Thermobarometric studies on the Levack Gneisses: Footwall rocks to the Sudbury Igneous Complex

Granulite and amphibolite facies gneisses and migmatites of the Levack Gneiss Complex occupy a zone up to 8 km wide around the northern part of the Sudbury Igneous Complex (SIC). Orthopyroxene- and garnet-bearing tonalitic and semipelitic assemblages of granulite facies grade occur within 3 km of the SIC together with lenses of mafic and pyroxenitic rock compositions normally represented by an amphibole +/- cpx-rich assemblage; amphibolite facies assemblages dominate elsewhere in this terrain. These 2.711-Ga gneisses were introduced by (1) the Cartier Granite Batholith during late Archaean to early Proterozoic time and (2) the SIC, at 1.85 Ga, which produced a contact aureole 1-1.5 km wide in which pyroxene hornfelses are common within 200-300 m of the contact. A suite of 12 samples including both the opx-gt and amphibole-rich rock compositions have been studied. Garnets in the semipelitic gneisses are variably replaced by a plg-bio assemblage. Thermobarometric calculations using a variety of barometers and thermometers reported in the literature suggest that the granulite facies assemblages formed at depths in the 21-28 km range (6-8 kbar). Textures and mineral chemistry in the garnet-bearing semipelitic rocks indicate that this terrain underwent a second metamorphic event during uplift to depth in the 5-11 km range (2-3 kbar) and at temperatures as low as 500-550 C. This latter event is distinct from thermal recrystallization caused by the emplacement of the SIC; it probably represents metamorphism attributable to intrusion of the Cartier Granite Batholith. These data allow two interpretations for the crustal uplift of the Levack Gneisses: (1) The gneisses were tectonically uplifted prior to the Sudbury Event (due to intrusion of the Cartier Batholith); or (2) the gneisses were raised to epizonal levels as a result of meteorite impact at 1.85 Ga

Novel pathogen introduction rapidly alters the evolution of movement, restructuring animal societies

Animal social interactions are the outcomes of evolved strategies that integrate the costs and benefits of being sociable. Using a novel mechanistic, evolutionary, individual-based simulation model, we examine how animals balance the risk of pathogen transmission against the benefits of social information about resource patches, and how this determines the emergent structure of spatial social networks. We study a scenario in which a fitness-reducing infectious pathogen is introduced into a population which has initially evolved movement rules in its absence. Pathogen introduction leads to a rapid evolutionary shift, within only a few generations, in animal social-movement strategies. Generally, animals adopt a dynamic social distancing behaviour, trading more movement away from individuals (and less intake) for lower infection risk, but there is considerable individual variation in these social movement strategies. Pathogen-adapted populations are more widely dispersed over the landscape, and thus have lessclustered social networks than their pre-introduction, pathogen-naive ancestors. Running simple epidemiological models on these emergent social networks, we show that diseases do indeed spread more slowly through pathogen-adapted animal societies. The post-introduction, pathogen-adapted movement strategy mix is stongly influenced by a combination of landscape productivity and diseasecost. Our model suggests how the introduction of an infectious pathogen to a population rapidly changes social structure. While such events might make populations more resilient to future disease outbreaks, this is at the cost of social information benefits. Overall, we offer both a general modelling framework and initial predictions for the evolutionary consequences of wildlife pathogen spillovers

Outcomes of Recurrent Head and Neck Cutaneous Squamous Cell Carcinoma

Recurrent, advanced stage cutaneous squamous cell carcinoma (cSCC) is uncommon with limited publications on patient outcomes. A retrospective study including patients who underwent surgical resection for recurrent, advanced stage cSCC of the head and neck was performed (n = 72). Data regarding tumor site, stage, treatment, parotid involvement, perineural invasion, positive margins, metastasis, and disease-free survival was analyzed. The majority of patients were male (85%) and presented with recurrent stage III (89%) cSCC. Two-year disease-free survival was 62% and decreased to 47% at 5 years. Parotid involvement, positive margins, nodal metastasis, or the presence of perineural invasion did not correlate with decreased survival (P > .05). Distant metastasis was a strong indicator of poor overall survival (P < .001). Adjuvant postoperative radiotherapy did not improve overall survival (P = .42). Overall survival was poor for patients with advanced recurrent cSCC despite the combined treatment with surgery and radiotherapy

Mining Disaggregase Sequence Space to Safely Counter TDP-43, FUS, and α-Synuclein Proteotoxicity.

