Fractal Graphene Patch Antennas and the THz Communications Revolution

Fractal antennas have and are continuing to receive attention in regard to the futureof wireless communications. This is because of their wide- and multi-band capabilities, theopportunity of fractal geometries to drive multiple resonances, and, the ability to make smallerand lighter antennas with fewer components and radiative elements with higher gains. Smallscale (i.e. on the micro- and nano-scale) and ultra high frequency (in the Terahertz or THz range)fractal antennas composed of Graphene have the potential to enhance wireless communicationsat a data rate that is unprecedented, i.e.∼1012bits per second. A Fractal Graphene antennais a high-frequency tuneable antenna for radio communications in the THz spectrum, enablingunique applications such as wireless nano-networks. This is because (mono-layer) Grapheneis a one-atom-thick two-dimensional allotrope of Carbon with the highest known electricalconductivity that is currently unavailable in any other material, including metals such as Goldand Silver. Thus, combining the properties of Graphene with the self-affine characteristics ofa fractal at the micro- and nano-scale, provides the potential to revolutionise communications,at least in the near field (the order of a few metres) for low power systems. In this paper, weconsider the basic physics and some of the principle mathematical models associated with thedevelopment of this new disruptive technology in order to provide a guide to those engagedin current and future research, a fractal Graphene antenna being an example of an advancedmaterial for demanding applications. This includes some example simulations on the THz fieldpatterns generated by a fractal patch antenna composed of Graphene whose conductivity istaken to scale with the inverse of the frequency according to a ‘Drude’ model. The approachto generating THz sources using Graphene is also explored based on Infrared laser pumping toinduce a THz photo-current

Fractal Graphene Patch Antennas and the THz Communications Revolution

Fractal antennas have and are continuing to receive attention in regard to the futureof wireless communications. This is because of their wide- and multi-band capabilities, theopportunity of fractal geometries to drive multiple resonances, and, the ability to make smallerand lighter antennas with fewer components and radiative elements with higher gains. Smallscale (i.e. on the micro- and nano-scale) and ultra high frequency (in the Terahertz or THz range)fractal antennas composed of Graphene have the potential to enhance wireless communicationsat a data rate that is unprecedented, i.e.∼1012bits per second. A Fractal Graphene antennais a high-frequency tuneable antenna for radio communications in the THz spectrum, enablingunique applications such as wireless nano-networks. This is because (mono-layer) Grapheneis a one-atom-thick two-dimensional allotrope of Carbon with the highest known electricalconductivity that is currently unavailable in any other material, including metals such as Goldand Silver. Thus, combining the properties of Graphene with the self-affine characteristics ofa fractal at the micro- and nano-scale, provides the potential to revolutionise communications,at least in the near field (the order of a few metres) for low power systems. In this paper, weconsider the basic physics and some of the principle mathematical models associated with thedevelopment of this new disruptive technology in order to provide a guide to those engagedin current and future research, a fractal Graphene antenna being an example of an advancedmaterial for demanding applications. This includes some example simulations on the THz fieldpatterns generated by a fractal patch antenna composed of Graphene whose conductivity istaken to scale with the inverse of the frequency according to a ‘Drude’ model. The approachto generating THz sources using Graphene is also explored based on Infrared laser pumping toinduce a THz photo-current

Expanding the epidemiological understanding of hepatitis C in South Africa: Perspectives from a patient cohort in a rural town

Background. The epidemiology of hepatitis C virus (HCV) in the general population of South Africa (SA) is incompletely understood. A high HCV prevalence in key populations is known, but data are limited in terms of a broader understanding of transmission risks in our general population.Objectives. To investigate a patient cohort with HCV infection clustering in a rural SA town, in order to identify possible HCV transmission risks, virological characteristics, phylogenetic data and treatment outcomes.Methods. A cluster of patients with positive HCV serology, previously identified from laboratory records, were contacted by a local district hospital and offered confirmatory testing for HCV viraemia where needed. Those with confirmed HCV RNA were invited to a local hospital visit, where relevant demographic information was recorded, clinical assessment performed and a confidential questionnaire administered. HCV population-based sequencing was performed on HCV NS3/4A, NS5A and NS5B using polymerase chain reaction-specific or M13 universal primers, and sequences were aligned using BioEdit 7.2.5. Phylogenetic trees were constructed. Clinical assessments included liver fibrosis determination with FibroScan (cut-off ≥12.5 kPa = F4). Patients were offered treatment, and sustained virological response (SVR) was confirmed by undetectable HCV RNA at least 12 weeks after the end of treatment.Results. Twenty-one patients, all from the same town, median (interquartile range (IQR)) age 64 (59 - 70) years, 57% female, were evaluated. Of these, 24% (n=5) were HIV co-infected, stable on antiretrovirals. The median (IQR) alanine aminotransferase level was 51 (31 - 89) U/L, with fibrosis distribution including 29% F1, 29% F2, 9% F3 and 33% F4 METAVIR fibrosis. Virologically, two genotypes were observed: 62% (n=13) genotype (GT) 1b and 38% (n=8) GT5a. No patient had ever used injecting drugs, 14% (n=3) had received blood products before 1992, and 9.5% (n=2) had undergone traditional healer-administered scarification. All (n=21) reported attendance at a single primary care clinic in the past, with most (n=20) recalling having received parenteral therapies at the clinic. Phylogenetic analysis of the HCV NS5A and NS5B regions confirmed GT1b and GT5a genotypes and formed two separate clusters within their respective genotypes, suggesting a common source for each genotype infection. Most patients received treatment with sofosbuvir/daclatasvir, 1 was treated with sofosbuvir/velpatasvir, and 1 was re-treated with sofosbuvir/velpatasvir/voxilaprevir. Per protocol SVR was 95%, with the non-SVR patient successfully re-treated.Conclusions. Data from a rural town cluster of patients suggest parenteral medical exposure as the probable common source of hepatitis C transmission risk. The cohort was of older age with a significant number having advanced fibrosis or cirrhosis, suggesting HCV acquisition in the distant past. Using a simplified care approach, treatment outcomes were very good

