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-Distribution of round goby Neogobius melanostomus in the southern Black Sea and the Sea of Marmara (black shadow area). [Distribution du gobie rond N. melanostomus dans le sud de la mer Noire et en mer de Marmara (figuré en noir).]

-Distribution of round goby Neogobius melanostomus in the southern Black Sea and the Sea of Marmara (black shadow area). [Distribution du gobie rond N. melanostomus dans le sud de la mer Noire et en mer de Marmara (figuré en noir).]

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Age and growth of the round goby Neogobius melanostomus (Pallas, 1814) were studied by examination of growth increments within otoliths of 868 specimens caught between October 2002 and March 2005 from offshore of Samsun city in the southern Black Sea. The values of intercept and slope in length-weight relationships were calculated as 0.0110 and 3.0...

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... the Black Sea and Caspian Sea, the Sea of Azov and Marmara and their tributaries are known as the native biogeographic range of this species. Though the map for European distribution of the round goby (Miller, 1986) indicates that this species does not exist along the southern shoreline of the Black Sea, it has a wide distribution in the region (Fig. 1). Kuru (1980) and Mater et al. (1989) reported its range along the whole Turkish coastline in the Black Sea and the Sea of Marmara at depths from 2-30 m. Geldiay and Balik (1996) represented a distribution map for this species including the lower to middle reaches of tributaries, freshwater lakes and lagoons in the Black Sea and Marmara ...

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... This commission is mostly concerned with turbot Scophthalmus maeoticus (Pallas, 1814), dogfish Squalus acanthias L., 1758, anchovy Engraulis encrasicolus (L., 1758), sprat Sprattus sprattus (L., 1758), horse mackerel Trachurus mediterraneus (Steindachner, 1868), red mullet (Mullus barbatus L., 1758) and whiting Merlangius merlangus (L., 1758) fisheries. In contrast, there has been little or no interest shown in the population status of gobies (Gobiidae) despite their local importance as a commercial fisheries species in the Black Sea, especially in Turkey and Bulgaria (Gümüş & Kurt 2009, Zarev et al. 2013, FAO 2020. In the recreational zone of the City of Odessa, e.g., anglers catch up to a tonne of gobies per day, even during the spawning period (Khutornoy 1998). ...
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... The sex composition is expected close 1:1 due to various reasons such as differences of natural and fishing mortality on sexes, spawning migration and, size and habitat differences between sexes (Nikolskii, 1980). Previous studies on population of N. melanostomus reported that male individuals were more abundant than female ones (Skora and Stolarski, 1996;Gözler et al., 2003;Gümüş and Kurt, 2009) as parallel to this study, that was found 1:1.77. ...
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... Translucent zone is characterized by less calcium carbonate rich and contain more concentrated proteins than opaque zone . The slower growth can be due to seasonal fluctuations in the water level, the photoperiod, the quality of the available food, a reduction in feeding activity, gonad maturation or spawning activity/behaviour (Yosef and Casselman, 1995;Jepsen et al., 1999;Gümüş and Kurt, 2009). In southeastern China, Liu et al. (2015) indicated an increase in the gonadosomatic index between January and April for a population of H. macrolepidota with a peak in June and a decrease in July. ...
... These age groups experienced a high variability in lengths, indicating a strong variability in growth. This observation could be explained by the fact that numerous populations of tropical fishes are able to reproduce all year (Gómez-Márquez, 1998;Bwanika et al., 2007;Gümüş and Kurt, 2009). A long reproduction period over the year can generate different growth rates due to seasonal changes of environmental conditions and due to a mixing of cohorts (Jiménez-Badillo, 2006). ...
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... Although males may not be capable of rapidly switching between tactics, it is currently not known if the two tactics represent sequential or fixed strategies. Second, numerous previous studies of N. melanostomus have revealed considerable variation in body size within age classes (Duan et al., 2016;French & Black, 2009;Gümüs & Kurt, 2009;Huo et al., 2014;MacInnis & Corkum, 2000;Sokołowska & Fey, 2011). Unfortunately, none of these previous studies accounted for the presence of male alternative reproductive tactics. ...
... For example, accounting for this variation is important when attempting to use otolith morphology to infer specific details about individual fish, such as their body size. Furthermore, it has been common practice for studies to estimate N. melanostomus size at age by using back-calculation techniques (Duan et al., 2016;French & Black, 2009;Gümüs & Kurt, 2009;Huo et al., 2014;MacInnis & Corkum, 2000;Sokołowska & Fey, 2011), the present study suggests that the efficiency of these techniques could be improved by considering guarder males separately from sneaker males. While alternative tactics are widespread among fishes and anthropogenic effects on aquatic ecosystems are a growing concern, their effects on otolith morphology have only rarely been studied. ...
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Round goby Neogobius melanostomus sagittal (saccular) otolith morphology was compared between males of the two alternative reproductive tactics (termed guarder and sneaker males) and between males captured from sites of high and low contamination. Otolith size increased with fish size and also displayed an ontogenetic shift in shape, becoming relatively taller as otoliths grew in size. Despite a considerable overlap in age between males adopting the two reproductive tactics, size‐at‐age measurements revealed that guarder males are significantly larger than sneakers at any given age and that they invest more into somatic growth than sneaker males. Controlling for body size, sneaker males possessed heavier sagittal otoliths than guarder males. Subtle otolith shape differences were also found between the two male tactics and between sites of high and low contaminant exposure. Sneaker males had relatively shorter otoliths with more pronounced notching than guarder males. Fish captured at sites of high contamination had otoliths showing slower growth rates in relation to body size and their shapes had more pronounced caudal points and ventral protrusions when compared with fish captured at sites of low contamination. The results are discussed in relation to life‐history tradeoffs between the male tactics in terms of reproductive and somatic investment as well as the putative metabolic costs of exposure to contaminants. Overall, this study reveals that male alternative reproductive tactics and environmental contaminants can have small, yet measurable, effects on otolith morphology and these factors should be accounted for in future research when possible. This article is protected by copyright. All rights reserved.
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The round goby ( Neogobius melanostomus Pallas, 1811) is one of the most invasive fish species in the world, including Poland. 300 fish of this species were collected in the waters of Szczecin lagoon between 2010 and 2014 and examination of the size, sex and age structures of the population and of the condition of the fish was performed. Total length and standard length of all the collected fish amounted to 149.2 mm (±42.21) and 128.1 mm (±38.65), respectively. The age structure of the fish consisted of nine generations, with clear prevalence of the fish aged 3+ and 4+. Mean values of condition factors for the whole fish sample amounted to 0.20 (±0.02). However, no statistically significant differences in particular years were observed (ANOVA, p > 0.05), but the condition of the fish between 2010 and 2011 was slightly higher than between 2013 and 2014. The obtained results indicate that the Szczecin Lagoon environment provides this species with favourable living conditions and it can be stipulated that the quantity of individuals of this fish species will increase.