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1

Jakšić, Goran, Margita Jadan, and Marina Piria. "The Review of Ecological and Genetic Research of Ponto-Caspian Gobies (Pisces, Gobiidae) in Europe." Croatian Journal of Fisheries 74, no. 3 (2016): 110–23. http://dx.doi.org/10.1515/cjf-2016-0015.

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Abstract Invasive Ponto-Caspian gobies (monkey goby Neogobius fluviatilis, round goby Neogobius melanostomus and bighead goby Ponticola kessleri) have recently caused dramatic changes in fish assemblage structure throughout European river systems. This review provides summary of recent research on their dietary habits, age and growth, phylogenetic lineages and gene diversity. The principal food of all three species is invertebrates, and more rarely fish, which depends on the type of habitat, part of the year, as well as the morphological characteristics of species. According to the von Bertalanffy growth model, size at age is specific for the region, but due to its disadvantages it is necessary to test other growth models. Phylogenetic analysis of monkey goby and round goby indicates separation between the Black Sea and the Caspian Sea haplotypes. The greatest genetic diversity is found among populations of the Black Sea, and the lowest among European invaders. The lack of molecular research on bighead goby requires further studies.
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2

Sasi, Huseyin, and Selcuk Berber. "Some Biological Characteristics of Monkey Goby in Anatolia." Asian Journal of Animal and Veterinary Advances 5, no. 3 (2010): 229–33. http://dx.doi.org/10.3923/ajava.2010.229.233.

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3

Kvach, Yuriy, Markéta Ondračková, Teodora Trichkova, Oleksandra Drobiniak, Veniamin Zamorov, and Pavel Jurajda. "Parasitization of monkey goby, Neogobius fluviatilis (Pallas, 1814) (Actinopterygii: Gobiidae), at localities with different salinity levels." Oceanological and Hydrobiological Studies 47, no. 4 (2018): 376–83. http://dx.doi.org/10.1515/ohs-2018-0035.

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Abstract Parasitism of monkey goby, Neogobius fliviatilis, was assessed at three brackish water localities with different salinity levels (Gulf of Odessa, Khadzibey Estuary, Lake Kytay) and one freshwater site along the Lower Danube River (Vidin). A total of 25 parasite taxa were identified, with minimum parasite richness recorded in the Khadzhibey Estuary (three species) and the maximum along the Lower Danube (11 species). Parasite richness in the mesohaline Gulf of Odessa and oligohaline Lake Kytay was lower, but still relatively high compared to the Khadzibey Estuary. Our study indicates that freshwater populations of monkey goby host richer and more abundant parasite communities than those inhabiting brackish waters with (more or less) stable salinity. Unstable abiotic conditions that probably affected the parasite’s intermediate hosts contributed to the reduction in parasite species in the estuarine zone of the Danube.
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4

Tarján, Zoltán, Judit Pénzes, Róza Tóth, and Mária Benkő. "First detection of circovirus-like sequences in amphibians and novel putative circoviruses in fishes." Acta Veterinaria Hungarica 62, no. 1 (2014): 134–44. http://dx.doi.org/10.1556/avet.2013.061.

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The negative samples of a collection, established originally for seeking new adeno- and herpesviruses in lower vertebrates, were screened for the pres-ence of circoviruses by a consensus nested PCR targeting the gene coding for the replication-associated protein. Six fish samples representing five species, namely asp (Aspius aspius), roach (Rutilus rutilus), common bream (Abramis brama), round goby (Neogobius melanostomus) and monkey goby (Neogobius fluviatilis), as well as three frog samples were found positive for circoviral DNA. Sequence analysis of the amplicons indicated the presence of three novel putative circo-like viruses and a circovirus in Hungarian fishes and one novel circovirus in a common toad (Bufo bufo), and another one in a dead and an alive specimen of green tree frog (Litoria caerulea), respectively. In phylogeny reconstruction, the putative bream circovirus clustered together with circoviruses discovered in other cyprinid fishes recently. Three other piscine circoviral sequences appeared closest to sequences derived from different environmental samples. Surprisingly, the nucleotide sequence derived from two fish samples (a bream and a monkey goby) proved to be from porcine circovirus 2 (PCV2), almost identical to a sequence detected in Sweden previously. This is the first report on the detection of PCV2 in fish and circoviral DNA in amphibian hosts.
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5

van Kessel, Nils. "First record of Pontian monkey goby, Neogobius fluviatilis (Pallas, 1814), in the Dutch Rhine." Aquatic Invasions 4, no. 2 (2009): 421–24. http://dx.doi.org/10.3391/ai.2009.4.2.24.

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6

Grabowska, Joanna, Michał Grabowski, and Anna Kostecka. "Diet and feeding habits of monkey goby (Neogobius fluviatilis) in a newly invaded area." Biological Invasions 11, no. 9 (2009): 2161–70. http://dx.doi.org/10.1007/s10530-009-9499-z.

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7

Top, Nildeniz, Uğur Karakuş, Erdi Gökhan Tepeköy, John Robert Britton, and Ali Serhan Tarkan. "Plasticity in habitat use of two native Ponto-Caspian gobies, Proterorhinus semilunaris and Neogobius fluviatilis: implications for invasive populations." Knowledge & Management of Aquatic Ecosystems, no. 420 (2019): 40. http://dx.doi.org/10.1051/kmae/2019031.

