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  • 1
    Publication Date: 2016-03-19
    Description: Systemic inflammation, which results from the massive release of proinflammatory molecules into the circulatory system, is a major risk factor for severe illness, but the precise mechanisms underlying its control are not fully understood. We observed that prostaglandin E2 (PGE2), through its receptor EP4, is down-regulated in human systemic inflammatory disease. Mice with reduced PGE2 synthesis develop systemic inflammation, associated with translocation of gut bacteria, which can be prevented by treatment with EP4 agonists. Mechanistically, we demonstrate that PGE2-EP4 signaling acts directly on type 3 innate lymphoid cells (ILCs), promoting their homeostasis and driving them to produce interleukin-22 (IL-22). Disruption of the ILC-IL-22 axis impairs PGE2-mediated inhibition of systemic inflammation. Hence, the ILC-IL-22 axis is essential in protecting against gut barrier dysfunction, enabling PGE2-EP4 signaling to impede systemic inflammation.〈br /〉〈br /〉〈a href="https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4841390/" target="_blank"〉〈img src="https://static.pubmed.gov/portal/portal3rc.fcgi/4089621/img/3977009" border="0"〉〈/a〉   〈a href="https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4841390/" target="_blank"〉This paper as free author manuscript - peer-reviewed and accepted for publication〈/a〉〈br /〉〈br /〉〈span class="detail_caption"〉Notes: 〈/span〉Duffin, Rodger -- O'Connor, Richard A -- Crittenden, Siobhan -- Forster, Thorsten -- Yu, Cunjing -- Zheng, Xiaozhong -- Smyth, Danielle -- Robb, Calum T -- Rossi, Fiona -- Skouras, Christos -- Tang, Shaohui -- Richards, James -- Pellicoro, Antonella -- Weller, Richard B -- Breyer, Richard M -- Mole, Damian J -- Iredale, John P -- Anderton, Stephen M -- Narumiya, Shuh -- Maizels, Rick M -- Ghazal, Peter -- Howie, Sarah E -- Rossi, Adriano G -- Yao, Chengcan -- 106122/Wellcome Trust/United Kingdom -- BB/K091121/1/Biotechnology and Biological Sciences Research Council/United Kingdom -- DK37097/DK/NIDDK NIH HHS/ -- Medical Research Council/United Kingdom -- New York, N.Y. -- Science. 2016 Mar 18;351(6279):1333-8. doi: 10.1126/science.aad9903.〈br /〉〈span class="detail_caption"〉Author address: 〈/span〉Medical Research Council (MRC) Centre for Inflammation Research, Queen's Medical Research Institute, The University of Edinburgh, Edinburgh EH16 4TJ, UK. ; Division of Pathway Medicine, Edinburgh Infectious Diseases, The University of Edinburgh, Edinburgh EH16 4SB, UK. ; Institute for Immunology and Infection Research, The University of Edinburgh, Edinburgh EH9 3JT, UK. ; MRC Centre for Regenerative Medicine, The University of Edinburgh, Edinburgh EH16 4UU, UK. ; Department of Gastroenterology, First Affiliated Hospital of Jinan University, Guangzhou 510630, China. ; Department of Veterans Affairs, Tennessee Valley Health Authority, Nashville, TN 37212, USA. Department of Medicine, Vanderbilt University Medical Center, Nashville, TN 37232, USA. ; Center for Innovation in Immunoregulative Technology and Therapeutics (AK Project), Kyoto University Graduate School of Medicine, Kyoto 606-8501, Japan. Core Research for Evolutional Science and Technology (CREST), Japan Science and Technology Agency (JST), Tokyo 102-0075, Japan. ; Division of Pathway Medicine, Edinburgh Infectious Diseases, The University of Edinburgh, Edinburgh EH16 4SB, UK. Centre for Synthetic and Systems Biology (SynthSys), The University of Edinburgh, Edinburgh EH9 3JD, UK. ; Medical Research Council (MRC) Centre for Inflammation Research, Queen's Medical Research Institute, The University of Edinburgh, Edinburgh EH16 4TJ, UK. chengcan.yao@ed.ac.uk.〈br /〉〈span class="detail_caption"〉Record origin:〈/span〉 〈a href="http://www.ncbi.nlm.nih.gov/pubmed/26989254" target="_blank"〉PubMed〈/a〉
    Keywords: Animals ; Bacterial Infections/genetics/immunology ; Dinoprostone/*immunology ; Gene Expression ; Humans ; Immunity, Innate ; Inflammation/drug therapy/*immunology/microbiology ; Interleukins/*immunology ; Intestines/*immunology/microbiology ; Lymphocytes/*immunology ; Mice ; Receptors, Prostaglandin E, EP4 Subtype/antagonists & ; inhibitors/genetics/*immunology ; Signal Transduction
    Print ISSN: 0036-8075
    Electronic ISSN: 1095-9203
