Skip to main content Skip to main navigation menu Skip to site footer
Type: Articles
Published: 2006-09-07
Page range: 53–68
Abstract views: 64
PDF downloaded: 4

Description of a new Fridericia species (Oligochaeta: Enchytraeidae) and its molecular comparison with two morphologically similar species by PCR-RFLP

Department of Systematic Zoology and Ecology, Eötvös Loránd University, Pázmány Péter sétány 1/C, H–1117 Budapest, Hungary
Department of Microbiology, Eötvös Loránd University, Pázmány Péter sétány 1/C, H–1117 Budapest, Hungary
Annelida Oligochaeta Enchytraeidae new Fridericia species ITS PCR-RFLP

Abstract

A new species, Fridericia crassiductata sp.n. was described and compared by DNA fragment analyses (PCR-RFLP), with two similar species, Fridericia ratzeli (Eisen,1872) sensu Nielsen & Christensen (1959) and F. eiseni Dózsa-Farkas, 2005. The main characteristics of the new species are: 13–20 mm long, 0.5–0.7 mm wide, segment number: (38)–40–56, spermatheca with 9–10 large, sessile, globular diverticula, long and thick ectal duct, and two very large (80–130 µ m long) egg shaped ectal glands. Maximum ten chaetae per bundle, typical brown reticulate epidermal gland cells noticeable on the body surface. The oesophageal appendage is variable between type-a and type-c (according to Möller 1971) the branches are located proximally. The seminal vesicle is large, the penial slit is longitudinal with more transverse components. Three subneural glands in XIV–XVI. The new species was collected only in the Zemplén Mountains in Hungary, in similar biotopes (between and under the leaf-litter) to those of the common F. ratzeli. It may be hypothesized that it fills the ecological role of F. ratzeli because, although all three compared species occurred in this area, F. ratzeli was very seldom found and never together with the new species. The three species were also examined by molecular methods. Which confirmed the existence of three distinct species. Both morphological and molecular studies indicate that F. ratzeli is still not a homogeneous species. It seems that the applied molecular methods help distinguish morphologically very similar species.

References

  1. Brockmeyer, V. (1991) Isosymes and general protein patterns for use in discrimination and identification of Enchytraeus species (Annelida, Oligochaeta). Zeitschrift für Zoologische Systematik und Evolutionsforschung 29, 343–361.

    Carvalho, O.S., Cardoso, P.C.M., Pollanah, M.L., Rumi, A., Roche, A., Berne, E., Müller, G. & Caldeira, R.L. (2004) The use of the polymerase chain reaction and restriction fragment length polymorphism technique associated with the classical morphology for characterization of Lymnea columella, L. viatrix, and L. diaphana (Mollusca: Lymnaeidae). Memórias do Instituto Oswaldo Cruz 99, 503–507.

    Cech, G. & Dózsa-Farkas, K. (2005) Identification of Fridericia schmelzi sp.n. combining morphological characters and PCR-RFLP analysis. In: Pop, V. & Pop, A. (Eds.), Advances in earthworm Taxonomy II (Annelida: Oligochaeta). University Press Cluj.(in press)

    Chen, C.A., Chen, C.P., Fan, T.Y., Yu, J.K. & Hsieh, H.L. (2002) Nucleotide sequences of ribosomal internal transcribed spacers and their utility in distinguishing closely related Perinereis Polychaets (Annelida; Polychaetea; Nereididae). Marine Biology 4, 17–29.

    Christensen, B., Berg, U. & Jelnes. J. (1976) A comparative study on enzyme polymorphism in sympatric diploid and triploid forms of Lumbricillus lineatus (Enchytraidae, Oligochaeta). Hereditas 84, 41–48.

    Christensen, B. & Jelnes, J. (1976) Sibling species in the oligochaete worm Lumbricillus rivalis (Enchtraeidae) revealed by enzyme polymorphisms and breeding experiments. Hereditas 83, 237–244.

    Christensen, B., Jelnes, J. & Berg, U. (1978) Long-term isosyme variation in parthenogenetic triploid forms of Lumbricillus lineatus (Enchytraeidae, Oligochaeta) in recently established environments. Hereditas 88, 65–73.

    Cutillas, C., Oliveros, R., de Rojas, M. & Guevera, D.C. (2002) Determination of Trichurus muris from murid hosts and T. arvicolae (Nematoda) from arvicolid rodents by amplification and sequentiation of the ITS1–5.8S–ITS2 segment of the ribosomal DNA. Parasitology Research 88, 574–582.

