Nd, Sr and stable isotope signatures of ancient methane-seep carbonates (Eocene, Washington, USA) as a record of incipient subduction at the Cascadia convergent margin

Author(s):  
Michał Jakubowicz ◽  
Steffen Kiel ◽  
James Goedert ◽  
Jolanta Dopieralska ◽  
Zdzislaw Belka

<p>Stratigraphic and structural context of the early evolution of the Cascadia convergent margin, following major subduction reconfiguration associated with accretion of the igneous Siletzia terrane at 50−45 Ma, remains insufficiently understood. Here, we have applied a novel approach that uses combined Nd, Sr and stable isotope analyses of ancient methane-seep carbonates to constrain the early hydrogeological regime of the Cascadia margin. Analyses included the oldest-known seep deposits of Cascadia, formed during mid-Eocene time (42.5−40.5 Ma). A combination of exceptionally high ε<sub>Nd</sub> and low <sup>87</sup>Sr/<sup>86</sup>Sr signatures observed in these carbonates consistently point to former interactions between the seeping fluids and mafic, igneous constituents of the forearc basement. Moderately negative δ<sup>13</sup>C<sub>carbonate</sub> values imply thermogenic origin of hydrocarbons at three out of four studied seeps, with likely contribution of biogenic methane at a single, landward-most site. When combined with structural constraints, the recorded signals point to discharges of fluids originating from deep portions of the young subduction wedge, and their channeled ascent through the Siletzia terrane. The results document the presence of a fluid expulsion system indicative of active convergence prior to maturation of typical arc magmatism in the Cascades at 40 Ma. The exceptionally pronounced role of exotic, <sup>143</sup>Nd-enriched, <sup>87</sup>Sr- and <sup>18</sup>O-depleted fluids recorded for early Cascadia reflects its distinctive structural architecture, including the relatively thin sedimentary cover of the young forearc, its extensional tectonics, and the near-trench position of the volcanic terrane that the descending plate-derived fluids must have migrated through prior to reaching the seafloor. </p>

2018 ◽  
Author(s):  
Casey Paquola ◽  
Reinder Vos De Wael ◽  
Konrad Wagstyl ◽  
Richard A.I. Bethlehem ◽  
Seok-Jun Hong ◽  
...  

SummaryWhile the role of cortical microstructure in organising neural function is well established, it remains unclear how structural constraints can give rise to more flexible elements of cognition. While non-human primate research has demonstrated a close structure-function correspondence, the relationship between microstructure and function remains poorly understood in humans, in part because of the reliance onpost mortemanalyses which cannot be directly related to functional data. To overcome this barrier, we developed a novel approach to model the similarity of microstructural profiles sampled in the direction of cortical columns. Our approach was initially formulated based on an ultra-high-resolution 3D histological reconstruction of an entire human brain and then translated to myelin-sensitive MRI data in a large cohort of healthy adults. This novel method identified a system-level gradient of microstructural differentiation traversing from primary sensory to limbic regions that followed shifts in laminar differentiation and cytoarchitectural complexity. Importantly, while microstructural and functional gradients described a similar hierarchy, they became increasingly dissociated in transmodal default mode and fronto-parietal networks. Meta analytic decoding of these topographic dissociations highlighted involvement in higher-level aspects of cognition such as cognitive control and social cognition. Our findings demonstrate a relative decoupling of macroscale functional from microstructural gradients in transmodal regions, which likely contributes to the flexible role these regions play in human cognition.


2020 ◽  
pp. jgs2020-193
Author(s):  
Simone Teloni ◽  
Chiara Invernizzi ◽  
Stefano Mazzoli ◽  
Pietro Paolo Pierantoni ◽  
Vincenzo Spina

A seismic sequence that affected the Durrës region in late 2019 to early 2020 sheds new light into the structural architecture and active tectonic setting of the northern outer Albanides. Stress inversion analysis using the focal mechanisms confirms that the area is dominated by ENE trending, horizontal maximum compression. Seismogenic sources consist mainly of ENE dipping thrust faults roughly parallel to the coastline. Hypocentre distribution indicates that most of the earthquakes, including the Mw = 6.4 main shock, nucleated within the basement, while only some of the shallow aftershocks tend to cluster around the deeper portion of previously identified seismogenic structures within the sedimentary cover. Our results, unravelling for the first time the fundamental role of deeply rooted, crustal ramp-dominated thrusting in seismogenesis, imply a profound reconsideration of the seismotectonic setting of the region in view of a correct assessment of seismic hazard in this densely populated area of Albania.


2018 ◽  
Vol 93 (1) ◽  
pp. 1-7 ◽  
Author(s):  
A.J.M. Sabadel ◽  
A.D. Stumbo ◽  
C.D. MacLeod

AbstractParasites are often overlooked in the construction of food webs, despite their ubiquitous presence in almost every type of ecosystem. Researchers who do recognize their importance often struggle to include parasites using classical food-web theory, mainly due to the parasites' multiple hosts and life stages. A novel approach using compound-specific stable-isotope analysis promises to provide considerable insight into the energetic exchanges of parasite and host, which may solve some of the issues inherent in incorporating parasites using a classical approach. Understanding the role of parasites within food webs, and tracing the associated biomass transfers, are crucial to constructing new models that will expand our knowledge of food webs. This mini-review focuses on stable-isotope studies published in the past decade, and introduces compound-specific stable-isotope analysis as a powerful, but underutilized, newly developed tool that may answer many unresolved questions regarding the role of parasites in food webs.