A preliminary study of a graphene fractal sierpinski antenna

We provide a preliminary study of a Graphene fractal antenna operating at THz frequencies with the opportunity to modulate the emission. There are many advantages of the fractal design, namely multiband/wideband ability, and, a smaller, lighter and simpler configuration for higher gain, that can benefit from the coupling with Graphene, the thinnest and strongest of materials exhibiting very high electrical conductivity and tunability. This paper proposes a conceptual background for the study and presents some preliminary results on the electromagnetic emission simulations undertake

Event-based Classification with Recurrent Spiking Neural Networks on Low-end Micro-Controller Units

Due to its intrinsic sparsity both in time and space, event-based data is optimally suited for edge-computing applications that require low power and low latency. Time varying signals encoded with this data representation are best processed with Spiking Neural Networks (SNN). In particular, recurrent SNNs (RSNNs) can solve temporal tasks using a relatively low number of parameters, and therefore support their hardware implementation in resource-constrained computing architectures. These premises propel the need of exploring the properties of these kinds of structures on low-power processing systems to test their limits both in terms of computational accuracy and resource consumption, without having to resort to full-custom implementations. In this work, we implemented an RSNN model on a low-end, resource-constrained ARM-Cortex-M4-based Micro Controller Unit (MCU). We trained it on a down-sampled version of the N-MNIST event-based dataset for digit recognition as an example to assess its performance in the inference phase. With an accuracy of 97.2%, the implementation has an average energy consumption as low as 4.1μJ and a worst-case computational time of 150.4μs per time-step with an operating frequency of 180 MHz, so the deployment of RSNNs on MCU devices is a feasible option for small image vision real-time tasks

Retroviral DNA—the silent winner: blood transfusion containing latent feline leukemia provirus causes infection and disease in naïve recipient cats

Additional File 7: Figure S5. Photo of a blood smear from cat R1 (group B) with lymphoblastic leukemia at the time of necropsy. Lymphoblast cells are marked with an arrow. a) The picture displays a large lymphoblast with moderate amounts of basophilic cytoplasm and a large, round nucleus with fine chromatin patterns and several large, indistinct nucleoli. There is also a medium-sized lymphocyte with moderate amounts of pale basophilic cytoplasm and a round nucleus with a coarse chromatin pattern. b) The picture shows a medium-sized to large lymphoblast with small amounts of basophilic cytoplasm and a large, round nucleus with a fine chromatin pattern and two prominent round nucleoli

Chronic "Candidatus Mycoplasma turicensis" infection

"Candidatus Mycoplasma turicensis" infects felids. The pathogenesis of "Candidatus M. turicensis" chronic infection is poorly understood. The goals of the present study were to (1) induce reactivation of the infection in chronic carrier cats by attempted immunosuppression, (2) identify potential tissue sequestration using real-time TaqMan® PCR and (3) monitor the humoral immune response by DnaK enzyme-linked immunosorbent assay (ELISA). Ten specified pathogen-free cats that had ostensibly recovered from experimental "Candidatus M. turicensis" infection were used: five cats (group 1) received high dose methylprednisolone (attempted immunosuppression), while five cats served as untreated controls (group 2). Besides weekly blood samples, tissue samples were collected from bone marrow, kidney, liver and salivary glands at selected time points. The cats in group 1 had significantly lower lymphocyte counts and higher blood glucose levels after methylprednisolone administration than the controls. After methylprednisolone administration one blood and three tissue samples from cats in group 1 tested PCR-positive; before the administration, only one sample was positive. All other samples tested PCR-negative. All cats stayed seropositive; the antibody levels of the cats in group 1 showed a significant transient decrease after methylprednisolone administration. This is the first study to report the presence of "Candidatus M. turicensis" in tissues of chronically infected cats and the persistence of anti-feline hemoplasma antibodies in the absence of detectable bacteremia. Methylprednisolone administration did not lead to a significant reactivation of the infection. Our results enhance the knowledge of "Candidatus M. turicensis" infection pathogenesis and are clinically relevant to the prognosis of hemoplasma-infected cats

