The method for determination of the molar absorption coefficient (MAC) of C 60 and C 70 fullerenes has been developed. The values of MAC obtained by the graphic method are refined there after by the mathematical method of successive approximation.The levels of analytical wavelengths, the ranges for concentrations of fullerene mixtures, solutions optimum for the qualitative analysis have been established.The spectra of C 60 solutions and solutions of its mixtures with C 70 containing C 60 0.5 10 -4 mol/l show the bathochromic shift of the absorption band with the maximum at =335 nm.
Aim. Although more than 80 fi sh species and some invertebrate aquatic organisms are known to be susceptible to in-
fectious pancreatic necrosis virus (IPNV) and aquatic birnaviruses, relatively little is known about its ability to infect
brown trout (Salmo trutta), zebrafi sh (Danio rerio), and a mollusk, swan mussel (Anodonta cygnea). Therefore, the aim
was to study in more detail the effects of IPNV on the said organisms. The information on the virulence of birnaviruses
for aquatic organisms is important for better understanding of their transmission and for the identifi cation of suscep-
tible or transient (symptomless) hosts. Methods. Cell culture method, using RTG-2 cells, was used for in vitro culti-
vation of IPNV as well as virus titer assessment. The supernatants from infected RTG-2 cells were used for artifi cial
inoculation to obtain experimental infection of the fi sh and mollusk. Fish and mollusk behaviour and mortality were
monitored daily. The infectious titer of the virus in experimental animals was assessed by cell culture assay and reverse
transcription PCR (RT-PCR). Results. This paper presents the results of IPNV experimental infection of brown trout
(Salmo trutta), zebrafi sh (Danio rerio), and an aquatic invertebrate mollusk - swan mussel (Anodonta cygnea). The
mortality of brown trout and zebrafi sh was 76.6 and 40 % respectively. Swan mussel was apparently resistant to the
virus, but it apparently accumulated and maintained substantial levels (up to 10 -10 ID 50 /ml -1 ) of the virus for the dura-
tion of the experiment (35 days). The highest infectious titer was found in brown trout (10 6 ID 50 /ml -1 ). In zebrafi sh and
swan mussels, it was up to 10 4.5 ID 50 /ml -1 and 10 2 ID 50 /ml -1 respectively. Conclusions. At the end of the experiments
the IPNV titers were higher than the initial viral doses in brown trout and zebrafi sh, indicating virus reproduction. In
diseasesd fi sh the blackening, whirling and anorexia were observed. It was shown that swan mussel accumulates and
maintains virus for at least 35 days under experimental conditions and that it may act as symptomless vector of IPNV
The paper contains the results of the studies into the ichthyopathological situation of the invasion and infectious diseases of salmonids carried out by the Ichthyopathology Laboratory of the Institute of Fisheries of Ukraine from 2013 to 2016. The investigated salmonid species included: the rainbow trout Oncorhynchus mykiss, the brown trout Salmo trutta morpha fario, the brook trout Salvelinus fontinalis, and the European grayling Thymallus thymallus. The fish were sampled from aquatculture farms as well as natural water bodies and their diseases included invasive (parasitic) and infectious (viral and bacterial). The most frequently encountered invasions in the brown and brook trout were ciliates: Chilodonella piscicola and Apiosoma conicum, Trichodina (in particular T. truttae and T. nigra), Ichtyophthirius multifiliis; monogenea Gyrodactylus birmani, and diplostoma Diplostomum spathaceum. Aeromonas and Flavobacterium bacteria were isolated from fry and young-of-the-year rainbow trout and brook trout. Y. ruckeri positive samples were isolated from the fish with the signs of yersiniosis. As for viral diseases, IPNV isolates (the first time in Ukraine) of the rainbow trout were first isolated in fish farms in the western regions of Ukraine. A phylogenetic analysis of these IPNV isolates was performed, which showed that they belonged to Sp strain and the European genotype.
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