411 research outputs found
Impacts of Spring-interseeded Cover Crops on Late-emerging Weed Suppression and Ground Cover in Corn (Zea mays L.) Production Systems
Any alternative crop management strategy will only be adopted by growers if yield is not negatively impacted, fits within a current management practice, is easily implementable with minimal cost, or provides other beneficial features such as weed control or suppression. Corn production that incorporates a cover crop as an alternative weed control strategy and ground cover may support a sustainable system that is less dependent on herbicidal weed control. In addition, the cover crop may be used as a fall forage, act as a slow release fertilizer source the following year, and provide ground cover to reduce soil erosion. In South Dakota, cover crop establishment cannot occur after corn harvest, as the growing season is too short, cold, and often dry. Therefore, interseeding cover crops into standing corn has the potential to establish, suppress late-emerging weeds, and provide late season ground cover. The purpose of this research was to examine if a cover crop mixture could be established in a standing corn crop at V5 growth stage, suppress weeds, and provide ground cover after corn harvest without negatively impacting corn yield. Crimson clover (Trifolium incarnatum), winter wheat (Triticum aestivum) and lentil (Lens culinaris) were planted using broadcast or drill methods, as a mixture at a rate of 5.4, 8.9, and 9.8 kg ha-1, respectively, into V5 corn in field studies from 2010 – 2012. In 2010 - 12, the mix was planted at summit (SMT) and toeslope (TSP) locations in corn fields near Andover, SD. In 2011 – 12 the mix also was planted at SMT and TSP locations near Trail City, and in a flat field near Aurora, SD. Corn and cover crop and weed biomass were collected each fall. Cover crops emerged about 14 d (days) after planting. Winter wheat and crimson clover were the only species that survived until corn harvest. The drill interseeding method had 76% more cover crop biomass than the broadcast method. Cover crops drill seeded reduced grass weed biomass by 38%. Regardless of seeding method, cover crops had no impact on corn grain yield. These results indicate that cover crops could be established in standing corn with no adverse yield impact. These crops provided ground cover during and after the corn growing season and suppressed late-emerging grass weed growth. Therefore, interseeding this cover crop mix into standing corn may be a feasible alternative management strategy for getting a cover crop established, as SD weather is too cold, dry, and season too short for after harvest planting
vital_sqi: A Python package for physiological signal quality control
Electrocardiogram (ECG) and photoplethysmogram (PPG) are commonly used to determine the vital signs of heart rate, respiratory rate, and oxygen saturation in patient monitoring. In addition to simple observation of those summarized indexes, waveform signals can be analyzed to provide deeper insights into disease pathophysiology and support clinical decisions. Such data, generated from continuous patient monitoring from both conventional bedside and low-cost wearable monitors, are increasingly accessible. However, the recorded waveforms suffer from considerable noise and artifacts and, hence, are not necessarily used prior to certain quality control (QC) measures, especially by those with limited programming experience. Various signal quality indices (SQIs) have been proposed to indicate signal quality. To facilitate and harmonize a wider usage of SQIs in practice, we present a Python package, named vital_sqi, which provides a unified interface to the state-of-the-art SQIs for ECG and PPG signals. The vital_sqi package provides with seven different peak detectors and access to more than 70 SQIs by using different settings. The vital_sqi package is designed with pipelines and graphical user interfaces to enable users of various programming fluency to use the package. Multiple SQI extraction pipelines can take the PPG and ECG waveforms and generate a bespoke SQI table. As these SQI scores represent the signal features, they can be input in any quality classifier. The package provides functions to build simple rule-based decision systems for signal segment quality classification using user-defined SQI thresholds. An experiment with a carefully annotated PPG dataset suggests thresholds for relevant PPG SQIs
Self-attraction effect and correction on three absolute gravimeters
The perturbations of the gravitational field due to the mass distribution of
an absolute gravimeter have been studied. The so called Self Attraction Effect
(SAE) is crucial for the measurement accuracy, especially for the International
Comparisons, and for the uncertainty budget evaluation. Three instruments have
