The Metabolic Transition in Japan

The notion of a (socio‐) metabolic transition has been used to describe fundamental changes in socioeconomic energy and material use during industrialization. During the last century, Japan developed from a largely agrarian economy to one of the world's leading industrial nations. It is one of the few industrial countries that has experienced prolonged dematerialization and recently has adopted a rigorous resource policy. This article investigates changes in Japan's metabolism during industrialization on the basis of a material flow account for the period from 1878 to 2005. It presents annual data for material extraction, trade, and domestic consumption by major material group and explores the relations among population growth, economic development, and material (and energy) use. During the observed period, the size of Japan's metabolism grew by a factor of 40, and the share of mineral and fossil materials in domestic material consumption (DMC) grew to more than 90%. Much of the growth in the Japanese metabolism was based on imported materials and occurred in only 20 years after World War II (WWII), when Japan rapidly built up large stocks of built infrastructure, developed heavy industry, and adopted patterns of mass production and consumption. The surge in material use came to an abrupt halt with the first oil crisis, however. Material use stabilized, and the economy eventually began to dematerialize. Although gross domestic product (GDP) grew much faster than material use, improvements in material intensity are a relatively recent phenomenon. Japan emerges as a role model for the metabolic transition but is also exceptional in many ways.     

遮光对刺梨果实和叶片中维生素C与糖含量以及相关酶活性的影响

为探究光照强度减弱对不同发育期的刺梨(Rosa roxburghii Tratt.)果实和叶片中维生素C与糖含量及相关酶活性的影响,以‘贵农5号’刺梨扦插苗为材料,采用遮阳网设置光强减弱20%、40%、60%的3个遮光处理,以自然光照强度为对照(CK),分析不同光照强度条件下刺梨果实和叶片中维生素C含量及相关酶活性以及糖含量的变化。结果表明：(1)光照强度减弱后,不同发育期的刺梨果实和叶片中维生素C含量均显著降低,对照及3个处理间的果实维生素C含量的差异在快速膨大期均达到显著水平。(2)随着光照强度的减弱,刺梨果实和叶片中L 半乳糖 1,4 内酯脱氢酶(GalLDH)、单脱氢抗坏血酸还原酶(MDHAR)和脱氢抗坏血酸还原酶(DHAR)活性均降低,而抗坏血酸氧化酶(AAO)和抗坏血酸过氧化物酶(APX)活性均增强,尤其是果实中MDHAR活性在快速膨大期迅速大幅增强。(3)刺梨果实和叶片中可溶性糖、蔗糖、葡萄糖、果糖含量随光照强度减弱而降低,但果实中葡萄糖含量在快速膨大期增加尤为迅速。(4)果实中维生素C含量与叶片中蔗糖、葡萄糖含量在不同发育期均呈极显著正相关关系,快速膨大期果实中GalLDH、MDHAR活性与维生素C含量呈极显著正相关关系且相关系数均达到最大值,而其APX活性与维生素C含量呈极显著负相关关系且相关系数达到最大值。研究认为,光照强度通过调控刺梨果实中维生素C合成及相关代谢关键酶的活性与叶片中光合产物的含量最终影响果实中维生素C的积累量;弱光环境不利于刺梨果实和叶片中维生素C及糖的积累,其影响在果实快速膨大期尤为明显;良好的光照是保证刺梨果实优良品质的基本条件。     

间伐强度对秦岭南坡栓皮栎种子库及实生苗生长的影响

2010年8-11月和2011年8月,以秦岭南坡商洛地区近自然经营的不同间伐强度(30％、20％和10％)下的栓皮栎纯林为对象,分析了间伐4～5年后栓皮栎种子库的种子数量,实生苗的存活率和生长状况,及其与环境因子的关系.结果表明:与对照相比,间伐后第4年,间伐10％、20％和30％强度下种子库中的种子总数分别增加了2.0％、21.1％和34.8％,翌年1年生实生苗数量分别增加了28.5％、99.7％和122.2％;间伐5年后,间伐10％、20％和30％样地内实生苗的存活率分别提高了25.5％、235.7％和480.0％.间伐使林地的光照、温度、土壤水分和养分等环境因子发生变化,促进了各年龄段实生苗的高度、新梢生长量及叶面积指数的增长,且随间伐强度的增加,3项生长指标均增加.在郁闭度≥0.85的栓皮栎林,间伐强度30％(郁闭度保留0.6)最有利于栓皮栎种子萌芽和实生苗生长.     

