114 research outputs found
Flavonoid Actions on Receptors for the Inhibitory Neurotransmitter GABA
- Publication venue
- 'IntechOpen'
- Publication date
- 23/08/2017
- Field of study
Flavonoids, both naturally occurring and synthetic, are known to have multiple effects on the activation of ionotropic receptors for Îł-aminobutyric acid (GABA), the major inhibitory neurotransmitter in our brains. They can act as positive or negative allosteric modulators, enhancing or reducing the effect of GABA. They can elicit a direct activation of the receptors. They can also act to modulate the action of other modulators. This ability to influence function via their actions on GABA receptors permits a range of effects of flavonoids, including relief of anxiety, anticonvulsant, analgesic and sedative actions
GABA-enriched Oolong Tea: Reducing Stress in a Student Cohort May Involve More than Just GABA
- Author
- Publication venue
- 'IntechOpen'
- Publication date
- 10/10/2022
- Field of study
We have previously shown that the consumption of GABA-enriched oolong tea is effective in reducing stress in a student cohort. However, key constituent content has not been previously investigated, especially as applied to a standard cup of tea. Further, it has not been substantiated whether it is the suggested GABA content or other constituents that lead to these observed changes in stress behaviour. Using reverse-phase HPLC, we determined the actual content of four chemicals known to influence stress in 200 mL cups of regular or GABA-enriched oolong tea brewed to manufacturerâs instructions. We found eight times as much Îł-aminobutyric acid (GABA) and 1.5 times as much caffeine in GABA-enriched oolong tea as in regular oolong tea. In contrast, there was 10 times less epigallocatechin gallate (EGCG), and half as much theanine in the GABA-enriched tea. Thus, there are changes in multiple constituents in GABA-enriched oolong tea that may contribute to the biological effects we observed in students consuming these teas
GABAA Receptors Containing Ï1 Subunits Contribute to In Vivo Effects of Ethanol in Mice
- Author
- Publication venue
- 'Public Library of Science (PLoS)'
- Publication date
- 01/01/2014
- Field of study
Yuri A. Blednov, Jillian M. Benavidez, Mendy Black, Courtney R. Leiter, Elizabeth Osterndorff-Kahanek, David Johnson, Cecilia M. Borghese, R. Adron Harris, Waggoner Center for Alcohol and Addiction Research, The University of Texas at Austin, Austin, Texas, United States of AmericaJane R. Hanrahan, Mary Chebib, Faculty of Pharmacy, The University of Sydney, Sydney NSW, AustraliaGraham A. R. Johnston, Department of Pharmacology, The University of Sydney, Sydney NSW, AustraliaGABAA receptors consisting of Ï1, Ï2, or Ï3 subunits in homo- or hetero-pentamers have been studied mainly in retina but are detected in many brain regions. Receptors formed from Ï1 are inhibited by low ethanol concentrations, and family-based association analyses have linked Ï subunit genes with alcohol dependence. We determined if genetic deletion of Ï1 in mice altered in vivo ethanol effects. Null mutant male mice showed reduced ethanol consumption and preference in a two-bottle choice test with no differences in preference for saccharin or quinine. Null mutant mice of both sexes demonstrated longer duration of ethanol-induced loss of righting reflex (LORR), and males were more sensitive to ethanol-induced motor sedation. In contrast, Ï1 null mice showed faster recovery from acute motor incoordination produced by ethanol. Null mutant females were less sensitive to ethanol-induced development of conditioned taste aversion. Measurement of mRNA levels in cerebellum showed that deletion of Ï1 did not change expression of Ï2, α2, or α6 GABAA receptor subunits. (S)-4-amino-cyclopent-1-enyl butylphosphinic acid (âÏ1â antagonist), when administered to wild type mice, mimicked the changes that ethanol induced in Ï1 null mice (LORR and rotarod tests), but the Ï1 antagonist did not produce these effects in Ï1 null mice. In contrast, (R)-4-amino-cyclopent-1-enyl butylphosphinic acid (âÏ2â antagonist) did not change ethanol actions in wild type but produced effects in mice lacking Ï1 that were opposite of the effects of deleting (or inhibiting) Ï1. These results suggest that Ï1 has a predominant role in two in vivo effects of ethanol, and a role for Ï2 may be revealed when Ï1 is deleted. We also found that ethanol produces similar inhibition of function of recombinant Ï1 and Ï2 receptors. These data indicate that ethanol action on GABAA receptors containing Ï1/Ï2 subunits may be important for specific effects of ethanol in vivo.This work was supported by NIH grants AA013520 and AA06399. The funders had no role in study design, data collection and analysis, decision to publish, or preparation of the manuscript.Waggoner Center for Alcohol and Addiction ResearchEmail: [email protected]
Overview of the JET results in support to ITER
- Author
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- ĆaszyĆska E.
