ALBERT

All Library Books, journals and Electronic Records Telegrafenberg

feed icon rss

Your email was sent successfully. Check your inbox.

An error occurred while sending the email. Please try again.

Proceed reservation?

Export
  • 1
    Publication Date: 2021-09-30
    Description: La revisione da parte degli analisti del BSI della sismicità registrata in Italia dal 1 gennaio al 30 aprile 2021 ha riguardato tutti i terremoti di magnitudo M≥1.5, mentre i parametri dei terremoti di magnitudo inferiore a tale soglia sono quelli calcolati in tempo reale, nella SALA DI SORVEGLIANZA SISMICA DI ROMA. I terremoti più forti (M≥3.5) e pochi altri di particolare interesse [vedi Marchetti et al., 2016, DOI: 10.4401/ag-6116], sono stati revisionati dagli analisti del BSI, mediamente nelle 24 ore successive al loro accadimento.
    Description: Istituto Nazionale di Geofisica e Vulcanologia - Dipartimento di Protezione Civile
    Description: Published
    Description: 4IT. Banche dati
    Keywords: Bollettino Sismico Italiano ; gennaio - aprile 2021 ; 04. Solid Earth
    Repository Name: Istituto Nazionale di Geofisica e Vulcanologia (INGV)
    Type: report
    Location Call Number Expected Availability
    BibTip Others were also interested in ...
  • 2
    Publication Date: 2012-04-03
    Description: IL-17-producing CD4+ T helper cells (TH17) have been extensively investigated in mouse models of autoimmunity. However, the requirements for differentiation and the properties of pathogen-induced human TH17 cells remain poorly defined. Using an approach that combines the in vitro priming of naive T cells with the ex vivo analysis of memory T cells, we describe here two types of human TH17 cells with distinct effector function and differentiation requirements. Candida albicans-specific TH17 cells produced IL-17 and IFN-gamma, but no IL-10, whereas Staphylococcus aureus-specific TH17 cells produced IL-17 and could produce IL-10 upon restimulation. IL-6, IL-23 and IL-1beta contributed to TH17 differentiation induced by both pathogens, but IL-1beta was essential in C. albicans-induced TH17 differentiation to counteract the inhibitory activity of IL-12 and to prime IL-17/IFN-gamma double-producing cells. In addition, IL-1beta inhibited IL-10 production in differentiating and in memory TH17 cells, whereas blockade of IL-1beta in vivo led to increased IL-10 production by memory TH17 cells. We also show that, after restimulation, TH17 cells transiently downregulated IL-17 production through a mechanism that involved IL-2-induced activation of STAT5 and decreased expression of ROR-gammat. Taken together these findings demonstrate that by eliciting different cytokines C. albicans and S. aureus prime TH17 cells that produce either IFN-gamma or IL-10, and identify IL-1beta and IL-2 as pro- and anti-inflammatory regulators of TH17 cells both at priming and in the effector phase.〈br /〉〈span class="detail_caption"〉Notes: 〈/span〉Zielinski, Christina E -- Mele, Federico -- Aschenbrenner, Dominik -- Jarrossay, David -- Ronchi, Francesca -- Gattorno, Marco -- Monticelli, Silvia -- Lanzavecchia, Antonio -- Sallusto, Federica -- England -- Nature. 2012 Apr 26;484(7395):514-8. doi: 10.1038/nature10957.〈br /〉〈span class="detail_caption"〉Author address: 〈/span〉Institute for Research in Biomedicine, Via Vincenzo Vela 6, 6500 Bellinzona, Switzerland. christina.zielinski@charite.de〈br /〉〈span class="detail_caption"〉Record origin:〈/span〉 〈a href="http://www.ncbi.nlm.nih.gov/pubmed/22466287" target="_blank"〉PubMed〈/a〉
    Keywords: Antigen Presentation/immunology ; Candida albicans/*immunology ; Cell Differentiation ; Down-Regulation ; Humans ; Immunologic Memory/immunology ; Interferon-gamma/*biosynthesis ; Interleukin-10/*biosynthesis ; Interleukin-17/biosynthesis ; Interleukin-1beta/*immunology ; Interleukin-2/antagonists & inhibitors/immunology ; Lymphocyte Activation ; Nuclear Receptor Subfamily 1, Group F, Member 3/genetics/metabolism ; STAT5 Transcription Factor/metabolism ; Staphylococcus aureus/*immunology ; Th17 Cells/cytology/*immunology/*metabolism/secretion ; Tumor Necrosis Factor-alpha/metabolism
    Print ISSN: 0028-0836
    Electronic ISSN: 1476-4687
    Topics: Biology , Chemistry and Pharmacology , Medicine , Natural Sciences in General , Physics
    Location Call Number Expected Availability
    BibTip Others were also interested in ...
