12 research outputs found

    Recording and automatic detection of African elephant (Loxodonta africana) infrasonic rumbles

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    The value of studying elephant vocalizations lies in the abundant information that can be retrieved from it. Recordings of elephant rumbles can be used by researchers to determine the size and composition of the herd, the sexual state, as well as the emotional condition of an elephant. It is a difficult task for researchers to obtain large volumes of continuous recordings of elephant vocalizations. Recordings are normally analysed manually to identify the location of rumbles via the tedious and time consuming methods of sped up listening and the visual evaluation of spectrograms. The application of speech processing on elephant vocalizations is a highly unexploited resource. The aim of this study was to contribute to the current body of knowledge and resources of elephant research by developing a tool for recording high volumes of continuous acoustic data in harsh natural conditions as well as examining the possibilities of applying human speech processing techniques to elephant rumbles to achieve automatic detection of these rumbles in recordings. The recording tool was designed and implemented as an elephant recording collar that has an onboard data storage capacity of 128 gigabytes, enough memory to record sound data continuously for a period of nine months. Data is stored in the wave file format and the device has the ability to navigate and control the FAT32 file system so that the files can be read and downloaded to a personal computer. The collar also has the ability to stamp sound files with the time and date, ambient temperature and GPS coordinates. Several different options for microphone placement and protection have been tested experimentally to find an acceptable solution. A relevant voice activity detection algorithm was chosen as a base for the automatic detection of infrasonic elephant rumbles. The chosen algorithm is based on a robust pitch determination algorithm that has been experimentally verified to function correctly under a signal-to-noise ratio as low as -8 dB when more than four harmonic structures exist in a sound. The algorithm was modified to be used for elephant rumbles and was tested with previously recorded elephant vocalization data. The results obtained suggest that the algorithm can accurately detect elephant rumbles from recordings. The number of false alarms and undetected calls increase when recordings are contaminated with unwanted noise that contains harmonic structures or when the harmonic nature of a rumble is lost. Data obtained from the recording collar is less prone to being contaminated than far field recordings and the automatic detection algorithm should provide an accurate tool for detecting any rumbles that appear in the recordings.Dissertation (MEng)--University of Pretoria, 2008.Electrical, Electronic and Computer Engineeringunrestricte

    Prevalence of amyloid blood clots in COVID-19 plasma

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    The rapid detection of COVID-19 uses genotypic testing for the presence of SARS-Cov-2 virus in nasopharyngeal swabs, but it can have a poor sensitivity. A rapid, host-based physiological test that indicated whether the individual was infected or not would be highly desirable. Coagulaopathies are a common accompaniment to COVID-19, especially micro-clots within the lungs. We show here that microclots can be detected in the native plasma of COVID-19 patient, and in particular that such clots are amyloid in nature as judged by a standard fluorogenic stain. This provides a rapid and convenient test (P<0.0001), and suggests that the early detection and prevention of such clotting could have an important role in therapy

    Prevalence of readily detected amyloid blood clots in 'unclotted' Type 2 Diabetes Mellitus and COVID-19 plasma: a preliminary report

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    CITATION: Pretorius, E., et al.2020. Prevalence of readily detected amyloid blood clots in unclotted Type 2 Diabetes Mellitus and COVID-19 plasma : a preliminary report. Cardiovasc Diabetol, 19:193, doi:10.1186/s12933-020-01165-7.The original publication is available at https://cardiab.biomedcentral.comBackground: Type 2 Diabetes Mellitus (T2DM) is a well-known comorbidity to COVID-19 and coagulopathies are a common accompaniment to both T2DM and COVID-19. In addition, patients with COVID-19 are known to develop micro-clots within the lungs. The rapid detection of COVID-19 uses genotypic testing for the presence of SARS-Cov-2 virus in nasopharyngeal swabs, but it can have a poor sensitivity. A rapid, host-based physiological test that indicated clotting severity and the extent of clotting pathologies in the individual who was infected or not would be highly desirable. Methods: Platelet poor plasma (PPP) was collected and frozen. On the day of analysis, PPP samples were thawed and analysed. We show here that microclots can be detected in the native plasma of twenty COVID-19, as well as ten T2DM patients, without the addition of any clotting agent, and in particular that such clots are amyloid in nature as judged by a standard fluorogenic stain. Results were compared to ten healthy age-matched individuals. Results: In COVID-19 plasma these microclots are significantly increased when compared to the levels in T2DM. Conclusions: This fluorogenic test may provide a rapid and convenient test with 100% sensitivity (P < 0.0001) and is consistent with the recognition that the early detection and prevention of such clotting can have an important role in therapy.https://cardiab.biomedcentral.com/articles/10.1186/s12933-020-01165-7Publisher's versio