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- Publication venue
- International Atomic Energy Agency
- Publication date
- 10/01/2018
- Field of study
Multiorgan MRI findings after hospitalisation with COVID-19 in the UK (C-MORE): a prospective, multicentre, observational cohort study
- Author
- Abel K
- Adamali H.
- Adeloye D
- Adeyemi Oluwaseun
- Adrego Rita
- Aguilar Jimenez Laura A.
- Ahmad Haider N
- Ahmad Shanaz
- Ahmed R
- Ahwireng Nyarko
- Ainsworth Mark
- Al-Sheklly B.
- Alamoudi Asma
- Alfaro-Almagro Fidel
- Ali Mariam
- Aljaroof M
- Allan L
- Allen R J
- Allerton Lisa
- Allsop Lynne
- Allt Ann Marie
- Almeida Paula
- Altmann Danny
- Alvarez Corral Maria
- Amoils S.
- Anderson David
- Antoniades C
- Arbane Gill
- Arias Ava Maria
- Armour C.
- Armstrong Lisa
- Armstrong Natalie
- Arnold David
- Arnold H
- Ashish A
- Ashworth Andrew
- Ashworth M
- Aslani S
- Assefa-Kebede Hosanna
- Atkin C
- Atkin Paul
- Aul Raminder
- Aung H
- Austin Liam
- Avram Cristina
- Ayoub A.
- Babores M.
- Baggott R
- Bagshaw J
- Baguley D
- Bailey L
- Baillie J.K.
- Bain S
- Bakali M
- Bakau M
- Baldry E
- Baldwin D
- Baldwin M
- Ballard C
- Bandula Steven
- Banerjee A
- Bang Dongchun
- Barker R E
- Barman L
- Barratt Shaney
- Barrett Fiona
- Basire Donna
- Basu N.
- Bates A
- Bates M
- Batterham R
- Baxendale H
- Bayes Hannah
- Beadsworth M.
- Beckett P
- Beggs Mark
- Begum M
- Beirne Paul
- Bell Murdina
- Bell R
- Bennett Kaytie
- Beranova Eva
- Bermperi Areti
- Berridge Anthony
- Berry C.
- Betts Sarah
- Bevan Emily
- Bhui K
- Bingham Michelle
- Birchall K
- Bishop L.
- Bisnauthsing Karen
- Blaikely J.
- Bloss Angela
- Bolger A.
- Bolton Charlotte E.
- Bonnington J.
- Botkai A
- Bourne Charlotte
- Bourne Michelle
- Bramham K.
- Brear Lucy
- Breen G
- Breeze Jonathon
- Briggs A.
- Bright E
- Brightling Christopher E
- Brill Simon
- Brindle K
- Broad Lauren
- Broadley A
- Brookes C
- Broome M
- Brown Ammani
- Brown Angela
- Brown J.
- Brown Jeremy S
- Brown Jo
- Brown M.
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- Brunskill Nigel
- Buch M.
- Buckley Phil
- Bularga A.
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- Burdett Tracy
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- Card Bethany
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- Carr Liesel
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- Carter Penny
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- Cassar Mark P.
- Cavanagh J
- Chablani Manish
- Chalder Trudie
- Chalmers James D.
- Chambers R C
- Chan Flora
- Channon K M
- Chapman Kerry
- Charalambou A
- Chaudhuri N
- Checkley A
- Chen Jin
- Cheng Yutung
- Chetham Luke
- Childs C
- Chilvers Edwin R
- Chinoy H
- Chiribiri Amedeo
- Chong-James K.
- Choudhury Gourab
- Choudhury N.
- Chowienczyk P
- Christie C
- Chrystal Melanie
- Clark Cameron
- Clark D
- Clarke Jude
- Clohisey S.
- Coakley G.
- Coburn Zach
- Coetzee S.
- Cole Joby
- Coleman C
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- Connell David
- Connolly B.
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- Coulding Martina
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- Cox Eleanor
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- Cristiano Daniele
- Crooks M.G.
- Cross Andy
- Cruz Isabel
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- Cuthbertson Dan J
- Daines L
- Dalton Matthhew
- Daly Patrick
- Daniels Alison
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- Davies Ellie
- Davies Ffyon
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- Edwards Sarah
- Edwardson C
- El-Taweel Hosni
- Elliott Anne
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- Ellis Y.
- Elmer Anne
- Elneima Omer
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- Evans Ranuromanana I.
