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Fig. 2 in Spatial Heterogeneity Of Steppe Bird Community In The Azov-Black Sea Enclave Of The European Dry-Steppe Zone (Southern Ukraine)

Fig. 2. Similarity of subregions of the dry-steppe enclave in the number of all steppe bird species: 1 — RB Prychornomoria, 2 — Lower Dnipro, 3 — LB Prychornomoria, 4 — N Prysyvashshia, 5 — NW Pryazovia, 6 — Syvash, 7 — Western Crimea, 8 — Central Crimea, 9 —Kerch Peninsula, 10 — Foothills.

Fig. 6 in Ostracodes (Crustacea, Ostracoda) In The Rocky Nearshore Water Area Of Zmiiniy Island (Black Sea)

Fig. 6. The results of CLUSTER analysis with the SIMPROF test based on the biomass on different substrates in Zmiiniy Island.

Fig. 1 in Distribution Of Sibling Species Yellow-Legged Gull, Larus Michahellis And Caspian Gull, Larus Cachinnans (Charadriiformes, Laridae), On The Black Sea Coast

Fig. 1. Differences in coloration of the outer primaries of Larus michahellis (left column) and Larus cachinnans (right column) from the Black Sea coast. A — Kobuleti, Georgia. August 20, 1910 (collection of the National Museum of Natural History, the National Academy of Sciences of Ukraine), B — Karadag, Crimean Peninsula, Ukraine, July 2, 1946; (collection of the Zoological Museum of Kyiv National University), C — Vilkovo, Danube Delta, Ukraine, April 26, 1948 (collection of the Zoological Museum of Kyiv National University), D — Swan Islands, Karkinitian Bay, Ukraine, February 22, 1972 (collection of the National Museum of Natural History of the National Academy of Sciences of Ukraine).

Fig. 3 in Spatial Heterogeneity Of Steppe Bird Community In The Azov-Black Sea Enclave Of The European Dry-Steppe Zone (Southern Ukraine)

Fig. 3. Similarity of subregions of the dry-steppe enclave in the number of rare steppe bird species: 1 — RB Prychornomoria, 2 — Lower Dnipro, 3 — LB Prychornomoria, 4 — N Prysyvashshia, 5 — NW Pryazovia, 6 — Syvash, 7 — Western Crimea, 8 — Central Crimea, 9 —Kerch Peninsula, 10 — Foothills.

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Fig. 3 in Transportation of microplastic during high-flow and low-flow seasons in southeastern Black Sea: A modelling approach

Fig. 3 — Snapshots of microplastic distribution on southeastern Black Sea in high-flow (S1, S2, and S3) and low-flow (S4, S5, and S6)

Fig. 9 in The black goby Gobius niger Linnaeus, 1758 in the Marchica Lagoon (Alboran Sea, Morocco): spatio-temporal distribution, its environmental drivers, and the site-related footprint

Fig. 9: Histogram of the Mantel test assessing the relationship between genetic and morphologic distance for Gobius niger. Sim: simulations; Frequency: frequency values of the correlation between the genetic and morphologic distances. The dot represents the original value of the correlation between the distance matrices.

Fig. 6 in The black goby Gobius niger Linnaeus, 1758 in the Marchica Lagoon (Alboran Sea, Morocco): spatio-temporal distribution, its environmental drivers, and the site-related footprint

Fig. 6: PCA of the morphological variables of Gobius niger (standard length, SL; body height, BH; head length, HL; snout length, SnL; eye diameter, ED; first dorsal fin, DF1; second dorsal fin, DF2; anal fin, AF; pectoral fin, PF; ventral fin, VF) with projection of phenotypic groups. PC1 vs. PC2 and PC2 vs. PC3. The percentage of variation explained by each PC axis is given within parentheses.

