A study of 25 cultures tentatively identified as Pseudo-nitzschia delicatissima (Cleve) Heiden, and originating from geographically widely distributed locations, showed both morphological and genetic variation among strains. Use of rRNA-targeted DNA probes on 17 different strains showed large variation in the hybridization patterns. Detailed morphological studies placed the isolates into three groups. The sample on which the neotype of P. delicatissima is based was also examined, and used to establish the morphological identity of P. delicatissima. Phylogenetic analyses of 16 strains, based on sequences of internal transcriber spacer 1 (ITS1), 5.8S and ITS2 of the nuclear-encoded rDNA, supported the morphological observations and the hybridization studies, and revealed large genetic variation among strains. A combination of the morphological and molecular findings resulted in the description of two new species, P. decipiens sp. nov. and P. dolorosa sp. nov. P. dolorosa has a mixture of one or two rows of poroids in the striae whereas P. delicatissima always has two rows. In addition, P. dolorosa has wider valves and a lower density of poroids. P. decipiens differs from P. delicatissima by a higher density of striae on the valve face as well as a higher density of poroids on the girdle bands. Among the strains referred to P. delicatissima, an epitype was selected. Large genetic variation was found among the P. delicatissima strains and a subdivision into two major clades represent cryptic species.

The role of geographic isolation in marine microbial speciation is hotly debated because of the high dispersal potential and large population sizes of planktonic microorganisms and the apparent lack of strong dispersal barriers in the open sea. Here, we show that gene flow between distant populations of the globally distributed, bloom-forming diatom species Pseudo-nitzschia pungens (clade I) is limited and follows a strong isolation by distance pattern. Furthermore, phylogenetic analysis implies that under appropriate geographic and environmental circumstances, like the pronounced climatic changes in the Pleistocene, population structuring may lead to speciation and hence may play an important role in diversification of marine planktonic microorganisms. A better understanding of the factors that control population structuring is thus essential to reveal the role of allopatric speciation in marine microorganisms.allopatric speciation | dispersal | marine cosmopolitan planktonic microorganisms | population structure | microsatellites

The effect of elevated pH on growth and on production of the neurotoxin domoic acid was studied in selected diatoms belonging to the genera Pseudo-nitzschia and Nitzschia. Growth of most of the 11 species studied stopped at pH values of 8.7 to 9.1. However, for P. delicatissima and N. navis-varingica the pH limit for growth was higher, 9.3 and 9.7 to 9.8, respectively. A compilation of all available data on the pH limits for growth of marine planktonic diatoms suggests that species from ponds and rock pools all have higher limits than coastal and oceanic species. Taking only coastal and oceanic species into account, the data suggest that smaller species have a higher upper pH limit for growth than larger species. Elevated pH induced production of domoic acid in P. multiseries in amounts comparable to those detected previously under silicate and phosphate limitation. As Pseudo-nitzschia species are found in high concentrations in nutrient-enriched areas, high pH and hence induction of the production of domoic acid would be expected during blooms. These results may help to understand when and why Pseudo-nitzschia species produce domoic acid in the field.KEY WORDS: Cell volume · Diatom · Domoic acid · Growth rate · pH · Phytoplankton · Pseudonitzschia · Toxin production Resale or republication not permitted without written consent of the publisherMar Ecol Prog Ser 273: [1][2][3][4][5][6][7][8][9][10][11][12][13][14][15] 2004 Pseudo-nitzschia spp. blooms are often found in coastal areas enriched by nutrient-rich freshwater runoff (Smith et al. 1990, Horner & Postel 1993, Dortch et al. 1997, Scholin et al. 2000, Odebrecht et al. 2001 or in upwelling areas (Abrantes & Moita 1999, Trainer et al. 2000, Villac & Tenenbaum 2001. A positive relationship between increasing eutrophication of coastal waters and the abundance of Pseudo-nitzschia spp. was found in present and historical data from the coast of Louisiana and Texas (Dortch et al. 1997, Parsons et al. 2002. Hence, nutrient enrichment may result in increased densities of phytoplankton organisms such as Pseudo-nitzschia spp.In seawater, pH has generally been recognised as being very stable (pH ≈ 8.2), as it is buffered by the carbonate system. However, uptake of dissolved inorganic carbon (DIC) during photosynthesis by high densities of phytoplankton may actually cause an increase in pH, and thus high pH values (around pH 9) have been recorded in natural environments during algal blooms (Hinga 1992, Macedo et al. 2001. For instance, in Narrangansett Bay, USA, 18% of the samples had pH values above 8.7 (Hinga 2002). Similarly, during the development of a bloom of the haptophyte Phaeocystis spp. in the North Sea, Brussard et al. (1996) found an increase in pH from 7.9 to 8.7. In fjords and coastal lagoons, pH values can attain even higher levels, and pH values up to around 10 may then be found during bloom periods (e.g. Marshall & Orr 1948, Macedo et al. 2001, Hansen 2002. The only study that we have been able to find in which pH, growth of potentially t...

