76 results on '"SHERIDAN, J"'
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2. Coronal Heating as Determined by the Solar Flare Frequency Distribution Obtained by Aggregating Case Studies
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James Paul Mason, Alexandra Werth, Colin G. West, Allison Youngblood, Donald L. Woodraska, Courtney L. Peck, Arvind J. Aradhya, Yijian Cai, David Chaparro, James W. Erikson, Koushik Ganesan, T. R. Geerdts, Thi D Hoang, Thomas M. Horning, Yan Jin, Haixin Liu, Noah Lordi, Zheng Luo, Thanmay S. Menon, Josephine C. Meyer, Emma E Nelson, Kristin A. Oliver, Jorge L Ramirez Ortiz, Andrew Osborne, Alyx Patterson, Nick Pellatz, John Pitten, Nanako Shitara, Daniel Steckhahn, Aseem Visal, Hongda Wang, Chaoran Wang, Evan Wickenden, John Wilson, Mengyu Wu, Nikolay Yegovtsev, Ingrid H Zimmermann, James Holland Aaron, Jumana T. Abdullah, Jonathan M. Abrams, Riley Abrashoff, Andres B. Acevedo, Iker Acha, Daniela M. Meza Acosta, Megan M. Adam, Dante Q. Adams, Kalvyn N Adams, Elena R Adams, Zainab A. Akbar, Ushmi H. Akruwala, Adel Al-Ghazwi, Batool H. Alabbas, Areej A. Alawadhi, Yazeed A. Alharbi, Mohammed S. Alahmed, Mohammed A. Albakr, Yusef J. Albalushi, Jonathan Albaum, Ahmed Aldhamen, Nolan Ales, Mohammad Alesmail, Abdulelah Alhabeeb, Dania Alhamli, Isehaq Alhuseini, Suhail Alkaabi, Tameem Alkhezzi, Mohamed Alkubaisi, Nasser Allanqawi, Martin Allsbrook, Yousef A. Almohsen, Justin Thomas Almquist, Teeb Alnaji, Yousef A Alnasrallah, Nicholas Alonzi, Meshal Alosaimi, Emeen Alqabani, Mohammad Alrubaie, Reema A. Alsinan, Ava L. Altenbern, Abdullah Altokhais, Saleh A. Alyami, Federico Ameijenda, Hamzi Amer, Meggan Amos, Hunter J. Anderson, Carter Andrew, Jesse C Andringa, Abigail Angwin, Gabreece Van Anne, Andrew Aramians, Camila Villamil Arango, Jack. W. Archibald, Brian A. Arias-Robles, Maryam Aryan, Kevin Ash, Justin Astalos, N. S. Atchley-Rivers, Dakota N. Augenstein, Bryce W. Austin, Abhinav Avula, Matthew C. Aycock, Abdulrahman A. Baflah, Sahana Balaji, Brian Balajonda, Leo M Balcer, James O. Baldwin, David J Banda, Titus Bard, Abby Barmore, Grant M. Barnes, Logan D. W. Barnhart, Kevin M. Barone, Jessica L. Bartman, Claire Bassel, Catalina S Bastias, Batchimeg Bat-Ulzii, Jasleen Batra, Lexi Battist, Joshua Bay, Simone Beach, Sara Beard, Quinn I Beato, Ryan Beattie, Thomas Beatty, Tristan De La Beaujardiere, Jacob N. Beauprez, M. G. Beck, Lily Beck, Simone E. Becker, Braden Behr, Timothy A. Behrer, Joshua Beijer, Brennan J. Belei, Annelene L. Belknap, Aislyn Bell, Caden Bence, Evan Benke, Naomi Berhanu, Zachary D. Berriman-Rozen, Chrisanna Bertuccio, Owen A. Berv, Blaine B. Biediger, Samuel J Biehle, Brennen Billig, Jacob Billingsley, Jayce A. Billman, Connor J. Biron, Gabrielle E. Bisacca, Cassidy A. Blake, Guillermo Blandon, Olivia Blevins, Ethan Blouin, Michal Bodzianowski, Taylor A. Boeyink, Matthew Bondar, Lauren Bone, Alberto Espinosa De Los Monteros Bonilla, William T Borelli, Luke R. Borgerding, Troy Bowen, Christine Boyer, Aidan Boyer, Aidan P. Boyle, Tom Boyne, Donovan Branch, Ariana E. Brecl, David J. Brennan, Alexander J Brimhall, Jennifer L. Brockman, Sarah Brookins, Gabriel T. Brown, Cameron L. Brown, Ryan Brown, Jordi Brownlow, Grant Brumage-Heller, Preston J. Brumley, Samuel Bryan, A. Brzostowicz, Maryam Buhamad, Gigi Bullard-Connor, J. R. Ramirez Bunsow, Annemarie C. Burns, John J. Burritt, Nicholas David Burton, Taylor Burton, Celeste Busch, Dylan R. Butler, B. W. Buxton, Malena C. Toups, Carter C. Cabbage, Breonna Cage, Jackson R. Cahn, Andrew J Campbell, Braden P. Canales, Alejandro R. Cancio, Luke Carey, Emma L. Carillion, Michael Andrew Carpender, Emily Carpenter, Shivank Chadda, Paige Chambers, Jasey Chanders, Olivia M. Chandler, Ethan C. Chang, Mitchell G. Chapman, Logan T. Chapman, S. Chavali, Luis Chavez, Kevin Chen, Lily Chen, Sam Chen, Judy Chen, Jenisha Chhetri, Bradyn Chiles, Kayla M. Chizmar, Katherine E Christiansen, Nicholas A. Cisne, Alexis Cisneros, David B. Clark, Evelyn Clarke, Peter C Clarkson, Alexis R. Clausi, Brooke Cochran, Ryan W. Coe, Aislinn Coleman-Plante, Jake R. Colleran, Zachary Colleran, Curran Collier, Nathaniel A. Collins, Sarah Collins, Jack C. Collins, Michael Colozzi, Aurora Colter, Rebecca A. Cone, Thomas C. Conroy, Reese Conti, Charles J. Contizano, Destiny J. Cool, Nicholas M. Cooper, Jessica S Corbitt, Jonas Courtney, Olivia Courtney, Corben L. Cox, Wilmsen B. Craig, Joshua B. Creany, Anastasia Crews, K. A. Crocker, A. J. Croteau, Christian J. Crow, Zoe Cruse, Avril Cruz, Tyler L. Curnow, Hayden Current, Riley T. Curry, Libby Cutler, Aidan St. Cyr, Frederick M. Dabberdt, Johnston Daboub, Olivia Damgaard, Swagatam Das, Emma A. B. Davis, Elyse Debarros, Sean Deel, Megan E. Delasantos, Tianyue Deng, Zachary Derwin, Om Desai, Kai Dewey, John S. Dias, Kenzie A. Dice, R. Dick, Cyrus A. Dicken, Henry Dietrick, Alexis M. Dinser, Alyssa M. Dixon, Thomas J. Dixon, Helen C. Do, Chris H Doan, Connor Doane, Joshua Dodrill, Timothy Doermer, Lizbeth Montoya Dominguez, J. Dominguez, Emerson N. Domke, Caroline R. Doran, Jackson A. Dorr, Philip Dorricott, Danielle C. Dresdner, Michael Driscoll, Kailer H. Driscoll, Sheridan J. Duncan, Christian Dunlap, Gabrielle M. Dunn, Tien Q. Duong, Tomi Oshima Dupeyron, Peter Dvorak, Andrew East, Andrew N. East, Bree Edwards, Lauren Ehrlich, Sara I. Elbashir, Rasce Engelhardt, Jacob Engelstad, Colin England, Andrew Enrich, Abbey Erickson, Benjamin Erickson, Nathan Evans, Calvin A Ewing, Elizabeth A. Eyeson, Ian Faber, Avery M. Fails, John T Fauntleroy, Kevin Fell, Zitian Feng, Logan D. Fenwick, Nikita Feoktistov, Ryann Fife, John Alfred D. Figueirinhas, Jean-Paul Fisch, Emmalee Fischer, Jules Fischer-White, Aidan F. Fitton, Alexander Fix, Lydia Flackett, Fernando Flores, Aidan Floyd, Leonardo Del Foco, Adeduni Folarin, Aidan E. Forbes, Elise Fortino, Benjamin L. Fougere, Alexandra A. Fowler, Margaret Fox, James M. French, Katherine V. French, Florian G. Frick, Calvin R. Fuchs, Bethany E. S. Fuhrman, Sebastian Furney, Moutamen Gabir, Gabriela Galarraga, Skylar Gale, Keala C. Gapin, A. J. Garscadden, Rachel Gasser, Lily Gayou, Emily E. Gearhart, Jane Geisman, Julianne R. Geneser, Sl Genne, Julia G Gentile, Eleanor Gentry, Jacob D. George, Nathaniel James Georgiades, Phillip Gerhardstein, Clint Gersabeck, Bandar Abu Ghaith, Dorsa Ghiassi, B. C. Giebner, Dalton Gilmartin, Connor B. Gilpatrick, Michael Gjini, Olivia Golden, Nathan T. Golding, C. A. Goldsberry, Angel R. Gomez, Angel A. Gomez, Sean Gopalakrishnan, Mariam Gopalani, Nicholas Gotlib, Alaina S. Graham, Michael J Gray, Alannah H. Gregory, Joshua A. Gregory, Kristyn Grell, Justus Griego, Nicholas F. Griffin, Kyle J. Griffin, Matt Guerrero, Nicole Gunderson, Mutian Guo, E. R. Gustavsson, Grace K. Hach, L. N. Haile, Jessica Haines, Jack J. Mc Hale, Ryder Buchanan Hales, Mark S. Haley, Jacqueline L. Hall, Sean R. Hamilton, Soonhee Han, Tyler Hand, Luke C. Hanley, Connor M Hansen, Joshua A. Hansen, Jonathan Hansson, Tony Yunfei Hao, Nicholas Haratsaris, Isabelle Hardie, Dillon F. Hardwick, Cameron T. Hares, Logan Swous Harris, Coyle M. Harris, Omer Hart, Kyle Hashiro, Elsie Hattendorf, Calder Haubrich, Elijah Hawat, Griffin A. Hayrynen, Danielle A. Heintz, Tim