Combined EISCAT radar and optical multispectral and tomographic observations of black aurora

Black auroras are recognized as spatially well-defined regions within a uniform diffuse auroral background where the optical emission is significantly reduced. Black auroras typically appear post-magnetic midnight and during the substorm recovery phase, but not exclusively so. We report on the first combined multimonochromatic optical imaging, bistatic white-light TV recordings and incoherent scatter radar observations of black aurora by EISCAT of the phenomenon. From the relatively larger reduction in luminosity at 4278 Å than at 8446 Å we show that nonsheared black auroras are most probably not caused by downward directed electrical fields at low altitude. From the observations, we determine this by relating the height and intensity of the black aurora to precipitating particle energy within the surrounding background diffuse aurora. The observations are more consistent with an energy selective loss cone. Hence the mechanism causing black aurora is most probably active in the magnetosphere rather than close to Earth

Chemoenzymatic Probes for Detecting and Imaging Fucose-α(1-2)-galactose Glycan Biomarkers

The disaccharide motif fucose-α(1-2)-galactose (Fucα(1-2)Gal) is involved in many important physiological processes, such as learning and memory, inflammation, asthma, and tumorigenesis. However, the size and structural complexity of Fucα(1-2)Gal-containing glycans have posed a significant challenge to their detection. We report a new chemoenzymatic strategy for the rapid, sensitive detection of Fucα(1-2)Gal glycans. We demonstrate that the approach is highly selective for the Fucα(1-2)Gal motif, detects a variety of complex glycans and glycoproteins, and can be used to profile the relative abundance of the motif on live cells, discriminating malignant from normal cells. This approach represents a new potential strategy for biomarker detection and expands the technologies available for understanding the roles of this important class of carbohydrates in physiology and disease

A Comparison of Lethal and Non-Lethal Management Approaches to Reduce Damage Associated with Urban Crow Roosts in New York and Virginia

Crow populations have steadily increased in many parts of the country since 1966. Although large winter congregations of crows in urban environments are not a new phenomenon, the number of complaints regarding damage associated with these large (2,000-20,000 individuals) roosts appears to be increasing. In an effort to assist the public in reducing impacts of urban crow roosts, USDA, APHIS, Wildlife Services in Virginia and New York implemented large-scale roost dispersal programs in the winter of 2001-2002. The goal of the programs were to manage local crow populations to minimize associated noise, accumulations of crow fecal droppings on and around residences, strong ammonia odors from fecal droppings, property damage, clean-up costs and threats to human health and safety. Multiple meetings involving the public and key stakeholders were convened where a variety of options and consequences of each option were discussed. Options considered were no action, habitat alteration, cultural methods, roost dispersal, and roost depopulation. Wildlife Services in each state took different approaches to managing crow roosting sites based on state regulations, available tools, scope of the problem, consequences of each management action, effectiveness of methods, and public input. In Virginia, a lethal control program was initiated targeting one roost site (2,000-6 ,000 crows/roost) using the avicide DRC-1339. The goals were to remove a significant percentage of the local crow population and disperse the remaining crows. This project resulted in an estimated 73% reduction in crow numbers at the primary roost site and altered roost dynamics at another roost. The cooperators satisfaction level was an immediate 75% reduction in damage based on a polling of affected property owners. This satisfaction level was based on a reduction in fecal droppings, maintenance costs to clean up fecal droppings, noise, and abundance of crows. In upstate New York, two roost sites (16,000-20,000 crows/roost) were successfully dispersed using a non-lethal hazing program (pyrotechnics, recorded crow distress calls and hand-held lasers). In New York, no avicides were registered at the time of this project and the Cities of Troy and Albany requested that WS try a non-lethal program prior to implementing a lethal control program. The number of crows in the primary roost in the cities of Albany and Troy were reduced by more than 95% over the course of an eight-day program. Significant reduction in crow numbers and damage remained more than eight weeks later. In this paper we will provide a comparison of crow management projects in Virginia and New York and discuss implications of different approaches for managing urban crows

Phase calibration of the EISCAT Svalbard Radar interferometer using optical satellite signatures

The link between natural ion-line enhancements in radar spectra and auroral activity has been the subject of recent studies but conclusions have been limited by the spatial and temporal resolution previously available. The next challenge is to use shorter sub-second integration times in combination with interferometric programmes to resolve spatial structure within the main radar beam, and so relate enhanced filaments to individual auroral rays. This paper presents initial studies of a technique, using optical and spectral satellite signatures, to calibrate the received phase of a signal with the position of the scattering source along the interferometric baseline of the EISCAT Svalbard Radar. It is shown that a consistent relationship can be found only if the satellite passage through the phase fringes is adjusted from the passage predicted by optical tracking. This required adjustment is interpreted as being due to the vector between the theoretical focusing points of the two antennae, i.e. the true radar baseline, differing from the baseline obtained by survey between the antenna foot points. A method to obtain a measurement of the true interferometric baseline using multiple satellite passes is outlined

A graphene-based glycan biosensor for electrochemical label-free detection of a tumor-associated antibody

