The Glenburgh Orogeny as a record of Paleoproterozoic continent-continent collision

The Gascoyne Province lies at the western end of the Capricorn Orogen, and includes a range of Paleoproterozoic gneisses and metasedimentary basins, known as the Glenburgh Terrane, that are exotic to both the Yilgarn and Pilbara Cratons. Here we present sensitive high-resolution ion microprobe (SHRIMP) U–Pb ages for a variety of detrital zircons and metamorphic zircon and monazite from several of these pre-collisional siliciclastic basins that were deformed and metamorphosed at high metamorphic grade during the Glenburgh Orogeny, when the Yilgarn Craton collided with a previously assembled Pilbara Craton – Glenburgh Terrane. The precursors to the Moogie Metamorphics were deposited sometime between 2240 and 2125 Ma in either a foreland basin to the Ophthalmian Orogeny, or a retro-arc that formed during the collision of the Glenburgh Terrane with the Pilbara Craton. The Quartpot Pelite of the Camel Hills Metamorphics was deposited between 2000 Ma and 1985 Ma as a fore-arc deposit to the Dalgaringa continental margin arc. The Petter Calc-silicate of the Camel Hills Metamorphics was deposited sometime between 2610 and 1965 Ma as part of the Yilgarn Craton passive margin. Metamorphic zircon and monazite ages indicate that continental collision and high-grade metamorphism during the Glenburgh Orogeny (D2g) took place between 1965 Ma and 1950 Ma

Pathology Associated with AAV Mediated Expression of Beta Amyloid or C100 in Adult Mouse Hippocampus and Cerebellum

Accumulation of beta amyloid (Ab) in the brain is a primary feature of Alzheimer’s disease (AD) but the exact molecular mechanisms by which Ab exerts its toxic actions are not yet entirely clear. We documented pathological changes 3 and 6 months after localised injection of recombinant, bi-cistronic adeno-associated viral vectors (rAAV2) expressing human Ab40- GFP, Ab42-GFP, C100-GFP or C100V717F-GFP into the hippocampus and cerebellum of 8 week old male mice. Injection of all rAAV2 vectors resulted in wide-spread transduction within the hippocampus and cerebellum, as shown by expression of transgene mRNA and GFP protein. Despite the lack of accumulation of Ab protein after injection with AAV vectors, injection of rAAV2-Ab42-GFP and rAAV2- C100V717F-GFP into the hippocampus resulted in significantly increased microgliosis and altered permeability of the blood brain barrier, the latter revealed by high levels of immunoglobulin G (IgG) around the injection site and the presence of IgG positive cells. In comparison, injection of rAAV2-Ab40-GFP and rAAV2-C100-GFP into the hippocampus resulted in substantially less neuropathology. Injection of rAAV2 vectors into the cerebellum resulted in similar types of pathological changes, but to a lesser degree. The use of viral vectors to express different types of Ab and C100 is a powerful technique with which to examine the direct in vivo consequences of Ab expression in different regions of the mature nervous system and will allow experimentation and analysis of pathological AD-like changes in a broader range of species other than mouse

Genome Sequence of Stenotrophomonas maltophilia PML168, Which Displays Baeyer-Villiger Monooxygenase Activity

Stenotrophomonas maltophilia PML168 was isolated from Wembury Beach on the English Coast from a rock pool following growth and selection on agar plates. Here we present the permanent draft genome sequence, which has allowed prediction of function for several genes encoding enzymes relevant to industrial biotechnology, including a novel flavoprotein monooxygenase

Using in situ SHRIMP U-Pb monazite and xenotime geochronology to determine the age of orogenic gold mineralization: An example from the Paulsens Mine, Southern Pilbara Craton

Paulsens is a mesothermal orogenic gold deposit located in the Wyloo Inlier on the southern margin of the Pilbara craton of Western Australia. Gold occurs in quartz-sulfide veins hosted within a folded and faulted gabbro dike, from which baddeleyite yields a U-Pb crystallization age of 2701 ± 11 Ma. Monazite and xenotime in the veins and from hydrothermally altered country rocks yield three distinct U-Pb dates of ca. 2400, 1730, and 1680 Ma. Textural relationships between euhedral xenotime and pyrite with rounded native gold inclusions from within the quartz-sulfide veins show that the primary gold mineralization was synchronous with xenotime crystallization at 2403 ± 5 Ma, and coeval with pervasive alteration of the host rocks, which yield monazite ages of 2398 ± 37 and 2403 ± 38 Ma. Regional-scale hydrothermal events at ca. 1730 and 1680 Ma are linked to the growth of monazite within phyllitic rocks at 1730 ± 28 and 1721 ± 32 Ma, carbonate veining at 1655 ± 37 Ma, and gold remobilization or introduction of new gold at 1680 ± 9 Ma. The ca. 2400 Ma age for mineralization and hydrothermal alteration does not correspond with any known deformation event in the region, indicating a significantly different and more complicated low-temperature tectonothermal evolution for the southern Pilbara region than previously recognized. The in situ secondary ion mass spectrometry dating of monazite and xenotime employed here will lead to better targeting of orogenic gold deposits in the northern Capricorn Orogen, and these techniques can be utilized for orogenic gold exploration worldwide