  • 3
    Publication Date: 2015-07-15
    Description: Human inborn errors of immunity mediated by the cytokines interleukin-17A and interleukin-17F (IL-17A/F) underlie mucocutaneous candidiasis, whereas inborn errors of interferon-gamma (IFN-gamma) immunity underlie mycobacterial disease. We report the discovery of bi-allelic RORC loss-of-function mutations in seven individuals from three kindreds of different ethnic origins with both candidiasis and mycobacteriosis. The lack of functional RORgamma and RORgammaT isoforms resulted in the absence of IL-17A/F-producing T cells in these individuals, probably accounting for their chronic candidiasis. Unexpectedly, leukocytes from RORgamma- and RORgammaT-deficient individuals also displayed an impaired IFN-gamma response to Mycobacterium. This principally reflected profoundly defective IFN-gamma production by circulating gammadelta T cells and CD4(+)CCR6(+)CXCR3(+) alphabeta T cells. In humans, both mucocutaneous immunity to Candida and systemic immunity to Mycobacterium require RORgamma, RORgammaT, or both.〈br /〉〈br /〉〈a href="https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4668938/" 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/PMC4668938/" target="_blank"〉This paper as free author manuscript - peer-reviewed and accepted for publication〈/a〉〈br /〉〈br /〉〈span class="detail_caption"〉Notes: 〈/span〉Okada, Satoshi -- Markle, Janet G -- Deenick, Elissa K -- Mele, Federico -- Averbuch, Dina -- Lagos, Macarena -- Alzahrani, Mohammed -- Al-Muhsen, Saleh -- Halwani, Rabih -- Ma, Cindy S -- Wong, Natalie -- Soudais, Claire -- Henderson, Lauren A -- Marzouqa, Hiyam -- Shamma, Jamal -- Gonzalez, Marcela -- Martinez-Barricarte, Ruben -- Okada, Chizuru -- Avery, Danielle T -- Latorre, Daniela -- Deswarte, Caroline -- Jabot-Hanin, Fabienne -- Torrado, Egidio -- Fountain, Jeffrey -- Belkadi, Aziz -- Itan, Yuval -- Boisson, Bertrand -- Migaud, Melanie -- Arlehamn, Cecilia S Lindestam -- Sette, Alessandro -- Breton, Sylvain -- McCluskey, James -- Rossjohn, Jamie -- de Villartay, Jean-Pierre -- Moshous, Despina -- Hambleton, Sophie -- Latour, Sylvain -- Arkwright, Peter D -- Picard, Capucine -- Lantz, Olivier -- Engelhard, Dan -- Kobayashi, Masao -- Abel, Laurent -- Cooper, Andrea M -- Notarangelo, Luigi D -- Boisson-Dupuis, Stephanie -- Puel, Anne -- Sallusto, Federica -- Bustamante, Jacinta -- Tangye, Stuart G -- Casanova, Jean-Laurent -- 8UL1TR000043/TR/NCATS NIH HHS/ -- HHSN272200900044C/AI/NIAID NIH HHS/ -- HHSN272200900044C/PHS HHS/ -- R37 AI095983/AI/NIAID NIH HHS/ -- R37AI095983/AI/NIAID NIH HHS/ -- T32 AI007512/AI/NIAID NIH HHS/ -- Canadian Institutes of Health Research/Canada -- Howard Hughes Medical Institute/ -- New York, N.Y. -- Science. 2015 Aug 7;349(6248):606-13. doi: 10.1126/science.aaa4282. Epub 2015 Jul 9.〈br /〉〈span class="detail_caption"〉Author address: 〈/span〉St. Giles Laboratory of Human Genetics of Infectious Diseases, Rockefeller Branch, The Rockefeller University, New York, NY 10065, USA. Department of Pediatrics, Hiroshima University Graduate School of Biomedical and Health Sciences, Hiroshima, Japan. ; St. Giles Laboratory of Human Genetics of Infectious Diseases, Rockefeller Branch, The Rockefeller University, New York, NY 10065, USA. jmarkle@rockefeller.edu jean-laurent.casanova@rockefeller.edu. ; Immunology Division, Garvan Institute of Medical Research, Darlinghurst, New