4,539 research outputs found
PiLa-CS Professional Learning Community - Workshop 2 Resources
During the Summer of 2021 and 2022, the Participating in Literacies and Computer Science (PiLa-CS) Research Practice Partnership convened and supported a community of practice to learn more about how to enable better CS teaching for emergent bilinguals. These are materials from Workshop 2 of the PLC.Sponsored by the National Science Foundation under NSF grant CNS-1738645 and DRL-1837446. Any opinions, findings, and conclusions or recommendations expressed in this material are those of the author(s) and do not necessarily reflect the views of the National Science Foundation
Translanguaging Pedagogy in CS Ed
Episode 3: Translanguaging pedagogy in CS Education
This video looks at how multilingual students already use translanguaging in their computer science classes and discusses how CS educators can further support them with translanguaging pedagogy, a framework that prompts teachers to consider their stance, design, and shifts.
Featuring team members from Participating in Literacies and Computer Science (PiLa-CS), https://www.pila-cs.orgEpisode 3: Translanguaging pedagogy in CS Education
This video looks at how multilingual students already use translanguaging in their computer science classes and discusses how CS educators can further support them with translanguaging pedagogy, a framework that prompts teachers to consider their stance, design, and shifts.
Featuring team members from Participating in Literacies and Computer Science (PiLa-CS), https://www.pila-cs.orgSponsored by the National Science Foundation under NSF grant CNS-1738645 and DRL-1837446. Any opinions, findings, and conclusions or recommendations expressed in this material are those of the author(s) and do not necessarily reflect the views of the National Science Foundation
PiLa-CS Professional Learning Community - Design Journal Template
During the Summer of 2021 and 2022, the Participating in Literacies and Computer Science (PiLa-CS) Research Practice Partnership convened and supported a community of practice to learn more about how to enable better CS teaching for emergent bilinguals. These are materials from from the PLC for a Design Journal to act as a planing template for teachers.Sponsored by the National Science Foundation under NSF grant CNS-1738645 and DRL-1837446. Any opinions, findings, and conclusions or recommendations expressed in this material are those of the author(s) and do not necessarily reflect the views of the National Science Foundation
Modified transmission and fluorescence in aperiodic and biomimetic photonic crystals
Complete photonic bandgaps (PBGs) are more readily achieved in highly-symmetric photonic crystals (Ph Cs). Aperiodic crystals (quasicrystals) with arbitrarily high orientational order are promising candidates to lower the dielectric contrast necessary to open PBGs. This thesis in- vestigates the connection between the structural and optical properties of four PhC lattices by studying the effects on transmission and fluorescence spectra. In order of increasing structural isotropy these lattices are: hexagonal, Archimedean-like, Stampfli, and a biomimetic 'sunflower'. High structural isotropy is associated with weaker diffraction. The sunflower's Fourier spectrum is defined by a dense ring of weak reciprocal lattice vectors. Its local morphology, which is everywhere unique, continuously transforms between localised 4- or 6-fold symmetry. All other crystals are spatially uniform with pure point spectra. Although structurally similar to the Archimedean, the Starnpfli improves isotropy without sacrificing diffraction efficiency. TM gaps of high-contrast (~c = 8.61) rod-type PhCs are shown to be nearly independent of the lattice geometry by FDTD simulations. The primary gaps are sensitive to random rod sizes, which disrupts the coherent coupling between the individual rod resonances. Transmission spectra for TE polarisation or hole-type Ph Cs are more dependent on Bragg reflection due to weak or non-existent Mie resonances. In small samples, the TM gap is typically wider in less isotropic crystals. Much larger samples demonstrate the importance of structural isotropy and long-range interactions in low ~c PhCs. The sunflower's 21% TM gap is, to date, the widest TM PBG reported for ~c = 1. The Stampfli also supports a TE gap in the same range as its 14% TM gap, thus yielding a 4.6% absolute PBG. Further band diagram calculations on an 'approximant' of the sunflower reveal the presence of intrinsic dipolar and monopolar defect states. Microwave characterisation of rod-type samples (~c = 8.61) showed complete TM PBGs (> 60dB) with gap ratios ranging from 37.28% (hexagonal) to 25.85% (sunflower). Low-contrast samples (~c = 1.6) showed complete TM PBGs (> 30dB) with gap ratios rising from 10.37% (hexagonal) to an ambiguous value of either 10.48% or 20.95% for the sunflower due to the unusual spiral structuring of the transmission spectra. The Stampfli also supports a complete TE gap (> 10dB) that coincides with its 14.19% TM gap for a 3.55% absolute gap that, to the author's knowledge, represents the first conclusive demonstration of an absolute PBG for ~c = 1.6. A larger sunflower sample was shown to have an extremely large experimental (simulated) TM gap of 33.33% (23.16%), erroneously broadened by the non-parallel rods. A new approach to enhance the efficiency of up conversion pumping in RE-doped media is pro- posed based on PBG suppression of emission from intermediate levels. Preliminary results indi- cate that visible emission from hexagonal and sunflower PhC slabs in 0.2 wt% Er:GLSO pumped at 808nm is enhanced by up to 1.6x at 550nm, or up to 4.5x at 525nm. Subsequent analysis appears to rule out suppression of IR emission, and suggests modified thermal properties as the cause.EThOS - Electronic Theses Online ServiceGBUnited Kingdo
Arizona Then and Now: Exploring Arizona's Five Cs Through Photography
abstract: Arizona Then and Now: Exploring Arizona's Five Cs Through Photography is a photographic exploration of the evolution of Arizona's five Cs: cotton, copper, citrus, cattle, and climate. This project first looks to the past to see how these five elements shaped the state of Arizona. Photographs were taken across the valley of these elements, or lack thereof, discovering what Arizona has transformed into in the process. Each chapter of the book begins with a brief history of the element focused on in that chapter, followed by an analytical thought about the photographs taken and how the element has evolved. Each chapter shows two historical photographs followed by a series of photographs taken during the project that the author thought depicted what is seen today. The book ends on a final positive note about how the five Cs are not dead, but soon could be completely taken over. This project was a way for a non-art major to explore the state that she grew up while also challenging herself by more than just taking pictures. The photographs displayed in the book depict a sampling of what the author saw that is left of the five Cs
IR-improved DGLAP-CS QCD parton showers in Pythia8
AbstractWe introduce the recently developed IR-improved DGLAP-CS theory into the showers in Pythia8, as this Monte Carlo event generator is in wide use at LHC. We show that, just as it was true in the IR-improved shower Monte Carlo Herwiri, which realizes the IR-improved DGLAP-CS theory in the Herwig6.5 environment, the soft limit in processes such as single heavy gauge boson production is now more physical in the IR-improved DGLAP-CS theory version of Pythia8. This opens the way to one’s getting a comparison between the actual detector simulations for some of the LHC experiments between IR-improved and unimproved showers as Pythia8 is used in detector simulations at LHC whereas Herwig6.5, the environment of the only other IR-improved DGLAP-CS QCD MC in the literature, Herwiri1.031, is not any longer so used. Our achieving the availability of the IR-improved DGLAP-CS Pythia8 then is an important step in the further development of the LHC precision theory program under development by the author and his collaborators
What CS Ed Can Offer Bi/Multilinguals
Episode 4: What can CS offer multilingual learners?