The study describes development of a glycan biosensor for detection of a tumor-associated antibody. The glycan biosensor is built on an electrochemically activated/oxidized graphene screen-printed electrode (GSPE). Oxygen functionalities were subsequently applied for covalent immobilization of human serum albumin (HSA) as a natural nanoscaffold for covalent immobilization of Thomsen-nouvelle (Tn) antigen (GalNAc-O-Ser/Thr) to be fully available for affinity interaction with its analyte—a tumor-associated antibody. The step by step building process of glycan biosensor development was comprehensively characterized using a battery of techniques (scanning electron microscopy, atomic force microscopy, contact angle measurements, secondary ion mass spectrometry, surface plasmon resonance, Raman and energy-dispersive X-ray spectroscopy). Results suggest that electrochemical oxidation of graphene SPE preferentially oxidizes only the surface of graphene flakes within the graphene SPE. Optimization studies revealed the following optimal parameters: activation potential of +1.5 V vs. Ag/AgCl/3 M KCl, activation time of 60 s and concentration of HSA of 0.1 g L−1. Finally, the glycan biosensor was built up able to selectively and sensitively detect its analyte down to low aM concentration. The binding preference of the glycan biosensor was in an agreement with independent surface plasmon resonance analysis.The financial support received from the Slovak Scientific Grant Agency VEGA 2/0137/18 and 2/0090/16 from the Slovak Research and Development Agency APVV 17-0300 is acknowledged. This publication is the result of the project implementation: Centre for materials, layers and systems for applications and chemical processes under extreme conditions—Stage I, ITMS no.: 26240120007, supported by the ERDF. This publication was supported by Qatar University Collaborative Grant QUCG-CAM-19/20-2. The findings achieved herein are solely the responsibility of the authors.Scopu

Atlantic salmon in regulated rivers: Understanding river management through the ecosystem services lens

Known as the "king of fishes," the Atlantic salmon (Salmo salar, Salmonidae) is an iconic freshwater species whose contribution to human well-being has long been recognized, as have widespread declines in its abundance, partly due to river regulation. To understand how salmon conservation has been addressed within the ecosystem services (ES) framework, we synthesized the peer-reviewed literature on ES provided by salmon in regulated rivers. We developed a search string to capture allusions to provisioning, regulating, supporting and cultural ES and assessed the results to identify knowledge gaps. The effects of hydropower on fisheries catches and on modelled populations were shown in several publications. Overall, few studies focused explicitly on ES from salmon and hydropower; this is surprising given the considerable body of literature on salmon in regulated rivers. Wild salmon as a food source and other provisioning services are less important today than historically. Because predators such as salmon are important for facilitating biodiversity by cycling nutrients and controlling food webs, there is a scope of work for future assessments of these regulating and supporting services. Few papers explicitly addressed cultural ES, despite the salmon's longstanding iconic status; this is a knowledge gap for future ES assessments in relation to hydropower. The influence of ES assessments for policy makers is growing through the Intergovernmental Panel for Biodiversity and Ecosystem Services (IPBES) and the post-2020 biodiversity strategy. Explicitly addressing ES poses an opportunity for river managers to raise awareness of aquatic conservation efforts and well-informed decision-making for sustaining ES

Chemically Defined Sialoside Scaffolds for Investigation of Multivalent Interactions with Sialic Acid Binding Proteins

Four glycodendrons and a glycocluster were synthesized from carbohydrate building blocks to form paucivalent (di- to tetravalent) structures of controlled scaffold architectures. Enzymatic sialylation of the functionalized cluster and dendrons, terminated in lactose residues, generated a library of paucivalent synthetic sialosides displaying sialic acids with different dispositions. These newly constructed bioactive sialic acid-based structures were differentially recognized by sialoadhesin, a mammalian macrophage sialic acid binding protein. The binding of the sialosides to sialoadhesin was evaluated by an enzyme-linked immunosorbant assay to investigate the complementarity of scaffold structure and binding to sialoadhesin. Modulating the interaction between sialoadhesin and its sialic acid ligands has important implications in immunobiology

Comparison of printed glycan array, suspension array and ELISA in the detection of human anti-glycan antibodies

Anti-glycan antibodies represent a vast and yet insufficiently investigated subpopulation of naturally occurring and adaptive antibodies in humans. Recently, a variety of glycan-based microarrays emerged, allowing high-throughput profiling of a large repertoire of antibodies. As there are no direct approaches for comparison and evaluation of multi-glycan assays we compared three glycan-based immunoassays, namely printed glycan array (PGA), fluorescent microsphere-based suspension array (SA) and ELISA for their efficacy and selectivity in profiling anti-glycan antibodies in a cohort of 48 patients with and without ovarian cancer. The ABO blood group glycan antigens were selected as well recognized ligands for sensitivity and specificity assessments. As another ligand we selected P1, a member of the P blood group system recently identified by PGA as a potential ovarian cancer biomarker. All three glyco-immunoassays reflected the known ABO blood groups with high performance. In contrast, anti-P1 antibody binding profiles displayed much lower concordance. Whilst anti-P1 antibody levels between benign controls and ovarian cancer patients were significantly discriminated using PGA (p = 0.004), we got only similar results using SA (p = 0.03) but not for ELISA. Our findings demonstrate that whilst assays were largely positively correlated, each presents unique characteristic features and should be validated by an independent patient cohort rather than another array technique. The variety between methods presumably reflects the differences in glycan presentation and the antigen/antibody ratio, assay conditions and detection technique. This indicates that the glycan-antibody interaction of interest has to guide the assay selection