- Evans Teriann
- Evenden Cerys
- Evison Lynsey
- Fabbri L
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- Goodwin Camelia
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- Gummadi Mahitha
- Gupta Ayushman
- Gurram Sambasivarao
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- Hainey Kera
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- Hall I
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- Hutchinson John
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- Ismail K.
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- Jarman Claire
- Jarrold I.
- Jarvis Hannah
- Jastrub Roman
- Jayaraman Bhagy
- Jenkins R Gisli
- Jezzard Peter
- Jiwa Kasim
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- Jones Mark G
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- Kaltsakas G.
- Kamwa V
- Kanellakis N.
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- Kausar Zunaira
- Keenan Natalie
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- Kelly S.
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- Kerr Steven
- Kerslake Helen
- Key Angela L.
- Khan F
- Khunti Kamlesh
- Kilroy Susan
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- Klenerman P
- Knibbs Lucy
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- Korszun A.
- Koychev Ivan
- Kurasz Claire
- Kurupati Prathiba
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- Lamlum Hanan
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- Langenberg C
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- Lawrie Allan
- Lawson C
- Lawson Cathy
- Layton Alison
- Lea A
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- Leitch Karen
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- Light Tessa
- Lightstone L.
- Lilaonitkul W
- Lim Lai
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- Lloyd Arwel
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- Lone Nazir I.
- Loosley Ronda
- Lord J M
- Lota Harpreet
- Lovegrove Wayne
- Lucey Alice
- Lukaschuk Elena
- Lye Alison
- Lynch Ceri
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- MacGowan G.
- Macharia Irene
- Mackie J
- Macliver L.
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- Madzamba Gladys
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- Magtoto Murphy M.
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- Malein Flora
- Malim M.
- Mallison Georgia
- Man William D-C.
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- Mariveles Myril
- Marks Michael
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- Marsh Sophie
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- Megson Clare
- Megson Sharon
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- Menzies Daniel
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- Munawar Unber
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- Wynter Inez
- Xie Cheng
- Xu M
- Yasmin Najira
- Yasmin S
- Yates Tom
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- Young B.
- Young Susan
- Yousuf A J
- Zawia Amira
- Zeidan Lisa
- Zhao Bang
- Zheng Bang
- Zongo O.
- Publication venue
- Elsevier
- Publication date
- 22/09/2023
- Field of study
Introduction:
The multiorgan impact of moderate to severe coronavirus infections in the post-acute phase is still poorly understood. We aimed to evaluate the excess burden of multiorgan abnormalities after hospitalisation with COVID-19, evaluate their determinants, and explore associations with patient-related outcome measures.
Methods:
In a prospective, UK-wide, multicentre MRI follow-up study (C-MORE), adults (aged â„18 years) discharged from hospital following COVID-19 who were included in Tier 2 of the Post-hospitalisation COVID-19 study (PHOSP-COVID) and contemporary controls with no evidence of previous COVID-19 (SARS-CoV-2 nucleocapsid antibody negative) underwent multiorgan MRI (lungs, heart, brain, liver, and kidneys) with quantitative and qualitative assessment of images and clinical adjudication when relevant. Individuals with end-stage renal failure or contraindications to MRI were excluded. Participants also underwent detailed recording of symptoms, and physiological and biochemical tests. The primary outcome was the excess burden of multiorgan abnormalities (two or more organs) relative to controls, with further adjustments for potential confounders. The C-MORE study is ongoing and is registered with ClinicalTrials.gov, NCT04510025.
Findings:
Of 2710 participants in Tier 2 of PHOSP-COVID, 531 were recruited across 13 UK-wide C-MORE sites. After exclusions, 259 C-MORE patients (mean age 57 years [SD 12]; 158 [61%] male and 101 [39%] female) who were discharged from hospital with PCR-confirmed or clinically diagnosed COVID-19 between March 1, 2020, and Nov 1, 2021, and 52 non-COVID-19 controls from the community (mean age 49 years [SD 14]; 30 [58%] male and 22 [42%] female) were included in the analysis. Patients were assessed at a median of 5·0 months (IQR 4·2â6·3) after hospital discharge. Compared with non-COVID-19 controls, patients were older, living with more obesity, and had more comorbidities. Multiorgan abnormalities on MRI were more frequent in patients than in controls (157 [61%] of 259 vs 14 [27%] of 52; p<0·0001) and independently associated with COVID-19 status (odds ratio [OR] 2·9 [95% CI 1·5â5·8]; padjusted=0·0023) after adjusting for relevant confounders. Compared with controls, patients were more likely to have MRI evidence of lung abnormalities (p=0·0001; parenchymal abnormalities), brain abnormalities (p<0·0001; more white matter hyperintensities and regional brain volume reduction), and kidney abnormalities (p=0·014; lower medullary T1 and loss of corticomedullary differentiation), whereas cardiac and liver MRI abnormalities were similar between patients and controls. Patients with multiorgan abnormalities were older (difference in mean age 7 years [95% CI 4â10]; mean age of 59·8 years [SD 11·7] with multiorgan abnormalities vs mean age of 52·8 years [11·9] without multiorgan abnormalities; p<0·0001), more likely to have three or more comorbidities (OR 2·47 [1·32â4·82]; padjusted=0·0059), and more likely to have a more severe acute infection (acute CRP >5mg/L, OR 3·55 [1·23â11·88]; padjusted=0·025) than those without multiorgan abnormalities. Presence of lung MRI abnormalities was associated with a two-fold higher risk of chest tightness, and multiorgan MRI abnormalities were associated with severe and very severe persistent physical and mental health impairment (PHOSP-COVID symptom clusters) after hospitalisation.
