[{"data":1,"prerenderedAt":-1},["ShallowReactive",2],{"_public_publisher_byId_4128dd95-92d7-462e-8061-2b7d930add0f":3,"_public_publication_all{\"sortAscending\":false,\"sortField\":\"updateTime\",\"page\":0,\"size\":10,\"facet\":true,\"searchKey\":\"publisherId:4128dd95-92d7-462e-8061-2b7d930add0f,\"}":32},{"code":4,"data":5,"meta":20},"SUCCESS",{"id":6,"createTime":7,"updateTime":8,"relativeEntities":9,"slug":10,"properties":11,"entityType":18,"verifyStatus":19,"verifyTime":20,"verifyNote":20,"syncStatus":19,"languages":20,"translateLanguages":20,"viewCount":21,"subjectFields":22,"manageAffiliations":23,"indexDatabases":24,"url":20,"thumbnailPath":20,"statistic":25,"gsStatistic":20,"type":20,"analyzePriority":20},"4128dd95-92d7-462e-8061-2b7d930add0f","2024-04-16T01:53:11.884+00:00","2024-12-25T09:55:31.967+00:00",[],"Springer-Science-and-Business-Media-LLC",{"issn":12,"eissn":14,"title":16},{"VOID":13},"0174-3597",{"VOID":15},"1438-3888",{"EN":17},"Springer Science and Business Media LLC","PUBLISHER","PENDING",null,0,[],[],[],{"impactFactor":21,"impactFactorByYear":26,"i10Index":27,"i10IndexLast5Year":21,"totalPublication":27,"totalPublicationByYear":28,"totalCitation":29,"totalCitationByYear":30,"totalCitationPerPublication":29,"totalCitationPerPublicationByYear":31,"hindexLast5Year":27,"hindex":27},{},1,{"1984":27},11,{"1984":29},{"1984":29},{"meta":33,"data":35},{"total":34},"1704",[36,97,227,331,520,653,708,807,861,940],{"id":37,"createTime":38,"updateTime":39,"relativeEntities":40,"slug":41,"properties":42,"entityType":51,"verifyStatus":52,"verifyTime":39,"verifyNote":53,"syncStatus":19,"languages":20,"translateLanguages":20,"viewCount":21,"primaryUrl":54,"fullTextUrl":20,"authors":55,"publicationType":73,"publisherRelationship":74,"citationCount":20,"citationInfo":20,"publishDate":94,"publishYear":95,"citationAnalyzeStatus":19,"lastCitationAnalyze":20,"indexDatabases":20,"openAccess":20,"references":20,"isForceReanalyzing":96},"99bf0cd5-49ac-4266-974d-2c2de8d1eb8a","2024-01-26T07:16:30.960+00:00","2025-01-07T23:59:11.991+00:00",[],"Reproduction-and-fecundity-of-the-musselmytilus-edulis-at-helgoland-North-sea-",{"references":43,"abstract":45,"title":47,"doi":49},{"VOID":44},"Baird, R. H., 1966. Factors affecting the growth and condition of mussels (Mytilus edulis L.). — Fishery Invest., Lond. (Ser. 2)25, 1–33.\nBayne, B. L., 1964. Primary and secondary settlement inMytilus edulis L. (Mollusca). — J. Anim. Ecol.33, 513–523.\nBayne, B. L. & Thompson, R. J., 1970. Some physiological consequences of keepingMytilus edulis in the laboratory. — Helgoländer wiss. Meeresunters.20, 526–552.\nBayne, B. L., Gabbott, P. A. & Widdows, J., 1975. Some effects of stress in the adult on the eggs and larvae ofMytilus edulis L. — J. mar. biol. Ass. U. K.55, 675–689.\nBayne, B. L., Holland, D. L., Moore, M. N., Lowe, D. M. & Widdows, J., 1978. Further studies on the effects of stress in the adult on the eggs ofMytilus edulis. — J. mar. biol. Ass. U. K.58, 825–842.\nBayne, B. L. & Worrall, C. M., 1980. Growth and production of musselsMytilus edulis from two populations. — Mar. Ecol. Prog. Ser.3, 317–328.\nBouxin, H., 1954. Observations sur le frai deMytilus edulis var.galloprovincialis Lmk. Dates précises de frai. Facteurs provoquant l'émission des produits génitaux. — ICES spec. scient. Meeting \"Oyster and Mussel Culture\"36.\nCampbell, S. A., 1969. Seasonal cycle in the carotenoid content inMytilus edulis. — Mar. Biol.4, 227–232.\nCheckley, D. M. Jr., 1982. Selective feeding by atlantic herring (Clupea harengus) larvae on zooplankton in natural assemblages. — Mar. Ecol. Prog. Ser.9, 245–253.\nChipperfield, P. N. J., 1953. Observations on the breeding and settlement ofMytilus edulis L. in British waters. — J. mar. biol. Ass. U. K.32, 449–476.\nCossa, D., Bourget, E. & Piuze, J., 1979. Sexual maturation as a source of variation in the relationship between cadmium concentration and body weight ofMytilus edulis L. — Mar. Pollut. Bull.10, 174–176.\nCrisp, D. J., 1974. Energy relations of marine invertebrate larvae. — Thalassia jugosl.10, 103–120.\nDare, P. J., 1976. Settlement, growth and production of the mussel,Mytilus edulis L. in Morecambe Bay, England. — Fishery Invest., Lond. (Ser. 2)28, 1–25.\nDayton, P., 1971. Competition, disturbance and community organization: the provision and subsequent utilization of space in a rocky intertidal community. — Ecol. Monogr.41, 351–389.\nField, I. A., 1909. The food value of the sea mussel. — Bull. U. S. Bur. Fish.29, 85–128.\nField, I. A., 1922. Biology and economic value of the sea musselMytilus edulis. — Bull. U. S. Bur. Fish.38, 127–259.\nFish, C. J. & Johnson, M. W., 1937. The biology of the zooplankton in the Bay of Fundy and the Gulf of Maine with special reference to production and distribution. — J. biol. Bd Can.3, 189–322.\nGiese, A. C., 1959. Comparative physiology. Annual reproductive cycles of marine invertebrates. — A. Rev. Physiol.21, 547–576.\nGriffiths, R. J., 1977. Reproductive cycles in littoral populations ofChoromytilus meridionalis Kr. andAulacomya ater Molina with a quantitative assessment of gamete production in the former. — J. exp. mar. Biol. Ecol.30, 53–71.\nGriffiths, R. J., 1981. Production and energy flow in relation to age and shore level in the bivalveChoromytilus meridionalis (Kr.). — Estuar. coast. mar. Sci.13, 477–493.\nHarger, J. R. E., 1972. Variation and relative \"niche\" size in the sea musselMytilus edulis in association withMytilus californianus. — Veliger14, 275–282.\nHernroth, L. & Ackefors, H., 1979. The zooplankton of the Baltic proper. A long-term investigation of the fauna, its biology and ecology. — Rep. Fishery Bd Sweden2, 1–66.\nJohnstone, J., 1898. The spawning of the mussel (Mytilus edulis). — Proc. Trans. Liverpool biol. Soc.13, 104–121.\nKändler, R., 1926. Muschellarven aus dem Helgoländer Plankton. — Wiss. Meeresunters. (Helgoland)16, 1–8.\nKautsky, N., 1982. Quantitative studies on gonad cycle, fecundity, reproductive output and recruitment in a balticMytilus edulis population. — Mar. Biol.68, 143–160.\nKühl, H., 1972. Hydrography and biology of the Elbe estuary. — Oceanogr. mar. Biol.10, 225–309.\nLebour, M. V., 1933. The importance of larval mollusca in the plankton. — J. Cons. perm. int. Explor. Mer8, 335–343.\nLowe, D. M., Moore, M. N. & Bayne, B. L., 1982. Aspects of gametogenesis in the marine musselMytilus edulis L. — J. mar. biol. Ass. U. K. 62, 133–145.\nLubet, P., 1956. Effets d'ablation des centres nerveux sur l'émission des gamètes chezMytilus edulis etChlamys varia L. — Annls Sci. nat.18, 175–183.\nLubet, P., 1957. Cycle sexuel deM. edulis etMytilus galloprovincialis dans le bassin d'Arcachon (Gironde). — Année biol.33, 19–29.\nLubet, P., 1959. Recherches sur le cycle de l'émission des gamètes chez les Mytilidés et les Pectinidés. — Revue Trav. Inst. scient. tech. Pêch. marit.23, 387–548.\nLunetta, J. E., 1969. Reproductive physiology of the musselMytilus perna. — Bolm Fac. Filos. Ciênc. Univ. S Paulo.26, 33–111.\nMateeva, T. A., 1948. The biology ofMytilus edulis L. in eastern Murman. — Trudy murmansk. biol. Inst.1, 215–241.\nMenge, B. A. & Sutherland, J. P., 1976. Species diversity gradients: synthesis of the roles of predation, competition, and temporal heterogeneity. — Am. Nat.110, 351–369.\nMix, C. M., Hemingway, S. J. & Schaffer, R. L., 1982. Benzo(a)pyrene concentrations in somatic and gonad tissues of bay mussels,Mytilus edulis. — Bull. environ. Contam. Toxicol.28, 46–51.\nOckelmann, K. W., 1965. Developmental types in marine bivalves and their distribution along the Atlantic coast of Europe. In: Proceedings of the European Malacological Congress. Ed. by L. R. Cox & J. F. Peake. Malacological Soc. of London, London1, 25–35.\nPelseneer, P., 1926. La proportion relative des sexes chez les animaux et particulièrement chez les mollusques. — Mém. Acad. r. Belg. Cl. Sci.8, 1–258.\nPilar-Aguirre, M. P., 1979. Biologia del mejillón (M. edulis) de cultivo de la Ria de Vigo. — Boln Inst. esp. Oceanogr.5, 109–159.\nRees, C. B., 1954. Continuous plankton records: the distribution of lamellibranch larvae in the North Sea, 1950–51. — Bull. mar. Ecol.4, 21–46.\nSchram, J. A., 1970. Studies on the meroplankton in the inner Oslofjord. II. Seasonal differences and seasonal changes in the specific distribution of larvae. — Nytt Mag. Zool.18, 1–21.\nSeed, R., 1969. The ecology ofMytilus edulis L. (Lamellibranchiata) on exposed rocky shores. I. Breeding and settlement. — Oecologia3, 277–316.\nSeed, R., 1975. Reproduction inMytilus (Mollusca: Bivalvia) in European waters. — Pubbl. Staz. zool. Napoli (Suppl.)39, 317–334.\nSeed, R. & Brown, R. A., 1975. The influence of reproductive cycle, growth, and mortality on population structure inModiolus modiolus (L.),Cerastoderma edule (L.) andMytilus edulis L. (Mollusca: Bivalvis). In: 9th European Marine Biology Symposium. Ed. by H. Barnes. Aberdeen Univ. Press, Aberdeen, 257–274.\nSprung, M., 1980. Das Frühjahrswachstum der Miesmuschel (Mytilus edulis L.) bei kontinuierlicher und diskontinuierlicher Nahrungszufuhr im Freiland-Biotop und unter Laborbedingungen. Dipl.-Arb., Univ. Kiel, 82 pp.\nSugiura, Y., 1959. Seasonal change in sexual maturity and sexuality ofMytilus edulis. — Bull. Jap. Soc. scient. Fish.25, 1–6.\nSunila, I., 1981. Reproduction ofMytilus edulis L. (Bivalvia) in a brackish water area, the Gulf of Finland. — Annls zool. Fenn.18, 121–128.\nTheisen, B. F., 1968. Growth and mortality of culture mussels in the Danish wadden sea. — Meddr Danm. Fisk. — og Havunders.6, 47–78.\nThompson, R. J., 1979. Fecundity and reproductive effort of the blue mussel (Mytilus edulis), the sea urchin(Strongylocentrotus droebachiensis), and the snow crab(Chionoectes opilio) from populations in Nova Scotia and Newfoundland. — J. Fish. Res. Bd Can.36, 955–964.\nThorson, G., 1946. Reproduction and larval development of Danish marine bottom invertebrates. — Meddr Kommn Danm. Fisk. — og Havunders. (Plankton)4, 1–523.\nWerner, B., 1940. Über die Entwicklung und Artunterscheidung von Muschellarven des Nordseeplanktons, unter gesonderter Berücksichtigung der Schalenentwicklung. — Zool. Jb. (Anat. Ontogenie Tiere)66, 1–54.\nWhite, K. M., 1937. Mytilus. — L. M. B. C. Mem. typ. Br. mar. Pl. Anim.31, 1–177.\nWiddows, J., 1978. Combined effects of body size, food concentration and season on the physiology ofMytilus edulis. — J. mar. biol. Ass. U. K.58, 109–124.\nWilson, B. R. & Hodgkin, E. P., 1967. A comparative account of the reproductive cycles of five species of marine mussels (Bivalvia: Mytilidae) in the vicinity of Freemantle, W. Australia. — Aust. J. mar. Freshwat. Res.18, 175–203.\nWilson, J., 1887. On the development of the common mussel (Mytilus edulis L.). — Rep. Fish. Bd Scotl.5, 247–256.",{"EN":46},"The reproductive cycle of aMytilus edulis population in the lower tidal zone at the island of Helgoland from Spring 1980 to Summer 1981 is described. In both years the spawning period extended from the end of April until the end of June at water temperatures between 6° and 14°C. The gametes were built up again in autumn and most individuals were mature in February. Sex ratio did not differ significantly from 1:1. Fecundity, egg diameter and gamete weight of this and another population in the subtidal zone were assessed and size frequency distribution of shell lengths was established. Based on data of body weight prior to spawning, the following tendencies could be outlined: animals of the intertidal population had significantly smaller eggs than those from the subtidal area. Although the soft body biomass per unit area of the subtidal population was nearly double that of the tidal, their annual egg output was nearly the same (2.3 × 109 eggs m−2). This was achieved by a smaller size at the onset of sexual maturation (18 mm instead of 30 mm shell length) and a higher egg output at comparable shell lengths in the intertidal. In both populations, large animals contributed most to gamete production, although they did not necessarily dominate in biomass.",{"EN":48},"Reproduction and fecundity of the musselmytilus edulis at helgoland (North sea)",{"VOID":50},"10.1007\u002FBF01983629","PUBLICATION","VERIFIED","Auto Verify","https:\u002F\u002Flink.springer.com\u002Farticle\u002F10.1007\u002FBF01983629",[56],{"id":57,"sortIndex":21,"researcher":20,"roles":58,"affiliations":60,"properties":70},"7f9bd0f2-69bb-4f86-8600-c0163b6ee85c",[59],"AUTHOR",[61],{"id":20,"sortIndex":21,"affiliation":62,"properties":20},{"id":63,"createTime":64,"updateTime":64,"relativeEntities":65,"slug":20,"properties":66,"entityType":69,"verifyStatus":19,"verifyTime":20,"verifyNote":20,"syncStatus":19,"languages":20,"translateLanguages":20,"viewCount":21},"bd35110c-38b8-4c0b-b3b4-26e48852c126","2024-01-26T07:16:30.971+00:00",[],{"title":67},{"VI":68},"Biologische Anstalt Helgoland (Meeresstation), Helgoland, Federal Republik of Germany","AFFILIATION",{"title":71},{"VI":72},"M. Sprung","ARTICLE",{"url":54,"publisher":75,"properties":89},{"id":6,"createTime":7,"updateTime":8,"relativeEntities":76,"slug":10,"properties":77,"entityType":18,"verifyStatus":19,"verifyTime":20,"verifyNote":20,"syncStatus":19,"languages":20,"translateLanguages":20,"viewCount":21,"subjectFields":81,"manageAffiliations":82,"indexDatabases":83,"url":20,"thumbnailPath":20,"statistic":84,"gsStatistic":20,"type":20,"analyzePriority":20},[],{"issn":78,"eissn":79,"title":80},{"VOID":13},{"VOID":15},{"EN":17},[],[],[],{"impactFactor":21,"impactFactorByYear":85,"i10Index":27,"i10IndexLast5Year":21,"totalPublication":27,"totalPublicationByYear":86,"totalCitation":29,"totalCitationByYear":87,"totalCitationPerPublication":29,"totalCitationPerPublicationByYear":88,"hindexLast5Year":27,"hindex":27},{},{"1984":27},{"1984":29},{"1984":29},{"volume":90,"pages":92},{"VOID":91},"36",{"VOID":93},"243-255","1983-09-01",1983,false,{"id":98,"createTime":99,"updateTime":99,"relativeEntities":100,"slug":101,"properties":102,"entityType":51,"verifyStatus":19,"verifyTime":20,"verifyNote":20,"syncStatus":19,"languages":20,"translateLanguages":20,"viewCount":21,"primaryUrl":113,"fullTextUrl":20,"authors":114,"publicationType":73,"publisherRelationship":210,"citationCount":20,"citationInfo":20,"publishDate":225,"publishYear":226,"citationAnalyzeStatus":19,"lastCitationAnalyze":20,"indexDatabases":20,"openAccess":20,"references":20,"isForceReanalyzing":96},"5b98a43a-c811-4737-bfc1-886a6faeef0e","2024-04-05T23:58:10.574+00:00",[],"Age-and-growth-of-Glycymeris-longior-Sowerby-1832-clam-at-the-southern-edge-of-its-distribution-Argentine-Sea-",{"references":103,"keywords":105,"abstract":107,"title":109,"doi":111},{"VOID":104},"Rhoads DC, Lutz RA. Skeletal growth of aquatic organisms: biological records of environmental change. New York: Plenum Press; 1980.