This video discusses how computer science education can benefit multilingual learners. You will meet a middle school ENL (English as a New Language) teacher who successfully incorporated both translanguaging pedagogy and CS education into her classroom, leading to a memorable experience for one of her students.
Featuring team members from Participating in Literacies and Computer Science (PiLa-CS), https://www.pila-cs.orgEpisode 4: What can CS offer multilingual learners?
This video discusses how computer science education can benefit multilingual learners. You will meet a middle school ENL (English as a New Language) teacher who successfully incorporated both translanguaging pedagogy and CS education into her classroom, leading to a memorable experience for one of her students.
Featuring team members from Participating in Literacies and Computer Science (PiLa-CS), https://www.pila-cs.orgSponsored by the National Science Foundation under NSF grant CNS-1738645 and DRL-1837446. Any opinions, findings, and conclusions or recommendations expressed in this material are those of the author(s) and do not necessarily reflect the views of the National Science Foundation
Microporous cesium salts of tetravalent Keggin-type polyoxotungstates Cs-4[SiW12O40], Cs-4[PW11O39(Sn-n-C4H9)], and Cs-4[PW11O39(Sn-OH)] and their adsorption properties
Microporous cesium salts of modified and unmodified tetravalent Keggin-type polyoxometalates, including Cs-4[SiW12O40], Cs-4[PW11O39(Sn-n-C4H9)], and Cs-4[PW11O39(Sn-OH)], were synthesized. The crystalline structures, which had body-centered cubic (bcc) arrangements, the lattice constants, and the pore-size distributions of the three Cs salts were similar, regardless of the presence or absence and types of functional groups introduced. The Cs salts had only micropores and no mesopores. The micropore size distributions were determined from adsorption isotherms of Ar, which showed a sharp peak at 0.59 nm and a shoulder at 0.62 nm. The fractions of the external surface areas to the total surface areas of the Cs salts were less than 6%. It is plausible that the micropores originate from the heteropoly anion defects in the crystallite, which form to avoid mismatches in the Cs+/(heteropoly anion) ratio required for charge balance (=4) and for a bcc structure (=3). The surface of the Cs salt introduced with n-butyl groups was hydrophobic, although the surface density of the n-butyl groups was low. On the other hand, the hydroxyl groups present on the surface of Cs-4[PW11O39(Sn-OH)] had little effect on the adsorption of water, methanol, ethanol, and hexane but a great impact on that for benzene due to the interactions between the -OH groups and the aromatic rings (-OH center dot center dot center dot pi). (C) 2013 Elsevier Inc. All rights reserved
Also By The Same Author: AKTiveAuthor, a Citation Graph Approach to Name Disambiguation
The desire for definitive data and the semantic web drive for inference over heterogeneous data sources requires co-reference resolution to be performed on those data. In particular, name disambiguation is required to allow accurate publication lists, citation counts and impact measures to be determined. This paper describes a graph-based approach to author disambiguation on large-scale citation networks. Using self-citation, co-authorship and document source analyses, AKTiveAuthor clusters papers, achieving precision of 0.997 and recall of 0.818 over a test group of eight surname clusters
INFRARED SPECTRA OF He--CS, Ne--CS, AND Ar--CS
Author Institution: Department of Physics and Astronomy, University of Calgary, Calgary, AB T2N; 1N4, CanadaInfrared spectra of weakly bound Rg--CS (Rg = He, Ne, and Ar) clusters formed in a pulsed supersonic slit-jet expansion have been recorded by exciting the CS fundamental band ( 1535 cm) using a tuneable diode laser. Spectra were well fitted to a conventional semi-rigid asymmetric rotor Hamiltonian. The He--CS spectrum was assigned to an a-type band, while spectra of Ne--CS and Ar--CS were well described by b-type bands, indicating a/b axis switching in transition from the He--CS complex to the Ne--CS and Ar--CS complexes. The results show that the complexes have vibrationally averged T-shaped structures. The determined structural parameters along with the observed vibrational shifts are and {\AA}, and 86.4^irc} and and cm for He--CS, Ne--CS and Ar--CS, respectively. Here, is the distance between the rare gas and the carbon atom, is the the angle between and and the CS axis and is the vibrational shift with respect to the free CS monomer
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