Fig. 3 in The black goby Gobius niger Linnaeus, 1758 in the Marchica Lagoon (Alboran Sea, Morocco): spatio-temporal distribution, its environmental drivers, and the site-related footprint

Fig. 3: Cluster analysis associated with the similarity profile test (SIMPROF), based on abundances of Gobius niger, reveals reciprocal relations among the 20 sampled stations in the Marchica Lagoon using the Bray–Curtis distance.

Fig. 2 in The black goby Gobius niger Linnaeus, 1758 in the Marchica Lagoon (Alboran Sea, Morocco): spatio-temporal distribution, its environmental drivers, and the site-related footprint

Fig. 2: Picture of Gobius niger from the Marchica Lagoon showing the main measurements taken: total length (TL), standard length (SL), head length (LT), snout length (SnL), body height (BH), and eye diameter (ED).

Fig. 7 in The black goby Gobius niger Linnaeus, 1758 in the Marchica Lagoon (Alboran Sea, Morocco): spatio-temporal distribution, its environmental drivers, and the site-related footprint

Fig. 7: Linear regression of the principal component score axis (PC1) from morphometric measurements on the log standard length of Gobius niger with projection of phenotypic groups.

Fig. 8 in The black goby Gobius niger Linnaeus, 1758 in the Marchica Lagoon (Alboran Sea, Morocco): spatio-temporal distribution, its environmental drivers, and the site-related footprint

Fig. 8: Haplotype network constructed from 16S rDNA sequences of Gobius niger. The size of a particular circle reflects the haplotype frequency. The numbers indicate the nodes.

Fig. 1 in The black goby Gobius niger Linnaeus, 1758 in the Marchica Lagoon (Alboran Sea, Morocco): spatio-temporal distribution, its environmental drivers, and the site-related footprint

Fig. 1: Map showing the geographical localization of the Marchica Lagoon and the sampling stations of Gobius niger.

Fig. 4 in The black goby Gobius niger Linnaeus, 1758 in the Marchica Lagoon (Alboran Sea, Morocco): spatio-temporal distribution, its environmental drivers, and the site-related footprint

Fig. 4: Two-dimensional redundancy analysis (RDA) ordination representing the spatial distribution of Gobius niger related to the predictor variables selected through the best linear models based on distance (DISTLM). SM: suspended matter.

Fig. 7 in The polyclad fauna (Platyhelminthes, Rhabditophora) of the Sinop Peninsula (Black Sea, Turkey) with a description of a new species of Cryptocelis Lang, 1884 Abstract

Fig. 7: A, Prosthiostomum siphunculus; B, Pleioplana okusi. The arrow points the sperm mass. Abbreviations to the figures: cg, cement glands; dLv, Lang's vesicle duct; fp, female gonopore; i, intestine; Lv, Lang´s vesicle; mp, male gonopore; pv1, prostatic vesicle 1; pv2, prostatic vesicle 2; st, stylet; sv, seminal vesicle; u, uterus; v, vagina. Scale bars: A: 200 µm; B: 200 µm.

Fig. 8 in The polyclad fauna (Platyhelminthes, Rhabditophora) of the Sinop Peninsula (Black Sea, Turkey) with a description of a new species of Cryptocelis Lang, 1884 Abstract

Fig. 8: Pleioplana okusi. A, sagittal section of the prostatic vesicle; B, sagittal section of the ovary; C-D, sagittal section of the vagina and female atrium. The arrows point the sperm mass. Abbreviations to the figures: ch, tubular chamber of the prostatic vesicle; ed, ejaculatory duct; fg, female gonopore; o, ovary; pi, epidermal pigment; pp, penis papilla; pv, prostatic vesicle. Scale bars: A: 100 µm; B: 50 µm; C: 30 µm; D: 50 µm.

