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The green algal family Chlorochytriaceae comprises relatively large coccoid algae with secondarily thickened cell walls. Despite its morphological distinctness, the family remained molecularly uncharacterized. In this study, we investigated the morphology and phylogenetic position of 16 strains determined as members of two Chlorochytriaceae genera, Chlorochytrium and Scotinosphaera. The phylogenetic reconstructions were based on the analyses of two data sets, including a broad, concatenated alignment of small subunit rDNA and rbcL sequences, and a 10-gene alignment of 32 selected taxa. All analyses revealed the distant relation of the two genera, segregated in two different classes: Chlorophyceae and Ulvophyceae. Chlorochytrium strains were inferred in two distinct clades of the Stephanosphaerinia clade within the Chlorophyceae. Whereas clade A morphologically fits the description of Chlorochytrium, the strains of clade B coincide with the circumscription of the genus Neospongiococcum. The Scotinosphaera strains formed a distinct and highly divergent clade within the Ulvophyceae, warranting the recognition of a new order, Scotinosphaerales. Morphologically, the order is characterized by large cells bearing local cell wall thickenings, pyrenoid matrix dissected by numerous anastomosing cytoplasmatic channels, sporogenesis comprising the accumulation of secondary carotenoids in the cell periphery and almost simultaneous cytokinesis. The close relationship of the Scotinosphaerales with other early diverging ulvophycean orders enforces the notion that nonmotile unicellular freshwater organisms have played an important role in the early diversification of the Ulvophyceae.

The coccoid green algae Coenochloris planoconvexa and Echinocoleum elegans are assigned to different families (Radiococcaceae and Oocystaceae, respectively), but display similar ray-like mucilaginous envelopes. Molecular analysis of the 18S rRNA gene of C. planoconvexa CAUP H 5502 and E. elegans SAG 37.93 revealed that they both belong to Oocystaceae. However, the two strains were not a part of a monophyletic cluster. Furthermore, their morphology differed, namely in the shape of their mucilaginous envelopes, and in their ability to form four-celled units in a broadened sporangial wall. Because the name Coenochloris cannot be used for members of Oocystaceae, a new genus Ooplanctella, with the type species O. planoconvexa comb. nova, is proposed.

A novel, combined approach to assessing species delimitation and biogeography within the well-known desmid species Micrasterias fimbriata and M. rotata (Desmidiales, Steptophyta) Abstract Morphological species of freshwater microalgae often have broad geographic distribution. However, traditional species concepts have been challenged by the results of molecular phylogenetic analyses that mostly indicate higher diversity than was previously recognized by purely morphological approaches. A degree of phenotypic differentiation or different geographic distribution of species defined by molecular data remains largely unknown. In this study, we analyzed a pair of well-known and widely distributed desmid species (Micrasterias fimbriata and M. rotata) and tested for their phylogenetic and Electronic supplementary material The online version of this article (

The morphological and molecular differentiation of the Micrasterias truncata (Corda) ex Bréb species complex was investigated. In total, 17 strains traditionally assigned to M. truncata were isolated from different European localities (Czech Republic, southwest France, Ireland), and obtained from public culture collections. In addition, strains of the morphologically similar species, M. decemdentata (Nägeli) W. Archer and M. zeylanica F. E. Fritsch, were also included. Molecular phylogenetic analysis based on trnG ucc intron sequences revealed five well supported clades. Two Australian strains assigned to M. truncata var. pusilla G. S. West formed a lineage sister to M. zeylanica. This was evident from a concatenated phylogeny based on small subunit rDNA and trnG ucc intron sequences. The isolated position of these strains was also illustrated by parallel landmark-based geometric morphometric analysis of cell shapes. The strains NIES 783 and NIES 784 probably represent a separate species. Particular analysis, including additional strains, is needed to resolve the relationship inside this lineage. The second phylogenetic lineage, containing two strains of M. truncata var. semiradiata (Kützing) Wolle, was also different from other strains on the basis of morphometric data. We suggest recognizing this variety as a separate species, Micrasterias semiradiata L.A. Brébisson ex F. T. Kützing. The remaining three clades formed a firmly supported group of the 'core' M. truncata recognized by both molecular markers. However, neither any morphological, morphometric, nor geographical pattern was detected among members of these three clades. This pattern could be caused by a relatively recent origin of these lineages that may represent a sympatric, truly cryptic species. Strains attributable to traditional morphologically defined variety M. truncata var. neodamensis were nested within the 'core' M. truncata.