Urban Growth, Resident Welfare, and Housing Markets: Evidence from China

Cities have become the principal platform of economic growth and residents’ settlements. The importance of urban growth in residents’ quality of life is increasingly evident, because of the intimate interaction between urban characteristics and human activities. Cities shape urban residents’ welfare, bringing benefits and disadvantages as well. The complex way in which urban growth and residents’ activities interact makes it difficult to figure out which kinds of urban features are positively or instead negatively associated with residents’ quality of life. This puzzle makes it harder to clarify whether cities can provide enough net welfare to their residents. Thus, there is a major challenge to understand and evaluate how and to what extent urban growth shapes the welfare of urban residents. The link between cities and welfare has been hotly debated, yet we still have a limited grasp of how urban growth may impact residents’ welfare. Most studies concentrate on a certain dimension of urban welfare and a specific geographical scale. However, the interaction between urban growth and resident welfare may touch upon multiple dimensions of welfare coincidently, and it may take different forms across geographical scales. This thesis focuses on urban growth in China, against the background of a newly industrializing and developing country. Through the housing market dynamic, its central claim is to explore the tensions between the positive and negative effects of urban growth on resident welfare at multiple dimensions (economic, social, environmental, and policy) and scales (intra-city, inter-city, and countrywide) from a spatial inequality perspective

Industrial agglomeration and industrial SO2 emissions in China's 285 cities: Evidence from multiple agglomeration types

The environmental externalities of industrial agglomeration have generated intense debate, yet few studies have considered their effects and inner influence mechanism based on varied agglomeration types. This study distinguished between industrial density and proximity (spatially) and industrial specialization and diversity, as well as related variety and unrelated variety (organizationally). Using the panel data from China's 285 cities from 2003 to 2013, we examined the different effects of multiple agglomeration types of industrial agglomeration on industrial SO2 emissions, and their inner influence mechanism from two aspects of industrial structure and technological progress. First, we found that various agglomeration types have different environmental externalities and that industrial density and proximity both have significant reduction effects on SO2 emissions; diversity and related variety effectively reduce SO2 discharges, but specialization and unrelated variety are linked to increased emissions. Second, technological progress and industrial structure are the critical channels of industrial agglomeration affecting pollution emissions while technological progress plays a greater role in the reducing emission effect of industrial agglomeration. Our findings reveal the importance of different agglomeration types and technological progress between industrial agglomeration and pollution emission

Energy consumption in China: Spatial effects of industrial concentration, localization, and diversity

This paper discusses the effects of industrial agglomeration on electrical energy consumption from a spatial perspective by highlighting multiple agglomeration types. It is argued that different types of industry agglomeration may exert differentiated effects on energy consumption and their possible spatial interactions. With city sector panel data of China's 285 prefecture-level cities for the period 2003–2013, we adopted the Spatial Durbin Model (SDM) with fixed effects to examine the spatial effects of industrial agglomeration types on energy consumption. The model found that all types of industrial agglomeration play significant and different roles in explaining overall local energy consumption. Second, geographical proximity, diversity, and related variety show the spatial spillover effects on surrounding areas. Third, the spatial energy effects of industrial agglomeration across regions are evidently heterogeneous. Diversity and one of its sub-forms-related variety maintains consumption-saving effects in regions with the initial or intermediate stage of an industry life cycle, while unrelated variety changes over different phases. The results suggest that policymakers scientifically discriminate regional features and guide the agglomerated types of industries in order to balance economic growth with energy conservation

Transcriptome profiling reveals the crucial biological pathways involved in cold response in Moso bamboo (Phyllostachys edulis).

Most bamboo species including Moso bamboo (Phyllostachys edulis) are tropical or subtropical plants that greatly contribute to human well-being. Low temperature is one of the main environmental factors restricting bamboo growth and geographic distribution. Our knowledge of the molecular changes during bamboo adaption to cold stress remains limited. Here, we provided a general overview of the cold-responsive transcriptional profiles in Moso bamboo by systematically analyzing its transcriptomic response under cold stress. Our results showed that low temperature induced strong morphological and biochemical alternations in Moso bamboo. To examine the global gene expression changes in response to cold, 12 libraries (non-treated, cold-treated 0.5, 1 and 24 h at -2 °C) were sequenced using an Illumina sequencing platform. Only a few differentially expressed genes (DEGs) were identified at early stage, while a large number of DEGs were identified at late stage in this study, suggesting that the majority of cold response genes in bamboo are late-responsive genes. A total of 222 transcription factors from 24 different families were differentially expressed during 24-h cold treatment, and the expressions of several well-known C-repeat/dehydration responsive element-binding factor negative regulators were significantly upregulated in response to cold, indicating the existence of special cold response networks. Our data also revealed that the expression of genes related to cell wall and the biosynthesis of fatty acids were altered in response to cold stress, indicating their potential roles in the acquisition of bamboo cold tolerance. In summary, our studies showed that both plant kingdom-conserved and species-specific cold response pathways exist in Moso bamboo, which lays the foundation for studying the regulatory mechanisms underlying bamboo cold stress response and provides useful gene resources for the construction of cold-tolerant bamboo through genetic engineering in the future

