115 research outputs found
Composing with Sounds: Designing an Object-Oriented DAW for the Teaching of Sound-Based Composition
This paper presents and discusses the ComposeWith Sounds (CwS) Digital AudioWorkstation (DAW) and its approach to sequencing musical materials. The system is designed to facilitate the composition within the realm of Sound-based
music wherein sound objects (real or synthesised) are main musical unit of construction over traditional musical notes. Unlike traditional DAW’s or graphical audio programming environments (such as Pure Data, Max MSP etc.) that are based around interactions with sonic materials within tracks or audio graphs, the implementation presented here is based solely around sound objects. To achieve this a bespoke cross-platform audio engine known FSOM (Free Sound Object Mixer) was created in C++. To enhance the learning experience, imagery, dynamic 3D animations and models are used to allow for efficient exploration and learning. All tools within the system are controlled by a flexible permissions system that allows users or workshop leaders to create sessions with specific features based on their requirements. The system is part of a suite of pedagogical tools currently in development for the creation of experimental electronic music
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Efficacy and safety of DFN-11 (sumatriptan injection, 3 mg) in adults with episodic migraine: a multicenter, randomized, double-blind, placebo-controlled study.
BackgroundIn a previous randomized, double-blind, proof-of-concept study in rapidly escalating migraine, a 3 mg dose of subcutaneous sumatriptan (DFN-11) was associated with fewer and shorter triptan sensations than a 6 mg dose. The primary objective of the study was to assess the efficacy and safety of acute treatment with DFN-11 compared with placebo in episodic migraine.MethodsThis was a multicenter, randomized, double-blind, placebo-controlled efficacy and safety study of DFN-11 in the acute treatment of adults with episodic migraine (study RESTOR). The primary endpoint was the proportion of subjects taking DFN-11 who were pain free at 2 h postdose in the double-blind period compared with placebo. Secondary endpoints included earlier postdose timepoints, assessments of pain relief and subjects' freedom from their most bothersome symptom (MBS) (among nausea, photophobia, and phonophobia). Safety and tolerability were assessed.ResultsA total of 392 subjects was screened, 268 (68.4%) were randomized, and 234 (87.3% of those randomized) completed the double-blind treatment period. The proportion of subjects who were pain free at 2 h postdose was significantly greater in the DFN-11 group than in the placebo group (51.0% vs 30.8%, P = 0.0023). Compared with placebo, significantly higher proportions of subjects treated with DFN-11 were also pain free at 30, 60, and 90 min postdose (P ≤ 0.0195). DFN-11 was significantly superior to placebo for pain relief at 60 min, 90 min, and 2 h postdose (P ≤ 0.0179). At 2 h postdose, DFN-11 was also significantly superior to placebo for freedom from photophobia (P = 0.0056) and phonophobia (P = 0.0167). Overall, 33.3% (37/111) who received DFN-11 and 13.4% (16/119) who received placebo experienced at least 1 treatment-emergent adverse event (TEAE), the most common of which were injection site swelling (7.2% vs 0.8%) and pain (7.2% vs 5.9%). Chest discomfort was about half as common in the DFN-11 treatment group as it was in the placebo group (0.9% vs 1.7%).ConclusionsThis study met its primary endpoint, pain freedom at 2 h postdose, with DFN-11 significantly better than placebo, and the incidence of TEAEs and triptan sensations with DFN-11 was low. The 3 mg dose of sumatriptan in DFN-11 appears to be an effective alternative to a 6 mg SC dose of sumatriptan, with good safety and tolerability. ( clinicaltrials.gov : NCT02569853; registered 07 October 2015)
The Luminosity Function of Galaxies in the Las Campanas Redshift Survey
We present the -band luminosity function for a sample of 18678 galaxies,
with average redshift , from the Las Campanas Redshift Survey. The
luminosity function may be fit by a Schechter function with , , and $\phi^* = 0.019 \pm 0.001 \
h^3^{-3}-23.0 \leq M - 5 \log h \leq -17.5b_J \approx 20b_J \approx 20\alpha = -0.7\alpha = -1W_{\lambda} = 5\alphaM^* =
-20.03 \pm 0.03 + 5 \log h\alpha = -0.9 \pm 0.1M^* = -20.22 \pm 0.02 + 5 \log h\alpha = -0.3
\pm 0.1$.
(abridged abstract)Comment: 41 pages, including 13 postscript figures, uses AASTEX v4.0 style
files. Important clarification of R-band definition, plus correction of
luminosity densities and updated references. Main conclusions unchanged.
