Katrine Worsaae

Prof. Dr. Katrine Worsaae

Marine Biological Section, Department of Biology, University of Copenhagen, Denmark
orcid

Research Focus & Metrics

Academic Career Length

26Years (2001-Present)

(Calculated once Scilit publication data is synced: current year − year of first publication + 1)

Representative Publications

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1 August 2015 in Current Biology
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Journal Article
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CLChristopher E. Laumer
Christopher E. Laumer
NBNicolas Bekkouche
Nicolas Bekkouche
AKAlexandra Kerbl
Alexandra Kerbl
FGFreya Goetz
Freya Goetz
RNRicardo C. Neves
Ricardo C. Neves
Katrine WorsaaeKatrine Worsaae
Katrine Worsaae

23 July 2015 in Molecular Biology and Evolution
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Journal Article
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SASónia Cristina Da Silva Andrade
Sónia Cristina Da Silva Andrade
MNMarta Novo
Marta Novo
GKGisele Y. Kawauchi
Gisele Y. Kawauchi
Katrine WorsaaeKatrine Worsaae
Katrine Worsaae
FPFredrik Pleijel
Fredrik Pleijel
Greg RouseGreg Rouse
Greg Rouse
Annelid disparity has resulted in morphological-based classifications that disagree with phylogenies based on Sanger sequencing and phylogenomic analyses. However, the data used for the latter studies came from various sources and technologies, involved poorly occupied matrices and lacked key lineages. Here, we generated a new Illumina-based data set to address annelid relationships from a fresh perspective, independent from previously generated data and with nearly fully occupied matrices. Our sampling reflects the span of annelid diversity, including two symbiotic annelid groups (Myzostomida and Spinther) and five meiofaunal groups once referred to as part of Archiannelida (three from Protodrilida, plus Dinophilus and Polygordius). As well as the placement of these unusual annelids, we sought to address the overall phylogeny of Annelida, and provide a new perspective for naming of major clades. Our results largely corroborate the phylogenomic results of Weigert et al. (2014; Illuminating the base of the annelid tree using transcriptomics. Mol Biol Evol. 31:1391-1401), with “Magelona + Owenia” and Chaetopteridae forming a grade with respect to all other annelids. Echiura and Sipuncula are supported as being annelid groups, with Sipuncula closest to amphinomids as sister group to Sedentaria and Errantia. We recovered the three Protodrilida terminals as sister clade to Phyllodocida and Eunicida (=clade Aciculata). We therefore place Protodrilida as part of Errantia. Polygordius was found to be sister group to the scaleworm terminal and the possibility that it is a simplified scaleworm clade, as has been shown for the former family Pisionidae, is discussed. Our results were equivocal with respect to Dinophilus, Myzostomida, and Spinther possibly owing to confounding long-branch effects.

17 March 2011 in Organisms Diversity & Evolution
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GEGregory D. Edgecombe
Gregory D. Edgecombe
GGGonzalo Giribet
Gonzalo Giribet
CDCasey W. Dunn
Casey W. Dunn
AHAndreas Hejnol
Andreas Hejnol
RKReinhardt M. Kristensen
Reinhardt M. Kristensen
MSMartin V. Sørensen
Martin V. Sørensen

23 March 2012 in PLOS ONE
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MCMarco Curini-Galletti
Marco Curini-Galletti
TATom Artois
Tom Artois
VDValentina Delogu
Valentina Delogu
WSWillem H De Smet
Willem H De Smet
Diego FontanetoDiego Fontaneto
Diego Fontaneto
Antonio TodaroAntonio Todaro
Antonio Todaro
Biogeographical and macroecological principles are derived from patterns of distribution in large organisms, whereas microscopic ones have often been considered uninteresting, because of their supposed wide distribution. Here, after reporting the results of an intensive faunistic survey of marine microscopic animals (meiofauna) in Northern Sardinia, we test for the effect of body size, dispersal ability, and habitat features on the patterns of distribution of several groups. As a dataset we use the results of a workshop held at La Maddalena (Sardinia, Italy) in September 2010, aimed at studying selected taxa of soft-bodied meiofauna (Acoela, Annelida, Gastrotricha, Nemertodermatida, Platyhelminthes and Rotifera), in conjunction with data on the same taxa obtained during a previous workshop hosted at Tjärnö (Western Sweden) in September 2007. Using linear mixed effects models and model averaging while accounting for sampling bias and potential pseudoreplication, we found evidence that: (1) meiofaunal groups with more restricted distribution are the ones with low dispersal potential; (2) meiofaunal groups with higher probability of finding new species for science are the ones with low dispersal potential; (3) the proportion of the global species pool of each meiofaunal group present in each area at the regional scale is negatively related to body size, and positively related to their occurrence in the endobenthic habitat. Our macroecological analysis of meiofauna, in the framework of the ubiquity hypothesis for microscopic organisms, indicates that not only body size but mostly dispersal ability and also occurrence in the endobenthic habitat are important correlates of diversity for these understudied animals, with different importance at different spatial scales. Furthermore, since the Western Mediterranean is one of the best-studied areas in the world, the large number of undescribed species (37%) highlights that the census of marine meiofauna is still very far from being complete.

16 November 2020 in Nature Ecology & Evolution
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JMJosé M. Martín-Durán
José M. Martín-Durán
BVBruno C. Vellutini
Bruno C. Vellutini
FMFerdinand Marlétaz
Ferdinand Marlétaz
VCViviana Cetrangolo
Viviana Cetrangolo
NCNevena Cvetesic
Nevena Cvetesic
AHAndreas Hejnol
Andreas Hejnol
The causes and consequences of genome reduction in animals are unclear because our understanding of this process mostly relies on lineages with often exceptionally high rates of evolution. Here, we decode the compact 73.8-megabase genome ofDimorphilus gyrociliatus, a meiobenthic segmented worm. TheD. gyrociliatusgenome retains traits classically associated with larger and slower-evolving genomes, such as an ordered, intact Hox cluster, a generally conserved developmental toolkit and traces of ancestral bilaterian linkage. Unlike some other animals with small genomes, the analysis of theD. gyrociliatusepigenome revealed canonical features of genome regulation, excluding the presence of operons andtrans-splicing. Instead, the gene-denseD. gyrociliatusgenome presents a divergent Myc pathway, a key physiological regulator of growth, proliferation and genome stability in animals. Altogether, our results uncover a conservative route to genome compaction in annelids, reminiscent of that observed in the vertebrateTakifugu rubripes.

10 June 2017 in Cladistics
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Brett C. GonzalezBrett C. Gonzalez
Brett C. Gonzalez
Alejandro MartínezAlejandro Martínez
Alejandro Martínez
EBElizabeth Borda
Elizabeth Borda
Thomas IliffeThomas Iliffe
Thomas Iliffe
DEDanny Eibye‐Jacobsen
Danny Eibye‐Jacobsen
Katrine WorsaaeKatrine Worsaae
Katrine Worsaae