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  • 1
    In: Aquatic invasions, Helsinki, Finland : Regional Euro-Asian Biological Invasions Centre, 2006, 3(2008), 2, Seite 113-124, 1818-5487
    In: volume:3
    In: year:2008
    In: number:2
    In: pages:113-124
    Description / Table of Contents: The distribution and abundance of the invasive ctenophore Mnemiopsis leidyi in the Bornholm Basin, an important spawning ground of several fish stocks, and in adjacent areas in the central Baltic Sea was studied in November 2007. The study showed that M. leidyi were relatively small (body length 18.6 ± 7.6 mm) and they were patchily distributed over a large part of the investigated area. Specimens were found on 68 and 59% of stations sampled with a Bongo net (n=39) and an Isaac-Kidd midwater trawl (n=51), respectively. Vertically, the highest densities of M. leidyi occurred at 40 to 60 m around the halocline. Horizontally, the highest abundances were found north and west of Bornholm, but relatively high densities were also observed in the Slupsk Furrow. The mean abundance was 1.58 ± 2.12 ind. m-2, the peak abundance was 8.92 ind. m-2, and the average and peak population density were 0.03 ± 0.05 and 0.28 ind. m-3, respectively. The abundances are low compared to densities recently observed in other areas of the Baltic region (e. g. Limfjorden, Åland Sea) and the estimated predation impact on zooplankton by M. leidyi was negligible in November 2007. However, because of the ctenophore’s wide distribution in the central Baltic Sea, its ability for rapid population growth, and its potential influence on fish stocks by competing for food and by preying on fish eggs and newly hatched larvae, close monitoring of the future development of M. leidyi in the Baltic Sea is strongly recommended.
    Type of Medium: Online Resource
    ISSN: 1818-5487
    Language: English
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  • 2
    Keywords: Hochschulschrift
    Type of Medium: Online Resource
    Pages: 1 Online-Ressource (111 Seiten = 8 MB) , Illustrationen, Graphen, Karten
    Edition: 2021
    Language: English
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  • 3
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    In:  Supplement to: Jaspers, Cornelia; Huwer, Bastian; Weiland-Bräuer, Nancy; Clemmesen, Catriona (2018): First record of the non-indigenous jellyfish Blackfordia virginica (Mayer, 1910) in the Baltic Sea. Helgoland Marine Research, 72(1), https://doi.org/10.1186/s10152-018-0513-7
    Publication Date: 2023-08-28
    Description: Positions, sampling times and occurence data for the non-indigenous jellyfish species Blackfordia virginica in NW Europe.
