Runoff Model Development and Validation for Afforestation in Arid Land of Western Australia

Abstract: As a countermeasure against global warming, large scale afforestation of arid land has been done by fixing atmospheric CO 2 into plants. In arid land, however most of the rainwater is lost by runoff and evaporation. Effective use of rainwater is required for afforestation. Thus, we made an original runoff model to evaluate water distribution in a research area. In this study, we report determination of parameters in the original runoff model with Digital Elevation Model (DEM) to estimate water movement for the selection of afforestation place. From the comparison of actual and numerical results, the two sensitive parameters were decided and the characteristics of runoff water movement were elucidated hydrologically. Moreover, validation on expansion of mesh size for application of this model in large scale area was done. However, numerical results with large size mesh hadn't been approximated to small size mesh, because of roughness information of large size mesh. It was our assignment of future investigation. Keywords: Afforestation, DEM, Mesh size, Runoff, Simulation Introduction For the mitigation of global warming issue, a large scale afforestation of arid land has been promoted to fix atmospheric carbon on land which is not effectively used. Arid land area is huge in the world but the most important problem is lack of water for afforestation because of the small amount of rainfall and occurrence of runoff on soil surface. Most of runoff water is evaporated without using for plants, therefore, it is necessary to use runoff water effectively for arid land afforestation. The authors have demonstrated the improve the land condition for afforestation by introducing artificial technologies The purpose of this study is to estimate the distribution of runoff water by using the original runoff model for selection of the best afforestation places. In this report, two sensitive parameters in the original runoff model were decided to estimate water movement for the selection of afforestation place. Moreover, expansion of mesh size by using our model was validated to calculate in large scale area

An ancillary study of participants in a randomized, placebo-controlled trial suggests that ingestion of bovine lactoferrin promotes expression of interferon alpha in the human colon

AbstractStudies using animal models have demonstrated that ingestion of bovine lactoferrin (bLF) is able to induce cytokine expression in the intestine and inhibit carcinogenesis in the colon and other organs of experimental animals. Consequently, a clinical trial was conducted in the National Cancer Center Hospital, Tokyo, Japan to determine whether ingestion of bLF affected the growth of colorectal polyps in humans. The Tokyo-trial found that ingestion of 3.0 g bLF suppressed the growth of colorectal polyps and increased the level of serum human lactoferrin in participants 63 years old or younger. The present study is a complementary study to the Tokyo-trial to determine if a change in the expression of one or more cytokines could be detected in the colon of the Tokyo-trial participants after ingesting bLF. We found that daily ingestion of 3.0 g bLF promoted the expression of interferon alpha in the colon of the Tokyo-trial participants

Litter carbon dynamics analysis in forests in an arid ecosystem with a model incorporating the physical removal of litter

金沢大学理工研究域自然システム学系Arid land afforestation could be a countermeasure for global warming, and a project for developing and evaluating techniques for arid land afforestation and reforestation has been carried out in Sturt Meadows near Leonora, Western Australia. As a part of this project, the litter carbon dynamics were investigated at three Acacia aneura forest sites, using a litter carbon model incorporating the physical removal of litter by winds, floods, etc. Based on the field observation data of above ground plant biomass, annual litter fall, existing amount of the litter, and also litter decomposition rate constants separately obtained for leaf litter and woody litter, we investigated the carbon flows at these forest sites, especially the annual amount of litter physically removed from the sites by floods or winds. As a result, it is estimated that annual physical removal of litter amounted to 59-75% of the annual litter fall, and the litter removal rate constants were from 0.38 to 0.55 year-1. Roughly one third to a half of the existing litter is removed annually from the sites. There was also a tendency that as the canopy coverage decreases, the litter removal rate constant increases. For this type of ecosystem, which is susceptible to the run-off of water and strong winds, we consider the taking into account of the physical removal of the litter is essential for analyzing the carbon dynamics in the ecosystem. © 2008 Elsevier B.V. All rights reserved

A combination of routine laboratory findings and vital signs can predict survival of advanced cancer patients without physician evaluation: a fractional polynomial model

IntroductionThere have been no reports about predicting survival of patients with advanced cancer constructed entirely with objective variables. We aimed to develop a prognostic model based on laboratory findings and vital signs using a fractional polynomial (FP) model.MethodsA multicentre prospective cohort study was conducted at 58 specialist palliative care services in Japan from September 2012 to April 2014. Eligible patients were older than 20 years and had advanced cancer. We developed models for predicting 7-day, 14-day, 30-day, 56-day and 90-day survival by using the FP modelling method.ResultsData from 1039 patients were analysed to develop each prognostic model (Objective Prognostic Index for advanced cancer [OPI-AC]). All models included the heart rate, urea and albumin, while some models included the respiratory rate, creatinine, C-reactive protein, lymphocyte count, neutrophil count, total bilirubin, lactate dehydrogenase and platelet/lymphocyte ratio. The area under the curve was 0.77, 0.81, 0.90, 0.90 and 0.92 for the 7-day, 14-day, 30-day, 56-day and 90-day model, respectively. The accuracy of the OPI-AC predicting 30-day, 56-day and 90-day survival was significantly higher than that of the Palliative Prognostic Score or the Prognosis in Palliative Care Study model, which are based on a combination of symptoms and physician estimation.ConclusionWe developed highly accurate prognostic indexes for predicting the survival of patients with advanced cancer from objective variables alone, which may be useful for end-of-life management. The FP modelling method could be promising for developing other prognostic models in future research

STING signalling is terminated through ESCRT-dependent microautophagy of vesicles originating from recycling endosomes

STING炎症シグナルの終結分子機構 --新規細胞内分解システムの発見--. 京都大学プレスリリース. 2023-03-14.Stimulator of interferon genes (STING) is essential for the type I interferon response against a variety of DNA pathogens. Upon emergence of cytosolic DNA, STING translocates from the endoplasmic reticulum to the Golgi where STING activates the downstream kinase TBK1, then to lysosome through recycling endosomes (REs) for its degradation. Although the molecular machinery of STING activation is extensively studied and defined, the one underlying STING degradation and inactivation has not yet been fully elucidated. Here we show that STING is degraded by the endosomal sorting complexes required for transport (ESCRT)-driven microautophagy. Airyscan super-resolution microscopy and correlative light/electron microscopy suggest that STING-positive vesicles of an RE origin are directly encapsulated into Lamp1-positive compartments. Screening of mammalian Vps genes, the yeast homologues of which regulate Golgi-to-vacuole transport, shows that ESCRT proteins are essential for the STING encapsulation into Lamp1-positive compartments. Knockdown of Tsg101 and Vps4, components of ESCRT, results in the accumulation of STING vesicles in the cytosol, leading to the sustained type I interferon response. Knockdown of Tsg101 in human primary T cells leads to an increase the expression of interferon-stimulated genes. STING undergoes K63-linked ubiquitination at lysine 288 during its transit through the Golgi/REs, and this ubiquitination is required for STING degradation. Our results reveal a molecular mechanism that prevents hyperactivation of innate immune signalling, which operates at REs