Abstract:For the first time, an otolith shape analysis was used to investigate the stocks of saddled bream (Oblada melanura, Linnaeus, 1758) in three fishing zones along the Tunisian coast (Bizerte, Kélibia and Sayada). Otolith shape analysis was used on 30 otoliths for each site, sampled during the spawning period. Using elliptic Fourier descriptors (EFD) the quantization of the shape otolith was investigated by SHAPE and multivariate statistical procedures. Considering the environmental and the genotypic aspects, the… Show more
“…Other factors can also be considered, such as the life-history traits associated with the otolith shape (Mérigot et al, 2007) and biological and behavioural characteristics, such as the type of swimming activity (Lord et al, 2012). This effect of environmental factors on the shape of otolith in Tunisian waters has also been previously recognized in P. erythrinus (Mejri et al, 2018), D. annularis (Trojette et al, 2015) and O. melanura (Barhoumi et al, 2018). Previous studies on the size and morphology of the otoliths have shown that the intra-population variation may reside in inter-and intra-individual and even inter-population variations (Mejri et al, 2018(Mejri et al, , 2020.…”
For the first time, saccular otolith shape and size were analysed in 254 samples of the bogue Boops boops collected from the marine stations of Bizerte and Kelibia situated in north-east Tunisia. The objectives were (1) to examine the inter- and intra-population variation in the otolith shape and size, including length (Lo), width (Wo) and area (Ao) measurements, and (2) to assess the relationship between otolith mass asymmetry (OMA) and total fish length (TL). In addition, the impact of pollution present in these two stations on the shape and size of the otolith in relation to the TL was discussed. Analyses of the otolith shape and biometric data showed a statistically significant asymmetry in the otolith shape (P < 0.0001) between the right and left sides within the population of Bizerte, as well as between the otoliths from the same right-right and left-left sides between the populations of Bizerte and Kelibia. Similarly, a significant Wo asymmetry (P < 0.05) was recorded within the population of Kelibia. Conversely, a significant symmetry was detected in Lo and Ao (P > 0.05) between the right and left sides within the populations of Bizerte and Kelibia. Moreover, the level of asymmetry of Ao was higher than that of Lo and Wo in both populations. Nevertheless, Student's t-test showed no statistically significant differences (P > 0.05) for Lo, Wo and Ao in relation to the means of TL between the three groups of the populations of Bizerte and Kelibia, although significant differences (P < 0.05) were found by using box plots. Furthermore, no statistically significant relationship (P > 0.05) was detected between OMA and TL within and between the populations of Bizerte and Kelibia. The possible cause of fluctuating asymmetry (FA) in the otolith shape and size both within and/or between populations of the two stations has been discussed in relation to the instability of development induced by environmental stress associated with the variation in water temperature, salinity, depth, feeding conditions and pollutants present in these stations.
“…Other factors can also be considered, such as the life-history traits associated with the otolith shape (Mérigot et al, 2007) and biological and behavioural characteristics, such as the type of swimming activity (Lord et al, 2012). This effect of environmental factors on the shape of otolith in Tunisian waters has also been previously recognized in P. erythrinus (Mejri et al, 2018), D. annularis (Trojette et al, 2015) and O. melanura (Barhoumi et al, 2018). Previous studies on the size and morphology of the otoliths have shown that the intra-population variation may reside in inter-and intra-individual and even inter-population variations (Mejri et al, 2018(Mejri et al, , 2020.…”
For the first time, saccular otolith shape and size were analysed in 254 samples of the bogue Boops boops collected from the marine stations of Bizerte and Kelibia situated in north-east Tunisia. The objectives were (1) to examine the inter- and intra-population variation in the otolith shape and size, including length (Lo), width (Wo) and area (Ao) measurements, and (2) to assess the relationship between otolith mass asymmetry (OMA) and total fish length (TL). In addition, the impact of pollution present in these two stations on the shape and size of the otolith in relation to the TL was discussed. Analyses of the otolith shape and biometric data showed a statistically significant asymmetry in the otolith shape (P < 0.0001) between the right and left sides within the population of Bizerte, as well as between the otoliths from the same right-right and left-left sides between the populations of Bizerte and Kelibia. Similarly, a significant Wo asymmetry (P < 0.05) was recorded within the population of Kelibia. Conversely, a significant symmetry was detected in Lo and Ao (P > 0.05) between the right and left sides within the populations of Bizerte and Kelibia. Moreover, the level of asymmetry of Ao was higher than that of Lo and Wo in both populations. Nevertheless, Student's t-test showed no statistically significant differences (P > 0.05) for Lo, Wo and Ao in relation to the means of TL between the three groups of the populations of Bizerte and Kelibia, although significant differences (P < 0.05) were found by using box plots. Furthermore, no statistically significant relationship (P > 0.05) was detected between OMA and TL within and between the populations of Bizerte and Kelibia. The possible cause of fluctuating asymmetry (FA) in the otolith shape and size both within and/or between populations of the two stations has been discussed in relation to the instability of development induced by environmental stress associated with the variation in water temperature, salinity, depth, feeding conditions and pollutants present in these stations.
