Background: Dragonflies and damselflies (Odonata) are important components in biomonitoring due to their amphibiotic lifecycle and specific habitat requirements. They are charismatic and popular insects, but can be challenging to identify despite large size and often distinct coloration, especially the immature stages. DNA-based assessment tools rely on validated DNA barcode reference libraries evaluated in a supraregional context to minimize taxonomic incongruence and identification mismatches.Methods: This study reports on findings from the analysis of the most comprehensive DNA barcode dataset for Central European Odonata to date, with 103 out of 145 recorded European species included and publicly deposited in the Barcode of Life Data System (BOLD). The complete dataset includes 697 specimens (548 adults, 108 larvae) from 274 localities in 16 countries with a geographic emphasis on Central Europe. We used BOLD to generate sequence divergence metrics and to examine the taxonomic composition of the DNA barcode clusters within the dataset and in comparison with all data on BOLD.Results: Over 88% of the species included can be readily identified using their DNA barcodes and the reference dataset provided. Considering the complete European dataset, unambiguous identification is hampered in 12 species due to weak mitochondrial differentiation and partial haplotype sharing. However, considering the known species distributions only two groups of five species possibly co-occur, leading to an unambiguous identification of more than 95% of the analysed Odonata via DNA barcoding in real applications. The cases of small interspecific genetic distances and the observed deep intraspecific variation inCordulia aenea(Linnaeus, 1758) are discussed in detail and the corresponding taxa in the public reference database are highlighted. They should be considered in future applications of DNA barcoding and metabarcoding and represent interesting evolutionary biological questions, which call for in depth analyses of the involved taxa throughout their distribution ranges.

Growing human-wildlife conflicts and legal conservation obligations increased the need for precise information on Eurasian otter (Lutra lutra) population parameters for species status assessment and wildlife management measures. Scat surveys have become the method of choice to monitor species distribution range, abundance and habitat use. Although methodological concerns exist, scat abundance is often used as main indicator for otter population estimates and trends. To evaluate whether scat counts serve as good proxy for otter densities in linear stream habitats, we modelled the relationship between old/fresh scat abundance and otter numbers on two spatial scales, including also seasonal effects. Actual otter densities and marking behaviour were ascertained by genotyping of otter faeces collected at 218 marking sites along 132.6 km of four salmonid streams. Otter densities in our study areas ranged from 0.16 to 0.28 otters per stream kilometre. The age of scats and the level of spatial scale were determining factors when evaluating the suitability of scat abundance as index for otter densities. Covering large parts of an otter’s territory, fresh scat abundance increased with otter density, irrespectively of season. On the spatial scale of single marking sites, the relationship was not well supported, and no relationship could be found when using old scats in the models. Otter marking behaviour and differences in marking site use intensity, as well as seasonal differences in traceability and accumulation of old scats were discussed to bias the relationship between scat abundance and otter numbers.

Monitoring of odonates has become an important instrument for ecological status assessment of (semi-)aquatic habitats. Besides information on presence and abundance, knowledge about a species´ autochthony at the surveyed waterbody is a significant information within the assessment process. Here, the finding of exuviae represents the ultimate proof of successful reproduction. Although feasible for most odonate species, morphological identification of exuviae is often time consuming, as it relies on small, fragile structures. To facilitate species identification of exuviae, a DNA barcoding approach was developed, including (1) non-destructive extraction of DNA using whole exuviae or their tracheal tubes, and (2) primer systems for long (< 600 bp) and short (< 200 bp) CO1 fragments. A total of 85 exuviae from 33 species were analysed and compared to results of morphological identification. Additionally, factors potentially influencing DNA quality and quantity, as well as PCR and sequencing success were investigated. Eighty-two exuviae matched the morphologically identified genus, and 60 matched at species level. Of the 33 species present in the data set, 82% could be identified to species level via DNA barcoding. The results show how DNA-based approaches can support fast and accurate species identification and therefore enhance monitoring of an ecologically important taxonomic group, with high relevance for conservation and habitat restoration. Moreover, the use of exuviae as DNA resource once more shows that non-invasive sampling offers great potential for molecular species identification, which is essential when studying rare and endangered species. Implications for insect conservation: Our results show how molecular tools, here DNA barcoding of odonate exuviae, can support species monitoring without the need of catching individuals, harming, or even killing them. Obtaining DNA from non-invasive sources can thus be a direct advantage to the conservation of insects, especially when dealing with rare and endangered species and/or populations. Using the example of odonates as bioindicator organisms for aquatic and semi-aquatic habitats, we highlight the importance of non-invasive genetic approaches for population studies and monitoring of insect species and/or species communities for ecosystem assessments and conservation management.

