We herein investigated the influence of temperature on the embryonic development (from fertilisation to hatching) of Mugil liza larvae. For this purpose, oocytes (>600 μm) and sperm were obtained from breeding stock at the laboratory of marine fish culture (LAPMAR). After fertilisation, 1200 eggs were distributed in 12 cylindrical experimental units of 400 mL under four different temperatures 18, 22, 26 and 30 ºC, all in triplicate. Every 15 min until hatching, about 10 eggs were randomly sampled in each treatment. The eggs were visualized and photographed, and the classification of embryonic stages was performed. Temperature influenced the main events of the embryonic development of M. liza. More accelerated development was observed according to the increase in temperature until the gastrula phase. At temperatures of 22 and 26 °C, embryonic development occurred from fertilisation to hatching of the larvae. In the 18 °C treatment, it was verified that most of the embryos ceased development during the final phase of cleavage and the beginning of blastula formation, while in the 30 °C treatment patterns of embryo malformation were also verified, with erratic divisions of the blastomeres, resulting in irregular cells. Unlike what was observed at a temperature of 18 °C, none of the embryos incubated at 30 °C reached the blastopore closure phase, stopping in the gastrula. The larvae hatched in the treatments at 22 and 26 °C were viable and exhibited intense swimming, with a large amount of reserve material (yolk) and an evident drop of oil.

This study documents the presence of crypsis in Mugil curema juveniles under laboratory culture. Initially, the juveniles were located in one brown tank (BT1), later almost half of the individuals were placed in a white tank (WT) where they showed a pigmentation change to white. After being moved to another brown tank (BT2), the juveniles changed to their brown original colour, but kept a few small white spots on the dorsal axis of the body. The ventral head melanophore pattern also changed in the white specimens. Temperature (°C), oxygen (mg l−1) and Illuminance light (Lux m−2), total length (mm) and total weight (g) were determined by tank. Chromaticity was measured in L*(relative luminance) a*(measurement relating to the redness or greenness of the light) b*(measurement relating to the yellowness or blueness of the light) coordinates where all three values are required to completely describe an object’s colour. One-way ANOVA showed no differences for temperature, oxygen and illuminance light among tanks. Length and weight were similar for BT1 and WT but both were different from BT2. The white juveniles depicted similar L* as the WT background as well as the dorsal area of the brown pigmentation and converted juveniles to the brown tanks BT1 and BT2, respectively. Therefore, the fish's body relative luminance matches the background. To our knowledge this behaviour has not been reported before for any fish mullet either cultured or living in the wild.

Mugil liza is distributed along the western Atlantic coast. It is a commercially exploited species in Argentina, supporting a small-scale fishery conducted by an artisanal fleet. Age determination of fishes constitutes an important key issue for fishery management. The age, growth and recruitment of M. liza juveniles in Mar Chiquita coastal lagoon and Las Brusquitas creek (Buenos Aires, Argentina), were estimated by means of the analysis of the sagittal otoliths of fish collected during January to December of 2014. Ages were estimated by counting and measuring daily growth increments in otoliths under a light microscope. A total of 735 specimens ranging from 19 to 71.5 mm SL and from 67 to 212 days age was analysed. Lengths at previous ages were determined by back-calculation, a linear growth model was fitted to the back-calculated data: SL = 0.2468 + 2.0516; R2 = 0.9945. Two peaks of recruiters were observed from February to March, and from October to November in 2014. Mean ages in days of Querimana and juveniles at the recruitment time were 84.07 ± 14.43 days and 87.56 ± 19.51 days, respectively. The hatching dates of specimens showed two spawning seasons. One was from December 2013 to January 2014, and the second one from July to August 2014. The assessment carried on this work generated age determination values that support previous findings, contributing to make a more accurate description of the life-history model currently used. In addition, valuable information has been generated to give better advice for improving the management of the fishery resource.

The long-finned mullet, Osteomugil perusii was caught along the eastern and western coasts of India. The finding of 12 specimens extends the current knowledge about the distribution of this mullet in the western Indo-Pacific to the Indian coast.

We applied a combined molecular and morphological approach to resolve the taxonomic status of Saccocoelium spp. parasitizing sympatric mullets (Mugilidae) in the Mediterranean. Eight morphotypes of Saccocoelium were distinguished by means of multivariate statistical analyses: 2 of Saccocoelium obesum ex Liza spp.; 4 of S. tensum ex Liza spp.; and 2 (S. cephali and Saccocoelium sp.) ex Mugil cephalus. Sequences of the 28S and ITS2 rRNA gene regions were obtained for a total of 21 isolates of these morphotypes. Combining sequence data analysis with a detailed morphological and multivariate morphometric study of the specimens allowed the demonstration of cryptic diversity thus rejecting the hypothesis of a single species of Saccocoelium infecting sympatric mullets in the Mediterranean. Comparative sequence analysis revealed 4 unique genotypes, thus corroborating the distinct species status of Saccocoelium obesum, S. tensum and S. cephali and a new cryptic species ex Liza aurata and L. saliens recognized by its consistent morphological differentiation and genetic divergence. However, in spite of their sharp morphological difference the 2 morphotypes from M. cephalus showed no molecular differentiation and 4 morphotypes of S. tensum were genetically identical. This wide intraspecific morphological variation within S. tensum and S. cephali suggests that delimiting species of Saccocoelium using solely morphological criteria will be misleading.