South Wales, Australia. St Vincent's Clinical School, University of New South Wales, Sydney, New South Wales, Australia. ; Institute for Research in Biomedicine, University of Italian Switzerland, Bellinzona, Switzerland. ; Department of Pediatrics, Hadassah University Hospital, Jerusalem, Israel. ; Department of Immunology, School of Medicine, Universidad de Valparaiso, Santiago, Chile. Department of Pediatrics, Padre Hurtado Hospital and Clinica Alemana, Santiago, Chile. ; Department of Pediatrics, King Faisal Specialist Hospital and Research Center, Riyadh, Saudi Arabia. ; Department of Pediatrics, King Faisal Specialist Hospital and Research Center, Riyadh, Saudi Arabia. Department of Pediatrics, Prince Naif Center for Immunology Research, College of Medicine, King Saud University, Riyadh, Saudi Arabia. ; Department of Pediatrics, Prince Naif Center for Immunology Research, College of Medicine, King Saud University, Riyadh, Saudi Arabia. ; Immunology Division, Garvan Institute of Medical Research, Darlinghurst, New South Wales, Australia. ; Institut Curie, INSERM U932, Paris, France. ; Division of Immunology, Boston Children's Hospital, Boston, MA 02115, USA. ; Caritas Baby Hospital, Post Office Box 11535, Jerusalem, Israel. ; Department of Immunology, School of Medicine, Universidad de Valparaiso, Santiago, Chile. ; St. Giles Laboratory of Human Genetics of Infectious Diseases, Rockefeller Branch, The Rockefeller University, New York, NY 10065, USA. ; Laboratory of Human Genetics of Infectious Diseases, Necker Branch, INSERM UMR 1163, Paris, France. Paris Descartes University, Imagine Institute, Paris, France. ; Trudeau Institute, Saranac Lake, NY 12983, USA. ; La Jolla Institute for Allergy and Immunology, La Jolla, CA 92037, USA. ; Department of Radiology, Assistance Publique-Hopitaux de Paris (AP-HP), Necker Hospital for Sick Children, Paris, France. ; Department of Microbiology and Immunology, Peter Doherty Institute for Infection and Immunity, University of Melbourne, Parkville, Victoria, Australia. ; Department of Biochemistry and Molecular Biology, School of Biomedical Sciences, Monash University, Clayton, Victoria, Australia. Australian Research Council Centre of Excellence for Advanced Molecular Imaging, Monash University, Clayton, Victoria, Australia. Institute of Infection and Immunity, Cardiff University, School of Medicine, Heath Park, Cardiff CF14 4XN, UK. ; Laboratoire Dynamique du Genome et Systeme Immunitaire, INSERM UMR 1163, Universite Paris Descartes-Sorbonne Paris Cite, Imagine Institute, Paris, France. ; Laboratoire Dynamique du Genome et Systeme Immunitaire, INSERM UMR 1163, Universite Paris Descartes-Sorbonne Paris Cite, Imagine Institute, Paris, France. Pediatric Hematology-Immunology Unit, AP-HP, Necker Hospital for Sick Children, Paris, France. ; Institute of Cellular Medicine, Newcastle University and Great North Children's Hospital, Newcastle upon Tyne NE4 6BE, UK. ; Laboratory of Lymphocyte Activation and Susceptibility to EBV Infection, INSERM UMR 1163, Universite Paris Descartes-Sorbonne Paris Cite, Imagine Institute, Paris, France. ; Department of Paediatric Allergy Immunology, University of Manchester, Royal Manchester Children's Hospital, Manchester, UK. ; St. Giles Laboratory of Human Genetics of Infectious Diseases, Rockefeller Branch, The Rockefeller University, New York, NY 10065, USA. Laboratory