Performance Enhancement in Copper Twisted Pair Cable Communications

The thesis focuses on the area of copper twisted pair based wireline communications. As one of the most widely deployed communication media, the copper twisted pair cable plays an important role in the communication network cabling infrastructure. This thesis looks to exploit diversity to improve twisted pair channels for data communications in two common application areas, namely Ethernet over Twisted Paris and digital subscriber line over twisted pair based telephone network. The first part of the thesis addresses new approaches to next generation Ethernet over twisted pair cable. The coming challenge for Ethernet over twisted pair cable is to realise a higher data rate beyond the 25/40GBASE-T standard, in relatively short reach scenarios. The straight-forward approaches, such as improving cable quality and extending frequency bandwidth, are unlikely to provide significant improvement in terms of data rate. However, other system diversities, such as spectrum utilization are yet to be fully exploited, so as to meet the desired data rate performance. The current balanced transmission over the structured twisted pair cable and its parallel single-in-single-out channel model is revisited and formulated as a full-duplex multiple-in-multiple-out (MIMO) channel model. With a common ground (provided by the cable shield), the balanced transmission is converted into unbalanced transmission, by replacing the differential-mode excitation with single-ended excitation. In this way, MIMO adoption may offer spectrum utilization advantages due to the doubled number of the channels. The S-parameters of the proposed MIMO channel model is obtained through the full wave electromagnetic simulation of a short CAT7A cable. The channel models are constructed from the resulting S-parameters, also the corresponding theoretical capacity is evaluated by exploiting different diversity scenarios. With higher spectrum efficiency, the orthogonal-frequency-division-multiplexing (OFDM) modulation can significantly improve the theoretical capacity compared with single-carrier modulation, where the channel frequency selectivity is aided. The MIMO can further enhance the capacity by minimising the impact of the crosstalk. When the crosstalk is properly handled under the unbalanced transmission, this thesis shows that the theoretical capacity of the EoTP cable can reach nearly 200GBit/s. In order to further extend the bandwidth capability of twisted pair cables, Phantom Mode transmission is studied, aiming at creating more channels under balanced transmission operation. The second part of the thesis focuses on the research of advanced scheduling algorithms for VDSL2 QoS enhancement. For VDSL2 broadband access networks, multi-user optimisation techniques have been developed, so as to improve the basic data rate performance. Spectrum balancing improves the network performance by optimising users transmit power spectra as the resource allocation, to mitigate the impact from the crosstalk. Aiming at enhancing the performance for the upstream VDSL2 service, where the users QoS demand is not known by all other users, a set of autonomous spectrum balancing algorithms is proposed. These optimise users transmit power spectra locally with only direct channel state information. To prevent selfish behaviour, the concept of a virtual user is introduced to represent the impact on both crosstalk interference and queueing status of other users. Moreover, novel algorithms are developed to determine the parameters and the weight of the virtual user. Another type of resource allocation in the VDSL2 network is crosstalk cancellation by centralised signal coordination. The history of the data queue is considered as a time series, on which different smooth filter characteristics are investigated in order to investigate further performance improvement. The use of filter techniques accounts for both the instantaneous queue length and also the previous data to determine the most efficient dynamic resource allocation. With the help of this smoothed dynamic resource allocation, the network will benefit from both reduced signalling communication and improved delay performance.The proposed algorithms are verified by numerical experiments

PPAR_2 expression in growth plate chondrocytes is regulated by p38 and GSK-3

Although peroxisome proliferator activated receptor (PPAR)_ remains a critical regulator of preadipocyte differentiation, new roles have been discovered in inflammation, bone morphogenesis, endothelial function, cancer, longevity and atherosclerosis. Despite the demonstration of PPAR expression in chondrocytes, its role and the pathways affecting its expression and activity in chondrocytes remain largely unknown. We investigated the effects of PPAR activation on chondrocyte differentiation and its participation in chondrocyte lipid metabolism. PPAR2 expression is highly regulated during chondrocyte differentiation in vivo and in vitro PPAR activation with troglitazone resulted in increased Indian hedgehog expression and reduced collagen X expression, confirming previously described roles in the inhibition of differentiation. However, the major effect of PPAR2 in chondrocytes appears to be on lipid metabolism. During differentiation chondrocytes increase expression of the lipid-associated metabolizing protein, Lpl, which is accompanied by increased gene expression of PPAR. PPAR expression is suppressed by p38 activity, but requires GSK-3 activity. Furthermore, Lpl expression is regulated by p38 and GSK-3 signalling. This is the first study demonstrating a relationship between PPAR2 expression and chondrocyte lipid metabolism and its regulation by p38 and GSK-3 signalling

Primordial Germ Cell-Like Cells Differentiated In Vitro from Skin-Derived Stem Cells

