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Fig. 3 in In situ experiments on the effect of low pH on the ultrastructure of the seagrasses Cymodocea nodosa and Posidonia oceanica Abstract
Fig. 3: A-E. Interphase epidermal cells of young leaves under different pH levels. In all figures, green represents tubulin immunofluorescence and blue represents Hoechst staining of DNA. A. Transfer of CN to pH 7.8 for 1 week: thick MT bundles showing a slightly aberrant orientation. B. Transfer of PO to pH 7.8 for 1 week: MT bundles oriented perpendicularly to the long leaf axis. C. Transfer of CN to pH 6.8 for 1 week: fragmented MT bundles with slightly aberrant orientations. D. Transfer of CN to pH 7.8 for 3 weeks: short, fragmented, and curved MT bundles with aberrant orientations. E. Transfer of PO at pH 7.8 for 3 weeks: depolymerization and disassembly of interphase MTs with loss of proper orientation. Scale bar = 10 μm.
Fig. 5 in Phenology of Anemonia viridis and Exaiptasia diaphana (Cnidaria: Anthozoa) from marine temperate ecosystems Abstract
Fig. 5: Scheme summarizing the life history traits of Anemonia viridis and Exaiptasia diaphana. Quadrants of the circle correspond to quarters; each quadrants shows phases of expansion (January-March and July-September) and regression (October-December and April-May) together with traits of the reproductive cycle (settlement, fission, gonad maturation, spawning etc.) and sea temperature ranges.
Fig. 3 in Phenology of Anemonia viridis and Exaiptasia diaphana (Cnidaria: Anthozoa) from marine temperate ecosystems Abstract
Fig. 3: Sex ratio of Anemonia viridis (A) and Exaiptasia diaphana (B) throughout the period July 2013-July 2014 with relative percentages of male, female and infertile individuals.
Fig. 4 in In situ experiments on the effect of low pH on the ultrastructure of the seagrasses Cymodocea nodosa and Posidonia oceanica Abstract
Fig. 4: A-C. TEM micrographs of young epidermal cells of C. nodosa after one week transfer at S2 area. A. Epidermal cell with undifferentiated chloroplasts and increased number of mitochondria. B. Higher magnification of a chloroplast with a few developing grana. C. Higher magnification of a mitochondrion with very few cristae. Scale bars = 0.5 μm (A, B, C).
Fig. 2 in Phenology of Anemonia viridis and Exaiptasia diaphana (Cnidaria: Anthozoa) from marine temperate ecosystems Abstract
Fig. 2: Temporal variations in abundance of Anemonia viridis (A) and Exaiptasia diaphana (B) expressed as cover percentage in relation to monthly fluctuations of surface water temperature (°C), irradiance (W/m2) and wave heights (m).
Fig. 1 in Phenology of Anemonia viridis and Exaiptasia diaphana (Cnidaria: Anthozoa) from marine temperate ecosystems Abstract
Fig. 1: Sampling area (Passetto, red frame) at Conero Promontory (Italy, Adriatic Sea). Anemonia viridis and Exaiptasia diaphana were collected from July 2013 to June 2014 at Site A (43.618639° N, 13.532489° W) and Site B (43.618069° N, 13.533586° W), respectively. QGIS elaboration (QGIS Development Team 2017).
Fig. 3 in The demersal fish assemblages of the infra and circalittoral coastal rocky bottoms of the Aeo- lian Archipelago (Central Mediterranean Sea) studied by Remotely Operated Vehicle (ROV) Abstract
Fig. 3: Variation (mean ± S.E.) in species richness, diversity (H') and total density among sectors and depth ranges.
