DIVERSITY IN THE GENUS SKELETONEMA (BACILLARIOPHYCEAE). II. AN ASSESSMENT OF THE TAXONOMY OF S. COSTATUM‐LIKE SPECIES WITH THE DESCRIPTION OF FOUR NEW SPECIES 1
By D. Sarno, Wiebe H. C. F. Kooistra, Linda K. Medlin, I. Percopo, Adriana Zingone. 2005
413 citations recorded by the source corpus.
Subfields: Biomaterials, Molecular Biology, Oceanography
View Paper: https://www.semanticscholar.org/paper/995911e4900ba3ea8e3f15c04449d901858f98b4
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In Biomaterials
- D. Sarno
- S. Balzano
- Wiebe H. C. F. Kooistra
- Linda K. Medlin
- David G. Mann
- K. Evans
- P. Hayes
- Marina Montresor
In Molecular Biology
- D. Sarno
- Wiebe H. C. F. Kooistra
- Linda K. Medlin
- S. Balzano
- U. John
- U. Tillmann
- David G. Mann
- A. Cembella
In Oceanography
- Wiebe H. C. F. Kooistra
- D. Sarno
- U. Tillmann
- Linda K. Medlin
- S. Balzano
- A. Cembella
- U. John
- Adriana Zingone
Citations in the corpus
- Tolerance of benthic diatoms from temperate aquatic and terrestrial habitats to experimental desiccation and temperature stress (2010, background): “In diatoms, it has recently become clear that a high (pseudo)cryptic species diversity exists (Sarno et al. 2005; Mann & Evans 2007; Vanormelingen et al. 2008a), and closely related species can occupy different niches (Vanelslander et al. 2009).”
- Molecular assessment of phylogenetic relationships in selected species/genera in the naviculoid diatoms (Bacillariophyta). I. The genus Placoneis. (2007, background): “…position within the heterokont algae (e.g., Daugbjerg & Andersen 1997), to reconstruct the evolution of the major classes (e.g., Medlin & Kaczmarska 2004) or to assess the monophyly of diatom orders or genera (e.g., Beszteri et al. 2001) and the presence of cryptic species (Sarno et al. 2005).”
- Effects of salinity on the growth rate and morphology of ten Skeletonema strains (2011, methodology): “These temperatures were chosen because they reflect conditions under which these strains were sampled, or because previous workers (Sarno et al., 2005, 2007) demonstrated rapid growth under these conditions.”
- Barcoding diatoms: evaluation of the V4 subregion on the 18S rRNA gene, including new primers and protocols (2011, methodology): “…small ribosomal subunit (SSU-rRNA gene), as the latter has been used widely for phylogenetic and taxonomic purposes (e.g. Behnke et al. 2004; Beszteri et al. 2001; Friedl and O’Kelly 2002; Kooistra and Medlin 1996; Medlin et al. 1996; Medlin and Kaczmarska 2004; Sarno et al. 2005; Sorhannus 2007).”
- INTER‐ AND INTRASPECIFIC VARIATION OF THE PSEUDO‐NITZSCHIA DELICATISSIMA COMPLEX (BACILLARIOPHYCEAE) ILLUSTRATED BY RRNA PROBES, MORPHOLOGICAL DATA AND PHYLOGENETIC ANALYSES 1 (2006, background): “It was recently shown, however, that at least some of the variation represent interspecific variation, and ‘‘S. costatum’’ has now been split into several species (Sarno et al. 2005).”
- Revision of the diatom genus Sellaphora: a first account of the larger species in the British Isles. (2008, background): “…et al. 2004, Evans et al. 2007, 2008) that what appear to be very small, though consistent, morphological differences can be correlated with significant molecular genetic divergence or sexual incompatibility (cf. Mann & chEpurnov 2005, sarno et al. 2005, TroBaJo et al. 2006, aMaTo et al. 2007).”
- The diversity and distribution of diatoms: from cosmopolitanism to narrow endemism (2008, background): “Clones assigned to the marine centric diatom Skeletonema marinoi (forming a clade with authenticated clones in analyses of LSU sequence data) were found in both the PaciWc and Atlantic Oceans and in the Mediterranean Sea (Sarno et al. 2005; Godhe et al. 2006).”
- Phytoplankton blooms in estuarine and coastal waters: Seasonal patterns and key species (2015, neutral): “costatum (Sarno et al., 2005).”
- MOLECULAR PHYLOGENY OF SELECTED MEMBERS OF THE ORDER THALASSIOSIRALES (BACILLARIOPHYTA) AND EVOLUTION OF THE FULTOPORTULA 1 (2006, background): “…global Skeletonema strains show that none of the living species named as Skeletonema costatum corresponds to the type material of S. costatum, and that the genetic diversity of the strains is so extensive worldwide that four new species have been described (Sarno et al. 2005, Zingone et al. 2005).”
- Evolution of the diatoms: insights from fossil, biological and molecular data (2006, background): “Weddell Sea but uncommon in more recent taxa. None of the other Weddell Sea diatoms seem to have rimoportulae but a rimoportula is illustrated on a pyritized specimen of Aulacodiscus sieminskae Geroch (Geroch 1978, pl. 3 figs 1–6) from the Lower Cretaceous of the Polish Carpatians. Foucault et al. (”
- INTRASPECIFIC GENETIC DIVERSITY IN THE MARINE COCCOLITHOPHORE EMILIANIA HUXLEYI (PRYMNESIOPHYCEAE): THE USE OF MICROSATELLITE ANALYSIS IN MARINE PHYTOPLANKTON POPULATION STUDIES 1 (2006, background): “Cryptic species have been documented in several coccolithophorid taxa, with molecular data supporting earlier morphological and geological evidence (Sáez et al. 2001), as well as in other cosmopolitan planktonic species (Sarno et al. 2005).”
- MORPHOLOGICAL AND ECOLOGICAL VARIATION WITHIN THE ACHNANTHIDIUM MINUTISSIMUM (BACILLARIOPHYCEAE) SPECIES COMPLEX 1 (2007, background): “Considering the growing evidence for the existence of cryptic diatom species (Mann et al. 2004, Sarno et al. 2005), it is reasonable to suggest that similar-looking taxa, such as A. jackii, A. minutissimum, A. lineare, and ‘‘A. linearis f. curta,’’ and other morphological groups that have not been…”