    Topics: Biology , Chemistry and Pharmacology , Computer Science , Medicine , Natural Sciences in General , Physics
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  • 2
    Publication Date: 2015-11-26
    Description: Skeletal growth relies on both biosynthetic and catabolic processes. While the role of the former is clearly established, how the latter contributes to growth-promoting pathways is less understood. Macroautophagy, hereafter referred to as autophagy, is a catabolic process that plays a fundamental part in tissue homeostasis. We investigated the role of autophagy during bone growth, which is mediated by chondrocyte rate of proliferation, hypertrophic differentiation and extracellular matrix (ECM) deposition in growth plates. Here we show that autophagy is induced in growth-plate chondrocytes during post-natal development and regulates the secretion of type II collagen (Col2), the major component of cartilage ECM. Mice lacking the autophagy related gene 7 (Atg7) in chondrocytes experience endoplasmic reticulum storage of type II procollagen (PC2) and defective formation of the Col2 fibrillary network in the ECM. Surprisingly, post-natal induction of chondrocyte autophagy is mediated by the growth factor FGF18 through FGFR4 and JNK-dependent activation of the autophagy initiation complex VPS34-beclin-1. Autophagy is completely suppressed in growth plates from Fgf18(-/-) embryos, while Fgf18(+/-) heterozygous and Fgfr4(-/-) mice fail to induce autophagy during post-natal development and show decreased Col2 levels in the growth plate. Strikingly, the Fgf18(+/-) and Fgfr4(-/-) phenotypes can be rescued in vivo by pharmacological activation of autophagy, pointing to autophagy as a novel effector of FGF signalling in bone. These data demonstrate that autophagy is a developmentally regulated process necessary for bone growth, and identify FGF signalling as a crucial regulator of autophagy in chondrocytes.〈br /〉〈span class="detail_caption"〉Notes: 〈/span〉Cinque, Laura -- Forrester, Alison -- Bartolomeo, Rosa -- Svelto, Maria -- Venditti, Rossella -- Montefusco, Sandro -- Polishchuk, Elena -- Nusco, Edoardo -- Rossi, Antonio -- Medina, Diego L -- Polishchuk, Roman -- De Matteis, Maria Antonietta -- Settembre, Carmine -- England -- Nature. 2015 Dec 10;528(7581):272-5. doi: 10.1038/nature16063. Epub 2015 Nov 23.〈br /〉〈span class="detail_caption"〉Author address: 〈/span〉Telethon Institute of Genetics and Medicine (TIGEM), Via Campi Flegrei, 34, 80078 Pozzuoli (NA), Italy. ; Dulbecco Telethon Institute, Via Campi Flegrei, 34, 80078 Pozzuoli (NA), Italy. ; Medical Genetics Unit, Department of Medical and Translational Science, Federico II University, Via Pansini 5, 80131 Naples, Italy. ; Department of Molecular Medicine, Biochemistry Unit, University of Pavia, 27100 Pavia, Italy.〈br /〉〈span class="detail_caption"〉Record origin:〈/span〉 〈a href="http://www.ncbi.nlm.nih.gov/pubmed/26595272" target="_blank"〉PubMed〈/a〉
    Keywords: Animals ; Autophagy/genetics/*physiology ; Bone Development/genetics/*physiology ; Cell Differentiation ; Cell Proliferation ; Cells, Cultured ; Chondrocytes/cytology/metabolism ; Collagen Type II/secretion ; Embryo, Mammalian ; Extracellular Matrix/genetics ; Fibroblast Growth Factors/*genetics/metabolism ; Growth Plate/cytology/metabolism ; MAP Kinase Signaling System ; Mice ; Microtubule-Associated Proteins/genetics/metabolism ; Receptor, Fibroblast Growth Factor, Type 4/genetics/metabolism ; *Signal Transduction
    Print ISSN: 0028-0836
    Electronic ISSN: 1476-4687
    Topics: Biology , Chemistry and Pharmacology , Medicine , Natural Sciences in General , Physics
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  • 3
    Publication Date: 2015-03-04