Hellweg, Angel Hernandez, Emanuel Herrera, Robert N. Herrington, Tim Herwig, Troy M. Hesse, Quinn Hiatt, Lea Pearl Hibbard, Imari R. Hicks, Andrew J. Hicks, Nigel Highhouse, Annalise K. Hildebrand, Paula Hill, Hallie Hill, Evan Hintsa, Anna E. Hirschmann, Travis Hitt, Ella Ho, Isabelle J. Hoff, Alex Hoffman, Blake A. Hogen, Linda Horne, Timothy J Houck, Noah H. Howell, E. M. Hrudka, J. Hu, Jianyang Huang, Chenqi Huang, Shancheng Huang, Zachary A. Hudson, Nathan C. Hudson, Tyler J. Huebsch, Owen Hull, Samuel C Hunter, Troy Husted, Abigail P. Hutabarat, Leslie Huynh, Antonio E. Samour Ii, Yolande Idoine, Julia A. Ingram, Taro Iovan, Samuel A. Isert, Antonio Salcido-Alcontar, Thomas Jacobsen, Alan A Jaimes, Connor Jameson, J. R. Jarriel, Sam Jarvis, Josh Jenkins, Alexander V. Jensen, Jacob Jeong, Luke A. Jeseritz, Trevor Jesse, Soo Yeun Ji, Yufan Jiang, Owen Johnson, Matthew Johnson, Sawyer Johnson, Julia Johnston, Braedon Y. Johnston, Olivia M. Jones, M. R. Jones, Tara Jourabchi, Tony A. House, Parker Juels, Sabrina J. H. T. Kainz, Emily Kaiser, Nicolas Ian Kallemeyn, Madison H. Kalmus, Etash Kalra, Margaret Kamenetskiy, Jeerakit Kanokthippayakun, Shaun D. Kapla, Brennan J. Karsh, Caden J. Keating, Morgan A. Kelley, Michael P. Kelley, Nicholas Kelly, James Kelly, Teagan Kelly, Christopher M Kelly, Kellen Kennedy, Cayla J. Kennedy, Forrest Kennedy, Abigail Kennedy, Liana Kerr-Layton, Marilyn Ketterer, Ibraheem A. Khan, Usman Khan, Sapriya Khanal, Jack L. Kiechlin, Dominic Killian, Kevin Kim, Brian T. Kim, Matthew M. Kim, Jake Kim, Aspen Kimlicko, Isabel M Kipp, Hunter B. Kirkpatrick, Natalie Kissner, Emily R. Kite, Olivia R. Kleinhaus, Philip Whiting Knott, Will Koch, Greta Koenig, Emily Koke, Thomas Kokes, Yash S. Kothamdi, Zack Krajnak, Zoe M. Kresek, Dylan Kriegman, Jake E. Kritzberg, Davis J. Krueger, Bartlomiej Kubiak, Kirsten Kuehl, Chrisanne Kuester, Nicolas A. Kuiper, Aman Priyadarshi Kumar, Connor Kuybus, Daniel Kwiatkowski, Quintin Y. Lafemina, Kevin Lacjak, Kyle Lahmers, Antonia Lam, Kalin Landrey, Maxwell B. Lantz, Zachary Larter, Benjamin P. Lau, Megan Lauzon, Rian Lawlor, Tyler Learned, E. C. Lee, Junwon Lee, Adrianna J. Lee, Justin Lee, Alexis Ying-Shan Lee, Christian J Lee, Nathaniel F. Lee, Linzhi Leiker, Dylan Lengerich, Cecilia Leoni, Adrienne R. Lezak, David Y. Li, Isaac Li, Ryan Z. Liao, Bridget Linders, Morgan I Linger, Katherine B. Linnane, Sam Lippincott, Barrett Lister, Shelby D Litton, Nianzi Liu, Steven Y. Liu, Timothy W. Logan, Nathan Londres, Mia C. Lonergan, Emily Lookhoff, N. E. Loomis, Christian Lopez, Justin Loring, Jeffrey Lucca, Dax Lukianow, Nathan M. Cheang, William Macdonald, Claire A. Madonna, Kasey O. Madsen, Tiffany E. Maksimuk, Macguire Mallory, Ryan A. Malone, Blake Maly, Xander R. Manzanares, Aimee S. Maravi, Serafima M. Marcus, Nasreen Marikar, Josie A. Marquez, Mathew J. Marquez, Lauren Marsh, Toni Marsh, Logan S. Martin, Alexa M. Martinez, Jose R. Martinez, Hazelia K. Martinez, Cara Martyr, Mirna Masri, Giorgio Matessi, Adam Izz Khan Mohd Reduan Mathavan, Randi M. Mathieson, Kabir P. Mathur, Graham Mauer, Victoria A. Mayer, Liam Mazzotta, Glen S. Mccammon, Rowan Mcconvey, Tyler Mccormick, Andrew Mccoy, Kelleen Mcentee, Meaghan V. Mcgarvey, Riley M. Mcgill, James K. Mcintyre, Finbar K. Mckemey, Zane Mcmorris, Jesse J. Mcmullan, Ella Mcquaid, Caden Mcvey, Kyle Mccurry, Mateo M. Medellin, Melissa Medialdea, Amar Mehidic, Stella Meillon, Jonah B. Meiselman-Ashen, Sarah Mellett, Dominic Menassa, Citlali Mendez, Patricia Mendoza-Anselmi, Riley Menke, Sarah Mesgina, William J. Mewhirter, Ethan Meyer, Aya M. Miften, Ethan J. Miles, Andrew Miller, Joshua B. Miller, Emily B. Millican, Sarah J. Millican, Dylan P. Mills, Josh Minimo, Jay H. Misener, Alexander J. Mitchell, Alexander Z. Mizzi, Luis Molina-Saenz, Tyler S Moll, Hayden Moll, Maximus Montano, Michael Montoya, Eli Monyek, Jacqueline Rodriguez Mora, Gavin Morales, Genaro Morales, Annalise M. Morelock, Cora Morency, Angel J. Moreno, Remy Morgan, Alexander P. Moss, Brandon A. Muckenthaler, Alexander Mueller, Owen T. Mulcahy, Aria T. Mundy, Alexis A. Muniz, Maxwell J. Murphy, Madalyn C. Murphy, Ryan C. Murphy, Tyler Murrel, Andrew J. Musgrave, Michael S. Myer, Kshmya Nandu, Elena R. Napoletano, Abdulaziz Naqi, Anoothi Narayan, Liebe Nasser, Brenna K Neeland, Molly Nehring, Maya Li Nelson, Lena P. Nguyen, Lena Nguyen, Leonardo Nguyen, Valerie A. Nguyen, Khoa D Nguyen, Kelso Norden, Cooper Norris, Dario Nunes-Valdes, Rosemary O. Nussbaum, Cian O’Sullivan, Ian O’Neill, S. H. Oakes, Anand Odbayar, Caleb Ogle, Sean Oishi-Holder, Nicholas Olguin, Nathaniel P. Olson, Jason Ong, Elena N. Opp, Dan Orbidan, Ryan Oros, Althea E. Ort, Matthew Osborn, Austin Osogwin, Grant Otto, Jessica Oudakker, Igor Overchuk, Hannah M. Padgette, Jacqueline Padilla, Mallory Palizzi, Madeleine L. Palmgren, Adler Palos, Luke J. Pan, Nathan L. Parker, Sasha R. Parker, Evan J. Parkinson, Anish Parulekar, Paige J. Pastor, Kajal Patel, Akhil Patel, Neil S. Patel, Samuel Patti, Catherine Patton, Genevieve K. Payne, Matthew P. Payne, Harrison M. Pearl, Charles B. Beck Von Peccoz, Alexander J. Pedersen, Lily M. Pelster, Munisettha E. Peou, J. S. Perez, Freddy Perez, Anneliese Pesce, Audrey J. Petersen, B. Peterson, Romeo S. L. Petric, Joshua Pettine, Ethan J. Phalen, Alexander V. Pham, Denise M. Phan, Callie C Pherigo, Lance Phillips, Justin Phillips, Krista Phommatha, Alex Pietras, Tawanchai P. Pine, Sedique Pitsuean-Meier, Andrew M. Pixley, Will Plantz, William C. Plummer, Kaitlyn E. Plutt, Audrey E. Plzak, Kyle Pohle, Hyden Polikoff, Matthew Pollard, Madelyn Polly, Trevor J. Porter, David Price, Nicholas K. Price, Gale H. Prinster, Henry Austin Propper, Josh Quarderer, Megan S. Quinn, Oliver Quinonez, Devon Quispe, Cameron Ragsdale, Anna L. Rahn, M. Rakhmonova, Anoush K Ralapanawe, Nidhi Ramachandra, Nathaniel Ramirez, Ariana C. Ramirez, Sacha Ramirez, Parker Randolph, Anurag Ranjan, Frederick C Rankin, Sarah Grace Rapaport, Nicholas O Ratajczyk, Mia G. V. Ray, Brian D. Reagan, John C. Recchia, Brooklyn J. Reddy, Joseph Reed, Charlie Reed, Justin Reeves, Eileen N. Reh, Ferin J. Von Reich, Andrea B. Reyna, Alexander Reynolds, Hope Reynolds, Matthew Rippel, Guillermo A. Rivas, Anna Linnea Rives, Amanda M. Robert, Samuel M. Robertson, Maeve Rodgers, Stewart Rojec, Andres C. Romero, Ryan Rosasco, Beth Rossman, Michael Rotter, Tyndall Rounsefell, Charlotte Rouse, Allie C. Routledge, Marc G. Roy, Zoe A. Roy, Ryan Ruger, Kendall Ruggles-Delgado, Ian C. Rule, Madigan Rumley, Brenton M. Runyon, Collin Ruprecht, Bowman Russell, Sloan Russell, Diana Ryder, David Saeb, J. Salazar, Violeta Salazar, Maxwell Saldi, Jose A. Salgado, Adam D. Salindeho, Ethan S. Sanchez, Gustavo Sanchez-Sanchez, Darian Sarfaraz, Sucheta Sarkar, Ginn A. Sato, Carl Savage, Marcus T. Schaller, Benjamin T. Scheck, Jared A. W. Schlenker, Matthew J Schofer, Stephanie H. Schubert, Courtney Schultze, Grace K Schumacher, Kasper Seglem, Lauren Serio, Octave Seux, Hannan Shahba, Callie D. Shannahan, Shajesh Sharma, Nathan Shaver, Timothy Shaw, Arlee K. Shelby, Emma Shelby, Grace Shelchuk, Tucker Sheldrake, Daniel P. Sherry, Kyle Z. Shi, Amanda M. Shields, Kyungeun Shin, Michael C. Shockley, Dominick Shoha, Jadon