Biology subjects

Malzahn, A.

Publications and source records attributed to Malzahn, A..

3 recordsLinked to original sources

bioRxiv2026

Exploring Warming Effects on lower food-web dynamics in the plankton of the River Elbe Estuarine Ecosystem in summer: Insights from a Mesocosm Experiment

Understanding how warming alters estuarine plankton communities is essential for predicting future changes in biodiversity and ecosystem functioning. We conducted a four-week indoor mesocosm experiment using natural summer plankton from the Elbe River to examine the effects of warming (+2 {degrees}C and +4 {degrees}C) on abiotic conditions and responses of the plankton community. In this study, oxygen concentrations, primary producer biomass (chlorophyll a, microphytoplankton) and microzooplankton abundances declined sharply during the first 10 days across all treatments while mesozooplankton abundances increased. This suggests a strong top-down control by mesozooplankton on lower trophic levels across all temperature treatments. Primary producers biomass and oxygen concentrations recovered after an initial decline, however to lower levels compared to the onset of the experiment while micro- and mesozooplankton remained low during the second half of the experiment. Nutrient dynamics indicated progressive remineralization, with increasing ammonium, NOx, and silicate concentrations, while phosphate concentrations remained low throughout the experiment. Complementary DNA and RNA metabarcoding revealed similar community turnover over time in all treatments and temperature effects became only pronounced at the end of the experiment. Overall, warming effects were subtle relative to the strong internal trophic dynamics likely caused by the artificial mesocosm setup. Our findings of changes in plankton community dynamics indicate that biotic interactions, changes in trophic diversity and other environmental factors, i.e. oxygen concentrations are likely the drivers of this estuarine system rather than warming alone.

ecology↗

bioRxiv2022

A de novo transcriptome assembly of the annelid worm Hediste diversicolor

The development of Next-Generation Sequencing (NGS) technologies has revolutionized multiple fields of Biology. The ability to sequence DNA and RNA in an automated, parallel and low-cost approach, was key to boost the applicability and acquisition efficiency of omics resources. In this context, the availability of these tools has become indispensable towards our understanding of biodiversity, deepening our knowledge on the distinct complexity levels, from cells to ecosystems. In this study we comprehensively characterised and annotated a whole-body transcriptome of Hediste diversicolor. This annelid worm species belongs to the family Nereididae and inhabits estuarine and lagoon areas on the Atlantic coasts of Europe and North America. Ecologically, this species plays an important role in benthic food webs. The ability of rework sediments through bioturbation activity makes this species essential to the estuarine mechanisms. Here, we used Illumina next-generation sequencing technology, to sequence a total 105 million (M) paired-end (PE) raw reads and produce the first multi-tissue transcriptome assembly of an adult of H. diversicolor. This transcriptome contains 69,335 transcripts with a N50 transcript length of 2,313 bp and a BUSCO gene completeness of 97.7% and 96% (S: 88.2%; D: 7.8%) in Eukaryota and Metazoa lineage-specific profile libraries. Our findings offer a valuable resource for multiple biological studies using this species.

genomics↗

bioRxiv2018

A large-scale whole-genome sequencing analysis reveals highly specific genome editing by both Cas9 and Cpf1 nucleases in rice

Targeting specificity has been an essential issue for applying genome editing systems in functional genomics, precise medicine and plant breeding. Understanding the scope of off-target mutations in Cas9 or Cpf1-edited crops is critical for research and regulation. In plants, only limited studies had used whole-genome sequencing (WGS) to test off-target effects of Cas9. However, the cause of numerous discovered mutations is still controversial. Furthermore, WGS based off-target analysis of Cpf1 has not been reported in any higher organism to date. Here, we conducted a WGS analysis of 34 plants edited by Cas9 and 15 plants edited by Cpf1 in T0 and T1 generations along with 20 diverse control plants in rice, a major food crop with a genome size of ~380 Mb. The sequencing depth ranged from 45X to 105X with reads mapping rate above 96%. Our results clearly show that most mutations in edited plants were created by tissue culture process, which caused ~102 to 148 single nucleotide variations (SNVs) and ~32 to 83 insertions/deletions (indels) per plant. Among 12 Cas9 single guide RNAs (sgRNAs) and 3 Cpf1 CRISPR RNAs (crRNAs) assessed by WGS, only one Cas9 sgRNA resulted in off-target mutations in T0 lines at sites predicted by computer programs. Moreover, we cannot find evidence for bona fide off-target mutations due to continued expression of Cas9 or Cpf1 with guide RNAs in T1 generation. Taken together, our comprehensive and rigorous analysis of WGS big data across multiple sample types suggests both Cas9 and Cpf1 nucleases are very specific in generating targeted DNA modifications and off-targeting can be avoided by designing guide RNAs with high specificity.

molecular biology↗