Biology subjects

Schuetz, R.

Publications and source records attributed to Schuetz, R..

6 recordsLinked to original sources

bioRxiv2026

eDNA metabarcoding provides scalable and continuous biodiversity monitoring across the tree of life

Environmental DNA (eDNA) metabarcoding has the potential to substantially expand our knowledge of global biodiversity beyond that provided by conventional approaches. However, the degree to which eDNA data provides real ecological insight, rather than primarily reflecting environmental factors that affect eDNA shedding and degradation, remains unclear. Additional uncertainties arise in terms of cost-effectiveness and whether the price is worth any extra biodiversity information that is gleaned. Here, we established a high-resolution, bi-weekly eDNA time-series in Germany across aquatic and riparian habitats to quantify seasonal biodiversity dynamics, to relate eDNA to different potential environmental drivers, and to parametrize cost estimates. Over one year, eDNA metabarcoding detected more than 1,000 species across multiple trophic levels and primarily revealed real, taxon-specific seasonal patterns, in addition to some relationships to water temperature, discharge, and conductivity. Compared to historical records dating back to 1891, year-round eDNA monitoring increased reported species numbers by 2.4-fold for invertebrates, 2.2-fold for mammals, 1.7-fold for diatoms, 1.2-fold for fish and lamprey, and 1.03-fold for birds. Cumulative biodiversity estimates increased strongly with sampling frequency, demonstrating the value of eDNA for high-frequency time-series monitoring. Moreover, eDNA monitoring was highly cost-effective, providing more than twice the biodiversity information of many conventional surveys for one-sixth the cost, enabling scalable, high-resolution freshwater biodiversity assessments.

ecology↗

bioRxiv2025

Unraveling long-term trends and drivers of fish biodiversity change using environmental DNA metabarcoding of archived samples

AbstractLong-term biodiversity data are critical for assessing, understanding, and predicting ecosystem change globally, but are often limited by their availability. We present the longest eDNA metabarcoding time series for freshwater fishes based on archived suspended particulate matter (SPM) from Germanys Environmental Specimen Bank, covering 17 years (2005-2021) across six major European river systems (Rhine, Danube, Elbe, and their tributaries). From 211 annual samples collected according to highly standardized procedures at 13 sites, we detected 63 fish and lamprey species and traced their spatio-temporal trajectories. eDNA metabarcoding captured significantly declining trends at multiple sites with no recoveries. Common and sensitive species declined at nearly half of sites while invasive species spread. Site occupancy and relative read abundance trends were correlated, providing semi-quantitative indicators. Alpha and beta diversity shifted over time and Bayesian hierarchical models revealed that 19% of species showed significant declines in relative read abundance. The eDNA-derived trends showed strong concordance with long-term regulatory fish monitoring data, validating the patterns across methodological approaches. Random forest models and multivariate analyses identified multiple anthropogenic pollutants, measured from the same SPM samples, as drivers of biodiversity patterns. Pesticides, heavy metals, temperature, and fine sediment negatively affected species richness, with site-specific stressor combinations explaining 29% of community variation. Our results demonstrate that archived SPM, originally collected for chemical monitoring, provides a reliable, dual-purpose monitoring matrix integrating pollution and biodiversity trend assessments simultaneously. This approach enables holistic monitoring of global freshwater ecosystem change and can provide an early warning framework supporting evidence-based environmental management.

ecology↗

bioRxiv2022

It`s raining species: Rainwash eDNA metabarcoding as a minimally invasive method to assess tree canopy invertebrate diversity

O_LIForest canopies are a highly diverse ecosystem, but despite several decades of intense research, there remain substantial gaps in our knowledge of their biodiversity and ecological interactions. One fundamental challenge in canopy research is the limited accessibility of the ecosystem. Consequently, previous studies have relied on the application of either highly invasive methods such as chemical knockdown, or on time-consuming and expensive setups such as canopy walkways or cranes. Therefore, time- and cost-efficient, ideally minimally invasive yet comprehensive applications are required to help close this knowledge gap. High-throughput metabarcoding of environmental DNA (eDNA) collected from water, soil, or air provides a minimally invasive method for biodiversity assessment, yet its potential for canopy biodiversity monitoring has not been explored. C_LIO_LIHerein, we conducted metabarcoding of eDNA washed off the canopy via rainwater to explore its monitoring potential. We placed four 1 m2 rain samplers beneath the canopies of four different tree taxa prior to a major rain event, filtered eDNA from the collected rainwater, and performed cytochrome c oxidase subunit I (COI) metabarcoding to profile the invertebrate community. Additionally, we collected and identified all specimens present in the rainwater for verification. C_LIO_LIWe detected 50 invertebrate species by eDNA metabarcoding, of which 43 were not physically present in the water sample, thus likely representing true canopy biodiversity signals. Furthermore, we observed distinct species occurrence patterns corresponding to the four tree taxa, suggesting that ecological patterns such as host specificity can be assessed using the method. C_LIO_LIIn conclusion, our study provides a proof of principle that rainwash eDNA metabarcoding offers a minimally invasive and comprehensive method for tree canopy diversity monitoring. C_LI

molecular biology↗

bioRxiv2021

Beyond fish eDNA metabarcoding: Field replicates disproportionately improve the detection of stream associated vertebrate species

