Torsten Hugo Struck

• Struck, T. H., Wey-Fabrizius, A. R., Golombek, A., Hering, L., Weigert, A., Bleidorn, C., Klebow, S., Iakovenko, N., Hausdorf, B., Petersen, M., Kück, P., Herlyn, H. & Hankeln, T. (2014). Platyzoan paraphyly based on phylogenomic data supports a non-coelomate ancestry of Spiralia. Molecular Biology and Evolution 31: 1833-1849.
• Weigert, A., Helm, C., Meyer, M., Nickel, B., Arendt, D., Hausdorf, B., Santos, S. R., Halanych, K. M., Purschke, G., Bleidorn, C. & Struck, T. H. (2014). Illuminating the base of the annelid tree using transcriptomics. Molecular Biology and Evolution 31: 1391-1401.
• Struck, T. H. (2014). TreSpEx – Detection of misleading signal in phylogenetic reconstructions based on tree information. Evolutionary Bioinformatics 10: 51-67.
• Struck, T. H. (2013). The impact of paralogy on phylogenomic studies – a case study on annelid relationships. PLoS ONE 8: e62892.
• Thornhill, D. J., Struck, T. H., Ebbe, B., Lee, R. W., Mendoza, G. F., Levin, L. A. & Halanych, K. M. (2012). Adaptive Radiation in Extremophilic Dorvilleids: Diversification of a Single Colonizer or Multiple Independent Lineages? Ecology & Evolution 2: 1958–1970.
• Struck, T. H., Paul, C., Hill, N., Hösel, C., Kube, M., Lieb, B., Meyer, A., Tiedemann, R., Purschke, G. & Bleidorn, C. (2011). Phylogenomic analyses unravel annelid evolution. Nature 471: 95-98.
• Struck, T. H. & Fisse, F. (2008). Phylogenetic position of Nemertea derived from phylogenomic data. Molecular Biology and Evolution 25: 728–736.
• Struck, T. H. (2007). Data congruence, paedomorphosis and salamanders. Frontiers in Zoology 4: 22.
• Struck, T. H., Schult, N., Kusen, T., Hickman, E., Bleidorn, C., McHugh, D. & Halanych, K. M. (2007). Annelida phylogeny and the status of Sipuncula and Echiura. BMC Evolutionary Biology 7:57.

• Cerca De Oliveira, Josè; Purschke, Günter & Struck, Torsten H (2018). Marine connectivity dynamics: clarifying cosmopolitan distributions of marine interstitial invertebrates and the meiofauna paradox. Marine Biology.  ISSN 0025-3162.  165(8) . doi: 10.1007/s00227-018-3383-2
• Elgetany, Asmaa H.; El-Ghobashy, Ahmed E.; Ghoneim, Ahmad & Struck, Torsten H (2018). Description of a new species of the genus Marphysa (Eunicidae), Marphysa aegypti sp.n., based on molecular and morphological evidence. Invertebrate Zoology.  ISSN 1812-9250.  15(1), s 71- 84 . doi: 10.15298/invertzool.15.1.05
• Ramey-Balci, Patricia; Fiege, Dieter & Struck, Torsten H (2018). Molecular phylogeny, morphology, and distribution of Polygordius (Polychaeta: Polygordiidae) in the Atlantic and Mediterranean. Molecular Phylogenetics and Evolution.  ISSN 1055-7903.  127, s 919- 930 . doi: https://doi.org/10.1016/j.ympev.2018.06.039
• Struck, Torsten H (2017). Phylogeny of Annelida, In Ponnampalam Gopalakrishnakone & Anita Malhotra (ed.),  Evolution of Venomous Animals and Their Toxins.  Springer Science+Business Media B.V..  ISBN 978-94-007-6457-6.  Chapter 18.  s 399 - 413
• Struck, Torsten H (2017). Spiralia/Lophotrochozoa, In Michel Laurin (ed.),  Evolution of Phylogenetic Tree of Life.  Eolss Publishing CO. Ltd..  ISBN 9781780215242.  Chapter.
• Struck, Torsten H; Feder, Jeffrey L.; Bendiksby, Mika; Birkeland, Siri; Cerca De Oliveira, Josè; Gusarov, Vladimir; Kistenich, Sonja; Larsson, Karl-Henrik; Liow, Lee Hsiang; Nowak, Michael; Stedje, Brita; Bachmann, Lutz & Dimitrov, Dimitar (2017). Finding Evolutionary Processes Hidden in Cryptic Species. Trends in Ecology & Evolution.  ISSN 0169-5347.  33(3), s 153- 163 . doi: 10.1016/j.tree.2017.11.007 Fulltekst i vitenarkiv. Vis sammendrag

  Cryptic species could represent a substantial fraction of biodiversity. However, inconsistent definitions and taxonomic treatment of cryptic species prevent informed estimates of their contribution to biodiversity and impede our understanding of their evolutionary and ecological significance. We propose a conceptual framework that recognizes cryptic species based on their low levels of phenotypic (morphological) disparity relative to their degree of genetic differentiation and divergence times as compared to non-cryptic species. We discuss how application of a more rigorous definition of cryptic species in taxonomic practice will lead to more accurate estimates of their prevalence in nature, better understanding of their distribution patterns on the tree of life, and increased abilities to resolve the processes underlying their evolution.

