90 research outputs found
A new pachyrhizodontid fish (Actinopterygii: Teleostei) from the Tarrant Formation (Cenomanian) of the Upper Cretaceous Eagle Ford Group of Texas, U.S.A.
SMU 76938 is a fossil skeleton of a large, nearly complete actinopterygian bony fish housed in Southern Methodist University in Dallas, Texas, USA. It was collected from the Upper Cretaceous Tarrant Formation (middle Cenomanian; ~96 Ma) of the Eagle Ford Group in Tarrant County, Texas, an area where it was near the western margin of the East Texas Embayment during the Late Cretaceous. Although parts of the skull and dorsal fin are damaged, SMU 76938 is relatively complete, especially in the preservation of the caudal fin with its soft tissue outline. The fish has a fusiform body and measures about 93, 109, and 119 cm in standard length, fork length, and total length, respectively, and about 17 cm in maximum body depth. Several features of SMU 76938 are reminiscent of Cretaceous crossognathiforms, yet many features, such as the villiform dentition, have yet to be seen in any taxa within the order. My phylogenetic analysis indicates that SMU 76938 is a pachyrhizodontid crossognathiform fish. The combination of villiform teeth and fused infraorbital 1 and 2 in SMU 76938 is unique, suggesting that the specimen belongs to a new genus and species within the family Pachyrhizodontidae. With a fusiform body, a large symmetrical caudal fin, and a mouth with numerous small conical teeth suited for grasping, the new taxon represented by SMU 76938 was most likely a fast swimming, open-ocean predator capable of high propulsion and quick bursts of speed, that likely pursued smaller, quick swimming animals, such as squid, crustaceans, and other fishes. Although the individual represented by SMU 76938 was about 14 years old at the time of its death, my vertebra-based theoretical growth model indicates that the species could have reached up to about 1.8 m TL and lived up to 37 years old in age
Microplastic in Surface Waters of Urban Rivers: Concentration, Sources, and Associated Bacterial Assemblages
The ecological dynamics of microplastic (\u3c5 mm) are well documented in marine ecosystems, but the sources, abundance, and ecological role of microplastic in rivers are unknown and likely to be substantial. Microplastic fibers (e.g., synthetic fabrics) and pellets (e.g., abrasives in personal care products) are abundant in wastewater treatment plant (WWTP) effluent, and can serve as a point source of microplastic in rivers. The buoyancy, hydrophobic surface, and long transport distance of microplastic make it a novel substrate for the selection and dispersal of unique microbial assemblages. We measured microplastic concentration and bacterial assemblage composition on microplastic and natural surfaces upstream and downstream of WWTP effluent sites at nine rivers in Illinois, United States. Microplastic concentration was higher downstream of WWTP effluent outfall sites in all but two rivers. Pellets, fibers, and fragments were the dominant microplastic types, and polymers were identified as polypropylene, polyethylene, and polystyrene. Mean microplastic flux was 1,338,757 pieces per day, although the flux was highly variable among nine sites (min = 15,520 per day, max = 4,721,709 per day). High-throughput sequencing of 16S rRNA genes showed bacterial assemblage composition was significantly different among microplastic, seston, and water column substrates. Microplastic bacterial assemblages had lower taxon richness, diversity, and evenness than those on other substrates, and microplastic selected for taxa that may degrade plastic polymers (e.g., Pseudomonas) and those representing common human intestinal pathogens (e.g., Arcobacter). Effluent from WWTPs in rivers is an important component of the global plastic “life cycle,” and microplastic serves as a novel substrate that selects and transports distinct bacterial assemblages in urban rivers. Rates of microplastic deposition, consumption by stream biota, and the metabolic capacity of microplastic biofilms in rivers are unknown and merit further research
Historical roots of gauge invariance
Gauge invariance is the basis of the modern theory of electroweak and strong
interactions (the so called Standard Model). The roots of gauge invariance go
back to the year 1820 when electromagnetism was discovered and the first
electrodynamic theory was proposed. Subsequent developments led to the
discovery that different forms of the vector potential result in the same
observable forces. The partial arbitrariness of the vector potential A brought
forth various restrictions on it. div A = 0 was proposed by J. C. Maxwell;
4-div A = 0 was proposed L. V. Lorenz in the middle of 1860's . In most of the
modern texts the latter condition is attributed to H. A. Lorentz, who half a
century later was one of the key figures in the final formulation of classical
electrodynamics. In 1926 a relativistic quantum-mechanical equation for charged
spinless particles was formulated by E. Schrodinger, O. Klein, and V. Fock. The
latter discovered that this equation is invariant with respect to
multiplication of the wave function by a phase factor exp(ieX/hc) with the
accompanying additions to the scalar potential of -dX/cdt and to the vector
potential of grad X. In 1929 H. Weyl proclaimed this invariance as a general
principle and called it Eichinvarianz in German and gauge invariance in
English. The present era of non-abelian gauge theories started in 1954 with the
paper by C. N. Yang and R. L. Mills.Comment: final-final, 34 pages, 1 figure, 106 references (one added with
footnote since v.2); to appear in July 2001 Rev. Mod. Phy
Can Charisma Be Taught? Tests of Two Interventions
We tested whether we could teach individuals to behave more charismatically, andwhether changes in charisma affected leader outcomes. In Study 1, a mixed-design fieldexperiment, we randomly assigned 34 middle-level managers to a control or anexperimental group. Three months later, we reassessed the managers using theircoworker ratings (Time 1 raters = 343; Time 2 raters = 321). In Study 2, a within-subjectslaboratory experiment, we videotaped 41 MBA participants giving a speech. We thentaught them how to behave more charismatically, and they redelivered the speech6 weeks later. Independent assessors (n = 135) rated the speeches. Results from thestudies indicated that the training had significant effects on ratings of leader charisma(mean D = .62) and that charisma had significant effects on ratings of leaderprototypicality and emergence...............................................................................................................................
