New records of rare deep-water fish species in the Eastern Ionian Sea (Mediterranean Sea)

We report new species records and information related to meristic, morphometric, bathymetric and biological characteristics that increase our knowledge of the deep ichthyofauna of the Ionian Sea (E. Mediterranean). The material was collected with long lines from 300 to 800 m deep in the Eastern Ionian Sea in June and October 2010. The fish species Schedophilus ovalis (Cuvier, 1833) (Osteichthyes: Centrolophidae), Sudis hyalina Rafinesque, 1810 (Osteicthyes: Paralepididae), Brama brama (Bonnaterre, 1788) (Osteichthyes: Bramidae) and Trachipterus trachypterus (Gmelin, 1789) (Osteichthyes: Trachipteridae) were recorded for the first time in the Eastern Ionian Sea. The absence of these new or rare species from the ichthyofauna of the study area to date is probably related to the absence of adequate sampling and catching techniques, although environmental factors could also be involved.     

Capacity allocation and coordination issues for the timely processing of outsourced operations

We consider dynamic capacity booking problems faced by multiple manufacturers each outsourcing certain operations to a common third-party firm. Each manufacturer, upon observing the current state of the third-party schedule, books capacity with the objective to jointly minimize holding costs that result from early deliveries, tardiness penalties due to late deliveries, and third-party capacity booking costs. When making a reservation, each manufacturer evaluates two alternative courses of action： （i） reserving capacity not yet utilized by other manufactures who booked earlier; or （ii） forming a coalition with a subset or all of other manufacturers to achieve a schedule minimizing coalition costs, i.e., a centralized schedule for that coalition. The latter practice surely benefits the coalition as a whole; however, some manufacturers may incur higher costs if their operations are either pushed back too much, or delivered too early. For this reason, a cost allocation scheme making each manufacturer no worse than they would be when acting differently （i.e., participating in a smaller coalition or acting on their own behalf,） must accompany centralized scheduling for the coalition. We model this relationship among the manufacturers as a cooperative game with transferable utility, and present optimal and/or heuristic algorithms to attain individually and eoalitionally optimal schedules as well as a linear program formulation to find a core allocation of the manufacturers＇ costs.     

Morphological and molecular separation between Macrocamptoptera grangeri Soyka and M. metotarsa (Girault) (Hymenoptera: Mymaridae)

ABSTRACT

Based on morphological and molecular evidence, the European fairyfly Herulia sundholmi Hedqvist syn. n. (Hymenoptera: Mymaridae) is removed from previous synonymy with the Nearctic Macrocamptoptera metotarsa (Girault), and synonymised with the Palaearctic M. grangeri Soyka, which is newly recorded from Georgia, Slovakia and Spain. Macrocamptoptera bulagarica (Donev) syn. n., known from Bulgaria and Italy, is also synonymised with M. grangeri. An updated key to females of the three currently recognised species of the rarely collected genus Macrocamptoptera Girault is given.     

Network robustness depth and topology management of networked dynamic systems

Networked control systems are subject to adversary conditions that affect their network topologies. To ensure reliable system operations, network topologies need to be characterized and managed for their impact on the overall system performance. This paper introduces the concept of network robustness depth for this pursuit. Discrete event systems are used as a foundation to model dynamic behavior of network topologies, support their analysis, and carry out their management. Stochastic analysis relates the link reliability probabilities to a probabilistic characterization of network robustness depth. Several topology management strategies are discussed, including passive methods, random strategies, and optimization methodologies. Their respective benefits and limitations are quantified. By using platoon control as a platform of hybrid (continuous and discrete event) systems and packet erasure channels as a communication protocol, the results are demonstrated with case studies.     

APJ acts as a dual receptor in cardiac hypertrophy

Cardiac hypertrophy is initiated as an adaptive response to sustained overload but progresses pathologically as heart failure ensues. Here we report that genetic loss of APJ, a G-protein-coupled receptor, confers resistance to chronic pressure overload by markedly reducing myocardial hypertrophy and heart failure. In contrast, mice lacking apelin (the endogenous APJ ligand) remain sensitive, suggesting an apelin-independent function of APJ. Freshly isolated APJ-null cardiomyocytes exhibit an attenuated response to stretch, indicating that APJ is a mechanosensor. Activation of APJ by stretch increases cardiomyocyte cell size and induces molecular markers of hypertrophy. Whereas apelin stimulates APJ to activate Gαi and elicits a protective response, stretch signals in an APJ-dependent, G-protein-independent fashion to induce hypertrophy. Stretch-mediated hypertrophy is prevented by knockdown of β-arrestins or by pharmacological doses of apelin acting through Gαi. Taken together, our data indicate that APJ is a bifunctional receptor for both mechanical stretch and the endogenous peptide apelin. By sensing the balance between these stimuli, APJ occupies a pivotal point linking sustained overload to cardiomyocyte hypertrophy.     