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The Ponto-Caspian region is an important source area for some invasive gobiid fishes. These fishes have colonised several freshwater ecosystems in Europe, as well as in North America. As knowledge on their habitat utilisation in their native range remains limited, the seasonal habitat uses of Western tubenose goby, Proterorhinus semilunaris and monkey goby Neogobius fluviatilis were studied in four natural lakes in the Marmara Region (NW Turkey). Habitat use of both species was highly variable between the lakes and seasons, with P. semilunaris showing higher plasticity. In general, the main habitats used by P. semilunaris were shallow waters in littoral areas that had vegetation cover, whereas N. fluviatilis consistently used sandy substratum in deeper waters that lacked vegetation. These results suggested there was high plasticity in the habitat utilisation of these two gobiids, especially in P. semilunaris, which potentially facilitates their ability to establish and invade novel environments. The habitats that are especially vulnerable to P. semilunaris invasion are medium size substrates which provide individuals with sufficient interstitial space for refuge. Waters providing differing habitats, such as sandy substrata, might inhibit their colonisation, but are potentially more vulnerable to N. fluviatilis invasion.
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8

Mineeva, O. V., and A. K. Mineev. "The First Data on Parasites of Monkey Goby Neogobius fluviatilis (Perciformes, Gobiidae) in the Saratov Reservoir." Russian Journal of Biological Invasions 11, no. 4 (2020): 341–47. http://dx.doi.org/10.1134/s2075111720040074.

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9

Sukharenko, E. V., R. А. Novitsky та V. S. Nedzvetsky. "Використання біомаркерів мозку донних риб для оцінки забруднення Керченської протоки Чорного моря". Visnyk of Dnipropetrovsk University. Biology, medicine 3, № 2 (2008): 81–88. http://dx.doi.org/10.15421/021236.

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Fish were sampled at the shallow part of the Kerch Strait, where the shipwreck brought to ecological emergency in 2007. There were used ichthyotoxicology, biochemistry and immunochemistry methods for the research of fish populations. Comparative investigation of samples from both polluted and uncontaminated regions (Vorskla River) shows the changes in metabolism of cytoskeleton proteins of astrocytes from the monkey goby Neogobius fluviatilis. The results are evidence of the neural cell pathology of ground fish from the polluted region. The neural system pathology could be a result of long-term effect of oil pollution in the Kerch Strait. There was shown the validity of the N. fluviatilis brain’s astroglial reactivity for the assessment of the population state. The presented data substantiate the necessity of ecological monitoring of the shallow biotopes of that region of the Black Sea.
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10

ZOGARIS, S., and A. APOSTOLOU. "First record of Pontian Monkey Goby, Neogobius fluviatilis (Pallas, 1814) in the Evros River (Greece); Is it an alien species?" Mediterranean Marine Science 12, no. 2 (2011): 454. http://dx.doi.org/10.12681/mms.47.

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The Pontian Monkey Goby,Neogobius fluviatilis (Pallas, 1814), was recorded for the first time in Greece in August 2011. Eight specimens were collected in the Greek-Turkish section of the Evros River, 65 kilometers upstream of its river-mouth. Although the species has been recently discovered in the Tundza, a tributary of the Evros in Bulgaria, it has never before been found in the Evros’ main stem. Although the lower Evros has been poorly researched by ichthyologists, it is unlikely that a conspicuous medium-sized fish would go unnoticed in this river; and, it is therefore suggested to be a probable alien. However, since the Evros basin has had geological connections to the Marmara Sea and Black Sea in the past and it is immediately adjacent to native populations of N. fluviatilis, the species status is categorized as questionable until genetic and morphological studies are completed.
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11

Ghomi, M. R., E. Von Elert, J. Borcherding, and P. Fink. "Fatty acid composition and content of round goby (Neogobius melanostomus Pallas 1814) and monkey goby (Neogobius fluviatilis Pallas 1814), two invasive gobiid species in the lower Rhine River (Germany)." Journal of Applied Ichthyology 30, no. 3 (2013): 527–31. http://dx.doi.org/10.1111/jai.12312.

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12

Piria, M., T. Treer, T. Tomljanović, et al. "First record of monkey goby, Neogobius fluviatilis (Pallas, 1814) in the barbel zone of the Sava River, Croatia." Journal of Applied Ichthyology 27, no. 6 (2011): 1383–84. http://dx.doi.org/10.1111/j.1439-0426.2011.01800.x.

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13

Čápová, Mária, Ivana Zlatnická, Vladimír Kováč, and Stanislav Katina. "Ontogenetic variability in the external morphology of monkey goby, Neogobius fluviatilis (Pallas, 1814) and its relevance to invasion potential." Hydrobiologia 607, no. 1 (2008): 17–26. http://dx.doi.org/10.1007/s10750-008-9361-9.

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14

Konečná, Markéta, and Pavel Jurajda. "Population structure, condition, and reproduction characteristics of native monkey goby, Neogobius fluviatilis (Actinopterygii: Perciformes Gobiidae), in the Bulgarian Danube." Acta Ichthyologica Et Piscatoria 42, no. 4 (2012): 321–27. http://dx.doi.org/10.3750/aip2012.42.4.05.