Shortman, Mitchell Shuttleworth, Lisa Sibrell, Molly G. Sickler, Nathan Siles, H. K. Silvester, Conor Simmons, Dylan M. Simone, Anna Simone, Savi Singh, Maya A. Singh, Madeline Sinkovic, Leo Sipowicz, Chris Sjoroos, Ryan Slocum, Colin Slyne, Korben Smart, Alexandra N. Smith, Kelly Smith, Corey Smith, Elena K. Smith, Samantha M. Smith, Percy Smith, Trevor J Smith, G. L. Snyder, Daniel A. Soby, Arman S. Sohail, William J. Solorio, Lincoln Solt, Caitlin Soon, Ava A Spangler, Benjamin C. Spicer, Ashish Srivastava, Emily Stamos, Peter Starbuck, Ethan K. Stark, Travis Starling, Caitlyn Staudenmier, Sheen L. Steinbarth, Christopher H. Steinsberger, Tyler Stepaniak, Ellie N. Steward, Trey Stewart, T. C. Stewart, Cooper N. Stratmeyer, Grant L. Stratton, Jordin L. Stribling, S. A Sulaiman, Brandon J Sullivan, M. E. Sundell, Sohan N. Sur, Rohan Suri, Jason R. Swartz, Joshua D. Sweeney, Konner Syed, Emi Szabo, Philip Szeremeta, Michael-Tan D. Ta, Nolan C. Tanguma, Kyle Taulman, Nicole Taylor, Eleanor Taylor, Liam C. Taylor, K. E. Tayman, Yesica Tellez, Richard Terrile, Corey D Tesdahl, Quinn N. Thielmann, Gerig Thoman, Daniel Thomas, Jeffrey J. Thomas, William N. Thompson, Noah R. Thornally, Darien P. Tobin, Kelly Ton, Nathaniel J. Toon, Kevin Tran, Bryn Tran, Maedee Trank-Greene, Emily D. Trautwein, Robert B. Traxler, Judah Tressler, Tyson R. Trofino, Thomas Troisi, Benjamin L. Trunko, Joshua K. Truong, Julia Tucker, Thomas D Umbricht, C. H. Uphoff, Zachary T. Upthegrove, Shreenija Vadayar, Whitney Valencia, Mia M. Vallery, Eleanor Vanetten, John D. Vann, Ilian Varela, Alexandr Vassilyev, Nicholas J. Vaver, Anjali A. Velamala, Evan Vendetti, Nancy Ortiz Venegas, Aditya V. Vepa, Marcus T. Vess, Jenna S. Veta, Andrew Victory, Jessica Vinson, Connor Maklain Vogel, Michaela Wagoner, Steven P. Wallace, Logan Wallace, Caroline Waller, Jiawei Wang, Keenan Warble, N. R. D. Ward-Chene, James Adam Watson, Robert J. Weber, Aidan B. Wegner, Anthony A Weigand, Amanda M. Weiner, Ayana West, Ethan Benjamin Wexler, Nicola H. Wheeler, Jamison R. White, Zachary White, Oliver S. White, Lloyd C. Whittall, Isaac Wilcove, Blake C. Wilkinson, John S. Willard, Abigail K. Williams, Sajan Williams, Orion K. Wilson, Evan M. Wilson, Timothy R. Wilson, Connor B. Wilson, Briahn Witkoff, Aubrey M. Wolfe, Jackson R. Wolle, Travis M. Wood, Aiden L. Woodard, Katelynn Wootten, Catherine Xiao, Jianing Yang, Zhanchao Yang, Trenton J. Young, Isabel Young, Thomas Zenner, Jiaqi Zhang, Tianwei Zhao, Tiannie Zhao, Noah Y. Zhao, Chongrui Zhou, Josh J Ziebold, Lucas J. Ziegler, James C. Zygmunt, Jinhua Zhang, and H. J. Lewandowski
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Astrophysics - Solar and Stellar Astrophysics ,Space and Planetary Science ,FOS: Physical sciences ,Astronomy and Astrophysics ,Solar and Stellar Astrophysics (astro-ph.SR) - Abstract
Flare frequency distributions represent a key approach to addressing one of the largest problems in solar and stellar physics: determining the mechanism that counter-intuitively heats coronae to temperatures that are orders of magnitude hotter than the corresponding photospheres. It is widely accepted that the magnetic field is responsible for the heating, but there are two competing mechanisms that could explain it: nanoflares or Alfv\'en waves. To date, neither can be directly observed. Nanoflares are, by definition, extremely small, but their aggregate energy release could represent a substantial heating mechanism, presuming they are sufficiently abundant. One way to test this presumption is via the flare frequency distribution, which describes how often flares of various energies occur. If the slope of the power law fitting the flare frequency distribution is above a critical threshold, $\alpha=2$ as established in prior literature, then there should be a sufficient abundance of nanoflares to explain coronal heating. We performed $>$600 case studies of solar flares, made possible by an unprecedented number of data analysts via three semesters of an undergraduate physics laboratory course. This allowed us to include two crucial, but nontrivial, analysis methods: pre-flare baseline subtraction and computation of the flare energy, which requires determining flare start and stop times. We aggregated the results of these analyses into a statistical study to determine that $\alpha = 1.63 \pm 0.03$. This is below the critical threshold, suggesting that Alfv\'en waves are an important driver of coronal heating., Comment: 1,002 authors, 14 pages, 4 figures, 3 tables, published by The Astrophysical Journal on 2023-05-09, volume 948, page 71
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- 2023
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3. CARD 2023: expanded curation, support for machine learning, and resistome prediction at the Comprehensive Antibiotic Resistance Database
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Brian P Alcock, William Huynh, Romeo Chalil, Keaton W Smith, Amogelang R Raphenya, Mateusz A Wlodarski, Arman Edalatmand, Aaron Petkau, Sohaib A Syed, Kara K Tsang, Sheridan J C Baker, Mugdha Dave, Madeline C McCarthy, Karyn M Mukiri, Jalees A Nasir, Bahar Golbon, Hamna Imtiaz, Xingjian Jiang, Komal Kaur, Megan Kwong, Zi Cheng Liang, Keyu C Niu, Prabakar Shan, Jasmine Y J Yang, Kristen L Gray, Gemma R Hoad, Baofeng Jia, Timsy Bhando, Lindsey A Carfrae, Maya A Farha, Shawn French, Rodion Gordzevich, Kenneth Rachwalski, Megan M Tu, Emily Bordeleau, Damion Dooley, Emma Griffiths, Haley L Zubyk, Eric D Brown, Finlay Maguire, Robert G Beiko, William W L Hsiao, Fiona S L Brinkman, Gary Van Domselaar, and Andrew G McArthur
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Genetics - Abstract
The Comprehensive Antibiotic Resistance Database (CARD; card.mcmaster.ca) combines the Antibiotic Resistance Ontology (ARO) with curated AMR gene (ARG) sequences and resistance-conferring mutations to provide an informatics framework for annotation and interpretation of resistomes. As of version 3.2.4, CARD encompasses 6627 ontology terms, 5010 reference sequences, 1933 mutations, 3004 publications, and 5057 AMR detection models that can be used by the accompanying Resistance Gene Identifier (RGI) software to annotate genomic or metagenomic sequences. Focused curation enhancements since 2020 include expanded β-lactamase curation, incorporation of likelihood-based AMR mutations for Mycobacterium tuberculosis, addition of disinfectants and antiseptics plus their associated ARGs, and systematic curation of resistance-modifying agents. This expanded curation includes 180 new AMR gene families, 15 new drug classes, 1 new resistance mechanism, and two new ontological relationships: evolutionary_variant_of and is_small_molecule_inhibitor. In silico prediction of resistomes and prevalence statistics of ARGs has been expanded to 377 pathogens, 21,079 chromosomes, 2,662 genomic islands, 41,828 plasmids and 155,606 whole-genome shotgun assemblies, resulting in collation of 322,710 unique ARG allele sequences. New features include the CARD:Live collection of community submitted isolate resistome data and the introduction of standardized 15 character CARD Short Names for ARGs to support machine learning efforts.