    Dózsa-Farkas, K. (2005) Fridericia eiseni sp. n., a new enchytraeid species close to the Fridericia ratzeli (Eisen, 1872). Proceedings of the Estonian Academy of Sciences Biology Ecology 54, 4, 279–291.

    Dózsa-Farkas, K. (2006) Comparative enchytraeid faunistic investigation of the Northeastern Mountain ranges in Hungary. In: Tajovsky, K., Schlaghamersky, J. & Pizl, V. (Eds.), Contributions to Soil Zoology in Central Europe II. ISB AS CR, Česke Budejovice, (in press)

    Dumont, H.J., Vanfleteren, J.R., De Jonckhere, J.F. & Weekers, P.H.H. (2005) Phylogenetic relationships, divergence time estimation, and global biogeographic patterns of calopteriygoid damselflies (Odonata, Zygoptera) inferred from ribosomal DNA sequences. Systematics Biology 54, 347–362.

    Gottschling, M. & Plötner, J. (2004) Secondary structure models of the nuclear internal transcribed spacer regions and 5.8S rRNA in Calciodinelloideae (Peridiniaceae) and other dinoflagellates. Nucleic Acids Research 32, 307–315.

    Möller, F. (1971) Systematische Untersuchungen an terricolen Enchytraeiden einiger Grünlandstandorte im Bezirk Potsdam. Mitt. Zool. Mus. Berlin, 47, 131–167.

    Nielsen, C.O. & Christensen, B. (1959) The Enchytraeidae. Critical revision and taxonomy of European species (studies on Enchytraeidae VII). Natura Jutlandica 8–9, 1–160.

    O’Connor, F.B. (1962) The extraction of Enchytraeidae from soil. In: Murphy, P,W. (Ed.), Progress in soil zoology, London: 279–285.

    Rojas, M. de, Mora. M.D., Ubeda, J.M., Cutillas, C., Navajas, M. & Guevera, D.C. (2002) Phylogenetic relationships in rhynonissid mites (Acari: Rhynonyssidae) based on ribosomal DNA sequences: insights for the discrimination of closely related species. Parasitology Research 88, 675–681.

    Schirmacher, A., Schmidt, H. & Westheide, W. (1998) RAPD-PCR investigations on sibling species of terrestrial Enchytraeus (Annelida: Oligochaeta). Biochemical Systematics and Ecology 26, 35–44.

    Schmelz. R.M., Collado, R. & Myohara. M. (2000) A taxonomic study of Enchytraeus japonensis (Enchtraeidae, (Oligochaeta): Morphological and Biochemical comparisons with E. bigeminus. Zoological Science 17, 505–516.

    Schmelz, R.M. (2003) Taxonomy of Fridericia (Oligochaeta, Enchytraeidae). Revision of species with morphological and biochemical methods. pp. 414, Fig 73. Naturwissenschaftlicher Verein in Hamburg.

    Stothard, J.R., Hughes, S. & Rollinson, D. (1996) Variation within the internal transcribed spacer (ITS) of ribosomal DNA genes of intermediate snail hosts within the genus Bulinus (Gastropoda. Planorbidae). Acta Tropica 61, 19–29.

    Subbotin S.A., Vierstraete A., De Ley P., Rowe J., Waeyenberge L., Moens M. & Vanfleteren J.R. (2001) Phylogenetic relationships within the cist-forming Nematodes (Nematoda, Heteroderidae) based on analysis of sequences from the ITS region of ribosomal DNA. Molecular Phylogenetics and evolution 21, 1–16.

    Vidigal, T.H.D.A., Spatz L., Kissinger, J.C., Redondo, R.A.F., Pires, E.C.R., Simpson, A.J.G. & Carvalho, O.S. (2004) Analysis of the first and second internal transcribed spacer sequences of the ribosomal DNA in Biomphalaria tenagophila complex (Mollusca: Planorbidae). Memórias do Instituto Oswaldo Cruz 99, 153–158.

    Weekers, P.H.H., De Jonckheere, J.F. & Dumont, H.J. (2001) Phylogenetic relationships inferred from ribosomal ITS sequences and biogeographic patterns in representatives of the genus Calopteryx (Insecta: Odonata) of the West Mediterranean and adjacent West European Zone. Molecular Phylogenetics and Evolution 20, 89–99.

    Westheide, W., Hass-Cordes, E., Krabusch, M. & Müller, M.C.M. (2003) Ctenodrilus serratus (Polychaeta: Ctenodrilidae) is a truly amphi-atlantic meiofauna species —evidence from molecular data. Marine Biology 142, 637–642.