Within-patch mobility and flight morphology reflect resource use and dispersal potential in the dryad butterfly Minois dryas

Knowledge of mobility is essential for understanding animal habitat use and dispersal potential, especially in the case of species occurring in fragmented habitats. We compared within-patch movement distances, turning angles, resting times, and flight-related morphological traits in the locally endangered butterfly, the dryad (Minois dryas), between its old populations occupying xerothermic grasslands and newly established ones in wet meadows. We expected that the latter group should be more mobile. Individuals living in both habitat types did not differ in their body mass and size, but those from xerothermic grasslands had wider thoraxes and longer wings, thus lower wing loading index (defined as body mass to wing length ratio). The majority of movements were short and did not exceed 10 m. Movement distances were significantly larger in males. However, there was no direct effect of habitat type on movement distances. Our results suggest that the dryads from xerothermic grasslands have better flight capabilities, whereas those from wet meadows are likely to invest more in reproduction. This implies that mobility is shaped by resource availability rather than by recent evolutionary history. Lower female mobility may have negative implications for the metapopulation persistence because only mated females are able to (re)colonise vacant habitat patches efficiently. Conservation efforts should thus be focused on maintaining large habitat patches that prevent stochastic local extinctions. Furthermore, the recommendation of promoting the exchange of individuals among patches through improving matrix permeability, as well as assisted reintroductions of the species into suitable vacant habitats should also improve its conservation

Expert consensus document: Clinical and molecular diagnosis, screening and management of Beckwith-Wiedemann syndrome: an international consensus statement.

Beckwith-Wiedemann syndrome (BWS), a human genomic imprinting disorder, is characterized by phenotypic variability that might include overgrowth, macroglossia, abdominal wall defects, neonatal hypoglycaemia, lateralized overgrowth and predisposition to embryonal tumours. Delineation of the molecular defects within the imprinted 11p15.5 region can predict familial recurrence risks and the risk (and type) of embryonal tumour. Despite recent advances in knowledge, there is marked heterogeneity in clinical diagnostic criteria and care. As detailed in this Consensus Statement, an international consensus group agreed upon 72 recommendations for the clinical and molecular diagnosis and management of BWS, including comprehensive protocols for the molecular investigation, care and treatment of patients from the prenatal period to adulthood. The consensus recommendations apply to patients with Beckwith-Wiedemann spectrum (BWSp), covering classical BWS without a molecular diagnosis and BWS-related phenotypes with an 11p15.5 molecular anomaly. Although the consensus group recommends a tumour surveillance programme targeted by molecular subgroups, surveillance might differ according to the local health-care system (for example, in the United States), and the results of targeted and universal surveillance should be evaluated prospectively. International collaboration, including a prospective audit of the results of implementing these consensus recommendations, is required to expand the evidence base for the design of optimum care pathways

Housing Expectations of Future Seniors Based on an Example of the Inhabitants of Poland

A longer life span, which entails a dynamic increase in the numbers of seniors, poses a wide range of global challenges, among others for engineers and architects. The said challenges include, among others, a well-organised medical care system, proper legislation and social education. The respective planning process should also recognise the important role of a well-designed environment. This paper is intended to analyse the current senior housing solutions in Poland and to define the desirable development of those housing forms that can successfully meet the needs of future seniors. For this purpose, we have analysed the current structure of elderly care. Further, this research was conducted using the diagnostic poll method (“Housing needs of the future seniors”), in order to define the current housing preferences of the young (future seniors). The results thereof provide relevant guidance in the search for spatial solutions that can ensure a high-quality housing environment for seniors in the future, which, at the same time, will facilitate their independent living

Modified Baby Milk—Bioelements Composition and Toxic Elements Contamination

Breast milk has the most suitable composition for the proper development in the first year of a child’s life. However, it is often replaced with artificial milk. The aim of the study was to analyze the composition of essential elements: Na, K, Ca, P, Mg, Fe, Zn, Cu, and Mn as well as toxic elements: Ni, Pb, Sr, Li, and In in 18 formulas available in Poland. The daily supply was also estimated. The study was performed by Inductively Coupled Plasma Optical Emission Spectrometry method. The results showed the presence of all essential elements tested, but the content of P and Mn significantly differed from the concentrations declared. Such discrepancies can have significant impact on the daily dose of the bioelements taken. However, the content of elements was within the reference standards established by the EU Directive with exception of P, the amount of which exceeded the norms 5.23–18.80-times. Daily supply of P in tested milk as well as Fe and Mn provided with first and hypoallergenic formula exceeded the adequate intake. Analysis revealed the contamination with harmful elements—Pb, Sr, Li, and In were detected in almost all products. The study confirms the data concerning some discrepancies in composition and the contamination of food and may provide information on the feeding quality of children and estimation of health risk associated with exposure to toxic elements

Characteristics of the patients carrying the m.3243A>G mutation patients 1–17 with multi-organ presentation (subgroup I), patients 18–29 with isolated hearing loss (subgroup II), and asymptomatic carriers 30–34 (subgroup III).

<p>Probands are shown in bold.</p><p>GC-MS = gas chromatography–mass spectroscopy; NMDAS = Newcastle Mitochondrial Disease Adult Scale; MGCA = 3-methylglutaconic aciduria; LA = lactic aciduria; HL = hearing loss; NP = not performed; NA = normal value; QoL = quality of life; CI = cochlear implant user; IMGP = increased mineralisation of globus pallidus; MCA = minimal cerebellar atrophy; MRS = magnetic resonance spectroscopy; MRS score: 0 = negative LA, 1 = uncertain LA, 2 = positive LA, 3 = strong LA.</p><p>C = cardiomyopathy; DM = diabetes mellitus; H = migraine; I = infertility; K = renal insufficiency; M = myopathy; N = peripheral neuropathy; RP = pigmentary degeneration of retina; S = stroke-like episodes; SS = short stature.</p><p>No HL = normal hearing.</p>*<p>Stress = hearing deterioration following stressful event; Aminogly = hearing deterioration following aminoglycoside administration; Noise = hearing deterioration following noise exposure; Pancreatitis = hearing deterioration following acute pancreatitis; Pregnancy = hearing deterioration after pregnancy.</p