Invasive alien species have extensively impacted the ecosystems, where they may affect the native biodiversity. The North American raccoon Procyon lotor is one of the most successful invaders in Europe since its introduction in the early twentieth century. In Italy, a wild population was first established in the North at the beginning of the 2000s following a local introduction event. A further self-sustaining population was reported ten years later in Central Italy. To support an official investigation by the authorities, who suspected a captive origin of the free-ranging raccoons in Central Italy, we used nuclear and mitochondrial DNA markers, combined with different statistical approaches, to characterise their gene pool and trace the source of the founders. Results revealed that founders came from a private zoo-park from which they had inadvertently escaped, soon establishing a reproductive population in the wild. Additionally, our mitochondrial DNA data were used to supplement the haplotype variability known to date in captive and wild raccoons from Europe, Asia and their native range. The comparisons allowed us to update previous networks based on the control region with a new mitochondrial lineage, which had not been detected so far.

The conservation of pure wolf populations in Europe is currently threatened by anthropogenic hybridization with dogs, through potential extinction of local gene pools due to replacement with domestic gene variants. Distinction of wolf–dog hybrids from wild ancestors is essential for development and implementation of management and conservation plans. Morphological traits are rarely helpful, and a genetic approach is the most effective to distinguish admixed individuals back to old backcrosses. To provide a molecular tool to address the issue, we optimized and validated a cost-effective protocol in multiplexed PCR format based on 22 STR canine loci, which allows us to distinguish genetically pure wolves from dogs, and, when used in association with a Bayesian assignment approach, is capable of statistically assigning admixed individuals to classes of hybrids with different levels of dog ancestry. Our method demonstrated high reliability, showing full repeatability and reproducibility of data with as little as 0.125 ng of genomic DNA, and was therefore suitable for the analysis of non-invasively collected samples and degraded DNA. The application of our STR panel to the appropriate assignment procedure unambiguously defined two genetically separated clusters for wolves and dogs, and successfully identified known hybrids as admixed individuals, which eventually were classified as recent hybrids and older backcrosses. The protocol, which is described here in detail, can be adopted by various laboratories that need this kind of diagnosis; furthermore, it would be capable of producing concordant results through inter-laboratory comparisons with wolf and dog control DNAs.

In the Falconidae, the genus Falco comprises species of large birds of prey with wide distribution worldwide. However, the European lanner falcon Falco biarmicus feldeggii is rapidly heading for global extinction following a dramatic decline caused by anthropogenic interference. Conservation projects are currently underway with the main purpose of increasing its population size in the Mediterranean basin through captive breeding and release of birds into the wild. To support the projects, and strengthen the legitimacy of conservation efforts consistently with the Evolutionary Significant Unit concept, we explored the possibility of characterising the gene pool of the European lanner and reliably distinguishing it from other falcon taxa inhabiting the Mediterranean area, which show morphological and genetic similarities. To address the issue, we examined genetic variability at the nuclear level through the analysis of 12 neutral Short Tandem Repeat loci, and, for the first time in these taxa, two single-copy functional genes, coding for the brain-derived neurotrophic factor precursor and the oocyte maturation factor, respectively. The second exon of the major histocompatibility complex class II B gene was also investigated. Additionally, to frame our data with previously published data, we assess variation at the mitochondrial level by sequencing portions of the cytochrome b, 12S rRNA gene, and the control region. Our results showed that the European lanner is highly distinct from other falcon taxa, as revealed by nuclear, but not by mitochondrial DNA. We discuss our findings focusing on their implications for the preservation of this highly endangered European bird, and highlighted the critical role of genetic information in planning and monitoring concrete interventions.

Reintroductions play a key role in conservation biology. Their long‐term success strongly depends on maximizing the genetic diversity of founders, as well as on ensuring ecological connectivity with adjacent populations. Accordingly, evaluating the conservation status of reintroduced populations to limit the loss of their genetic diversity requires long‐term genetic monitoring. The griffon vulture population of central Italy originated from 93 birds sourced from wildlife rehabilitation centers in Spain from 1994 to 2002, without prior genetic characterization. To conduct a post‐release genetic assessment, feather samples from 155 free‐living individuals, collected from 2013 to 2018 were analyzed at biparental short tandem repeat loci (STRs). Genetic diversity parameters, mean number of alleles (A), mean effective number of alleles (Ae), expected heterozygosity (He), and observed heterozygosity (Ho), were estimated and compared with those reported for native and reintroduced European griffon vulture populations. Individual inbreeding coefficient (F _IS ) and effective population size (Ne) were also assessed. Genetic variability (A = 7.8; Ae = 3.69; He = 0.64; Ho = 0.63) and effective population size (Ne ≈ 125) are consistent with medium‐term viability. Furthermore, field observations and genetic data suggest connectivity with other populations, including those in Spain, France and the Balkans, supporting the potential role of this population as a genetic bridge between western and eastern populations. This study represents the first population‐level genetic assessment based on nuclear markers of the reintroduced continental griffon vulture population in Italy, providing a baseline for future genetic monitoring and assessments of gene flow and connectivity among European populations.

Background/Objectives: The gene pool of the Apennine wolf is affected by admixture with domestic variants due to anthropogenic hybridisation with dogs. Genetic monitoring at the population level involves assessing the extent of admixture in single individuals, ranging from pure wolves to recent hybrids or wolf backcrosses, through the analysis of nuclear and mitochondrial DNA (mtDNA) markers. Although individually non-diagnostic, mtDNA is nevertheless essential for completing the final diagnosis of genetic admixture. Typically, the identification of wolf mtDNA haplotypes is carried out via sequencing of coding genes and non-coding DNA stretches. Our objective was to develop a fast real-time PCR assay to detect the mtDNA haplotypes that occur exclusively in the Apennine wolf population, as a valuable alternative to the demanding sequence-based typing. Methods: We validated a qualitative duplex real-time PCR that exploits the combined presence of diagnostic point mutations in two mtDNA segments, the NDH-4 gene and the control region, and is performed in a single-tube step through TaqMan-MGB chemistry. The aim was to detect mtDNA multi-fragment haplotypes that are exclusive to the Apennine wolf, bypassing sequencing. Results: Basic validation of 149 field samples, consisting of pure Apennine wolves, dogs, wolf × dog hybrids, and Dinaric wolves, showed that the assay is highly specific and sensitive, with genomic DNA amounts as low as 10⁻⁵ ng still producing positive results. It also proved high repeatability and reproducibility, thereby enabling reliable high-throughput testing. Conclusions: The results indicate that the assay presented here provides a valuable alternative method to the time- and cost-consuming sequencing procedure to reliably diagnose the maternal lineage of the still-threatened Apennine wolf, and it covers a wide range of applications, from scientific research to conservation, diagnostics, and forensics.