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      Genus level molecular phylogeny of Aegisthidae Gisbrecht, 1893 (Copepoda: Harpacticoida) reveals morphological adaptations to deep-sea and plagic habitats

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      BMC Evolutionary Biology
      BioMed Central

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          Abstract

          Background

          The family Aegisthidae is known as typical component of deep-sea hyperbenthic waters that gradually colonized other marine environments. The phylogenetic relationships within this family have been examined here including hyperbenthic, planktonic, benthic forms and two associated Aegisthidae species.

          Results

          Ninety four specimens belong to 14 genera were studied using 18S and 28S rRNA and COI mtDNA. Bayesian analysis supports the monophyly of 10 genera whereas Andromastax, Jamstecia, Nudivorax and Aegisthus revealed to be paraphyletic. The first offshoot of the phylogenetic tree is a clade consists of the undescribed genus Aegisthidae gen.1 sister to the two monophyletic genera Cerviniella and Hase, whereas the other Cerviniinae members (represented by Cervinia and Expansicervinia) assemble a monophylum, sister to the hyperbenthic and planktonic aegisthid genera, resulting in the paraphyly of the subfamily Cerviniinae. Hence, we defined the new subfamily Cerviniellinae subfam. nov. encompassing the three benthic genera Cerviniella, Hase and Eucanuella. The subfamily Cerviniinae has been re-defined to include Cervinia, Expansicervinia and Paracerviniella. Members of the subfamily Pontostratiotinae were clustered into two clades, one consists of the genus Stratiopontotes sister to an undescribed genus + Cerviniopsis and Siphonis. The second contains Pontostratiotes sister to the members of the planktonic subfamily Aegisthinae, resulting in the paraphyly of the Pontostratiotinae. Therefore, the Pontostratiotinae has been re-defined to include only members of the genus Pontostratiotes; whereas the subfamily Cerviniopseinae has been re-erected and re-defined containing Stratiopontotes, Cerviniopsis, Siphonis, Aegisthidae gen. 2, Herdmaniopsis, Hemicervinia and Tonpostratiotes. Within this subfamily, the associated Siphonis clusters as sister to the Cerviniopsis represents an example of convergent evolution in which the possession of a stylet-like mandible and an oral cone reminiscent of the Siphonostomatoida. The planktonic Aegisthus, Andromastax, Jamstecia, Nudivorax and Scabrantenna confirm the monophylom Aegisthinae, sister to the Pontostratiotinae.

          Conclusions

          Our DNA based phylogeny reveals the deep-sea origin of Aegisthidae by placing benthic Aegisthidae gen.1 and Cerviniellinae subfam. nov. as the most basal lineages. Secondary adaptations to hyperbenthic and planktonic realms, as well as associated lifestyle were discovered here by the derived positions of Pontostratiotinae, Aegisthinae and Siphonis respectively.

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          Most cited references18

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          Unresolved cases of type fixation, synonymy and homonymy in harpacticoid copepod nomenclature (Crustacea: Copepoda)