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15

Czeglédi, István, Bálint Preiszner, Zoltán Vitál, et al. "Habitat use of invasive monkey goby (Neogobius fluviatilis) and pumpkinseed (Lepomis gibbosus) in Lake Balaton (Hungary): a comparison of electrofishing and fyke netting." Hydrobiologia 846, no. 1 (2019): 147–58. http://dx.doi.org/10.1007/s10750-019-04060-9.

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16

Mekhtiev, A. A., G. M. Palatnikov, S. K. Movsum-zadeh, and R. Yu Kasimov. "A rise of mutation level in tissues of monkey goby and sturgeon fry under conditions of block by antibodies to the serotonin-modulated anticonsolidation protein." Journal of Evolutionary Biochemistry and Physiology 46, no. 5 (2010): 447–52. http://dx.doi.org/10.1134/s0022093010050038.

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17

Pauen, Sabina, Lena Heilig, Daniel Danner, Johann Haffner, Andrea Tettenborn, and Jeanette Roos. "Milestones of Normal Development in Early Years (MONDEY)." Frühe Bildung 1, no. 2 (2012): 64–70. http://dx.doi.org/10.1026/2191-9186/a000032.

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Standardisierte Instrumente zur Dokumentation der frühkindlichen Entwicklung für den Altersbereich 0 – 3 Jahre liegen im deutschen Sprachraum kaum vor. Der vorliegende Beitrag diskutiert zunächst Anforderungen an geeignete Verfahren und stellt anschließend ein neues Dokumentationsprogramm (MONDEY; Pauen, 2011 ) vor. MONDEY enthält Beschreibungen von 111 Meilensteinen, die acht unterschiedlichen Entwicklungsbereichen (Gob- und Feinmotorik, Wahrnehmung und Denken, Sprache, Soziale Beziehungen, Selbstregulation, Emotionen) zugeordnet sind, welche ihrerseits die allgemeine Entwicklung in der frühen Kindheit widerspiegeln sollen. Strukturgleichungsmodelle, die mit einer Pilotversion des Instrumentes ( Pauen, 2008 ) durchgeführt wurden, bestätigen die hierarchische Konzeption von MONDEY und dokumentieren eine überraschend gute Modellanpassung. Der allgemeine Entwicklungswert korreliert zudem hoch mit dem Alter der Kinder. Auf dieser Grundlage schließen wir, dass das neue Programm eine hohe Konstruktvalidität aufweist.
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18

Reading, Richard P., Sukhiin Amgalanbaatar, Henry Mix, and Badamjaviin Lhagvasuren. "Argali Ovis ammon surveys in Mongolia's South Gobi." Oryx 31, no. 4 (1997): 285–94. http://dx.doi.org/10.1046/j.1365-3008.1997.d01-17.x.

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The argali, Ovis ammon, a species of wild sheep, is threatened in Mongolia, suffering from poaching and competition with domestic livestock. The authors conducted ground and aerial surveys of argali in Dundgobi, Omnogobi and Dornogobi aimags (or provinces) of the South Gobi region of Mongolia. Ground surveys were conducted by vehicle and on foot, while aerial surveys were conducted using two Soviet AN-2 aircraft flying 40-km parallel transects. The interactive computer programme Distance was used to estimate population size and density. The authors observed a total of 423 argali in 85 groups (mean group size = 5.0 ± 0.6 SE), including 300 individuals in 61 groups on the ground survey (mean size = 4.9 ± 0.8 SE) and 123 animals in 24 groups during the aerial survey (mean size = 5.1 ± 1.2 SE). Population structure of the groups observed during the ground survey was 14.3 per cent males, 53.3 per cent females, 19.7 per cent lambs, and 12.7 per cent animals of undetermined sex (means = 0.7 ± 0.2 SE males, 2.6 ± 0.6 SE females, 1.0 ± 0.2 SE lambs, and 0.6 ± 0.4 SE undetermined). We estimated a population size of 3900 ± 1132 SE argali in the study area for a population density of 0.0187 ± 0.0054 SE animals/sq km. More rigorous and comprehensive surveys for argali, preferably for each distinct population, should be conducted for more accurate estimates. Argali require more active conservation and management, especially with respect to poaching and competition with domestic livestock. If sport hunting is to continue, a large portion of all money
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19

Steele, James, Marina Gkiasta, and Stephen Shennan. "The Neolithic transition and European population history – a response." Antiquity 78, no. 301 (2004): 711–13. http://dx.doi.org/10.1017/s0003598x00113353.

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We thank Crombé and Van Strydonck for their comments on our earlier paper (Gkiasta et al. 2003). They kindly draw attention to recent surveys of radiocarbon data from Belgium, most of which were published subsequent to our own work, which was carried out in 1999. Even at the time we were under no illusion that our compilation was complete: “It became clear in the course of the project that, despite the large sums of money which have been spent over the years on radiocarbon dating in Europe, the state of public availability of the dates, their context and associations and details which enable users to judge the reliability of dates is in general very poor. Thus, no claim is made that the database is in any sense complete” (Gkiasta et al. 2003: 48). It would probably also be as well to correct the impression that the dates we used were mainly derived from Gob (1990). Over half those finally included were extracted from the University of Lyon Banadora database; the remainder came from a wide range of other sources. The new dates from Belgium may well shed new light on the chronology of the transition in that region. New discoveries frequently do cause old interpretations to be modified or revised; we look forward to their analysis and demonstration of the implications of the new data to which they refer.
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20

Sharkova, Iryna. "Image of Good Faith Subjects of Law in Legal Cultural History: Definition of Universal Standards." Law Review of Kyiv University of Law, no. 3 (November 10, 2020): 56–59. http://dx.doi.org/10.36695/2219-5521.3.2020.08.