\nRichardson C. Molluscs as archives of environmental change. Oceanogr Mar Biol Annu Rev. 2001;39:103–64.\nBeamish RJ, McFarlane GA. The forgotten requirement for age validation in fisheries biology. Trans Am Fish Soc. 1983;112(6):735–43.\nCampana SE. Accuracy, precision and quality control in age determination, including a review of the use and abuse of age validation methods. J Fish Biol. 2001;59:197–242.\nSchöne BR. The curse of physiology—challenges and opportunities in the interpretation of geochemical data from mollusk shells. Geo Mar Lett. 2008;28:269–85.\nThomas RDK. Functional morphology, ecology, and evolutionary conservatism in the Glycymerididae (Bivalvia). Palaeontology. 1975;18:217–54.\nFAO. http:\u002F\u002Fwww.fao.org. Accessed 1 Nov 2019.\nPoutiers JM. Bivalves (Acéphales, Lamellibranches, Péléccypodes). In: Fisher W, Bauchot ML, Scheider M, editors. Fiches FAO d´identification des espèces pour les besoins de la pêche 37. Volume 1. Végétaux et Invertébrés. Rome: FAO; 1987. p. 369–512.\nBeaver PE, Bucher DJ, Joannes-Boyau R. Growth patterns of three bivalve species targeted by the Ocean Cockle Fishery, southern New South Wales: Eucrassatella kingicola (Lamarck, 1805); Glycymeris grayana (Dunker, 1857); and Callista (Notocallista) kingii (Gray, 1827). Molluscan Res. 2017;37:104–12.\nAbbot RT. Bivalves. In: Fischer W, Bianchi G, Scott WB, editors. FAO species identification sheets for fishery purposes Eastern Central Atlantic (Fishing Areas 34, 47 in part). Rome: FAO; 1982. p. 1–17.\nArguelles J, Taipe A, Srmiento M, Valdez R. Prospección del recurso mejillón Glycymeris ovata en el área del callao (12–13 Mayo 2013). Instituto del Mar del Perú. 2014.\nPoutiers JM. Bivalves of the world. Annotaed list of marine and brackish water species of interest to fisheries. FAO Catalogue. 1992 (Unpublished).\nBerthou P, Blanchard M, Noël P, Vergnaud-Grazzini C. Stable isotope analysis of shells for age determination in four bivalve species from the Normand-Breton Gulf (western English Channel). International Council for the Exploration of the Sea Shellfish Committed, report. 1986.\nPeharda M, Crnčević M, Bušelić I, Richardson CA, Ezgeta-Balić D. Growth and longevity of Glycymeris nummaria (Linnaeus, 1758) from the eastern Adriatic, Croatia. J Shellfish Res. 2012;31:947–50.\nBrocas WM, Reynolds DJ, Butler PG, Richardson CA, Scourse JD, Ridgway ID, Ramsay K. The dog cockle, Glycymeris glycymeris (L.), a new annually-resolved sclerochronological archive for the Irish Sea. Palaeogeogr Palaeoclimatol Palaeoecol. 2013;373:133–40.\nRoyer C, Thébault J, Chauvaud L, Olivier F. Structural analysis and paleoenvironmental potential of dog cockle shells (Glycymeris glycymeris) in Brittany, northwest France. Palaeogeogr Palaeoclimatol Palaeoecol. 2013;373:123–32.\nBušelić I, Peharda M, Reynolds DJ, Butler PG, González AR, Ezgeta-Balić D, Vilibić I, Grbec B, Hollyman P, Richardson CA. Glycymeris bimaculata (Poli, 1795)—a new sclerochronological archive for the Mediterranean? J Sea Res. 2015;95:139–48.\nPeharda M, Thébault J, Markulin K, Schöne BR, Janeković I, Chauvaud L. Contrasting shell growth strategies in two Mediterranean bivalves revealed by oxygen-isotope ratio geochemistry: the case of Pecten jacobaeus and Glycymeris pilosa. Chem Geol. 2017. https:\u002F\u002Fdoi.org\u002F10.1016\u002Fj.chemgeo.2017.09.029.\nReynolds DJ, Hall IR, Slater SM, Scourse JD, Halloran PR, Sayer MDJ. Reconstructing past seasonal to multicentennial-scale variability in the NE atlantic ocean using the long-lived marine bivalve mollusk Glycymeris glycymeris. Paleoceanography. 2017;32:1153–73.\nScarabino V. Moluscos del golfo San Matías (provincia de Río Negro, República Argentina). Inventario y claves para su identificación. Comunicaciones de la Sociedad Malacológica del Uruguay. 1977;4:177–285.\nZelaya DG. Marine bivalves from the Argentine coast and continental shelf: species diversity and assessment of the historical knowledge. Am Malacol Bull. 2015;33:245–62.\nRocha VP, Matthews Cascon H. The family glycymerididae (Mollusca: Bivalvia) from North and Northeast Brazil. Arquivos de Ciências do. 2014;47(2):64–71.\nBayer MS, Gordillo S. A new Pleistocene species of Glycymeris (Bivalvia, Glycymerididae) from northern Patagonia, Argentina. Ameghiniana. 2013;50(2):265–9.\nDoldan MS. Patrones y procesos de la dinámica poblacional de la ostra puelche, Ostrea puelchana, (D’ Orbigny, 1842). PhD thesis. Universidad de Buenos Aires, Argentina. 2013.\nRivas AL, Beier EJ. Temperature and salinity fields in the North Patagonian gulfs. Oceanol Acta. 1990;13:15–20.\nPiola AR, Scasso LM. Circulación en el golfo San Matías. Geoacta. 1988;15:33–51.\nGagliardini DA, Rivas AL. Environmental characteristics of San Matías Gulf obtained from LANDSAT-TM and ETM + data. Gayana. 2004;68:186–93.\nWilliams GN, Zaidman PC, Glembocki NG, Narvarte MA, González RA, Esteves JL, Gagliardini DA. Comparison between remotely-sensed sea-surface temperature (AVHRR) and in situ records in San Matías Gulf (Patagonia, Argentina). LAJAR. 2014;2:192–203.\nWilliams GN, Dogliotti AI, Zaidman P, Solis M, Narvarte MA, Gonzalez RC, Esteves JL, Gagliardini DA. Assessment of remotely-sensed sea-surface temperature and chlorophyll-a concentration in San Matías Gulf (Patagonia, Argentina). Cont Shelf Res. 2013;52:159–71.\nMorsan EM, Pappalardo P, Doldan MS. Growth compensation as a regulatory mechanism of purple clam Amiantis purpurata population dynamics in Patagonia. Mar Ecol Prog Ser. 2011;443:207–16.\nGenchi SA, Carbone ME, Piccolo MC, Perillo ME. Déficit hídrico en San Antonio Oeste, Argentina. Revista de Climatología. 2010;10:29–43.\nServicio Meteorológico Nacional http:\u002F\u002Fwww.smn.gob.ar\u002F.\nYamaguchi DK. A simple method for cross-dating increment cores from living trees. Can J For Res. 1991;21(3):414–6.\nPanfili, J, Morales-Nin, B. Semi-direct validation. In: Panfili J, Pontual H, Troadec H, Wright PJ, eds. Manual of fish sclerochronology. Ifremer-IRD coedition, Brest (France). 2002. p. 129–34.\nQuinn TJ, Deriso RB. Quantitative fish dynamics. Oxford: Oxford University Press; 1999.\nPinheiro JC, Bates DM. Mixed-effects models in S and S-PLUS. New York: Springer-Verlag; 2002 (Corrected third printing).\nLindstrom MJ, Bates DM. Nonlinear mixed effects models for repeated measures data. Biometrics. 1990;46:673–87.\nMunro JL, Pauly D. A simple method for comparing the growth of fishes and invertebrates. Fishbyte. 1983;1:5–6.\nPauly D. Gill size and temperature as governing factors in fish growth: a generalization of von Bertalanffy’s growth formula. 1979.\nPenttila J, Dery LM. Age determination methods for Northwest Atlantic species. NOAA Technical Report. NMFS. 1988;72:129–32.\nNémeth A, Kern Z. Sclerochronological study of a Glycymeris vangentsumi population from the Madeira Islands. Front Earth Sci. 2018;6:76.\nWalliser EO, Schöne BR, Tütken T, Zirkel J, Grimm KI, Pross J. The bivalve Glycymeris planicostalis as a high-resolution paleoclimate archive for the Rupelian (Early Oligocene) of central Europe. Clim Past. 2015;11:653–68.\nArendt JD. Adaptive intrinsic growth rates: an integration across taxa. Q Rev Biol. 1997;72:149–77.\nSavina M. Modélisation écologique des populations de palourdes roses (Paphia rhomboïdes) et d’amandes de mer (Glycymeris glycymeris) en Manche. Ph.D. Thesis, Université d’Aix-Marseille II. 2004.\nPeharda M, Black BA, Purroy A, Mihanović H. The bivalve Glycymeris pilosa as a multidecadal environmental archive for the Adriatic and Mediterranean Seas. Mar Environ Res. 2016;119:79–87.\nPaparazzo FE, Crespi-Abril AC, Gonçalves RJ, Barbieri ES, Gracia Villalobos LL, Solís ME, Soria G. Patagonian dust as a source of macronutrients in the Southwest Atlantic Ocean. Oceanography. 2018;31(4):33–9.\nGalap C, Netchitaı̈lo P, Leboulenger F, Grillot J-P. Variations of fatty acid contents in selected tissues of the female dog cockle (Glycymeris glycymeris L., Mollusca, Bivalvia) during the annual cycle. Comp Biochem Physiol A: Mol Integr Physiol. 1999;122:241–54.\nNajdek M, Ezgeta-Balić D, Blažina M, Crnčević M, Peharda M. Potential food sources of Glycymeris nummaria (Mollusca: Bivalvia) during the annual cycle indicated by fatty acid analysis. Sci Mar. 2016;80:123–9.\nFeatherstone AM, Butler PG, Peharda M, Chauvaud L, Thébault J. Influence of riverine input on the growth of Glycymeris glycymeris in the Bay of Brest, North-West France. PLoS ONE. 2017;12:e0189782.\nNaidu KS, Anderson JT. Aspects of scallop recruitment on St. Pierre Bank in relation to oceanography and implications for resource management. CAFSAC Res. Doc. 84\u002F29. 1984. 15 pp.\nMorsan EM, Orensanz J. Age structure and growth in an unusual population of purple clams, Amiantis purpuratus (Lamarck, 1818) (Bivalvia; Veneridae), from Argentine Patagonia. J Shellfish Res. 2004;2004(23):73–80.\nArnold WS, Marelli DC, Bray CP, Harrison MM. Recruitment of bay scallops Argopecten irradians in Floridan Gulf of Mexico waters: scales of coherence. Mar Ecol Prog Ser. 1998;170:143–57.\nOrensanz JL, Parma AM, Smith SJ. Dynamics, assessment, and management of exploited natural scallop populations. Developments in aquaculture and fisheries science. New York: Elsevier; 2016. p. 611–95.\nItuarte CF. Sobre la sexualidad de Glycymeris longior (Sowerby) (Mollusca Pelecypoda). Neotropica. 1979;25:161–5.\nNakaoka M. Yearly variation in recruitment and its effect on population dynamics in Yoldia notabilis (Mollusca: Bivalvia), analyzed using projection matrix model. Res Popul Ecol. 1993;35:199–213.\nEckman JE. Closing the larval loop: linking larval ecology to the population dynamics of marine benthic invertebrates. J Exp Mar Biol Ecol. 1996;200:207–37.\nRoughgarden J, Gaines S, Possingham H. Recruitment dynamics in complex life cycles. Science. 1988;241:1460–6.\nAmor A. The larval development of Arenicola brasiliensis Nonato Polychaeta, Arenicolidae. Physis. 1981;39:79–83.\nPiacentino GL, Luzzatto DC. Hippocampus patagonicus sp. nov., nuevo caballito de mar para la Argentina (Pisces, Syngnathiformes). Revista del Museo Argentino de Ciencias Naturales. 2004;6:339–49.\nMorsan EM, Kroeck MA. Reproductive cycle of purple clam, Amiantis purpurata (Bivalvia: Veneridae) in northern Patagonia (Argentina). J Mar Biol Assoc UK. 2005;85:367–73.\nPascual MS, Zampatti EA, Iribarne OO. Population structure and demography of the puelche oyster (Ostrea puelchana, D’Orbigny, 1841) grounds in Northern Patagonia, Argentina. J Shellfish Res. 2001;20:1003–10.",{"EN":106},"",{"EN":108},"Even though Glycymeris longior is a clam widely distributed in the SW Atlantic Ocean, little is known about its biology and life history. The present study assessed the periodicity of the internal growth increments of G. longior using thin shell sections. Each internal growth increment was composed of two alternating bands: a translucent band (light-coloured when viewed with transmitted light) and an opaque band (dark-coloured). Annual formation for each pair of bands was demonstrated. The formation of the annual growth increments was synchronous among individuals. Growth was determined from live clams collected at El Sótano, Argentine Sea (age range = 29 to 69 years). According to the growth model, G. longior grows fast during the first 5 years of life and then growth becomes slower in later years; individuals reached 50% and 90% of maximum size at 5 and 13 years of age, respectively. High variability was found in shell height for the first 10 years: differences up to 5–7 mm among individuals were registered for the first 2 years of age, and up to 11 mm between the ages of 3 and 9 years. The growth performance index phi-prime (φ′) and the index of growth performance (P) of G. longior were compared with those of other Glycymeris species. Our results indicate that G. longior is a slow-growing species with a long lifespan (maximum longevity = 69 years).",{"EN":110},"Age and growth of Glycymeris longior (Sowerby, 1832) clam at the southern edge of its distribution (Argentine Sea)",{"VOID":112},"10.1186\u002Fs10152-020-0534-x","https:\u002F\u002Fhmr.biomedcentral.com\u002Farticles\u002F10.1186\u002Fs10152-020-0534-x",[115,138,160,188],{"id":116,"sortIndex":21,"researcher":20,"roles":117,"affiliations":118,"properties":135},"dd9982c5-56dd-41b9-976b-926f6c2211b7",[59],[119,127],{"id":20,"sortIndex":21,"affiliation":120,"properties":20},{"id":121,"createTime":122,"updateTime":122,"relativeEntities":123,"slug":20,"properties":124,"entityType":69,"verifyStatus":19,"verifyTime":20,"verifyNote":20,"syncStatus":19,"languages":20,"translateLanguages":20,"viewCount":21},"45ccca4c-bd4f-4207-9195-d85794700fbd","2024-01-09T17:01:24.588+00:00",[],{"title":125},{"VI":126},"Departamento de Ecología, Universidad Católica de la Santísima Concepción, Concepción, Chile",{"id":20,"sortIndex":21,"affiliation":128,"properties":20},{"id":129,"createTime":130,"updateTime":130,"relativeEntities":131,"slug":20,"properties":132,"entityType":69,"verifyStatus":19,"verifyTime":20,"verifyNote":20,"syncStatus":19,"languages":20,"translateLanguages":20,"viewCount":21},"191d815b-3c4c-4312-a20b-639d48f69f74","2024-01-29T17:58:07.414+00:00",[],{"title":133},{"VI":134},"Escuela Superior de Ciencias Marinas, Universidad Nacional del Comahue, San Antonio Oeste, Argentina",{"title":136},{"VI":137},"Lucas