1,814 research outputs found

    Energy and low-income tropical housing in Tanzania

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    Low-income housing in Tanzania is traditionally made from mud and thatch. With thatch having a typical life span of 2-7 years and mangrove poles 5-15 years, low durability is identified as the key issue with the traditional low-income house design. This paper studies the financial and social implications, embodied energy (EE) and human energy (HE) of a variety of materials in a bid to identify both the positive and negative impacts of each material substitution on the overall design, the environment and the local community. Using primary data collected from houses in the Mbweni district of Dar es Salaam and The Inventory of Carbon and Energy to calculate EE, a qualitative and quantitative assessment of each material is made. 47% of residents questioned in Tanzania, identified low durability to be the key issue with their mud house, with design changes which address this issue therefore affecting the largest share of the population. Stabilised bricks are identified as the key material substitution that should be adopted by local people, they perform well in terms of improved durability, financial and environmental considerations, and have the potential to be socially beneficial as well. This research identifies the social considerations to be key to understanding how local people will respond to the suggested material substitutions and whether they are likely to be adopted in the future. Whilst the environmental considerations are important, this is not a concept local people can relate to and does not affect their day-to-day lives as much as financial and social implications. It is extremely difficult and ethically questionable, especially in communities with people living close to poverty, to expect someone to adopt a design which requires more effort/money on their part, just because it is better for the environment

    Model for coiling and meandering instability of viscous threads

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    A numerical model is presented to describe both the transient and steady-state dynamics of viscous threads falling onto a plane. The steady-state coiling frequency w is calculated as a function of fall height H. In the case of weak gravity, w ~ H^{-1} and w ~ H are obtained for lower and higher fall heights respectively. When the effect of gravity is significant, the relation w ~ H^2 is observed. These results agree with the scaling laws previously predicted. The critical Reynolds number for coil-uncoil transition is discussed. When the gravity is weak, the transition occurs with hysteresis effects. If the plane moves horizontally at a constant speed, a variety of meandering oscillation modes can be observed experimentally. The present model also can describe this phenomenon. The numerically obtained state diagram for the meandering modes qualitatively agrees with the experiment.Comment: 12 pages, 10 figure

    Hazards of handling

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    A study of the bacterial flora among infants, mothers, staff (nursing and medical), and the environment of a neonatal unit is outlined. On admission to the unit, 60,5% of babies were already infected, presumably from contact with medical staff. By day 15 this number had increased significantly. A large number of mothers (40% on day 1, and 91% on day 15) were found to be carrying pathogenic organisms, providing a significant bacterial reservoir in the unit. Few pathogens were isolated from the environment.S. Afr. Med. J., 48, 1165 (1974)

    Rigidity of Linearly Constrained Frameworks

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    We consider the problem of characterising the generic rigidity of bar-joint frameworks in R d in which each vertex is constrained to lie in a given affine subspace. The special case when d = 2 was previously solved by I. Streinu and L. Theran in 2010. We will extend their characterisation to the case when d ≄ 3 and each vertex is constrained to lie in an affine subspace of dimension t, when t = 1, 2 and also when t ≄ 3 and d ≄ t(t−1). We then point out that results on body-bar frameworks obtained by N. Katoh and S. Tanigawa in 2013 can be used to characterise when a graph has a rigid realisation as a d-dimensional body-bar framework with a given set of linear constraints

    Evaluation of SIP Signalling and QoS for VoIP over OLSR MANET Routing Protocol

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    Abstract: This paper evaluates the SIP based VoIP applications over the Optimized Link State Routing protocol (OLSR) as a proactive routing protocol for Mobile Ad Hoc Networks (MANET) using Static, Uniform, and Random mobility models. The evaluation considered PCM, LQS, IPTelephony, and GSM voice codecs to study the SIP signaling performance and the voice Quality of Service (QoS) for VoIP calls over OLSR MANET. The simulation efforts performed in OPNET Modeler 17.1. The results show that VoIP over OLSR MANET has good performance over Static and Uniform mobility models while it has variable performance with Random models. SIP signaling has large delays compared with the voice signaling which reduce the VoIP performance and increases the call's duration. In addition, GSM and LQS based VoIP calls have an acceptable level of QoS while PCM and IP-Telephony based VoIP calls have a low level of QoS over different types of mobility models. Furthermore, the location and the mobility of SIP server affect the number of hops and the SIP signaling performance between the different parties of the VoIP call

    Hematopoietic arginase 1 deficiency results in decreased leukocytosis and increased foam cell formation but does not affect atherosclerosis