    Keywords: 19-13; AL324; AL324_698-1; AL324_699-3; AL324_700-1; AL324_701-3; AL324_702-1; AL324_703-3; AL324_704-1; AL324_705-2; AL324_706-1; AL324_707-2; AL324_708-1; AL324_709-3; AL324_710-1; AL324_713-1; AL324_714-3; AL324_715-1; AL324_716-3; AL324_717-3; AL324_718-1; AL324_719-2; AL324_720-1; AL324_721-2; AL324_722-1; AL324_723-2; AL324_724-1; AL324_725-2; AL324_726-1; AL324_727-2; AL324_728-1; AL324_729-3; AL324_730-1; AL324_731-2; AL324_738-1; AL324_739-2; AL324_740-1; AL324_741-3; AL324_742-1; AL324_743-2; AL324_744-1; AL324_745-2; AL324_746-1; AL324_747-2; AL324_748-1; AL324_749-2; AL324_750-1; AL358; AL358_522-1; AL358_523-2; AL358_524-1; AL358_525-2; AL358_526-1; AL358_527-2; AL358_528-1; AL358_529-2; AL358_530-1; AL358_531-2; AL358_532-1; AL358_533-2; AL358_534-1; AL358_535-2; AL358_535-3; AL358_537-2; AL358_538-1; AL358_539-2; AL358_540-1; AL358_541-2; AL358_546-2; AL358_547-1; AL358_548-2; AL358_549-1; AL358_550-2; AL358_551-1; AL358_552-2; AL358_553-1; AL358_555-2; AL358_556-1; AL358_557-2; AL358_559-2; AL358_560-1; AL358_561-2; AL358_562-1; AL358_563-2; AL358_564-1; AL358_565-2; AL358_570-1; AL358_571-2; AL358_572-1; AL358_573-2; AL358_574-1; AL358_575-2; AL358_576-1; AL421; AL421_481-1; AL421_482-2; AL421_483-1; AL421_484-2; AL421_485-1; AL421_486-2; AL421_487-1; AL421_488-2; AL421_489-1; AL421_490-2; AL421_491-1; AL421_492-2; AL421_493-1; AL421_494-2; AL421_495-1; AL421_496-2; AL421_497-1; AL421_498-1; AL421_499-2; AL421_500-1; AL421_501-2; AL421_502-1; AL421_503-2; AL421_504-1; AL421_505-2; AL421_506-1; AL421_507-1; AL421_508-2; AL421_509-1; AL421_510-2; AL421_511-1; AL421_512-2; AL421_513-1; AL421_514-2; AL421_515-1; AL421_516-2; AL421_517-1; AL421_518-2; AL421_519-1; AL421_519-2; AL421_521-1; AL421_522-2; AL421_523-1; AL421_524-2; AL421_525-1; AL442; AL442_1055-1; AL442_1056-2; AL442_1057-1; AL442_1058-2; AL442_1059-1; AL442_1060-3; AL442_1061-1; AL442_1062-2; AL442_1063-1; AL442_1064-2; AL442_1065-1; AL442_1066-2; AL442_1067-1; AL442_1068-2; AL442_1069-1; AL442_1070-2; AL442_1071-1; AL442_1072-2; AL442_1074-1; AL442_1075-2; AL442_1076-1; AL442_1077-3; AL442_1078-1; AL442_1079-2; AL442_1080-1; AL442_1081-2; AL442_1082-1; AL442_1083-2; AL442_1084-1; AL442_1085-2; AL442_1086-1; AL442_1087-2; AL442_1088-1; AL442_1089-2; AL442_1090-1; AL442_1091-2; AL442_1092-1; AL442_1093-2; AL442_1094-1; AL442_1095-2; AL442_1096-1; AL442_1097-2; AL442_1098-1; AL442_1099-2; AL442_1100-1; AL461; AL461_605-2; AL461_606-1; AL461_607-2; AL461_608-1; AL461_609-2; AL461_610-1; AL461_611-2; AL461_612-1; AL461_613-2; AL461_614-1; AL461_615-2; AL461_616-1; AL461_617-2; AL461_618-1; AL461_619-2; AL461_620-1; AL461_621-2; AL461_622-1; AL461_623-2; AL461_624-1; AL461_625-2; AL461_626-1; AL461_627-2; AL461_628-1; AL461_629-2; AL461_630-1; AL461_631-2; AL461_632-1; AL461_633-2; AL461_634-1; AL461_635-2; AL461_636-1; AL461_637-2; AL461_638-1; AL461_639-2; AL461_640-1; AL461_641-2; AL461_642-1; AL461_643-2; AL461_644-1; AL461_645-2; AL461_646-1; AL461_647-2; AL461_648-1; AL461_649-2; AL499; AL499_10-2; AL499_11-2; AL499_12-2; AL499_1-3; AL499_13-2; AL499_14-2; AL499_15-2; AL499_16-2; AL499_17-2; AL499_18-2; AL499_19-2; AL499_20-2; AL499_2-1; AL499_21-2; AL499_22-2; AL499_23-1; AL499_24-2; AL499_25-1; AL499_26-2; AL499_27-1; AL499_28-2; AL499_29-1; AL499_30-2; AL499_31-1; AL499_3-2; AL499_32-2; AL499_33-1; AL499_34-2; AL499_35-1; AL499_36-2; AL499_37-1; AL499_38-2; AL499_39-1; AL499_40-2; AL499_4-1; AL499_41-1; AL