Final version to appear in Ap
Increasing Multiyear Sea Ice Loss in the Beaufort Sea: A New Export Pathway for the Diminishing Multiyear Ice Cover of the Arctic Ocean
Historically, multiyear sea ice (MYI) covered a majority of the Arctic and circulated through the Beaufort Gyre for years. However, increased ice melt in the Beaufort Sea during the early 2000s was proposed to have severed this circulation. Constructing a regional MYI budget from 1997 to 2021 reveals that MYI import into the Beaufort Sea has increased year-round, yet less MYI now survives through summer and is transported onwards in the Gyre. Annual average MYI loss quadrupled over the study period and increased from ∼7% to ∼33% of annual Fram Strait MYI export, while the peak in 2018 (385,000 km2) was similar in magnitude to Fram Strait MYI export. The ice-albedo feedback coupled with the transition toward younger thinner MYI is responsible for the increased MYI loss. MYI transport through the Beaufort Gyre has not been severed, but it has been reduced so severely to prevent it from being redistributed throughout the Arctic Ocean
Loose Groups of Galaxies in the Las Campanas Redshift Survey
A ``friends-of-friends'' percolation algorithm has been used to extract a
catalogue of dn/n = 80 density enhancements (groups) from the six slices of the
Las Campanas Redshift Survey (LCRS). The full catalogue contains 1495 groups
and includes 35% of the LCRS galaxy sample. A clean sample of 394 groups has
been derived by culling groups from the full sample which either are too close
to a slice edge, have a crossing time greater than a Hubble time, have a
corrected velocity dispersion of zero, or contain a 55-arcsec ``orphan'' (a
galaxy with a mock redshift which was excluded from the original LCRS redshift
catalogue due to its proximity to another galaxy -- i.e., within 55 arcsec).
Median properties derived from the clean sample include: line-of-sight velocity
dispersion sigma_los = 164km/s, crossing time t_cr = 0.10/H_0, harmonic radius
R_h = 0.58/h Mpc, pairwise separation R_p = 0.64/h Mpc, virial mass M_vir =
(1.90x10^13)/h M_sun, total group R-band luminosity L_tot = (1.30x10^11)/h^2
L_sun, and R-band mass-to-light ratio M/L = 171h M_sun/L_sun; the median number
of observed members in a group is 3.Comment: 32 pages of text, 27 figures, 7 tables. Figures 1, 4, 6, 7, and 8 are
in gif format. Tables 1 and 3 are in plain ASCII format (in paper source) and
are also available at http://www-sdss.fnal.gov:8000/~dtucker/LCLG . Accepted
for publication in the September 2000 issue of ApJ
Willingness to Use a Wearable Device Capable of Detecting and Reversing Overdose Among People Who Use Opioids in Philadelphia
Background: The incidence of opioid-related overdose deaths has been rising for 30 years and has been further exacerbated amidst the COVID-19 pandemic. Naloxone can reverse opioid overdose, lower death rates, and enable a transition to medication for opioid use disorder. Though current formulations for community use of naloxone have been shown to be safe and effective public health interventions, they rely on bystander presence. We sought to understand the preferences and minimum necessary conditions for wearing a device capable of sensing and reversing opioid overdose among people who regularly use opioids.
Methods: We conducted a combined cross-sectional survey and semi-structured interview at a respite center, shelter, and syringe exchange drop-in program in Philadelphia, Pennsylvania, USA during the COVID-19 pandemic in August and September 2020. The primary aim was to explore the proportion of participants who would use a wearable device to detect and reverse overdose. Preferences regarding designs and functionalities were collected via a questionnaire with items having Likert-based response options and a semi-structured interview intended to elicit feedback on prototype designs. Independent variables included demographics, opioid use habits, and previous experience with overdose.
Results: A total of 97 adults with an opioid-use history of at least 3 months were interviewed. A majority of survey participants (76%) reported a willingness to use a device capable of detecting an overdose and automatically administering a reversal agent upon initial survey. When reflecting on the prototype, most respondents (75.5%) reported that they would wear the device always or most of the time. Respondents indicated discreetness and comfort as important factors that increased their chance of uptake. Respondents suggested that people experiencing homelessness and those with low tolerance for opioids would be in greatest need of the device.
Conclusions: The majority of people sampled with a history of opioid use in an urban setting were interested in having access to a device capable of detecting and reversing an opioid overdose. Participants emphasized privacy and comfort as the most important factors influencing their willingness to use such a device.
Trial Registration: NCT0453059
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