been analysed: MPG-2, FG5-238 and IMPG-02. The SAE has been calculated using a
numerical method based on FEM simulation. The observed effect has been treated
as an additional vertical gravity gradient. The correction (SAC) to be applied
to the computed g value has been associated with the specific height level,
where the measurement result is typically reported. The magnitude of the
obtained corrections is of order 1E-8 m/s2.Comment: 14 pages, 8 figures, submitted to Metrologi
Numerical modeling of thermal dust polarization from aligned grains in the envelope of evolved stars with updated POLARIS
Magnetic fields are thought to influence the formation and evolution of
evolved star envelopes. Thermal dust polarization from magnetically aligned
grains is potentially a powerful tool for probing magnetic fields and dust
properties in these circumstellar environments. In this paper, we present
numerical modeling of thermal dust polarization from the envelope of IK Tau
using the magnetically enhanced radiative torque (MRAT) alignment theory
implemented in our updated POLARIS code. Due to the strong stellar radiation
field, the minimum size required for RAT alignment of silicate grains is . Additionally, ordinary paramagnetic grains can achieve
perfect alignment by MRAT in the inner regions of due to
stronger magnetic fields of mG - 1G, producing thermal dust
polarization degree of . The polarization degree can be enhanced
to for grains with embedded iron inclusions. We also find that
the magnetic field geometry affects the alignment size and the resulting
polarization degree due to the projection effect in the plane-of-sky. We also
study the spectrum of polarized thermal dust emission and find the increased
polarization degree toward due to the alignment of
small grains by MRAT. Furthermore, we investigate the impact of rotational
disruption by RATs (RAT-D) and find the RAT-D effect cause a decrease in the
dust polarization fraction. Finally, we compare our numerical results with
available polarization data observed by SOFIA/HAWC+ for constraining dust
properties, suggesting grains are unlikely to have embedded iron clusters and
might have slightly elongated shapes. Our modeling results suggest further
observational studies at far-infrared/sub-millimeter wavelengths to understand
the properties of magnetic fields and dust in AGB envelopes.Comment: 27 pages, 23 figures, 1 table, to be submitte
Silicon resonant microcantilevers for absolute pressure measurement
This work is focused on the developing of silicon resonant microcantilevers for the measurement of the absolute pressure. The microcantilevers have been fabricated with a two-mask bulk micromachining process. The variation in resonance response of microcantilevers was investigated as a function of pressure 10−1-105 Pa, both in terms of resonance frequency and quality factor. A theoretical description of the resonating microstructure is given according to different molecular and viscous regimes. Also a brief discussion on the different quality factors contributions is presented. Theoretical and experimental data show a very satisfying agreement. The microstructure behavior demonstrates a certain sensitivity over a six decade range and the potential evolution of an absolute pressure sensor working in the same rang
Sample size requirements for separating out the effects of combination treatments: Randomised controlled trials of combination therapy vs. standard treatment compared to factorial designs for patients with tuberculous meningitis
<p>Abstract</p> <p>Background</p> <p>In certain diseases clinical experts may judge that the intervention with the best prospects is the addition of two treatments to the standard of care. This can either be tested with a simple randomized trial of combination versus standard treatment or with a 2 × 2 factorial design.</p> <p>Methods</p> <p>We compared the two approaches using the design of a new trial in tuberculous meningitis as an example. In that trial the combination of 2 drugs added to standard treatment is assumed to reduce the hazard of death by 30% and the sample size of the combination trial to achieve 80% power is 750 patients. We calculated the power of corresponding factorial designs with one- to sixteen-fold the sample size of the combination trial depending on the contribution of each individual drug to the combination treatment effect and the strength of an interaction between the two.</p> <p>Results</p> <p>In the absence of an interaction, an eight-fold increase in sample size for the factorial design as compared to the combination trial is required to get 80% power to jointly detect effects of both drugs if the contribution of the less potent treatment to the total effect is at least 35%. An eight-fold sample size increase also provides a power of 76% to detect a qualitative interaction at the one-sided 10% significance level if the individual effects of both drugs are equal. Factorial designs with a lower sample size have a high chance to be underpowered, to show significance of only one drug even if both are equally effective, and to miss important interactions.