    Erythrocyte, Platelet, Serum Ferritin, and P-Selectin Pathophysiology Implicated in Severe Hypercoagulation and Vascular Complications in COVID-19

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    CITATION: Venter, C. et al. 2020. Erythrocyte, Platelet, Serum Ferritin, and P-Selectin Pathophysiology Implicated in Severe Hypercoagulation and Vascular Complications in COVID-19. International Journal of Molecular Sciences, 21(21). doi:10.3390/ijms21218234The original publication is available at https://www.mdpi.com/journal/ijmsProgressive respiratory failure is seen as a major cause of death in severe acute respiratory syndrome coronavirus 2 (SARS-Cov-2)-induced infection. Relatively little is known about the associated morphologic and molecular changes in the circulation of these patients. In particular, platelet and erythrocyte pathology might result in severe vascular issues, and the manifestations may include thrombotic complications. These thrombotic pathologies may be both extrapulmonary and intrapulmonary and may be central to respiratory failure. Previously, we reported the presence of amyloid microclots in the circulation of patients with coronavirus disease 2019 (COVID-19). Here, we investigate the presence of related circulating biomarkers, including C-reactive protein (CRP), serum ferritin, and P-selectin. These biomarkers are well-known to interact with, and cause pathology to, platelets and erythrocytes. We also study the structure of platelets and erythrocytes using fluorescence microscopy (using the markers PAC-1 and CD62PE) and scanning electron microscopy. Thromboelastography and viscometry were also used to study coagulation parameters and plasma viscosity. We conclude that structural pathologies found in platelets and erythrocytes, together with spontaneously formed amyloid microclots, may be central to vascular changes observed during COVID-19 progression, including thrombotic microangiopathy, diffuse intravascular coagulation, and large-vessel thrombosis, as well as ground-glass opacities in the lungs. Consequently, this clinical snapshot of COVID-19 strongly suggests that it is also a true vascular disease and considering it as such should form an essential part of a clinical treatment regime.https://www.mdpi.com/1422-0067/21/21/8234Publishers versio

    Roeping en stryd in die kerklike bediening van H.Ph.J. Pasch en G.B.S. Pasch

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    MTh (Church and Dogma History), North-West University, Potchefstroom Campus, 2015This study aims to focus on the importance of vocation in the ministry of two extraordinary reformed ministers of the GKSA. The two protagonists that were researched in this study are Reverend Hendrikus Philippus Josef (H.Ph.J. Pasch 1865-1936) and his son, Reverend Gerhardus Barthlomeus Schutteus Pasch (G.B.S. Pasch 1916-1960; also known as Rabbo Pasch). Both had lived a life of struggle against the calling before answering to the vocation of becoming a minister. The essence of being truly called is the continuous incentive to the motive to being truly called and living this calling as ministers. The exceptional circumstances and challenges that were unusual in their lives are highlighted. These challenges often resulted in intense conflict to stay true to their calling is unequalled. The weakness of men and the broken human existence, as well as the harshness of human relations, even between people within the church, are pointed out. This study has shown that calling has to be the main motive and driving force in the ministry of a pastor for lifelong perseverance in this specific calling with its struggles and challenges.Master

    Trace element dispersion in wallrocks of copper-bearing bodies, Namaqualand

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    Thesis (M. Sc.) -- University of Stellenbosch, 1970.Full text to be digitised and attached to bibliographic record