of Human Genetics of Infectious Diseases, Necker Branch, INSERM UMR 1163, Paris, France. Paris Descartes University, Imagine Institute, Paris, France. Pediatric Hematology-Immunology Unit, AP-HP, Necker Hospital for Sick Children, Paris, France. Center for the Study of Primary Immunodeficiencies, AP-HP, Necker Hospital for Sick Children, Paris, France. ; Department of Pediatrics, Hiroshima University Graduate School of Biomedical and Health Sciences, Hiroshima, Japan. ; St. Giles Laboratory of Human Genetics of Infectious Diseases, Rockefeller Branch, The Rockefeller University, New York, NY 10065, USA. Laboratory of Human Genetics of Infectious Diseases, Necker Branch, INSERM UMR 1163, Paris, France. Paris Descartes University, Imagine Institute, Paris, France. ; Division of Immunology, Boston Children's Hospital, Boston, MA 02115, USA. Manton Center for Orphan Disease Research, Children's Hospital, Boston, MA 02115, USA. ; Institute for Research in Biomedicine, University of Italian Switzerland, Bellinzona, Switzerland. Center of Medical Immunology, Institute for Research in Biomedicine, University of Italian Switzerland, Bellinzona, Switzerland. ; St. Giles Laboratory of Human Genetics of Infectious Diseases, Rockefeller Branch, The Rockefeller University, New York, NY 10065, USA. Laboratory of Human Genetics of Infectious Diseases, Necker Branch, INSERM UMR 1163, Paris, France. Paris Descartes University, Imagine Institute, Paris, France. Center for the Study of Primary Immunodeficiencies, AP-HP, Necker Hospital for Sick Children, Paris, France. ; St. Giles Laboratory of Human Genetics of Infectious Diseases, Rockefeller Branch, The Rockefeller University, New York, NY 10065, USA. Laboratory of Human Genetics of Infectious Diseases, Necker Branch, INSERM UMR 1163, Paris, France. Paris Descartes University, Imagine Institute, Paris, France. Pediatric Hematology-Immunology Unit, AP-HP, Necker Hospital for Sick Children, Paris, France. Howard Hughes Medical Institute, New York, NY 10065, USA. jmarkle@rockefeller.edu jean-laurent.casanova@rockefeller.edu.〈br /〉〈span class="detail_caption"〉Record origin:〈/span〉 〈a href="http://www.ncbi.nlm.nih.gov/pubmed/26160376" target="_blank"〉PubMed〈/a〉
    Keywords: Alleles ; Animals ; Candida albicans/*immunology ; Candidiasis, Chronic Mucocutaneous/complications/*genetics/immunology ; Cattle ; Child ; Child, Preschool ; DNA Mutational Analysis ; Exome/genetics ; Female ; Gene Rearrangement, alpha-Chain T-Cell Antigen Receptor ; Humans ; Immunity/*genetics ; Interferon-gamma/immunology ; Interleukin-17/immunology ; Mice ; Mutation ; Mycobacterium bovis/immunology/isolation & purification ; Mycobacterium tuberculosis/immunology/isolation & purification ; Nuclear Receptor Subfamily 1, Group F, Member 3/*genetics ; Pedigree ; Receptors, Antigen, T-Cell, alpha-beta/genetics/immunology ; Receptors, Antigen, T-Cell, gamma-delta/genetics/immunology ; Severe Combined Immunodeficiency/*genetics ; T-Lymphocytes/immunology ; Thymus Gland/abnormalities/immunology ; Tuberculosis, Bovine/*genetics/immunology ; Tuberculosis, Pulmonary/*genetics/immunology
    Print ISSN: 0036-8075
    Electronic ISSN: 1095-9203
    Topics: Biology , Chemistry and Pharmacology , Computer Science , Medicine , Natural Sciences in General , Physics
    Location Call Number Expected Availability
    BibTip Others were also interested in ...