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- 2022
4. Regulation and functional consequences of mGlu4 RNA editing
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Christopher S. Hofmann, Karen J. Gregory, Colleen M. Niswender, Sheridan J. S. Carrington, and Andrew N. Keller
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RNA editing ,G protein ,Metabotropic glutamate receptor 4 ,ADAR ,Glutamate receptor ,RNA ,Biology ,Heteroreceptor ,Receptor ,Molecular Biology ,Cell biology - Abstract
Metabotropic glutamate receptor 4 (mGlu4) is one of eight mGlu receptors within the Class C G protein-coupled receptor superfamily. mGlu4 is primarily localized to the presynaptic membrane of neurons where it functions as an auto and heteroreceptor controlling synaptic release of neurotransmitter. mGlu4 is implicated in numerous disorders and is a promising drug target; however, more remains to be understood about its regulation and pharmacology. Using high-throughput sequencing, we have validated and quantified an adenosine-to-inosine (A-to-I) RNA editing event that converts glutamine 124 to arginine in mGlu4; additionally, we have identified a rare but novel K129R site. Using an in vitro editing assay, we then validated the pre-mRNA duplex that allows for editing by ADAR enzymes and predicted its conservation across the mammalian species. Structural modeling of the mGlu4 protein predicts the Q124R substitution to occur in the B helix of the receptor that is critical for receptor dimerization and activation. Interestingly, editing of a receptor homodimer does not disrupt G protein activation in response to the endogenous agonist, glutamate. Using an assay designed to specifically measure heterodimer populations at the surface, however, we found that Q124R substitution decreased the propensity of mGlu4 to heterodimerize with mGlu2 and mGlu7. Our study is the first to extensively describe the extent and regulatory factors of RNA editing of mGlu4 mRNA transcripts. In addition, we have proposed a novel functional consequence of this editing event that provides insights regarding its effects in vivo and expands the regulatory capacity for mGlu receptors.
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- 2021
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5. The small-sized telescope of CTAO
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Gianpiero Tagliaferri, Angelo Antonelli, Tora Arnesen, Jann Aschersleben, Primo Attina', Matteo Balbo, Sunghyun Bang, Miquel Barcelo, Andrey Baryshev, Giancarlo Bellassai, David Berge, Chris Bicknell, Ciro Bigongiari, Giacomo Bonnoli, Frederic Bouley, Anthony Brown, Andrea Bulgarelli, Massimo Cappi, Patrizia Caraveo, Salvatore Caschera, Paula Chadwick, Francesco Conte, Garret Cotter, Pierre Cristofari, Fatima De Frondat, Elisabete De Gouveia Dal Pino, Nico De Simone, Davide Depaoli, Jean Laurent Dournaux, Connor Duffy, Sabrina Einecke, Carlos E. Fermino, Stefan Funk, Carmelo Gargano, Gianluca Giavitto, Andrea Giuliani, Tim Greenshaw, Jim Hinton, Jean-Michel Huet, Simone Iovenitti, Nicola la Palombara, Jon S. Lapington, Philippe Laporte, Steve Leach, Luigi Lessio, Giuseppe Leto, Sheridan J. Lloyd, Fabrizio Lucarelli, Saverio Lombardi, Alberto Macchi, Eugenio Martinetti, Antonio Micciche', Rachele Millul, Teresa Mineo, Takahashi Mitsunari, Amrit P. Nayak, Gaetano Nicotra, Akira Okumura, Giovanni Pareschi, Marek Penno, Heike Prokoph, Emma Rebert, Chiara Righi, Cameron B. Rulten, Federico Russo, Ricardo Zanmar Sanchez, Francesco G. Saturni, Johannes Schaefer, Benni Schwab, Salvatore Scuderi, Giorgia Sironi, Vitalii Sliusar, Helene Sol, Samuel Spencer, Antonio Stamerra, Hiro Tajima, Fabrizio tavecchio, Gino Tosti, Alessio Trois, Manuela Vecchi, Stefano Vercellone, Jacco Vink, Roland Walter, Jason Watson, Richard White, Roberta Zanin, Luca Zampieri, Andreas Zech, Adrian Zink, and Astronomy
- Abstract
The Cherenkov Telescope Array Observatory (CTAO) consists of three types of telescopes: large-sized (LST), mediumsized (MST), and small-sized (SST), distributed in two observing sites (North and South). For the CTA South "Alpha Configuration" the construction and installation of 37 (+5) SST telescopes (a number that could increase up to 70 in future upgrades) are planned. The SSTs are developed by an international consortium of institutes that will provide them as an in-kind contribution to CTAO. The SSTs rely on a Schwarzschild-Couder-like dual-mirror polynomial optical design, with a primary mirror of 4 m diameter, and are equipped with a focal plane camera based on SiPM detectors covering a field of view of ~9°. The current SST concept was validated by developing the prototype dual-mirror ASTRI-Horn Cherenkov telescope and the CHEC-S SiPM focal plane camera. In this contribution, we will present an overview of the SST key technologies, the current status of the SST project, and the planned schedule.
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- 2022
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6. Axion constraints from quiescent soft gamma-ray emission from magnetars
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Sheridan J. Lloyd, P. M. Chadwick, Kuver Sinha, Huai-Ke Guo, and Anthony M. Brown
- Subjects
High Energy Astrophysical Phenomena (astro-ph.HE) ,Physics ,Photon ,010308 nuclear & particles physics ,Scattering ,Astrophysics::High Energy Astrophysical Phenomena ,Gamma ray ,FOS: Physical sciences ,Flux ,Magnetosphere ,Astrophysics ,Magnetar ,01 natural sciences ,Physics::Geophysics ,High Energy Physics - Phenomenology ,High Energy Physics - Phenomenology (hep-ph) ,0103 physical sciences ,Astrophysics - High Energy Astrophysical Phenomena ,010306 general physics ,Gamma-ray burst ,Axion - Abstract
Axion-like-particles (ALPs) emitted from the core of a magnetar can convert to photons in its magnetosphere. The resulting photon flux is sensitive to the product of $(i)$ the ALP-nucleon coupling $G_{an}$ which controls the production cross section in the core and $(ii)$ the ALP-photon coupling $g_{a\gamma \gamma}$ which controls the conversion in the magnetosphere. We study such emissions in the soft-gamma-ray range (300 keV to 1 MeV), where the ALP spectrum peaks and astrophysical backgrounds from resonant Compton upscattering are expected to be suppressed. Using published quiescent soft-gamma-ray flux upper limits in 5 magnetars obtained with $CGRO$ COMPTEL and $INTEGRAL$ SPI/IBIS/ISGRI, we put limits on the product of the ALP-nucleon and ALP-photon couplings. We also provide a detailed study of the dependence of our results on the magnetar core temperature. We further show projections of our result for future $Fermi$-GBM observations. Our results motivate a program of studying quiescent soft-gamma-ray emission from magnetars with the $Fermi$-GBM., Comment: 14 pages, 4 figures. Version accepted in Physical Review D. More conservative benchmark core temperature assumed, details of production in the core provided, new constraints on ALP couplings based on spectral analysis presented. Extensive supplementary material added, future projections discussed, overall conclusions unchanged
- Published
- 2021
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7. 60 YEARS OF POMC: Regulation of feeding and energy homeostasis by α-MSH
- Author
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Roger D. Cone, Michael J Litt, Sheridan J. S. Carrington, Isin Cakir, Masoud Ghamari-Langroudi, Taneisha Gillyard, Luis E. Gimenez, and Erica J. P. Anderson
- Subjects
0301 basic medicine ,endocrine system ,medicine.medical_specialty ,Pro-Opiomelanocortin ,Biology ,Article ,Energy homeostasis ,03 medical and health sciences ,Endocrinology ,Central melanocortin system ,Internal medicine ,Genetic model ,medicine ,Animals ,Homeostasis ,Humans ,Protein Isoforms ,Agouti-Related Protein ,Cloning, Molecular ,Receptor ,Molecular Biology ,Melanocortins ,Neurons ,integumentary system ,Receptors, Melanocortin ,digestive, oral, and skin physiology ,Membrane Proteins ,Feeding Behavior ,Melanocortin 3 receptor ,Cell biology ,Optogenetics ,030104 developmental biology ,medicine.anatomical_structure ,alpha-MSH ,Melanocortin ,Signal transduction ,Energy Metabolism ,hormones, hormone substitutes, and hormone antagonists ,Signal Transduction - Abstract
The melanocortin peptides derived from pro-opiomelanocortin (POMC) were originally understood in terms of the biological actions of α-melanocyte-stimulating hormone (α-MSH) on pigmentation and adrenocorticotrophic hormone on adrenocortical glucocorticoid production. However, the discovery of POMC mRNA and melanocortin peptides in the CNS generated activities directed at understanding the direct biological actions of melanocortins in the brain. Ultimately, discovery of unique melanocortin receptors expressed in the CNS, the melanocortin-3 (MC3R) and melanocortin-4 (MC4R) receptors, led to the development of pharmacological tools and genetic models leading to the demonstration that the central melanocortin system plays a critical role in the regulation of energy homeostasis. Indeed, mutations in MC4R are now known to be the most common cause of early onset syndromic obesity, accounting for 2–5% of all cases. This review discusses the history of these discoveries, as well as the latest work attempting to understand the molecular and cellular basis of regulation of feeding and energy homeostasis by the predominant melanocortin peptide in the CNS, α-MSH.
