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Fig. 4 in On the biology of blackbellied angler, Lophius budegassa Spinola, 1807, in the north-western Mediterranean Abstract

Fig. 4: Length-weight relationship of L. budegassa for males (black dots), females (dark grey triangle) and undetermined (light grey square) specimens.

Fig. 7 in On the biology of blackbellied angler, Lophius budegassa Spinola, 1807, in the north-western Mediterranean Abstract

Fig. 7: Von Bertalanffy growth curves (dashed lines) for females (black) and males (grey) of L. budegassa in the study area. Dots and triangles represent observations for females and males, respectively.

Fig. 3 in On the biology of blackbellied angler, Lophius budegassa Spinola, 1807, in the north-western Mediterranean Abstract

Fig. 3: Heatmap representing the spatial distribution of blackbellied angler in terms of biomass per spatial unit, obtained from MEDITS survey data (1994-2021).

Fig. 6 in On the biology of blackbellied angler, Lophius budegassa Spinola, 1807, in the north-western Mediterranean Abstract

Fig. 6: Sections of illicia of L. budegassa (magnification 100x). Left: Female, 28.0 cm TL; Right: Female, 42.5 cm TL.

Fig. 2 in On the biology of blackbellied angler, Lophius budegassa Spinola, 1807, in the north-western Mediterranean Abstract

Fig. 2: Temporal evolution of biomass and density indices from MEDITS survey data (1994 2021). Shaded areas are standard deviations.

Fig. 8 in On the biology of blackbellied angler, Lophius budegassa Spinola, 1807, in the north-western Mediterranean Abstract

Fig. 8: Age bias plots between two readers with the mean age recorded (black points) and 95% confidence intervals (bars). Red points represent mean age estimates that differ significantly between readers.

Fig. 5 in Using spatial indicators to investigate fish spawning strategies from ichthyoplankton surveys: A case study on co-occurring pelagic species from the North-East Aegean Sea Abstract

Fig. 5: Distribution and abundance maps of eggs during May (A, B) and July 2010 (C-E), in the NE Aegean Sea. The major patches are indicated by different colours, while the size of the circles is scaled by the maximum abundance per species and period (Table 2). The number of each patch indicates the ranking according to the abundance of individuals in each patch. The small black cross symbols show the centres of gravity (CG) of each major patch (i.e. those patches having more than 10% of the overall abundance; Table 3). The large cross indicates the CG of the population. The length of the cross axes indicate the isotropy of the egg distribution. The 200m isobaths are also shown (dark contour line).

Fig. 4 in Using spatial indicators to investigate fish spawning strategies from ichthyoplankton surveys: A case study on co-occurring pelagic species from the North-East Aegean Sea Abstract

Fig. 4: Box-and-whisker plots for temperature (oC; at 10 m depth), salinity (at 10 m depth), log-transformed integrated fluorescence (μg l-1) and log-transformed mesozooplankton biomass (mg m-2) between three groups of sampling stations: L – Lemnos plateau, O – offshore pelagic area north of Lemnos island, and T- Thracian Sea shelf. Boxes indicate median and interquartile ranges, whiskers delineate full ranges. F-values are provided for comparisons of the parameters between the three groups (L, O, T) and within each season. For comparisons that did not meet the assumptions of the analysis of variance, the Kruskal-Wallis statistic H is provided. Asterisks indicate significant differences: *p <0.05, **p <0.01, ***p <0.001. Post-hoc multiple comparisons were performed with a Student-Newman-Keul's test, where statistically significant differences among groups are indicated by letters a, b, c on the left side of each box. Groups with the same letter do not differ significantly.

Fig. 3 in Using spatial indicators to investigate fish spawning strategies from ichthyoplankton surveys: A case study on co-occurring pelagic species from the North-East Aegean Sea Abstract

Fig. 3: Contour maps of the vertical distribution of temperature (oC; left column), salinity (middle column) and fluorescence (μg Chlα l-1; right column) during May 2010 along transect A (A-C) and transect B (D-F), and during July 2010 along transects A (H-J) and B (K-M). Y-axis: depth of the water column; X-axis: distance (nmi) from the northern sampling station (0 nmi) to the southern station. The position (distance, nmi) of the sampling stations along the transects are shown in white, dashed lines on top of the temperature contour maps.

Fig. 2 in Using spatial indicators to investigate fish spawning strategies from ichthyoplankton surveys: A case study on co-occurring pelagic species from the North-East Aegean Sea Abstract

Fig. 2: Temperature (oC, 10 m depth; A, E), salinity (10 m; B, F), integrated fluorescence (μg Chl-a l-1, 0-100 m; C, G) and mesozooplankton biomass (mg m-2; D, H) during May (A-D) and July 2010 (E-H) in the study area.

Fig. 1 in Using spatial indicators to investigate fish spawning strategies from ichthyoplankton surveys: A case study on co-occurring pelagic species from the North-East Aegean Sea Abstract

Fig. 1: Ichthyoplankton (shown as open red circles) and CTD sampling stations (shown as filled red circles) during May and July 2010. The isobaths of 100 and 200 m are shown (light and dark blue lines, respectively). Black arrows indicate the main circulation pattern in the area: LIS - Lemnos-Imvros stream, SG - Samothraki gyre (Somarakis et al., 2002). The sampling stations of transects A and B (grey lines) show the vertical structure of the water column in Figure 3.