Fig. 7 in In situ experiments on the effect of low pH on the ultrastructure of the seagrasses Cymodocea nodosa and Posidonia oceanica Abstract
Fig. 7: A-D. TEM micrographs of young epidermal cells of P. oceanica after three weeks transfer at S1 area. A. Part of an epidermal cell of P. oceanica with warped cell walls, distorted cytoplasm, and a large nucleus with condensed chromatin masses. B. Chloroplast with remnants of disorganized cisternae and round plastoglobuli. C. Chloroplasts with large starch grains surrounded by a system of electron-dense elongated and/or round plastoglobuli. Mitochondria with a few broken dilated cristae are visible. D. Fragmented ER membranes arranged along the cell periphery. Scale bars = 1 μm (A), 0.5μm (B, C) and 0.2μm (D).
Fig. 1 in The demersal fish assemblages of the infra and circalittoral coastal rocky bottoms of the Aeo- lian Archipelago (Central Mediterranean Sea) studied by Remotely Operated Vehicle (ROV) Abstract
Fig. 1: Map of the study area in the southern Tyrrhenian Sea. The three sectors of the Aeolian Archipelago (1=Western sector; 2=Central sector; 3=Eastern sector) and locations of the ROV transects () and the main fishing ports () are indicated in the inset maps.
Fig. 2 in The demersal fish assemblages of the infra and circalittoral coastal rocky bottoms of the Aeo- lian Archipelago (Central Mediterranean Sea) studied by Remotely Operated Vehicle (ROV) Abstract
Fig. 2: Scatter plot of the canonical discriminant analysis on the effects of (a) sector and (b) depth range. Species contribution to the observed patterns is shown with directional vectors. Aant=Anthias anthias, Afil=Aulopus filamentosus, Crub=Callanthias ruber, Cchr=Chromis chromis, Cjul=Coris julis, Dgib=Dentex gibbosus, Dvul=Diplodus vulgaris, Gkol=Gobius kolombatovici, Hdac=Helicolenus dactylopterus, Mhel=Muraena helena, Scab=Serranus cabrilla, Teph=Thorogobius ephippiatus.
Fig. 5 in Evidence of a second nursery area of the sandbar shark, Carcharhinus plumbeus (Nardo, 1827) in the Eastern Mediterranean Sea Abstract
Fig. 5: Frequency of sandbar sharks Carcharhinus plumbeus observations caught as accidentally by pelagic longlines and commercial trawling from depths of 25 and 125 m of Mersin Bay and Iskenderun Bay, eastern Mediterranean Turkish coasts between August 2010 and March 2014 (BaŞusta, 2016). The bars represent the number of observations and dots (○) represent the size of sandbar sharks.
Fig. 1 in Evidence of a second nursery area of the sandbar shark, Carcharhinus plumbeus (Nardo, 1827) in the Eastern Mediterranean Sea Abstract
Fig. 1: Map of the Yumurtalik Bight in the Iskenderun Bay, the north-eastern Mediterranean Sea with an inset depicting the location where the sandbar sharks Carcharhinus plumbeus were caught accidentally by a pelagic bluefish longline on 24–27 July 2017. The location of the first nursery (Boncuk bay) is also shown on the left that is based on the coordinate obtained from Google Map.
Fig. 13 in Spatio-temporal distribution of pufferfish (Tetraodontidae) along the Turkish coast of the Mediterranean Sea Abstract
Fig. 13: CCA triplot of Tetraodontidae species (A) abundance and (B) biomass; stations classified by the bottom depths, environmental parameters (see Appendix 1 for abbreviations) and the species (L sce = Lagocephalus sceleratus, L spa = Lagocephalus guentheri, L sue = Lagocephalus suezensis, T fla = Torquigener flavimaculosus, S pac = Sphoeroides pachygaster, and T spi = Tylerius spinosissimus).
Fig. 10 in Spatio-temporal distribution of pufferfish (Tetraodontidae) along the Turkish coast of the Mediterranean Sea Abstract
Fig. 10: Length-weight relationships of males (blue), females (pink), and pooled data (red) of Lagocephalus suezensis.
