Nadine Küchenmeister’s scientific contributions

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Publications (2)


Figure 1. Examples of species identified with light microscopy. (a): Euastrum humerosum terias truncata, (c): Euastrum verrucosum, (d): Micrasterias americana.
Figure 5. A comparison of the total alpha diversity of microalgal genera in 5 different ponds in the Eifel National Park. Light microscopy: the algae were determined by light microscopical identification. Silva: algal genera were determined by aligning metagenomic reads with the Silva database. Cyanobacteria were not counted in this comparison.
Microalgal Diversity and Molecular Ecology: A Comparative Study of Classical and Metagenomic Approaches in Ponds of the Eifel National Park, Germany
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August 2024

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209 Reads

Phycology

Karl-Heinz Linne von Berg

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Nadine Küchenmeister

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While molecular methods have begun to transform ecology, most algal biodiversity is still studied using the classical approach of identifying microalgae by light microscopy directly in sample material or using cultures. In this study, we compare both approaches (light microscopy and metagenomics as a molecular approach) using the freshwater ponds of the Eifel National Park in Germany as a case study. The ponds were found to be rich in desmids by light microscopy. A total of 299 species representing 81 genera were identified by light microscopy. While the molecular method does not currently allow species identification in most cases, we were able to identify 207 different algal genera. In total, 157 genera were detected only by metagenomics, 50 genera were found with both methods, and 31 genera were found by light microscopy, highlighting the need to continue using light microscopy in addition to a molecular approach. The metagenomics method has several advantages over the light microscopy method: (1) deeper assessment of alpha biodiversity, (2) better abundance numbers, and (3) complete coverage of all living matter. The latter is also a significant improvement over metabarcoding, as universal PCR primers are not available.

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Figure 1. Examples of species identified with light microscopy a: Euastrum humerosum, b: Micrasterias truncata, c: Euastrum verrucosum, d: Micrasterias americana.
Figure 2. Non metric multidimensional scaling (NMDS) based on algae species, identified with light microscopy, in different sites. Vectors indicate significant correlations between algae diversity and environmental variables (p-value for depth = 0.0029, p-value for nitrite = 0.0215, and the p-value for pH = 0.0042), (p < 0.05). HT = Himmelteiche, KG= Kleingewässer, and SU = Schürhübelteiche. Sampling sites used for metagenomic studies are indicated with their abbreviations.
Figure 5. Comparison of the total alpha diversity of micro algal genera in 5 different ponds in the Eifel National Park. Light microscopy: algae were determined by light microscopical identification. Silva: Algal genera were determined by aligning metagenomic reads with the Silva database. Cyanobacteria are not counted in this comparison.
Microalgal Diversity and Molecular Ecology: A Comparative Study of Classical and Metagenomic Approaches in Ponds of the Eifel National Park, Germany

June 2024

·

57 Reads

While molecular methods have begun to transform ecology, most algal biodiversity is still studied using the classical approach of identifying microalgae by light microscopy directly in sample material or using cultures. In this study, we compare both approaches (light microscopy and metagenomics as a molecular approach) using freshwater ponds of the Eifel National Park in Germany as a case study. The ponds were found to be rich in desmids by light microscopy. A total of 299 species representing 81 genera were identified by light microscopy. While the molecular method does not currently allow species identification in most cases, we were able to identify 207 different algal genera. 157 genera were detected only by metagenomics, 50 genera with both methods and 31 genera were found by light microscopy, highlighting the need to continue using light microscopy in addition to a molecular approach. The metagenomics method has several advantages over the light microscopy method: 1) deeper assessment of alpha biodiversity 2) better abundance numbers 3) complete coverage of all living matter. The latter is also a significant improvement over metabarcoding, as universal PCR primers are not available.