- Published
- 2016
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8. Reply to 'Comment on ‘Understanding the γ -ray emission from the globular cluster 47 Tuc: Evidence for dark matter?'’
- Author
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Céline Bœhm, Anthony M. Brown, Sheridan J. Lloyd, P. M. Chadwick, Thomas Lacroix, Laboratoire Univers et Particules de Montpellier (LUPM), Université Montpellier 2 - Sciences et Techniques (UM2)-Institut National de Physique Nucléaire et de Physique des Particules du CNRS (IN2P3)-Université de Montpellier (UM)-Centre National de la Recherche Scientifique (CNRS), Laboratoire d'Annecy-le-Vieux de Physique Théorique (LAPTH), Université Savoie Mont Blanc (USMB [Université de Savoie] [Université de Chambéry])-Centre National de la Recherche Scientifique (CNRS), and Université de Montpellier (UM)-Université Montpellier 2 - Sciences et Techniques (UM2)-Institut National de Physique Nucléaire et de Physique des Particules du CNRS (IN2P3)-Centre National de la Recherche Scientifique (CNRS)
- Subjects
Physics ,High Energy Astrophysical Phenomena (astro-ph.HE) ,010308 nuclear & particles physics ,Astrophysics::High Energy Astrophysical Phenomena ,Spectral properties ,Dark matter ,FOS: Physical sciences ,Astrophysics ,01 natural sciences ,Spectral line ,Black hole ,Millisecond pulsar ,Globular cluster ,0103 physical sciences ,010306 general physics ,[PHYS.ASTR]Physics [physics]/Astrophysics [astro-ph] ,Astrophysics - High Energy Astrophysical Phenomena - Abstract
Analysing 9 years of Fermi-LAT observations, we recently studied the spectral properties of the prominent globular cluster 47 Tuc (Brown et al. 2018). In particular, we investigated several models to explain the observed gamma-ray emission, ranging from millisecond pulsars (MSP) to Dark Matter (DM), with the motivation for the latter model driven by recent evidence that 47 Tuc harbours an intermediate-mass black hole (IMBH). This investigation found evidence that the observed gamma-ray emission from 47 Tuc is due to two source populations of MSPs and DM. In Bartels \& Edwards (2018), the authors comment that this evidence is an artifact of the MSP spectra used in (Brown et al. 2019). Here we reply to this comment and argue that the authors of Bartels \& Edwards (2018) (i) do not give due consideration to a very important implication of their result and (ii) there is tension between our MSP fit and their MSP fit when taking uncertainties into consideration. As such, we still conclude there is evidence for a DM component which motivates a deeper radio study of the prominent globular cluster 47 Tuc., 3 pages, accepted for publication in PRD
- Published
- 2019
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9. Constraining Axion Mass through Gamma-ray Observations of Pulsars
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P. M. Chadwick, Anthony M. Brown, and Sheridan J. Lloyd
- Subjects
Physics ,High Energy Astrophysical Phenomena (astro-ph.HE) ,Range (particle radiation) ,Field (physics) ,010308 nuclear & particles physics ,Astrophysics::High Energy Astrophysical Phenomena ,High Energy Physics::Phenomenology ,Bremsstrahlung ,Gamma ray ,Flux ,FOS: Physical sciences ,Astrophysics ,01 natural sciences ,Pulsar ,0103 physical sciences ,Astrophysics - High Energy Astrophysical Phenomena ,010303 astronomy & astrophysics ,Axion ,Energy (signal processing) - Abstract
We analyze 9 years of PASS 8 $\textit{Fermi}$-LAT data in the 60$-$500 MeV range and determine flux upper limits (UL) for 17 gamma-ray dark pulsars as a probe of axions produced by nucleon-nucleon Bremsstrahlung in the pulsar core. Using a previously published axion decay gamma-ray photon flux model for pulsars which relies on a high core temperature of 20 MeV, we improve the determination of the UL axion mass ($m_a$), at 95 percent confidence level, to 9.6 $\times$ 10$^{-3}$ eV, which is a factor of 8 improvement on previous results. We show that the axion emissivity (energy loss rate per volume) at realistic lower pulsar core temperatures of 4 MeV or less is reduced to such an extent that axion emissivity and the gamma-ray signal becomes negligible. We consider an alternative emission model based on energy loss rate per mass to allow $m_a$ to be constrained with $Fermi$-LAT observations. This model yields a plausible UL $m_a$ of 10$^{-6}$ eV for pulsar core temperature $, Comment: 13 pages, 5 figures, Accepted for publication in Physical Review D
- Published
- 2019
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10. G protein-coupled receptors differentially regulate glycosylation and activity of the inwardly rectifying potassium channel Kir7.1
- Author
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Ciria C. Hernandez, Daniel R. Swale, Oluwatosin A. Aluko, Jerod S. Denton, Roger D. Cone, and Sheridan J. S. Carrington
- Subjects
0301 basic medicine ,Glycosylation ,G protein ,Leber Congenital Amaurosis ,Biochemistry ,03 medical and health sciences ,chemistry.chemical_compound ,Neurobiology ,Humans ,G protein-coupled inwardly-rectifying potassium channel ,Potassium Channels, Inwardly Rectifying ,Receptor ,Molecular Biology ,Ion channel ,G protein-coupled receptor ,Sequence Deletion ,Cell Biology ,Potassium channel ,Cell biology ,Protein Transport ,030104 developmental biology ,HEK293 Cells ,chemistry ,Receptors, Adrenergic, beta-3 ,Mutation ,Receptors, Adrenergic, beta-2 ,Signal transduction ,Protein Multimerization ,Receptors, Adrenergic, beta-1 ,Ion Channel Gating - Abstract
Kir7.1 is an inwardly rectifying potassium channel with important roles in the regulation of the membrane potential in retinal pigment epithelium, uterine smooth muscle, and hypothalamic neurons. Regulation of G protein–coupled inwardly rectifying potassium (GIRK) channels by G protein–coupled receptors (GPCRs) via the G protein βγ subunits has been well characterized. However, how Kir channels are regulated is incompletely understood. We report here that Kir7.1 is also regulated by GPCRs, but through a different mechanism. Using Western blotting analysis, we observed that multiple GPCRs tested caused a striking reduction in the complex glycosylation of Kir7.1. Further, GPCR-mediated reduction of Kir7.1 glycosylation in HEK293T cells did not alter its expression at the cell surface but decreased channel activity. Of note, mutagenesis of the sole Kir7.1 glycosylation site reduced conductance and open probability, as indicated by single-channel recording. Additionally, we report that the L241P mutation of Kir7.1 associated with Lebers congenital amaurosis (LCA), an inherited retinal degenerative disease, has significantly reduced complex glycosylation. Collectively, these results suggest that Kir7.1 channel glycosylation is essential for function, and this activity within cells is suppressed by most GPCRs. The melanocortin-4 receptor (MC4R), a GPCR previously reported to induce ligand-regulated activity of this channel, is the only GPCR tested that does not have this effect on Kir7.1.
- Published
- 2018
11. Assessing the Capacity and Resilience of Melbourne’s Foodbowl: The Foodprint Melbourne project
- Author
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Carey, R, Sheridan, J, Candy, S, and Larsen, K
- Abstract
The city of Melbourne is located in a highly productive agricultural region with the capacity to meet approximately 41% of the city population’s food needs. Melbourne’s “foodbowl” is an important building block in a resilient and sustainable food system for this rapidly growing city. This article presents some findings of the Foodprint Melbourne initiative led by University of Melbourne researchers who worked in partnership with local governments to investigate the significance of periurban food production to the city’s long-term food security and the regional economy. They identified risks to city fringe food production from urban sprawl and the impacts of water scarcity, and generated an important evidence base to support the development of a vision and roadmap to strengthen the resilience of Melbourne’s foodbowl.
- Published
- 2018
12. A citizen science approach to obtain quantitative measurements of urban agriculture inputs and outputs in Melbourne
- Author
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Candy, S, Sheridan, J, and Jackson, S
- Abstract
There are many advocates and critics of urban agriculture’s role in a sustainable food system but little quantitative data, potentially due the difficulties in collecting it. Urban food production is an example of a distributed system intrinsically linked to urban farmers and urban lifestyles and therefore cannot be recreated in a lab. Citizen science (CS) is identified as a potential method to measure aspects of urban agriculture but has potential issues associated with maintaining participation in data collection. This paper presents the development of a citizen science methodology combining general CS project design methods with methods for engaging and retaining participants in CS projects, based on motivation, for the design of a citizen science project measuring the sustainability performance of urban food gardens in Melbourne, Australia. It was found that an additional motivation emerged that is not yet documented in existing literature and is particular to citizen science projects. Other conclusions were also drawn related to timeline management, potential cost reductions conflicting with reducing barriers to participation and diversifying recruitment methods to attract participants with more time to be involved.