</p> <p>Conclusions</p> <p>Pragmatic combination trials of multiple interventions versus standard therapy are valuable in diseases with a limited patient pool if all interventions test the same treatment concept, it is considered likely that either both or none of the individual interventions are effective, and only moderate drug interactions are suspected. An adequately powered 2 × 2 factorial design to detect effects of individual drugs would require at least 8-fold the sample size of the combination trial.</p> <p>Trial registration</p> <p>Current Controlled Trials <a href="http://www.controlled-trials.com/ISRCTN61649292">ISRCTN61649292</a></p
MyCTC chip: microfluidic-based drug screen with patient-derived tumour cells from liquid biopsies
Cancer patients with advanced disease are characterized by intrinsic challenges in predicting drug response patterns, often leading to ineffective treatment. Current clinical practice for treatment decision-making is commonly based on primary or secondary tumour biopsies, yet when disease progression accelerates, tissue biopsies are not performed on a regular basis. It is in this context that liquid biopsies may offer a unique window to uncover key vulnerabilities, providing valuable information about previously underappreciated treatment opportunities. Here, we present MyCTC chip, a novel microfluidic device enabling the isolation, culture and drug susceptibility testing of cancer cells derived from liquid biopsies. Cancer cell capture is achieved through a label-free, antigen-agnostic enrichment method, and it is followed by cultivation in dedicated conditions, allowing on-chip expansion of captured cells. Upon growth, cancer cells are then transferred to drug screen chambers located within the same device, where multiple compounds can be tested simultaneously. We demonstrate MyCTC chip performance by means of spike-in experiments with patient-derived breast circulating tumour cells, enabling >95% capture rates, as well as prospective processing of blood from breast cancer patients and ascites fluid from patients with ovarian, tubal and endometrial cancer, where sensitivity to specific chemotherapeutic agents was identified. Together, we provide evidence that MyCTC chip may be used to identify personalized drug response patterns in patients with advanced metastatic disease and with limited treatment opportunities
Studying Magnetic Fields and Dust in M17 Using Polarized Thermal Dust Emission Observed by SOFIA/HAWC
We report on the highest spatial resolution measurement to date of magnetic fields (B-fields) in M17 using thermal dust polarization measurements taken by SOFIA/HAWC+ centered at a wavelength of 154 μm. Using the Davis–Chandrasekhar–Fermi method, in which the polarization angle dispersion calculated using the structure function technique is the quantity directly observed by SOFIA/HAWC+, we found the presence of strong B-fields of 980 ± 230 and 1665 ± 885 μG in the lower-density M17-N and higher-density M17-S regions, respectively. The B-field morphology in M17-N possibly mimics the fields in gravitationally collapsing molecular cores, while in M17-S the fields run perpendicular to the density structure. M17-S also displays a pillar feature and an asymmetric large-scale hourglass-shaped field. We use the mean B-field strengths to determine Alfvénic Mach numbers for both regions, finding that B-fields dominate over turbulence. We calculate the mass-to-flux ratio, λ, finding λ = 0.07 for M17-N and 0.28 for M17-S. These subcritical λ values are consistent with the lack of massive stars formed in M17. To study dust physics, we analyze the relationship between dust polarization fraction, p, emission intensity, I, gas column density, N(H2), polarization angle dispersion function, S, and dust temperature, T
d. p decreases with intensity as I
−α
with α = 0.51. p tends to first increase with T
d, but then decreases at higher T
d. The latter feature, seen in M17-N at high T
d when N(H2) and S decrease, is evidence of the radiative torque disruption effect
Point-of-care C-reactive protein testing to reduce inappropriate use of antibiotics for non-severe acute respiratory infections in Vietnamese primary health care: a randomised controlled trial
Background Inappropriate antibiotic use for acute respiratory tract infections is common in primary health care, but
distinguishing serious from self-limiting infections is diffi cult, particularly in low-resource settings. We assessed
whether C-reactive protein point-of-care testing can safely reduce antibiotic use in patients with non-severe acute
respiratory tract infections in Vietnam.
