Static compression of porous dust aggregates

Context: In protoplanetary disks, dust grains coagulate with each other and grow to form aggregates. As these aggregates grow by coagulation, their filling factor \phi decreases down to \phi << 1. However, comets, the remnants of these early planetesimals, have \phi ~ 0.1. Thus, static compression of porous dust aggregates is important in planetesimal formation. However, the static compression strength has been investigated only for relatively high density aggregates (\phi > 0.1). Aims: We investigate and find the compression strength of highly porous aggregates (\phi << 1). Methods: We perform three dimensional N-body simulations of aggregate compression with a particle-particle interaction model. We introduce a new method of static compression: the periodic boundary condition is adopted and the boundaries move with low speed to get closer. The dust aggregate is compressed uniformly and isotropically by themselves over the periodic boundaries. Results: We empirically derive a formula of the compression strength of highly porous aggregates (\phi << 1). We check the validity of the compression strength formula for wide ranges of numerical parameters, such as the size of initial aggregates, the boundary speed, the normal damping force, and material. We also compare our results to the previous studies of static compression in the relatively high density region (\phi > 0.1) and confirm that our results consistently connect to those in the high density region. The compression strength formula is also derived analytically.Comment: 12 pages, 14 figures, accepted for publication in A&

Interpopulation variation of behavioural and morphological traits that affect downstream displacement of the juvenile white‐spotted charr Salvelinus leucomaenis

Downstream displacement is a riverine phenomenon in which organisms are advected by water flow from their home river section to a downstream area. Water flows that cause downstream displacement can be divided into two types: flood flows (Chapman & Kramer, 1991; Good et al., 2001; Meffe, 1984; Sato, 2006; Weese et al., 2011; Yamada & Wada, 2021) and flows under ordinary river conditions (i.e., ordinary flows; Lechner et al., 2016; Nagel et al., 2021; Thiesmeier & Schuhmacher, 1990). Although flood flows can cause catastrophic downstream displacement (Meffe, 1984; Sato, 2006; Weese et al., 2011), occurrences of such downstream displacement are often trait-dependent in riverine fishes (Blondel et al., 2021; Chapman & Kramer, 1991; Good et al., 2001; Meffe, 1984; Yamada & Wada, 2021). For example, smaller individuals are more likely to be displaced by strong floods from their home river section in populations of the molly Poecilia gillii (Kner 1863) (Chapman & Kramer, 1991) and the Trinidadian guppy Poecilia reticulata Peters 1859 (Blondel et al., 2021). Downstream displacement due to ordinary flows can also remove individuals with vulnerable traits from upstream populations. For example, reduced use of low-current habitats in the stickleback Gasterosteus aculeatus (Linnaeus 1758) is correlated with increased downstream displacement under ordinary flow conditions (Jiang et al., 2015). Thus, downstream displacement can be a general evolutionary pressure that removes individuals with low resistance to flow-driven displacement from their home river reaches (Yamada & Wada, 2021)

Morphological evolution reduces downstream displacement in juvenile landlocked salmon

Severe flooding often leads to downstream displacement of aquatic animals. Despite this, many salmonid populations persist in habitats located upstream of tall barriers, such as artificial check dams and/or natural waterfalls, that completely block fishes from returning to the upstream areas after flooding. The evolution of such populations may be affected by spatial sorting due to differential rates of downstream displacement. This study examined whether a morphological trait (increased body depth) that allows individuals to better maintain their position during flooding has evolved in juvenile amago salmon Oncorhynchus masou ishikawae inhabiting above-barrier habitats in two rivers. In both rivers, juveniles collected at the stations with multiple downstream barriers had deeper bodies than those collected at other stations. Similar differences were found in juveniles reared in a common-garden experiment. Field experiments with natural flooding also indicated that deep bodies help juveniles resist downstream displacement. These results consistently suggest that juveniles in some above-barrier habitats have evolved deep bodies to resist downstream displacement due to flooding. Our study is the first to show the evolutionary outcomes of passive spatial sorting during severe climate events