Field sampling was undertaken to investigate the occurrence of Pseudo-nitzschia Peragallo species in eight locations along the coast of Malaysian Borneo. A total of 108 strains of Pseudo-nitzschia species were isolated, and their morphology examined with SEM and TEM. Additionally, molecular data from nuclear-encoded partial LSU rDNA, and ITS regions, were characterized. A total of five species were confidently identified based on a combination of distinct morphological characteristics and supporting molecular evidence: P. brasiliana Lundholm, Hasle & Fryxell, P. cuspidata (Hasle) Hasle, P. dolorosa Lundholm & Moestrup, P. micropora Priisholm, Moestrup & Lundholm, and P. pungens (Grunow) Hasle var. pungens. However, one morphotype from Sarawak, while somewhat similar to P. caciantha, showed significant morphological distinction from this and any other of the currently described species. Most notably this morphotype possessed a characteristic pore arrangement in the poroids, with the fine pores in each perforation sector arranged in circles. Pair-wise sequence comparison of the LSU rDNA between this unidentified morphotype and P. caciantha Lundholm, Moestrup & Hasle, revealed 2.7% genetic divergence. Phylogenetic analyses strongly supported the monophyly of the morphotype. Based upon these supporting data it is here described as a new species, Pseudo-nitzschia circumpora sp. nov. A key to the six species of Pseudo-nitzschia from Malaysian Borneo is presented. Molecular signatures for all species were established based on structural comparisons of ITS2 rRNA transcripts.

No abstract

Domoic acid (DA), a neuroexcitatory amino acid, was detected in batch culture of the newly recognized species Nitzschia navis‐varingica Lundholm et Moestrup. The production of DA by this diatom was confirmed by electrospray ionization mass spectrometry. The diatom was collected from a shrimp‐culture pond in Do Son, Vietnam. The production of DA (1.7 pg·cell−1) is within the levels reported for Pseudo‐nitzschia multiseries (Hasle) Hasle. The DA production started during the late exponential growth phase and reached a maximum during the early stationary growth phase. Maximum DA levels in the axenic culture decreased to about half that of the nonaxenic culture (0.9 pg·cell−1 vs. 1.7 pg·cell−1), suggesting that DA production by the new species is influenced by bacteria.

We identified and investigated the potential toxicity of oceanic Pseudo-nitzschia species from Ocean Station Papa (OSP), located in a high-nitrate, low-chlorophyll (HNLC) region of the northeast (NE) subarctic Pacific Ocean. Despite their relatively low abundances in the indigenous phytoplankton assemblage, Pseudo-nitzschia species richness is high. The morphometric characteristics of five oceanic Pseudo-nitzschia isolates from at least four species are described using SEM and TEM. The species identified are Pseudo-nitzschia dolorosa Lundholm et Moestrup, P. granii Hasle, P. heimii Manguin, and P. cf. turgidula (Hust.) Hasle. Additional support for the taxonomic classifications based on frustule morphology is provided through the sequencing of the internal transcribed spacer 1 (ITS1) rDNA. Pseudo-nitzschia species identification was also assessed by the construction of ITS1 clone libraries and using automated ribosomal intergenic spacer analysis (ARISA) for environmental samples collected during the Subarctic Ecosystem Response to Iron Enrichment Study (SERIES), conducted in close proximity to OSP in July of 2002. Based on ITS1 sequences, the presence of P. granii, P. heimii, P. cf. turgidula, and at least five other putative, unidentified Pseudo-nitzschia ITS1 variants was confirmed within iron-enriched phytoplankton assemblages at OSP. None of the oceanic isolates produced detectable levels of particulate domoic acid (DA) when in prolonged stationary phase due to silicic acid starvation. The lack of detectable concentrations of DA suggests that either these strains produce very little or no toxin, or that the physiological conditions required to promote particulate DA production were not met and thus differ from their coastal, toxigenic congeners.

No abstract