Marine mammal hotspots across the circumpolar Arctic

Aim: Identify hotspots and areas of high species richness for Arctic marine mammals. Location: Circumpolar Arctic. Methods: A total of 2115 biologging devices were deployed on marine mammals from 13 species in the Arctic from 2005 to 2019. Getis-Ord Gi* hotspots were calculated based on the number of individuals in grid cells for each species and for phyloge-netic groups (nine pinnipeds, three cetaceans, all species) and areas with high spe-cies richness were identified for summer (Jun-Nov), winter (Dec-May) and the entire year. Seasonal habitat differences among species’ hotspots were investigated using Principal Component Analysis. Results: Hotspots and areas with high species richness occurred within the Arctic continental-shelf seas and within the marginal ice zone, particularly in the “Arctic gateways” of the north Atlantic and Pacific oceans. Summer hotspots were generally found further north than winter hotspots, but there were exceptions to this pattern, including bowhead whales in the Greenland-Barents Seas and species with coastal distributions in Svalbard, Norway and East Greenland. Areas with high species rich-ness generally overlapped high-density hotspots. Large regional and seasonal dif-ferences in habitat features of hotspots were found among species but also within species from different regions. Gap analysis (discrepancy between hotspots and IUCN ranges) identified species and regions where more research is required. Main conclusions: This study identified important areas (and habitat types) for Arctic marine mammals using available biotelemetry data. The results herein serve as a benchmark to measure future distributional shifts. Expanded monitoring and teleme-try studies are needed on Arctic species to understand the impacts of climate change and concomitant ecosystem changes (synergistic effects of multiple stressors). While efforts should be made to fill knowledge gaps, including regional gaps and more com-plete sex and age coverage, hotspots identified herein can inform management ef-forts to mitigate the impacts of human activities and ecological changes, including creation of protected areas

INTRODUCTION POPULATIONS OF USEFUL PLANTS IN THE YAKUT BOTANICAL GARDEN

Aim. The aim is to study the ontogeny and structure of introduced populations of useful plants in Central Yakutia. Methods. Description of the ontogeny of the plants under study was carried out with the determination of ontogenetic states according to generally accepted methods. After planting, current measures were taken to care for plants with elimination of weeds and preservation of the undergrowth. The number of plants at the planting sites was calculated annually. Results. In plants, there is a polyvariety of the rate of development, in which the life cycle is shortened in individuals, the rate of development is accelerated or the ontogenetic states are missed, and there is also transition of plants to a temporarily non-flowering state. All studied introductory populations were left-sided and had different absolute maxima, which depended on the life form and duration of plant stay in culture. Conclusions. Among young monocentric plants we saw the development and attenuation of the population (Delphinium grandiflorum, Linum komarovii, Plantago major, Redowskia sophiifolia). In them, absolute maximums fall on juvenile, immitric, virginile and young generative groups. In populations of monocentric perennial plants, Lilium pensylvanicum and Adonis sibirica, absolute maxima fall on virginile groups. For studied years, the nature of the developmental spectrum in populations of Clausia aprica and Tussilago farfara has not changed with the absolute maximum in the virginal group

Estimation of pion-emitting source in symmetric and asymmetric collisions using the UrQMD model

The femtoscopy technique allows one to measure spatial and temporal characteristics of the particle-emitting source produced in high-energy collisions. In non-central ultrarelativistic heavy-ion collisions the emission source can be tilted in the reaction plane. In the current analysis, the orientation of freeze-out distributions with respect to the first-order event plane in symmetric (Au+Au) and asymmetric (Cu+Au) collisions at $$\sqrt {{s_{NN}}} = 200$$ GeV was studied using the UrQMD model to extract information about the emission source tilt. The effect of the initial geometry on the femtoscopic radii of small systems was measured at the same number of charged particles and transverse momentum was studied in d+Au and 3He+Au collisions at $$\sqrt {{s_{NN}}} = 200$$ GeV. The implications of the results are discussed

Estimation of pion-emitting source in symmetric and asymmetric collisions using the UrQMD model

The femtoscopy technique allows one to measure spatial and temporal characteristics of the particle-emitting source produced in high-energy collisions. In non-central ultrarelativistic heavy-ion collisions the emission source can be tilted in the reaction plane. In the current analysis, the orientation of freeze-out distributions with respect to the first-order event plane in symmetric (Au+Au) and asymmetric (Cu+Au) collisions at sNN=200$$\sqrt {{s_{NN}}} = 200$$ GeV was studied using the UrQMD model to extract information about the emission source tilt. The effect of the initial geometry on the femtoscopic radii of small systems was measured at the same number of charged particles and transverse momentum was studied in d+Au and 3He+Au collisions at sNN=200$$\sqrt {{s_{NN}}} = 200$$ GeV. The implications of the results are discussed

Complex Diagnostics of Non-Specific Intellectual Developmental Disorder

Intellectual development disorder (IDD) is characterized by a general deficit in intellectual and adaptive functioning. In recent years, there has been a growing interest in studying the genetic structure of IDD. Of particular difficulty are patients with non-specific IDD, for whom it is impossible to establish a clinical diagnosis without complex genetic diagnostics. We examined 198 patients with non-specific IDD from 171 families using whole-exome sequencing and chromosome microarray analysis. Hereditary forms of IDD account for at least 35.7% of non-specific IDD, of which 26.9% are monogenic forms. Variants in the genes associated with the BAF (SWI/SNF) complex were the most frequently identified. We were unable to identify phenotypic features that would allow differential diagnosis of monogenic and microstructural chromosomal rearrangements in non-specific IDD at the stage of clinical examination, but due to its higher efficiency, exome sequencing should be the diagnostic method of the highest priority study after the standard examination of patients with NIDD in Russia