Method We did a multicentre open-label randomised controlled trial in ten primary health-care centres in northern
Vietnam. Patients aged 1–65 years with at least one focal and one systemic symptom of acute respiratory tract infection
were assigned 1:1 to receive either C-reactive protein point-of-care testing or routine care, following which antibiotic
prescribing decisions were made. Patients with severe acute respiratory tract infection were excluded. Enrolled
patients were reassessed on day 3, 4, or 5, and on day 14 a structured telephone interview was done blind to the
intervention. Randomised assignments were concealed from prescribers and patients but not masked as the test
result was used to assist treatment decisions. The primary outcome was antibiotic use within 14 days of follow-up. All
analyses were prespecifi ed in the protocol and the statistical analysis plan. All analyses were done on the intention-totreat
population and the analysis of the primary endpoint was repeated in the per-protocol population. This trial is
registered under number NCT01918579.
Findings Between March 17, 2014, and July 3, 2015, 2037 patients (1028 children and 1009 adults) were enrolled and
randomised. One adult patient withdrew immediately after randomisation. 1017 patients were assigned to receive
C-reactive protein point-of-care testing, and 1019 patients were assigned to receive routine care. 115 patients in the
C-reactive protein point-of-care group and 72 patients in the routine care group were excluded in the intention-to-treat
analysis due to missing primary endpoint. The number of patients who used antibiotics within 14 days was 581 (64%)
of 902 patients in the C-reactive protein group versus 738 (78%) of 947 patients in the control group (odds ratio
[OR] 0·49, 95% CI 0·40–0·61; p<0·0001). Highly signifi cant diff erences were seen in both children and adults, with
substantial heterogeneity of the intervention eff ect across the 10 sites (I²=84%, 95% CI 66–96). 140 patients in the
C-reactive protein group and 137 patients in the routine care group missed the urine test on day 3, 4, or 5. Antibiotic
activity in urine on day 3, 4, or 5 was found in 267 (30%) of 877 patients in the C-reactive protein group versus
314 (36%) of 882 patients in the routine treatment group (OR 0·78, 95% CI 0·63–0·95; p=0·015). Time to resolution
of symptoms was similar in both groups. Adverse events were rare, with no deaths and a total of 14 hospital admissions
(six in the C-reactive protein group and eight in the control group).
Interpretation C-reactive protein point-of-care testing reduced antibiotic use for non-severe acute respiratory tract
infection without compromising patients’ recovery in primary health care in Vietnam. Health-care providers might
have become familiar with the clinical picture of low C-reactive protein, leading to reduction in antibiotic prescribing
in both groups, but this would have led to a reduction in observed eff ect, rather than overestimation. Qualitative
analysis is needed to address diff erences in context in order to implement this strategy to improve rational antibiotic
use for patients with acute respiratory infection in low-income and middle-income countries
Rapid Enzyme-linked Immunosorbent Assay for Detection of the Algal Toxin Domoic Acid
Domoic acid (DA) is a potent toxin produced by bloom-forming phytoplankton in the genus Pseudo-nitzschia, which is responsible for causing amnesic shellfish poisoning (ASP) in humans. ASP symptoms include vomiting, diarrhea, and in more severe cases confusion, loss of memory, disorientation, and even coma or death. This paper describes the development and validation of a rapid, sensitive, enzyme linked immunosorbent assay test kit for detecting DA using a monoclonal antibody. The assay gives equivalent results to those obtained using standard high performance liquid chromatography, fluorenylmethoxycarbonyl high performance liquid chromatography, or liquid chromatography—mass spectrometry methods. It has a linear range from 0.1–3 ppb and was used successfully to measure DA in razor clams, mussels, scallops, and phytoplankton. The assay requires approximately 1.5 h to complete and has a standard 96-well format where each strip of eight wells is removable and can be stored at 4°C until needed. The first two wells of each strip serve as an internal control eliminating the need to run a standard curve. This allows as few as 3 or as many as 36 duplicate samples to be run at a time enabling real-time sample processing and limiting degradation of DA, which can occur during storage. There was minimal cross-reactivity in this assay with glutamine, glutamic acid, kainic acid, epi- or iso-DA. This accurate, rapid, cost-effective, assay offers environmental managers and public health officials an effective tool for monitoring DA concentrations in environment samples
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