Title
A mixed seismic-aseismic stress release episode in the Andean subduction zone
Date Issued
01 February 2016
Access level
open access
Resource Type
journal article
Author(s)
Nocquet J.M.
Rolandone F.
Vallee M.
Bondoux F.
Tran T.
Martin X.
Chlieh M.
Publisher(s)
Nature Publishing Group
Abstract
In subduction zones, stress is released by earthquakes and transient aseismic slip. The latter falls into two categories: slow slip and afterslip. Slow-slip events emerge spontaneously during the interseismic phase, and show a progressive acceleration of slip with a negligible contribution of synchronous tremors or microseismicity to the energy, or moment release. In contrast, afterslip occurs immediately after large and moderate earthquakes, decelerates over time, and releases between 20 and 400% of the moment released by the preceding earthquake. Here we use seismic and GPS data to identify transient aseismic slip that does not fit into either of these categories. We document a seismic-aseismic slip sequence which occurred at shallow depths along a weakly coupled part of the Andean subduction zone in northern Peru and lasted seven months. The sequence generated several moderate earthquakes that together account for about 25% of the total moment released during the full sequence, equivalent to magnitude 6.7. Transient slip immediately followed two of the earthquakes, with slip slowing at a logarithmic rate. Considered separately, the moment released by transient slip following the second earthquake was more than 1,000% of the moment released during the earthquake itself, a value incompatible with classical models of afterslip. Synchronous seismic swarms and aseismic slip may therefore define a stress-release process that is distinct from slow-slip events and afterslip.
Start page
150
End page
154
Volume
9
Issue
2
Language
English
OCDE Knowledge area
Geografía física
Sensores remotos
Geología
DOI
Scopus EID
2-s2.0-84957071929
Source
Nature Geoscience
ISSN of the container
17520894
Sponsor(s)
ACKNOWLEDGMENTS. We thank Lily F. Lee, Xinyue Liu, and Jiwoo Ha for their comments. Support for this research was provided by a grant from the UCLA FSPH High-Impact Data Initiative (A.N. and Y.T.). A.E. was financially supported by The Nakajima Foundation and The Alan Turing Institute. Additional support for A.N., J.D.S., and S.D.Y. was provided by Grant P30DA027828 from the National Institute on Drug Abuse, awarded to C. Hendricks Brown, and, for S.D.Y., from grants from the National Institute of Mental Health, National Institute of Allergy and Infectious Diseases, and National Center for Complementary and Alternative Medicine. G.I. acknowledges support from Science Foundation Ireland through Grant 16/IA/4610. The opinions expressed herein are the views of the authors and do not necessarily reflect the official policy or position of the National Institute on Drug Abuse, or any other part of the US Department of Health and Human Services.
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