    NEW PRODUCT DEVELOPMENT WITH DYNAMIC DECISION SUPPORT

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    The development of new and improved management methods for new product development is important. Existing methods suffer from a number of shortcomings, especially their inability to deal with a mixture of quantitative and qualitative data. The objective of this study is to apply decision support techniques (especially Bayesian networks) to the area of new product development management in order to address some of the shortcomings.The research approach is one of decision structuring and modeling. The literature shows the criteria that are important during the management of new product development. These criteria are used in a three-step decision structuring framework to develop a conceptual model based on a Bayesian network, in support of new product development management. The result is a Bayesian network that incorporates the knowledge of experts into a decision support model. The model is shown to be requisite because it contains all the essential elements of the problem on which decision-makers can base their action.The model can be used to perform 'what-if' analyses in various ways, thereby supporting the management of risk in new product development. This research not only contributes a model to support new product development management, but also provides insight into how decision support — especially Bayesian networks — can enhance technology management methods.Product development, dynamic decision support

    Early management of severe COVID-19 coagulopathy should be guided by TEG<sup>®</sup>, microclot and platelet mapping

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    An important component of severe COVID-19 disease is virus-induced endothelilitis. This leads to disruption of normal endothelial function, initiating a state of failing normal clotting physiology. Massively increased levels of von Willebrand Factor (VWF) lead to overwhelming platelet activation, as well as activation of the enzymatic (intrinsic) clotting pathway. In addition, there is an impaired fibrinolysis, caused by, amongst others, increased levels of alpha-(2) antiplasmin. The end result is hypercoagulation [proven by thromboelastography ® (TEG ® )] and reduced fibrinolysis, inevitably leading to a difficult-to-overcome hypercoagulated physiological state. Platelets in circulation also plays a significant role in clot formation, but themselves may also drive hypercoagulation when they are overactivated due to the interactions of their receptors with the endothelium, immune cells or circulating inflammatory molecules. From the literature it is clear that the role of platelets in severely ill COVID-19 patients has been markedly underestimated or even ignored. We here highlight the value of early management of severe COVID-19 coagulopathy as guided by TEG ® , microclot and platelet mapping. We also argue that the failure of clinical trials, where the efficacy of prophylactic versus therapeutic clexane (low molecular weight heparin (LMWH)) were not always successful, might be because the significant role of platelet activation was not taken into account during the planning of the trial. We conclude that, because of the overwhelming alteration of clotting, the outcome of any trial evaluating an any single anticoagulant, including thrombolytic, would be negative. Here we suggest the use of the degree of platelet dysfunction and presence of microclots in circulation, together with TEG ® , should be used as a guideline for disease severity. A multi-pronged approach, guided by TEG ® and platelet mapping, would be required to maintain normal clotting physiology in severe COVID-19 disease

    TEG(R), Microclot and Platelet Mapping for Guiding Early Management of Severe COVID-19 Coagulopathy

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    An important component of severe COVID-19 disease is virus-induced endothelilitis. This leads to disruption of normal endothelial function, initiating a state of failing normal clotting physiology. Massively increased levels of von Willebrand Factor (VWF) lead to overwhelming platelet activation, as well as activation of the enzymatic (intrinsic) clotting pathway. In addition, there is an impaired fibrinolysis, caused by, amongst others, increased levels of alpha-(2) antiplasmin. The end result is hypercoagulation (proven by thromboelastography® (TEG®)) and reduced fibrinolysis, inevitably leading to a difficult-to-overcome hypercoagulated physiological state. Platelets in circulation also plays a significant role in clot formation, but they themselves may also drive hypercoagulation when they are overactivated due to the interactions of their receptors with the endothelium, immune cells or circulating inflammatory molecules. From the literature it is clear that the role of platelets in severely ill COVID-19 patients has been markedly underestimated or even ignored. We here highlight the value of early management of severe COVID-19 coagulopathy as guided by TEG®, microclot and platelet mapping. We also argue that the failure of clinical trials, where the efficacy of prophylactic versus therapeutic clexane (low molecular weight heparin (LMWH)) were not always successful, which may be because the significant role of platelet activation was not taken into account during the planning of the trial. We conclude that, because of the overwhelming alteration of clotting, the outcome of any trial evaluating an any single anticoagulant, including thrombolytic, would be negative. Here we suggest the use of the degree of platelet dysfunction and presence of microclots in circulation, together with TEG®, might be used as a guideline for disease severity. A multi-pronged approach, guided by TEG® and platelet mapping, would be required to maintain normal clotting physiology in severe COVID-19 disease
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