• Struck, Torsten H; Koczula, Jens; Stateczny, Dave; Meyer, Christian & Purschke, Günter (2017). Two new species in the annelid genus Stygocapitella (Orbiniida, Parergodrilidae) with comments on their biogeography. Zootaxa.  ISSN 1175-5326.  4286(3), s 301- 332 . doi: 10.11646/zootaxa.4286.3.1
• Aguado, Maria Teresa; Richter, Sandy; Sontowski, Rebekka; Golombek, Anja; Struck, Torsten Hugo & Bleidorn, Christoph (2016). Syllidae mitochondrial gene order is unusually variable for Annelida. Gene.  ISSN 0378-1119.  594(1), s 89- 96 . doi: 10.1016/j.gene.2016.08.050 Fulltekst i vitenarkiv. Vis sammendrag

  Complete mitochondrial genomes of five syllids (Streptosyllis sp., Eusyllis blomstrandi, Myrianida brachycephala, Typosyllis antoni and Typosyllis sp.) have been obtained using Illumina sequencing. Together with two previous studied taxa (Ramisyllis multicaudata and Trypanobia cryptica), the analysed sequences represent most of the main lineages within the family Syllidae (Anoplosyllinae, Eusyllinae, Autolytinae and Syllinae). The genomic features, gene order and phylogenetic relationships are examined. Unusual for annelids, syllid mitochondrial genomes are highly variable in their gene order. Considering genomic features, such as length, skewness, gene content, and codon bias, most similar to the rest of annelids are the genomes of E. blomstrandi and M. brachycephala, while Streptosyllis sp. and the analysed sylline taxa (R. multicaudata, T. cryptica, T. antoni and Typosyllis sp.) are the most dissimilar. Two methionine tRNA's (trnM) have been found in T. antoni and Typosyllis sp. The mt genomes of these latter taxa are the longest with numerous non-coding regions. The 13 protein coding genes, as well as the rRNA's are used to perform phylogenetic analyses that recovered the relationships within the family explored before by previous authors. The gene order in Syllidae shows very different patterns. E. blomstrandi and M. prolifera show a similar pattern to the one found in Pleistoannelida; however this might have changed at least twice within Syllidae: in Streptosyllis sp. and within Syllinae. All analysed Syllinae show different gene orders, thereby illustrating more variability as all other pleistoannelids analysed so far. The information provided herein allows a more accurate reconstruction of the possible evolutionary scenarios in Syllidae.

• Kocot, Kevin M.; Struck, Torsten H; Merkel, Julia; Waits, Damien S.; Todt, Christiane; Bannock, Pamela M.; Weese, David A.; Cannon, Johanna T.; Moroz, Leonid L.; Lieb, Bernhard & Halanych, Kenneth M. (2016). Phylogenomics of Lophotrochozoa with consideration of systematic error. Systematic Biology.  ISSN 1063-5157.  66(2), s 256- 282 . doi: 10.1093/sysbio/syw079 Fulltekst i vitenarkiv. Vis sammendrag

  Abstract.—Phylogenomic studies have improved understanding of deep metazoan phylogeny and show promise for resolving incongruences among analyses based on limited numbers of loci. One region of the animal tree that has been especially difficult to resolve, even with phylogenomic approaches, is relationships within Lophotrochozoa (the animal clade that includes molluscs, annelids, and flatworms among others). Lack of resolution in phylogenomic analyses could be due to insufficient phylogenetic signal, limitations in taxon and/or gene sampling, or systematic error. Here, we investigated why lophotrochozoan phylogeny has been such a difficult question to answer by identifying and reducing sources of systematic error. We supplemented existing data with 32 new transcriptomes spanning the diversity of Lophotrochozoa and constructed a new set of Lophotrochozoa-specific core orthologs. Of these, 638 orthologous groups (OGs) passed strict screening for paralogy using a tree-based approach. In order to reduce possible sources of systematic error, we calculated branch-length heterogeneity, evolutionary rate, percent missing data, compositional bias, and saturation for each OG and analyzed increasingly stricter subsets of only the most stringent (best) OGs for these five variables. Principal component analysis of the values for each factor examined for each OG revealed that compositional heterogeneity and average patristic distance contributed most to the variance observed along the first principal component while branch-length heterogeneity and, to a lesser extent, saturation contributed most to the variance observed along the second. Missing data did not strongly contribute to either. Additional sensitivity analyses examined effects of removing taxa with heterogeneous branch lengths, large amounts of missing data, and compositional heterogeneity. Although our analyses do not unambiguously resolve lophotrochozoan phylogeny, we advance the field by reducing the list of viable hypotheses. Moreover, our systematic approach for dissection of phylogenomic data can be applied to explore sources of incongruence and poor support in any phylogenomic data set.

• Sielaff, Malte; Schmidt, Hanno; Struck, Torsten Hugo; Rosenkranz, David; Mark Welch, David B.; Hankeln, Thomas & Herlyn, Holger (2016). Phylogeny of Syndermata (syn. Rotifera): Mitochondrial gene order verifies epizoic Seisonidea as sister to endoparasitic Acanthocephala within monophyletic Hemirotifera. Molecular Phylogenetics and Evolution.  ISSN 1055-7903.  96, s 79- 92 . doi: 10.1016/j.ympev.2015.11.017

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• Struck, Torsten H; Feder, Jeffrey L.; Bendiksby, Mika; Birkeland, Siri; Cerca De Oliveira, Josè; Gusarov, Vladimir; Kistenich, Sonja; Larsson, Karl-Henrik; Liow, Lee Hsiang; Nowak, Michael; Stedje, Brita; Bachmann, Lutz & Dimitrov, Dimitar (2018). Cryptic Species ? More Than Terminological Chaos: A Reply to Heethoff. Trends in Ecology & Evolution.  ISSN 0169-5347.  33(5), s 310- 312 . doi: 10.1016/j.tree.2018.02.008

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