Lack of cross-protection against Mycoplasma haemofelis infection and signs of enhancement in "Candidatus Mycoplasma turicensis"-recovered cats

"Mycoplasma haemofelis" and "Candidatus Mycoplasma turicensis" are feline hemoplasmas that induce hemolytic anemia. Protection from homologous re-challenge was recently demonstrated in cats recovered from primary infection. Here, we determined if cats recovered from "Cand. M. turicensis" infection were protected against infections with the more pathogenic M. haemofelis. Ten specified pathogen-free cats were exposed to M. haemofelis. Five of the ten cats had recovered from "Cand. M. turicensis" bacteremia (group A), and five cats were naïve controls (group B). No cross-protection was observed. By contrast, the "Cand. M. turicensis"-recovered cats displayed faster M. haemofelis infection onset (earlier PCR-positive and anemic) than the controls. No "Cand. M. turicensis" was detected in any cat. M. haemofelis shedding was observed in saliva, feces and urine. In both groups, evidence of a Th1 response was observed (high IFN-γ, low IL-4), but IL-10 levels were also high. In group A, total, CD4+ and CD8+ T cells increased within days after M. haemofelis exposure. At times of maximal bacteremia, macrocytic hypochromic anemia, neutropenia, monocytosis and a decrease in leukocyte, eosinophil, and lymphocyte counts and subsets thereof (B- and T-cells, CD4+, CD8+ and CD4+CD25+ cells) were particularly significant in group A. Moreover, an increase in protein concentrations, hypoalbuminemia and a polyclonal hypergammaglobulinemia were observed. Five of ten M. haemofelis-infected cats subsequently cleared bacteremia without antibiotic treatment. In conclusion, the study suggests that a previous hemoplasma infection, even when the cat has ostensibly recovered, may influence subsequent infections, lead to an enhancement phenomenon and other differences in infection kinetics

Forest ecosystem monitoring in Tuscany (Italy): past activities, present status and future perspectives

Since 1987 the Region of Tuscany has been actively monitoring crown status in its forests, in order to protect them from atmospheric pollution, biotic factors and environmental change. Over this period the Region has performed periodical inventories on crown condition in publicly-owned forests (Level I network) and established a network of permanent plots (MON.I.TO., Level II – III) to study long-term changes occurring in forest ecosystems. Some of these permanent plots were later included in the national programme CONECOFOR, managed by the Ministry for Policy in Agriculture and Forest. Currently a further development of MON.I.TO. is being implemented, called MONITO III – TOpModel, the aim of which is to broaden the information potential of the monitoring system to include carbon stocks and biodiversity evaluation. This paper provides an up-to-date report on the status of the various surveys and recommends a closer connection between MON.I.TO. and the other regional information systems, especially the Regional Forest Inventory, in order to produce information that may be useful in forest planning and in Sustainable Forest Management

Modified-live feline calicivirus vaccination elicits cellular immunity against a current feline calicivirus field strain in an experimental geline challenge study

Feline calicivirus (FCV) is a common cat virus associated with oral ulcerations and virulent-systemic disease. Efficacious FCV vaccines protect against severe disease but not against infection. The high genetic diversity of FCV poses a challenge in vaccine design. Protection against FCV has been related to humoral and cellular immunity; the latter has not been studied in detail. This study investigates the cellular and humoral immune response of specified pathogen-free (SPF) cats after modified-live FCV F9 vaccinations and two heterologous FCV challenges by the analysis of lymphocyte subsets, cytokine mRNA transcription levels, interferon (IFN)-γ release assays in peripheral blood mononuclear cells (PBMCs), anti-FCV antibodies, and neutralisation activity. Vaccinated cats developed a Th1 cytokine response after vaccination. Vaccination resulted in antibodies with neutralising activity against the vaccine but not the challenge viruses. Remarkably, IFN-γ-releasing PBMCs were detected in vaccinated cats upon stimulation with the vaccine strain and the first heterologous FCV challenge strain. After the first experimental infection, the mRNA transcription levels of perforin, granzyme B, INF-γ, and antiviral factor MX1 and the number of IFN-γ-releasing PBMCs when stimulated with the first challenge virus were higher in vaccinated cats compared to control cats. The first FCV challenge induced crossneutralising antibodies in all cats against the second challenge virus. Before the second challenge, vaccinated cats had a higher number of IFN-γ-releasing PBMCs when stimulated with the second challenge virus than control cats. After the second FCV challenge, there were less significant differences detected between the groups regarding lymphocyte subsets and cytokine mRNA transcription levels. In conclusion, modified-live FCV vaccination induced cellular but not humoral crossimmunity in SPF cats; innate immune mechanisms, secretory and membranolytic pathways, and IFN-γ-releasing PBMCs seem to be important in the host immune defence against FCV