499_42-2; AL499_43-1; AL499_44-2; AL499_45-1; AL499_47-2; AL499_48-1; AL499_49-2; AL499_50-1; AL499_51-2; AL499_5-2; AL499_52-3; AL499_53-1; AL499_54-1; AL499_55-2; AL499_56-1; AL499_57-2; AL499_58-1; AL499_59-2; AL499_60-1; AL499_61-2; AL499_62-1; AL499_6-3; AL499_63-2; AL499_64-2; AL499_65-3; AL499_66-3; AL499_67-2; AL499_68-2; AL499_69-3; AL499_70-2; AL499_7-1; AL499_71-3; AL499_74-2; AL499_75-2; AL499_76-2; AL499_77-1; AL499_78-2; AL499_8-2; AL499_9-2; Alkor (1990); BB01; BB02; BB03; BB04; BB05; BB06; BB07; BB08; BB09; BB10; BB11; BB12; BB13; BB14; BB15; BB16; BB17; BB18; BB19; BB20; BB21; BB22; BB23; BB24; BB25; BB26; BB27; BB28; BB29; BB30; BB31; BB32; BB33; BB34; BB35; BB36; BB37; BB38; BB39; BB40; BB41; BB42; BB43; BB44; BB45; BONGO; Bongo net; Bornholm Basin; BY1; BY15; BY2; BY20A; BY32; BY5; CTD/Rosette; CTD-RO; GB96; GD56; GD57; GD58; GD59; GD59a; GD60; GD60a; GD63; H14; H18; KB03; KB12; Kiel-Canal; Monitoring station; MONS; MSN; MULT; Multiple investigations; Multiple opening/closing net; N1; N2; SW14; SW4; T4; T5; T6; T7; T8
    Type: Dataset
    Format: application/zip, 2 datasets
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  • 4
    Publication Date: 2023-08-28
    Keywords: Blackfordia virginica; Comment; Kiel-Canal; Monitoring station; MONS; Month; Salinity; Salinity, standard deviation; Sampling date; Standard deviation; Temperature, water; Temperature, water, standard deviation
    Type: Dataset
    Format: text/tab-separated-values, 298 data points
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  • 5
    Publication Date: 2023-08-28
    Keywords: 19-13; AL324; AL324_698-1; AL324_699-3; AL324_700-1; AL324_701-3; AL324_702-1; AL324_703-3; AL324_704-1; AL324_705-2; AL324_706-1; AL324_707-2; AL324_708-1; AL324_709-3; AL324_710-1; AL324_713-1; AL324_714-3; AL324_715-1; AL324_716-3; AL324_717-3; AL324_718-1; AL324_719-2; AL324_720-1; AL324_721-2; AL324_722-1; AL324_723-2; AL324_724-1; AL324_725-2; AL324_726-1; AL324_727-2; AL324_728-1; AL324_729-3; AL324_730-1; AL324_731-2; AL324_738-1; AL324_739-2; AL324_740-1; AL324_741-3; AL324_742-1; AL324_743-2; AL324_744-1; AL324_745-2; AL324_746-1; AL324_747-2; AL324_748-1; AL324_749-2; AL324_750-1; AL358; AL358_522-1; AL358_523-2; AL358_524-1; AL358_525-2; AL358_526-1; AL358_527-2; AL358_528-1; AL358_529-2; AL358_530-1; AL358_531-2; AL358_532-1; AL358_533-2; AL358_534-1; AL358_535-2; AL358_535-3; AL358_537-2; AL358_538-1; AL358_539-2; AL358_540-1; AL358_541-2; AL358_546-2; AL358_547-1; AL358_548-2; AL358_549-1; AL358_550-2; AL358_551-1; AL358_552-2; AL358_553-1; AL358_555-2; AL358_556-1; AL358_557-2; AL358_559-2; AL358_560-1; AL358_561-2; AL358_562-1; AL358_563-2; AL358_564-1; AL358_565-2; AL358_570-1; AL358_571-2; AL358_572-1; AL358_573-2; AL358_574-1; AL358_575-2; AL358_576-1; AL421; AL421_481-1; AL421_482-2; AL421_483-1; AL421_484-2; AL421_485-1; AL421_486-2; AL421_487-1; AL421_488-2; AL421_489-1; AL421_490-2; AL421_491-1; AL421_492-2; AL421_493-1; AL421_494-2; AL421_495-1; AL421_496-2; AL421_497-1; AL421_498-1; AL421_499-2; AL421_500-1; AL421_501-2; AL421_502-