H. Gimenez",{"id":139,"sortIndex":140,"researcher":20,"roles":141,"affiliations":142,"properties":157},"46d2593c-08fa-4ed0-b60f-f4b06c780500",3,[59],[143,152],{"id":20,"sortIndex":21,"affiliation":144,"properties":20},{"id":145,"createTime":146,"updateTime":146,"relativeEntities":147,"slug":148,"properties":149,"entityType":69,"verifyStatus":19,"verifyTime":20,"verifyNote":20,"syncStatus":19,"languages":20,"translateLanguages":20,"viewCount":21},"9e50bda3-c8f1-41c5-aadf-27d58c5762bf","2024-04-05T23:58:10.592+00:00",[],"Centro-de-Investigaci%C3%B3n-Aplicada-y-Transferencia-Tecnol%C3%B3gica-en-Recursos-Marinos-Almirante-Storni-CIMAS-Universidad-Nacional-del-Comahue-CONICET-MAGyP-R%C3%ADo-Negro-G%C3%BCemes-San-Antonio-Oeste-Argentina",{"title":150},{"VI":151},"Centro de Investigación Aplicada y Transferencia Tecnológica en Recursos Marinos “Almirante Storni” (CIMAS), Universidad Nacional del Comahue – CONICET – MAGyP Río Negro. Güemes, San Antonio Oeste, Argentina",{"id":20,"sortIndex":21,"affiliation":153,"properties":20},{"id":129,"createTime":130,"updateTime":130,"relativeEntities":154,"slug":20,"properties":155,"entityType":69,"verifyStatus":19,"verifyTime":20,"verifyNote":20,"syncStatus":19,"languages":20,"translateLanguages":20,"viewCount":21},[],{"title":156},{"VI":134},{"title":158},{"VI":159},"Enrique M. Morsan",{"id":161,"sortIndex":162,"researcher":20,"roles":163,"affiliations":164,"properties":185},"a6404355-3419-4f88-aa66-c6721805f10c",2,[59],[165,170,180],{"id":20,"sortIndex":21,"affiliation":166,"properties":20},{"id":145,"createTime":146,"updateTime":146,"relativeEntities":167,"slug":148,"properties":168,"entityType":69,"verifyStatus":19,"verifyTime":20,"verifyNote":20,"syncStatus":19,"languages":20,"translateLanguages":20,"viewCount":21},[],{"title":169},{"VI":151},{"id":20,"sortIndex":21,"affiliation":171,"properties":20},{"id":172,"createTime":173,"updateTime":174,"relativeEntities":175,"slug":176,"properties":177,"entityType":69,"verifyStatus":19,"verifyTime":20,"verifyNote":20,"syncStatus":19,"languages":20,"translateLanguages":20,"viewCount":21},"ceceaa3c-bf29-4365-a0bf-ccc6b749f9e9","2023-12-07T04:31:35.727+00:00","2024-09-26T17:08:38.498+00:00",[],"Consejo-Nacional-de-Investigaciones-Cient%C3%ADficas-y-T%C3%A9cnicas-CONICET-Ciudad-Aut%C3%B3noma-de-Buenos-Aires-Argentina",{"title":178},{"VI":179},"Consejo Nacional de Investigaciones Científicas y Técnicas (CONICET), Ciudad Autónoma de Buenos Aires, Argentina",{"id":20,"sortIndex":21,"affiliation":181,"properties":20},{"id":129,"createTime":130,"updateTime":130,"relativeEntities":182,"slug":20,"properties":183,"entityType":69,"verifyStatus":19,"verifyTime":20,"verifyNote":20,"syncStatus":19,"languages":20,"translateLanguages":20,"viewCount":21},[],{"title":184},{"VI":134},{"title":186},{"VI":187},"Paula C. Zaidman",{"id":189,"sortIndex":27,"researcher":20,"roles":190,"affiliations":191,"properties":207},"45f78a58-1838-4717-85e4-09a4992d0347",[59],[192,197,202],{"id":20,"sortIndex":21,"affiliation":193,"properties":20},{"id":172,"createTime":173,"updateTime":174,"relativeEntities":194,"slug":176,"properties":195,"entityType":69,"verifyStatus":19,"verifyTime":20,"verifyNote":20,"syncStatus":19,"languages":20,"translateLanguages":20,"viewCount":21},[],{"title":196},{"VI":179},{"id":20,"sortIndex":21,"affiliation":198,"properties":20},{"id":129,"createTime":130,"updateTime":130,"relativeEntities":199,"slug":20,"properties":200,"entityType":69,"verifyStatus":19,"verifyTime":20,"verifyNote":20,"syncStatus":19,"languages":20,"translateLanguages":20,"viewCount":21},[],{"title":201},{"VI":134},{"id":20,"sortIndex":21,"affiliation":203,"properties":20},{"id":145,"createTime":146,"updateTime":146,"relativeEntities":204,"slug":148,"properties":205,"entityType":69,"verifyStatus":19,"verifyTime":20,"verifyNote":20,"syncStatus":19,"languages":20,"translateLanguages":20,"viewCount":21},[],{"title":206},{"VI":151},{"title":208},{"VI":209},"María del Socorro Doldan",{"url":20,"publisher":211,"properties":20},{"id":6,"createTime":7,"updateTime":8,"relativeEntities":212,"slug":10,"properties":213,"entityType":18,"verifyStatus":19,"verifyTime":20,"verifyNote":20,"syncStatus":19,"languages":20,"translateLanguages":20,"viewCount":21,"subjectFields":217,"manageAffiliations":218,"indexDatabases":219,"url":20,"thumbnailPath":20,"statistic":220,"gsStatistic":20,"type":20,"analyzePriority":20},[],{"issn":214,"eissn":215,"title":216},{"VOID":13},{"VOID":15},{"EN":17},[],[],[],{"impactFactor":21,"impactFactorByYear":221,"i10Index":27,"i10IndexLast5Year":21,"totalPublication":27,"totalPublicationByYear":222,"totalCitation":29,"totalCitationByYear":223,"totalCitationPerPublication":29,"totalCitationPerPublicationByYear":224,"hindexLast5Year":27,"hindex":27},{},{"1984":27},{"1984":29},{"1984":29},"2020-01-13",2020,{"id":228,"createTime":229,"updateTime":230,"relativeEntities":231,"slug":232,"properties":233,"entityType":51,"verifyStatus":52,"verifyTime":230,"verifyNote":53,"syncStatus":19,"languages":20,"translateLanguages":20,"viewCount":21,"primaryUrl":240,"fullTextUrl":20,"authors":241,"publicationType":73,"publisherRelationship":309,"citationCount":20,"citationInfo":20,"publishDate":329,"publishYear":330,"citationAnalyzeStatus":19,"lastCitationAnalyze":20,"indexDatabases":20,"openAccess":20,"references":20,"isForceReanalyzing":96},"6a862553-a84e-4824-90bf-8e2bd86b2ef3","2024-01-29T18:08:33.563+00:00","2024-12-27T23:57:08.935+00:00",[],"Investigation-of-the-effects-of-current-velocity-on-mussel-feeding-and-mussel-bed-stability-using-an-annular-flume",{"abstract":234,"title":236,"doi":238},{"EN":235}," An annular flume was used to measure the effect of increasing current velocity on mussel (Mytilus edulis) feeding rate and the stability of mussel beds sampled from the mouth of the Exe estuary (SW England). It was found that, in contrast to earlier flume studies, the feeding rates of mussels from open coast sites were unaffected by current velocities up to 0.8 m s–1. Algal cell depletion in the water column above mussels was a function of current velocity, increasing with declining currents below 0.05 m s–1. The erodability\u002Fstability of the mussel bed, measured in terms of critical erosion velocity, sediment mass eroded and mean erosion rate, was found to be a function of the nature of the substrate and the density of the mussels. Erosion of mussel beds on sandy substrate showed a non-linear relationship with mussel bed density. In comparison with the sand (0% mussel cover), sediment resuspension was about five and four times higher for 25% and 50% cover, respectively. This was due to the increased turbulence and scouring around the clumps of mussels in low-density parts of the bed, and this resulted in some mussels detaching from the bed. At ~100% mussel cover, the sandy bed was more protected by the dense surface layer of mussels, and none became detached during erosion due to the high number of byssal attachments between individuals. The sediment resuspension from the 100% mussel cover was about three times lower than the 0% cover. Erosion of the bed with 50% cover resulted in burial of a large proportion of the mussels, with a 6 cm increase in sediment level. However, the mussels returned to the surface and recovered in 1–2 days, due to a combination of migration upwards and substrate settlement. Channels on the edge of the main Exmouth mussel bed were characterised by a more stable substrate comprising pebbles and sand with varying mussel densities. At these sites, where mussels experience high current velocities on spring tides (up to 0.9 m s–1), there was no difference between the erodability of pebble\u002Fsand substrate with 0% and 100% mussel cover. The sediment erosion was also lower than the 100% mussel cover on the sandy substrate, particularly at currents >0.4 m s–1. Sampling of different parts of the mussel bed at Exmouth showed mussels at low densities were made up of smaller clumps with a lower mass ratio of mussels to attached substrate (pebbles\u002Fsand), thus providing a greater degree of anchorage.",{"EN":237},"Investigation of the effects of current velocity on mussel feeding and mussel bed stability using an annular flume",{"VOID":239},"10.1007\u002Fs10152-001-0100-0","https:\u002F\u002Fhmr.biomedcentral.com\u002Farticles\u002F10.1007\u002Fs10152-001-0100-0",[242,257,272,284,296],{"id":243,"sortIndex":162,"researcher":20,"roles":244,"affiliations":245,"properties":254},"abfc2a5a-702e-46e7-8612-a3c598e0c254",[59],[246],{"id":20,"sortIndex":21,"affiliation":247,"properties":20},{"id":248,"createTime":249,"updateTime":249,"relativeEntities":250,"slug":20,"properties":251,"entityType":69,"verifyStatus":19,"verifyTime":20,"verifyNote":20,"syncStatus":19,"languages":20,"translateLanguages":20,"viewCount":21},"e4e7d024-a164-417f-a88c-786c5ad7bb15","2024-01-29T18:08:33.582+00:00",[],{"title":252},{"VI":253},"Plymouth Marine Laboratory, Prospect Place, The Hoe, Plymouth PL1 3DH, UK, UK",{"title":255},{"VI":256},"Mary D. Brinsley",{"id":258,"sortIndex":27,"researcher":20,"roles":259,"affiliations":260,"properties":269},"a38b5d1e-7751-42d0-9f0e-4f8b46a23909",[59],[261],{"id":20,"sortIndex":21,"affiliation":262,"properties":20},{"id":263,"createTime":264,"updateTime":264,"relativeEntities":265,"slug":20,"properties":266,"entityType":69,"verifyStatus":19,"verifyTime":20,"verifyNote":20,"syncStatus":19,"languages":20,"translateLanguages":20,"viewCount":21},"7a4fc397-d613-4b04-91ad-904a931e641f","2024-01-29T18:08:33.604+00:00",[],{"title":267},{"VI":268},"School of Marine Biology and Aquaculture, James Cook University, Queensland 4811, Australia, Australia",{"title":270},{"VI":271},"John S. Lucas",{"id":273,"sortIndex":140,"researcher":20,"roles":274,"affiliations":275,"properties":281},"8ba49021-ea55-4c5d-93e0-705f1b827c63",[59],[276],{"id":20,"sortIndex":21,"affiliation":277,"properties":20},{"id":248,"createTime":249,"updateTime":249,"relativeEntities":278,"slug":20,"properties":279,"entityType":69,"verifyStatus":19,"verifyTime":20,"verifyNote":20,"syncStatus":19,"languages":20,"translateLanguages":20,"viewCount":21},[],{"title":280},{"VI":253},{"title":282},{"VI":283},"Peter N. Salkeld",{"id":285,"sortIndex":21,"researcher":20,"roles":286,"affiliations":287,"properties":293},"a8c566ac-41cb-458a-87ce-63581a219d25",[59],[288],{"id":20,"sortIndex":21,"affiliation":289,"properties":20},{"id":248,"createTime":249,"updateTime":249,"relativeEntities":290,"slug":20,"properties":291,"entityType":69,"verifyStatus":19,"verifyTime":20,"verifyNote":20,"syncStatus":19,"languages":20,"translateLanguages":20,"viewCount":21},[],{"title":292},{"VI":253},{"title":294},{"VI":295},"John Widdows",{"id":297,"sortIndex":298,"researcher":20,"roles":299,"affiliations":300,"properties":306},"db02d4bb-68c1-4e44-882e-1ad68ed389ac",4,[59],[301],{"id":20,"sortIndex":21,"affiliation":302,"properties":20},{"id":248,"createTime":249,"updateTime":249,"relativeEntities":303,"slug":20,"properties":304,"entityType":69,"verifyStatus":19,"verifyTime":20,"verifyNote":20,"syncStatus":19,"languages":20,"translateLanguages":20,"viewCount":21},[],{"title":305},{"VI":253},{"title":307},{"VI":308},"Fred J. Staff",{"url":240,"publisher":310,"properties":324},{"id":6,"createTime":7,"updateTime":8,"relativeEntities":311,"slug":10,"properties":312,"entityType":18,"verifyStatus":19,"verifyTime":20,"verifyNote":20,"syncStatus":19,"languages":20,"translateLanguages":20,"viewCount":21,"subjectFields":316,"manageAffiliations":317,"indexDatabases":318,"url":20,"thumbnailPath":20,"statistic":319,"gsStatistic":20,"type":20,"analyzePriority":20},[],{"issn":313,"eissn":314,"title":315},{"VOID":13},{"VOID":15},{"EN":17},[],[],[],{"impactFactor":21,"impactFactorByYear":320,"i10Index":27,"i10IndexLast5Year":21,"totalPublication":27,"totalPublicationByYear":321,"totalCitation":29,"totalCitationByYear":322,"totalCitationPerPublication":29,"totalCitationPerPublicationByYear":323,"hindexLast5Year":27,"hindex":27},{},{"1984":27},{"1984":29},{"1984":29},{"volume":325,"pages":327},{"VOID":326},"56",{"VOID":328},"3-12","2002-02-09",2002,{"id":332,"createTime":333,"updateTime":334,"relativeEntities":335,"slug":336,"properties":337,"entityType":51,"verifyStatus":52,"verifyTime":334,"verifyNote":53,"syncStatus":19,"languages":348,"translateLanguages":20,"viewCount":21,"primaryUrl":350,"fullTextUrl":20,"authors":351,"publicationType":73,"publisherRelationship":419,"citationCount":434,"citationInfo":435,"publishDate":437,"publishYear":438,"citationAnalyzeStatus":19,"lastCitationAnalyze":20,"indexDatabases":20,"openAccess":20,"references":439,"isForceReanalyzing":96},"01ce1298-c786-4d13-866f-a82b02f4d5fe","2024-04-16T04:22:00.674+00:00","2024-12-10T23:55:54.755+00:00",[],"Codium-fragile-rhizomatous-growth-in-the-Zostera-thief-of-eastern-Canada",{"mag":338,"keywords":340,"openalex":341,"abstract":343,"title":344,"doi":346},{"VOID":339},"2078153009",{},{"VOID":342},"W2078153009",{},{"EN":345},"Codium fragile: rhizomatous growth in the Zostera thief of eastern Canada",{"VOID":347},"10.1007\u002Fs10152-004-0173-7",[349],"EN","https:\u002F\u002Fhmr.biomedcentral.com\u002Farticles\u002F10.1007\u002Fs10152-004-0173-7",[352,369,389,405],{"id":353,"sortIndex":162,"researcher":20,"roles":354,"affiliations":355,"properties":364},"89cbb07c-e0ab-49f8-be52-520b6be1387e",[],[356],{"id":20,"sortIndex":21,"affiliation":357,"properties":20},{"id":358,"createTime":359,"updateTime":359,"relativeEntities":360,"slug":20,"properties":361,"entityType":69,"verifyStatus":19,"verifyTime":20,"verifyNote":20,"syncStatus":19,"languages":20,"translateLanguages":20,"viewCount":21},"260cbb1f-63fb-4c35-bafd-cfd92324a177","2023-12-02T09:01:34.171+00:00",[],{"title":362},{"VI":363},"Department of Biology, St. Francis Xavier University, Antigonish, Canada",{"openalex":365,"title":367},{"VOID":366},"A5045471434",{"EN":368},"Charlene B. Hubbard",{"id":370,"sortIndex":140,"researcher":20,"roles":371,"affiliations":372,"properties":382},"bbe1a05b-f072-4f8a-9641-40e66c6316f2",[],[373],{"id":20,"sortIndex":21,"affiliation":374,"properties":20},{"id":375,"createTime":376,"updateTime":376,"relativeEntities":377,"slug":378,"properties":379,"entityType":69,"verifyStatus":19,"verifyTime":20,"verifyNote":20,"syncStatus":19,"languages":20,"translateLanguages":20,"viewCount":21},"cffe4810-7c6d-49d8-a336-0c420e19040f","2024-04-09T11:50:23.747+00:00",[],"Department-of-Oceanography-Chonnam-National-University-Kwangju-Korea",{"title":380},{"EN":381},"Department of Oceanography, Chonnam National