Global link between deformation and volcanic eruption quantified by satellite imagery

A key challenge for volcanological science and hazard management is that few of the world’s volcanoes are effectively monitored. Satellite imagery covers volcanoes globally throughout their eruptive cycles, independent of ground-based monitoring, providing a multidecadal archive suitable for probabilistic analysis linking deformation with eruption. Here we show that, of the 198 volcanoes systematically observed for the past 18 years, 54 deformed, of which 25 also erupted. For assessing eruption potential, this high proportion of deforming volcanoes that also erupted (46%), together with the proportion of non-deforming volcanoes that did not erupt (94%), jointly represent indicators with ‘strong’ evidential worth. Using a larger catalogue of 540 volcanoes observed for 3 years, we demonstrate how this eruption–deformation relationship is influenced by tectonic, petrological and volcanic factors. Satellite technology is rapidly evolving and routine monitoring of the deformation status of all volcanoes from space is anticipated, meaning probabilistic approaches will increasingly inform hazard decisions and strategic development

Systematics of the Neotropical Genus Leptodactylus Fitzinger, 1826 (Anura: Leptodactylidae): Phylogeny, the Relevance of Non-molecular Evidence, and Species Accounts

A phylogeny of the species-rich clade of the Neotropical frog genus Leptodactylus sensu stricto is presented on the basis of a total evidence analysis of molecular (mitochondrial and nuclear markers) and non-molecular (adult and larval morphological and behavioral characters) sampled from > 80% of the 75 currently recognized species. Our results support the monophyly of Leptodactylus sensu stricto, with Hydrolaetare placed as its sister group. The reciprocal monophyly of Hydrolaetare and Leptodactylus sensu stricto does not require that we consider Hydrolaetare as either a subgenus or synonym of Leptodactylus sensu lato. We recognize Leptodactylus sensu stricto, Hydrolaetare, Adenomera, and Lithodytes as valid monophyletic genera. Our results generally support the traditionally recognized Leptodactylus species groups, with exceptions involving only a few species that are easily accommodated without proposing new groups or significantly altering contents. The four groups form a pectinate tree, with the Leptodactylus fuscus group diverging first, followed by the L. pentadactylus group, which is sister to the L. latrans and L. melanonotus groups. To evaluate the impact of non-molecular evidence on our results, we compared our total evidence results with results obtained from analyses using only molecular data. Although non-molecular evidence comprised only 3.5% of the total evidence matrix, it had a strong impact on our total evidence results. Only one species group was monophyletic in the molecular-only analysis, and support differed in 86% of the 54 Leptodactylus clades that are shared by the results of the two analyses. Even though no non-molecular evidence was included for Hydrolaetare, exclusion of that data partition resulted in that genus being nested within Leptodactylus, demonstrating that the inclusion of a small amount of non-molecular evidence for a subset of species can alter not only the placement of those species, but also species that were not scored for those data. The evolution of several natural history and reproductive traits is considered in the light of our phylogenic framework. Invasion of rocky outcrops, larval oophagy, and use of underground reproductive chambers are restricted to species of the Leptodactylus fuscus and L. pentadactylus groups. In contrast, larval schooling, larval attendance, and more complex parental care are restricted to the L. latrans and L. melanonotus groups. Construction of foam nests is plesiomorphic in Leptodactylus but their placement varies extensively (e.g., underground chambers, surface of waterbodies, natural or excavated basins). Information on species synonymy, etymology, adult and larval morphology, advertisement call, and geographic distribution is summarized in species accounts for the 30 species of the Leptodactylus fuscus group, 17 species of the L. pentadactylus group, eight species of the L. latrans group, and 17 species of the L. melanonotus group, as well as the three species that are currently unassigned to any species group.Se presenta una filogenia del género Leptodactylus, un ciado neotropical rico en especies, basada en análises combinados de datos moleculares (marcadores nuclear y mitocondriales) y no moleculares (caracteres de la morfología de adultos y larvas así como de comportamiento) se muestrearon > 80% de las 75 especies reconocidas. Los resultados apoyan la monofília de Leptodactylus sensu stricto, con Hydrolaetare como su grupo hermano. La monofília recíproca de Hydrolaetare y Leptodactylus no requiere considerar a Hydrolaetare como un subgénero o sinónimo de Leptodactylus sensu lato. Se reconocen Leptodactylus sensu stricto, Hydrolaetare, Adenomera y Lithodytes como géneros monofiléticos válidos. Los resultados en general resuelven los grupos tradicionalmente reconocidos de Leptodactylus, con excepciones de algunas especies que son reasignadas sin la necesidad de proponer nuevos grupos o alterar significativamente el contenido de los grupos tradicionales. Los cuatro grupos de especies forman una topología pectinada donde el grupo de L. fuscus tiene una posición basal, seguido por el grupo de L. pentadactylus que es el grupo hermano al clado formado por los grupo de L. latrans y L. melanonotus. Se estimó el impacto de los datos no moleculares en los resultados, comparándose los resultados de evidencia total con los de los análises de datos moleculares solamente. Los datos no moleculares representan un 3.5% de la matriz de evidencia total, pero estos datos tuvieron un impacto significativo en los resultados del análisis de evidencia total. En el análisis estrictamente molecular solamente un grupo de especies resultó monofilético, y el apoyo difirió en 86% de los 54 ciados de Leptodactylus compartidos entre los dos análises. A pesar que datos no moleculares no fueron incluidos para Hydrolaetare, la exclusión de evidencia no molecular resultó en el género estar dentro de Leptodactylus, demostrando que la inclusión de evidencia no molecular pequeña para un subgrupo de especies altera no solamente la posición topológica de esas especies, sino tambien de las especies para las cuales dichos datos no fueron codificados. La evolución de patrones de historia natural y reprodución se evalúan en el contexto filogenético. La invasión de afloramientos rocosos y la construción de cámaras de reprodución subterraneas está limitada a los grupos de Leptodactylus fuscus y L. pentadactylus, mientras que la oofagia larval está restringida al grupo de L. pentadactylus. Por otro lado, los cárdumenes larvales, la proteción del cárdumen, y otros comportamientos parentales complejos carecterizan al clado formado por los grupos de especies de L. latrans y L. melanonotus. Los resúmenes de especies incluyen información de sinonimias, etimología, morfología de adultos y larvas, cantos, y distribución geográfica para las 30 especies del grupo de Leptodactylus fuscus, 17 especies del grupo L. pentadactylus, ocho especies del grupo de L. latrans, 17 especies del grupo de L. melanonotus, así como para las tres especies que actualmente no se encuentran asociadas a ninguno de los grupos de especies.Taran Grant was supported by Conselho Nacional de Desenvolvimento Científico e Tecnológico Proc. 307001/2011-3 and Fundação de Amparo à Pesquisa do Estado de São Paulo Proc. 2012/10000-5

