Selected hybrids of the wine grape variety Seibel 5279

In the resistance breeding programme of our Institute, which was begun after World War II, the French resistant hybrids Seyve Villard and Seibel, both of which resulted from crosses involving American species, were used for resistance sources. In the resistance breeding programme at Kecskemet, the variety Seibel 5279 was used first as a male parent to transfer resistance. From the resulting hybrid families the variety candidates RF 5 (Reflex), RF 16 (Refren) and RF 48 (Reform) were selected because of their valuable characters. Data collected over several years demonstrate the value of these selections from both a breeding and production point of view. This generation represents the first step in the breeding programme and the results encourage us to continue our work

The potential negative impact of antibiotic pack on antibiotic stewardship in primary care in Switzerland: a modelling study.

BACKGROUND: In Switzerland, oral antibiotics are dispensed in packs rather than by exact pill-count. We investigated whether available packs support compliance with recommended primary care treatment regimens for common infections in children and adults. METHODS: Hospital-based guidelines for oral community -based treatment of acute otitis media, sinusitis, tonsillopharyngitis, community-acquired pneumonia and afebrile urinary tract infection were identified in 2017 in an iterative process by contacting hospital pharmacists and infectious diseases specialists. Furthermore, newly available national guidelines published in 2019 were reviewed. Available pack sizes for recommended solid, dispersible and liquid antibiotic formulations were retrieved from the Swiss pharmaceutical register and compared with recommended regimens to determine optimal (no leftovers) and adequate (optimal +/- one dose) matches. RESULTS: A large variety of recommended regimens were identified. For adults, optimal and adequate packs were available for 25/70 (36%) and 8/70 (11%) regimens, respectively. Pack-regimen matching was better for WHO Watch (optimal: 15/24, 63%) than Access antibiotics (optimal: 7/39, 18%). For the four paediatric weight-examples and 42 regimens involving child-appropriate formulations, optimal and adequate packs were available for only 14/168 (8%) and 27/168 (16%), respectively. Matching was better for older children with higher body and for longer treatment courses > 7 days. CONCLUSIONS: Fixed antibiotic packs often do not match recommended treatment regimens, especially for children, potentially resulting in longer than necessary treatments and leftover doses in the community. As part of national stewardship, a move to an exact pill-count system, including for child-appropriate solid formulations, should be considered

Die gesundheitsbezogene Lebensqualität

Zusammenfassung: Die Messung der Lebensqualität gewinnt zunehmend an Bedeutung. Obwohl eine Definition des Begriffs fehlt, wurden unzählige Messinstrumente zu ihrer Erfassung entwickelt, vorwiegend subjektive Fragebogen. In der Medizin wird die Lebensqualität eingeschränkt, man spricht von der gesundheitsbezogenen Lebensqualität ["health-related quality of life" (HRQoL)]. Ihre Messung ist heute Teil der Beurteilung von medizinischen Interventionen. Im vorliegenden Beitrag wird das Konstrukt der (gesundheitsbezogenen) Lebensqualität beleuchtet und eine Auswahl von Instrumenten zur Erfassung der HRQoL vorgestellt. Herausforderungen im Umgang mit der HRQoL werden besprochen und der Einbezug von objektiv gemessenen Parametern diskutiert