University, Kwangju, Korea",{"openalex":383,"orcid":385,"title":387},{"VOID":384},"A5077401920",{"VOID":386},"https:\u002F\u002Forcid.org\u002F0000-0002-5401-3515",{"EN":388},"Kwang Young Kim",{"id":390,"sortIndex":21,"researcher":20,"roles":391,"affiliations":392,"properties":398},"8d61613d-95cd-4da6-839b-6b5b39f7788d",[],[393],{"id":20,"sortIndex":21,"affiliation":394,"properties":20},{"id":358,"createTime":359,"updateTime":359,"relativeEntities":395,"slug":20,"properties":396,"entityType":69,"verifyStatus":19,"verifyTime":20,"verifyNote":20,"syncStatus":19,"languages":20,"translateLanguages":20,"viewCount":21},[],{"title":397},{"VI":363},{"openalex":399,"orcid":401,"title":403},{"VOID":400},"A5062636945",{"VOID":402},"https:\u002F\u002Forcid.org\u002F0000-0001-5126-6608",{"EN":404},"David J. Garbary",{"id":406,"sortIndex":27,"researcher":20,"roles":407,"affiliations":408,"properties":414},"20ec94b0-5b2b-4e86-bf1c-546a1d0517b7",[],[409],{"id":20,"sortIndex":21,"affiliation":410,"properties":20},{"id":358,"createTime":359,"updateTime":359,"relativeEntities":411,"slug":20,"properties":412,"entityType":69,"verifyStatus":19,"verifyTime":20,"verifyNote":20,"syncStatus":19,"languages":20,"translateLanguages":20,"viewCount":21},[],{"title":413},{"VI":363},{"openalex":415,"title":417},{"VOID":416},"A5091787126",{"EN":418},"Stephen Fraser",{"url":20,"publisher":420,"properties":20},{"id":6,"createTime":7,"updateTime":8,"relativeEntities":421,"slug":10,"properties":422,"entityType":18,"verifyStatus":19,"verifyTime":20,"verifyNote":20,"syncStatus":19,"languages":20,"translateLanguages":20,"viewCount":21,"subjectFields":426,"manageAffiliations":427,"indexDatabases":428,"url":20,"thumbnailPath":20,"statistic":429,"gsStatistic":20,"type":20,"analyzePriority":20},[],{"issn":423,"eissn":424,"title":425},{"VOID":13},{"VOID":15},{"EN":17},[],[],[],{"impactFactor":21,"impactFactorByYear":430,"i10Index":27,"i10IndexLast5Year":21,"totalPublication":27,"totalPublicationByYear":431,"totalCitation":29,"totalCitationByYear":432,"totalCitationPerPublication":29,"totalCitationPerPublicationByYear":433,"hindexLast5Year":27,"hindex":27},{},{"1984":27},{"1984":29},{"1984":29},33,{"total":434,"publishYear":20,"statisticByYear":436},{"2012":27,"2013":140,"2014":162,"2015":162,"2016":140,"2019":27,"2021":27,"2023":27},"2004-10-01",2004,[440,443,447,451,455,458,462,466,470,474,477,480,484,487,491,494,498,502,506,509,512,516],{"id":20,"text":441,"url":20,"identifiers":442},"Bird CJ, Dadswell MJ, Grund DW (1993) First record of the potential nuisance alga Codium fragile ssp. tomentosoides (Chlorophyta, Caulerpales) in Atlantic Canada. Proc Nova Scotia Inst Sci 40:11?17",{},{"id":20,"text":444,"url":20,"identifiers":445},"Borden CA, Stein JR (1969) Reproduction and early development in Codium fragile (Suringar) Hariot: Chlorophyceae. Phycologia 8:91?99",{"doi":446},"10.2216\u002Fi0031-8884-8-2-91.1",{"id":20,"text":448,"url":20,"identifiers":449},"Carlton JT, Scanlon JA (1985) Progression and dispersal of an introduced alga: Codium fragile ssp. tomentosoides (Chlorophyta) on the Atlantic coast of North America. Bot Mar 28:155?165",{"doi":450},"10.1515\u002Fbotm.1985.28.4.155",{"id":20,"text":452,"url":20,"identifiers":453},"Ceccherelli G, Cinelli F (1999) The role of vegetative fragmentation in dispersal of the invasive alga Caulerpa taxifolia in the Mediterranean. Mar Ecol Prog Ser 182:299?303",{"doi":454},"10.3354\u002Fmeps182299",{"id":20,"text":456,"url":20,"identifiers":457},"Chapman AS, Scheibling RE, Chapman ARO (2004) Species introductions and changes in marine vegetation of Atlantic Canada. In: Claudi R (ed) Alien invasive species: threat to Canadian biodiversity. Natural Resources Canada, Ottawa (in press)",{},{"id":20,"text":459,"url":20,"identifiers":460},"Dromgoole FI (1982) The buoyant properties of Codium. Bot Mar 25:391?397",{"doi":461},"10.1515\u002Fbotm.1982.25.8.391",{"id":20,"text":463,"url":20,"identifiers":464},"Fralick RA, Mathieson AC (1972) Winter fragmentation of Codium fragile (Suringar) Hariot ssp. tomentosoides (van Goor) Silva (Chlorophyceae, Siphonales) in New England. Phycologia 11:67?70",{"doi":465},"10.2216\u002Fi0031-8884-11-1-67.1",{"id":20,"text":467,"url":20,"identifiers":468},"Garbary DJ, Vandermeulen H, Kim KY (1997) Codium fragile ssp. tomentosoides (Chlorophyta) invades the Gulf of St. Lawrence, Atlantic Canada. Bot Mar 40:537?540",{"doi":469},"10.1515\u002Fbotm.1997.40.1-6.537",{"id":20,"text":471,"url":20,"identifiers":472},"Hubbard CB, Garbary DJ (2002) Morphological variation of Codium fragile (Chlorophyta) in eastern Canada. Bot Mar 45:476?485",{"doi":473},"10.1515\u002FBOT.2002.050",{"id":20,"text":475,"url":20,"identifiers":476},"Locke A, Hanson JM, Ellis KM, Klassen GJ, Garbary DJ, MacNair NG (2002) Effects of recent invasions on ecosystems in the southern gulf of St. Lawrence: predictions and early observations. In: Proceedings of the 11th International Invasive Species Conference, 25?28 February 2002, Alexandria, Canada, pp 143?153",{},{"id":20,"text":478,"url":20,"identifiers":479},"Loosanoff VL (1975) Introduction of Codium in New England waters. Fish Bull 73:215?218",{},{"id":20,"text":481,"url":20,"identifiers":482},"Malinowski KC, Ramus J (1973) Growth of the green alga Codium fragile in a Connecticut estuary. J Phycol 9:102?110",{"doi":483},"10.1111\u002Fj.0022-3646.1973.00102.x",{"id":20,"text":485,"url":20,"identifiers":486},"Mathieson AC, Dawes CJ, Harris LG, Hehre EJ (2003) Expansion of the Asiatic green alga Codium fragile ssp.tomentosoides in the Gulf of Maine. Rhodora 105:1?53",{},{"id":20,"text":488,"url":20,"identifiers":489},"Scheibling RE, Anthony SX (2001) Feeding, growth and reproduction of sea urchins (Strongylocentrotus droebachiensis) on single and mixed diets of kelp (Laminaria spp.) and the invasive alga Codium fragile ssp. tomentosoides. Mar Biol 139:139?146",{"doi":490},"10.1007\u002Fs002270100567",{"id":20,"text":492,"url":20,"identifiers":493},"Schmidt AL, Scheibling RE (2003) Density, recruitment, growth, and survival of the invasive green alga Codium fragile ssp. tomentosoides in tidepools on a rocky shore in Nova Scotia. Abstract Book, Plant Canada 2003, 25?29 June 2003, St. Francis Xavier University, Antigonish, Nova Scotia, p 33",{},{"id":20,"text":495,"url":20,"identifiers":496},"Seymour NR, Miller AG, Garbary DJ (2002) Decline of Canada geese (Branta canadensis) and common goldeneye (Bucephala clangula) associated with collapse of eelgrass (Zostera marina) in a Nova Scotia estuary. Helgol Mar Res 56:198?202",{"doi":497},"10.1007\u002Fs10152-002-0112-4",{"id":20,"text":499,"url":20,"identifiers":500},"Smith CM, Walters LJ (1999) Fragmentation as a strategy for Caulerpa species: fates of fragments and implications for management of an invasive weed. Mar Ecol 20:307?319",{"doi":501},"10.1046\u002Fj.1439-0485.1999.2034079.x",{"id":20,"text":503,"url":20,"identifiers":504},"Trowbridge CD (1993) Interactions between an ascoglossan sea slug and its green algal host: branch loss and role of epiphytes. Mar Ecol Prog Ser 101:263?273",{"doi":505},"10.3354\u002Fmeps101263",{"id":20,"text":507,"url":20,"identifiers":508},"Trowbridge CD (1998) Ecology of the green macroalga Codium fragile (Suringar) Hariot 1889: invasive and non-invasive subspecies. Annu Rev Oceanogr Mar Biol 36:1?64",{},{"id":20,"text":510,"url":20,"identifiers":511},"Wassman R, Ramus J (1973) Seaweed invasion. Nat Hist 82:24?36",{},{"id":20,"text":513,"url":20,"identifiers":514},"Williams SL (1984) The uptake of sediment ammonium and translocation in the marine green macroalga Caulerpa cupressoides. Limnol Oceanogr 29:374?379",{"doi":515},"10.4319\u002Flo.1984.29.2.0374",{"id":20,"text":517,"url":20,"identifiers":518},"Williams SL, Fisher TR (1985) Kinetics of the nitrogen-15 labeled ammonium uptake by Caulerpa cupressoides (Chlorophyta). J Phycol 21:287?296",{"doi":519},"10.1111\u002Fj.0022-3646.1985.00287.x",{"id":521,"createTime":522,"updateTime":523,"relativeEntities":524,"slug":525,"properties":526,"entityType":51,"verifyStatus":52,"verifyTime":523,"verifyNote":53,"syncStatus":19,"languages":20,"translateLanguages":20,"viewCount":21,"primaryUrl":535,"fullTextUrl":20,"authors":536,"publicationType":73,"publisherRelationship":631,"citationCount":20,"citationInfo":20,"publishDate":651,"publishYear":652,"citationAnalyzeStatus":19,"lastCitationAnalyze":20,"indexDatabases":20,"openAccess":20,"references":20,"isForceReanalyzing":96},"9b41d9ca-59b0-4df4-9cbf-6599c9e612b4","2023-11-25T20:13:45.756+00:00","2025-01-16T23:55:24.739+00:00",[],"Interrelationships-of-bacteria-meiofauna-and-macrofauna-in-a-Mediterranean-sedimentary-beach-Maremma-Park-NW-Italy-",{"references":527,"abstract":529,"title":531,"doi":533},{"VOID":528},"Albertelli G, Covazzi-Harriague A, Danovaro R, Fabiano M, Fraschetti S, Pusceddu A (1999) Differential responses of bacteria, meiofauna and macrofauna in a shelf area (Ligurian Sea, NW Mediterranean): role of food availability. J Sea Res 42:11–26\nBell SS (1980) Meiofauna–macrofauna interactions in a high salt marsh habitat. Ecol Monogr 50:487–505\nBell SS, Coull BC (1978) Field evidence that shrimp predation regulates meiofauna. Oecologia 35:141–148\nBrazeiro A (2001) Relationship between species richness and morphodynamics in sandy beaches: what are the underlying factors? Mar Ecol Prog Ser 224:35–44\nBrown AC (1971) The ecology of the sandy beaches of the Cape Peninsula, South Africa. Part 1: Introduction. Trans Roy Soc S Afr 39:247–279\nBrown AC, McLachlan A (1990) Ecology of sandy shores. Elsevier, Amsterdam\nBuchanan JB (1984) Sediment analysis. In: Holme NM, McIntyre AD (eds) Methods for the study of marine benthos. Blackwell Scientific, Oxford, pp 41–64\nClarke KR, Ainsworth M (1993) A method for linking multivariate community structure to environmental variables. Mar Ecol Prog Ser 92:205–209\nClarke KR, Green RH (1988) Statistical design and analysis for a “biological effects” study. Mar Ecol Prog Ser 46:213–226\nClarke KR, Warwick RM (1994) Change in marine communities: an approach to statistical analysis and interpretation. Natural Environmental Research Council, Plymouth Marine Laboratory, Plymouth\nDanovaro R, Fabiano M (1995) Seasonal and interannual variation of benthic bacteria in a seagrass bed of the Mediterranean Sea: relationship with labile organic compounds and other environmental factors. Aquat Micr Ecol 9:17–26\nDefeo O, Brazeiro A, de Alava A, Riestra G (1997) Is sandy beach macrofauna only physically controlled? Role of substrate and competition in Isopods. Estuar Coast Shelf Sci 45:3–462\nDubois M, Gilles K, Hamilton JK, Rebers PA, Smith F (1956) Colorimetric method for determination of sugars and related substances. Anal Chem 28:350–356\nEleftheriou A, Nicholson MD (1975) The effects of exposure on beach fauna. Cah Biol Mar 16:695–710\nFabiano M, Danovaro R, Fraschetti S (1995) A three-year time series of elemental and biochemical composition of organic matter in subtidal sandy sediments of the Ligurian Sea (NW Mediterranean). Cont Shelf Res 15:1453–1469\nFabiano M, Marin V, Misic C, Moreno M, Salvo VS, Vezzulli L (2004) Sedimentary organic matter and bacterial community in microtidal mixed beaches of the Ligurean Sea (NW Mediterranean). Chem Ecol 20:423–435\nFry JC (1990) Direct methods and biomass estimation. In: Grigorova R, Norris JR (eds) Methods in microbiology, vol 22. Academic Press, New York, pp 41–85\nFruin P (2000) Effects of anthropogenic disturbances of tropical soft-bottom benthic communities. Mar Ecol Prog Ser 194:39–53\nGrasshoff K, Ehrhard M, Kremmling K (1983) Methods of seawater analysis. Verlag Chemie, Berlin\nGray JS (1981) The ecology of marine sediments. An introduction to the structure and function of benthic communities. Camb Stud Mod Biol 2:1–185\nHartree EF (1972) Determination of proteins: a modification of the Lowry method that give a linear photometric response. Anal Biochem 48:422–427\nHeip C, Vinx M, Vranken G (1985) The ecology of marine nematodes. Oceanogr Mar Biol Annu Rev 23:399–489\nHiggins RP, Thiel H (1988) Introduction to the study of meiofauna. Smithsonian Institution Press, Washington\nHobbie JE, Daley RJ, Jasper S (1977) Use of Nuclepore filters for counting bacteria by fluorescence microscopy. Appl Environ Microbiol 33:1225–1228\nIncera M, Cividanes SP, Lastra M, Lopez J (2003) Temporal and spatial variability of sedimentary organic matter in sandy beaches on the northwest coast of the Iberian Peninsula. Estuar Coast Shelf Sci 58:55–61\nJedrzejczak MF (2002) Stranded Zostera marina L. vs wrack fauna community interactions on a Baltic sandy beach (Hel, Poland): a short-term pilot study. Part I. Driftline effects of fragmented detritivory, leaching and decay rates. Oceanologia 44:273–286\nKoop K, Griffiths L (1982) The relative significance of bacteria, meio- and macrofauna on an exposed sandy beach. Mar Biol 66:295–300\nKotwicki L, De Troch M, Urban-Malinga B, Gheskiere T, Weslawsky JM (2005) Horizontal and vertical distribution of meiofauna on sandy beaches of the North Sea (The Netherlands, Belgium, France). Helg Mar Res 59:255–264\nMarques JC, Goncalves SC, Pardal MA, Chelazzi L, Colombini I, Fallaci M, Bouslama MF, ElGtari M, Charfi-Cheikhrouha F, Scapini F (2003) Comparison of Talitrus saltator (Amphipoda, Talitridae) biology, dynamics, and secondary production in Atlantic (Portugal) and Mediterranean (Italy and Tunisia) populations. Estuar Coast Shelf Sci 58:127–148\nMcLachlan A, Jaramillo E (1995) Zonation on sandy beaches. Oceanogr Mar Biol Annu Rev 33:305–335\nMcLachlan A, Jaramillo E, Defeo O, Dugan J, de Ruyck A, Coetzee P (1995) Adaptations of bivalves to different beach types. J Exp Mar Biol Ecol 187:147–160\nMoreno M, Granelli V, Albertelli G, Fabiano M (2005a) Meiofaunal distribution in microtidal mixed mixed beaches of the Ligurian Sea (NW Mediterranean). Meiofauna Mar 14:131–137\nMoreno M, Ferrero TJ, Granelli V, Marin V, Albertelli G, Fabiano M (2005b) Across shore variability and trophodynamic features of meiofauna in microtidal beach of the NW Mediterranean. Estuar Coast Shelf Sci 66:357–367\nNovitsky JA, MacSween MC (1989) Microbiology of a high energy beach sediment: evidence for an active and growing community. Mar Ecol Prog Ser 52:71–75\nOlsgard F, Somerfield