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190 results for “Aegean Sea”
Figure 7 in A new species of the genus Echinolaophonte Nicholls, 1941 (Copepoda, Harpacticoida, Laophontidae) from the Aegean Sea coast of Turkey
Figure 7. Echinolaophonte mordoganensis sp. nov., a–b) holotype ♀; c–f) allotype ♂, antennule: a), penultimate somite, anal somite, and caudal rami, dorsal; b) urosome, ventral; c) antennule; d) distal part of the fifth segment; e) 3-dimensional spinous process of the sixth segment; f) seventh and eighth segments.
Figure 4 in A new species of the genus Echinolaophonte Nicholls, 1941 (Copepoda, Harpacticoida, Laophontidae) from the Aegean Sea coast of Turkey
Figure 4. Echinolaophonte mordoganensis sp. nov., SEM micrographs, ♀: a) antennule; b) maxilliped; c) P1 endopod claw; d) antenna; e) dorsal process of the penultimate somite; f) caudal rami.
Figure 6 in A new species of the genus Echinolaophonte Nicholls, 1941 (Copepoda, Harpacticoida, Laophontidae) from the Aegean Sea coast of Turkey
Figure 6. Echinolaophonte mordoganensis sp. nov., SEM micrographs, ♂: a) habitus, dorsal; b) cephalothorax; c) somites 1–6, dorsal; d) somites 8–11, dorsal; e) somite 2–6, dorsal; f) antennule.
Figure 9 in A new species of the genus Echinolaophonte Nicholls, 1941 (Copepoda, Harpacticoida, Laophontidae) from the Aegean Sea coast of Turkey
Figure 9. Echinolaophonte mordoganensis sp. nov., a ♂, b–d ♀, variation of pseudo-operculum on paratypes.
Figure 3 in A new species of the genus Echinolaophonte Nicholls, 1941 (Copepoda, Harpacticoida, Laophontidae) from the Aegean Sea coast of Turkey
Figure 3. Echinolaophonte mordoganensis sp. nov., ♀, holotype: a) antennule and rostrum; b) antenna; c) mandible; d) cutting edge of the mandibular gnathobase, e–f; mandibular palp; e) posterior; f) anterior; g) maxillule, h) maxilla; i) maxilliped.
Figure 8 in A new species of the genus Echinolaophonte Nicholls, 1941 (Copepoda, Harpacticoida, Laophontidae) from the Aegean Sea coast of Turkey
Figure 8. Echinolaophonte mordoganensis sp. nov., a) ♀, holotype; b–e) ♂, allotype; a) P5; b) P5; c) P6; d) P3; e) P4.
Figure 1 in A new species of the genus Echinolaophonte Nicholls, 1941 (Copepoda, Harpacticoida, Laophontidae) from the Aegean Sea coast of Turkey
Figure 1. Echinolaophonte mordoganensis sp. nov., SEM micrographs, ♀: a) habitus, dorsal; b) habitus, ventral; c) somites 7–9, dorsal; d) somites 2–6, dorsal.
Figure 2 in Ecomorphological patterns and shape indices of otoliths in the Pagellus acarne (Actinopterygii, Sparidae) from the Aegean and Marmara Seas
Figure 2. Explanation of morphometric otolith measurements on the proximal otolith surface of Pagellus acarne.
Figure 4 in Ecomorphological patterns and shape indices of otoliths in the Pagellus acarne (Actinopterygii, Sparidae) from the Aegean and Marmara Seas
Figure 4. Principal component analysis (PCA) plot showing similarities/ differences between both Pagellus acarne stocks and left and right side otoliths: (AS) Aegean Sea and (MS) Sea of Marmara.
Figure 3 in Reproductive biology of Lophius budegassa (Lophiidae) in the North Aegean Sea
Figure 3. - Monthly percentage of each maturity stage for males (A) and females (B) black-bellied anglerfish. Maturity stages: I, Immature; II, Maturing; III, Mature; IV, Spawning; V, Post-Spawning.
Figure 2 in Reproductive biology of Lophius budegassa (Lophiidae) in the North Aegean Sea
Figure 2. - Length-number distribution of Lophius budegassa sampled in the Saros Bay by commercial vessel between September 2006 and September 2008.