Knowledge on predator diet and drivers of prey selection is particularly of interest for an efficient management of predator and prey populations where predators potentially compete with humans for resources. Actual or perceived predation by Eurasian otter (Lutra lutra) on fish stocks generates conflicts in many countries. Recently, conflicts are heating up in riverine habitats, where multiple stressors affect stream fish populations. We combined dietary analysis of otter faeces and prey fish availability in three Austrian streams to assess spatial and seasonal differences in diet composition, the extent of (salmonid) fish consumption and the selection for specific salmonid fish sizes relative to their availability. Otters in upper reaches of temperate salmonid streams occupied a narrow trophic niche. Overall, otters fed predominantly on fish with salmonids dominating diet, both in terms of frequency and ingested biomass measures. Within the category of salmonids, otters selected for specific size classes. Concurrently, otters also displayed an opportunistic feeding behaviour, and seasonally and locally non-fish prey and other fish species than salmonids became key resources. Diet composition and salmonid size selection varied significantly within and between streams, which we relate to spatio-temporal variations of prey community composition and stream-specific habitat characteristics affecting prey vulnerability.

The use of non-invasively collected DNA source material for genetic and genomic applications is usually characterized by low target DNA concentration and quality, genotyping errors and cost-intensive lab procedures. However, for otters (Lutrinae) as elusive species of conservation concern, genetic non-invasive sampling has become an important tool to study their ecology and demography. To increase cost-efficiency of monitoring programmes and to promote the expansion of genomic approaches to non-invasive samples, we aimed to refine sample collection and preparation. Therefore, we examined the effects of intrinsic sample characteristics (including diet), environmental conditions in the field and sample treatment in the molecular laboratory on the success of genotyping and allelic dropout (ADO) rates using microsatellite markers in 1970 fresh Eurasian otter (Lutra lutra) scats. Using fresh samples only, we probably eliminated one of the most important impediments of genotyping DNA from otter faecal samples beforehand. But, we observed higher genotyping success and lower ADO rates for anal glad secretions and faecal samples containing high proportions of mucus. Moist conditions during sample collection may promote DNA degradation and PCR inhibition, leading to decreased genotyping success rates. ADO was further affected by the type of extraction kit. However, a high proportion of variance remaining unexplained by our models implied that additional parameters were acting (amount of PCR inhibitors, non-uniform distribution of intestinal cells, efficiency of PCRs, specific microclimate at marking sites). We summarized influential factors maximizing genotyping quality of otter scats and give recommendations for sample collection, storage and DNA extraction based on our results and current literature.

Understanding genetic consequences of habitat fragmentation is crucial for the management and conservation of wildlife populations, especially in case of species sensitive to environmental changes and landscape alteration. In central Europe, the Alps are the core area of black grouse Tetrao tetrix distribution. There, black grouse dispersal is limited by high altitude mountain ridges and recent black grouse habitats are known to show some degree of natural fragmentation. Additionally, substantial anthropogenic fragmentation has occurred within the past ninety years. Facing losses of peripheral subpopulations and ongoing range contractions, we explored genetic variability and the fine‐scale genetic structure of the Alpine black grouse metapopulation at the easternmost fringe of the species’ Alpine range. Two hundred and fifty tissue samples and non‐invasive faecal and feather samples of eleven a priori defined subpopulations were used for genetic analysis based on nine microsatellite loci. Overall, eastern Alpine black grouse show similar amounts of genetic variation ( H _O = 0.65, H _E = 0.66) to those found in more continuous populations like in Scandinavia. Despite of naturally and anthropogenically fragmented landscapes, genetic structuring was weak (global F _ST < 0.05), suggesting that the actual intensity of habitat fragmentation does not completely hamper dispersal, but probably restricts it to some extent. The most peripheral subpopulations at the edge of the species range show signs of genetic differentiation. The present study gives new insights into the population genetic structure of black grouse in the eastern Alps and provides a more fine‐scale view of genetic structure than previously available. Our findings will contribute to monitor the current and future status of the population under human pressures and to support supra‐regional land use planning as well as decision making processes in responsibilities of public administration.