Background: We have previously demonstrated that stem cells isolated from fetal porcine skin have the potential to form oocyte-like cells (OLCs) in vitro. However, primordial germ cells (PGCs), which must also be specified during the stem cell differentiation to give rise to these putative oocytes at more advanced stages of culture, were not systematically characterized. The current study tested the hypothesis that a morphologically distinct population of cells derived from skin stem cells prior to OLC formation corresponds to putative PGCs, which differentiate further into more mature gametes. Methodology/Principal Findings: When induced to differentiate in an appropriate microenvironment, a subpopulation of morphologically distinct cells, some of which are alkaline phosphatase (AP)-positive, also express Oct4, Fragilis, Stella, Dazl, and Vasa, which are markers indicative of germ cell formation. A known differentially methylated region (DMR) within the H19 gene locus, which is demethylated in oocytes after establishment of the maternal imprint, is hypomethylated in PGClike cells compared to undifferentiated skin-derived stem cells, suggesting that the putative germ cell population undergoes imprint erasure. Additional evidence supporting the germ cell identity of in vitro-generated PGC-like cells is that, when labeled with a Dazl-GFP reporter, these cells further differentiate into GFP-positive OLCs. Significance: The ability to generate germ cell precursors from somatic stem cells may provide an in vitro model to stud

Smoothed Complexity Theory

Smoothed analysis is a new way of analyzing algorithms introduced by Spielman and Teng (J. ACM, 2004). Classical methods like worst-case or average-case analysis have accompanying complexity classes, like P and AvgP, respectively. While worst-case or average-case analysis give us a means to talk about the running time of a particular algorithm, complexity classes allows us to talk about the inherent difficulty of problems. Smoothed analysis is a hybrid of worst-case and average-case analysis and compensates some of their drawbacks. Despite its success for the analysis of single algorithms and problems, there is no embedding of smoothed analysis into computational complexity theory, which is necessary to classify problems according to their intrinsic difficulty. We propose a framework for smoothed complexity theory, define the relevant classes, and prove some first hardness results (of bounded halting and tiling) and tractability results (binary optimization problems, graph coloring, satisfiability). Furthermore, we discuss extensions and shortcomings of our model and relate it to semi-random models.Comment: to be presented at MFCS 201

Tracking crystal-melt segregation and magma recharge using zircon trace element data

The Cretaceous Yunshan caldera complex in SE China consists of an unusual coexisting assemblage of peraluminous and peralkaline rhyolites and a resurgent intra-caldera porphyritic quartz monzonite. In this study, we use zircon trace element data to study the compositional differences of zircons from cogenetic magmas and to track the evolution of the entire magmatic system. Our results indicate that the zircons from the peraluminous and peralkaline rhyolites formed from highly evolved compositions with high Hf concentrations and low Ti contents, and low Th/U and Zr/Hf ratios, which are distinct from those of the intrusive porphyritic quartz monzonite. Zircons from the peraluminous and peralkaline rhyolites display overlapping Zr/Hf and Hf, but the zircons from the peralkaline rhyolites have extremely low Eu/Eu* ratios (Peer reviewe

Structure–function analysis of the kinase-CPD domain of yeast tRNA ligase (Trl1) and requirements for complementation of tRNA splicing by a plant Trl1 homolog

Trl1 is an essential 827 amino acid enzyme that executes the end-healing and end-sealing steps of tRNA splicing in Saccharomyces cerevisiae. Trl1 consists of two domains—an N-terminal ligase component and a C-terminal 5′-kinase/2′,3′-cyclic phosphodiesterase (CPD) component—that can function in tRNA splicing in vivo when expressed as separate polypeptides. To understand the structural requirements for the kinase-CPD domain, we performed an alanine scan of 30 amino acids that are conserved in Trl1 homologs from other fungi. We thereby identified four residues (Arg463, His515, Thr675 and Glu741) as essential for activity in vivo. Structure–function relationships at these positions, and at four essential or conditionally essential residues defined previously (Asp425, Arg511, His673 and His777), were clarified by introducing conservative substitutions. Biochemical analysis showed that lethal mutations of Asp425, Arg463, Arg511 and His515 in the kinase module abolished polynucleotide kinase activity in vitro. We report that a recently cloned 1104 amino acid Arabidopsis RNA ligase functions in lieu of yeast Trl1 in vivo and identify essential side chains in the ligase, kinase and CPD modules of the plant enzyme. The plant ligase, like yeast Trl1 but unlike T4 RNA ligase 1, requires a 2′-PO(4) end for tRNA splicing in vivo

Geology, U-Pb geochronology and stable isotope geochemistry of the Heihaibei gold deposit in the southern part of the Eastern Kunlun Orogenic Belt, China : A granitic intrusion-related gold deposit?