Interpretation:
After hospitalisation for COVID-19, people are at risk of multiorgan abnormalities in the medium term. Our findings emphasise the need for proactive multidisciplinary care pathways, with the potential for imaging to guide surveillance frequency and therapeutic stratification
Search for gravitational-wave transients associated with magnetar bursts in advanced LIGO and advanced Virgo data from the third observing run
- Author
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- Yang Yang
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- Yeeles D.W
- Yeh S.-W
- Yelikar A.B
- Ying M
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- Yokozawa T
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- Yoshioka T
- Yu Hang
- Yu Haocun
- Yuzurihara H
- ZadroĆŒny A
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- Zhu Z.-H
- Zucker M.E
- Zweizig J
- Publication venue
- American Astronomical Society
- Publication date
- 01/01/2024
- Field of study
Gravitational waves are expected to be produced from neutron star oscillations associated with magnetar giant f lares and short bursts. We present the results of a search for short-duration (milliseconds to seconds) and longduration (âŒ100 s) transient gravitational waves from 13 magnetar short bursts observed during Advanced LIGO, Advanced Virgo, and KAGRAâs third observation run. These 13 bursts come from two magnetars, SGR1935 +2154 and SwiftJ1818.0â1607. We also include three other electromagnetic burst events detected by FermiGBM which were identified as likely coming from one or more magnetars, but they have no association with a known magnetar. No magnetar giant flares were detected during the analysis period. We find no evidence of gravitational waves associated with any of these 16 bursts. We place upper limits on the rms of the integrated incident gravitational-wave strain that reach 3.6 Ă 10âÂČÂł Hz at 100 Hz for the short-duration search and 1.1 Ă10âÂČÂČ Hz at 450 Hz for the long-duration search. For a ringdown signal at 1590 Hz targeted by the short-duration search the limit is set to 2.3 Ă 10âÂČÂČ Hz. Using the estimated distance to each magnetar, we derive upper limits upper limits on the emitted gravitational-wave energy of 1.5 Ă 1044 erg (1.0 Ă 1044 erg) for SGR 1935+2154 and 9.4 Ă 10^43 erg (1.3 Ă 1044 erg) for Swift J1818.0â1607, for the short-duration (long-duration) search. Assuming isotropic emission of electromagnetic radiation of the burst ïŹuences, we constrain the ratio of gravitational-wave energy to electromagnetic energy for bursts from SGR 1935+2154 with the available ïŹuence information. The lowest of these ratios is 4.5 Ă 103
A joint Fermi-GBM and Swift-BAT analysis of gravitational-wave candidates from the third gravitational-wave observing run
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- Abbott R.
- Abe H.
- Acernese F.
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- Zweizig J.
- Publication venue
- American Astronomical Society
- Publication date
- 01/04/2024
- Field of study
We present Fermi Gamma-ray Burst Monitor (Fermi-GBM) and Swift Burst Alert Telescope (Swift-BAT) searches for gamma-ray/X-ray counterparts to gravitational-wave (GW) candidate events identified during the third observing run of the Advanced LIGO and Advanced Virgo detectors. Using Fermi-GBM onboard triggers and subthreshold gamma-ray burst (GRB) candidates found in the Fermi-GBM ground analyses, the Targeted Search and the Untargeted Search, we investigate whether there are any coincident GRBs associated with the GWs. We also search the Swift-BAT rate data around the GW times to determine whether a GRB counterpart is present. No counterparts are found. Using both the Fermi-GBM Targeted Search and the Swift-BAT search, we calculate flux upper limits and present joint upper limits on the gamma-ray luminosity of each GW. Given these limits, we constrain theoretical models for the emission of gamma rays from binary black hole mergers
Constraints on the cosmic expansion history from GWTCâ3
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- Zucker M.E.