PJ, Carr MR (1997) Relationships between taxonomic resolution and data transformations in analyses of a macrobenthic community along an established pollution gradient. Mar Ecol Prog Ser 149:173–181\nParsons TR, Maita Y, Lali CM (1984) A manual of chemical and biological methods for seawater analysis. Pergamon, New York\nRouse G, Pleijel F (2001) Polychaetes. Oxford University Press, Oxford, p 364\nSomerfield PJ, Clarke KR (1995) Taxonomic levels, in marine community studies, revisited. Mar Ecol Prog Ser 127:113–119\nStrickland JD, Parsons TR (1972) A practical handbook of seawater analysis. Bull Fish Res Board Canada 167:1–310\nSundbaeck K, Nilsson P, Nilsson C, Joensson B (1996) Balance between autotrophic and heterotrophic components and processes in microbenthic communities of sandy sediments: a field study. Estuar Coast Shelf Sci 43:689–706\nTsutsumi H, Fukunaga S, Fujita N, Sumida M (1990) Relationship between growth of Capitella sp. and organic enrichment of the sediment. Mar Ecol Prog Ser 63:157–162\nTurner SJ, Thrudh SF, Pridmore RD, Hewitt JE, Cummings VJ, Maskery M (1995) Are soft-sediment communities stable? An example from a windy harbour. Mar Ecol Prog Ser 120:219–230\nWarwick RM, Clarke KR (1991) A comparison of some methods for analyzing changes in benthic community structure. J Mar Biol Ass UK 71:225–244",{"EN":530},"Collelungo beach (Maremma Park, NW Italy), was sampled quantitatively for macrofauna, meiofauna and bacteria in May 2003; several physicochemical variables and variables associated with food availability and sediment structure were also measured. Replicated samples were collected from three sites representing natural conditions, an erosion regime, and the influence of the Ombrone River, respectively, as well as from four stations each located in the surf and sublittoral zones. Both uni- and multivariate techniques were used to assess the benthic community structure and the associated environmental variables. Different diversity indices revealed no pattern; in contrast, multivariate techniques applied on the macrobenthic fauna and the polychaete taxocommunity distinguished between the sites located in natural and eroding conditions from the one located nearby the discharges of the Ombrone river. Τhe community patterns deriving from meio- and macrofauna are clearly divergent. The overall benthic faunal community appears to be influenced by both groups of organisms. The patterns of the meio- and macrofaunal communities seem to be affected synergistically by a number of environmental variables, in accordance with the multicausal environmental severity hypothesis. Meiofaunal patterns are more often correlated with bacteria and the protein concentration than are macrofaunal patterns, indicating a potential utilization of bacteria as a food source by the meiofaunal organisms. Total bacterial numbers are associated with the macrofaunal pattern under the erosion regime, probably as a consequence of competition for food between macrofauna and meiofauna.",{"EN":532},"Interrelationships of bacteria, meiofauna and macrofauna in a Mediterranean sedimentary beach (Maremma Park, NW Italy)",{"VOID":534},"10.1007\u002Fs10152-006-0051-6","https:\u002F\u002Fhmr.biomedcentral.com\u002Farticles\u002F10.1007\u002Fs10152-006-0051-6",[537,553,565,578,594,607,619],{"id":538,"sortIndex":140,"researcher":20,"roles":539,"affiliations":540,"properties":550},"8b56c531-3f19-4db9-b548-769815a7fb7f",[59],[541],{"id":20,"sortIndex":21,"affiliation":542,"properties":20},{"id":543,"createTime":544,"updateTime":544,"relativeEntities":545,"slug":546,"properties":547,"entityType":69,"verifyStatus":19,"verifyTime":20,"verifyNote":20,"syncStatus":19,"languages":20,"translateLanguages":20,"viewCount":21},"702057d9-1dd0-4825-92fc-3c3a0b4afcb4","2023-11-25T20:13:45.784+00:00",[],"Department-of-Study-of-the-Territory-and-its-Resources-University-of-Genoa-Genoa-Italy",{"title":548},{"VI":549},"Department of Study of the Territory and its Resources, University of Genoa, Genoa, Italy",{"title":551},{"VI":552},"Susanna Baiardo",{"id":554,"sortIndex":162,"researcher":20,"roles":555,"affiliations":556,"properties":562},"0fb0bf5f-25c8-4186-b317-d74b530358b8",[59],[557],{"id":20,"sortIndex":21,"affiliation":558,"properties":20},{"id":543,"createTime":544,"updateTime":544,"relativeEntities":559,"slug":546,"properties":560,"entityType":69,"verifyStatus":19,"verifyTime":20,"verifyNote":20,"syncStatus":19,"languages":20,"translateLanguages":20,"viewCount":21},[],{"title":561},{"VI":549},{"title":563},{"VI":564},"Valentina Marin",{"id":566,"sortIndex":567,"researcher":20,"roles":568,"affiliations":569,"properties":575},"bc3c3674-e706-4308-9e87-a41b85c46148",5,[59],[570],{"id":20,"sortIndex":21,"affiliation":571,"properties":20},{"id":543,"createTime":544,"updateTime":544,"relativeEntities":572,"slug":546,"properties":573,"entityType":69,"verifyStatus":19,"verifyTime":20,"verifyNote":20,"syncStatus":19,"languages":20,"translateLanguages":20,"viewCount":21},[],{"title":574},{"VI":549},{"title":576},{"VI":577},"Mauro Fabiano",{"id":579,"sortIndex":21,"researcher":20,"roles":580,"affiliations":581,"properties":591},"165ce41c-6421-4279-b8b8-b39936473dfd",[59],[582],{"id":20,"sortIndex":21,"affiliation":583,"properties":20},{"id":584,"createTime":585,"updateTime":585,"relativeEntities":586,"slug":587,"properties":588,"entityType":69,"verifyStatus":19,"verifyTime":20,"verifyNote":20,"syncStatus":19,"languages":20,"translateLanguages":20,"viewCount":21},"d7253e97-2933-42bd-bca4-7b20d3eeb1cf","2023-11-25T20:13:45.767+00:00",[],"Institute-of-Marine-Biology-and-Genetics-Hellenic-Centre-for-Marine-Research-Crete-Greece",{"title":589},{"VI":590},"Institute of Marine Biology and Genetics, Hellenic Centre for Marine Research, Crete, Greece",{"title":592},{"VI":593},"Nafsika Papageorgiou",{"id":595,"sortIndex":596,"researcher":20,"roles":597,"affiliations":598,"properties":604},"06fc85ea-2701-4bfc-b571-11dd9272da69",6,[59],[599],{"id":20,"sortIndex":21,"affiliation":600,"properties":20},{"id":584,"createTime":585,"updateTime":585,"relativeEntities":601,"slug":587,"properties":602,"entityType":69,"verifyStatus":19,"verifyTime":20,"verifyNote":20,"syncStatus":19,"languages":20,"translateLanguages":20,"viewCount":21},[],{"title":603},{"VI":590},{"title":605},{"VI":606},"Anastasios Eleftheriou",{"id":608,"sortIndex":298,"researcher":20,"roles":609,"affiliations":610,"properties":616},"77ecae5d-c59e-46e1-990f-3ee291cd204d",[59],[611],{"id":20,"sortIndex":21,"affiliation":612,"properties":20},{"id":584,"createTime":585,"updateTime":585,"relativeEntities":613,"slug":587,"properties":614,"entityType":69,"verifyStatus":19,"verifyTime":20,"verifyNote":20,"syncStatus":19,"languages":20,"translateLanguages":20,"viewCount":21},[],{"title":615},{"VI":590},{"title":617},{"VI":618},"Christos Arvanitidis",{"id":620,"sortIndex":27,"researcher":20,"roles":621,"affiliations":622,"properties":628},"51d9a5e3-da72-4aac-91aa-218cdf900190",[59],[623],{"id":20,"sortIndex":21,"affiliation":624,"properties":20},{"id":543,"createTime":544,"updateTime":544,"relativeEntities":625,"slug":546,"properties":626,"entityType":69,"verifyStatus":19,"verifyTime":20,"verifyNote":20,"syncStatus":19,"languages":20,"translateLanguages":20,"viewCount":21},[],{"title":627},{"VI":549},{"title":629},{"VI":630},"Mariapaola Moreno",{"url":535,"publisher":632,"properties":646},{"id":6,"createTime":7,"updateTime":8,"relativeEntities":633,"slug":10,"properties":634,"entityType":18,"verifyStatus":19,"verifyTime":20,"verifyNote":20,"syncStatus":19,"languages":20,"translateLanguages":20,"viewCount":21,"subjectFields":638,"manageAffiliations":639,"indexDatabases":640,"url":20,"thumbnailPath":20,"statistic":641,"gsStatistic":20,"type":20,"analyzePriority":20},[],{"issn":635,"eissn":636,"title":637},{"VOID":13},{"VOID":15},{"EN":17},[],[],[],{"impactFactor":21,"impactFactorByYear":642,"i10Index":27,"i10IndexLast5Year":21,"totalPublication":27,"totalPublicationByYear":643,"totalCitation":29,"totalCitationByYear":644,"totalCitationPerPublication":29,"totalCitationPerPublicationByYear":645,"hindexLast5Year":27,"hindex":27},{},{"1984":27},{"1984":29},{"1984":29},{"volume":647,"pages":649},{"VOID":648},"61",{"VOID":650},"31-42","2006-12-21",2006,{"id":654,"createTime":655,"updateTime":656,"relativeEntities":657,"slug":658,"properties":659,"entityType":51,"verifyStatus":52,"verifyTime":668,"verifyNote":53,"syncStatus":19,"languages":20,"translateLanguages":20,"viewCount":162,"primaryUrl":669,"fullTextUrl":20,"authors":670,"publicationType":73,"publisherRelationship":686,"citationCount":20,"citationInfo":20,"publishDate":706,"publishYear":707,"citationAnalyzeStatus":19,"lastCitationAnalyze":20,"indexDatabases":20,"openAccess":20,"references":20,"isForceReanalyzing":96},"d836d37b-0944-4563-82b6-5be299e5c0ca","2023-12-05T07:57:23.313+00:00","2024-06-30T23:52:12.009+00:00",[],"Zur-Morphologie-und-%C3%96kologie-vonPolydora-ciliata-undP-ligni-Polychaeta-Spionidae-",{"references":660,"abstract":662,"title":664,"doi":666},{"VOID":661},"Ankel, W. E., 1937. Prosobranchia. Tierwelt Nord- u. Ostesee9b1, 1–240.\nBanse, K., 1955. Über das Verhalten von meroplanktischen Larven in geschichtetem Wasser. Kieler Meeresforsch.11, 188–200.\nBlake, J. A., 1969. Reproduction and larval development ofPolydora from northern New England (Polychaeta: Spionidae). Ophelia7, 1–63.\n— & Evans, J. W., 1973.Polydora and related genera as borers in mollusc shells and other calcareous substrates (Polychaeta: Spionidae). Veliger15, 235–242.\nBøggild, O. B., 1930. The shell syructure of the molluscs. K. danske Vidensk. Selsk. Skr. (Naturv. og mathem. Afd. 9. Raekke 2)2, 231–326.\nCarazzi, D., 1895. Revisione del generePolydora Bosc e cenni su due specie che vivono, sulle ostriche. Mitt. zool. Stn Neapel11, 4–45.\nDaro, M. H. & Polk, P., 1973. The autecology ofPolydora ciliata along the Belgian coast. Neth. J. Sea Res.6 (1–2), 130–140.\nDollfuss, R.-Ph., 1932. Sur l'attaque de la coquille des bigorneauxLittorina littorea (L.) de Hollande parPolydora. Revue Trav. Inst. scient. tech. Pêch. marit.5 (18), 273–277.\nFriedrich, H., 1937. Polychaetenstudien. I–III. Kieler Meeresforsch.1 (2), 343–351.\nHaigler, S. A., 1969. Boring mechanism ofPolydora websteri inhabitingCrassostrea virginica. Am. Zool.9, 821–828.\nHannerz, L., 1956. Larval development of the polychaete families Spionidae Sars, Disomidae Mesnil, and Poecilochaetidae n. fam. in the Gullmar Fjord (Sweden). Zool. Bidr. Uppsala31, 1–204.\nHauser, B. & Michaelis, H., 1975. Die Makrofauna der Watten, Strände Riffe und Wracks um den Hohen Knechtsand in der Wesermündung. Jber. Forschungsstelle Norderney26, 85–119.\nHempel, C., 1957a. Über den Röhrenbau und die Nahrungsaufnahme einiger Spioniden (Polychaeta sedentaria) der deutschen Küsten. Helgoländer wiss. Meeresunters.6, 100–135.\n—, 1957b. Zur Ökologie einiger Spioniden (Polychaeta sedentaria) der deutschen Küsten. Kieler Meeresforsch.13, 275–288.\n— (1961. Über das Festsetzen der Larven und die Bohrtätigkeit der Jugendstadien vonPolydora ciliata (Polychaeta sedentaria). Helgoländer wiss. Meeresunters.7, 80–92.\nHertweck, G., 1971. Aktuopaläontologische Urkunden, 1.Polydora ciliata auf lebenden Herzmuscheln. Natur Mus., Frankf.101, 458–466.\nJacobi, R., 1883. Anatomisch-histologische Untersuchung der Polydoren der Kieler Bucht. Diss. Kiel, 37 pp.\nKorringa, P., 1954. The shell ofOstrea edulis as a habitat. Observations on the epifauna of oysters living in the Oosterschelde, Holland, with some notes on polychaete worms occuring there in other habitats. Archs néerl. Zool.10, 32–135.\nLamy, E. & André, M., 1937. Annelides perforant les Coquilles des Mollusques. Int. Congr. Zool.12, 946–968.\nLanders, W. S., 1967. Infestation of the hard clam,Mercenaria mercenaria, by the boring polychaete wormPolydora ciliata. Proc. natn. Shellfish. Ass.57, 63–66.\nLeschke, M., 1903. Beiträge zur Kenntniss der pelagischen Polychaetenlarven der Kieler Föhrde. Wiss. Meeresunters. (Abt. Kiel)7, 113–134.\nMesnil, F., 1896. Etudes de morphologie externe chez les Annélides I. Les Spionidiens des côtes de la Manche. Bull. scient. Fr. Belg.29, 110–287.\nMichaelis, H., 1976. Die Makrofauna des nördlichen Eversandes (Wesermündung). Jber. Forsschungsstelle Norderney27, 167–179.\nPrell, H., 1926. Fossile Wurmröhren. Beiträge zur paläobiologischen Beurteilung der Polydorinen-Horizonte. Neues Jb. Miner. Geol. Paläont.53 (Bei.-Bd), 325–396.\nRasmussen, E., 1973. Systematics and ecology of the Isefjord marine fauna (Denmark). Ophelia11, 1–507.\nSchäfer, W., 1962. Aktuo-PalÖaontologie nach Studien in der Nordsee. Kramer, Frankfurt a. M., 666 pp.\nSöderström, A., 1920. Studien über die Polychaetenfamilie Spionidae. Diss. Uppsala, 286 pp.\n— 1923. Über das Bohren derPolydora ciliata. zool. Bidr. Uppsala8, 319–326.\nTauber, A. F., 1944. Über prämortalen Befall von rezenten und fossilen Molluskenschalen durch tubicole Polychaeten (Spionidae). Palaeobiol.8, 154–172.\nThorson, G., 1946. Reproduction and larval development of Danish marine bottom invertebrates, with special reference to the planctonic larvae in the Sound (Øresund). Meddr Kommn Danm. Fisk.-og Havunders. (Plankton)4, 1–523.\nWebster, H. E., 1879. Annelida Chaetopoda of New Jersey. Rep. N.Y. St. Mus. nat. Hist.32, 101–128.\n— & Benedict, J. E., 1884. The Annelida Chaetopoda from Princetown and Wellfleet, Mass. Rep. U.S. Commn Fish.1884, 699–747.\nWilson, D.P., 1928. The larvae ofPolydora ciliata Johnston andPolydora hoplura Claparède. J. mar. biol. Ass. U. K.15, 567–603.