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The article is devoted to the problem of Good Faith Subjects` status in law. For a better understanding of the problem, image ofgood faith subjects of law in Ancient Rome was analyzed. In particular, it was found that in roman law, the term bonus pater familias(good family father) refers to a standard of good faith subjects of law. In the English version, this concept was translated as «that of aman of ordinary prudence in managing his own affairs».The concept of a gentleman in the English legal tradition is specially studied.English noun ‘gentleman’ dates back to the Old French word ‘gentilz hom’ (graceful, refined man). That was why the social ca -te gory of gentleman is considered as “the nearest, contemporary English equivalent of the noblesse of France.” (Maurice Hugh Keen).Now, a gentleman is not just any man of good and courteous conduct, but a certain person having legal personality in accordancewith the standard of common law.In conformity with the dimension of public law, the English social category of gentleman captures a right of certen classe of theBritish nobility.But in accordance with modern private law the connotation of the term gentleman corresponds to the Rome legal institute ofbonus pater familias.The double origin of this term from the status of a knight and the social position of the merchant causes a controversial interpretationsof its meaning.In contemporary usage, the word gentleman is ambiguously defined, because “to behave like a gentleman” communicates as littlepraise or as much criticism as the speaker means to imply; thus, “to spend money like a gentleman” is criticism, but “to conduct a businesslike a gentleman” is praise (Walter Alison Phillips).In modern International Trade Law a gentleman is essentially a ‘man of sense’, ‘а man of judgment’ or a reasonable person.So United Nations Convention on Contracts for the International Sale of Goods (1980), The UNIDROIT Principles of InternationalCommercial Contract and the Principles of European Contract Law provided a rule, which offers an opportunity for such an interpretation.‘the contract is to be interpreted according to the meaning that reasonable persons of the same kind as the parties would giveto it in the same circumstances’.It led to the conclusion that the modern image of a good faith subject to the greatest extent actualizes the criterion of commonsense.
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21

Choudhury, H., J. Coleman, C. T. De Rosa, and J. F. Stara. "Pentachlorophenol: Health and Environmental Effects Profile." Toxicology and Industrial Health 2, no. 4 (1986): 483–571. http://dx.doi.org/10.1177/074823378600200409.