Foliar N application at anthesis alters grain protein composition and enhances baking quality in winter wheat only under a low N fertiliser regimen

Wheat is the second biggest staple crop worldwide and is mainly consumed in the form of baked goods, requiring a specific flour quality. Grain protein concentration (GPC) is an underpinning parameter for baking quality and therefore strongly influences the value of wheat. It is a common strategy to increase GPC by combining high protein varieties with the application of a late dose of nitrogen. However, the late use of N fertilisers can cause environmental problems, such as nitrate leaching and gaseous losses. Furthermore, recent studies show, that there is only a weak relationship between GPC and bread volume. The aim of this study was to re-evaluate the merits of a late N application by investigating the effects of a late foliar N application, not only on GPC, but also on the gluten protein composition and on bread volume. In this study, an increasing GPC did not necessarily lead to improved baking quality. Baking performance rather depended on the grain protein composition. Only at a low N fertiliser level (100 kg N ha-1), the foliar N application decreased the HMW-GS/LMW-GS ratio and increased the gliadin/HMW-GS ratio, which led to an improved bread volume. These results imply that a late foliar N application can be used to effectively improve baking quality when the total N uptake was low due to low fertilisation or unfavourable weather conditions. The results also show that quality cannot be evaluated by measuring GPC alone but also needs information of storage protein composition as well as bread volume

Southward re-distribution of tropical tuna fisheries activity can be explained by technological and management change

There is broad evidence of climate change causing shifts in fish distribution worldwide, but less is known about the response of fisheries to these changes. Responses to climate-driven shifts in a fishery may be constrained by existing management or institutional arrangements and technological settings. In order to understand how fisheries are responding to ocean warming, we investigate purse seine fleets targeting tropical tunas in the east Atlantic Ocean using effort and sea surface temperature anomaly (SSTA) data from 1991 to 2017. An analysis of the spatial change in effort using a centre of gravity approach and empirical orthogonal functions is used to assess the spatiotemporal changes in effort anomalies and investigate links to SSTA. Both analyses indicate that effort shifts southward from the equator, while no clear pattern is seen northward from the equator. Random forest models show that while technology and institutional settings better explain total effort, SSTA is playing a role when explaining the spatiotemporal changes of effort, together with management and international agreements. These results show the potential of management to minimize the impacts of climate change on fisheries activity. Our results provide guidance for improved understanding about how climate, management and governance interact in tropical tuna fisheries, with methods that are replicable and transferable. Future actions should take into account all these elements in order to plan successful adaptation. © 2020 The Authors. Fish and Fisheries published by John Wiley & Sons Ltd.This research is supported by the project CLOCK, under the European Horizon 2020 Program, ERC Starting Grant Agreement nº679812 funded by the European Research Council. It is also supported by the Basque Government through the BERC 2018-2021 programme and by the Spanish Ministry of Economy and Competitiveness MINECO through the BC3 María de Maeztu excellence accreditation MDM- 2017-0714. We thank, without implicating, C. Palma for his helpful advice on the ICCAT database and M. Gabantxo and H. Gabantxo for their knowledge transfer about tropical tuna fisheries. Also, we thank I. Arostegui for her comments during the design of the random forest; F. Saborido, A. Tidd and H. Arrizabalaga for scientific advice and H. Murua and M. Ortiz for providing ICCAT data. Elena Ojea thanks the Xunta the Galicia GAIN Oportunius programme and Consellería de Educación (Galicia, Spain) for additional financial support

Reproducibility of adenosine stress cardiovascular magnetic resonance in multi-vessel symptomatic coronary artery disease