Fast, reliable, and comprehensive biodiversity monitoring data are needed for environmental decision making and management. Recent work on fish environmental DNA (eDNA) metabarcoding shows that aquatic diversity can be captured fast, reliably, and non-invasively at moderate costs. Because water in a catchment flows to the lowest point in the landscape, often a stream, it can often collect traces of terrestrial species via surface or subsurface runoff along its way or when specimens come into direct contact with water (e.g., for drinking purposes). Thus, fish eDNA metabarcoding data can provide information on fish but also on other vertebrate species that live in riparian habitats. This additional data may offer a much more comprehensive approach for assessing vertebrate diversity at no additional costs. Studies on how the sampling strategy affects species detection especially of stream-associated communities, however, are scarce. We therefore performed an analysis on the effects of biological replication on both fish as well as (semi-)terrestrial species detection. Along a 2 km stretch of the river Mulde (Germany), we collected 18 1-L water samples and analyzed the relation of detected species richness and quantity of biological replicates taken. We detected 58 vertebrate species, of which 25 were fish and lamprey, 18 mammals, and 15 birds, which account for 50%, 24%, and 7% of all native species to the German federal state of Saxony-Anhalt. However, while increasing the number of biological replicates resulted in only 25% more detected fish and lamprey species, mammal, and bird species richness increased disproportionately by 69% and 84%, respectively. Contrary, PCR replicates showed little stochasticity. We thus emphasize to increase the number of biological replicates when the aim is to improve general species detections. This holds especially true, when the focus is on rare aquatic taxa or on (semi-)terrestrial species, the so-called bycatch. As a clear advantage, this information can be obtained without any additional sampling or laboratory effort when the sampling strategy is chosen carefully. With the increased use of eDNA metabarcoding as part of national fish bioassessment and monitoring programs, the complimentary information provided on bycatch can be used for biodiversity monitoring and conservation on a much broader scale.

molecular biology↗

bioRxiv2020

Social signaling via bioluminescent blinks drives schooling behavior in the flashlight fish Anomalops katoptron

The bioluminescent flashlight fish Anomalops katoptron live in schools of several hundred specimens. To understand how flashlight fish, integrate bioluminescent signaling into their schooling behavior, we analyzed movement profiles and blink frequencies. Isolated specimen of A. katoptron show a high motivation to align with fixed or moving artificial light organs. Depending on presented frequencies A. katoptron responds with a reduction in swimming speed and its own blink frequency. Higher presented blink frequencies reduce the nearest neighbor distance. In the natural environment A. katoptron is changing its blink frequencies and nearest neighbor distance in a context specific manner. Blink frequencies are increased from day to night and during avoidance behavior, while nearest neighbor distance is decreased with increasing blink frequencies. A. katoptron changes its blink frequencies by modifying light organ occlusion. Our results suggest that visually transmitted information via specific blink patterns determine intraspecific communication and group cohesion in schooling A. katoptron.Competing Interest StatementThe authors have declared no competing interest.View Full Text

animal behavior and cognition↗

bioRxiv2019

Posttranscriptional regulation of ribosomal and multiresistance genes by the bacterial leader peptide peTrpL

The ribosome-dependent attenuator located upstream of bacterial tryptophan biosynthesis genes harbors a small ORF trpL containing tryptophan codons. When tryptophan is available, efficient trpL translation causes transcription termination and release of the attenuator RNA rnTrpL. In Sinorhizobium meliloti, rnTrpL is a trans-acting sRNA. Here, we identified an evolutionary conserved function for the trpL-encoded 14-aa leader peptide peTrpL. Upon exposure to tetracycline, the cellular peTrpL levels were increased and rnTrpL was generated independently of tryptophan availability. Both peTrpL and rnTrpL were found to be involved in tetracycline-dependent destabilization of rplUrpmA mRNA encoding ribosomal proteins L21 and L27. We provide evidence for redirection of the sRNA rnTrpL from its antibiotic-independent target trpDC to rplUrpmA by formation of an antibiotic-dependent ribonucleoprotein complex (ARNP). ARNPs comprising peTrpL, rnTrpL, rplUrpmA and antisense RNA were also observed for other translation-inhibiting antibiotics, suggesting that bacteria evolved mechanisms to utilize antibiotics for mRNA destabilization.

microbiology↗