  • 4
    Publication Date: 2014-12-06
    Description: Distinct types of CD4(+) T cells protect the host against different classes of pathogens. However, it is unclear whether a given pathogen induces a single type of polarized T cell. By combining antigenic stimulation and T cell receptor deep sequencing, we found that human pathogen- and vaccine-specific T helper 1 (T(H)1), T(H)2, and T(H)17 memory cells have different frequencies but comparable diversity and comprise not only clones polarized toward a single fate, but also clones whose progeny have acquired multiple fates. Single naive T cells primed by a pathogen in vitro could also give rise to multiple fates. Our results unravel an unexpected degree of interclonal and intraclonal functional heterogeneity of the human T cell response and suggest that polarized responses result from preferential expansion rather than priming.〈br /〉〈span class="detail_caption"〉Notes: 〈/span〉Becattini, Simone -- Latorre, Daniela -- Mele, Federico -- Foglierini, Mathilde -- De Gregorio, Corinne -- Cassotta, Antonino -- Fernandez, Blanca -- Kelderman, Sander -- Schumacher, Ton N -- Corti, Davide -- Lanzavecchia, Antonio -- Sallusto, Federica -- New York, N.Y. -- Science. 2015 Jan 23;347(6220):400-6. doi: 10.1126/science.1260668. Epub 2014 Dec 4.〈br /〉〈span class="detail_caption"〉Author address: 〈/span〉Institute for Research in Biomedicine, Bellinzona, Universita della Svizzera Italiana, Lugano, Switzerland. Institute of Microbiology, ETH Zurich, Zurich, Switzerland. ; Institute for Research in Biomedicine, Bellinzona, Universita della Svizzera Italiana, Lugano, Switzerland. ; Division of Immunology, Netherlands Cancer Institute, Amsterdam, Netherlands. ; Institute for Research in Biomedicine, Bellinzona, Universita della Svizzera Italiana, Lugano, Switzerland. federica.sallusto@irb.usi.ch.〈br /〉〈span class="detail_caption"〉Record origin:〈/span〉 〈a href="http://www.ncbi.nlm.nih.gov/pubmed/25477212" target="_blank"〉PubMed〈/a〉
    Keywords: Amino Acid Sequence ; CD4-Positive T-Lymphocytes/*immunology ; Candida albicans/*immunology ; Cells, Cultured ; Clone Cells ; High-Throughput Nucleotide Sequencing ; Host-Pathogen Interactions/*immunology ; Humans ; *Immunologic Memory ; Lymphocyte Activation ; Molecular Sequence Data ; Mycobacterium tuberculosis/*immunology ; Receptors, Antigen, T-Cell/genetics ; T-Lymphocyte Subsets/*immunology ; Th1 Cells/immunology ; Th17 Cells/immunology ; Th2 Cells/immunology ; Vaccines/*immunology
    Print ISSN: 0036-8075
    Electronic ISSN: 1095-9203
    Topics: Biology , Chemistry and Pharmacology , Computer Science , Medicine , Natural Sciences in General , Physics
    Location Call Number Expected Availability
    BibTip Others were also interested in ...