1; AL421_503-2; AL421_504-1; AL421_505-2; AL421_506-1; AL421_507-1; AL421_508-2; AL421_509-1; AL421_510-2; AL421_511-1; AL421_512-2; AL421_513-1; AL421_514-2; AL421_515-1; AL421_516-2; AL421_517-1; AL421_518-2; AL421_519-1; AL421_519-2; AL421_521-1; AL421_522-2; AL421_523-1; AL421_524-2; AL421_525-1; AL442; AL442_1055-1; AL442_1056-2; AL442_1057-1; AL442_1058-2; AL442_1059-1; AL442_1060-3; AL442_1061-1; AL442_1062-2; AL442_1063-1; AL442_1064-2; AL442_1065-1; AL442_1066-2; AL442_1067-1; AL442_1068-2; AL442_1069-1; AL442_1070-2; AL442_1071-1; AL442_1072-2; AL442_1074-1; AL442_1075-2; AL442_1076-1; AL442_1077-3; AL442_1078-1; AL442_1079-2; AL442_1080-1; AL442_1081-2; AL442_1082-1; AL442_1083-2; AL442_1084-1; AL442_1085-2; AL442_1086-1; AL442_1087-2; AL442_1088-1; AL442_1089-2; AL442_1090-1; AL442_1091-2; AL442_1092-1; AL442_1093-2; AL442_1094-1; AL442_1095-2; AL442_1096-1; AL442_1097-2; AL442_1098-1; AL442_1099-2; AL442_1100-1; AL461; AL461_605-2; AL461_606-1; AL461_607-2; AL461_608-1; AL461_609-2; AL461_610-1; AL461_611-2; AL461_612-1; AL461_613-2; AL461_614-1; AL461_615-2; AL461_616-1; AL461_617-2; AL461_618-1; AL461_619-2; AL461_620-1; AL461_621-2; AL461_622-1; AL461_623-2; AL461_624-1; AL461_625-2; AL461_626-1; AL461_627-2; AL461_628-1; AL461_629-2; AL461_630-1; AL461_631-2; AL461_632-1; AL461_633-2; AL461_634-1; AL461_635-2; AL461_636-1; AL461_637-2; AL461_638-1; AL461_639-2; AL461_640-1; AL461_641-2; AL461_642-1; AL461_643-2; AL461_644-1; AL461_645-2; AL461_646-1; AL461_647-2; AL461_648-1; AL461_649-2; AL499; AL499_10-2; AL499_11-2; AL499_12-2; AL499_1-3; AL499_13-2; AL499_14-2; AL499_15-2; AL499_16-2; AL499_17-2; AL499_18-2; AL499_19-2; AL499_20-2; AL499_2-1; AL499_21-2; AL499_22-2; AL499_23-1; AL499_24-2; AL499_25-1; AL499_26-2; AL499_27-1; AL499_28-2; AL499_29-1; AL499_30-2; AL499_31-1; AL499_3-2; AL499_32-2; AL499_33-1; AL499_34-2; AL499_35-1; AL499_36-2; AL499_37-1; AL499_38-2; AL499_39-1; AL499_40-2; AL499_4-1; AL499_41-1; AL499_42-2; AL499_43-1; AL499_44-2; AL499_45-1; AL499_47-2; AL499_48-1; AL499_49-2; AL499_50-1; AL499_51-2; AL499_5-2; AL499_52-3; AL499_53-1; AL499_54-1; AL499_55-2; AL499_56-1; AL499_57-2; AL499_58-1; AL499_59-2; AL499_60-1; AL499_61-2; AL499_62-1; AL499_6-3; AL499_63-2; AL499_64-2; AL499_65-3; AL499_66-3; AL499_67-2; AL499_68-2; AL499_69-3; AL499_70-2; AL499_7-1; AL499_71-3; AL499_74-2; AL499_75-2; AL499_76-2; AL499_77-1; AL499_78-2; AL499_8-2; AL499_9-2; Alkor (1990); Area/locality; BB01; BB02; BB03; BB04; BB05; BB06; BB07; BB08; BB09; BB10; BB11; BB12; BB13; BB14; BB15; BB16; BB17; BB18; BB19; BB20; BB21; BB22; BB23; BB24; BB25; BB26; BB27; BB28; BB29; BB30; BB31; BB32; BB33; BB34; BB35; BB36; BB37; BB38; BB39; BB40; BB41; BB42; BB43; BB44; BB45; BONGO; Bongo net; Bornholm Basin; BY1; BY15; BY2; BY20A; BY32; BY5; Cruise/expedition; CTD/Rosette; CTD-RO; Event label; GB96; GD56; GD57; GD58; GD59; GD59a; GD60; GD60a; GD63; H14; H18; KB03; KB12; LATITUDE; LONGITUDE; MSN; MULT; Multiple investigations; Multiple opening/closing net; N1; N2; Presence/absence; Sampling date; Species; Station label; SW14; SW4; T4; T5; T6; T7; T8