Genome-wide association and Mendelian randomisation analysis provide insights into the pathogenesis of heart failure
Heart failure (HF) is a leading cause of morbidity and mortality worldwide. A small proportion of HF cases are attributable to monogenic cardiomyopathies and existing genome-wide association studies (GWAS) have yielded only limited insights, leaving the observed heritability of HF largely unexplained. We report results from a GWAS meta-analysis of HF comprising 47,309 cases and 930,014 controls. Twelve independent variants at 11 genomic loci are associated with HF, all of which demonstrate one or more associations with coronary artery disease (CAD), atrial fibrillation, or reduced left ventricular function, suggesting shared genetic aetiology. Functional analysis of non-CAD-associated loci implicate genes involved in cardiac development (MYOZ1, SYNPO2L), protein homoeostasis (BAG3), and cellular senescence (CDKN1A). Mendelian randomisation analysis supports causal roles for several HF risk factors, and demonstrates CAD-independent effects for atrial fibrillation, body mass index, and hypertension. These findings extend our knowledge of the pathways underlying HF and may inform new therapeutic strategies
Search for Eccentric Black Hole Coalescences during the Third Observing Run of LIGO and Virgo
Despite the growing number of confident binary black hole coalescences
observed through gravitational waves so far, the astrophysical origin of these
binaries remains uncertain. Orbital eccentricity is one of the clearest tracers
of binary formation channels. Identifying binary eccentricity, however, remains
challenging due to the limited availability of gravitational waveforms that
include effects of eccentricity. Here, we present observational results for a
waveform-independent search sensitive to eccentric black hole coalescences,
covering the third observing run (O3) of the LIGO and Virgo detectors. We
identified no new high-significance candidates beyond those that were already
identified with searches focusing on quasi-circular binaries. We determine the
sensitivity of our search to high-mass (total mass ) binaries
covering eccentricities up to 0.3 at 15 Hz orbital frequency, and use this to
compare model predictions to search results. Assuming all detections are indeed
quasi-circular, for our fiducial population model, we place an upper limit for
the merger rate density of high-mass binaries with eccentricities at Gpc yr at 90\% confidence level.Comment: 24 pages, 5 figure
Intravenous alteplase for stroke with unknown time of onset guided by advanced imaging: systematic review and meta-analysis of individual patient data
Background: Patients who have had a stroke with unknown time of onset have been previously excluded from thrombolysis. We aimed to establish whether intravenous alteplase is safe and effective in such patients when salvageable tissue has been identified with imaging biomarkers. Methods: We did a systematic review and meta-analysis of individual patient data for trials published before Sept 21, 2020. Randomised trials of intravenous alteplase versus standard of care or placebo in adults with stroke with unknown time of onset with perfusion-diffusion MRI, perfusion CT, or MRI with diffusion weighted imaging-fluid attenuated inversion recovery (DWI-FLAIR) mismatch were eligible. The primary outcome was favourable functional outcome (score of 0–1 on the modified Rankin Scale [mRS]) at 90 days indicating no disability using an unconditional mixed-effect logistic-regression model fitted to estimate the treatment effect. Secondary outcomes were mRS shift towards a better functional outcome and independent outcome (mRS 0–2) at 90 days. Safety outcomes included death, severe disability or death (mRS score 4–6), and symptomatic intracranial haemorrhage. This study is registered with PROSPERO, CRD42020166903. Findings: Of 249 identified abstracts, four trials met our eligibility criteria for inclusion: WAKE-UP, EXTEND, THAWS, and ECASS-4. The four trials provided individual patient data for 843 individuals, of whom 429 (51%) were assigned to alteplase and 414 (49%) to placebo or standard care. A favourable outcome occurred in 199 (47%) of 420 patients with alteplase and in 160 (39%) of 409 patients among controls (adjusted odds ratio [OR] 1·49 [95% CI 1·10–2·03]; p=0·011), with low heterogeneity across studies (I2=27%). Alteplase was associated with a significant shift towards better functional outcome (adjusted common OR 1·38 [95% CI 1·05–1·80]; p=0·019), and a higher odds of independent outcome (adjusted OR 1·50 [1·06–2·12]; p=0·022). In the alteplase group, 90 (21%) patients were severely disabled or died (mRS score 4–6), compared with 102 (25%) patients in the control group (adjusted OR 0·76 [0·52–1·11]; p=0·15). 27 (6%) patients died in the alteplase group and 14 (3%) patients died among controls (adjusted OR 2·06 [1·03–4·09]; p=0·040). The prevalence of symptomatic intracranial haemorrhage was higher in the alteplase group than among controls (11 [3%] vs two [<1%], adjusted OR 5·58 [1·22–25·50]; p=0·024). Interpretation: In patients who have had a stroke with unknown time of onset with a DWI-FLAIR or perfusion mismatch, intravenous alteplase resulted in better functional outcome at 90 days than placebo or standard care. A net benefit was observed for all functional outcomes despite an increased risk of symptomatic intracranial haemorrhage. Although there were more deaths with alteplase than placebo, there were fewer cases of severe disability or death. Funding: None
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