“…Similar results have previously been reported in a range of sparids, including D . annularis (Trojette et al ., 2015), Oblada melanura (Barhoumi et al ., 2018), Pagellus erythrinus (Mejri et al ., 2020) and B . boops (Ider et al ., 2017; Ben Labidi et al ., 2020 a ).…”
Saccular otolith shape and size were analysed for the first time in 120 adult individuals of D. vulgaris collected from two localities, the Bizerte and Ghar El Melh lagoons (north-east Tunisia). The objectives were (1) to examine the specific inter- and intra-individual variation in the otolith shape using elliptical Fourier analysis combined with measures of length (LO), width (WO) and area (AO); (2) to use the otolith shape and size analysis as a phenotypic-based approach to discriminate the stock structure of this species in the two localities to investigate whether they represent two separate stocks to inform on appropriate management procedures; and (3) to test for biases resulting from potential fluctuating asymmetry (FA) in the otolith size on the discrimination of stock structure. Discriminant function analysis performed with the normalized elliptical Fourier descriptors coefficients showed statistically significant differences (P < 0.0001) in the otolith contour shape, i.e. asymmetry, either between the left and right sides or between the same sides (left-left and right-right) within and among individuals of the two localities. Besides, a significant asymmetry (P < 0.05) was found in WO and AO among individuals within the Bizerte locality and in WO only within the Ghar El Melh locality. Moreover, significant FA was observed in the otolith size parameters among individuals of the two localities. This significant asymmetry detected in the otolith shape, as well as in the size due to FA, within and among individuals of D. vulgaris collected from the Bizerte and Ghar El Melh localities confirms that the two stocks could be discriminated from each other and should be managed separately. This asymmetry is discussed in light of the instability of development caused either by environmental stress associated with the variation in water temperature, salinity, depth, feeding conditions and pollutants that have led to abnormalities in the development of individuals or by the presence of poor living conditions for the larvae resulting from unfavourable environments.
“…In recent years, cage-reared L. maculatus have been imported from China into Korea and Japan for human consumption (An et al 2014). Germplasm degradation and a reduction in disease resistance of cultured L. maculatus restricts its sustainable development (Wang et al 2017), and calls for an assessment of the population structure of this fish (Barhoumi et al 2017). The results of such study can be used to prevent overfishing and ultimately declines in the numbers of L. maculatus.…”
The whole mitochondrial genome of Lateolabrax maculatus (Cuvier, 1828) was used to investigate the reasons for the observed patterns of genetic differentiation among 12 populations in northern and southern China. The haplotype diversity and nucleotide diversity of L. maculatus were 0.998 and 0.00169, respectively. Pairwise FST values between populations ranged from 0.001 to 0.429, correlating positively with geographic distance. Genetic structure analysis and haplotype network analysis indicated that these populations were split into two groups, in agreement with geographic segregation and environment. Tajima’s D values, Fu’s Fs tests and Bayesian skyline plot (BSP) indicated that a demographic expansion event may have occurred in the history of L. maculatus. Through selection pressure analysis, we found evidence of significant negative selection at the ATP6, ND3, Cytb, COX3, COX2 and COX1 genes. In our hypotheses, this study implied that demographic events and selection of local environmental conditions, including temperature, are responsible for population divergence. These findings are a step forward toward the understanding of the genetic basis of differentiation and adaptation, as well as conservation of L. maculatus.
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