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219 results for “Marmara”
Fig. 5 in Ponto-Caspian And Mediterranean Faunal And Floral Records Of Upper Pleistocene-Holocene Sediments From The İzmit Gulf (Marmara Sea, Turkey)
Fig. 5 Scanning electron micrographs of selected benthic foraminiferal species identified from the İzmit Gulf drilling cores. a. Asterigerinata mamilla, 206/37.5 m: a1, spiral view; a2, peripheral view; a3, umbilical view. b. Aubignyna perlucida, 208/37.5 m: b1, spiral view; b2, umbilical view. c. Aubignyna perlucida, 207/31 m: c1, spiral view; c2, peripheral view; c3, umbilical view. d. Biloculinella labiata, 204/13 m. e. Bolivina alata, 207/22 m. f. Bolivina dilatata, 206/37.5 m. g. Bolivina dilatata, 208/18 m. h. Bolivina ordinaria, 207/22.75 m. i. Bolivina ordinaria, 206/8 m: i1, side view; i2, apertural edge view. j. Bolivina pseudoplicata, 206/37.5 m. k. Bolivina spathulata, 206/37.5 m. l. Bolivina striatula, 206/14 m. m. Bolivina striatula, 208/25 m. n. Bulimina aculeata, 208/33 m. o. Bulimina elongata, 208/18 m. p. Bulimina marginata, 207/18 m. q. Bulimina marginata, 207/22.75 m.
Fig. 10 in Ponto-Caspian And Mediterranean Faunal And Floral Records Of Upper Pleistocene-Holocene Sediments From The İzmit Gulf (Marmara Sea, Turkey)
Fig. 10 Total Benthic Foraminifera (TBF) and Species Number (SN) in drillings a. Dilovası and b. Hersek Burnu. TBF indicates numbers of specimens per 10 g dry sediment. The lower intervals of drillings 10MB-204 (120-80 m), 10MB-205 (117.2-40 m), 10MB- 206 (122-80 m), 10MB-207 (120.9-50 m) and 10MB-208 (200-40 m) are not shown due to absence of sample.
Figure 6 in Age, growth, and reproductive biology of Atlantic bonito (Sarda sarda Bloch, 1793) from the Turkish coasts of the Black Sea and the Sea of Marmara
Figure 6. Micrographs from gonad cross-sections of immature stage (a), nonspawning mature stage (b), spawning stage (c), and postovulatory stage (d).
Figure 1 in Age, growth, and reproductive biology of Atlantic bonito (Sarda sarda Bloch, 1793) from the Turkish coasts of the Black Sea and the Sea of Marmara
Figure 1. Length–frequency distribution for females, males, unidentified specimens, and all samples of S. sarda (n = 212).
Figures 2–13 in Limoniidae (Diptera) fauna of the Marmara region with 23 new records for Turkey
Figures 2–13. Diagnostic characters of the new records of Limoniidae. Wings: 2- Crypteria (s. str.) limnophiloides Bergroth, 1913; 3- Ellipteroides (Protogonomyia) alboscutellatus (von Roser, 1840); 4-. Erioptera (s. str.) tenuirama Savchenko, 1972; 5- Gnophomyia lugubris (Zetterstedt, 1838); 6- Gonomyia (s. str.) tenella (Meigen, 1818); 7- Molophilus (s. str.) directidens Stary, 1976; 8- Molophilus (s. str.) lackschewitzianus lackschewitzianus Alexander, 1953; 9- Molophilus (s. str.) serpentiger Edwards, 1938; 10- Ormosia (s. str.) furcata Savchenko, 1973; 11- Rhypholophus varius (Meigen, 1818); 12- Dactylolabis (s. str.) sexmaculata (Macquart, 1826); 13- Eloeophila submarmorata (Verrall, 1887).
Figures 14–24 in Limoniidae (Diptera) fauna of the Marmara region with 23 new records for Turkey
Figures 14–24. Diagnostic characters of the new records of Limoniidae. Wings: 14- Euphylidorea aperta (Verrall, 1887); 15- Prionolabis hospes (Egger, 1863); 16- Achyrolimonia decemmaculata (Loew, 1873); 17- Atypophthalmus (s. str.) inustus (Meigen, 1818); 18- Dicranomyia (s. str.) autumnalis (Staeger, 1840); 19- Dicranoptycha paralivescens Stary, 1972; 20- Helius (s. str.) flavus (Walker, 1856); 21- Helius (s. str.) longirostris longirostris (Meigen, 1818); 22- Helius (s. str.) pallirostris Edwards, 1921; 23- Limonia albifrons (Meigen, 1818); 24- Neolimonia dumetorum (Meigen, 1804).
Figures 37–47 in Limoniidae (Diptera) fauna of the Marmara region with 23 new records for Turkey
Figures 37–47. Diagnostic characters of the new records of Limoniidae. Male terminalia: 37- Euphylidorea aperta (Verrall, 1887); 38- Prionolabis hospes (Egger, 1863); 39- Achyrolimonia decemmaculata (Loew, 1873); 40- Atypophthalmus (s. str.) inustus (Meigen, 1818); 41- Dicranomyia (s. str.) autumnalis (Staeger, 1840); 42- Dicranoptycha paralivescens Stary, 1972; 43- Helius (s. str.) flavus (Walker, 1856); 44- Helius (s. str.) longirostris longirostris (Meigen, 1818); 45- Helius (s. str.) pallirostris Edwards, 1921; 46- Limonia albifrons (Meigen, 1818); 47- Neolimonia dumetorum (Meigen, 1804).