- Published
- 2018
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13. Fermi-LAT Studies of Globular Clusters
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P. M. Chadwick, Anthony M. Brown, and Sheridan J. Lloyd
- Subjects
Physics ,Range (particle radiation) ,Millisecond pulsar ,Globular cluster ,Gamma ray ,Astrophysics ,Galactic plane ,Lower energy ,Spectral line ,Fermi Gamma-ray Space Telescope - Abstract
We analyse 30 Galactic globular clusters ( GC ) located off the Galactic plane, using 8 years of Pass 8 Fermi-LAT data in the range 60 MeV - 300 GeV with the analysis down to lower energy being performed for the first time. We refine the prior detections of 5 GC, 47 Tuc, NGC 6093, NGC 6218, NGC 6752 and NGC 7078. We also detect NGC 6254 for the first time. NGC 6093 and NGC 6218 exhibit flat hard spectra in the range 1 - 10 GeV. The lack of a spectral cut-off between 1-4 GeV in NGC 6093 and NGC 6218, suggests other sources of gamma ray emission apart from millisecond pulsars may be important in these GCs.
- Published
- 2017
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14. Australia's city food bowls: Fertile ground for investigating biomes and food security
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Carey, R and Sheridan, J
- Published
- 2017
15. What does a low carbon local diet look like for Melbourne?
- Author
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Candy, S and Sheridan, J
- Abstract
Food systems in cities are under increasing pressure. Food production is occurring further and further from the point of consumption and extreme weather events due to climate change are impacting on food supply networks. It is possible that cities will have to rely on their local regions to meet at least some of their food needs in the future. Although large amounts of food are produced on the outskirts of cities, it is not clear the extent to which the nutritional needs of inhabitants could be met sustainably. This paper aims to investigate if it is possible to feed the city of Melbourne a healthy diet from the local area (i.e. achieve direct food availability) and what that diet might look like. It tests a new methodology using linear programming to find the optimal mix of food types to produce a diet profile that meets the Australian Dietary Guidelines within theproduction capacity of the local ‘region’. Results from three region scenarios are presented – Greater Melbourne, Foodbowl and Rest of Victoria. No solution could be found that satisfied all constraints for any region, however this identified issues surrounding availability of certain food types, particularly fruit, vegetables and legumes. Systematically increasing certain constraints provided insight into how diets could be composed to meet requirements and where it might be necessary to increase production within a region or future proof food supply networks. It also highlighted conflicts between sourcing food locally and reducing carbon emissions.
- Published
- 2017
16. Further exploration of M1 allosteric agonists: Subtle structural changes abolish M1 allosteric agonism and result in pan-mAChR orthosteric antagonism
- Author
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Hyekyung P. Cho, Michael R. Wood, Kimberly M. Lovell, James C. Tarr, Christian Sevel, Sheridan J. S. Carrington, Douglas J. Sheffler, Uyen M. Le, Craig W. Lindsley, Colleen M. Niswender, P. Jeffrey Conn, Gregory J. Digby, and Corey R. Hopkins
- Subjects
Agonist ,medicine.drug_class ,Stereochemistry ,Clinical Biochemistry ,Allosteric regulation ,Pharmaceutical Science ,CHO Cells ,Transfection ,Biochemistry ,Article ,Structure-Activity Relationship ,Cricetulus ,Allosteric Regulation ,Piperidines ,Cricetinae ,Drug Discovery ,Muscarinic acetylcholine receptor ,medicine ,Animals ,Humans ,Structure–activity relationship ,Agonism ,Molecular Biology ,Molecular switch ,biology ,Chemistry ,Receptor, Muscarinic M1 ,Organic Chemistry ,biology.organism_classification ,Receptors, Muscarinic ,Acetylcholine ,Rats ,Benzamides ,Molecular Medicine ,Benzimidazoles ,Calcium ,Antagonism ,Allosteric Site - Abstract
This letter describes the further exploration of two series of M(1) allosteric agonists, TBPB and VU0357017, previously reported from our lab. Within the TPBP scaffold, either electronic or steric perturbations to the central piperidine ring led to a loss of selective M(1) allosteric agonism and afforded pan-mAChR antagonism, which was demonstrated to be mediated via the orthosteric site. Additional SAR around a related M(1) allosteric agonist family (VU0357017) identified similar, subtle 'molecular switches' that modulated modes of pharmacology from allosteric agonism to pan-mAChR orthosteric antagonism. Therefore, all of these ligands are best classified as bi-topic ligands that possess high affinity binding at an allosteric site to engender selective M(1) activation, but all bind, at higher concentrations, to the orthosteric ACh site, leading to non-selective orthosteric site binding and mAChR antagonism.
- Published
- 2013
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17. Development of a novel, CNS-penetrant, metabotropic glutamate receptor 3 (mGlu3) NAM probe (ML289) derived from a closely related mGlu5 PAM
- Author
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Sheridan J. S. Carrington, Nicholas D. P. Cosford, P. Jeffrey Conn, Colleen M. Niswender, Ryan D. Morrison, Douglas J. Sheffler, Anna L. Blobaum, Kiran Gogi, Shaun R. Stauffer, Joshua A. Bruner, Paige N. Vinson, J. Scott Daniels, Cody J. Wenthur, Mitchell Vamos, and Craig W. Lindsley
- Subjects
Central Nervous System ,animal structures ,Allosteric modulator ,Receptor, Metabotropic Glutamate 5 ,Clinical Biochemistry ,Allosteric regulation ,Glutamic Acid ,Pharmaceutical Science ,Pharmacology ,Receptors, Metabotropic Glutamate ,Sensitivity and Specificity ,Biochemistry ,Article ,Permeability ,Cell Line ,Structure-Activity Relationship ,chemistry.chemical_compound ,Allosteric Regulation ,Piperidines ,Drug Discovery ,Humans ,Structure–activity relationship ,Receptor ,Molecular Biology ,health care economics and organizations ,Chemistry ,Drug discovery ,Organic Chemistry ,food and beverages ,Liver metabolism ,Molecular Probes ,Microsomes, Liver ,Molecular Medicine ,Metabotropic glutamate receptor 3 ,Penetrant (biochemical) - Abstract
Herein we report the discovery and SAR of a novel metabotropic glutamate receptor 3 (mGlu(3)) NAM probe (ML289) with 15-fold selectivity versus mGlu(2). The mGlu(3) NAM was discovered via a 'molecular switch' from a closely related, potent mGlu(5) positive allosteric modulator (PAM), VU0092273. This NAM (VU0463597, ML289) displays an IC(50) value of 0.66 μM and is inactive against mGlu(5).
- Published
- 2012
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18. Melbourne’s food future: Planning a resilient city foodbowl. A summary briefing from the Foodprint Melbourne project
- Author
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Carey, R, Larsen, K, and SHERIDAN, J
- Published
- 2016
19. Melbourne’s food future: Planning a resilient city foodbowl
- Author
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Carey, R, Larsen, K, SHERIDAN, J, and Candy, S
- Abstract
Melbourne is surrounded by a highly productive foodbowl that currently grows a wide variety of fresh foods, but it faces challenges. • Melbourne’s foodbowl grows 47% of the vegetables produced in Victoria and has the capacity to meet around 41% of Melbourne’s total food needs. • As Melbourne grows to a population of 7-8 million people by 2050, it will need at least 60% more food. • If the city’s footprint continues to grow as it has in the past, the capacity of Melbourne’s foodbowl to meet the city’s food needs could fall to around 18% by 2050, due to population growth and urban sprawl. • Loss of production in the foodbowl is likely to contribute to higher food prices. • Melbourne’s foodbowl contributes $2.45 billion per annum to Melbourne’s regional economy and 21,000 full time equivalent jobs. • Melbourne’s food supply faces future challenges from the impacts of climate change, including water scarcity and extreme weather events. • Other major Australian state capitals also have productive foodbowls that contribute to fresh food supplies, but they are all under similar pressure from population growth and urban expansion. They are unlikely to be able to meet future deficits in Melbourne’s food needs. Melbourne’s foodbowl is an important building block in a resilient and sustainable food future for the city. • Ensuring a resilient food supply for Melbourne requires a precautionary planning approach that retains – or strengthens – the capacity of the city’s foodbowl. • The loss of Melbourne’s foodbowl is not inevitable as the city grows. If growth on the city fringe can be limited to existing growth corridors and strong targets are set for urban infill and increased urban density, the impact on the city’s foodbowl can be reduced. • Melbourne can plan for a resilient city foodbowl that provides healthy food for a growing population, promotes a vibrant regional food economy and acts as a buffer against future food system shocks. • Increased investment in delivery of recycled water from water treatment plants could create ‘drought-proof’ areas of food production. • A ‘joined up’ policy framework is required to plan for a resilient city foodbowl. Policy is needed to protect farmland, increase water access, reduce and reuse food waste, strengthen the regional food economy and attract farmers to farm in the city’s foodbowl.
