Phylogenetic reconstructions of the Haptophyta inferred from 18S ribosomal DNA sequences and available morphological data
By Bente Edvardsen, W. Eikrem, J. C. Green, R. Andersen, S. Y. Moon-van der Staay, Linda K. Medlin. 2000
212 citations recorded by the source corpus.
Subfields: Ecology, Molecular Biology, Oceanography
View Paper: https://www.semanticscholar.org/paper/c02b5ba3bb518e6a55ea1a3f1935a2f5b2e3287c
How researchers see this paper
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In Ecology
- Daniel Vaulot
- Fabrice Not
- Ian Probert
- N. Simon
- Wiebe H. C. F. Kooistra
- N. Dijkman
- J. Kromkamp
- A. Worden
In Molecular Biology
- Daniel Vaulot
- Fabrice Not
- Ian Probert
- Wiebe H. C. F. Kooistra
- Linda K. Medlin
- N. Simon
- J. Young
- Alberto Sáez
In Oceanography
- Ian Probert
- Daniel Vaulot
- M. Geisen
- J. Young
- Fabrice Not
- Linda K. Medlin
- Wiebe H. C. F. Kooistra
- Alberto Sáez
Citations in the corpus
- Phospholipid-derived fatty acids as chemotaxonomic markers for phytoplankton: application for inferring phytoplankton composition (2006, background): “Phylogenetic trees show that the division of Haptophyta is split into 2 classes, being the Pavlovophyceae (which contains all Pavlova species), and the Prymnesiophyceae containing all other haptophyte species (Edvardsen et al. 2000).”
- On the description of Tisochrysis lutea gen. nov. sp. nov. and Isochrysis nuda sp. nov. in the Isochrysidales, and the transfer of Dicrateria to the Prymnesiales (Haptophyta) (2013, background): “…corroborates published information that shows that D. inornata and Imantonia rotunda are very similar in ultrastructure (Green and Pienaar 1977; Edvardsen et al. 2000) and pigment signatures (Jeffrey and Wright 1994; Zapata et al. 2004), and the fact that neither produces alkenones (Marlowe et…”
- Ribosomal DNA phylogenies and a morphological revision provide the basis for a revised taxonomy of the Prymnesiales (Haptophyta) (2011, methodology): “, 2000 ; Edvardsen & Medlin, 2007 ) and rbc L DNA sequence analysis (Inouye, 1997 ; Fujiwara et al.”
- Holococcolithophore‐heterococcolithophore (Haptophyta) life cycles: Flow cytometric analysis of relative ploidy levels (2004, unknown): “NB. Molecular genetic data on haptophytes is being actively compiled but studies to date (Edvardsen et al., 2000; Fujiwara et al., 2001, Sáez et al., 2003; Sáez et al., in press) show a high degree of congruence between analyses based on different genes (18S, Rubisco, tufA) and between molecular…”
- Diversity and Ecology of Eukaryotic Marine Phytoplankton (2012, background): “The organic scales of Pavlovophyceae, when present, consist of small dense bodies (‘knob scales’) in contrast to the plate scales of the Prymnesiophyceae.”
- What is new in coccolithophore biology (2004, background): “Using flow cytometric DNA analysis, they confirm that Coccolithus cells are diploid whereas the alternate holococcolithophorid stage is haploid; other species were analyzed in this study (see below) confirming the earlier hypothesis based on body scale morphologies, that heterococcolithophores are d”