Hsp104 is an AAA+ protein disaggregase, which can be potentiated via diverse mutations in its autoregulatory middle domain (MD) to mitigate toxic misfolding of TDP-43, FUS, and α-synuclein implicated in fatal neurodegenerative disorders. Problematically, potentiated MD variants can exhibit off-target toxicity. Here, we mine disaggregase sequence space to safely enhance Hsp104 activity via single mutations in nucleotide-binding domain 1 (NBD1) or NBD2. Like MD variants, NBD variants counter TDP-43, FUS, and α-synuclein toxicity and exhibit elevated ATPase and disaggregase activity. Unlike MD variants, non-toxic NBD1 and NBD2 variants emerge that rescue TDP-43, FUS, and α-synuclein toxicity. Potentiating substitutions alter NBD1 residues that contact ATP, ATP-binding residues, or the MD. Mutating the NBD2 protomer interface can also safely ameliorate Hsp104. Thus, we disambiguate allosteric regulation of Hsp104 by several tunable structural contacts, which can be engineered to spawn enhanced therapeutic disaggregases with minimal off-target toxicity

Auger Recombination in Semiconductor Quantum Wells

The principal mechanisms of Auger recombination of nonequilibrium carriers in semiconductor heterostructures with quantum wells are investigated. It is shown for the first time that there exist three fundamentally different Auger recombination mechanisms of (i) thresholdless, (ii) quasi-threshold, and (iii) threshold types. The rate of the thresholdless Auger process depends on temperature only slightly. The rate of the quasi-threshold Auger process depends on temperature exponentially. However, its threshold energy essentially varies with quantum well width and is close to zero for narrow quantum wells. It is shown that the thresholdless and the quasi-threshold Auger processes dominate in narrow quantum wells, while the threshold and the quasi-threshold processes prevail in wide quantum wells. The limiting case of a three-dimensional (3D)Auger process is reached for infinitely wide quantum wells. The critical quantum well width is found at which the quasi-threshold and threshold Auger processes merge into a single 3D Auger process. Also studied is phonon-assisted Auger recombination in quantum wells. It is shown that for narrow quantum wells the act of phonon emission becomes resonant, which in turn increases substantially the coefficient of phonon-assisted Auger recombination. Conditions are found under which the direct Auger process dominates over the phonon-assisted Auger recombination at various temperatures and quantum well widths.Comment: 38 pages, 7 figure

Quantum Monte Carlo Loop Algorithm for the t-J Model

We propose a generalization of the Quantum Monte Carlo loop algorithm to the t-J model by a mapping to three coupled six-vertex models. The autocorrelation times are reduced by orders of magnitude compared to the conventional local algorithms. The method is completely ergodic and can be formulated directly in continuous time. We introduce improved estimators for simulations with a local sign problem. Some first results of finite temperature simulations are presented for a t-J chain, a frustrated Heisenberg chain, and t-J ladder models.Comment: 22 pages, including 12 figures. RevTex v3.0, uses psf.te

Double Blind Study Investigating the Effect of Different Voice Prostheses on Ease of Swallowing and Residue Post Laryngectomy.

Voice prostheses have been examined for their effect on voice production but there is little datum on their effect on swallow function. This study investigated the difference between six commonly available voice prostheses in terms of swallowing. Laryngectomy patients had up to six voice prostheses placed in a random order over two visits. Swallowing was evaluated for each prosthesis using FEES (Fibreoptic Endoscopic Evaluation of Swallowing). After each prosthesis trial, patients self-evaluated their experience of swallowing. Three independent experts indicated which prosthesis they considered best for swallowing for each patient and judged residue on the voice prosthesis and in the upper esophagus. Raters were blinded to participant details, voice prosthesis type and scores of other raters. On patient self-evaluation, scores were equally distributed across all prostheses for swallowing. Experts most frequently chose the Blom Singer Low pressure and Blom Singer Classic Indwelling voice prostheses as best for swallowing but consensus was poor for most patients. Experts found that the Blom Singer Classic Indwelling and the Provox Vega had least residue on the voice prosthesis on thin liquid (p ≤ 0.001) and soft (p = 0.001), respectively. Experts also found that the Blom Singer Low Pressure had least residue in the upper esophagus on soft consistency (p ≤ 0.001). While self-evaluation by patients did not identify a consistently preferred prosthesis for swallow, many patients expressed personal preferences, suggesting benefits to involving patients in the choice of prosthesis. Some voice prostheses may be associated with lower levels of residue on the prosthesis and upper esophagus with certain consistencies

Evolutionary consequences of feedbacks between within-host competition and disease control

Lay Summary: Competition often occurs among diverse parasites within a single host, but control efforts could change its strength. We examined how the interplay between competition and control could shape the evolution of parasite traits like drug resistance and disease severity