The Heihaibei gold deposit is a newly discovered gold deposit in the southern part of the Eastern Kunlun Orogenic Belt. Its most distinctive features are that the gold mineralization is hosted in monzogranite, and that the presence of pre-ore (possibly syn-ore) monzogranite and post-ore gabbro allows to constrain the minerali-zation's formation age. Zircons from the monzogranites yield U-Pb ages of 454 +/- 3 Ma, while zircons separated from the gabbro dikes cutting the monzogranites and gold mineralized body yield U-Pb ages of 439 +/- 3 Ma, which is interpreted to be the minimum age of the Au mineralizing event. Combined with the regional geological background, we proposed that the Heihaibei Au mineralization occurred during the subduction stage of the Early Paleozoic Proto-Tethys ocean. The ore assemblage is dominated by pyrite, arsenopyrite and native gold. The hydrothermal alteration that has led to the peculiar enrichment of Au is not systematically distributed and displays no clear concentric zoning pattern. The main mineralization formed during three stages: the K-feldspar-quartz-pyrite (Py1)-arsenopyrite-sericite-epidote stage (I), the quartz-pyrite (Py2)-native gold-chlorite stage (II), and the quartz-carbonate stage (III). The main gold mineralization occurred during stage II. Fluid inclusion homogenization temperature and salinities decrease from stage I (Th., 268-412 C; W., 6.87-16.63 wt% NaCl equiv.) to stage II (Th., 183-288 C; W., 3.69-14.84 wt% NaCl equiv.). The 818O and 8D values (818OH2O = 4.9 to 9.7%o; 8DV-SMOW =-84.1%o to -81.1%o) of quartz samples from stage I and stage II are comparable to a magmatic-hydrothermal ore-forming fluid that possibly underwent fluid-rock interaction with the Nachitai Group metamorphic rocks during the early ore-forming stage. The relatively uniform 834S values (834SV-CDT = 7.7 to 8.5%o) are slightly elevated compared to magmatic 834S values, but could be derived from a magma if a significant crustal melt component is present. Moreover, the 834S values are within the S isotopic composition range of a granitic reservoir, suggesting that they are probably inherited from the Heihaibei monzogranites. The Pb and Hf isotope compositions imply a close genetic association between the gold mineralization and granitic magmatism, which are both the products of the mixing of crustal and mantle sources. The trace element compositions of pyrite provide additional evidence that the gold mineralization in the Heihaibei deposit was related to the magmatism. Compared with the typical characteristics of orogenic gold and intrusion-related gold systems (IRGS) deposits, the Heihaibei gold deposit may instead be classified as a granitic intrusion-related gold deposit.Peer reviewe

75%-efficiency blue generation from an intracavity PPKTP frequency doubler

We report on a high-efficiency 461 nm blue light conversion from an external cavity-enhanced second-harmonic generation of a 922 nm diode laser with a quasi-phase-matched KTP crystal (PPKTP). By choosing a long crystal (LC=20 mm) and twice looser focusing (w0=43 $\mu$m) than the "optimal" one, thermal lensing effects due to the blue power absorption are minimized while still maintaining near-optimal conversion efficiency. A stable blue power of 234 mW with a net conversion efficiency of eta=75% at an input mode-matched power of 310 mW is obtained. The intra-cavity measurements of the conversion efficiency and temperature tuning bandwidth yield an accurate value d33(461 nm)=15 pm/V for KTP and provide a stringent validation of some recently published linear and thermo-optic dispersion data of KTP

Reduced EGFR signaling enhances cartilage destruction in a mouse osteoarthritis model

Osteoarthritis (OA) is a degenerative joint disease and a major cause of pain and disability in older adults. We have previously identified epidermal growth factor receptor (EGFR) signaling as an important regulator of cartilage matrix degradation during epiphyseal cartilage development. To study its function in OA progression, we performed surgical destabilization of the medial meniscus (DMM) to induce OA in two mouse models with reduced EGFR activity, one with genetic modification (Egfr Wa5/+ mice) and the other one with pharmacological inhibition (gefitinib treatment). Histological analyses and scoring at 3 months post-surgery revealed increased cartilage destruction and accelerated OA progression in both mouse models. TUNEL staining demonstrated that EGFR signaling protects chondrocytes from OA-induced apoptosis, which was further confirmed in primary chondrocyte culture. Immunohistochemistry showed increased aggrecan degradation in these mouse models, which coincides with elevated amounts of ADAMTS5 and matrix metalloproteinase 13 (MMP13), the principle proteinases responsible for aggrecan degradation, in the articular cartilage after DMM surgery. Furthermore, hypoxia-inducible factor 2α (HIF2α), a critical catabolic transcription factor stimulating MMP13 expression during OA, was also upregulated in mice with reduced EGFR signaling. Taken together, our findings demonstrate a primarily protective role of EGFR during OA progression by regulating chondrocyte survival and cartilage degradation