Predominantly Non-Solar Origin of Nitrogen in Lunar Soils

Simultaneous static-mode mass spectrometric measurements of nitrogen, carbon, helium, neon, and argon, extracted from the same aliquot of sample by high-resolution stepped combustion, have been made for a suite of five lunar soils. Noble gas isotope ratios show that the majority of noble gases are derived from a solar wind source; for example, at peak release temperatures of 500–600 °C,21Ne/22Ne = 0.0313 ± 0.0007 to 0.0333 ± 0.0007, and 20Ne/22Ne = 11.48 ± 0.05 to 12.43 ± 0.07, with values at the lowest temperature steps less fractionated during implantation from, and therefore even closer to, solar values (21Ne/22NeSW = 0.03361 ± 0.00018 and 20Ne/22NeSW = 14.001 ± 0.042 (Pepin et al., 2012)). Despite the co-release of nitrogen and solar wind argon, measured nitrogen isotopic signatures at each temperature step, whilst variable, are significantly more enriched in 15N compared to the measured solar wind nitrogen value from the Genesis mission. Therefore, mixing between a 15N-enriched non-solar planetary nitrogen source with solar wind nitrogen is required to explain the measured isotopic values from the stepped combustion analysis of lunar soils. Binary mixing calculations, made under different assumptions about the degree of loss of solar wind 36Ar, reveal that the majority (up to 98%) of the nitrogen released is derived from a non-solar source. The range of modelled non-solar end-member nitrogen compositions required to satisfy the measuredδ15N values varies between samples and temperature steps from +5‰ up to +300‰, or between +87‰ and +160‰ for bulk samples. This range of modelled isotopic compositions for the non-solar source of nitrogen encompasses measured values for several different groups of carbonaceous chondrite, as well as IDPs

Simultaneous analysis of abundance and isotopic composition of nitrogen, carbon, and noble gases in lunar basalts: insights into interior and surface processes on the Moon

Simultaneous static-mode mass spectrometric measurements of nitrogen, carbon, helium, neon, and argon extracted from the same aliquot of sample by high-resolution stepped combustion have been made for a suite of six lunar basalts. Collecting abundance and isotopic data for several elements simultaneously from the same sample aliquot enables more detailed identification of different volatile components present in the basalts by comparing release patterns for volatiles across a range of temperature steps. This approach has yielded new data, from which new insights can be gained regarding the indigenous volatile inventory of the Moon. By taking into account N and C data for mid-temperature steps, unaffected by terrestrial contamination or cosmogenic additions, it is possible to determine the indigenous N and C signatures of the lunar basalts. With an average δ15N value of around +0.35‰, the indigenous N component seen in these samples is similar within error to other (albeit limited in number) isotopic measurements of indigenous lunar N. Average C/N ratios for indigenous volatiles in these six basalt samples are much lower than those of the terrestrial depleted mantle, or bulk silicate Earth, possibly suggesting much less C in the lunar interior, relative to N, than on Earth. Cosmogenic isotopes in these samples are well-correlated with published sample exposure ages, and record the rate of in situ production of spallogenic volatiles within material on the lunar surface

Multiple reservoirs of volatiles in the Moon revealed by the isotopic composition of chlorine in lunar basalts

The isotopes of chlorine (37Cl and 35Cl) are highly fractionated in lunar samples compared to most other Solar System materials. Recently, the chlorine isotope signatures of lunar rocks have been attributed to large-scale degassing processes that occurred during the existence of a magma ocean. In this study we investigated how well a suite of lunar basalts, most of which have not previously been analyzed, conform to previous models. The Cl isotope compositions (δ37Cl (‰) = [(37Cl/35Clsample/37Cl/35ClSMOC)-1]×1000, where SMOC refers to standard mean ocean chloride) recorded range from ∼+7 to +14 ‰ (Apollo 15), +10 to +19 ‰ (Apollo 12), +9 to +15 ‰ (70017), +4 to +8 ‰ (MIL 05035), and +15 to +22 ‰ (Kalahari 009). The Cl isotopic data from the present study support the mixing trends previously reported by Boyce et al., 2015, Barnes et al., 2016, as the Cl isotopic composition of apatites are positively correlated with bulk-rock incompatible trace element abundances in the low-Ti basalts, inclusive of low-Ti and KREEP basalts. This trend has been interpreted as evidence that incompatible trace elements, including Cl, were concentrated in the urKREEP residual liquid of the lunar magma ocean, rather than the mantle cumulates, and that urKREEP Cl had a highly fractionated isotopic composition. The source regions for the basalts were thus created by variable mixing between the mantle (Cl-poor and relatively unfractionated) and urKREEP. The high-Ti basalts show much more variability in measured Cl isotope ratios and scatter around the trend formed by the low-Ti basalts. Most of the data for lunar meteorites also fits the mixing of volatiles in their sources, but Kalahari 009, which is highly depleted in incompatible trace elements, contains apatites with heavily fractionated Cl isotopic compositions. Given that Kalahari 009 is one of the oldest lunar basalts and ought to have been derived from very early-formed mantle cumulates, a heavy Cl isotopic signature is likely not related to its mantle source, but more likely to magmatic or secondary alteration processes, perhaps via impact-driven vapor metasomatism of the lunar crust

