Regulatory changes in the EU for safety purposes require strict control and high safety standards for essential oils obtained by steam distillation, as they are classified as chemical mixtures with potential toxic effects. Subcritical water extracts (SWEs) are considered safer. This study evaluated the cytotoxicity and genotoxicity of SWEs from Rosa damascena Mill. and Rosa alba L. in three test systems at different hierarchical levels: higher plants (root meristems of Hordeum vulgare), somatic cells of Mus musculus ICR strain, and human lymphocytes in vitro. The chromatographic fingerprint of the extracts revealed the presence of key components such as flavonoids, phenolic acids, and glycoside derivatives, with species-dependent variations and concentrations. No significant cytotoxicity was detected in the concentration range of 6–20%. SWE from R. alba showed a higher level of safety at high doses. Genotoxicity tests showed a weak, dose-dependent induction of chromosomal aberrations and micronuclei in barley and lymphocytes (greater in R. alba), a lack of genotoxicity in mouse bone marrow, and a slight increase in micronuclei in mouse erythrocytes after exposure to R. alba extract. The results highlight the suitability of SWEs from R. damascena and R. alba for safe application in the medical, food, and cosmetic industries.

This study aimed to reveal intraspecific variations in two Dryomys species distributed in Türkiye, based on mitochondrial DNA cytochrome b gene sequences, and to discuss the factors driving these variations in the context of phylogeography and genetic species concepts. As a result of Maximum Likelihood, Bayesian Inference, and Network analyses, which included haplogroups or lineages from Italy, Russia, the Caucasus, and Iran identified in previous studies, along with Turkish haplotypes, three major clades (MC1, MC2, and MC3) were identified within Dryomys nitedula. These clades began to diverge evolutionarily in the middle of the Late Miocene (8.82 million years ago) and exhibit significant genetic differences from one another. The Turkish haplotypes were divided into five distinct lineages (N1–N5), each within five subclades (SC1–SC5), which were nested within these MCs. These lineages, their geographical distributions, and the subspecies defined in previous studies that correspond to these lineages are as follows: N1 from the Thrace region (Dryomys nitedula wingei), N2 from the Black Sea region (potentially a new subspecies), N3 from western and central Anatolia (Dryomys nitedula phrygius), N4 from northeastern Anatolia (Dryomys nitedula tichomirowi), and N5 from eastern Anatolia (Dryomys nitedula pictus). The N2 lineage, distributed in areas close to the coastal side of the Eastern Black Sea region and with a range close to both N3 (D. n. phrygius) and N4 (D. n. tichomirowi), exhibited high genetic differentiation from these two lineages and was a candidate to be treated as a new subspecies of Dryomys nitedula in Türkiye. The N5 lineage, which includes haplotypes from the distribution areas of the populations initially classified as Dryomys pictus and later as Dryomys nitedula pictus in previous studies, was found to be more closely related to Dryomys nitedula kurdistanicus from the Zagros Mountains than to D. n. pictus from the central regions of Iran. Combining the results of this study with previous research, it is clear that the D. nitedula lineages in Türkiye, along with haplogroups or subspecies in neighboring regions diverged between the middle Late Miocene and Middle Pleistocene. This divergence is believed to have been driven by climatic cycles and geomorphological processes that shaped the topography of their distribution range. The high genetic diversity observed in the lineages of Anatolia suggests that the region may have served as a glacial refuge for D. nitedula. Similarly to the processes and factors shaping the evolution of D. nitedula, Dryomys laniger was found to have diverged into two lineages, western (L1) and eastern (L2 or Dryomys anatolicus), within its distribution range during the Late Pliocene (2.94 Mya). To make a more accurate taxonomic assessment of D. laniger, a larger number of samples is needed, and the distribution limits should be more clearly defined.

The study aimed to determine the age structure of male capercaillies Tetrao urogallus L., 1758 in Bulgaria based on specimens preserved in collections. We studied 206 birds from the museum collections of the Sitnyakovo Palace (Rila Mnt.) and the National Museum of Natural History, (Bulgarian Academy of Sciences). The age of the birds was determined by the shape of the beak, the shape of the outer feathers of tail, the length of the beak, the length of the beak furrow and the height of the beak at the base. For each of the characteristics used, we divided the birds into three age classes: juvenile (up to 14 months), subadult (between 14 and 60 months) and adult (over 60 months). Of all individuals studied, 92 (44.7%) were juveniles, 64 (31.1%) were subadults and 50 (24.3%) were adults. We found an inconsistency in determining the age of individuals using only one of the characteristics. We proposed to use the angle of curvature of the beak for the age determination. We recommend introducing the requirement to examine more somatometric characteristics in the rare cases when shooting of capercaillies is allowed. This will allow the correct estimation of the age of capercaillies and the accumulation of database information, which will be useful for the management of this difficult to be studied and economically important species.