- Zweizig J.
- Publication venue
- 'American Astronomical Society'
- Publication date
- 01/06/2023
- Field of study
We use 47 gravitational wave sources from the Third LIGOâVirgoâKamioka Gravitational Wave Detector Gravitational Wave Transient Catalog (GWTCâ3) to estimate the Hubble parameter H(z), including its current value, the Hubble constant H0. Each gravitational wave (GW) signal provides the luminosity distance to the source, and we estimate the corresponding redshift using two methods: the redshifted masses and a galaxy catalog. Using the binary black hole (BBH) redshifted masses, we simultaneously infer the source mass distribution and H(z). The source mass distribution displays a peak around 34 Mâ, followed by a drop-off. Assuming this mass scale does not evolve with the redshift results in a H(z) measurement, yielding H0â=68â8+12âkm  sâ1Mpcâ1 (68% credible interval) when combined with the H0 measurement from GW170817 and its electromagnetic counterpart. This represents an improvement of 17% with respect to the H0 estimate from GWTCâ1. The second method associates each GW event with its probable host galaxy in the catalog GLADE+, statistically marginalizing over the redshifts of each event's potential hosts. Assuming a fixed BBH population, we estimate a value of H0â=68â6+8âkm  sâ1Mpcâ1 with the galaxy catalog method, an improvement of 42% with respect to our GWTCâ1 result and 20% with respect to recent H0 studies using GWTCâ2 events. However, we show that this result is strongly impacted by assumptions about the BBH source mass distribution; the only event which is not strongly impacted by such assumptions (and is thus informative about H0) is the well-localized event GW190814
Open data from the third observing run of LIGO, Virgo, KAGRA, and GEO
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- Publication venue
- American Astronomical Society
- Publication date
- 01/01/2023
- Field of study
The global network of gravitational-wave observatories now includes five detectors, namely LIGO Hanford, LIGO Livingston, Virgo, KAGRA, and GEO 600. These detectors collected data during their third observing run, O3, composed of three phases: O3a starting in 2019 April and lasting six months, O3b starting in 2019 November and lasting five months, and O3GK starting in 2020 April and lasting two weeks. In this paper we describe these data and various other science products that can be freely accessed through the Gravitational Wave Open Science Center at https://gwosc.org. The main data set, consisting of the gravitational-wave strain time series that contains the astrophysical signals, is released together with supporting data useful for their analysis and documentation, tutorials, as well as analysis software packages
Search for eccentric black hole coalescences during the third observing run of LIGO and Virgo
- Author
- Abac A.G.
- Abbott R.
- Abe H.
- Acernese F.
- Ackley K.
- Adamcewicz C.
- Adhicary S.
- Adhikari N.
- Adhikari R.X.
- Adkins V.K.
- Adya V.B.
- Affeldt C.
- Agarwal D.
- Agathos M.
- Aguiar O.D.
- Aguilar I.
- Aiello L.
- Ain A.
- Ajith P.
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- Al-Jodah A.
- Albanesi S.
- Alfaidi R.A.
- Allocca A.
- Alléné C.
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- Arellano F.E.P.
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- Assiduo M.
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- Yeung T.Y.
- Yokoyama J.
- Yokozawa T.
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- Yuzurihara H.
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- Zweizig J.
- Ălvarez-LĂłpez S.
- Publication venue
- American Astronomical Society
- Publication date
- 01/10/2024
- Field of study
Despite the growing number of binary black hole coalescences confidently observed through gravitational waves so far, the astrophysical origin of these binaries remains uncertain. Orbital eccentricity is one of the clearest tracers of binary formation channels. Identifying binary eccentricity, however, remains challenging due to the limited availability of gravitational waveforms that include the effects of eccentricity. Here, we present observational results for a waveform-independent search sensitive to eccentric black hole coalescences, covering the third observing run (O3) of the LIGO and Virgo detectors. We identified no new high-significance candidates beyond those that have already been identified with searches focusing on quasi-circular binaries. We determine the sensitivity of our search to high-mass (total source-frame mass M > 70 Mâ) binaries covering eccentricities up to 0.3 at 15 Hz emitted gravitational-wave frequency, and use this to compare model predictions to search results. Assuming all detections are indeed quasi-circular, for our fiducial population model, we place a conservative upper limit for the merger rate density of high-mass binaries with eccentricities 0 < e †0.3 at 16.9 Gpcâ3 yrâ1 at the 90% confidence level
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