The origin of water in the primitive Moon as revealed by the lunar highlands samples

The recent discoveries of hydrogen (H) bearing species on the lunar surface and in samples derived from the lunar interior have necessitated a paradigm shift in our understanding of the water inventory of the Moon, which was previously considered to be a ‘bone-dry’ planetary body. Most sample-based studies have focused on assessing the water contents of the younger mare basalts and pyroclastic glasses, which are partial-melting products of the lunar mantle. In contrast, little attention has been paid to the inventory and source(s) of water in the lunar highlands rocks which are some of the oldest and most pristine materials available for laboratory investigations, and that have the potential to reveal the original history of water in the Earth–Moon system. Here, we report in-situ measurements of hydroxyl (OH) content and H isotopic composition of the mineral apatite from four lunar highlands samples (two norites, a troctolite, and a granite clast) collected during the Apollo missions. Apart from troctolite in which the measured OH contents in apatite are close to our analytical detection limit and its H isotopic composition appears to be severely compromised by secondary processes, we have measured up to ~2200 ppm OH in the granite clast with a weighted average δD of ~-105±130‰, and up to ~3400 ppm OH in the two norites (77215 and 78235) with weighted average δD values of -281±49‰ and -27±98‰, respectively. The apatites in the granite clast and the norites are characterised by higher OH contents than have been reported so far for highlands samples, and have H isotopic compositions similar to those of terrestrial materials and some carbonaceous chondrites, providing one of the strongest pieces of evidence yet for a common origin for water in the Earth–Moon system. In addition, the presence of water, of terrestrial affinity, in some samples of the earliest-formed lunar crust suggests that either primordial terrestrial water survived the aftermath of the putative impact-origin of the Moon or water was added to the Earth–Moon system by a common source immediately after the accretion of the Moon

The noble gas and nitrogen relationship between Ryugu and carbonaceous chondrites