Crowding induces live cell extrusion to maintain homeostatic cell numbers in epithelia

For an epithelium to provide a protective barrier, it must maintain homeostatic cell numbers by matching the number of dividing cells with the number of dying cells. Although compensatory cell division can be triggered by dying cells, it is unknown how cell death might relieve overcrowding due to proliferation. When we trigger apoptosis in epithelia, dying cells are extruded to preserve a functional barrier. Extrusion occurs by cells destined to die signalling to surrounding epithelial cells to contract an actomyosin ring that squeezes the dying cell out. However, it is not clear what drives cell death during normal homeostasis. Here we show in human, canine and zebrafish cells that overcrowding due to proliferation and migration induces extrusion of live cells to control epithelial cell numbers. Extrusion of live cells occurs at sites where the highest crowding occurs in vivo and can be induced by experimentally overcrowding monolayers in vitro. Like apoptotic cell extrusion, live cell extrusion resulting from overcrowding also requires sphingosine 1-phosphate signalling and Rho-kinase-dependent myosin contraction, but is distinguished by signalling through stretch-activated channels. Moreover, disruption of a stretch-activated channel, Piezo1, in zebrafish prevents extrusion and leads to the formation of epithelial cell masses. Our findings reveal that during homeostatic turnover, growth and division of epithelial cells on a confined substratum cause overcrowding that leads to their extrusion and consequent death owing to the loss of survival factors. These results suggest that live cell extrusion could be a tumour-suppressive mechanism that prevents the accumulation of excess epithelial cells.     

Accurate whole-genome sequencing and haplotyping from 10 to 20 human cells

Recent advances in whole-genome sequencing have brought the vision of personal genomics and genomic medicine closer to reality. However, current methods lack clinical accuracy and the ability to describe the context (haplotypes) in which genome variants co-occur in a cost-effective manner. Here we describe a low-cost DNA sequencing and haplotyping process, long fragment read (LFR) technology, which is similar to sequencing long single DNA molecules without cloning or separation of metaphase chromosomes. In this study, ten LFR libraries were made using only ～100?picograms of human DNA per sample. Up to 97% of the heterozygous single nucleotide variants were assembled into long haplotype contigs. Removal of false positive single nucleotide variants not phased by multiple LFR haplotypes resulted in a final genome error rate of 1 in 10?megabases. Cost-effective and accurate genome sequencing and haplotyping from 10-20 human cells, as demonstrated here, will enable comprehensive genetic studies and diverse clinical applications.     

Domain structure and function of matrix metalloprotease 23 (MMP23): role in potassium channel trafficking

MMP23 is a member of the matrix metalloprotease family of zinc- and calcium-dependent endopeptidases, which are involved in a wide variety of cellular functions. Its catalytic domain displays a high degree of structural homology with those of other metalloproteases, but its atypical domain architecture suggests that it may possess unique functional properties. The N-terminal MMP23 pro-domain contains a type-II transmembrane domain that anchors the protein to the plasma membrane and lacks the cysteine-switch motif that is required to maintain other MMPs in a latent state during passage to the cell surface. Instead of the C-terminal hemopexin domain common to other MMPs, MMP23 contains a small toxin-like domain (TxD) and an immunoglobulin-like cell adhesion molecule (IgCAM) domain. The MMP23 pro-domain can trap Kv1.3 but not closely-related Kv1.2 channels in the endoplasmic reticulum, preventing their passage to the cell surface, while the TxD can bind to the channel pore and block the passage of potassium ions. The MMP23 C-terminal IgCAM domain displays some similarity to Ig-like C2-type domains found in IgCAMs of the immunoglobulin superfamily, which are known to mediate protein–protein and protein–lipid interactions. MMP23 and Kv1.3 are co-expressed in a variety of tissues and together are implicated in diseases including cancer and inflammatory disorders. Further studies are required to elucidate the mechanism of action of this unique member of the MMP family.     

2019年熔盐电解法制备硅基能源材料热点回眸

 介绍熔盐电解法制备硅材料及其在能源领域的应用，并回顾其2019年的基础研究进展。熔盐电解方法可以在较温和的温度下通过电化学还原氧化硅实现硅纳米材料的大规模制备，得到的硅纳米材料纯度和形貌可控，能够用于硅基光伏材料以及锂离子电池负极材料。     

交换环上的Galois扩张的G－同态

定义了交换环Ｒ的关于自同构群Ｇ的Ｇ－自同态，给出有关Ｇ－自同态的一些基本性质，证明了Ｇａｌｏｉｓ扩张的Ｇ－自同态象仍为Ｇａｌｏｉｓ扩张，并且还得到它的逆命题．