Neurophysiological studies on the control mechanisms of the pheromone-triggered behavior in the silkmoth

Male Silkmoths, Bombyx mori exhibit a characteristic zigzagging behavior consisting of a straight-line walking, zigzagging turns and a looping. The timing for shifting the turning direction is synchronized to the sideways head movements controlled by neck motor neurons (NMNs) including a cervical ventral NMN (cvl-NMN). ...Thesis (Ph. D. in Science)--University of Tsukuba, (A), no. 3720, 2005.3.25Includes bibliographical referencesTitlepage,Table of Contents -- 1.List of Abbreviations -- 2.Abstract -- 3.Introduction -- 4.Material and Methods -- 5.Results -- 6.Discussion -- 7.Acknowledgements -- 8.References -- 9.Figures and Legends -- 10.Table

Soluble PD-L1 changes in advanced non-small cell lung cancer patients treated with PD-1 inhibitors: an individual patient data meta-analysis

IntroductionCurrently, first-line immune checkpoint inhibitors (ICIs), including programmed cell death protein-1 (PD-1) inhibitors, are utilized as monotherapy in advanced non-small cell lung cancer (NSCLC) patients with high programmed death ligand-1 (PD-L1) expression (≧50%). Pre-treatment or post-treatment serum soluble PD-L1 (sPD-L1) has been identified as a potential biomarker for assessing ICI efficacy through fixed-point observations. However, existing studies on sPD-L1 changes have produced inconsistent results or have had sample sizes too small to detect clinically meaningful effect sizes. To elucidate the role of sPD-L1, we conducted a collaborative individual patient data meta-analysis of PD-1 inhibitor treatments.MethodsWe conducted a thorough search of articles in PubMed via Medline, Embase, Scopus, and Cochrane databases from inception to October 20, 2023. Trials were deemed eligible if they contained individual datasets for advanced NSCLC patients, including data on overall survival (OS)/progression-free survival (PFS), as well as pre- and post-treatment sPD-L1 levels after 3-4 cycles of PD-1 inhibitor treatments. Our analysis focused on patients who completed 3-4 cycles of PD-1 inhibitor treatments. The primary outcome measure was OS/PFS, and we assessed changes in sPD-L1 concentration pre- and post-treatment through ELISA analyses.ResultsFrom our search, we identified a potential seven trials, encompassing 256 patients. Among these, two trials with 26 patients met the criteria for inclusion in our primary analyses. Over a median follow-up period of 10 months, pooled univariate analysis revealed that increases in sPD-L1 levels during PD-1 inhibitor treatment were not associated with OS (HR = 1.25; CI: 0.52–3.02)/PFS (HR = 1.42; CI: 0.61–3.30) when compared to cases with sPD-L1 decreases. Subgroup analyses indicated that the impact of sPD-L1 changes on overall mortality/progression-related mortality remained consistent regardless of gender, age, or the type of treatment (nivolumab or pembrolizumab).ConclusionOur findings suggest that changes in sPD-L1 levels during PD-1 inhibitor treatment do not significantly influence the prognosis of advanced NSCLC patients, regardless of gender, age, or treatment type. Continuous monitoring of sPD-L1 may not offer significant advantages compared to fixed-point observations

Phase structure of linear quiver gauge theories from anomaly matching

We consider the phase structure of the linear quiver gauge theory, using the 't Hooft anomaly matching condition. This theory is characterized by the length $K$ of the quiver diagram. When $K$ is even, the symmetry and its anomaly are the same as those of massless QCD. Therefore, one can expect that the spontaneous symmetry breaking similar to the chiral symmetry breaking occurs. On the other hand, when $K$ is odd, the anomaly matching condition is satisfied by the massless composite fermions. We also consider the thermal partition function under the twisted boundary conditions. When $K$ is even, from the anomaly at finite temperature, we estimate the relation between the critical temperatures associated with the confinement/deconfinement and the breaking of the global symmetry. Finally we discuss the anomaly matching at finite temperature when $K$ is odd.Comment: 20 pages, 6 figure