Carbonaceous chondrites are considered to have originated from C-type asteroids and represent some of the most primitive material in our solar system. Furthermore, since carbonaceous chondrites can contain significant quantities of volatile elements, they may have played a crucial role in supplying volatiles and organic material to Earth and other inner solar system bodies. However, a major challenge of unravelling the volatile composition of chondritic meteorites is distinguishing between which features were inherited from the parent body, and what may be a secondary feature attributable to terrestrial weathering. In December 2020, the Hayabusa2 mission of the Japan Aerospace Exploration Agency (JAXA) successfully returned surface material from the C-type asteroid (162173) Ryugu to Earth. This material has now been classified as closely resembling CI-type chondrites, which are the most chemically pristine meteorites. The analysis of material from the surface of Ryugu therefore provides a unique opportunity to analyse the volatile composition of material that originated from a CI-type asteroid without the complications arising from terrestrial contamination. Given their highly volatile nature, the noble gas and nitrogen inventories of chondrites are highly sensitive to different alteration processes on the asteroid parent body, and to terrestrial contamination. Here, we investigate the nitrogen and noble gas signature of two pelletized grains collected from the first and second touchdown sites (Okazaki et al., 2022a), to provide an insight into the formation and alteration history of Ryugu. The concentration of trapped noble gas in the Ryugu samples is greater than the average composition of previously measured CI chondrites and are primarily derived from phase Q, although a significant contribution of presolar nanodiamond Xe-HL is noted. The large noble gas concentrations coupled with a significant contribution of presolar nanodiamonds suggests that the Ryugu samples may represent some of the most primitive unprocessed material from the early solar system. In contrast to the noble gases, the abundance of nitrogen and δ15N composition of the two Ryugu pellets are lower than the average CI chondrite value. We attribute the lower nitrogen abundances and δ15N measured in this study to the preferential loss of a 15N-rich phase from our samples during aqueous alteration on the parent planetesimal. The analyses of other grains returned from Ryugu have shown large variations in nitrogen concentrations and δ15N indicating that alteration fluids heterogeneously interacted with material now present on the surface of Ryugu. Finally, the ratio of trapped noble gases to nitrogen is higher than CI chondrites, and is closer to refractory phase Q and nanodiamonds. This indicates that Ryugu experienced aqueous alteration that led to the significant and variable loss of nitrogen, likely from soluble organic matter, without modification of the noble gas budget, which is primarily hosted in insoluble organic matter and presolar diamonds and is therefore more resistant to aqueous alteration.ISSN:0016-7037ISSN:1872-953

Water in evolved lunar rocks: Evidence for multiple reservoirs

We have measured the abundance and isotopic composition of water in apatites from several lunar rocks representing Potassium (K), Rare Earth Elements (REE), and Phosphorus (P) − KREEP − rich lithologies, including felsites, quartz monzodiorites (QMDs), a troctolite, and an alkali anorthosite. The H-isotope data from apatite provide evidence for multiple reservoirs in the lunar interior. Apatite measurements from some KREEP-rich intrusive rocks display moderately elevated δD signatures, while other samples show δD signatures similar to the range known for the terrestrial upper mantle. Apatite grains in Apollo 15 quartz monzodiorites have the lowest δD values measured from the Moon so far (as low as −749‰), and could potentially represent a D-depleted reservoir in the lunar interior that had not been identified until now. Apatite in all of these intrusive rocks contains 6500 ppm H2O). Complexities in partitioning of volatiles into apatite make this comparison uncertain, but measurements of residual glass in KREEP basalt fragments in breccia 15358 independently show that the KREEP basaltic magmas were low in water. The source of 15358 contained ∼10 ppm H2O, about an order of magnitude lower than the source of the Apollo 17 pyroclastic glass beads, suggesting potential variations in the distribution of water in the lunar interior

On the origin and evolution of the material in 67P/Churyumov-Gerasimenko

International audiencePrimitive objects like comets hold important information on the material that formed our solar system. Several comets have been visited by spacecraft and many more have been observed through Earth- and space-based telescopes. Still our understanding remains limited. Molecular abundances in comets have been shown to be similar to interstellar ices and thus indicate that common processes and conditions were involved in their formation. The samples returned by the Stardust mission to comet Wild 2 showed that the bulk refractory material was processed by high temperatures in the vicinity of the early sun. The recent Rosetta mission acquired a wealth of new data on the composition of comet 67P/Churyumov-Gerasimenko (hereafter 67P/C-G) and complemented earlier observations of other comets. The isotopic, elemental, and molecular abundances of the volatile, semi-volatile, and refractory phases brought many new insights into the origin and processing of the incorporated material. The emerging picture after Rosetta is that at least part of the volatile material was formed before the solar system and that cometary nuclei agglomerated over a wide range of heliocentric distances, different from where they are found today. Deviations from bulk solar system abundances indicate that the material was not fully homogenized at the location of comet formation, despite the radial mixing implied by the Stardust results. Post-formation evolution of the material might play an important role, which further complicates the picture. This paper discusses these major findings of the Rosetta mission with respect to the origin of the material and puts them in the context of what we know from other comets and solar system objects