    Description: Inflammation promotes regeneration of injured tissues through poorly understood mechanisms, some of which involve interleukin (IL)-6 family members, the expression of which is elevated in many diseases including inflammatory bowel diseases and colorectal cancer. Here we show in mice and human cells that gp130, a co-receptor for IL-6 cytokines, triggers activation of YAP and Notch, transcriptional regulators that control tissue growth and regeneration, independently of the gp130 effector STAT3. Through YAP and Notch, intestinal gp130 signalling stimulates epithelial cell proliferation, causes aberrant differentiation and confers resistance to mucosal erosion. gp130 associates with the related tyrosine kinases Src and Yes, which are activated on receptor engagement to phosphorylate YAP and induce its stabilization and nuclear translocation. This signalling module is strongly activated upon mucosal injury to promote healing and maintain barrier function.〈br /〉〈br /〉〈a href="https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4447318/" target="_blank"〉〈img src="https://static.pubmed.gov/portal/portal3rc.fcgi/4089621/img/3977009" border="0"〉〈/a〉   〈a href="https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4447318/" target="_blank"〉This paper as free author manuscript - peer-reviewed and accepted for publication〈/a〉〈br /〉〈br /〉〈span class="detail_caption"〉Notes: 〈/span〉Taniguchi, Koji -- Wu, Li-Wha -- Grivennikov, Sergei I -- de Jong, Petrus R -- Lian, Ian -- Yu, Fa-Xing -- Wang, Kepeng -- Ho, Samuel B -- Boland, Brigid S -- Chang, John T -- Sandborn, William J -- Hardiman, Gary -- Raz, Eyal -- Maehara, Yoshihiko -- Yoshimura, Akihiko -- Zucman-Rossi, Jessica -- Guan, Kun-Liang -- Karin, Michael -- CA118165-09/CA/NCI NIH HHS/ -- CA132809/CA/NCI NIH HHS/ -- DP2 OD008469/OD/NIH HHS/ -- EY022611/EY/NEI NIH HHS/ -- R00 DK088589/DK/NIDDK NIH HHS/ -- R01 CA118165/CA/NCI NIH HHS/ -- England -- Nature. 2015 Mar 5;519(7541):57-62. doi: 10.1038/nature14228. Epub 2015 Feb 25.〈br /〉〈span class="detail_caption"〉Author address: 〈/span〉1] Laboratory of Gene Regulation and Signal Transduction, University of California, San Diego, La Jolla, California 92093, USA [2] Departments of Pharmacology and Pathology, University of California, San Diego, La Jolla, California 92093, USA [3] Department of Surgery and Science, Graduate School of Medical Sciences, Kyushu University, Fukuoka 812-8582, Japan [4] Department of Microbiology and Immunology, Keio University School of Medicine, Tokyo 160-8582, Japan. ; 1] Laboratory of Gene Regulation and Signal Transduction, University of California, San Diego, La Jolla, California 92093, USA [2] Institute of Molecular Medicine, College of Medicine, National Cheng Kung University, Tainan 70101, Taiwan. ; 1] Laboratory of Gene Regulation and Signal Transduction, University of California, San Diego, La Jolla, California 92093, USA [2] Fox Chase Cancer Center, Cancer Prevention and Control Program, Philadelphia, Pennsylvania 19111, USA. ; Department of Medicine, University of California, San Diego, La Jolla, California 92093, USA. ; 1] Departments of Pharmacology and Pathology, University of California, San Diego, La Jolla, California 92093, USA [2] Moores Cancer Center, University of California, San Diego, La Jolla, California 92093, USA [3] Department of Biology, Lamar University, PO Box 10037, Beaumont, Texas 77710, USA. ; 1] Departments of Pharmacology and Pathology, University of California, San Diego, La Jolla, California 92093, USA [2] Moores Cancer Center, University of California, San Diego, La Jolla, California 92093, USA [3] Children's Hospital and Institutes of Biomedical Sciences, Fudan University, Shanghai 200032, China. ; Laboratory of Gene Regulation and Signal Transduction, University of California, San Diego, La Jolla, California 92093, USA. ; Department of Medicine, VA San Diego Healthcare System, San Diego, California 92161, USA. ; Inflammatory Bowel Disease Center, Division of Gastroenterology, Department of Medicine, School of Medicine, University of California, San Diego, La Jolla, California 92093, USA. ; 1] Department of Medicine, Medical University of South Carolina, Charleston, South Carolina 29425, USA [2] CSRC and BIMRC, San Diego State University, San Diego, California 92182, USA. ; Department of Surgery and Science, Graduate School of Medical Sciences, Kyushu University, Fukuoka 812-8582, Japan. ; 1] Department of Microbiology and Immunology, Keio University School of Medicine, Tokyo 160-8582, Japan [2] Japan Science and Technology Agency, CREST, Tokyo 102-0076, Japan. ; 1] Inserm, UMR 1162, Genomique fonctionnelle des tumeurs solides, IUH, Paris 75010, France [2] Universite Paris Descartes, Labex Immuno-oncology, Sorbonne Paris Cite, Faculte de Medicine, Paris 75006, France. ; 1] Departments of Pharmacology and Pathology, University of California, San Diego, La Jolla, California 92093, USA [2] Moores Cancer Center, University of California, San Diego, La Jolla, California 92093, USA. ; 1] Laboratory of Gene Regulation and Signal Transduction, University of California, San Diego, La Jolla, California 92093, USA [2] Departments of Pharmacology and Pathology, University of California, San Diego, La Jolla, California 92093, USA [3] Moores Cancer Center, University of California, San Diego, La Jolla, California 92093, USA.〈br /〉〈span class="detail_caption"〉Record origin:〈/span〉 〈a href="http://www.ncbi.nlm.nih.gov/pubmed/25731159" target="_blank"〉PubMed〈/a〉