          RONY HUYS (2009)
          Type fixation for each of the 601 valid genera (17 placed incertae sedis) and 13 genera of doubtful identity (genera inquirenda) in the Harpacticoida (Crustacea, Copepoda) has been verified. Twenty-four genus-group names published after 1930 lack the mandatory type fixation and are therefore unavailable. With the exception of Kliopsyllus Kunz, 1962 which is replaced by its senior synonym Emertonia Wilson, 1932, such names are made available here by either attributing the original name to the first author(s) who explicitly fixed a type species (Psammastacus Nicholls, 1935; Alteuthellopsis Lang, 1944; Idyellopsis Lang, 1944; Paralaophonte Lang, 1944; Robertgurneya Lang, 1944; Cladorostrata Shen & Tai, 1963; Micropsammis Mielke, 1975; and the subgenera Rheocamptus Borutzky, 1948 and Scottopsyllus Kunz, 1962;) or by adopting the name taking the present authorship and date (Paranannopus Lang, 1936a; Paraidya Sewell, 1940; Apodopsyllus Kunz, 1962; Scottolana Por, 1967; Barbaracletodes Becker, 1979; Ameiropsyllus Bodin, 1979; Chilaophonte Mielke, 1985; Psammonitocrella Rouch, 1992; Tectacingulum Harris, 1994; and the subgenera Intermedopsyllus Kunz, 1962 (corrected spelling Intermediopsyllus) and Fiersiella Suárez Morales & Iliffe, 2005). In two cases a ruling by the International Commission on Zoological Nomenclature will be required to avoid upsetting a long-accepted name in its accustomed meaning (Halectinosoma Lang, 1944; Heterolaophonte Lang, 1944). The recently proposed generic name Pilocamptus Wells, 2007 does not satisfy the provisions of ICZN Art. 13.1 and is here made available by explicit citation of a bibliographic reference that provides a diagnosis purported to differentiate the taxon. Rhizothrix Brady & Robertson, 1876 is an unavailable name which was first made available by Sars (1909a). The unavailable generic name Scottopsyllus Kunz, 1962 has no potentially valid synonym and is replaced by the next oldest available name from among its subgenera, i.e. Wellsopsyllus Kunz, 1981 (ICZN Art. 23.3.5). The unavailable subgeneric name Psyllocamptus (Langpsyllocamptus) Kunz, 1975b is not reinstated because it denotes a taxon that is based exclusively on plesiomorphies. New replacement names have been proposed for preoccupied generic names in the harpacticoid families Canthocamptidae (Poria Lang, 1965; Dahlakia Por, 1986a), Dactylopusiidae (Sewellia Lang, 1965), and Leptopontiidae (Ichnusella Cottarelli, 1971). The preoccupied generic name Anoplosoma Sars, 1911c (family Ameiridae) is replaced by a previously proposed, but subsequently forgotten, replacement name, Anoplosomella Strand, 1929. Nomina nova are also suggested for Parathalassius Dussart, 1986 (Calanoida: Centropagidae) and Berea Yamaguti, 1963 (Cyclopoida: Chondracanthidae) which have entered into homonymy with previously established names. The junior synonym Alteutha Baird, 1846b is considered valid, taking precedence as a nomen protectum over the older names Sterope Goodsir, 1845 and Carillus Goodsir, 1845 (nomina oblita). Similar reversal of precedence applies to the family-group names Peltidiidae Claus, 1860 and Tisbidae Stebbing, 1910 which are junior subjective synonyms of Steropinae Dana, 1854 and Scutellidiinae Claus, 1889, respectively. Since the type of Idomene Philippi, 1843 is identified as a member of the Clausidiidae (Cyclopoida), the generic name Xouthous Thomson, 1883 is reinstated to accommodate all remaining species currently placed in Idomene. The forgotten copepod genus Microchelonia Brady, 1918 is placed in the family Laophontidae and considered a senior subjective synonym of Namakosiramia Ho & Perkins, 1977. The family-group name Pontostratiotidae A. Scott, 1909 (type: Pontostratiotes Brady, 1883) is a senior subjective synonym of Cerviniopseinae Brotskaya, 1963 (type: Cerviniopsis Sars, 1903) and the former is consequently reinstated at the subfamilial level. The family-group name Huntemanniidae Por, 1986a (type: Huntemannia Poppe, 1884) is a junior subjective synonym of Nannopinae Brady, 1880a (type: Nannopus Brady, 1880a) and the latter is reinstated as the valid name at family rank and with the spelling corrected to Nannopodidae. The family-name Paranannopinae Por, 1986a is a nomen nudum based on an unavailable generic name and is replaced by Danielsseniinae Huys & Gee in Huys et al., 1996. Four orphaned taxonomic groupings created by the removal of the type species – but not of the remaining species included in a genus – require an existing (previously invalid) or new generic name. Amphiascus Sars, 1905a is a senior objective synonym of Paramphiascopsis Lang, 1944 and must be restricted to the species currently included in the latter; a new genus Sarsamphiascus (type: Dactylopus minutus Claus, 1863) is proposed to receive all remaining Amphiascus species. The new generic names Monardius gen. nov. and Glabrotelson gen. nov. are proposed for the orphaned taxonomic groupings resulting from the removal of the types of Teissierella Monard, 1935a to Robertsonia Brady, 1880a, and of Hastigerella Nicholls, 1935 to Arenosetella Wilson, 1932, respectively. Leptomesochra Sars, 1911b is a senior subjective synonym of Interleptomesochra Lang, 1965 and must be restricted to the latter’s taxonomic concept; the previously unavailable generic name Leptameira Lang, 1936d is reinstated under the present authorship and date to assemble all remaining Leptomesochra species.
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            Ribosomal RNA sequences for inferring phylogeny within the grass family (Poaceae)

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              Species diversity and faunal affinities of meiobenthic Copepoda in the deep sea

              B. Coull (1972)
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                Author and article information

                Contributors
                sahar.khodami@senckenberg.de
                nancy.mercado@senckenberg.de
                pedro.martinez@senckenberg.de
                Journal
                BMC Evol Biol
                BMC Evol. Biol
                BMC Evolutionary Biology
                BioMed Central (London )
                1471-2148
                14 March 2020
                14 March 2020
                2020
                : 20
                : 36
                Affiliations
                GRID grid.500026.1, ISNI 0000 0004 0487 6958, Senckenberg am Meer, German Centre for Marine Biodiversity Research, ; Südstrand 44, 26382 Wilhelmshaven, Germany
                Author information
                http://orcid.org/0000-0002-7944-4004
                Article
                1594
                10.1186/s12862-020-1594-x
                7071595
                32171237
                1bd1d5ba-61d1-4c07-8d88-e0e99fcec651
                © The Author(s). 2020

                Open AccessThis article is distributed under the terms of the Creative Commons Attribution 4.0 International License ( http://creativecommons.org/licenses/by/4.0/), which permits unrestricted use, distribution, and reproduction in any medium, provided you give appropriate credit to the original author(s) and the source, provide a link to the Creative Commons license, and indicate if changes were made. The Creative Commons Public Domain Dedication waiver ( http://creativecommons.org/publicdomain/zero/1.0/) applies to the data made available in this article, unless otherwise stated.

                History
                : 10 October 2018
                : 5 February 2020
                Categories
                Research Article
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                © The Author(s) 2020

                Evolutionary Biology
                Evolutionary Biology

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