Pulmonary alveolar type I cell population consists of two distinct subtypes that differ in cell fate.

Pulmonary alveolar type I (AT1) cells cover more than 95% of alveolar surface and are essential for the air-blood barrier function of lungs. AT1 cells have been shown to retain developmental plasticity during alveolar regeneration. However, the development and heterogeneity of AT1 cells remain largely unknown. Here, we conducted a single-cell RNA-seq analysis to characterize postnatal AT1 cell development and identified insulin-like growth factor-binding protein 2 (Igfbp2) as a genetic marker specifically expressed in postnatal AT1 cells. The portion of AT1 cells expressing Igfbp2 increases during alveologenesis and in post pneumonectomy (PNX) newly formed alveoli. We found that the adult AT1 cell population contains both Hopx+Igfbp2+ and Hopx+Igfbp2- AT1 cells, which have distinct cell fates during alveolar regeneration. Using an Igfbp2-CreER mouse model, we demonstrate that Hopx+Igfbp2+ AT1 cells represent terminally differentiated AT1 cells that are not able to transdifferentiate into AT2 cells during post-PNX alveolar regeneration. Our study provides tools and insights that will guide future investigations into the molecular and cellular mechanism or mechanisms underlying AT1 cell fate during lung development and regeneration

Enzyme Biosensors for Point-of-Care Testing

Biosensors are devices that integrate a variety of technologies, containing biology, electronics, chemistry, physics, medicine, informatics, and correlated technology. Biosensors act as transducer with a biorecognition element and transform a biochemical reaction on the transducer surface directly into a measurable signal. The biosensors have the advantages of rapid analysis, low cost, and high precision, which are widely used in many fields, such as medical care, disease diagnosis, food detection, environmental monitoring, and fermentation industry. The enzyme biosensors show excellent application value owing to the development of fixed technology and the characteristics of specific identification, which can be combined with point-of-care testing (POCT) technology. POCT technology is attracting more and more attention as a very effective method of clinic detection. We outline the recent advances of biosensors in this chapter, focusing on the principle and classification of enzyme biosensor, immobilization method of biorecognition layers, and fabrication of amperometric biosensors, as well as the applications of POCT. A summary of glucose biosensor development and integrated setups is included. The latest applications of enzyme biosensors in diagnostic applications focusing on POCT of biomarkers in real samples were described

The Energy Crisis in CPT II Variant Fibroblasts

Carnitine palmitoyltransferase II (CPT II) deficiency is one of the most common causes of fatty acid oxidation metabolism disorders. However, the molecular mechanism between CPT2 gene polymorphisms and metabolic stress has not been fully clarified. We previously reported that a number of patients show a thermal instable phenotype of compound hetero/homozygous variants of CPT II. To understand the mechanism of the metabolic disorder resulting from CPT II deficiency, the present study investigated CPT II variants in patient fibroblasts, [c.1102 G>A (p.V368I)] (heterozygous), [c.1102 G>A (p.V368I)] (homozygous), and [c.1055 T>G (p.F352C)] (heterozygous) + [c.1102 G>A (p.V368I)] (homozygous) compared with fibroblasts from healthy controls. CPT II variants exerted an effect of dominant negative on the homotetrameric proteins that showed thermal instability, reduced residual enzyme activities and a short half-life. Moreover, CPT II variant fibroblasts showed a significant decrease in fatty acid β-oxidation and adenosine triphosphate generation, combined with a reduced mitochondrial membrane potential, resulting in cellular apoptosis. Collectively, our data indicate that the CPT II deficiency induces an energy crisis of the fatty acid metabolic pathway. These findings may contribute to the elucidation of the genetic factors involved in metabolic disorder encephalopathy caused by the CPT II deficiency