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    Background and aimsArginase1 (Arg1), an M2 macrophage marker, plays a critical role in a number of immunological functions in macrophages, which are the main cell type facilitating atherosclerotic lesion development. Arg1 uses the substrate l-arginine to create l-ornithine, a precursor molecule required for collagen formation and vascular smooth muscle cell differentiation. By reducing l-arginine availability, Arg1 limits the production of nitric oxide (NO), a pro-atherogenic factor in macrophages. In endothelial cells, conversely, NO is strongly anti-atherogenic. However, until now, the role of Arg1 in atherosclerosis is largely unknown. The aim of this study is to specifically investigate the effect of Arg1 deletion in hematopoietic cells on atherosclerosis susceptibility.MethodsLdlr KO mice were transplanted with Arg1flox/flox;Tie2-Cre (Arg1 KO) bone marrow (BM) or wildtype (WT) BM. After 8 weeks of recovery on chow diet, recipients mice were fed a Western-Type Diet (WTD) for 10 weeks to induce atherosclerosis.ResultsAfter 10-week WTD challenge, blood leukocyte counts were decreased by 25% (p p = 0.05) in Ldlr KO mice transplanted with Arg1 KO BM compared to mice transplanted with WT BM. The decrease in leukocytes was due to lower B lymphocyte counts. However, oxLDL-specific antibodies were increased in plasma of Ldlr KO mice transplanted with Arg1 KO BM compared to WT BM transplanted controls, whereas oxLDL-specific IgM was not affected. On the other hand, peritoneal foam cells in Arg1 KO BM recipients were increased 3-fold (p ConclusionsDeletion of Arg1 in hematopoietic cells adversely affects blood leukocyte counts and increases foam cell formation. However, no effects on atherosclerosis could be demonstrated, indicating that hematopoietic Arg1 function is not a decisive factor in atherosclerotic plaque formation.Article / Letter to editorLeiden Academic Centre for Drug Researc

    Hematopoietic arginase 1 deficiency results in decreased leukocytosis and increased foam cell formation but does not affect atherosclerosis

    Get PDF
    Background and aimsArginase1 (Arg1), an M2 macrophage marker, plays a critical role in a number of immunological functions in macrophages, which are the main cell type facilitating atherosclerotic lesion development. Arg1 uses the substrate l-arginine to create l-ornithine, a precursor molecule required for collagen formation and vascular smooth muscle cell differentiation. By reducing l-arginine availability, Arg1 limits the production of nitric oxide (NO), a pro-atherogenic factor in macrophages. In endothelial cells, conversely, NO is strongly anti-atherogenic. However, until now, the role of Arg1 in atherosclerosis is largely unknown. The aim of this study is to specifically investigate the effect of Arg1 deletion in hematopoietic cells on atherosclerosis susceptibility.MethodsLdlr KO mice were transplanted with Arg1flox/flox;Tie2-Cre (Arg1 KO) bone marrow (BM) or wildtype (WT) BM. After 8 weeks of recovery on chow diet, recipients mice were fed a Western-Type Diet (WTD) for 10 weeks to induce atherosclerosis.ResultsAfter 10-week WTD challenge, blood leukocyte counts were decreased by 25% (p p = 0.05) in Ldlr KO mice transplanted with Arg1 KO BM compared to mice transplanted with WT BM. The decrease in leukocytes was due to lower B lymphocyte counts. However, oxLDL-specific antibodies were increased in plasma of Ldlr KO mice transplanted with Arg1 KO BM compared to WT BM transplanted controls, whereas oxLDL-specific IgM was not affected. On the other hand, peritoneal foam cells in Arg1 KO BM recipients were increased 3-fold (p ConclusionsDeletion of Arg1 in hematopoietic cells adversely affects blood leukocyte counts and increases foam cell formation. However, no effects on atherosclerosis could be demonstrated, indicating that hematopoietic Arg1 function is not a decisive factor in atherosclerotic plaque formation.Article / Letter to editorLeiden Academic Centre for Drug Researc

    Hematopoietic arginase 1 deficiency results in decreased leukocytosis and increased foam cell formation but does not affect atherosclerosis

    Get PDF
    Background and aimsArginase1 (Arg1), an M2 macrophage marker, plays a critical role in a number of immunological functions in macrophages, which are the main cell type facilitating atherosclerotic lesion development. Arg1 uses the substrate l-arginine to create l-ornithine, a precursor molecule required for collagen formation and vascular smooth muscle cell differentiation. By reducing l-arginine availability, Arg1 limits the production of nitric oxide (NO), a pro-atherogenic factor in macrophages. In endothelial cells, conversely, NO is strongly anti-atherogenic. However, until now, the role of Arg1 in atherosclerosis is largely unknown. The aim of this study is to specifically investigate the effect of Arg1 deletion in hematopoietic cells on atherosclerosis susceptibility.MethodsLdlr KO mice were transplanted with Arg1flox/flox;Tie2-Cre (Arg1 KO) bone marrow (BM) or wildtype (WT) BM. After 8 weeks of recovery on chow diet, recipients mice were fed a Western-Type Diet (WTD) for 10 weeks to induce atherosclerosis.ResultsAfter 10-week WTD challenge, blood leukocyte counts were decreased by 25% (p p = 0.05) in Ldlr KO mice transplanted with Arg1 KO BM compared to mice transplanted with WT BM. The decrease in leukocytes was due to lower B lymphocyte counts. However, oxLDL-specific antibodies were increased in plasma of Ldlr KO mice transplanted with Arg1 KO BM compared to WT BM transplanted controls, whereas oxLDL-specific IgM was not affected. On the other hand, peritoneal foam cells in Arg1 KO BM recipients were increased 3-fold (p ConclusionsDeletion of Arg1 in hematopoietic cells adversely affects blood leukocyte counts and increases foam cell formation. However, no effects on atherosclerosis could be demonstrated, indicating that hematopoietic Arg1 function is not a decisive factor in atherosclerotic plaque formation.Article / Letter to editorLeiden Academic Centre for Drug Researc
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