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Pentachlorophenol is used as an industrial wood preservative for utility poles, crossarms, fence posts, and other purposes (79%);for NaPCP (12%); and miscellaneous, including mill uses, consumer wood preserving formulations and herbicide intermediate (9%) (CMR, 1980). As a wood preservative, pentachlorophenol acts as both a fungicide and insecticide (Freiter, 1978). The miscellaneous mill uses primarily involve the application of pentachlorophenol as a slime reducer in paper and pulp milling and may constitute ∼6% of the total annual consumption of pentachlorophenol (Crosby et al., 1981). Sodium pentachlorophenate (NaPCP) is also used as an antifungal and antibacterial agent (Freiter, 1978). Pentachlorophenol also is used as a general herbicide (Martin and Worthing, 1977). Photolysis and microbial degradation are the important chemical removal mechanisms for pentachlorophenol in water. In surface waters, pentachlorophenol photolyzes rapidly (ECETOC, 1984; Wong and Crosby. 1981; Zepp et al., 1984); however, the photolytic rate decreases as the depth in water increases (Pignatello et al., 1983). Pentachlorophenol is readily biodegradable in the presence of accli-mated microorganisms; however, biodegradation in natural waters requires the presence of microbes that can become acclimated. A natural river water that had been receiving domestic and industrial effluents significantly biodegraded pentachlorophenol after a 15-day lag period, while an unpolluted natural river water was unable to biodegrade the compound (Banerjee et al., 1984). Even though pentachlorophenol is in ionized form in natural waters, sorption to organic particulate matter and sediments can occur (Schellenberg et al., 1984), with desorption contributing as a continuing source of pollution in a contaminated environment (Pierce and Victor, 1978). Experimentally determined BCFs have shown that pentachlorophenol can significantly accumulate in aquatic organisms (Gluth et al., 1985; Butte et al., 1985; Statham et al., 1976; Veith et al., 1979a,b; Ernst and Weber, 1978), which is consistent with its widespread detection in fish and other organisms. Direct photolysis may be an important environmental sink for pen tachlorophenol present in the atmosphere. The detection of pen tachlorophenol in snow and rain water (Paasivirta et al., 1985; Bevenue et al., 1972) suggests that removal from air by dissolution is possible. Soil degradation studies indicate that pentachlorophenol is biodegrad able; microbial decomposition is an important and potentially domin ant removal mechanism in soil (Baker et al., 1980; Baker and Mayfield, 1980; Edgehill and Finn, 1983; Kirsch and Etzel, 1973; Ahlborg and Thunberg, 1980). The degree to which pentachlorophenol leaches in soil is dependent on the type of soil. In soils of neutral pH, leaching may be significant, but in acidic soils, adsorption to soil generally increases (Callahan et al. , 1979; Sanborn et al. , 1977). The ionized form of pentachlorophenol may be susceptible to adsorption in some soils (Schellenberg et al., 1984). In laboratory soils, pen tachlorophenol decomposes faster in soils of high organic content as compared with low organic content, and faster when moisture content is high and the temperature is conducive to microbial activity. Half- lives are usually ∼2-4 weeks (Crosby et al., 1981). Monitoring studies have confirmed the widespread occurrence of pentachlorophenol in surface waters, groundwater, drinking water and industrial effluents (see Table 2). The U.S. EPA's National Urban Runoff Program and National Organic Monitoring Survey reported frequent detections in storm water runoff and public water supplies (Cole et al., 1984; Mello, 1978). Primary sources by which pen tachlorophenol may be emitted to environmental waters may be through its use in wood preservation and the associated effluents and its pesticidal applications. Pentachlorophenol can be emitted to the atmosphere by evaporation from treated wood or water surfaces, by releases from cooling towers using pentachlorophenol biocides or by incineration of treated wood (Skow et al., 1980; Crosby et al., 1981). Pentachlorophenol has been detected in ambient atmospheres (Caut reels et al., 1977), in snow and rain water (Paasivirta et al,. 1985; Bevenue et al., 1972) and in emissions from hazardous waste incinera tion (Oberg et al., 1985). The U.S. Food and Drug Administration's Total Diet Study (conducted between 1964 and 1977) found pen tachlorophenol residues in 91/4428 ready-to-eat food composites (See Tables 4 and 5). The average American dietary intake of pen tachlorophenol during 1965-1969 was estimated to range from <0.001-0.006 mg/day (Duggan and Corneliussen, 1972). The most likely source of pentachlorophenol contamination in many food prod ucts may be the exposure of the food to pentachlorophenol-treated wood materials such as storage containers (Dougherty, 1978). Acute toxicity data indicated that salmonids are more sensitive to the toxic effects of pentachlorophenol than other fish species, with LC50 values of 34-128 μ g/l for salmonids and 60-600 μ g/l for other species. More recent data showed that carp larvae, bluegills, channel catfish and knifefish also had LC50 values < 100 μ gl (see Table 10). The most sensitive marine fishes were pinfish larvae, the goby, Gobius minutus, and eggs and larvae of the flounder, Pleuronectes platessa, all with LC50 values <100 μ g/l (Adema and Vink, 1981). The most sensitive freshwater invertebrate species were the chironomid, Chironomus gr. thummi (Slooff, 1983) and the snail, Lymnaea luteola (Gupta et al., 1984). The most sensitive marine invertebrates were the Eastern oyster (Borthwick and Schimmel, 1978), larvae of the crusta ceans, Crangon crangon and Palaemon elegans (VanDijk et al. , 1977), and the copepod, Pseudodiaptomus coronatus (Hauch et al., 1980), all with LC50 values <200 μ g/l. In chronic toxicity tests, the lowest concentration reported to cause adverse effects was 1.8 μ g/l (NaPCP), which inhibited growth of sockeye salmon (Webb and Brett, 1973). The marine species tested displayed similar thresholds for chronic toxicity. Both acute and chronic toxicity increased at lower pH, probably because a lower pH favors the un-ionized form of pentachlorophenol, which is taken up more readily and is therefore more toxic than ionized pentachlorophenol (Kobayashi and Kishino, 1980; Spehar et al., 1985). Data concerning the effects of pentachlorophenol on aquatic plants were highly variable. Therefore, it was difficult to draw conclusions from these data. Pentachlorophenol did not appear to bioaccumulate in aquatic or ganisms to very high concentrations. BCFs for pentachlorophenol were <1000 for most species tested. The highest BCF was 3830 for the polychaete, Lanice conchilega (Ernst, 1979). Some species appear to have an inducible pentachlorophenol-detoxification mechanism, as evidenced in several experiments in which pentachlorophenol tissue levels peaked in 