  • 5
    Publication Date: 2021-04-16
    Description: Nel periodo che va dal 1 gennaio al 30 aprile 2020, gli analisti del BSI hanno effettuato la revisione di tutti gli eventi di magnitudo M≥1.5, registrati dalle stazioni sismiche dell’INGV. I terremoti di magnitudo inferiore a tale soglia di revisione vengono localizzati in tempo reale, nella sala di sorveglianza sismica di Roma. I terremoti di M≥3.5, e pochi altri di particolare interesse (vedi Marchetti et al., 2016, DOI: 10.4401/ag-7169), vengono revisionati dagli analisti del BSI, contestualmente al loro accadimento.
    Description: Istituto Nazionale di Geofisica e Vulcanologia - Dipartimento di Protezione Civile
    Description: Published
    Description: 4IT. Banche dati
    Keywords: Bollettino Sismico Italiano ; gennaio - aprile 2020 ; 04. Solid Earth
    Repository Name: Istituto Nazionale di Geofisica e Vulcanologia (INGV)
    Type: report
    Location Call Number Expected Availability
    BibTip Others were also interested in ...
  • 6
    Publication Date: 2021-05-18
    Description: La revisione da parte degli analisti del BSI della sismicità registrata in Italia dal 1 settembre al 31 dicembre 2020 ha riguardato tutti i terremoti di magnitudo M≥1.5, mentre i parametri dei terremoti di magnitudo inferiore a tale valore sono quelli calcolati in tempo reale, nella sala di sorveglianza sismica di Roma. I terremoti più forti (M≥3.5), e pochi altri di particolare interesse [vedi Marchetti et al., 2016, DOI: 10.4401/ag-6116], sono stati revisionati dagli analisti del BSI, mediamente nelle 24 ore successive al loro accadimento.
    Description: Istituto Nazionale di Geofisica e Vulcanologia - Dipartimento di Protezione Civile
    Description: Published
    Description: 4IT. Banche dati
    Keywords: Bollettino Sismico Italiano ; settembre - dicembre 2020 ; 04. Solid Earth
    Repository Name: Istituto Nazionale di Geofisica e Vulcanologia (INGV)
    Type: report
    Location Call Number Expected Availability
    BibTip Others were also interested in ...
  • 7
    Publication Date: 2019-12-02
    Description: In questo lavoro presentiamo il catalogo completo delle localizzazioni dei terremoti appartenenti alla più importante sequenza sismica avvenuta in Italia negli ultimi 30 anni, ovvero la sequenza sismica di Amatrice-Visso-Norcia (AVN) iniziata il 24 Agosto del 2016 in Appennino centrale. Si tratta di 102582 eventi sismici registrati dalle 129 stazioni della Rete Sismica Nazionale (RSN, http://doi.org/10.13127/SD/X0FXNH7QFY) e della rete temporanea installata nella regione epicentrale (Moretti et al., 2016), dal 14 agosto 2016 al 31 agosto 2018 e analizzati manualmente dagli analisti del Bollettino Sismico Italiano (BSI, http://cnt.rm.ingv.it/bsi). Le fasi P ed S e le ampiezze di questi terremoti, stimate in tempo reale nella sala di sorveglianza dell’Istituto Nazionale di Geofisica e Vulcanologia (INGV) di Roma, sono state successivamente riviste in dettaglio, per tutti gli eventi di M≽ 2.3, con l’intento di aumentare la qualità dei parametri di localizzazione e della stima della magnitudo. Gli analisti hanno inoltre inserito le fasi P ed S osservate a quelle stazioni che il sistema di acquisizione non aveva eventualmente incluso nelle soluzioni automatiche in real-time. Per i primi mesi della sequenza l'analisi ha riguardato anche l’integrazione delle registrazioni di 9 stazioni temporanee standalone che non entravano automaticamente nelle localizzazioni della sala sismica; per i