Fig. 5 in The polyclad fauna (Platyhelminthes, Rhabditophora) of the Sinop Peninsula (Black Sea, Turkey) with a description of a new species of Cryptocelis Lang, 1884 Abstract

Fig. 5: Cryptocelis sinopae sp. nov. Sagittal reconstruction of reproductive system. Abbreviations to the figures: cg, cement gland; cmw, cirrus muscular wall; ed, ejaculatory duct; ep, epidermis; fa, female atrium; fg, female gonopore: gf, musculo-glandular fold; ma, male atrium; mb, muscular bulb; mg, male gonopore; pv, prostatic vesicle; se, secretory epithelium; vd, vas deferens; vf, vaginal fold. Scale bar: 1000 µm.

Fig. 3 in The polyclad fauna (Platyhelminthes, Rhabditophora) of the Sinop Peninsula (Black Sea, Turkey) with a description of a new species of Cryptocelis Lang, 1884 Abstract

Fig. 3: Cryptocelis sinopae sp. nov. A, sagittal section of the male copulatory organ (vas deferens and prostatic vesicle); B, sagittal section of the ejaculatory duct, the arrow points the projection of the ejaculatory duct into the proximal prostatic vesicle; C, sagittal section of the male copulatory organ (cirrus and male atrium); D, sagittal section of the male copulatory apparatus (cirrus); E and E´, sagittal sections of the musculo-glandular folds; F, transversal diagram of the male atrium. Abbreviations to the figures: co, cirrus opening; cr, cirrus; ed, ejaculatory duct; gce, glandular cells; gf, musculo-glandular fold; gf 1, right musculo-glandular fold; gf 2, left musculo-glandular fold; ma, male atrium; mg, male gonopore; ppv, proximal prostatic vesicle; vd, vas deferens. Scale bars: A: 100 µm; B: 30 µm; C: 200 µm; D: 200 µm; E: 200 µm; E΄: 30 µm.

Fig. 1 in The polyclad fauna (Platyhelminthes, Rhabditophora) of the Sinop Peninsula (Black Sea, Turkey) with a description of a new species of Cryptocelis Lang, 1884 Abstract

Fig. 1: Map of the coast of Turkey and the Black Sea showing the sampling site of the biodiversity studies carried out in the area, chronologically ordered. 1, Czerniavsky (1880); 2, Jacubowa (1909); 3, Murina et al. (1995); 4, Bulnes et al. (2009); 5, Bulnes (2010); 6, Çinar (2014); 7, Gözcelioğlu (2011); 8, Teker et al. (2017); 9, this study; M1, Liman-İskele; M2, Gazi Kayası; M3, Asma Kaya; M4, İnceburun-Başoz; M5, Üzümlü Dere.

Fig. 6 in The polyclad fauna (Platyhelminthes, Rhabditophora) of the Sinop Peninsula (Black Sea, Turkey) with a description of a new species of Cryptocelis Lang, 1884 Abstract

Fig. 6: Sagittal sections of the reproductive system of A, Echinoplana celerrima; B, Leptoplana mediterranea; C, Leptoplana tremellaris. Abbreviations to the figures: cb, cirrus bulb; cg, cement glands; cr, cirrus; ed, ejaculatory duct; mp, male gonopore; ph, pharynx; pv, prostatic vesicle; sv, seminal vesicle; vd, vas deferens. Scale bars: A: 500 µm; B: 200 µm; C: 500 µm.

Fig. 4 in The polyclad fauna (Platyhelminthes, Rhabditophora) of the Sinop Peninsula (Black Sea, Turkey) with a description of a new species of Cryptocelis Lang, 1884 Abstract

Fig. 4: Cryptocelis sinopae sp. nov. A-C, sagittal section of the female reproductive system; D, sagittal section of the uterus and vas deferens; E, sagittal section of an oocyte; F, sperm cells immersed in body parenchyma. The black arrows point sperm cells. Abbreviations to the figures: cg, cement glands; ev, external vagina; fa, female atrium; i, intestine; iv, internal vagina; mg, male gonopore; mv, median vagina; ov, oviduct; vd, vas deferens; vf, vaginal fold. Scale bars: A: 100 µm; B: 100 µm; C: 100 µm; D: 100 µm; E: 30 µm; F: 15 µm.