    Keywords: Adaptor Proteins, Signal Transducing/*metabolism ; Animals ; Body Weight ; Cell Differentiation ; Cell Proliferation ; Cytokine Receptor gp130/*metabolism ; Disease Models, Animal ; Enzyme Activation ; Epithelial Cells/*cytology/metabolism/pathology ; HEK293 Cells ; Homeostasis ; Humans ; Inflammation/*metabolism/pathology ; Inflammatory Bowel Diseases/metabolism/pathology ; Intestinal Mucosa/*cytology/metabolism/pathology ; Mice ; Phosphoproteins/*metabolism ; Proto-Oncogene Proteins c-yes/metabolism ; Proto-Oncogene Proteins pp60(c-src)/*metabolism ; Receptors, Notch/metabolism ; *Regeneration ; Signal Transduction ; Up-Regulation
    Print ISSN: 0028-0836
    Electronic ISSN: 1476-4687
    Topics: Biology , Chemistry and Pharmacology , Medicine , Natural Sciences in General , Physics
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  • 4
    Publication Date: 2020-12-03
    Description: We present the first high-quality catalog of early aftershocks of the three mainshocks of the 2016 central Italy Amatrice-Visso-Norcia normal faulting sequence. We located 10,574 manually picked aftershocks with a robust probabilistic, non-linear method achieving a significant improvement in the solution accuracy and magnitude completeness with respect to previous studies. Aftershock distribution and relocated mainshocks give insight into the complex architecture of major causative and subsidiary faults, thus providing crucial constraints on multi-segment rupture models. We document reactivation and kinematic inversion of a WNW-dipping listric structure, referable to the inherited Mts Sibillini Thrust (MST) that controlled segmentation of the causative normal faults. Spatial partitioning of aftershocks evidences that the MST lateral ramp had a dual control on rupture propagation, behaving as a barrier for the Amatrice and Visso mainshocks, and later as an asperity for the Norcia mainshock. We hypothesize that the Visso mainshock re-activated also the deep part of an optimally oriented preexisting thrust. Aftershock patterns reveal that the Amatrice Mw5.4 aftershock and the Norcia mainshock ruptured two distinct antithetic faults 3-4 km apart. Therefore, our results suggest to consider both the MST cross structure and the subsidiary antithetic fault in the finite-fault source modelling of the Norcia earthquake.
    Description: Published
    Description: 6921
    Description: 4T. Sismicità dell'Italia
    Description: JCR Journal
    Keywords: 2016 Amatrice-Visso-Norcia seismic sequence (central Italy) ; high-quality catalog of early Aftershocks ; 04.06. Seismology
    Repository Name: Istituto Nazionale di Geofisica e Vulcanologia (INGV)
    Type: article
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  • 5
    Publication Date: 2018-03-23
    Description: The 24 August 2016 earthquake very heavily struck the central sector of the Apennines among the Lazio,Umbria, Marche and Abruzzi regions, devastating the town of Amatrice, the nearby villages and other localities along the Tronto valley. In this paper we present the results of the macroseismic field survey carried out using the European Macroseismic Scale (EMS) to take the heterogeneity of the building stock into account. We focused on the epicentral area, where geological conditions may also have contributed to the severity of damage. On the whole, we investigated 143 localities; the maximum intensity 10 EMS has been estimated for Amatrice, Pescara del Tronto and some villages in between. The severely damaged area (8-9 EMS) covers a strip trending broadly N-S and extending 15 km in length and 5 km in width; minor damage occurred over an area up to 35 km northward from the epicenter.
