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Map of the Czech Republic showing the main rivers and sites where samples of Carassius were collected. The occurrence of five species of Carassius was confirmed using molecular analysis: Ca – Carassius auratus (orange circle), Cg – C. gibelio (green circle), Clan – C. langsdorfii (blue circle), Cc – C. carassius (brownish circle), C “M” – Carassius sp. (purple circle). For details of occurrence see Table 1. 

Map of the Czech Republic showing the main rivers and sites where samples of Carassius were collected. The occurrence of five species of Carassius was confirmed using molecular analysis: Ca – Carassius auratus (orange circle), Cg – C. gibelio (green circle), Clan – C. langsdorfii (blue circle), Cc – C. carassius (brownish circle), C “M” – Carassius sp. (purple circle). For details of occurrence see Table 1. 

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Molecular markers have recently been used to change the taxonomical status of many species of fish. Fishes of the genus Carassius (Nilsson, 1832) were subjected to phylogenetic analyses when it was recognized that differences in morphology could not be used for identifying species. Four species of Carassius are known to occur in waters of the Czec...

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... sixty five samples of Carassius fishes originating from the Czech Republic ( Fig. 1) were included in this study. Sixty three samples came from our previous studies, one is original to this study and one was obtained from GenBank database. As an outgroup we used a sequence of Common carp (Cyprinus carpio Linnaeus, 1758) obtained from GenBank acc. No. HM008692. Detailed information on the material sampled is listed in ...

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... On the other hand, the diversity loss of diploids may be due to the strong selection in the extreme environmental conditions of the QTP. Previous studies have observed high genetic diversity in invasive C. auratus from Croatia (Jakovlic & Gui, 2011), Czechia (Bohem, 2013) ...
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... A wide spectrum of ecological tolerance and extraordinary resistance to adverse environmental conditions enabled C. gibelio to successively and progressively spread to various water bodies (Kottelat & Freyhof, 2007;Grabowska, Kotusz, & Witkowski, 2010;Boroń et al., 2011). Moreover, this species frequently hybridizes with other cyprinids, especially with the crucian carp, Carassius carassius (Linnaeus, 1758), which is native in Europe as well as with C. auratus and common carp, Cyprinus carpio (Linnaeus, 1758) (Sayer et al., 2011Mezhzerin, Kokodii, Kulish, Verlatii, & Fedorenko, 2012;Wouters, Janson, Lusková, & Olsén, 2012;Rylková & Kalous, 2013). These hybrids show high morphological similarity and reveal better adaptations to unfavourable conditions than their parental species. ...
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Background Invasive gibel carp, Carassius gibelio (Bloch, 1782) has become well-established in the Hungarian waters and now are spreading in the European waters. On major concern now is the potential hybridization between gibel carp and the other invasive species in the Carassius auratus complex (CAC), which may further accelerate the spread of the whole invasive species complex. The identification of gibel carp and their hybrids is difficult because of its morphological similarity to the other species in CAC. Here we carry out a genomic assessment to understand the history of gibel carp invasion and its phylogenetic relationship with the other species in CAC. Three loci of the mitochondrial genome (D-loop, CoI, Cytb) were used to determine the phylogenetic origin of individuals and relarionship among six gibel carp populations and the other species in the CAC. Methodolgy A total of 132 gibel carp samples from six locations in Southern Transdanubia (Hungary) were collected after phenotypic identification to measure the genetic diversity within and among gibel carp populations of Southern Transdanubia (Hungary). The genetic background was examined by the sequences of the mitochondrial genome: D-loop, Cytochrome c oxidase I (CoI) and Cytochrome b (Cytb). Mitochondrial genetic markers are excellent tools for phylogenetic studies because they are maternally inherited. Successfully identified haplotypes were aligned and with reference sequences in nucleotide databases ( i.e., NCBI-BLAST: National Centre for Biotechnology Information and BOLD: Barcode of Life Data System). The phylogenetic relationships among gibel carp populations were then analyzed together with the reference sequences to understand the relationship and the level of hybridization with the species in CAC. Results Among the 132 aligned D-loop sequences 22 haplotypes were identified. Further examination of representative individuals of the 22 haplotypes, six Cytb and four CoI sequences were detected. The largest number of haplotypes of all three loci were found in Lake Balaton, the largest shallow lake in Central Europe. Based on the NCBI-BLAST alignment of the D-loop, haplotypes of Carassius auratus auratus and Carassius a. buergeri in CAC were identified in the C. gibelio samples. Further analysis of haplotypes with the other two mitochondrial markers confirmed the occurrence of intragenus hybridization of C. gibelio in the Hungarian waters. Conclusion By using three mitochondrial markers (D-loop, Cytb, CoI), we genomically characterized a gibel carp-complex in Hungarian waters and assessed the C. gibelio phylogenetic status between them. Hybrid origin of locally invasive Carassius taxon was detected in Hungary. It points out that invasive species are not only present in Hungary but reproduce with each other in the waters, further accelerating their spread.
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The present study was carried out to demonstrate the baseline values for some serum biochemical parameters for 64 adult freshwater fish including seven species belong to family Cyprinidae, have been collected in Dukan Lake, Kurdistan region-Iraq. Fishes were weighed, measured, and collect blood for blood chemistry. Serum biochemical analyses were determined using (Cobas C 311) full automatic chemical analyzer. The result of comparative study of serum biochemical parameters of all Cyprinidae species showed that serum glucose was (459.10±106.99 mg/dl) and direct bilirubin was (0.056±0.021mg/dl) in Barbus grypus, serum total protein (3.511± 0.0484gm/dl) and HDL (133.11±0.4231mg/dl) in Cyprinus carpio, serum cholesterol (338.33±43.923 mg/dl) and LDL (86.11±11.871mg/dl) in Carassius carassius, serum triglyceride (420.0±28.8mg/dl) and ALK (113.93±20.65U/L) in Chondrostoma regium, serum AST and serum ALT in Capoeta trutta, were significantly higher when compared to other species. In a conclusion there is variation in biochemical values among species of same family.