\nZottoli, R. A. & Carriker, M. R. 1974. Burrow Morphology, Tube Formation and Microarchitecture of Shell Dissolution by the Spionid PolychaetePolydora websteri. Mar. Biol.27, 307–316.",{"EN":663},"The polychaete wormsPolydora ciliata andP. ligni were investigated with regard to the morphology of their fifth chaetigerous segment, bearing bundles of modified bristles in a special arrangement. The development of these chaetae from late larval to adult stages is described, considering the loss of provisional bristles, the variation of shape caused by the wear and the shedding of old chaetae after losing their function. In addition an epidemic shell disease of the mussel,Mytilus edulis, induced by infestation withP. ciliata is reported.P. ligni was observed to regularly inhabit the inflorescenses of the eelgrass,Zostera marina. The relationships between this plant andP. ligni are discussed.",{"EN":665},"Zur Morphologie und Ökologie vonPolydora ciliata undP. ligni (Polychaeta, Spionidae)",{"VOID":667},"10.1007\u002FBF02296992","2024-06-30T23:52:12.008+00:00","https:\u002F\u002Flink.springer.com\u002F10.1007\u002FBF02296992",[671],{"id":672,"sortIndex":21,"researcher":20,"roles":673,"affiliations":674,"properties":683},"811d94bc-a0e3-4c92-b257-6174fdda1075",[59],[675],{"id":20,"sortIndex":21,"affiliation":676,"properties":20},{"id":677,"createTime":678,"updateTime":678,"relativeEntities":679,"slug":20,"properties":680,"entityType":69,"verifyStatus":19,"verifyTime":20,"verifyNote":20,"syncStatus":19,"languages":20,"translateLanguages":20,"viewCount":21},"ea8deca1-e1c7-4d79-9c8a-1fe1034e7d03","2023-12-05T07:57:23.324+00:00",[],{"title":681},{"VI":682},"Forschungsstelle für Insel- und Küstenschutz, Norderney, Bundesrepublik Deutschland",{"title":684},{"VI":685},"H. Michaelis",{"url":669,"publisher":687,"properties":701},{"id":6,"createTime":7,"updateTime":8,"relativeEntities":688,"slug":10,"properties":689,"entityType":18,"verifyStatus":19,"verifyTime":20,"verifyNote":20,"syncStatus":19,"languages":20,"translateLanguages":20,"viewCount":21,"subjectFields":693,"manageAffiliations":694,"indexDatabases":695,"url":20,"thumbnailPath":20,"statistic":696,"gsStatistic":20,"type":20,"analyzePriority":20},[],{"issn":690,"eissn":691,"title":692},{"VOID":13},{"VOID":15},{"EN":17},[],[],[],{"impactFactor":21,"impactFactorByYear":697,"i10Index":27,"i10IndexLast5Year":21,"totalPublication":27,"totalPublicationByYear":698,"totalCitation":29,"totalCitationByYear":699,"totalCitationPerPublication":29,"totalCitationPerPublicationByYear":700,"hindexLast5Year":27,"hindex":27},{},{"1984":27},{"1984":29},{"1984":29},{"volume":702,"pages":704},{"VOID":703},"31",{"VOID":705},"102-116","1978-04-01",1978,{"id":709,"createTime":710,"updateTime":711,"relativeEntities":712,"slug":713,"properties":714,"entityType":51,"verifyStatus":52,"verifyTime":711,"verifyNote":53,"syncStatus":19,"languages":20,"translateLanguages":20,"viewCount":21,"primaryUrl":723,"fullTextUrl":20,"authors":724,"publicationType":73,"publisherRelationship":786,"citationCount":20,"citationInfo":20,"publishDate":806,"publishYear":438,"citationAnalyzeStatus":19,"lastCitationAnalyze":20,"indexDatabases":20,"openAccess":20,"references":20,"isForceReanalyzing":96},"b5475ecf-df76-4107-99c3-91e2818a7398","2024-02-07T18:39:05.402+00:00","2025-01-11T23:50:38.724+00:00",[],"Using-HPLC-pigment-analysis-to-investigate-phytoplankton-taxonomy-the-importance-of-knowing-your-species",{"references":715,"abstract":717,"title":719,"doi":721},{"VOID":716},"Barlow RG, Cummings DG, Gibb S (1997) Improved resolution of mono and divinyl chlorophylls a and b and zeaxanthin and lutein in phytoplankton extracts using reverse phase C-8 HPLC. Mar Ecol Prog Ser 161:303–307\nBelviso S, Claustre H, Marty JC (2001) Evaluation of the utility of chemotaxonomic pigments as a surrogate for particulate DMSP. Limnol Oceanogr 46:989–995\nBrown MR, Dunstan GA, Jeffrey SW, Volkman JK, Barrett SM, LeRoi JM (1993) The influence of irradiance on the biochemical composition of the prymensiophyte Isochrysis sp. (clone T-iso). J Phycol 29:601–612\nCasotti R, Brunet C, Aronne B, D’Alcala R (2000) Mesoscale features of phytoplankton and planktonic bacteria in a coastal area as induced by external water masses. Mar Ecol Prog Ser 195:15–27\nDescy JP, Higgins HW, Mackey DJ, Hurley JP, Frost TM (2000) Pigment ratios and phytoplankton assessment in northern Wisconsin lakes. J Phycol 36:274–286\nGibb SW, Barlow RG, Cummings DG, Rees NW, Trees CC, Holligan P, Suggett D (2000) Surface phytoplankton pigment distributions in the Atlantic Ocean: an assessment of basin scale variability between 50°N and 50°S. Prog Oceanogr 45:339–368\nGill CW, Harris RP (1987) Behavioural responses of the copepods Calanus helgolandicus and Temora longicornis to dinoflagellates diets. J Mar Biol Assoc UK 67:785–801\nHiggins HW, Mackey DJ (2000) Algal class abundances, estimated from chlorophyll and carotenoid pigments, in the western equatorial Pacific under El Nino and non-El Nino conditions. Deep-Sea Res I 8:1461–1483\nHolligan PM, Harbour DS (1977) The vertical distribution and succession of phytoplankton in the western English Channel in 1975 and 1976. J Mar Biol Assoc UK 57:1075–1093\nJeffrey SW, Wright SW (1994) Photosynthetic pigments in the Haptophyta. In: Green JC, Leadbeater BSC (eds) The haptophyte algae. Systematic Association, Clarendon Press, Oxford, pp 111–132\nJohnsen G, Sakshaug E (1993) Bio-optical characteristics and photoadaptive responses in toxic and bloom-forming dinoflagellates Gyrodinium aureolum, Gymnodinium galatheanum, and two strains of Prorocentrum minimum. J Phycol 29:627–642\nLandry MR, Ondrusek ME, Tanner SJ, Brown SL, Constantinou J, Bidigare RR, Coale KH, Fitzwater S (2000) Biological response to iron fertilization in the eastern equatorial Pacific (IronEx II). Microplankton community abundances and biomass. Mar Ecol Prog Ser 201:27–42\nMackey MD, Mackey DJ, Higgins HW, Wright SW (1996) CHEMTAX—a program for estimating class abundance from chemical markers: application to HPLC measurements of phytoplankton. Mar Ecol Prog Ser 144:265–283\nMoal J, Martin-Jezequel V, Harris RP, Samain JF, Poulet SA (1987) Interspecific and intraspecific variability of the chemical composition of marine phytoplankton. Oceanol Acta 10:339–346\nOernolfsdottir EB, Pinckney JL, Tester PA (2003) Quantification of the relative abundance of the toxic dinoflagellate, Karenia brevis (Dinophyta), using unique photopigments. J Phycol 39:449–457\nPartensky F, Le Botterff J, Verbist JF (1989) Does the fish-killing dinoflagellate Gymnodinium cf. nagasakiense produce cytotoxins? J Mar Biol Assoc UK 69:501–509\nPeterson DH, Festa JF (1984) Numerical simulation of phytoplankton productivity in partially mixed estuaries. Estuar Coast Shelf Sci 19:563–589\nRiegman R, Kraay GW (2001) Phytoplankton community structure derived from HPLC analysis of pigments in the Faroe-Shetland Channel during summer 1999: the distribution of taxonomic groups in relation to physical\u002Fchemical conditions in the photic zone. J Plankton Res 23:191–205\nSchlueter L, Moehlenberg F, Havskum H, Larsen S (2000) The use of phytoplankton pigments for identifying and quantifying phytoplankton groups in coastal areas: Testing the influence of light and nutrients on pigment\u002Fchlorophyll a ratios. Mar Ecol Prog Ser 192:49–63\nSmith WO Jr, Asper VL (2001) The influence of phytoplankton assemblage composition on biogeochemical characteristics and cycles in the Southern Ross Sea, Antarctica. Deep Sea Res I 48:137–161\nStrathmann RR (1967) Estimating the organic carbon content of phytoplankton from cell volume or plasma volume. Limnol Oceanogr 12:411–418\nTurner SM, Malin G, Nightingale PD, Liss PS (1996) Seasonal variation of dimethyl sulphide in the North Sea and an assessment of fluxes to the atmosphere. Mar Chem 54:245–262\nWright SW, Jeffrey SW (1997) High-resolution HPLC system for chlorophylls and carotenoids of marine phytoplankton. In: Jeffrey SW, Mantoura RFC, Wright SW (eds) Phytoplankton pigments in oceanography. UNESCO, pp 327–360\nWright SW, Van den Enden RL (2000) Phytoplankton community structure and stocks in the East Antarctic marginal ice zone determined by Chemtax analysis of HPLC pigment signatures. Deep Sea Res II 47:2363–2400",{"EN":718},"Phytoplankton microscopic enumerations and HPLC analyses of their pigments were performed weekly for a complete year at a coastal station in the English Channel. The taxonomic composition of the phytoplankton community was assessed using the HPLC results combined with the mathematical tool CHEMTAX in two different ways. Firstly, without using the species level taxonomic information obtained at the microscopic level (blind analyses), and secondly by including the information from the microscopic taxonomic analysis (directed analyses). The results indicate that, due to the particular pigment composition of some species (for example, the dinoflagellate, Karenia mikimotoi and the haptophyte, Phaeocystis pouchetii), a blind analysis would result in very significant errors in the taxonomic determination of the bloom events at this station. Major blooms of Karenia mikimotoi and P. pouchetii were mistaken for blooms of diatoms on the basis of a blind HPLC-CHEMTAX analysis. Only with the information from the microscopic observations was it possible to obtain an accurate representation of the phytoplankton community.",{"EN":720},"Using HPLC pigment analysis to investigate phytoplankton taxonomy: the importance of knowing your species",{"VOID":722},"10.1007\u002Fs10152-004-0171-9","https:\u002F\u002Fhmr.biomedcentral.com\u002Farticles\u002F10.1007\u002Fs10152-004-0171-9",[725,740,757,774],{"id":726,"sortIndex":21,"researcher":20,"roles":727,"affiliations":728,"properties":737},"8a36f81d-d880-4695-850e-190f9f0b8956",[59],[729],{"id":20,"sortIndex":21,"affiliation":730,"properties":20},{"id":731,"createTime":732,"updateTime":732,"relativeEntities":733,"slug":20,"properties":734,"entityType":69,"verifyStatus":19,"verifyTime":20,"verifyNote":20,"syncStatus":19,"languages":20,"translateLanguages":20,"viewCount":21},"bb649b78-3480-4fd1-9db3-0545d620874c","2024-02-08T16:02:54.444+00:00",[],{"title":735},{"VI":736},"AZTI, Pasaia, Spain",{"title":738},{"VI":739},"Xabier Irigoien",{"id":741,"sortIndex":27,"researcher":20,"roles":742,"affiliations":743,"properties":754},"84e78ec8-831f-4843-b932-d6d300f3a7e7",[59],[744],{"id":20,"sortIndex":21,"affiliation":745,"properties":20},{"id":746,"createTime":747,"updateTime":748,"relativeEntities":749,"slug":750,"properties":751,"entityType":69,"verifyStatus":19,"verifyTime":20,"verifyNote":20,"syncStatus":19,"languages":20,"translateLanguages":20,"viewCount":21},"181ccfa6-7a36-4c6c-ba08-4bbe7a684509","2024-01-25T20:05:41.065+00:00","2024-12-25T19:27:38.424+00:00",[],"Alfred-Wegener-Institute-for-Polar-and-Marine-Research-Bremerhaven-Germany",{"title":752},{"VI":753},"Alfred Wegener Institute for Polar and Marine Research, Bremerhaven, Germany",{"title":755},{"VI":756},"Bettina Meyer",{"id":758,"sortIndex":140,"researcher":20,"roles":759,"affiliations":760,"properties":771},"6a6d072e-309b-4554-b271-95d3e5e78e5a",[59],[761],{"id":20,"sortIndex":21,"affiliation":762,"properties":20},{"id":763,"createTime":764,"updateTime":765,"relativeEntities":766,"slug":767,"properties":768,"entityType":69,"verifyStatus":19,"verifyTime":20,"verifyNote":20,"syncStatus":19,"languages":20,"translateLanguages":20,"viewCount":21},"66231596-c3f8-47ff-8143-0fa4238d6170","2023-12-28T06:05:51.960+00:00","2025-02-10T16:43:11.984+00:00",[],"Plymouth-Marine-Laboratory-Plymouth-UK",{"title":769},{"VI":770},"Plymouth Marine Laboratory, Plymouth, UK",{"title":772},{"VI":773},"Derek Harbour",{"id":775,"sortIndex":162,"researcher":20,"roles":776,"affiliations":777,"properties":783},"acc29320-fd32-416e-9e51-d93287897671",[59],[778],{"id":20,"sortIndex":21,"affiliation":779,"properties":20},{"id":763,"createTime":764,"updateTime":765,"relativeEntities":780,"slug":767,"properties":781,"entityType":69,"verifyStatus":19,"verifyTime":20,"verifyNote":20,"syncStatus":19,"languages":20,"translateLanguages":20,"viewCount":21},[],{"title":782},{"VI":770},{"title":784},{"VI":785},"Roger Harris",{"url":723,"publisher":787,"properties":801},{"id":6,"createTime":7,"updateTime":8,"relativeEntities":788,"slug":10,"properties":789,"entityType":18,"verifyStatus":19,"verifyTime":20,"verifyNote":20,"syncStatus":19,"languages":20,"translateLanguages":20,"viewCount":21,"subjectFields":793,"manageAffiliations":794,"indexDatabases":795,"url":20,"thumbnailPath":20,"statistic":796,"gsStatistic":20,"type":20,"analyzePriority":20},[],{"issn":790,"eissn":791,"title":792},{"VOID":13},{"VOID":15},{"EN":17},[],[],[],{"impactFactor":21,"impactFactorByYear":797,"i10Index":27,"i10IndexLast5Year":21,"totalPublication":27,"totalPublicationByYear":798,"totalCitation":29,"totalCitationByYear":799,"totalCitationPerPublication":29,"totalCitationPerPublicationByYear":800,"hindexLast5Year":27,"hindex":27},{},{"1984":27},{"1984":29},{"1984":29},{"volume":802,"pages":804},{"VOID":803},"58",{"VOID":805},"77-82","2004-02-12",{"id":808,"createTime":809,"updateTime":810,"relativeEntities":811,"slug":812,"properties":813,"entityType":51,"verifyStatus":52,"verifyTime":810,"verifyNote":53,"syncStatus":19,"languages":20,"translateLanguages":20,"viewCount":21,"primaryUrl":822,"fullTextUrl":20,"authors":823,"publicationType":73,"publisherRelationship":839,"citationCount":20,"citationInfo":20,"publishDate":859,"publishYear":860,"citationAnalyzeStatus":19,"lastCitationAnalyze":20,"indexDatabases":20,"openAccess":20,"references":20,"isForceReanalyzing":96},"8090085b-e443-46f5-af4a-6a0e731cfc5d","2024-02-12T09:11:14.820+00:00","2025-02-16T23:48:26.479+00:00",[],"Bay-scale-assessment-of-eelgrass-beds-using-sidescan-and-video",{"references":814,"abstract":816,"title":818,"doi":820},{"VOID":815},"Barrell J, Grant J (2013) Detecting hot and cold spots in a seagrass landscape using local indicators of spatial association. Landsc Ecol 28:2005–2018\nBekkby T, Rinde E, Erikstad L, Bakkestuen V, Longva O, Christensen O, Isaeus M, Isachsen PE (2008) Spatial probability modelling of eelgrass (Zostera marina) distribution on the west coast of Norway. ICES J Mar Sci 65:1093–1101\nBernard G, Boudouresque CF, Picon P (2007) Long term changes in Zostera meadows in the Berre lagoon (Provence, Mediterranean Sea). Estuar Coast Shelf S 73:617–629\nDFO (2009) Does eelgrass (Zostera marina) meet the criteria as an ecologically significant species? Fisheries and Oceans, Canadian Science Advisory Secretariat, Science Advisory Report 2009\u002F018, p 11. http:\u002F\u002Fwww.dfo-mpo.gc.ca\u002Fcsas-sccs\u002Fpublications\u002Fsar-as\u002F2009\u002F2009_018-eng.htm\nElliott JK, Spear E, Wyllie-Echeverria S (2006) Mats of Beggiatoa bacteria reveal that organic pollution from lumber mills inhibits growth of