giorni nei quali si sono verificati gli eventi di M≽ 5.5 la revisione è stata particolarmente accurata anche per eventi di magnitudo inferiore a 2.3 (Improta et al. 2019) Il dataset così costruito consiste in 25496 terremoti rivisti dagli analisti del bollettino (versione 1000) e 77426 eventi elaborati dai turnisti in sala sismica (versione 100). Le 1705987 fasi P che ne sono derivate, e le 1271757 fasi S, sono disponibili nel database ISIDe (DOI: 10.13127/ISIDe). Tutte le letture dei tempi di arrivo sono state utilizzate per localizzare gli ipocentri della sequenza utilizzando il codice di inversione non lineare NonLinLoc (NLL, Lomax et al., 2001): l’utilizzo di questa tecnica ha migliorato, rispetto ai lavori precedenti, la stima dei parametri ipocentrali fornendo delle soluzioni più robuste ai fini della ricostruzione sismotettonica dell’area interessata dalla sequenza sismica AVN. Rispetto ai dati forniti in tempo reale dal personale in servizio di sorveglianza sismica dell’INGV, questo nuovo catalogo presenta un notevole miglioramento in termini di omogeneità della stima della ML, almeno nel range definito dalla soglia inferiore di revisione pari a ML≽ 2.3. Questa maggiore omogeneità del catalogo permetterà ulteriori analisi per la stima della Mc (Magnitudo di completezza). Inoltre, all’interno del catalogo sono presenti 75 terremoti con ML≽4.0: per 47 di questi eventi sismici abbiamo calcolato il meccanismo focale a partire dalle prime polarità utilizzando il codice FPFIT (Reasenberg and Oppenheimer, 1985). Un catalogo di questo tipo, di alta qualità, basato quindi su un imponente numero di fasi e ampiezze riviste manualmente, ha una particolare importanza e può essere un valido riferimento per l’applicazione per esempio di tecniche di detection basate sulla crosscorrelazione di registrazioni di terremoti templates, per la validazione di cataloghi composti da letture automatiche dei tempi di arrivo, o anche per l’ottimizzazione di algoritmi di picking automatici. La qualità delle localizzazioni dei mainshocks e degli aftershocks della sequenza sismica AVN diventa fondamentale per capire l'analisi dell'evoluzione spazio-temporale della sismicità, anche di bassa magnitudo, e le complesse geometrie delle faglie attivate durante la sequenza sismica, contestualmente alle relazioni tra esse esistenti.
    Description: Published
    Description: Roma - Italia
    Description: 4IT. Banche dati
    Keywords: Bollettino Sismico Italiano ; Catalogo ; sequenza sismica ; Amatrice-Visso-Norcia ; 04.06. Seismology
    Repository Name: Istituto Nazionale di Geofisica e Vulcanologia (INGV)
    Type: Conference paper
    Location Call Number Expected Availability
    BibTip Others were also interested in ...
  • 8
    Publication Date: 2020-07-02
    Description: Gli analisti del BSI hanno revisionato tutti gli eventi di magnitudo M≥1.5, localizzati dal 1 MAGGIO AL 31 AGOSTO 2019. I parametri dei terremoti di magnitudo inferiore a tale soglia di revisione, sono quelli calcolati in tempo reale, nella sala di sorveglianza sismica di Roma.
    Description: Istituto Nazionale di Geofisica e Vulcanologia - Dipartimento di Protezione Civile
    Description: Published
    Description: 4IT. Banche dati
    Keywords: Bollettino Sismico Italiano ; maggio - agosto 2019 ; 04. Solid Earth
    Repository Name: Istituto Nazionale di Geofisica e Vulcanologia (INGV)
    Type: report
    Location Call Number Expected Availability
    BibTip Others were also interested in ...
