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Figure 3 in Merluccius polli and M. senegalensis (Merlucciidae) as first records from the Canary Islands (north-eastern Atlantic), with morphology data

Figure 3. – Radiographs of M. senegalensis from the Canary Islands (TFMCBM-VP/01449, adult, 804 mm TL). Insert: Detail of five cervical vertebrae.

Figure 2 in Merluccius polli and M. senegalensis (Merlucciidae) as first records from the Canary Islands (north-eastern Atlantic), with morphology data

Figure 2. – Radiographs of M. polli from the Canary Islands (TFMCBM-VP/01952, maturing female, 624 mm TL). Insert: Detail of five cervical vertebrae.

Figure 1 in Merluccius polli and M. senegalensis (Merlucciidae) as first records from the Canary Islands (north-eastern Atlantic), with morphology data

Figure 1. – The Canary Islands. Collection locations for the first records. Ì: Merluccius polli; ■: Merluccius senegalensis.

Figure 1. – Merluccius merluccius. A in Figure 1. - A in Junior synonymy of Mulloides armatus and intraspecific comparisons of the yellowstripe goatfish Mulloidichthys flavolineatus (Mullidae) using a comprehensive alpha-taxonomy approach

Figure 1. – Merluccius merluccius. A: Normal pigmentation; B: Yellowalbino phenotype 616 mm TL; C: Dark spots on dorsal part; D: Black marks on the dorsal fin margin.

Figure 5 in Growth estimation of Merluccius merluccius off the northern coast of Tunisia

Figure 5. - Von Bertalanffy model for hake combined sex off the northern coast in Tunisia fitted to the data, compared to those observed in the Bay of Biscay and in the Gulf of Lion.

Fig. 3 in Age and growth of the Argentine hake Merluccius hubbsi Marini, 1933 in the Brazilian South-Southeast Region during 1996-2001

Fig. 3. Merluccius hubbsi: scheme of a sliced otolith showing core, demersal I (De I), demersal II (De II), 1 to 3 rings and opaque edge (OP).

Fig. 5 in Age and growth of the Argentine hake Merluccius hubbsi Marini, 1933 in the Brazilian South-Southeast Region during 1996-2001

Fig. 5. Merluccius hubbsi: plot for total length (mm) and ring radius (mm) showing the constancy of otolith readings.

Fig. 4 in Age and growth of the Argentine hake Merluccius hubbsi Marini, 1933 in the Brazilian South-Southeast Region during 1996-2001

Fig. 4. Merluccius hubbsi: seasonal length class distribution obtained from surveys and commercial landings during the period 1996-2001.

Fig. 7 in Age and growth of the Argentine hake Merluccius hubbsi Marini, 1933 in the Brazilian South-Southeast Region during 1996-2001

Fig. 7. Merluccius hubbsi: seasonal average marginal incre- Fig. 9. Merluccius hubbsi: seasonal frequency of opaque (OP) ment (MI, mm) and confidence limits obtained for all fish with and translucent (TR) edges for fish otoliths with three rings. three rings.

Fig. 6 in Age and growth of the Argentine hake Merluccius hubbsi Marini, 1933 in the Brazilian South-Southeast Region during 1996-2001

Fig. 6. Merluccius hubbsi: seasonal average marginal increment (MI, mm) and confidence limits obtained for all fish with two rings.

Fig. 1 in Identification of the stages of ovarian maturation of the Argentine hake Merluccius hubbsi Marini, 1933 (Teleostei: Merlucciidae): advantages and disadvantages of the use of the macroscopic and microscopic scales

Fig. 1. Merluccius hubbsi: area of collection of samples obtained during surveys and the operations of the commercial fishing fleet of Santos and Guarujá in the period from 1996 to 2002.

Fig. 10 in Identification of the stages of ovarian maturation of the Argentine hake Merluccius hubbsi Marini, 1933 (Teleostei: Merlucciidae): advantages and disadvantages of the use of the macroscopic and microscopic scales

Fig. 10. Merluccius hubbsi: relative frequency of females by stage of gonadal maturation identified microscopically by class of total lenght (n = 326).

Fig. 2 in Identification of the stages of ovarian maturation of the Argentine hake Merluccius hubbsi Marini, 1933 (Teleostei: Merlucciidae): advantages and disadvantages of the use of the macroscopic and microscopic scales

Fig. 2. Merluccius hubbsi: relative frequency of females by stage of gonadal maturation identified macroscopically by class of total lenght (n = 326).

Figure 3 in Growth estimation of Merluccius merluccius off the northern coast of Tunisia

Figure 3. - Length distribution of sample by sex.

Figure 4 in Growth estimation of Merluccius merluccius off the northern coast of Tunisia

Figure 4. - Ponderal and somatic growth for hake for each sex off the northern coast in Tunisia.

Figure 2 in Growth estimation of Merluccius merluccius off the northern coast of Tunisia

Figure 2. - Age determination of Merluccius merluccius from otolith section.

Figure 1 in Growth estimation of Merluccius merluccius off the northern coast of Tunisia

Figure 1. - Location (■) of main sampling areas.

Fig. 1 in Age and growth of the Argentine hake Merluccius hubbsi Marini, 1933 in the Brazilian South-Southeast Region during 1996-2001

Fig. 1. Study area showing the location of Merluccius hubbsi samples collected during 1996-2001.

Fig. 6 in Identification of the stages of ovarian maturation of the Argentine hake Merluccius hubbsi Marini, 1933 (Teleostei: Merlucciidae): advantages and disadvantages of the use of the macroscopic and microscopic scales

Fig. 6. Merluccius hubbsi: oocyte with complete vitellogenesis (1.5mm length field).

Fig. 4 in Identification of the stages of ovarian maturation of the Argentine hake Merluccius hubbsi Marini, 1933 (Teleostei: Merlucciidae): advantages and disadvantages of the use of the macroscopic and microscopic scales

Fig. 4. Merluccius hubbsi: oocyte in cortical alveolar stage (arrow) (1.5mm length field).