- Published
- 2016
20. Foodprint Melbourne: What does it take to feed a city?
- Author
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SHERIDAN, J, Carey, R, and Candy, S
- Abstract
This report explores Melbourne’s ‘foodprint’ – the environmental footprint of feeding the city. It takes a lot of land, water and energy to feed a rapidly growing city like Melbourne, and a significant amount of food waste and GHG emissions are generated as a result. As supplies of the natural resources underpinning food production become more constrained, the city will need to explore new approaches to increase the sustainability and resilience of its food supply. This report aims to provide an evidence base to support this process. The principal findings of this research are: • It takes over 475L of water per capita per day to feed Melbourne, around double the city’s household usage. • 16.3 million hectares of land is required to feed Melbourne each year, an area equivalent to 72% of the state of Victoria. • Feeding Melbourne generates over 907,537 tonnes of edible food waste, which represents a waste of 3.6 million hectares of land and 180 GL of water. • Around 4.1 million tonnes of GHG emissions are emitted in producing the city’s food, and a further 2.5 million tonnes from food waste. • Melbourne is likely to grow rapidly between now and 2050, and its foodprint will increase significantly as a result. • Melbourne’s city foodbowl could play an important role in increasing the resilience and sustainability of the city’s food supply. • The city foodbowl has significant capacity for production of fresh foods. It also has access to recycled water and organic waste streams, and could reduce the city’s dependence on distant sources of fresh foods. • Key vulnerabilities in Melbourne’s regional food supply include loss of agricultural land, water scarcity and the impacts of climate change. • Potential strategies to increase the sustainability and resilience of Melbourne’s regional food supply include increasing urban density, shifting to regenerative agriculture, increasing the use of recycled water for agriculture, reducing food waste and modifying our diets. • Multiple strategies are likely to be needed to increase the sustainability and resilience of Melbourne’s regional food supply. • Around 10% of the available recycled water from Melbourne’s water treatment plants would be enough to grow half of the vegetables that Melbourne eats. • Increasing urban density as Melbourne grows could reduce urban sprawl by about 50% over the next 20 years, saving 180,000 hectares of land in Melbourne’s foodbowl – an area equivalent to almost 5 times Victoria’s vegetable growing land.
- Published
- 2016
21. Melbourne's Foodbowl: Now and at seven million
- Author
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SHERIDAN, J, Larsen, K, and Carey, R
- Published
- 2015
22. Roles of cities in climate resilient food systems: A Foodprint Melbourne briefing
- Author
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Carey, R, Larsen, K, and SHERIDAN, J
- Published
- 2015
23. Defining the nature of participation in rural Australian communities: A qualitative approach
- Author
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Sheridan J. Coakes and Brian Bishop
- Subjects
Politics ,Qualitative analysis ,Social Psychology ,Structured interview ,Community life ,Gender studies ,Community or ,Sociology ,Social science ,Social engagement - Abstract
Within the literature, theories and analyses of social involvement or participation have focussed primarily on the political and formal role of participation within the community or neighborhood. This study illustrates, through qualitative inquiry, that within small rural communities, individuals find it difficult to separate formal and informal participation, when both have an equally important role to play in community life. Fifty-five structured interviews were conducted with women across six rural shires in the southwest region of Western Australia. Qualitative analysis revealed that approximately 50% of women, when asked about their involvement in their community, referred initially to their informal participation within the community, rather than their participation in formal community groups or associations. These results are discussed in relation to life in small rural towns. © 2002 Wiley Periodicals, Inc.
- Published
- 2002
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24. The experience of moral community in a rural community context
- Author
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Sheridan J. Coakes and Brian Bishop
- Subjects
Community studies ,Social Psychology ,Feeling ,Community building ,Turnover ,Community organization ,media_common.quotation_subject ,Moral community ,Community psychology ,Context (language use) ,Sociology ,Social psychology ,media_common - Abstract
This paper examines the concept of moral community within a rural context. The theory of moral community is discussed in relation to research in the social justice and community psychology literatures, and is related to participation in voluntary community organizations. A total of 388 women, located across six rural shires in the Great Southern Region of Western Australia, participated in the study. Results suggest that individuals participating within different community organizations or groups differ in their intensity of moral community feelings, and that sporting groups have much lower feelings of moral community than most other community organizations. The results of the study are then discussed in relation to the literature on group structure and climate. © 1996 John Wiley & Sons, Inc.
- Published
- 1996
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25. Measuring Multimodal Synchrony for Human-Computer Interaction
- Author
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England, D., Dennis Reidsma, Sheridan, J., Anton Nijholt, Crane, B., Wolfgang Tschacher, and Fabian Ramseyer
- Subjects
HCI ,Synchrony ,Measurement ,Non-verbal communication ,IR-75064 - Abstract
Nonverbal synchrony is an important element in human-human interaction. It can also play various roles in human-computer interaction. This paper surveys some of these uses, and presents a quantitative method for measuring the level of nonverbal synchrony in an interaction.
- Published
- 2010
26. The effects of age on platelet intracellular free calcium concentration in normotensives and hypertensives
- Author
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Joseph Duggan, S. Kilfeather, ET O'Brien, Kevin O'Malley, and Sheridan J
- Subjects
Adult ,Blood Platelets ,Male ,Aging ,medicine.medical_specialty ,Mean arterial pressure ,Physiology ,chemistry.chemical_element ,Calcium ,Calcium in biology ,Reference Values ,Internal medicine ,Intracellular free calcium ,Internal Medicine ,medicine ,Humans ,Platelet ,Aged ,business.industry ,Middle Aged ,Pathophysiology ,Endocrinology ,Blood pressure ,chemistry ,Hypertension ,Regression Analysis ,Female ,Cardiology and Cardiovascular Medicine ,business ,Intracellular - Abstract
We have investigated relationships between age, blood pressure and intracellular calcium concentration in platelets from normotensives and hypertensives. In normotensives, there were positive correlations between age and platelet intracellular calcium concentration (r = 0.76, P less than 0.001), age and mean arterial pressure (MAP; r = 0.55, P less than 0.01) and MAP and platelet intracellular calcium concentration (r = 0.45, P less than 0.01). Multiple regression analysis revealed that age was the primary determinant of platelet intracellular calcium concentration in normotensives. The effect of MAP on platelet intracellular calcium concentration when adjusted for age was not significant (P = 0.73). In hypertensives, there was no significant relationship between age and platelet intracellular calcium concentration (r = 0.15, P = 0.43), age and MAP (r = 0.17, P = 0.37) or MAP and platelet intracellular calcium concentration (r = -0.27, P = 0.15). Overall, platelet intracellular calcium concentration was significantly higher in hypertensives than in age-matched normotensives (P less than 0.05). Within the age groups examined, platelet intracellular calcium concentration was significantly higher only in younger hypertensives when compared with controls of a similar mean age (P less than 0.001). Thus, age, in addition to hypertension, is an important determinant of platelet intracellular calcium concentration.
- Published
- 1991
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27. Beyond evidence‐based guidelines to implementation: A model for integrating care for people with diabetes
- Author
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Sheridan J, Close G, and Boyages Sc
- Subjects
Evidence-Based Medicine ,Evidence-based practice ,Delivery of Health Care, Integrated ,Leadership and Management ,business.industry ,Best practice ,Early detection ,Pilot Projects ,Evidence-based medicine ,Continuity of Patient Care ,medicine.disease ,Community Health Planning ,Chronic disease ,Nursing ,Models, Organizational ,Diabetes mellitus ,Health care ,Diabetes Mellitus ,Humans ,Medicine ,New South Wales ,business ,Patient education - Abstract
There is a growing realization in the health system that integration of effort may be the best way of ensuring optimal outcomes of management both for clinicians and for people using the health system. It is also hypothesized that the impact of diabetes (chronic disease) and its sequelae could be reduced by the provision of well-organized care, based on agreed evidence-based guidelines for best practice, incorporating patient education and early detection of complication. This paper defines the characteristics of an integrated model of providing care to people with diabetes.
- Published
- 1999
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28. Radiocarbon dating results from the Beaker people project : Scottish samples
- Author
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Sheridan, J. A., Parker Pearson, M., Jay, M., Richards, M., and Curtis, N.
- Published
- 2006
29. Sense of Community in Rural Communities
- Author
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Pamela N. D’Rozario, Brian Bishop, and Sheridan J. Coakes
- Subjects
Emotional support ,Action (philosophy) ,Community organization ,Sense of community ,Community psychology ,Alienation ,Risk factor (computing) ,Social issues ,Psychology ,Social psychology - Abstract
Psychological sense of community (SOC) was proposed to be the central aspect of community psychology by Sarason (1974). At the Society for Community Research and Action conference at Yale in 1999, Sarason was asked by Bob Newbrough why he had formulated the concept of SOC. He stated that as a child during the depression he experienced the terror of being at the point of having no physical and emotional support. Sustained experiences of this kind then form the basis of alienation that individuals and groups in our societies experience. Sarason argued that this was a profound experience and is a considerable risk factor for psychological and social problems. Understanding SOC, thus, is an essential aspect of community psychology.
- Published
- 2002
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30. Caregiver stress, mortality and immunity
- Author
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Glaser, R, Sheridan, J, Malarkey, W, MacCallum, R, Kiecolt-Glaser, J, Schulz, R, Beach, SR, Vedhara, K, Cox, N, Wilcock, G, Perks, P, Hunt, M, Anderson, S, Lightman, S, and Shanks, N
- Published
- 2001
31. Community competence and empowerment: strategies for rural change in women's health service planning and delivery
- Author
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Sheridan J. Coakes and Gail J. Kelly
- Subjects
Economic growth ,Health Knowledge, Attitudes, Practice ,media_common.quotation_subject ,Health services ,Nursing ,Mental strain ,Humans ,Empowerment ,Competence (human resources) ,media_common ,Rural health ,Public Health, Environmental and Occupational Health ,Community Participation ,Western Australia ,Organizational Innovation ,Health Planning ,Women's Health Services ,Rural management ,Female ,Business ,Rural Health Services ,Rural area ,Rural change ,Power, Psychological ,Family Practice ,Delivery of Health Care - Abstract
Rural women face a variety of health-related problems, some of which they share with their city sisters. However, the multiple responsibilities of women on the land, and their geographical isolation and lack of support, can lead to physical decline and increased mental strain. It is these factors which are often overlooked in the planning and allocation of funding and services to rural areas. This paper examines the application of community competence and empowerment measures in developing and implementing health services for women in rural Australian communities. A study conducted in the south-west region of Western Australia illustrates the ability of women within rural communities to identify and respond constructively to health issues of concern.