    Description: Published
    Description: 3T. Storia Sismica
    Description: 4T. Sismologia, geofisica e geologia per l'ingegneria sismica
    Description: 1IT. Reti di monitoraggio
    Description: 4IT. Banche dati
    Description: JCR Journal
    Keywords: Macroseismic survey ; EMS intensity ; Amatrice 2016 earthquake ; 04.06. Seismology ; 05.02. Data dissemination
    Repository Name: Istituto Nazionale di Geofisica e Vulcanologia (INGV)
    Type: article
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  • 6
    Publication Date: 2019-05-06
    Description: Il 24 agosto 2016 un terremoto di magnitudo 6.0 ha dato inizio ad una sequenza sismica in Italia centrale, che ha generato decine di migliaia di eventi sismicitra cui un evento Mw=6.5 il 30 ottobre. Per l’analisi elarevisione di questa sequenza si rimanda ad unauscitaspeciale del BSI previstanei primi mesi del 2019(S_BSI_CI). In questo quadrimestre,così come nel precedente e nei successivi,gli eventi nella zona della sequenza (rettangolo in mappa; lat=42.2-43.2, lon=12.4-14.1) sono quelli localizzati nella sala di sorveglianza. Solo gli eventi con M〉=3.5, e pochi altri (vedi Marchetti et al.,Annals of Geophys. DOI: 10.4401/ag-7169) sono stati rivisti.
    Description: Istituto Nazionale di Geofisica - Dipartimento di Protezione Civile
    Description: Published
    Description: 4IT. Banche dati
    Keywords: Bollettino Sismico Italiano ; gennaio–aprile 2017 ; 04.06. Seismology
    Repository Name: Istituto Nazionale di Geofisica e Vulcanologia (INGV)
    Type: report
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  • 7
    Publication Date: 2019-08-19
    Description: La sequenza sismica Amatrice-Visso-Norcia (AVN s.s. nel seguito) include il terremoto più forte avvenuto negli ultimi 30 anni in Italia ed è caratterizzata da molteplici eventi di magnitudo superiore a 5.0. La sequenza sismica è iniziata il 24 agosto 2016 con due terremoti di Mw 6.0 e Mw 5.4 nella zona di Amatrice (RI) ed è proseguita con altri due terremoti forti avvenuti il 26 ottobre, Mw 5.4 e Mw 5.9 nell’area compresa tra i comuni di Visso (MC), Castel S.Angelo sul Nera (MC), Norcia (PG) e Arquata del Tronto (AP). Il 30 ottobre si è verificato l’evento più forte della sequenza (Mw 6.5), con epicentro non lontano da Norcia, che ha colpito un vasto settore dell'Italia centrale, interessando ben quattro regioni (Umbria, Marche, Lazio e Abruzzo). Nel mese di gennaio 2017 ed in particolare il 18 gennaio quattro eventi con magnitudo maggiore o uguale a 5.0 si sono verificati nell’area meridionale della sequenza nei pressi dei paesi di Capitignano e Barete. Gli analisti del Bollettino Sismico Italiano (BSI) hanno deciso di revisionare tutta la sequenza dal 24 agosto 2016 al 31 agosto 2018 considerando solo gli eventi con magnitudo maggiore o uguale a ML=2.3 mentre, come già era stato riportato nel precedente report del BSI, i terremoti che hanno seguito immediatamente i principali eventi della sequenza: quelli del 24 agosto, del 26 e del 30 ottobre 2016 sono stati rivisti anche per magnitudo più basse. A partire dal 1 settembre 2018 gli eventi nella zona della sequenza sono stati revisionati dagli analisti del BSI a partire da ML≥1.5 come nel resto del territorio italiano.