Zostera marina. Mar Ecol 27:372–380\nFonseca MS, Bell SS (1998) Influence of physical setting on seagrass landscapes near Beaufort, North Carolina, USA. Mar Ecol Prog Ser 171:109–121\nFonseca M, Whitfield PE, Kelly NM, Bell SS (2002) Modeling seagrass landscape pattern and associated ecological attributes. Ecol Appl 12:218–237\nFrederiksen M, Krause-Jensen D, Holmer M, Laursen JS (2004) Long-term changes in area distribution of eelgrass (Zostera marina) in Danish coastal waters. Aquat Bot 78:167–181\nGarono RJ, Simenstad CA, Robinson R, Ripley H (2004) Using high spatial resolution hyperspectral imagery to map intertidal habitat structure in Hood Canal, Washington, USA. Can J Remote Sens 30:54–83\nGullstrom M, Lunden B, Bodin M, Kangwe J, Ohman MC, Mtolera MSP, Bjork M (2006) Assessment of changes in the seagrass-dominated submerged vegetation of tropical Chwaka Bay (Zanzibar) using satellite remote sensing. Estuar Coast Shelf S 67:399–408\nHale JA, Frazer TK, Tomasko DA, Hall MO (2004) Changes in the distribution of seagrass species along Florida’s central Gulf Coast: Iverson and Bittaker revisited. Estuaries 27:36–43\nHovel KA, Fonseca MS, Myer DL, Kenworthy WJ, Whitfield PE (2002) Effects of seagrass landscape structure, structural complexity and hydrodynamic regime on macrofaunal densities in North Carolina seagrass beds. Mar Ecol Prog Ser 243:11–24\nKelly MG (1980) Remote sensing of seagrass beds. In: Phillips RC, McRoy CP (eds) Handbook of seagrass biology: an ecosystem perspective. Garland STPM Press, New York, pp 69–85\nKiparissis S, Fakiris E, Papatheodorou G, Geraga M, Kornaros M, Kapareliotis A, Ferentinos G (2011) Illegal trawling and induced invasive algal spread as collaborative factors in a Posidonia oceanica meadow degradation. Biol Invasions 13:669–678\nKirkman H (1996) Baseline and monitoring methods for seagrass meadows. J Environ Manage 47:191–201\nKusel K, Trinkwalter T, Drake HL, Devereux R (2006) Comparative evaluation of anaerobic bacterial communities associated with roots of submerged macrophytes growing in marine or brackish water sediments. J Exp Mar Biol Ecol 337:49–58\nLeriche A, Boudouresque CF, Bernard G, Bonhomme P, Denis J (2004) A one-century suite of seagrass bed maps: can we trust ancient maps? Estuar Coast Shelf S 59:353–362\nLeriche A, Pasqualini V, Boudouresque CF, Bernard G, Bonhomme P, Clabaut P, Denis J (2006) Spatial, temporal and structural variations of a Posidonia oceanica seagrass meadow facing human activities. Aquat Bot 84:287–293\nMcKenzie LJ, Finkbeiner MA, Kirkman H (2001) Methods for mapping seagrass distribution. In: Short FT, Coles RG (eds) Global seagrass research methods. Elsevier Science B.V., Amsterdam, pp 101–121\nMontefalcone M, Albertelli G, Bianchi CN, Mariani M, Morri C (2006) A new synthetic index and a protocol for monitoring the status of Posidonia oceanica meadows: a case study at Sanremo (Ligurian Sea, NW Mediterranean). Aquat Conserv 16:29–42\nMontefalcone M, Rovere A, Parravicini V, Albertelli G, Morri C, Bianchi CN (2013) Evaluating change in seagrass meadows: a time-framed comparison of side scan sonar maps. Aquat Bot 104:204–212\nMoore CG, Bates CR, Mair JM, Saunders GR, Harries DB, Lyndon AR (2009) Mapping serpulid worm reefs (Polychaeta: Serpulidae) for conservation management. Aquat Conserv 19:226–236\nMulhearn PJ (2001) Mapping seabed vegetation with sidescan sonar. Australian Department of Defence, Defence Science and Technology Organisation, Aeronautical and Maritime Research Laboratory. DSTO-TN-0381. p 28. http:\u002F\u002Fwww.dtic.mil\u002Fcgi-bin\u002FGetTRDoc?AD=ADA395552\nNeckles HA, Kopp BS, Peterson BJ, Pooler PS (2012) Integrating scales of seagrass monitoring to meet conservation needs. Estuar Coast 35:23–46\nNienhuis PH, De Bree BHH, Herman PMJ, Holland AMB, Verschuure JM, Wessel EGJ (1996) Twenty-five years of changes in the distribution and biomass of eelgrass, Zostera marina, in Grevelingen Lagoon, The Netherlands. Neth J Aquat Ecol 30:107–117\nOakley BA, Alvarez JD, Boothroyd JC (2012) Benthic geologic habitats of shallow estuarine environments: Greenwich Bay and Wickford Harbor, Narragansett Bay, Rhode Island, USA. J Coast Res 28:760–773\nRaineault NA, Trembanis AC, Miller DC (2012) Mapping benthic habitats in Delaware Bay and the coastal Atlantic: acoustic techniques provide greater coverage and high resolution in complex, shallow-water environments. Estuar Coast 35:682–699\nSánchez-Carnero N, Rodríguez-Pérez D, Couñago E, Aceñaand S, Freire J (2012) Using vertical sidescan sonar as a tool for seagrass cartography. Estuar Coast Shelf S 115:334–344\nShao G, Wu J (2008) On the accuracy of landscape pattern analysis using remote sensing data. Landsc Ecol 23:505–511\nShort FT, Burdick DM (1996) Quantifying eelgrass habitat loss in relation to housing development and nitrogen loading in Waquoit Bay, Massachusetts. Estuaries 19:730–739\nStevens T, Connolly RM (2005) Local-scale mapping of benthic habitats to assess representation in a marine protected area. Mar Freshw Res 56:111–123\nTaylor BR, Garbary DJ, Miller A, Bärlocher F (2009) Metabolism and ecology of the water mould, Leptomitus lacteus (Oomycota), blooming in winter in a Nova Scotia stream. Fundam Appl Limnol 175:171–180\nValle M, Borja A, Chust G, Galparsoro I, Garmendia JM (2011) Modelling suitable estuarine habitats for Zostera noltii, using ecological niche factor analysis and bathymetric LiDAR. Estuar Coast Shelf S 94:144–154\nvan Overmeeren R, Craeymeersch J, van Dalfsen J, Fey F, van Heteren S, Meesters E (2009) Acoustic habitat and shellfish mapping and monitoring in shallow coastal water—sidescan sonar experiences in The Netherlands. Estuar Coast Shelf S 85:437–448\nVandermeulen H (2005) Assessing marine habitat sensitivity: a case study with eelgrass (Zostera marina L.) and kelps (Laminaria, Macrocystis). Fisheries and Oceans, Canadian Science Advisory Secretariat, Research Document 2005\u002F032, p 57. http:\u002F\u002Fwww.dfo-mpo.gc.ca\u002Fcsas-sccs\u002Fpublications\u002Fresdocs-docrech\u002F2005\u002F2005_032-eng.htm\nVandermeulen H (2009) An introduction to eelgrass (Zostera marina L.): the persistent ecosystem engineer. Fisheries and Oceans, Canadian Science Advisory Secretariat, Research Document 2009\u002F085, p 11. http:\u002F\u002Fwww.dfo-mpo.gc.ca\u002Fcsas-sccs\u002Fpublications\u002Fresdocs-docrech\u002F2009\u002F2009_085-eng.htm\nVandermeulen H (2011) Mapping the nearshore using a unique towfish. Canadian Technical Report of Fisheries and Aquatic Sciences 2959, p 18. http:\u002F\u002Fwww.dfo-mpo.gc.ca\u002FLibrary\u002F344627.pdf\nVandermeulen H, Jamieson G, Ouellette M (2006) Shellfish aquaculture and marine habitat sensitivity case studies. Fisheries and Oceans, Canadian Science Advisory Secretariat, Research Document 2006\u002F036, p 62. http:\u002F\u002Fwww.dfo-mpo.gc.ca\u002Fcsas-sccs\u002Fpublications\u002Fresdocs-docrech\u002F2006\u002F2006_036-eng.htm\nVandermeulen H, Surette J, Skinner M (2012) Responses of eelgrass (Zostera marina L.) to stress. Fisheries and Oceans, Canadian Science Advisory Secretariat, Research Document 2011\u002F095, p 43. http:\u002F\u002Fwww.dfo-mpo.gc.ca\u002Fcsas-sccs\u002FPublications\u002FResDocs-DocRech\u002F2011\u002F2011_095-eng.html\nVela A, Pasqualini V, Leoni V, Djelouli A, Langar H, Pergent G, PergentMartini C, Ferrat L, Ridha M, Djabou H (2008) Use of SPOT 5 and IKONOS imagery for mapping biocenoses in a Tunisian Coastal Lagoon (Mediterranean Sea). Estuar Coast Shelf S 79:591–598",{"EN":817},"The assessment of the status of eelgrass (Zostera\n                marina) beds at the bay-scale in turbid, shallow estuaries is problematic. The bay-scale assessment (i.e., tens of km) of eelgrass beds usually involves remote sensing methods such as aerial photography or satellite imagery. These methods can fail if the water column is turbid, as is the case for many shallow estuaries on Canada’s eastern seaboard. A novel towfish package was developed for the bay-scale assessment of eelgrass beds irrespective of water column turbidity. The towfish consisted of an underwater video camera with scaling lasers, sidescan sonar and a transponder-based positioning system. The towfish was deployed along predetermined transects in three northern New Brunswick estuaries. Maps were created of eelgrass cover and health (epiphyte load) and ancillary bottom features such as benthic algal growth, bacterial mats (Beggiatoa) and oysters. All three estuaries had accumulations of material reminiscent of the oomycete Leptomitus, although it was not positively identified in our study. Tabusintac held the most extensive eelgrass beds of the best health. Cocagne had the lowest scores for eelgrass health, while Bouctouche was slightly better. The towfish method proved to be cost effective and useful for the bay-scale assessment of eelgrass beds to sub-meter precision in real time.",{"EN":819},"Bay-scale assessment of eelgrass beds using sidescan and video",{"VOID":821},"10.1007\u002Fs10152-014-0412-5","https:\u002F\u002Fhmr.biomedcentral.com\u002Farticles\u002F10.1007\u002Fs10152-014-0412-5",[824],{"id":825,"sortIndex":21,"researcher":20,"roles":826,"affiliations":827,"properties":836},"263e4cb5-44a2-4be7-b7f8-7f997da00aac",[59],[828],{"id":20,"sortIndex":21,"affiliation":829,"properties":20},{"id":830,"createTime":831,"updateTime":831,"relativeEntities":832,"slug":20,"properties":833,"entityType":69,"verifyStatus":19,"verifyTime":20,"verifyNote":20,"syncStatus":19,"languages":20,"translateLanguages":20,"viewCount":21},"5e9da72b-e0d2-43dc-88f1-ce09d5bbc4d8","2024-02-12T09:11:14.838+00:00",[],{"title":834},{"VI":835},"St. Andrews Biological Station, St. Andrews, Canada",{"title":837},{"VI":838},"Herb Vandermeulen",{"url":822,"publisher":840,"properties":854},{"id":6,"createTime":7,"updateTime":8,"relativeEntities":841,"slug":10,"properties":842,"entityType":18,"verifyStatus":19,"verifyTime":20,"verifyNote":20,"syncStatus":19,"languages":20,"translateLanguages":20,"viewCount":21,"subjectFields":846,"manageAffiliations":847,"indexDatabases":848,"url":20,"thumbnailPath":20,"statistic":849,"gsStatistic":20,"type":20,"analyzePriority":20},[],{"issn":843,"eissn":844,"title":845},{"VOID":13},{"VOID":15},{"EN":17},[],[],[],{"impactFactor":21,"impactFactorByYear":850,"i10Index":27,"i10IndexLast5Year":21,"totalPublication":27,"totalPublicationByYear":851,"totalCitation":29,"totalCitationByYear":852,"totalCitationPerPublication":29,"totalCitationPerPublicationByYear":853,"hindexLast5Year":27,"hindex":27},{},{"1984":27},{"1984":29},{"1984":29},{"volume":855,"pages":857},{"VOID":856},"68",{"VOID":858},"559-569","2014-09-21",2014,{"id":862,"createTime":863,"updateTime":863,"relativeEntities":864,"slug":20,"properties":865,"entityType":51,"verifyStatus":19,"verifyTime":20,"verifyNote":20,"syncStatus":19,"languages":20,"translateLanguages":20,"viewCount":21,"primaryUrl":874,"fullTextUrl":20,"authors":875,"publicationType":73,"publisherRelationship":918,"citationCount":20,"citationInfo":20,"publishDate":938,"publishYear":939,"citationAnalyzeStatus":19,"lastCitationAnalyze":20,"indexDatabases":20,"openAccess":20,"references":20,"isForceReanalyzing":96},"5d310076-e16d-487c-bdf4-dd657e0a12a5","2024-02-07T23:48:17.264+00:00",[],{"references":866,"abstract":868,"title":870,"doi":872},{"VOID":867},"Albrecht A (1998) Soft bottom versus hard rock: community ecology of macroalgae on intertidal mussel beds in the Wadden Sea. J Exp Mar Biol Ecol 229:85–109\nAnderson MJ, Underwood AJ (1997) Effects of gastropod grazers on recruitment and succession of an estuarine assemblage: a multivariate and univariate approach. Oecologia 109:442–453\nAusten I (1992) Geologisch-sedimentologische Kartierung des Königshafens (List\u002FSylt). Meyniana 44:45–52\nAusten G (1994a) Hydrodynamics and particulate matter budget of Königshafen, southeastern North Sea. Helgol Mar Res 48:183–200\nAusten I (1994b) The surficial sediments of Königshafen; variations over the past 50 years. Helgol Mar Res 48:163–171\nBartsch I, Tittley I (2004) The rocky intertidal biotopes of Helgoland: present and past. Helgol Mar Res 58:289–302\nBayerl KA, Higelke B (1994) The development of northern Sylt during the last Holocene. Helgol Mar Res 48:145–171\nBayne BL, Worrall CM (1980) Growth and production of mussel Mytilus edulis from two populations. Mar Ecol Prog Ser 3:317–328\nBrown KM, Quinn JF (1988) The effect of wave action on growth in three species of intertidal gastropods. Oecologia 75:420–425\nBuschbaum C (2000) Direct and indirect effects of Littorina littorea (L.) on barnacles growing on mussel beds in the Wadden Sea. Hydrobiologia 440:119–128\nBuschbaum C (2002) Predation on barnacles of intertidal and subtidal mussel beds in the Wadden Sea. Helgol Mar Res 56:37–43\nBuschbaum C, Reise K (1999) Effects of barnacle epibionts on the periwinkle Littorina littorea (L.). Helgol Mar Res 53:56–61\nBuschbaum C, Buschbaum G, Schrey I, Thieltges DW (2007) Shell boring polychaetes affect gastropod shell strength and crab predation. Mar Ecol Prog Ser 329:123–130\nByers JE (2000) Effects of body size and resource availability on dispersal in a native and a non-native estuarine snail. J Exp Mar Biol Ecol 248:133–150\nDavies MS, Knowles AJ (2001) Effects of trematode parasitism on the behaviour and ecology of a common marine snail (Littorina littorea (L.)). J Exp Mar Biol Ecol 260:155–167\nFenske C (1997) The importance of intraspecific competition in a Littorina littorea population in the Wadden Sea. Hydrobiologia 355:29–39\nFretter V, Graham A (1980) The prosobranch molluscs of Britain and Denmark; Part 5 marine Littorinacea. J Moll Stud Suppl 7:241–284\nGeller JB (1991) Gastropod grazers and algal colonization on a rocky shore in northern California—the importance of the body size of grazers. J Exp Mar Biol Ecol 150:1–17\nGiménez L, Dick S (2007) Settlement of shore crab Carcinus maenas on a mesotidal open habitat as a function of transport mechanisms. Mar Ecol Prog Ser 338:159–168\nHadlock RP (1980) Alarm response of the intertidal snail Littorina littorea (L.) to predation by the crab Carcinus maenas (L.). Biol Bull 159:269–279\nHagmeier A (1930) Die Besiedlung des Felsstrandes und der Klippen von