<p>Abstract</p> <p>Purpose</p> <p>First-pass perfusion cardiovascular magnetic resonance (CMR) is increasingly being utilized in both clinical practice and research. However, the reproducibility of this technique remains incompletely evaluated, particularly in patients with severe coronary artery disease (CAD). The purpose of this study was to determine the inter-study reproducibility of adenosine stress CMR in patients with symptomatic multi-vessel CAD and those at low risk for CAD.</p> <p>Methods</p> <p>Twenty patients (10 with CAD, 10 low risk CAD) underwent two CMR scans 8 ± 2 days apart. Basal, mid and apical left ventricular short axis slices were acquired using gadolinium 0.05 mmol/kg at peak stress (adenosine, 140 μ/kg/min, 4 min) and rest. Myocardial perfusion was evaluated qualitatively by assessing the number of ischemic segments, and semi-quantitatively by determining the myocardial perfusion reserve index (MPRi) using a normalized upslope method. Inter-study and observer reproducibility were assessed--the latter being defined by the coefficient of variation (CoV), which was calculated from the standard deviation of the differences of the measurements, divided by the mean. Additionally, the percentage of myocardial segments with perfect agreement and inter- and intra-observer MPRi correlation between studies, were also determined.</p> <p>Results</p> <p>The CoV for the number of ischemic segments was 31% with a mean difference of -0.15 ± 0.88 segments and 91% perfect agreement between studies. MPRi was lower in patients with CAD (1.13 ± 0.21) compared to those with low risk CAD (1.59 ± 0.58), p = 0.02. The reproducibility of MPRi was 19% with no significant difference between patients with CAD and those with low risk CAD (p = 0.850). Observer reproducibility for MPRi was high: inter-observer CoV 9%, r = 0.93 and intra-observer CoV 5%, r = 0.94. For trials using perfusion CMR as an endpoint, an estimated sample size of 12 subjects would be required to detect a two-segment change in the number of ischemic segments (power 0.9, α 0.05).</p> <p>Conclusions</p> <p>Adenosine stress CMR, by qualitative and semi-quantitative normalized upslope analyses are reproducible techniques in both patients with multi-vessel CAD and those without known CAD. The robust inter-study reproducibility of perfusion CMR supports its clinical and research application.</p

Trophic Ecology of Atlantic Bluefin Tuna (Thunnus thynnus) Larvae from the Gulf of Mexico and NW Mediterranean Spawning Grounds: A Comparative Stable Isotope Study

The present study uses stable isotopes of nitrogen and carbon (δ15Nandδ13C) as trophic indicators for Atlantic bluefin tuna larvae (BFT) (6–10mm standard length) in the highly contrasting environmental conditions of the Gulf of Mexico (GOM) and the Balearic Sea (MED). These regions are differentiated by their temperature regime and relative productivity, with the GOM being significantly warmer and more productive. MED BFT larvae showed the highest δ15N signatures, implying an elevated trophic position above the underlyingmicrozooplankton baseline. Ontogenetic dietary shifts were observed in the BFT larvae from the GOM and MED which indicates early life trophodynamics differences between these spawning habitats. Significant trophic differences between the GOM and MED larvae were observed in relation to δ15N signatures in favour of the MED larvae, which may have important implications in their growth during their early life stages. These low δ15N levels in the zooplankton from the GOM may be an indication of a shifting isotopic baseline in pelagic food webs due to diatrophic inputs by cyanobacteria. Lack of enrichment for δ15N in BFT larvae compared to zooplankton implies an alternative grazing pathway from the traditional food chain of phytoplankton— zooplankton—larval fish. Results provide insight for a comparative characterization of the trophic pathways variability of the two main spawning grounds for BFT larvaeVersión del editor4,411

Ex-vivo changes in amino acid concentrations from blood stored at room temperature or on ice: implications for arginine and taurine measurements

Background: Determination of the plasma concentrations of arginine and other amino acids is important for understanding pathophysiology, immunopathology and nutritional supplementation in human disease. Delays in processing of blood samples cause a change in amino acid concentrations, but this has not been precisely quantified. We aimed to describe the concentration time profile of twenty-two amino acids in blood from healthy volunteers, stored at room temperature or on ice.Methods: Venous blood was taken from six healthy volunteers and stored at room temperature or in an ice slurry. Plasma was separated at six time points over 24 hours and amino acid levels were determined by high-performance liquid chromatography.Results: Median plasma arginine concentrations decreased rapidly at room temperature, with a 6% decrease at 30 minutes, 25% decrease at 2 hours and 43% decrease at 24 hours. Plasma ornithine increased exponentially over the same period. Plasma arginine was stable in blood stored on ice, with a &lt; 10% change over 24 hours. Plasma taurine increased by 100% over 24 hours, and this change was not prevented by ice. Most other amino acids increased over time at room temperature but not on ice.Conclusion: Plasma arginine concentrations in stored blood fall rapidly at room temperature, but remain stable on ice for at least 24 hours. Blood samples taken for the determination of plasma amino acid concentrations either should be placed immediately on ice or processed within 30 minutes of collection

Detection of porcine circovirus type 1 in commercial porcine vaccines by loop-mediated isothermal amplification

A loop-mediated isothermal amplification (LAMP) method with a real-time monitoring system was developed for the detection of porcine circovirus type 1 (PCV1) in commercial swine vaccines. This method was highly specific for PCV1. No cross-reaction to porcine circovirus type 2, porcine parvovirus, pseudorabies virus, classical swine fever virus, and porcine reproductive and respiratory syndrome virus was observed. The analytical sensitivity of the LAMP for PCV1 DNA was 10 copies/μl in the case of positive recombinant plasmid comparable to that obtained from the nested polymerase chain reaction (nested PCR). Furthermore, 25 commercial swine vaccines were tested by both the LAMP and the nested PCR, and three of them were tested positive for PCV1 DNA. These results indicate that PCV1 DNA can be real-time detected by the LAMP; the method was highly specific, sensitive, and rapid for the detection of PCV1 DNA, particularly in commercial swine vaccines