Fig. 6 in Spatio-temporal distribution of pufferfish (Tetraodontidae) along the Turkish coast of the Mediterranean Sea Abstract
Fig. 6: Distribution of (A) biomass, (B) abundance (circles square-rooted), and (C) percent sex composition of Lagocephalus suezensis in time (months) and space (regions and depths). Seasonal colors on the figures are: blue = May 2014, green = August 2014, red = October 2014, and magenta = February 2015. Colors for sex composition: females follow seasonal color scheme, males are black, and juveniles are white in seasons.
Fig. 9 in Spatio-temporal distribution of pufferfish (Tetraodontidae) along the Turkish coast of the Mediterranean Sea Abstract
Fig. 9: Post-hoc test (least significant difference, LSD) in total length in cm of Lagocephalus suezensis among (A) regions, (B) seasons (1 = May, 2 = August, 3 = October, and 4 = February), (C) bottom depths, and (D) sex (F = female, M = male, NI = sex not identified, and J = juvenile). Circle = mean, horizontal bar = standard deviation, blue mark = to be tested among the regions, months, and depths, red = significantly different, gray = not significantly different between vertical discrete gray lines.
Fig. 7 in Spatio-temporal distribution of pufferfish (Tetraodontidae) along the Turkish coast of the Mediterranean Sea Abstract
Fig. 7: Post-hoc test (least significant difference, LSD) of biomasses in kg/km2 of Lagocephalus suezensis among (A) regions, (B) seasons (1 = May, 2 = August, 3 = October, and 4 = February), and (C) bottom depths. Circle = mean, horizontal bar = standard deviation, blue mark = to be tested for biomasses among regions, months and depths, red = significant difference, gray = no significant difference between vertical discrete gray lines.
Fig. 12 in Spatio-temporal distribution of pufferfish (Tetraodontidae) along the Turkish coast of the Mediterranean Sea Abstract
Fig. 12: Length-weight relationships of males (blue), females (pink), and unisex pooled data (red) of Torquigener flavimaculosus.
Fig. 4 in Spatio-temporal distribution of pufferfish (Tetraodontidae) along the Turkish coast of the Mediterranean Sea Abstract
Fig. 4: Distribution of (A) biomass, (B) abundance (circles square-rooted), and (C) percent sex composition of Lagocephalus guentheri in time (months) and space (regions and depths). Seasonal colors on figures are: blue = May 2014, green = August 2014, red = October 2014, and magenta = February 2015. Colors for sex ratio: females follow seasonal color scheme, males are black, and juveniles are white in seasons.
Fig. 2 in Spatio-temporal distribution of pufferfish (Tetraodontidae) along the Turkish coast of the Mediterranean Sea Abstract
Fig. 2: Distribution of (A) biomass, (B) abundance (circles square-rooted), and (C) percent sex ratio of Lagocephalus sceleratus in time (months) and space (regions and depths). Seasonal colors on the figures are: blue for May 2014, green for August 2014, red for October 2014, and magenta for February 2015. Colors for sex ratio: females follow seasonal color scheme, males are black, and juveniles are white in seasons.
ScienceDex guides
Understand access before you commit
These curated guides explain access requirements, typical timelines, costs, and reuse considerations for widely used research datasets.
Allen Brain Atlas
Allen Brain Atlas is an Allen Institute collection of brain map atlases, datasets, APIs, and analysis tools covering mouse, human, and non-human primate brain resources.
Annotated Behaviour and Observability Dataset (ABODe)
ABODe is a University of Edinburgh DataShare dataset for behavior classification in group-housed mice using home-cage video, identities, bounding boxes, ground-plate positions, and annotator labels.
DANDI Archive for NWB datasets
DANDI is a BRAIN Initiative archive for publishing and sharing neurophysiology data, including electrophysiology, optophysiology, and behavioral data packaged as NWB and related standards.
International Brain Laboratory public data
The International Brain Laboratory public data releases expose standardized mouse decision-making experiments, including Neuropixels recordings, widefield calcium imaging, behavior, and session metadata accessed through the ONE API.
OpenNeuro
OpenNeuro is a free, open platform for sharing neuroimaging datasets, with public search, dataset pages, and download paths for web, S3, DataLad, and the OpenNeuro CLI.