Project objectives
O1: To assess genetic diversity and ecological requirements of the idle crayfish populations
We aimed for this project to move forward to next-generation sequencing (NGS) approaches to
evaluate the genetic diversity and the relationship between populations with molecular analysis
based on genome single-nucleotide polymorphisms (SNPs). This method has the advantage of
no requirement for genomic resources background. Within this objective, we will extend the
approach of corroborating the population genetics with the species’ ecology, to address
scientifically sound hypotheses in the field of evolutionary aspects of this endemic crayfish
species (e.g., allopatric speciation by isolation or spatial patterns driven purely by recent
environmental variables). Each of these approaches, taken separately, would lead to results of
significantly lower scientific relevance.
O2: To establish the conservation measures for idle crayfish populations
Here we aims to find the best way to sustain the long-term protection of A. bihariensis
populations. In this regard, identification of some ecologically stabile sites, which exhibit the
best quality of biological populations with the lowest invasion risk, is targeted. Further
identification of these natural ark sites will guarantee a ‘bank of specimens’ - highly valuable
assets available for re-colonization in the event of worst-case scenarios . Being a newly
described species, no conservation status is available yet for A. bihariensis. Hence, according
to IUCN Red List of Threatened Species™ relevant criteria, trends in population and the quality
of habitat are critical in establishing the appropriate status. Our plan is to estimate population
trends by using molecular data obtained in O1, followed by specific analyses to assess the
habitat fragmentation, the pressure of invasive crayfish species and the carried pathogen A.
astaci, explored by applying distribution modelling methods. To enhance detectability, the field
distribution will be investigated by both traditional and eDNA methods, reducing the amount of
false negative records.
Project website: http://www.idle.crayfish.ro
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