    Type: Dataset
    Format: text/tab-separated-values, 5280 data points
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  • 6
    Publication Date: 2018-08-01
    Repository Name: EPIC Alfred Wegener Institut
    Type: Article , isiRev
    Format: application/pdf
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  • 7
    Publication Date: 2021-02-08
    Description: Highlights: • First long-term study on microplastic in the marine environment • Case study based on a unique sample set from the highly human impacted Baltic Sea • Water column microplastic concentration constant over past three decades • Microplastic concentration in forage fish constant over past three decades • We hypothesise that household waste is the dominant source of Baltic marine plastics. Abstract Microplastic is considered a potential threat to marine life as it is ingested by a wide variety of species. Most studies on microplastic ingestion are short-term investigations and little is currently known about how this potential threat has developed over the last decades where global plastic production has increased exponentially. Here we present the first long-term study on microplastic in the marine environment, covering three decades from 1987 to 2015, based on a unique sample set originally collected and conserved for food web studies. We investigated the microplastic concentration in plankton samples and in digestive tracts of two economically and ecologically important planktivorous forage fish species, Atlantic herring (Clupea harengus) and European sprat (Sprattus sprattus), in the Baltic Sea, an ecosystem which is under high anthropogenic pressure and has undergone considerable changes over the past decades. Surprisingly, neither the concentration of microplastic in the plankton samples nor in the digestive tracts changed significantly over the investigated time period. Average microplastic concentration in the plankton samples was 0.21±0.15particlesm-3. Of 814 fish examined, 20% contained plastic particles, of which 95% were characterized as microplastic (〈5mm) and of these 93% were fibres. There were no significant differences in the plastic content between species, locations, or time of day the fish were caught. However, fish size and microplastic in the digestive tracts were positively correlated, and the fish contained more plastic during summer than during spring, which may be explained by increased food uptake with size and seasonal differences in feeding activity. This study highlights that even though microplastic has been present in the Baltic environment and the digestive tracts of fishes for decades, the levels have not changed in this period. This underscores the need for greater understanding of how plastic is cycled through marine ecosystems. The stability of plastic concentration and contamination over time observed here indicates that the type and level of microplastic pollution may be more closely correlated to specific human activities in a region than to global plastic production and utilization as such.