4-8 days and declined thereafter despite continued exposure (Pruitt et al., 1977; Trujillo et al., 1982). A study by Niimi and Cho (1983) indicated that uptake of waterborne pentachlorophenol from gills was much greater than uptake from food, indicating that bioconcentration of pentachlorophenol through the food chain is unlikely. Biomonitoring data of Lake Ontario fishes showed that similar pentachlorophenol levels were found in predators andforage species. Studies with experimental ecosystems have indicated that ecological effects may occur at pentachlorophenol levels as low as those causing chronic toxicity in sensitive species in single-species tests. The lowest concentration that caused adverse effects in these studies was 15.8 μ g/l, which caused a reduction in numbers of individuals and species in a marine benthic community (Tagatz et al., 1978). Pentachlorophenol is readily absorbed from the gastrointestinal tract of rats, mice, monkeys and humans (Braun et al. , 1977, 1978; Ahlborg et al., 1974; Braun and Sauerhoff, 1976). Peak plasma concentrations are reached within 12-24 hours after oral administration to monkeys (Braun and Sauerhoff, 1976), but 4-6 hours after oral administration to rats (Braun et al., 1977). After oral administration, the highest concentration of radioactivity was found in the liver and gastrointesti nal tract of monkeys (Braun et al., 1977). In rats and mice, tet rachlorohydroquinone was identified in the urine (Jakobson and Yllner, 1971; Braun et al., 1977; Ahlborg et al., 1974) as well as unmetabolized pentachlorophenol and glucuronide-conjugated pen tachlorophenol. Although Ahlborg et al. (1974) reported that oxidative dechlorination of pentachlorophenol occurs in humans, as evidenced by the presence of tetrachlorohydroquinone in the urine of workers occupationally exposed (probably by inhalation), analysis of human urine after ingestion of pentachlorophenol revealed the presence of conjugated pentachlorophenol and unmetabolized pentachlorophenol (Braun et al., 1978). The primary route of excretion after oral administrtation of all species studied is in the urine (Braun et al. , 1977, 1978; Ahlborg et al., 1974; Larsen et al., 1972; Braun and Sauerhoff, 1976). Although urinary excretion followed second-order kinetics in rats (Larsen et al., 1972; Braun et al., 1977) except in females receiving a single high dose (100 mg/kg) of pentachlorophenol, urinary excretion of pentachlorophenol in humans and monkeys followed first-order kinetics (Braun and Sauerhoff, 1976; Braun et al., 1978). Enterohepatic circulation played an importation role in the pharmacokinetics of pen tachlorophenol. The half-life of pentachlorophenol in the plasma is longer in female rats and monkeys than it is in male rats and monkeys (Braun et al. , 1978; Braun and Sauerhoff, 1976). Because many preparations of pentachlorophenol are contaminated with small but measurable amounts of highly toxic substances, such as dibenzodioxins, special attention must be paid to the composition of the pentachlorophenol solution tested. In studies where technical and purified pentachlorophenol have been evaluated (Schwetz et al., 1974; Goldstein et al., 1977; Kimbrough and Linder, 1978; Knudsen et al., 1974; Johnson et al., 1973; Kerkvliet et al., 1982), only the results of the experiments using purified pentachlorophenol were reported in detail. Oral exposure to pentachlorophenol was not carcinogenic in mice (BRL, 1968; Innes et al., 1969) or rats (Schwetz et al., 1977), regardless of the composition of the pentachlorophenol solution tested. Although there are a few studies that suggest pentachlorophenol may be mutagenic in B. subtilis (Waters et al., 1982; Shirasu, 1976), in yeast, Saccharomyces cerevisiae (Fahrig et al., 1977) and in mice, as evidenced by the coat-color spot test (Fahrig et al., 1977), no evidence of mutagenicity was reported in S. typhimurium (Anderson et al. , 1972; Simmon et al., 1977; Lemma and Ames, 1975; Moriya et al. , 1983; Waters et al., 1982; Buselmaier et al., 1973) or in E. coli (Simmon et al., 1977; Fahrig, 1974; Moriya et al., 1983; Waters et al., 1982) with or without metabolic activation. Three teratogenicitylreproductive toxicity studies (Schwetz et al., 1974, 1977; Courtney et al., 1976) indicate that pentachlorophenol is fetotoxic in rats at oral dose levels ≥5 mg/kg/day. At the highest dose tested (500 ppm) in a fourth teratogenicity/reproductive toxicity study (Exon and Koller, 1982), there was a statistically nonsignificant decrease in litter size. The lowest dose tested (5 mg/kg/day) by Schwetz et al. (1977) was the lowest dose at which any evidence offetotoxicity, as indicated by delayed ossification, was observed. No adverse fetal or reproductive effects were reported at ≤3 mg/kg/day (Schwetz et al., 1977; Exon and Koller, 1982). In subchronic and chronic toxicity studies, adverse effects occurred primarily in the liver (Kerkvliet et al., 1982; Johnson et al., 1973; Knudsen et al. , 1974; Goldstein et al. , 1977; Kimbrough and Linder, 1978; Schwetz et al., 1977), the kidney (Johnson et al., 1973; Kimbrough and Linder, 1978; Schwetz et al., 1977) and the immune system (Kerkvliet et al., 1982). Knudsen et al. (1974) reported increased liver weights in female rats and centrilobu lar vacuolization in male rats exposed to diets containing ≧50 ppm commercial pentachlorophenol, which contained 282 ppm dioxins. In the remaining studies, increased liver weight (Johnson et al., 1973) and increased pigmentation of hepatocytes (Schwetz et al., 1977) were observed at oral doses of≥10 mg/kg/day (∼90%), and SGPT levels significantly increased in rats ingesting 30 mg/kg/day pentachloro phenol (∼90%) for 2 years (Schwetz et al., 1977). Increased kidney weight unaccompanied by renal histopathology was reported in rats exposed to dietary concentration ≧20 ppm of pentachlorophenol (>99%) for 8 months (Kimbrough and Linder, 1978) and in rats ingesting 30 mg/kg/day (∼90%) for 90 days (Johnson et al., 1973). Increased pigmentation of the renal tubular epithelial cells was re ported in rats ingesting 10 or 30 mg/kg/day pentachlorophenol for 2 years (Schwetz et al., 1977). Although decreased immunocompetence was reported in mice exposed to dietary levels of 50 or 500 ppm of pentachlorophenol (>99%) for 34 weeks (Kerkvliet et al., 1982), the decrease was statistically significant only at the higher dose. An ADI of 0.03 mg/kg/day or 2.1 mg/day for a 70 kg human was derivedfrom the NOAEL of 3 mg/kg/day in rats in the chronic dietary study by Schwetz et al. (1977). An uncertainty factor of 100 was used. An RQ of 100 was derived based on the fetotoxic effects of pen tachlorophenol in rats in the study by Schwetz et al. (1974). Based on guidelines for carcinogen risk assessment (U.S. EPA, 1984b) and inadequate evidence for animal carcinogenicity or absence of human cancer data, pentachlorophenol is classified as Group D, meaning that it is not classified as a human carcinogen.
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22