Interaction Between Climate and Tectonics in the Northern Lesser Antilles Inferred From the Last Interglacial Shoreline on Barbuda Island

International audienceIn the context of increasing evidence of plate interface coupling variability in subduction zones, there is a need to extend the short time window given by instrumental data and to gather data over multiple time and spatial scales. We hence investigated the long-term topography on Barbuda island, located in the northern part of the Lesser Antilles, west of the Caribbean subduction zone. Following pioneering work using a set of marine terraces on the eastern side of the island, we performed the first U-Th dating on 10 corals in growth position from the lowest terrace, for which the highest relative sea-level (RSL) indicator is found at 9 ± 1 m above the mean sea level. We find that this terrace corresponds to the Last Interglacial (LIG) (ages between 122.8 ± 0.3 ka and 128.1 ± 0.3 ka) and we estimate a paleo RSL of 7 ± 2 m above the current mean sea level. The present elevation of the LIG shoreline on Barbuda might imply tectonics as an additional mechanism to eustatic sea level, mantle dynamic topography and glacial isostatic adjustment. East-west morphological asymmetry of Barbuda and difference in LIG shoreline elevation between Barbuda and Antigua suggest a regional tectonic process. As with the proposed westward tilting from the forearc to the volcanic arc of the Guadeloupe archipelago, vertical deformation on Barbuda could be related to plate-scale subduction processes. Long-term uplift of Barbuda might be related to the accumulation of residual coseismic deformation not fully recovered by interseismic subsidence and the corresponding seismogenic segment would extend below the Moho

Earthquake supercycles on the Mentawai segment of the Sunda megathrust in the seventeenth century and earlier

Over at least the past millennium, the Mentawai segment of the Sunda megathrust has failed in sequences of closely timed events rather than in single end-to-end ruptureseach the culmination of an earthquake supercycle. Here we synthesize the sixteenth- and seventeenth-century coral microatoll records into a chronology of interseismic and coseismic vertical deformation. We identify at least five discrete uplift events in about 1597, 1613, 1631, 1658, and 1703 that likely correspond to large megathrust ruptures. This sequence contrasts with the following supercycle culmination, which involved only two large ruptures in 1797 and 1833. Fault slip modeling suggests that together the five cascading ruptures involved failure of the entire Mentawai segment. Interseismic deformation rates also changed after the onset of the rupture sequence, as they did after the 1797 earthquake. We model this change as an altered distribution of fault coupling, presumably triggered by the similar to 1597 rupture. We also analyze the far less continuous microatoll record between A.D. 1 and 1500. While we cannot confidently delineate the extent of any megathrust rupture during that period, all evidence suggests that individual major ruptures involve only part of the Mentawai segment, often overlap below the central Mentawai Islands, often trigger coupling changes, and occur in clusters that cumulatively cover the entire Mentawai segment at the culmination of each supercycle. It is clear that each Mentawai rupture sequence evolves uniquely in terms of the order and grouping of asperities that rupture, suggesting heterogeneities in fault frictional properties at the similar to 100km scale