Author(s):  
Peta Wellstead

This paper reports part of an ongoing study exploring the information behaviour of New Zealand men during periods of diminished health and wellbeing. Focus groups were used for this iteration of the study. Results indicate that New Zealand men face both personal and structural constraints to their information-seeking during periods when their health and wellbeing may be compromised. This study highlights that service providers need to develop more effective information delivery mechanisms and support services for men. These services need to be appealing to men and reflect men’s information seeking preferences. The role of LIS professionals in supporting this endeavour is discussed. Cet article présente une étude en cours explorant le comportement informationnel d’ hommes néo-zélandais durant des périodes où leur état de santé et de bien-être est amoindri. Des groupes de discussion ont été utilisés pour cette itération de l'étude. Les résultats indiquent que les hommes en Nouvelle-Zélande font face à des contraintes à la fois  personnelles et structurelles dans leur recherche d'information pendant les périodes où leur santé et leur bien-être peuvent être affaiblis. Cette étude met en évidence le besoin pour les fournisseurs de services de développer des mécanismes de diffusion de l'information plus efficaces et des services de soutien pour les hommes. Ces services doivent être attrayants et refléter les préférences des hommes dans leurs recherches d’information. Le rôle des professionnels de l'information dans le soutien à cette entreprise est discuté.


Polymers ◽  
2021 ◽  
Vol 13 (12) ◽  
pp. 1900
Author(s):  
Ramin Hosseinnezhad ◽  
Iurii Vozniak ◽  
Fahmi Zaïri

The paper discusses the possibility of using in situ generated hybrid polymer-polymer nanocomposites as polymeric materials with triple shape memory, which, unlike conventional polymer blends with triple shape memory, are characterized by fully separated phase transition temperatures and strongest bonding between the polymer blends phase interfaces which are critical to the shape fixing and recovery. This was demonstrated using the three-component system polylactide/polybutylene adipateterephthalate/cellulose nanofibers (PLA/PBAT/CNFs). The role of in situ generated PBAT nanofibers and CNFs in the formation of efficient physical crosslinks at PLA-PBAT, PLA-CNF and PBAT-CNF interfaces and the effect of CNFs on the PBAT fibrillation and crystallization processes were elucidated. The in situ generated composites showed drastically higher values of strain recovery ratios, strain fixity ratios, faster recovery rate and better mechanical properties compared to the blend.


Lupus ◽  
2019 ◽  
Vol 28 (12) ◽  
pp. 1468-1472 ◽  
Author(s):  
N Yoshida ◽  
F He ◽  
V C Kyttaris

Signal transducer and activator of transcription (STAT) 3 is a regulator of T-cell responses to external stimuli, such as pro-inflammatory cytokines and chemokines. We have previously shown that STAT3 is activated (phosphorylated) at high levels in systemic lupus erythematosus (SLE) T cells and mediates chemokine-induced migration and T:B cell interactions. Stattic, a small molecular STAT3 inhibitor, can partially ameliorate lupus nephritis in mice. To understand the role of STAT3 better in T-cell pathophysiology in lupus nephritis and its potential as a treatment target, we silenced its expression in T cells using a cd4-driven CRE-Flox model. We found that lupus-prone mice that do not express STAT3 in T cells did not develop lymphadenopathy, splenomegaly, or glomerulonephritis. Moreover, the production of anti-dsDNA antibodies was decreased in these mice compared to controls. To dissect the mechanism, we also used a nephrotoxic serum model of nephritis. In this model, T cell–specific silencing of STAT3 resulted in amelioration of nephrotoxic serum-induced kidney damage. Taken together, our results suggest that in mouse models of autoimmune nephritis, T cell–specific silencing of STAT3 can hamper their ability to help B cells to produce autoantibodies and induce cell tissue infiltration. We propose that STAT3 inhibition in T cells represents a novel approach in the treatment of SLE and lupus nephritis in particular.


2020 ◽  
Vol 22 (Supplement_3) ◽  
pp. iii401-iii401
Author(s):  
Sarah Injac ◽  
L Frank Huang ◽  
Stephen Mack ◽  
Frank Braun ◽  
Yuchen Du ◽  
...  

Abstract Medulloblastoma (MB) is the most common malignant brain tumor of childhood. Despite major advances in our understanding of the biology of MB, novel treatments remain urgently needed. Using a chemical-genomics driven drug repositioning strategy, we identified the cardiac glycoside family of compounds as potential treatments for Group 3 MB. We subsequently demonstrated that single-agent treatment with digoxin prolongs survival in a patient-derived xenograft model (PDOX) of Group 3 MB to a degree comparable to radiation therapy, a mainstay in the treatment of MB. Finally, we examined the mechanism of digoxin-mediated cell killing using RNA-seq. This work identified LHX9, a member of the LIM homeobox family of transcription factors, as the gene most significantly down-regulated following treatment (Huang and Injac et al, Sci Trans Medicine, 2018). Homologs of LHX9 play key roles in cerebellar development via spatially and temporally restricted expression and LHX9 has been proposed as a core transcription factor (TF) in the regulatory circuitry of Group 3 tumors. Loss of function of other core TFs has been shown to impact MB growth. The role of LHX9 in MB, however, has not been previously experimentally evaluated. We now report that knockdown of LHX9 in MB-derived cell lines results in marked growth inhibition raising the possibility that loss of LHX9 plays a major role in digoxin-mediated cell killing and that LHX9 represents a key dependency required for the growth of Group 3 MB. Clinical targeting of core TFs would represent a novel approach to targeting this devastating disease.


Sign in / Sign up

Export Citation Format

Share Document