    Description: Istituto Nazionale di Geofisica e Vulcanologia
    Description: Published
    Description: 4IT. Banche dati
    Keywords: La sequenza sismica Amatrice-Visso-Norcia ; Bollettino Sismico Italiano ; 04.06. Seismology
    Repository Name: Istituto Nazionale di Geofisica e Vulcanologia (INGV)
    Type: report
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  • 8
    Publication Date: 2018-03-20
    Description: The Italian Parametric Earthquake Catalogue (CPTI) represents the most extensive and reliable source of parameters for earthquakes in Italy and surrounding areas. Since its first introduction in 1999, CPTI benefits from the results of the 30-years-long Italian tradition in historical earthquake research that, still today, keeps on providing a wealth of studies and macroseismic data. Such data have been collected, homogenized and made available through several releases of the related macroseismic database (DBMI). In 2016, the fourth release of CPTI and DBMI, has been finalized. They provide the most advanced and updated sets of macroseismic and instrumental data and parameters, and cover the time-span 1000-2014 with earthquakes with maximum intensity I ≥ 5 or magnitude Mw ≥ 4.0. The catalogue lists 4574 events, 70% of which accompa- nied by intensity data points (about 125’000 as a whole). Macroseismic data derive from 185 studies, 54 of them are new with respect to the previous version CPTI11. Parameters related to historical earthquakes are completely re-assessed, and magnitudes from macroseismic data are derived with new intensity-to-Mw relationships. Such relationships are based on the same dataset that contributes updated instrumental magnitudes to the catalogue. Either Mw from moment tensor solutions or proxies calculated with new published conversion relationship are considered. If available, both macroseismic and instrumental parameters are provided, together with a set of “preferred ones”, which consist of a selection between the macroseismic and the instrumental epicentres, and the weighted average of the macroseismic and instrumental magnitudes.
    Description: Published
    Description: Trieste, Italy
    Description: 3T. Storia Sismica
    Description: 4T. Sismologia, geofisica e geologia per l'ingegneria sismica
    Description: 4IT. Banche dati
    Keywords: seismicity ; historical seismology ; earthquake catalogue ; seismic history ; 05.02. Data dissemination ; 04.04. Geology ; 04.06. Seismology
    Repository Name: Istituto Nazionale di Geofisica e Vulcanologia (INGV)
    Type: Abstract
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  • 9
    Publication Date: 2019-02-19
    Description: La sequenza sismica Amatrice-Visso-Norcia (AVN s.s. nel seguito) include il terremoto più forte avvenuto negli ultimi 30 anni in Italia ed è caratterizzata da molteplici eventi di magnitudo superiore a 5.0. La sequenza sismica è iniziata il 24 agosto 2016 con due terremoti di Mw 6.0 e Mw 5.4 nella zona di Amatrice (RI) ed è proseguita con altri due terremoti forti avvenuti il 26 ottobre, Mw 5.4 e Mw 5.9 nell’area compresa tra i comuni di Visso (MC), Castel S.Angelo sul Nera (MC), Norcia (PG) e Arquata del Tronto (AP). Il 30 ottobre si è verificato l’evento più forte della sequenza (Mw 6.5), con epicentro non lontano da Norcia, che ha colpito un vasto settore dell'Italia centrale, interessando ben quattro regioni (Umbria, Marche, Lazio e Abruzzo).
    Description: Istituto Nazionale di Geofisica e Vulcanologia
    Description: Unpublished
    Description: 1SR. TERREMOTI - Servizi e ricerca per la Società
    Keywords: La sequenza sismica Amatrice-Visso-Norcia ; Bollettino Sismico Italiano ; early aftershocks ; 04.06. Seismology
    Repository Name: Istituto Nazionale di Geofisica e Vulcanologia (INGV)
    Type: report
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  • 10
    Publication Date: 2019-06-18
    Description: I parametri dei terremoti registrati dalla Rete Sismica Nazionale Italiana, localizzati nelle sale di monitoraggio di Roma, Napoli e Catania, sono immediatamente disponibili sul web, alla pagina http://terremoti.ingv.it/, e nell’Italian Seismological Instrumental and parametric Data-base (ISIDe working group (2016) version 1.0, DOI: 10.13127/ISIDe). Gli analisti del Bollettino Sismico Italiano (BSI) ricontrollano i parametri dei terremoti localizzati, inserendo pesi e polarità degli arrivi delle onde sismiche e integrando, inoltre, i dati letti in sala con tutti quelli disponibili nel sistema di acquisizione. Dal 1985 i dati del bollettino sono consultabili nel data-base ISIDe.
    Description: Istituto Nazionale di Geofisica - Dipartimento di Protezione Civile
    Description: Published
    Description: 4IT. Banche dati
    Keywords: Bollettino Sismico Italiano ; maggio – agosto 2017 ; 04.06. Seismology
    Repository Name: Istituto Nazionale di Geofisica e Vulcanologia (INGV)
    Type: report
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