4.2 Article

Using geometric morphometrics to disentangle Didymosphenia hullii and D. geminata (Bacillariophyceae) from Connecticut, USA, and two congeneric relatives

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EUROPEAN JOURNAL OF PHYCOLOGY
卷 58, 期 1, 页码 99-109

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TAYLOR & FRANCIS LTD
DOI: 10.1080/09670262.2022.2068075

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Benthic diatoms; brown algae; diatom; Didymosphenia; fine structure; invasive species; morphometrics; nuisance species; stalk-forming diatoms

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This research used geometric morphometrics analysis to successfully distinguish between two populations of Didymosphenia in the Farmington River, Connecticut, and confirmed the identity of the second population as D. geminata. The study highlights the enhanced ability of geometric morphometrics, in combination with scanning electron microscopy and light microscopy, to differentiate between morphologically similar species of Didymosphenia.
Two morphologically similar populations of Didymosphenia were reported from the West Branch of the Farmington River, Connecticut, USA in 2014 and 2016. We described one of them as a new species, D. hullii. The other was observed subsequently in late 2016 and resembled D. geminata, but given the worldwide nuisance characteristic of this species, the identification required confirmation. In this work we used geometric morphometrics analysis to test for quantitative distinctions between the two Connecticut populations, along with two morphologically similar taxa from the literature, D. laticollis and D. pumila. We successfully separated the four entities and confirmed the identity of the second blooming diatom in the Farmington River, Connecticut, as D. geminata, which is the first confirmed report of this species for the state. We conclude that geometric morphometrics, in combination with features viewed with scanning electron microscopy and light microscopy, enhances the ability to distinguish among these morphologically similar species of Didymosphenia. We summarize these findings and pinpoint morphological distinctions that can be used to separate the taxa during routine light microscopy analyses.

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