INTER‐ AND INTRASPECIFIC VARIATION OF THE PSEUDO‐NITZSCHIA DELICATISSIMA COMPLEX (BACILLARIOPHYCEAE) ILLUSTRATED BY RRNA PROBES, MORPHOLOGICAL DATA AND PHYLOGENETIC ANALYSES 1

By Nina Lundholm, Ø. Moestrup, Y. Kotaki, Kerstin Hoef-Emden, C. Scholin, P. Miller. 2006

199 citations recorded by the source corpus.

Subfields: Cell Biology, Food Science, Plant Science

View Paper: https://www.semanticscholar.org/paper/7f9149530c5126028222391969427f468569e316

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In Food Science

1. Wim Vyverman
2. E. Verleyen
3. P. Vanormelingen

In Plant Science

1. O. De Clerck
2. G. Zuccarello
3. Heroen Verbruggen
4. Frederik Leliaert

Citations in the corpus

• Pseudo-nitzschia physiological ecology, phylogeny, toxicity, monitoring and impacts on ecosystem health (2012, background): “This has revealed that cryptic and pseudo-cryptic species are a more commonly encountered phenomenon than previously considered (Orsini et al., 2004; Lundholm et al., 2003, 2006, in press; Amato et al., 2007; Quijano-Scheggia et al., 2009b).”
• Application of environmental sample processor (ESP) methodology for quantifying Pseudo‐nitzschia australis using ribosomal RNA‐targeted probes in sandwich and fluorescent in situ hybridization formats (2006, background): “For example, distinguishing between species of pennate diatoms within the genus Pseudo-nitzschia H. Peragallo requires electron microscopy (e.g., Hasle 1965, 1994; Smith et al. 1990; Lundholm et al. 2006).”
• The diversity and distribution of diatoms: from cosmopolitanism to narrow endemism (2008, background): “…taxonomic signiWcance, are instead generally correlated with variation in reproductive, moleculargenetic, physiological, and ecological characters (see review by Mann 1999 and references therein; Behnke et al. 2004; Beszteri et al. 2005; Créach et al. 2006; Lundholm et al. 2006; Amato et al. 2007).”
• Morphology, physiology, molecular phylogeny and sexual compatibility of the cryptic Pseudo-nitzschia delicatissima complex (Bacillariophyta), including the description of P. arenysensis sp. nov. (2009, methodology): “On the contrary, our strains from the northwestern Mediterranean strains did not reveal such differences and in this respect agree with Lundholm et al. (2006).”
• Intense stratification leads to phytoplankton nutrient limitation and reduced microzooplankton grazing in the southeastern Bering Sea (2008, unknown): “Light microscopy followed by SEM analysis showed that two cell types were present, a large cell identified as P. seriata, and a smaller cell consistent in frustule morphology with the P. delicatissima complex (Lundholm et al., 2006).”
• Morphological, genetic and mating diversity within the widespread bioindicator Nitzschia palea (Bacillariophyceae) (2009, background): “Molecular sequencing has revealed the presence of genetically distinct entities within morphologically delineated diatom species in a variety of genera, including Pseudo-nitzschia (e.g. Lundholm et al. 2006; Amato et al. 2007), Skeletonema (Sarno et al. 2005) and Sellaphora (Evans et al. 2007, 2008)”
• Pseudo-nitzschia (Bacillariophyceae) species, domoic acid and amnesic shellfish poisoning: revisiting previous paradigms (2012, background): “…P. caciantha (Lundholm & Moestrup 2002), P. antarctica (Marchant & Thomas 2005), P. obtusa (Hasle & Lundholm 2005), P. decipiens, P. dolorosa (Lundholm et al. 2006), P. roundii (HernándezBecerril & Dı́az-Almeyda 2006), P. mannii (Amato & Montresor 2008), P. arenysensis (Quijano-Scheggia et…”
• Comparative molecular and morphological phylogenetic analyses of taxa in the Chaetocerotaceae (Bacillariophyta) (2010, background): “…often consist of sets of genetically distinct groups of specimens that are reproductively isolated (Montresor et al. 2003; Behnke et al. 2004; Sarno et al. 2005, 2007; Lundholm et al. 2006; Amato et al. 2007; Beszteri et al. 2007; Evans et al. 2008; Kooistra et al. 2008; Vanormelingen et al. 2008).”
• DNA-based species delimitation in algae (2014, background): “…Transcribed Spacer (ITS) of the nuclear rDNA are much higher than those of the rRNA genes, and this region has been advocated as a marker for species level phylogenetics for macro- and microalgae (e.g., van der Strate et al., 2002; Lundholm et al., 2006; Gile et al., 2010; Pröschold et al., 2011).”
• Morphology, phylogeny, and sexual cycle of Pseudo-nitzschia mannii sp. nov. (Bacillariophyceae): a pseudo-cryptic species within the P. pseudodelicatissima complex (2008, methodology): “On the basis of the present and previous phylogenies and morphological investigations (Lundholm et al. 2003, 2006; Amato et al. 2007; present work), it emerges that P. caciantha, P. calliantha, and P. mannii are phylogenetically more closely related with one another than with P. pseudodelicatissima…”
• Tolerance of benthic diatoms from temperate aquatic and terrestrial habitats to experimental desiccation and temperature stress (2010, background): “…are generally correlated with differences in reproductive, molecular, physiological and ecological char- acters (e.g. Mann 1999; Behnke et al. 2004; Lundholm et al. 2006; Vanormelingen et al. 2008a), these isolates were divided in different morphotypes (Table 2) and treated as separate species.”