- Published
- 1997
32. Mechanisms of VCAM-1 and fibronectin binding to integrin alpha 4 beta 1: implications for integrin function and rational drug design
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Martin Humphries, Sheridan J, Ap, Mould, and Newham P
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Inflammation ,Integrins ,Binding Sites ,Sequence Homology, Amino Acid ,Drug Design ,Molecular Sequence Data ,Receptors, Lymphocyte Homing ,Animals ,Humans ,Vascular Cell Adhesion Molecule-1 ,Amino Acid Sequence ,Integrin alpha4beta1 ,Fibronectins - Abstract
Integrin alpha 4 beta 1 can mediate both cell-cell and cell-extracellular matrix adhesion by binding to either fibronectin or vascular cell adhesion molecule 1 (VCAM-1). Both interactions are important for extravasation of leukocytes from the blood implying that rationally designed inhibitors of alpha 4 beta 1 function may be useful for treating a various inflammatory conditions. The mechanisms of ligand binding by alpha 4 beta 1 are complicated by the fact that alternative splicing can generate different isoforms of the receptor-binding domains in both fibronectin and VCAM-1. Therefore, in addition to developing alpha 4 beta 1 antagonists, we have also been interested in identifying isoform-specific functions. Recombinant ligand variants have been tested in adhesion and direct receptor-binding assays and each molecule was found to have a different inherent affinity for alpha 4 beta 1 that endows them with different adhesive activities. This suggests that alternative splicing may regulate alpha 4 beta 1-dependent motility in vivo. The initial strategy that we have adopted to develop alpha 4 beta 1 inhibitors has been to identify key amino acid residues and peptide sequences participating in the receptor-ligand binding event and to use this information to generate synthetic mimetics. Three active sites have been identified in fibronectin by testing truncated proteins, expressing recombinant fragments and screening synthetic peptides. Two of these sites employ versions of a novel integrin-binding motif, LDVP/IDAP. A key active site in VCAM-1 has been identified by similar approaches as the related sequence IDSP. Since IDSP-like sequences are probably used by other integrin-binding immunoglobulins, derivatives of these peptides may turn out to be the forerunners of a new generation of therapeutic agents with multiple applications.
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- 1995
33. Providing adequate instruction to data processing students spread over a wide geographical area
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Sheridan J. West
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Data processing ,Work (electrical) ,Multimedia ,Computer science ,ComputingMilieux_COMPUTERSANDEDUCATION ,Mathematics education ,General Materials Science ,computer.software_genre ,computer - Abstract
Students are spread out over approximately 20 European U.S. military installations.The objective of the course of study is the Data Processing Core and Advanced Certificates awarded after 12 and 24 semester hours of course work, respectively.Instruction is provided by U.S. military and civilian personnel qualified in data processing and the language being taught.Purpose: To give students the fundamentals of programming in several of the most common programming languages in use today. They are not expected to become full fledged programmers. In the introductory courses, an important objective is to provide a general appreciation of data processing and how it is affecting the lives of everyone. In addition, it is hoped that students will apply this understanding so that data processing is seen as a tool to make jobs more meaningful—as opposed to the threat people feel as their job is “automated.”
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- 1972
- Full Text
- View/download PDF
34. Development of an air purifier for personnel cubicles
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Sheridan J. Rodgers and Ferdinand Roehlich
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Waste management ,business.industry ,Respiratory Tract Diseases ,Public Health, Environmental and Occupational Health ,Environmental engineering ,Air pollution ,Scrubber ,Particulates ,medicine.disease_cause ,law.invention ,Occupational Diseases ,HEPA ,Air conditioning ,law ,Air Pollution ,medicine ,Environmental science ,Air purifier ,Humans ,Air Conditioning ,business ,Air quality index ,Filtration - Abstract
An air purifier was developed for tunnel, toll and garage booths or cubicles. Catalytic oxidation, activated carbon and a HEPA filter are used to scrub out CO, hydrocarbons, NO2 and particulates. Tunnel tests showed these air impurities were adequately removed.
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- 1976
35. Application of cusums to ambulatory blood pressure data: a simple statistical technique for detecting trends over time
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O'Brien E, Perry I, Sheridan J, Neil Atkins, and O'Malley K
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Reference Values ,Statistics as Topic ,Humans ,Blood Pressure ,Blood Pressure Monitors ,Circadian Rhythm ,Monitoring, Physiologic - Published
- 1989
36. Études de conjugaison et d'hyperconjugaison dans quelques molécules par la spectroscopie ultrahertzienne
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Thomas, L.F., Heeks, J.S., and Sheridan, J.
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- 1957
- Full Text
- View/download PDF
37. Études récentes de structure de quelques molécules simples par la spectroscopie ultrahertzienne
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Sheridan, J., Cox, A.P., and Tyler, J.K.
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- 1960
- Full Text
- View/download PDF
38. Gems of New Zealand Primary Health Care Research: Pharmacists' perceptions of roles and accreditation
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Jeff Harrison, Scahill, S., and Sheridan, J.
39. Characteristics of flow over a double backward-facing step
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Wang, S., David Burton, Sheridan, J., and Thompson, M. C.
40. Separation of yawed turbulent flows over a forward-facing ramp
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Xie, D. F., Hugh Blackburn, and Sheridan, J.
41. Decide rationale/design: daclizumab high yield process monotherapy in relapsing remitting multiple sclerosis (RRMS)
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Kappos, L., Wiendl, H., Kaufman, M., Rose, J., Havrdova, E., Boyko, A., Eraksoy, M., Sheridan, J., Elkins, J., and O Neil, G.
42. Comparison of fluid forces and wake modes between free vibration and tracking motion of a circular cylinder
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Zhao, J., Nemes, A., David Lo Jacono, and Sheridan, J.
43. Generation, evolution and breakdown of helical vortex wakes
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Nemes, A., Sherry, M., David Lo Jacono, Blackburn, H. M., and Sheridan, J.
44. A phase-averaged analysis of the pedalling cyclist wake
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Crouch, T. N., Burton, D., Thompson, M. C., Martin, D. T., Nicholas Brown, and Sheridan, J.
45. Control of scabies, skin sores and haematuria in children in the Solomon Islands: another role for ivermectin
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Lawrence, G., Leafasia, J., Sheridan, J., Hills, S., Wate, J., Wate, C., Montgomery, J., Nirmala Pandeya, and Purdie, D.
46. Social stress induces glucocorticoid resistance in macrophages
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Stark, J. L., Ronit Avitsur, Padgett, D. A., Campbell, K. A., Beck, F. M., and Sheridan, J. F.
47. Embedding fiber-optic strain sensors using ultrasonic additive manufacturing
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Christian Petrie, Sridharan, N., Hehr, A., Norfolk, M., and Sheridan, J.
48. Flow separation characterisation of a forward facing step immersed in a turbulent boundary layer
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Sherry, M. J., Jacono, D. L., Sheridan, J., Mathis, R., and Ivan Marusic
49. Holographic photopolymer materials with non-local and non-linear responses
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Kelly, J. V., O Neill, F. T., Sheridan, J. T., Neipp, C., Sergi Gallego, and Ortuno, M.
50. Vortex-induced vibration of a transversely rotating sphere
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Sareen, A., Zhao, J., Lo Jacono, D., Sheridan, J., Kerry Hourigan, Thompson, M. C., Centre National de la Recherche Scientifique - CNRS (FRANCE), Institut National Polytechnique de Toulouse - Toulouse INP (FRANCE), Université Toulouse III - Paul Sabatier - UT3 (FRANCE), Monash University (AUSTRALIA), and Institut de Mécanique des Fluides de Toulouse - IMFT (Toulouse, France)
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Mécanique des fluides ,Fluid-structure interaction ,Vortex ,VIV - Abstract
Vortex-induced vibration (VIV) of a sphere is one of the most basic fluid-structure interaction problems. Since such vibrations can lead to fatal structural failures, numerous studies have focused on suppressing such flow-induced vibrations. In this study, for the first time, the effect of an imposed transverse rotation on the dynamics of the VIV of an elastically mounted sphere has been investigated. It was observed that the non-dimensional vibration amplitude for a rotating sphere (A∗ = √2yrms/D, where yrms is the root mean square of the displacement in the transverse direction and D = sphere diameter) exhibits a bell-shaped evolution as a function of reduced velocity, similar to the classic VIV response of a non-rotating sphere. The sphere is found to oscillate freely up to a rotation ratio α (ratio of the equatorial velocity of the sphere to the free-stream velocity) close to 0.5. For lower rotation ratios (α ≤ 0.3), the response looks similar to the non-rotating case but with slightly smaller vibration amplitude. For higher α values, the amplitude was found to decrease significantly with the rotation up to α = 0.5. The amplitude dropped drastically after it reached the peak amplitude. This is unlike the VIV response of a rotating circular cylinder where the vibration amplitude increases up to three times the maximum vibration amplitude in the non- rotating case due to a novel asymmetric wake pattern (see [1])
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