  • 9
    Publication Date: 2020-07-20
    Description: DAL 1 SETTEMBRE AL 31 DICEMBRE 2019 la revisione della sismicità fatta dagli analisti del BSI ha riguardato tutti gli eventi di magnitudo M≥1.5. I parametri dei terremoti di magnitudo inferiore a tale soglia di revisione, sono quelli calcolati in tempo reale, nella sala di sorveglianza sismica di Roma. Tutti gli eventi con M≥3.5, e pochi altri di particolare interesse (vedi Marchetti et al., 2016, DOI: 10.4401/ag-7169), sono stati rianalizzati dagli analisti del BSI, contestualmente al loro accadimento.
    Description: Istituto Nazionale di Geofisica e Vulcanologia - Dipartimento di Protezione Civile
    Description: Published
    Description: 4IT. Banche dati
    Keywords: Bollettino Sismico Italiano ; settembre - dicembre 2019 ; 04. Solid Earth
    Repository Name: Istituto Nazionale di Geofisica e Vulcanologia (INGV)
    Type: report
    Location Call Number Expected Availability
    BibTip Others were also interested in ...
  • 10
    Publication Date: 2018-03-22
    Description: The Amatrice-Visso-Norcia seismic sequence is the most important of the last 30 years in Italy. The seismic sequence started on 24 August, 2016 and still is ongoing in central Apennines. At the end of February 2017 more than 57,000 events were located, 80,000 events up to the end of September 2017 (Fig. 1). The mainshocks of the sequence occurred on 24 August 2016 (Mw 6.0 and Mw 5.4), 26 October 2016 (Mw 5.4 and Mw 5.9), 30 October 2016 (Mw 6.5), 18 January 2017 (four earthquakes Mw≥ 5.0). In this seismic sequence, all the waveforms recorded by temporary stations deployed by the SISMIKO emergency group (stations T12**; Moretti et al., 2016) where available in real- time at the surveillance room of INGV. Because of the high level of seismicity and the dense seismic network installed in the region, more than 150 events per day were located at the end of February 2017; still 60 events per day were located up to the end of August 2017.The Amatrice-Visso-Norcia is the most important seismic sequence since 2015, the time when the analysis procedures of the BSI group (Bollettino Sismico Italiano) were revised (Nardi et al., 2015). BSI is now available every four months on the web: bulletins contain revised earthquakes (location and magnitude) with ML≥ 1.5, quasi-real time revision of ML≥ 3.5 earthquakes and phase arrivals from waveforms recorded on seismic stations available from the European Integrated Data Archive (EIDA), (Mazza et al., 2012). These last procedures allow the integration of signals from temporary seismic stations (Moretti et al., 2014) installed by the emergency group SISMIKO (Moretti and Sismiko working group, 2016), even when they are not in real time transmission, if they are rapidly archived in EIDA, together with real time signals from the seismic stations of the permanent INGV network. The analysis strategy of the BSI group for the Amatrice -Visso - Norcia seismic sequence (AVN.s.s in the following) was to select the earthquakes located in the box with min/max latitude: 42.2/43.2 - and min/max longitude: 12.4/14.1 to prepare a special volume of BSI on the seismic sequence.
    Description: Published
    Description: Trieste, Italy
    Description: 1SR. TERREMOTI - Servizi e ricerca per la Società
    Keywords: seismic data analysis ; Central Italy 2016 seismic sequence ; Bollettino Sismico Italiano
    Repository Name: Istituto Nazionale di Geofisica e Vulcanologia (INGV)
    Type: Conference paper
    Location Call Number Expected Availability
    BibTip Others were also interested in ...
Close ⊗
This website uses cookies and the analysis tool Matomo. More information can be found here...