApr 2022View details →

FIG. 4 in A new Nitzschia Hassall species (Bacillariaceae, Bacillariophyta) from saline ponds in Serbia

FIG. 4. — Nitzschia austriaca Hust. SEM and LM images taken from Bela Bara saline pond. A-C, SEM external valve views of a frustule; C, arrow indicates more widely spaced center fibulae; D-W, LM valve views of a population arranged in decreasing length. Scale bars: A-C, 5 µm; D-W, 10 µm.

opencc-zeroApr 2022View details →

FIG. 1 in A new Nitzschia Hassall species (Bacillariaceae, Bacillariophyta) from saline ponds in Serbia

FIG. 1. — Location of the four study saline ponds in the Vojvodina Region, Serbia. A, Bela Bara; B, Čoka Kopovo; C, Velika Rusanda; D, Slatina.

opencc-zeroApr 2022View details →

FIG. 3 in A new Nitzschia Hassall species (Bacillariaceae, Bacillariophyta) from saline ponds in Serbia

FIG. 3. — Nitzschia haloserbica Vidaković, Ector, C.E.Wetzel & Krizmanić, sp. nov., SEM images taken from the type material (Bela Bara saline pond): A, C, E, SEM views of a frustule in valve view; B, SEM internal view of two valves from the same frustule; D, SEM internal view of the center of the valve with fibulae regularly distributed; F, SEM internal view of valve apex with helictoglossa and raphe; G, SEM internal detail view of valve apex with helictoglossa. Scale bars: A-C, 5 µm; D, G, 1 µm; E, 3 µm; F, 2 µm.

opencc-zeroFeb 2020View details →

FIG. 3 in An annotated list of hornwort and liverwort species of Serbia

FIG. 3. — The graphical representation of total number of hornwort and liverworts present in Serbia in time.

opencc-by-4.0May 2023View details →

FIGURE 8 in A new perspective on the molecular dating of the brown trout complex with an extended phylogeographic information on the species in Serbia

FIGURE 8 Simplified palinspastic map for the Pliocene (compiled and modified after Popov et al., 2004, 2006; Neubauer et al., 2015) with the indication of hypothetic BT colonization routes (arrows). Interrupted lines mark migration routes that are, in our opinion, less likely. Green areas represent brackish environments, light blue freshwater lakes or marshes and rivers, dark blue seas, dark gray mountain ranges, and light gray land mass; all geographic features are tentatively positioned. 1 – Ancestral trout originated in the Ponto-Caspian system and crossed from the paleo-Danube into the Western Mediterranean basin via stream capture of Alpine rivers in Pliocene; 2 – Ancestral trout originated in the Balkans basin and colonized other parts of the Mediterranean Basin from here; 3 – Colonization of the Central Alps took place in the Pliocene after the paleo-Rhône separated from the paleo-Danube and reached the Mediterranean; 4 – Atlantic basin was colonized when the Rhine captured Central Alpine rivers; 5 – Atlantic basin was colonized along the Mediterranean coastline and via Gibraltar; 6 – Ponto-Caspian basin was colonized from the Mediterranean basin following a presumed sea corridor in the upper Euphrates valley or using the paleo-Euphrates, which might have been connected with the Mediterranean until the Middle Pliocene; 7 – Ponto-Caspian basin was colonized via a possible Pliocene gateway that connected the Dacic basin and the Aegean Sea; 8 – Ponto-Caspian basin was colonized through the Bosphorus gateway.