    Type: Article , PeerReviewed
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  • 8
    Publication Date: 2021-03-19
    Description: Marine invasions are of increasing concern for biodiversity conservation worldwide. Gelatinous macrozooplankton contain members, which have become globally invasive, for example the ctenophore Mnemiopsis leidyi or the hydromedusae Blackfordia virginica. B. virginica is characterised by a large salinity tolerance, with a brackish-water habitat preference, and by a metagenic life history strategy with an alternation between sexually reproducing planktonic medusae and asexually reproducing benthic polyps to complete the life cycle. In this study we analysed 8 years of ichthyoplankton survey data (2010–2017) from the Kiel Canal and 14 ichthyoplankton summer surveys in the central Baltic Sea (2008–2017). We report the first presence of B. virginica in northern Europe, namely from the southwestern Baltic Sea and the Kiel Canal. In the Kiel Canal, B. virginica was first sporadically sighted in 2014 and 2015 and has developed persistent populations since summer 2016. Changes in size-frequency distributions during summer 2016 indicate active recruitment in the Kiel Canal at salinities between 7 and 13 and temperatures 〉 14 °C. Close vicinity to and direct connection with the southwestern Baltic Sea, where B. virginica was observed during 2017, indicate that the Baltic Sea and other brackish-water habitats of Northern Europe are at risk for colonisation of this non-indigenous species. Our results highlight that monitoring activities should consider gelatinous macrozooplankton for standard assessments to allow for the detection of non-indigenous species at an early stage of their colonisation.
    Type: Article , PeerReviewed
    Format: text
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  • 9
    Publication Date: 2019-01-23
    Description: The European sprat (Sprattus sprattus) was a main target species of the German GLOBEC program that investigated the trophodynamic structure and function of the Baltic and North Seas under the influence of physical forcing. This review summarizes literature on the ecophysiology of sprat with an emphasis on describing how environmental factors influence the life-history strategy of this small pelagic fish. Ontogenetic changes in feeding and growth, and the impacts of abiotic and biotic factors on vital rates are discussed with particular emphasis on the role of temperature as a constraint to life-history scheduling of this species in the Baltic Sea. A combination of field and laboratory data suggests that optimal thermal windows for growth and survival change during early life and are wider for eggs (5–17 °C) than in young (8- to 12-mm) early feeding larvae (5–12 °C). As larvae become able to successfully capture larger prey, thermal windows expand to include warmer waters. For example, 12- to 16-mm larvae can grow well at 16 °C and larger, transitional-larvae and early juveniles display the highest rates of feeding and growth at ~18–22 °C. Gaps in knowledge are identified including the need for additional laboratory studies on the physiology and behavior of larvae (studies that will be particularly critical for biophysical modeling activities) and research addressing the role of overwinter survival as a factor shaping phenology and setting limits on the productivity of this species in areas located at the northern limits of its latitudinal range (such as the Baltic Sea). Based on stage- and temperature-specific mortality and growth potential of early life stages, our analysis suggests that young-of-the year sprat would benefit from inhabiting warmer, near-shore environments rather than the deeper-water spawning grounds such as the Bornholm Basin (central Baltic Sea). Utilization of warmer, nearshore waters (or a general increase in Baltic Sea temperatures) is expected to accelerate growth rates but also enhance the possibility for density-dependent regulation of recruitment (e.g., top-down control of zooplankton resources) acting during the late-larval and juvenile stages, particularly when sprat stocks are at high levels.
    Type: Article , PeerReviewed
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  • 10
    Publication Date: 2019-09-23
    Description: Variations in oxygen conditions in the Baltic are influenced by several mechanisms. Generally, the frequency and magnitude of major inflows have been identified as the most crucial process for the renewal of oxygen-depleted water masses in the Baltic Sea. Furthermore, enhanced degradation of suspended organic matter by bacteria over the past few decades has increased oxygen consumption. Finally, the effects of large-scale climate warming are causing long-term variations in oxygen content and saturation as an observed increase in temperature has led to a general decrease in oxygen solubility of water masses. Oxygen-dependent relationships based on field data and laboratory experiments were used to analyse the impact of the observed decrease in oxygen content on eastern Baltic cod (Gadus morhua) stock-specific processes (e.g. survival rates of eggs, settlement probability of juveniles, habitat utilization of spawning fish, age structure of successful spawners, food consumption rates of adult fish). The observed long-term decline in oxygen conditions in the Baltic Sea has had a seemingly generally negative impact on oxygen-related processes for the different life stages of eastern Baltic cod. Experimentally derived results of oxygen-driven processes were validated by field data.
    Type: Article , PeerReviewed
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