Figure 4 in Reproductive biology of Lophius budegassa (Lophiidae) in the North Aegean Sea
Figure 4. - Monthly variation of gonadosomatic index for males (A) Figure 5. - Percentage of sexually mature males (A) and females and females (B) Lophius budegassa between September 2006 and (B) Lophius budegassa according to total length. September 2008. Vertical bars represent standard error with sample size values indicated between brackets. and GSI values in females and males. Therefore, the results suggest a main spawning period from December to March decreases with increasing depth that may reflect a seasonal for blackbellied anglerfish. In females, spawning and postsegregation (García-Rodríguez et al., 2005). Laurenson et spawning stages have been seen from December to March al. (2008) found that the proportion of L. piscatorius varies and in males from January to March (Fig. 3A, B). At the same with both depth and season in Scottish waters. Several state- time, GSI values in males were high except in August and ments can explain this difference. Differentiation in growth November, while female GSI values were the highest in Janrate between sexes can cause an unbalanced proportion, uary (Fig. 4A, B). The spawning males can be seen almost all since the sex presenting faster growth rate will go through year around (Duarte et al., 2001; Landa et al., 2014), and this the most vulnerable smaller size phase quickly and, there- could increase the chances for a mature female to encounter fore decrease the predation proportion. Conversely, the sex with slower growth rate will be more likely to pass predation, with its abundance decreased disproportion- Table I. - Length at 50% maturity (L50) of Lophius budegassa obtained by other authors. ately in next development phases (Vicentini and Araújo,
Figure 3. Simognathus adriaticus Viets, 1940 in Halacaridae (Acari: Prostigmata) of the Aegean Sea of Turkey (Çanakkale and Izmir)
Figure 3. Simognathus adriaticus Viets, 1940 (female) – A. dorsal view of idiosoma; B. ventral view of idiosoma; C. lateral view of; D. lateral view of chelicera; E. lateral view of leg I. Scale bars: 50 µm.
Figure 2 in Halacaridae (Acari: Prostigmata) of the Aegean Sea of Turkey (Çanakkale and Izmir)
Figure 2. Halacaropsis hirsuta (Trouessart, 1889) (deutonymph) – A. Dorsal view of idiosoma; B. Ventral view of idiosoma; C. Lateral view of gnathosoma; D. Ocular plate; E. Lateral view of leg I; F. Genitoanal plate (AP: anal plate; co: corneae; ep: eye pigment; gac: genital acetabula; pgs. perigenital setae). Scale bars: 50 µm.
Datasets associated with a study of extensional faulting around Kolumbo Volcano, Aegean Sea
<p>This contribution of data includes 56 different data files of various formats, plus one excel file ("Data_Inventory_and_Descriptions_Kolumbo_Faulting.xlsx") which provides all of the necessary metadata for each of the 56 data files. The excel file should be used as a readme file, detailing key information for each file including format, georeferencing information, and relevant software for loading and viewing the data. The excel file also shows how each file is related to an associated figure in a manuscript currently being submitted for peer review. Once that paper is published, this description will be updated with the doi of the paper.</p>
Fig. 8 in The cytotoxic activity of Sponges and Tunicates from Turkish Aegean Sea
Fig. 8 — Microscopic images of PC-3 cells treated with extracts for 24 h (Scale bar: 100 µm)
Fig. 7 in The cytotoxic activity of Sponges and Tunicates from Turkish Aegean Sea
Fig. 7 — Cell viability of PC-3 cell line with various extract concentrations treatment for 24 h
Fig. 6 in The cytotoxic activity of Sponges and Tunicates from Turkish Aegean Sea
Fig. 6 — Microscopic images of SH-SY5Y cells treated with extracts for 24 h (Scale bar: 200 µm)
Fig. 4 in The cytotoxic activity of Sponges and Tunicates from Turkish Aegean Sea
Fig. 4 — Microscopic images of AGS cells treated with extracts for 24 h (Scale bar: 200 µm)
Fig. 5 in The cytotoxic activity of Sponges and Tunicates from Turkish Aegean Sea
Fig. 5 — Cell viability of SH-SY5Y cell line with various extract concentrations treatment for 24 h
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International Brain Laboratory public data
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OpenNeuro
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