Helgoland. I. Der Lebensraum. Wiss Meeresunters (Abt. Helgoland) 15:1–35\nHarger JRE (1970) The effect of wave impact on some aspects of the biology of sea mussels. Veliger 12:401–414\nHawkins SJ, Hartnoll RG (1983) Grazing of intertidal algae by marine invertebrates. Oceanogr Mar Biol Annu Rev 21:195–282\nHuxham M, Raffaelli D, Pike A (1993) The influence of Cryptocotyle lingua (Digenea: Plathyelminthes) infections on the survival and fecundity of Littorina littorea (Gastropoda: Prosobranchia); an ecological approach. J Exp Mar Biol Ecol 168:223–238\nHylleberg J, Christensen JT (1978) Factors affecting the intra-specific competition and size distribution of the periwinkle Littorina littorea (L.). Natura Jütl 20:193–202\nJanke K (1986) Die Makrofauna und ihre Verteilung im Nordost-Felswatt von Helgoland. Helgoländer Meeresunters 40:1–55\nJanke K (1990) Biological interactions and their role in community structure in the rocky intertidal of Helgoland (German Bight, North Sea). Helgoländer Meeresunters 44:219–263\nJanson K (1987) Allozyme and shell variation in two marine snails (Littorina, Prosobranchia) with different dispersal abilities. Biol J Linn Soc 30:245–256\nKemp P, Bertness MD (1984) Snail shape and growth rates: Evidence for plastic shell allometry in Littorina littorea. Proc Natl Acad Sci USA 81:811–813\nLauckner G (1984) Impact of trematode parasitism on the fauna of a North Sea tidal flat. Helgoländer Meeresunters 37:185–199\nLubchenco J (1978) Plant species diversity in a marine intertidal community: importance of herbivore food preference on algal competitive abilities. Am Nat 112:23–29\nMouritson KN, Poulin R (2002) Parasitism, community structure and biodiversity in intertidal ecosystems. Parasitology 124:101–117\nPalmer AR (1990) Effect of crab effluent and scent of damaged conspecifics on feeding, growth and shell morphology of the Atlantic dogwhelk Nucella lapillus (L.). Hydrobiologia 193:155–182\nRaffaelli D (1982) Recent ecological research on some European species of Littorina. J Moll Stud 48:342–354\nReichert K, Buchholz F (2006) Changes in the macrozoobenthos of the intertidal zone at Helgoland (German Bight, North Sea): a survey of 1984 repeated in 2002. Helgol Mar Res 60:213–223\nReid DG (1996) Systematics and evolution of Littorina. Ray Society, London\nReise K (1985) Tidal flat ecology. Springer, Berlin\nReise K, Herre E, Sturm M (1994) Biomass and abundance of macrofauna in intertidal sediments of Königshafen in the northern Wadden Sea. Helgoländer Meeresunters 48:201–215\nSaier B (2000) Age-dependent zonation of the periwinkle Littorina littorea (L.) in the Wadden Sea. Helgol Mar Res 54:224–229\nScherer B, Reise K (1981) Significant predation on micro- and macrobenthos by the crab Carcinus maenas L. in the Wadden Sea. Kiel Meeresforsch Sonderh 5:490–500\nSeed R (1968) Factors influencing shell shape in the mussel Mytilus edulis. J Mar Biol Assoc UK 48:561–584\nSeed R, Suchanek TH (1992) Population and community ecology of Mytilus. In: Gosling E (ed) The mussel Mytilus: ecology, physiology, genetics and culture. Elsevier, Amsterdam, pp 87–169\nSherrell RM (1981) Intraspecific competition in the periwinkle, Littorina littorea. Biol Bull 161(2):331\nThieltges DW, Buschbaum C (2007) Vicious circle in the intertidal: Facilitation between barnacle epibionts, a shell boring polychaete and trematode parasites in the periwinkle Littorina littorea. J Exp Mar Biol Ecol 340:90–95\nTrussel GC (1996) Phenotypic plasticity in an intertidal snail: the role of a common crab predator. Evolution 50:448–454\nTrussel GC, Nicklin MO (2002) Cue sensitivity, inducible defence, and trade-offs in a marine snail. Ecology 83:1635–1647\nTrussell GC, Ewanchuk PJ, Bertness MD (2002) Field evidence of trait-mediated indirect interactions in a rocky intertidal food web. Ecol Lett 5:241–245\nTrussell GC, Ewanchuk PJ, Bertness MD (2003) Trait-mediated effects in rocky intertidal food chains: predator risk cues alter prey feeding rates. Ecology 84:629–640\nTrussell GC, Ewanchuk PJ, Bertness MD, Silliman BR (2004) Trophic cascades in rocky shore tide pools: distinguishing lethal and nonlethal effects. Oecologia 139:427–432\nWahl M (1996) Fouled snails in flow: potential of epibionts on Littorina littorea to increase drag and reduce snail growth rates. Mar Ecol Prog Ser 138:157–168\nWarner GF (1997) Occurrence of epifauna on the periwinkle Littorina littorea (L.), and interactions between the polychaete Polydora ciliata (Johnston). Hydrobiologia 355:41–47\nWilhelmsen U (1998) Populationsgenetik und -ökologie von drei Littorina-Arten (Gastropoda) der Nord- und Ostseeküste. Ph.D. thesis, University of Hamburg, Germany\nWilhelmsen U, Reise K (1994) Grazing on green algae by the periwinkle Littorina littorea in the Wadden Sea. Helgoländer Meeresunters 48:233–242\nWurster P (1962) Geologisches Portrait Helgolands. Die Natur 70:135–150\nYamada SB, Navarrete SA, Needham C (1998) Predation induced changes in behavior and growth rate in three populations of the intertidal snail, Littorina sitkana (Philippi). J Exp Mar Biol Ecol 220:213–226",{"EN":869},"Shell size distribution patterns of marine gastropod populations may vary considerably across different environments. We investigated the size and density structure of genetically continuous periwinkle populations (Littorina littorea) on an exposed rocky and a sheltered sedimentary environment on two nearby islands in the south-eastern North Sea (German Bight). On the sedimentary shore, periwinkle density (917 ± 722 individuals m−2) was about three times higher than on the rocky shore (296 ± 168 individuals m−2). Mean (9.8 ± 3.9 mm) and maximum (22 mm) shell size of L. littorea on the sedimentary shore were smaller than on the rocky shore (21.5 ± 4.2 and 32 mm, respectively), where only few small snails were found. Additionally, periwinkle shells were thicker and stronger on the rocky than on the sedimentary shore. To ascertain mechanisms responsible for differences in population structures, we examined periwinkles in both environments for growth rate, predation pressure, infection with a shell boring polychaete (Polydora ciliata) and parasitic infestation by trematodes. A crosswise transplantation experiment revealed better growth conditions on the sedimentary than on the rocky shore. However, crab abundance and prevalence of parasites and P. ciliata in adult snails were higher on the sedimentary shore. Previous investigations showed that crabs prefer large periwinkles infested with P. ciliata. Thus, we suggest that parasites and shell boring P. ciliata in conjunction with an increased crab predation pressure are responsible for low abundances of large periwinkles on the sedimentary shore while high wave exposure may explain low densities of juvenile L. littorea on the rocky shore. We conclude that biotic factors may strongly contribute to observed differences in size structure of the L. littorea populations studied on rocky and sedimentary shores.",{"EN":871},"Habitat-specific size structure variations in periwinkle populations (Littorina littorea) caused by biotic factors",{"VOID":873},"10.1007\u002Fs10152-008-0131-x","https:\u002F\u002Fhmr.biomedcentral.com\u002Farticles\u002F10.1007\u002Fs10152-008-0131-x",[876,891,903],{"id":877,"sortIndex":21,"researcher":20,"roles":878,"affiliations":879,"properties":888},"93a22614-0705-49ea-b1c3-26b9eef49f7e",[59],[880],{"id":20,"sortIndex":21,"affiliation":881,"properties":20},{"id":882,"createTime":883,"updateTime":883,"relativeEntities":884,"slug":20,"properties":885,"entityType":69,"verifyStatus":19,"verifyTime":20,"verifyNote":20,"syncStatus":19,"languages":20,"translateLanguages":20,"viewCount":21},"5eaa045d-2d8d-4da3-9cfc-f75d2ef0f603","2024-02-07T23:48:17.527+00:00",[],{"title":886},{"VI":887},"Wadden Sea Station Sylt, Alfred Wegener Institute for Polar and Marine Research, List\u002FSylt, Germany",{"title":889},{"VI":890},"Nina Eschweiler",{"id":892,"sortIndex":162,"researcher":20,"roles":893,"affiliations":894,"properties":900},"9fac7acc-c992-4641-8ecf-ffd08d92b75c",[59],[895],{"id":20,"sortIndex":21,"affiliation":896,"properties":20},{"id":882,"createTime":883,"updateTime":883,"relativeEntities":897,"slug":20,"properties":898,"entityType":69,"verifyStatus":19,"verifyTime":20,"verifyNote":20,"syncStatus":19,"languages":20,"translateLanguages":20,"viewCount":21},[],{"title":899},{"VI":887},{"title":901},{"VI":902},"Christian Buschbaum",{"id":904,"sortIndex":27,"researcher":20,"roles":905,"affiliations":906,"properties":915},"ee091c54-367c-49b1-b9ab-cfbc6477f3f1",[59],[907],{"id":20,"sortIndex":21,"affiliation":908,"properties":20},{"id":909,"createTime":910,"updateTime":910,"relativeEntities":911,"slug":20,"properties":912,"entityType":69,"verifyStatus":19,"verifyTime":20,"verifyNote":20,"syncStatus":19,"languages":20,"translateLanguages":20,"viewCount":21},"5b05866e-3693-4d80-8eb1-58c061789040","2024-02-07T23:48:17.439+00:00",[],{"title":913},{"VI":914},"Section Seaweed Biology, Biologische Anstalt Helgoland, Alfred Wegener Institute for Polar and Marine Research, Helgoland, Germany",{"title":916},{"VI":917},"Markus Molis",{"url":874,"publisher":919,"properties":933},{"id":6,"createTime":7,"updateTime":8,"relativeEntities":920,"slug":10,"properties":921,"entityType":18,"verifyStatus":19,"verifyTime":20,"verifyNote":20,"syncStatus":19,"languages":20,"translateLanguages":20,"viewCount":21,"subjectFields":925,"manageAffiliations":926,"indexDatabases":927,"url":20,"thumbnailPath":20,"statistic":928,"gsStatistic":20,"type":20,"analyzePriority":20},[],{"issn":922,"eissn":923,"title":924},{"VOID":13},{"VOID":15},{"EN":17},[],[],[],{"impactFactor":21,"impactFactorByYear":929,"i10Index":27,"i10IndexLast5Year":21,"totalPublication":27,"totalPublicationByYear":930,"totalCitation":29,"totalCitationByYear":931,"totalCitationPerPublication":29,"totalCitationPerPublicationByYear":932,"hindexLast5Year":27,"hindex":27},{},{"1984":27},{"1984":29},{"1984":29},{"volume":934,"pages":936},{"VOID":935},"63",{"VOID":937},"119-127","2008-10-15",2008,{"id":941,"createTime":942,"updateTime":943,"relativeEntities":944,"slug":945,"properties":946,"entityType":51,"verifyStatus":52,"verifyTime":943,"verifyNote":53,"syncStatus":19,"languages":20,"translateLanguages":20,"viewCount":21,"primaryUrl":955,"fullTextUrl":20,"authors":956,"publicationType":73,"publisherRelationship":972,"citationCount":20,"citationInfo":20,"publishDate":992,"publishYear":993,"citationAnalyzeStatus":19,"lastCitationAnalyze":20,"indexDatabases":20,"openAccess":20,"references":20,"isForceReanalyzing":96},"b7f9fb64-c1d3-4b3b-b414-ea7d5607bd80","2024-02-22T02:29:09.730+00:00","2025-02-24T23:46:55.690+00:00",[],"Die-Entwicklung-vonMonostroma-grevillei",{"references":947,"abstract":949,"title":951,"doi":953},{"VOID":948},"Carter, Nellie, 1926: An investigation into the cytology and biology of the Ulvaceae. Ann. Bot.40, 665–689.\nFöyn, B., 1934: Lebenszyklus, Cytologic und Sexualität der ChlorophyceeCladophora Suhriana Kützing. Arch. Protistenkde83, 1–56\nKornmann, P., 1959: Die heterogene GattungGomontia. I. Der sporangiale Anteil,Codiolum polyrhizum. Helgol. Wiss. Meeresunters.6, 229–238.\n-- 1962: Zur Entwicklung vonMonostroma grevillei und zur systematischen Stellung vonGomontia polyrhiza. Algensymposium Göttingen, Oktober 1961 (im Druck).\nPapenfuss, G. F., 1960: On the genera of the Ulvales and the status of the order. J. Linn. Soc. (Bot.),56, 303–318.\nSchreiber, E., 1942: Über die geschlechtliche Fortpflanzung vonMonostroma Grevillei (Thur.) undCladophora rupestris (L.). Planta32, 414–417.\nSuneson, S., 1947: Notes on the life-history ofMonostroma. Svensk Bot. Tidskrift41, 235–246.\nYamada, Y., and Saito, E., 1938: On some culture experiments with the swarmers of certain species belonging to the Ulvaceac. Sci. Papers Inst. Algol. Res., Fac. Sci. Hokkaido Imp. Univ.2, 35–51.",{"EN":950},"Die Entwicklung vonMonostroma grevillei zeichnet sich durch eine ungewöhnliche Variabilität aus (Schema Abb. 5). Der Lebenszyklus ist heteromorph mit einem einzelligen, kalkbohrenden Sporophyten (a). Parthenogenetische Gameten entwickeln sich zur Gestalt von Sporophyten; ihre Nachkommenschaft behält das Geschlecht der Ursprungspflanze bei (b). Ein kleiner Teil der zweigeißeligen Schwärmer kann unmittelbar wieder zu Gametophyten führen (c). Ganz ungewöhnlich ist die durch besondere Versuchsbedingungen bewirkte Entstehung beider Phänotypen sowie morphologischer Zwischenformen in der Nachkommenschaft eines einzelnen Sporophyten.",{"EN":952},"Die Entwicklung vonMonostroma grevillei",{"VOID":954},"10.1007\u002FBF01609436","https:\u002F\u002Flink.springer.com\u002Farticle\u002F10.1007\u002FBF01609436",[957],{"id":958,"sortIndex":21,"researcher":20,"roles":959,"affiliations":960,"properties":969},"2085aefe-8b5b-4f3b-94a6-fbc731d50217",[59],[961],{"id":20,"sortIndex":21,"affiliation":962,"properties":20},{"id":963,"createTime":964,"updateTime":964,"relativeEntities":965,"slug":20,"properties":966,"entityType":69,"verifyStatus":19,"verifyTime":20,"verifyNote":20,"syncStatus":19,"languages":20,"translateLanguages":20,"viewCount":21},"69078043-0183-4024-80f2-94c1beb67009","2023-12-07T13:35:22.023+00:00",[],{"title":967},{"VI":968},"Aus der Biologischen Anstalt Helgoland, Germany",{"title":970},{"VI":971},"Peter Kornmann",{"url":955,"publisher":973,"properties":987},{"id":6,"createTime":7,"updateTime":8,"relativeEntities":974,"slug":10,"properties":975,"entityType":18,"verifyStatus":19,"verifyTime":20,"verifyNote":20,"syncStatus":19,"languages":20,"translateLanguages":20,"viewCount":21,"subjectFields":979,"manageAffiliations":980,"indexDatabases":981,"url":20,"thumbnailPath":20,"statistic":982,"gsStatistic":20,"type":20,"analyzePriority":20},[],{"issn":976,"eissn":977,"title":978},{"VOID":13},{"VOID":15},{"EN":17},[],[],[],{"impactFactor":21,"impactFactorByYear":983,"i10Index":27,"i10IndexLast5Year":21,"totalPublication":27,"totalPublicationByYear":984,"totalCitation":29,"totalCitationByYear":985,"totalCitationPerPublication":29,"totalCitationPerPublicationByYear":986,"hindexLast5Year":27,"hindex":27},{},{"1984":27},{"1984":29},{"1984":29},{"volume":988,"pages":990},{"VOID":989},"8",{"VOID":991},"195-202","1962-11-01",1962]