Ghomi, Mohammad, Eric Elert, Jost Borcherding, Andreas Uhde, and Patrick Fink. "Correlation between body size and fatty acid and essential amino acid composition of round goby (Neogobius melanostomus) and monkey goby (Neogobius fluviatilis) from the Rhine River (Germany)." Biologia 69, no. 6 (2014). http://dx.doi.org/10.2478/s11756-014-0374-8.

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AbstractIn this study correlations between body size and muscle fatty and amino acid content of two species of goby, round goby (Neogobius melanostomus) and monkey goby (Neogobius fluviatilis) caught from river Rhine (Germany) were investigated. Among saturated fatty acids (SFAs), mono- (MUFA) and polyunsaturated fatty acids (PUFAs) only SFAs were significantly higher in round goby than monkey goby (P < 0.05). In general, the correlation between body size of both gobies and the content of most of the individual fatty acids was not significant. In monkey goby, the content of palmitic acid (C16:0) and oleic acid (C18:1 n-9) was positively correlated with weight (r = 0.43) and total length (r = −0.58), respectively, and the content of docosahexaenoic acid (DHA) increased with condition factor (r = 0.50). The content of threonine, arginine, valine, phenylalanine and isoleucine in monkey goby was higher than those of round goby (P < 0.05). In round goby the three essential amino acids arginine, valine and leucine were positively (P < 0.05) correlated with body length, which indicates that longer round gobies are of higher nutritional value.
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23

Kvach, Yuriy, Vasily Boldyrev, Rachel Lohner, and Carol A. Stepien. "The parasite community of gobiid fishes (Actinopterygii: Gobiidae) from the Lower Volga River region." Biologia 70, no. 7 (2015). http://dx.doi.org/10.1515/biolog-2015-0108.

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AbstractThe parasitic fauna in the lower Volga River basin was investigated for four gobiid species: the nonindigenous monkey goby Neogobius fluviatilis (Pallas, 1814), the round goby N. melanostomus (Pallas, 1814), the Caspian bighead goby Ponticola gorlap (Iljin, 1949), and the tubenose goby Proterorhinus cf. semipellucidus (Kessler, 1877). In total, 19 species of goby parasites were identified, of which two - Bothriocephalus opsariichthydis Yamaguti, 1934 and Nicolla skrjabini (Iwanitzki, 1928) - appeared to have been introduced from other geographic regions. The monkey goby had significantly fewer parasitic species (6), but relatively high levels of infection, in comparison to the native species. Parasitism of the Caspian bighead goby, which is the only predatory fish among the studied gobies, differed from the others according to the results of discriminant analysis. The parasitic fauna of the tubenose goby more closely resembled those of Caspian Sea gobiids, rather than the Black Sea monkey goby.
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24

Semenchenko, Vitaliy, Joanna Grabowska, Michal Grabowski, Viktor Rizevsky, and Michail Pluta. "Non-native fish in Belarusian and Polish areas of the European central invasion corridor." Oceanological and Hydrobiological Studies 40, no. 1 (2011). http://dx.doi.org/10.2478/s13545-011-0007-6.

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AbstractThis is the first comprehensive review to examine the role of the central European invasion corridor on fish introductions into Belarusian and Polish inland waters (Dnieper-Bug-Vistula-Oder-Elbe-Spree-Havel). Historical and recent data were assessed, including the results of a 2003–2008 survey along the Belarusian and Polish sections of the corridor. Since the eighteenth century, at least six fish species of Ponto-Caspian origin have spread via the corridor and migrated westwards to the Baltic basin, with five species found in recent surveys, namely the monkey goby Neogobius fluviatilis, round goby N. melanostomus, racer goby N. gymnotrachelus, tubenose goby Proterorhinus marmoratus and the white eye-bream Abramis sapa. Four other non-native species were also found within the corridor — the Amur sleeper Perccottus glenii, gibel carp Carassius gibelio, brown bullhead Ameiurus nebulosus and the topmouth gudgeon Pseudorasbora parva. Their presence is related to numerous accidental introductions to many localities in Belarus and Poland, rather than from using the corridor as an invasion route. One species, the ninespine stickleback, Pungitius pungitius, has migrated from the Baltic basin to the Black Sea drainage systems.
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25

Stepanova, Irina Pavlovn, Dmitriy Viktorovich Mikhaylichenko, and Andrey Mikhailovich Tikhomirov. "METHODS OF ASSESSING WATER QUALITY USING BEHAVIORAL RESPONSE OF FISH SPECIES." Vestnik of Astrakhan State Technical University. Series: Fishing industry, June 25, 2017, 80–85. http://dx.doi.org/10.24143/2073-5529-2017-2-80-85.

