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      Context of diversification of the viviparous Gyrodactylidae (Platyhelminthes, Monogenoidea)

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      Zoologica Scripta
      Blackwell Science Ltd

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          Abstract

          Using four criteria proposed a decade ago by Brooks & McLennan to identify a case of adaptive radiation indicates that the evolutionary history of the viviparous clade of the Gyrodactylidae is dominated by nonvicariant processes. The viviparous clade, with 446 species, has significantly more species than its sister clade (one species), and high species richness was shown to be an apomorphic trait of only the viviparous gyrodactylids within the Gyrodactylidae. Reconciliation of the phylogenetic tree of the viviparous Gyrodactylidae with that of its hosts showed a low probability for cospeciation suggesting that adaptive modes of speciation and not vicariance were predominant during the historical diversification of the clade. The proposed hypothesis suggests that the Gyrodactylidae originated on the South American continent about 60 Mya after geographical dispersal and host switching of its common ancestor to demersal freshwater catfishes by a marine ancestor. Development of hyperviviparity and the consequent loss of ‘sticky’ eggs in conjunction with other symplesiomorphic and apomorphic features allowed rapid diversification coupled with high dispersal to new host groups and geographical areas by viviparous members of the Gyrodactylidae.

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          Interactions between monogenean parasites and their fish hosts.

          Parasite factors associated with recognition and selection of the host and the mechanisms in the host responsible for acceptance or rejection of the invading organism were evaluated. Sensory structures in parasites are able to detect differences between different fish species and this ability to discern between fishes may be based on both chemical and mechanical stimuli on the host surface. Complex glycoproteins, proteins, carbohydrates and simple molecules attract parasites or modify their behaviour. Furthermore, attachment of the monogenean parasite to a host is dependent on both mechanical structures and chemical factors in the parasite. These systems comprise anterior pads, posterior haptors, gland secretions, and muscular elements. The parasite needs access to appropriate nutrients which can be absorbed and used for reproduction and in this context signals from the host are needed for an optimal physiological response of the parasite. The innate and adaptive immune systems of the host are important elements in this question. Investigations have indicated that innate host factors (complement, lectins, acute phase reactants, macrophages) can bind to monogeneans and elicit severe damage to the parasites. The targets for these hostile products are not only the monogenean tegument, but may involve the gastrodermis and glands. However, the parasite's ability to avoid and even exploit the wide array of immunological elements of the host may be an important player in the dynamic interactions between host and monogenean determining host specificity. Even fish hosts susceptible to a certain parasite show an ability to mount a protective response at post-infection periods. Elevation of the host's production of adaptive and non-adaptive factors following monogenean infections of a certain duration may explain the acquired response.
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            Testing whether certain traits have caused amplified diversification: an improved method based on a model of random speciation and extinction.

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              Maps between Trees and Cladistic Analysis of Historical Associations Among Genes, Organisms, and Areas

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                Author and article information

                Journal
                Zool Scr
                Zool. Scr
                10.1111/(ISSN)1463-6409
                ZSC
                Zoologica Scripta
                Blackwell Science Ltd (Oxford, UK )
                0300-3256
                1463-6409
                13 August 2003
                September 2003
                : 32
                : 5 ( doiID: 10.1111/zsc.2003.32.issue-5 )
                : 437-448
                Author notes
                [*] [* ] Walter A. Boeger, Departamento de Zoologia, Universidade Federal do Paraná, Caixa Postal 19020, Curitiba, Paraná 81530, Brazil, and Conselho Nacional de Desenvolvimento Cientifíco e Tecnológico (CNPq). E‐mail: wboeger@bio.ufpr.br wboeger@ 123456bio.ufpr.br

                Delane C. Kritsky, Department of Health and Nutrition Sciences, Campus Box 8090, Idaho State University, Pocatello, ID 83209, USA. E‐mail: kritdela@ 123456isu.edu

                Marcio R. Pie, Department of Biology, Boston University, 5 Cummington St., Boston, MA 02215. E‐mail: pie@ 123456bu.edu

                Article
                ZSC130
                10.1046/j.1463-6409.2003.00130.x
                7165889
                32336863
                15199efb-3b2f-450f-ae70-491236d5947d

                This article is being made freely available through PubMed Central as part of the COVID-19 public health emergency response. It can be used for unrestricted research re-use and analysis in any form or by any means with acknowledgement of the original source, for the duration of the public health emergency.

                History
                : 30 January 2003
                Page count
                Figures: 4, Tables: 5, Equations: 0, References: 43, Pages: 12, Words: 5483
                Categories
                Original Articles
                Custom metadata
                2.0
                September 2003
                Converter:WILEY_ML3GV2_TO_JATSPMC version:5.8.0 mode:remove_FC converted:15.04.2020

                Animal science & Zoology
                Animal science & Zoology

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