Apical groove type and molecular phylogeny suggests reclassification of Cochlodinium geminatum as Polykrikos geminatum

PLoS One. 2013 Aug 19;8(8):e71346. doi: 10.1371/journal.pone.0071346. eCollection 2013.

Abstract

Traditionally Cocholodinium and Gymnodinium sensu lato clade are distinguished based on the cingulum turn number, which has been increasingly recognized to be inadequate for Gymnodiniales genus classification. This has been improved by the combination of the apical groove characteristics and molecular phylogeny, which has led to the erection of several new genera (Takayama, Akashiwo, Karenia, and Karlodinium). Taking the apical groove characteristics and molecular phylogeny combined approach, we reexamined the historically taxonomically uncertain species Cochlodinium geminatum that formed massive blooms in Pearl River Estuary, China, in recent years. Samples were collected from a bloom in 2011 for morphological, characteristic pigment, and molecular analyses. We found that the cingulum in this species wraps around the cell body about 1.2 turns on average but can appear under the light microscopy to be >1.5 turns after the cells have been preserved. The shape of its apical groove, however, was stably an open-ended anticlockwise loop of kidney bean shape, similar to that of Polykrikos. Furthermore, the molecular phylogenetic analysis using 18S rRNA-ITS-28S rRNA gene cistron we obtained in this study also consistently placed this species closest to Polykrikos within the Gymnodinium sensu stricto clade and set it far separated from the clade of Cochlodinium. These results suggest that this species should be transferred to Polykrikos as Polykrikos geminatum. Our results reiterate the need to use the combination of apical groove morphology and molecular phylogeny for the classification of species within the genus of Cochlodinium and other Gymnodiniales lineages.

Publication types

  • Research Support, Non-U.S. Gov't

MeSH terms

  • Cell Nucleus / genetics
  • Cell Separation
  • China
  • Classification
  • Dinoflagellida / classification*
  • Dinoflagellida / cytology
  • Dinoflagellida / genetics
  • Estuaries
  • Microscopy, Electron, Scanning
  • Microscopy, Electron, Transmission
  • Mitochondria / genetics
  • Phylogeny
  • RNA, Ribosomal, 18S / genetics
  • RNA, Ribosomal, 28S / genetics
  • Sequence Analysis, DNA

Substances

  • RNA, Ribosomal, 18S
  • RNA, Ribosomal, 28S

Grants and funding

This research is supported by the National Science Foundation of China (41129001, 41130855, 41006067) (http://www.nsfc.gov.cn/). The funders had no role in study design, data collection and analysis, decision to publish, or preparation of manuscript.