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The proposed technique of water quality assessment is intended for monitoring and measuring the behavioral responses of fishes in minimally structured environment, and further evaluating the reactivity of the fish nervous system. Tests were conducted in the period from 11 May to 7 June, 2016 at the sea coast station of the Southern Scientific Center of the Russian Academy of Sciences (Kagalnik village, the Rostov region). As test-objects (bioindicators), there were selected three species of gobies: round goby ( Neogobius melanostomus ), monkey goby ( Neogobius fluviatilis ) and goby Shearman ( Neogobius syrman ). Fish behavior was assessed by response to external stimuli, which is manifested by increased or decreased locomotor activity. Expected and phone activity has been defined. As the test stimuli there were used: a low-frequency sonic boom, a sinusoidal audio signal, a high-frequency sonic boom, an electrical stimulus. Testing water samples were taken from three stations in the water area of the Gulf of Taganrog (estuary of the Don, middle section of the bay and section of the river close to the coastal base). The results showed that the developed method is sensitive to changes of natural water pollutants and can be used in the monitoring system, as a component for coastal stations on the test areas of the Azov Sea in terms of bioindication data matching techniques to identify natural and anthropogenic sources of pollution.
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26

Stanek, Magdalena, Zbigniew Borejszo, Janusz Dąbrowski, and Bogdan Janicki. "SELECTED MEAT QUALITY PARAMETERS OF PONTIAN MONKEY GOBY ( NEOGOBIUS FLUVIATILIS PALLAS) FISHED IN THE VISTULA RIVER." Zywnosc.Nauka.Technologia.Jakosc/Food.Science.Technology.Quality, no. 5(96) (2014). http://dx.doi.org/10.15193/zntj/2014/96/101-110.

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27

Płąchocki, Dariusz, Jarosław Kobak, and Tomasz Kakareko. "First report on the importance of alien gobiids in the diet of native piscivorous fishes in the lower Vistula River (Poland)." Oceanological and Hydrobiological Studies 41, no. 2 (2012). http://dx.doi.org/10.2478/s13545-012-0020-4.

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AbstractWe conducted a snapshot study to check the importance of non-native Ponto-Caspian gobies (monkey and racer goby) in the diet of native obligate (northern pike, pikeperch) and facultative (Eurasian perch) predators in the Vistula River 3–4 years after the appearance of aliens. In total 71 fish with non-empty stomachs, taken randomly from net catches from various parts of the river were analyzed, including 32 pike, 20 pikeperch and 19 perch specimens. We found that gobiids prevailed in the diet of smaller (<30 cm standard length, SL) individuals of pike and pikeperch, as well as larger (>15 cm SL) specimens of perch, although the effect of predator size on the presence of gobiids in the diet was not significant in the case of perch. Our results indicate that gobiids as a prey fish can stimulate considerable changes in local food webs, which require further studies.
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28

Onoprienko, V. P., and I. S. Mytai. "COMPARATIVE CHARACTERISTICS OF MORPHOMETRIC PARAMETERS OF MONKEY GOBY (NEOGOBIUS FLUVIATILIS PALLAS) OF FRESH AND SALINE WATER RESERVOIRS IN UKRAINE." Biological Bulletin of Bogdan Chmelnitskiy Melitopol State Pedagogical University 4, no. 1 (2014). http://dx.doi.org/10.7905/bbmspu.v4i1.794.

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29

"Monogeneans of fish of the Mingechevir Reservoir of the Kura River basin." Journal of V. N. Karazin Kharkiv National University, Series "Biology", no. 32 (2019). http://dx.doi.org/10.26565/2075-5457-2019-32-10.

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In 2010–2013, a study on fish of the Mingechevir Reservoir of the Kura River basin, for infestation with parasites belonging to the Monogenea class was conducted. 297 specimens of fish were subjected to parasitological dissections. These fish belong to the following 23 species: roach – Rutilus rutilus caspius, Caucasian chub – Leuciscus cephalus orientalis, asp – Aspius aspius taeniatus, tench – Tinca tinca, Kura nase – Chondrostoma cyri, Kura khramulya – Capoeta capoeta, chanari-barbel – Luciobarbus capito, goldfish – Carassius auratus gibelio, carp – Cyprinus carpio, Kura beardie – Barbatula brandti, Transcaucasica spined loach – Cobitis taenia satunini, catfish – Silurus glanis, mosquito fish – Gambusia affinis, pike – Sander lucioperca, big headed goby – Neogobius kessleri gorlap, monkey goby – N. fluviatilis pallasi. As a result of the research, 34 species of monogeneans belonging to 3 orders of 4 families and 5 genera were identified. The overwhelming majority (32 species) of monogeneans found are parasitic on the gill petals of fish, from two to six species are also found on the surface of the body and fins, in the nasal cavity of fish. Of the found monogeneans, 24 species (70.6%) are specific for one species or one genus of fish. It has been established that monogeneans parasitizing on several hosts infect the main of them more than others fish, and the intensity of invasion of fish with large sizes was higher than that of relatively small fish. By their origin, 23 species or 67.7% of all species belong to the boreal lowland faunistic complex. According to the ecological groups of this complex, they are distributed as follows: in the Ponto-Caspian group – 17 species, in the Palaearctic and amphiboreal groups – 3 species each. The Middle East faunistic complex is represented by six, the Indian lowland complex is represented by three, and the Ponto-Caspian marine complex by two species. Among the monogeneans of fish of the Mingechevir Reservoir, two species, Dactylogyrus extensus and D. vastator destroy gill petals of their hosts and cause their diseases. They are the cause of the mass death of juvenile fish.
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