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Dataset: Peoples Bancorp of North Carolina, Inc. (PEBK) Stock Performance

This dataset provides historical stock market performance data for specific companies. It enables users to analyze and understand the past trends and fluctuations in stock prices over time. This information can be utilized for various purposes such as investment analysis, financial research, and market trend forecasting.

Fig. 5 in Molecular and morpho-anatomical assessment of the family Dorididae (Mollusca, Nudibranchia) in the Mediterranean and North-East Atlantic

Fig. 5. Scanning electron micrographs of the radular teeth. A–C. Doris ocelligera (Bergh, 1881) (ZSM20240260). D–F. Doris berghi (Vayssière, 1901) comb. rest. (ZSM20240261). Showing first (fl) and subsequent (cl) lateral teeth.

Fig. 7. A–B in Molecular and morpho-anatomical assessment of the family Dorididae (Mollusca, Nudibranchia) in the Mediterranean and North-East Atlantic

Fig. 7. A–B. Scanning electron micrographs of the radular teeth of Doris verrucosa Linnaeus, 1758, showing first (fl) and subsequent (cl) lateral teeth.

Fig. 6 in Molecular and morpho-anatomical assessment of the family Dorididae (Mollusca, Nudibranchia) in the Mediterranean and North-East Atlantic

Fig. 6. Schematic drawing of the reproductive systems. A. Doris ocelligera (Bergh, 1881). B. Doris berghi (Vayssière, 1901) comb. rest. Abbreviations: A = ampulla; Bc = bursa copulatrix; Fgl = female glands; Ps = penial sheath; R = seminal receptacle; Vd = vas deferens; Vdu = vaginal duct. The black arrowheads represent the connection of the ampulla to the gonad.

Fig. 8 in Molecular and morpho-anatomical assessment of the family Dorididae (Mollusca, Nudibranchia) in the Mediterranean and North-East Atlantic

Fig. 8. Doris marmorata (Risso, 1818). A. Specimen from Blanes, NE Spain (ZSM20240263). B. Specimen from Sant Feliu de Guíxols, NE Spain (ZSMMol20210023).

Fig. 3 in Molecular and morpho-anatomical assessment of the family Dorididae (Mollusca, Nudibranchia) in the Mediterranean and North-East Atlantic

Fig. 3. Results from ASAP for both COI (top) and 16S (bottom) markers of the alignment of the species within the genus Doris Linnaeus, 1758 based on the phylogenetic tree results. Colour boxes refer to species hypotheses and the dash-line is the threshold (representing a 5–10% genetic divergence distance) in which species hypotheses were selected.

Fig. 1 in Molecular and morpho-anatomical assessment of the family Dorididae (Mollusca, Nudibranchia) in the Mediterranean and North-East Atlantic

Fig. 1. Map of the Iberian Peninsula and North-West Africa showing the sampling localities where specimens of Doris ocelligera (Bergh, 1881) were collected. The purple triangles show the locations where the blueish morphotype specimens were taken, whereas the yellow circles show the locations where the yellow morphotype specimens were collected. Map generated at https://www.simplemappr.net

Fig. 4. A. Doris verrucosa Linnaeus, 1758 in Molecular and morpho-anatomical assessment of the family Dorididae (Mollusca, Nudibranchia) in the Mediterranean and North-East Atlantic

Fig. 4. A. Doris verrucosa Linnaeus, 1758 (ZSM20210044) from Thau, SE France. B–E. Doris berghi (Vayssière, 1901) comb. rest. B. Specimen from Sant Feliu de Guíxols, NE Spain (ZSMMol20210024). C. Specimen from Begur, NE Spain (MCZMal395161).D. Specimen from Gran Canaria (ZSM20240262). E. Specimen from Galicia, NW Spain (ZSM20240261). F–H. Doris ocelligera (Bergh, 1881). F. Specimen from l'Escala, NE Spain (MCZ395160). G. Specimen from Sant Feliu de Guíxols, NE Spain (ZSM20240260). H. Specimen from Sant Feliu de Guíxols, NE Spain (ZSM20240259).

Fig. 2 in Molecular and morpho-anatomical assessment of the family Dorididae (Mollusca, Nudibranchia) in the Mediterranean and North-East Atlantic

Fig. 2. Bayesian phylogenetic tree of Dorididae Rafinesque, 1815 based on the concatenated alignment of COI, 16S, and H3 markers. Posterior probabilities and bootstrap support values are shown above and below branches, respectively. The outgroup used to root the tree was the genus Aphelodoris Bergh, 1879. Green dots indicate nodes with maximum branch support in both analyses. The scale bar indicates substitutions per site. Names of the sequences downloaded from GenBank have not been modified, yet taxa that may belong to a different identity are specified between quotation marks. Specimens sequenced in this study are highlighted in bold.