Figure 1 in Exploring the dynamics of small pelagic fish catches in the Marmara Sea in relation to changing environmental and bio-optical parameters
Figure 1. Time series of deseasonalised Chl-a, net primary productivity (NPP), and sea surface temperature (SST). Solid lines show the time series, dash-dot lines show the deseasonalised time series, dashed lines indicate their respective nonlinear trends, and flat solid lines show linear trend components.
Figure 2 in Exploring the dynamics of small pelagic fish catches in the Marmara Sea in relation to changing environmental and bio-optical parameters
Figure 2. Time series of fisheries catches (tons) and fishing effort in the Marmara Sea between 2000 and 2019. Flat solid lines indicate linear trends.
Figure 5. Sentinel 3 in Marine mucilage in the Sea of Marmara and its effects on the marine ecosystem: mass deaths
Figure 5. Sentinel 3 imagery of the chlorophyll-a concentration in the study area on April 22, 2021.
Figure 3 in Marine mucilage in the Sea of Marmara and its effects on the marine ecosystem: mass deaths
Figure 3. Some dead species were collected during sampling. The orange circle indicates Atherina sp., and the yellow square indicates other affected species.
Figure 2 in Marine mucilage in the Sea of Marmara and its effects on the marine ecosystem: mass deaths
Figure 2. Regional map and sampling stations in the southern of Sea of Marmara (1: Misakça, 2: Şirinçavuş, 3: Narlı, 4: Tatlısu)
Figure 1 in Marine mucilage in the Sea of Marmara and its effects on the marine ecosystem: mass deaths
Figure 1. Mucilage aggregation examples on the water surface in the Sea of Marmara, a) on April 23, 2021, on the coast of Misakça and b) on May 25, 2021, in Erdek Harbor.
Figure 3 in Occlusal surface variations in genetically-identified specimens of the genus Apodemus (Mammalia: Rodentia) distributed in the Northern Anatolia region and three Turkish islands: Gökçeada, Marmara Island, and Bozcaada
Figure 3. The variations observed in the left upper teeth and their locations. D1: Presence of a bis structure immediately adjacent to the t2 cusp in UM1, D2: Presence of the t12 cusp in UM1, D3: Presence of a spur structure extending posteriorly from the t3 cusp in UM1 but not merging with the t5 cusp, D4: Existence of a bridge between the t1 cusp and t5 cusp in UM1, D5: Connection through a bridge between the t4 cusp and t7 cusp in UM1, D6: Structural swelling and island-like condition of the t7 cusp in UM1, D7: Structural line-like condition of the t7 cusp in UM1, D8: Structural swelling and island-like condition of the t7 cusp in UM2, D9: Line-like structural condition of t7 in UM2, D10: Presence or absence of the t12 cusp in UM2, D11: Presence of a bridge-like structure between the t1 cusp and t5 cusp in UM2, D12: Presence of a bridge between the t4 cusp and t7 cusp in UM2, D13: Existence of a bridge structure between the t1 cusp and t5 cusp in UM3, D14: Presence of a connection between the t6 cusp and t8 cusp in UM3.
Figure 4 in Occlusal surface variations in genetically-identified specimens of the genus Apodemus (Mammalia: Rodentia) distributed in the Northern Anatolia region and three Turkish islands: Gökçeada, Marmara Island, and Bozcaada
Figure 4. The intra- and interspecies schematic diagram of left lower dental variations. Diagram A: refers to the island population of A. sylvaticus, while B: refers to the mainland population of A. sylvaticus. Numbers represent species; 1: A. flavicollis, 2: A. witherbyi, 3: A. sylvaticus, 4: A. uralensis, 5: A. mystacinus. Lowercase letters have been selected as variation characteristics; a: number of cingula in LM1, b: tma in LM1, c: central distoconid in LM1, d: aneroconid complex in LM1, e: number of cingula in LM2, f: central distoconid in LM2.
Figure 1 in Occlusal surface variations in genetically-identified specimens of the genus Apodemus (Mammalia: Rodentia) distributed in the Northern Anatolia region and three Turkish islands: Gökçeada, Marmara Island, and Bozcaada
Figure 1. Map of the locations where the samples were collected and main locations (modified from Çolak et al., 2013) A: The Dardanelles, B: The Bosphorus, C: Kızılırmak, D: Melet River, E: Çoruh River, a: Marmara Adası, b: Gökçeada, c: Bozcaada, 1-Ardahan, 2-Artvin, 3-Rize, 4-Trabzon, 5-Giresun, 6-Ordu, 7-Tokat, 8-Samsun, 9-Sinop, 10-Çorum, 11-Kastamonu, 12-Zonguldak, 13-Bolu, 14-Düzce, 15-Kocaeli, 16-İstanbul, 17-Bursa, 18-Tekirdağ, 19-Kırklareli, 20-Balıkesir, 21-Edirne, 22-Çanakkale.
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 2 in First record of shrimp scad Alepes djedaba (Carangidae) from the Sea of Marmara, Turkey
Figure 2. - Alepes djedaba, female, 116 mm TL, caught from the Sea of Marmara (Photo by M.L. Artüz).
Figure 1 in Changes in abundance and community structure of the zooplankton population during the 2008 mucilage event in the northeastern Marmara Sea
Figure 1. Study area.
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