Entrainment to light of circadian activity rhythms in tench (Tinca tinca)

The present article analyzes locomotor activity rhythms in Tinca tinca. To that end, three different experiments were conducted on 24 animals (20 g body weight) kept in pairs in 60-liter aquaria fitted with infrared sensors connected to a computer to continuously record fish movements. The first experiment was designed to study the endogenous circadian clock under free-running conditions [ultradian 40:40 min LD pulses and constant dark (DD)] and after shifting the LD cycle. Our results demonstrate that tench has a strictly nocturnal activity pattern, an endogenous rhythm being evident in 45.8% of the fish analyzed. The second experiment was conducted to test the influence of different photoperiods (LD 6:18, 12:12, 18:6, and 22:2) on locomotor activity, the results showing that even under an extremely long photoperiod, tench activity is restricted to dark hours. The third experiment examined the effect of light intensity on locomotor activity rhythms. When fish were exposed to decreasing light intensities (from 300:0 lux to 30:0, 3:0, and 0.3:0 lux) while maintaining a constant photoperiod (LD 12:12), the highest percentage of locomotor activity was in all cases associated with the hours of complete darkness (0 lux). In short, our results clearly show that (a) tench is a species with a strictly nocturnal behavior, and (b) daily activity rhythms gradually entrain after shifting the LD cycle and persist under free-running conditions, pointing to their circadian nature. However, light strongly influences activity rhythms, since (c) the length of the active phase is directly controlled by the photophase, and (d) strictly nocturnal behavior persists even under very dim light conditions (0.3 lux). The above findings deepen our knowledge of tench behavior, which may help to optimize the aquacultural management of this species, for example, by adjusting feeding strategies to their nocturnal behavior.     

中国特有植物血水草开花物候与生殖特性

于2008年3-5月对分布在井冈山的血水草(Eomecon chionantha Hance )5个自然种群的开花物候进行了观察,运用开花振幅、相对开花强度和开花同步性等指数研究了其开花物候特征及其对该种生殖成功的影响.结果表明:血水草开花时间为3月下旬-5月上旬,种群花期历时24 ～46 d,个体平均开花持续时间为11～21 d,单花花期一般为3～5d;井冈山血水草种群的开花物候进程呈单峰曲线模式具有一个开花高峰期,表现出一种“集中开花模式”;与大多数亚热带植物一样,血水草具有较低的相对开花强度,分布频率集中在10％ ～30％.开花物候指数与生殖间的相关分析结果表明:始花时间与花期持续时间呈显著负相关,而与开花数和坐果率呈显著正相关;花期持续时间与开花数和坐果率呈显著正相关;同步性指数与始花时间、开花数、花期持续时间呈负相关.血水草“集中开花模式”是其在长期的进化过程中适应周围气候条件及生境的一种生殖保障.     

Rapid degradation of longer DNA fragments enables the improved estimation of distribution and biomass using environmental DNA

The advent of environmental DNA (eDNA) analysis methods has enabled rapid and wide‐range ecological monitoring in aquatic ecosystems, but there is a dearth of information on eDNA degradation. The results of previous studies suggest that the decay rate of eDNA varies depending on the length of DNA fragments. To examine this hypothesis, we compared temporal change in copy number of long eDNA fragments (719 bp) with that of short eDNA fragments (127 bp). First, we isolated rearing water from a target fish species, Japanese Jack Mackerel (Trachurus japonicus), and then quantified the copy number of the long and short eDNA fragments in 1 L water samples after isolating the water from the fish. Long DNA fragments showed a higher decay rate than short fragments. Next, we measured the eDNA copy numbers of long and short DNA fragments using field samples, and compared them with fish biomass as measured by echo intensity. Although a previous study suggested that short eDNA fragments could be overestimated because of nontarget eDNA from a nearby fish market and carcasses, the eDNA concentrations of long fragments were correlated with echo intensity. This suggests that the concentration of longer eDNA fragments reflects fish biomass more accurately than the previous study by removing the effects of the fish market and carcasses. The length‐related differences in eDNA have a substantial potential to improve estimation of species biomass.     

藏北高寒草地植被和土壤对不同放牧强度的响应

放牧压力在时间和空间的不均衡分布导致局部土地过度利用和生态退化,然而当前对放牧强度的量化多采用替代性指标或对照试验,缺乏直接监测数据,也缺乏不同草地类型对放牧强度变化的响应差异性研究。以西藏自治区那曲市为研究区,利用佩戴式GPS牛羊定位器构建高精度放牧轨迹数据集模拟放牧强度,构建栅格尺度放牧强度空间分布和划分方法,结合草地群落样方调查,通过Duncan法（Duncan''s multiple comparative analysis）进行多重比较分析,探究自由放牧模式下高寒草甸和高寒草原两类区域植被和土壤对不同放牧强度的响应方式及差异性。本研究可为放牧行为环境效应监测提供新思路,并根据不同草地状况因地制宜提出放牧优化管理策略,助力高寒传统牧区的可持续发展。主要结论有：1）随着放牧强度的增大,高寒草原地上生物量先升高后降低,高强度放牧对高寒草原植被的影响大于高寒草甸。2）高放牧强度下,高寒草原土壤水分显著高于中低强度,高寒草甸土壤容重显著低于低强度。可能原因是放牧压力多集聚于水源附近。高寒草原区土壤的砂粒含量随放牧强度的增大而增加。放牧强度的增大导致草甸上层土壤有机质增加,草甸下层、草原上层、草原下层土壤有机质先增加后减小。草甸上下层土壤全磷含量在低放牧强度下显著低于中高强度。3）植被土壤变化受到自然因子和放牧活动的共同影响。高寒草甸更加耐牧,高强度放牧对高寒草原的负面影响更大,而中度放牧有利于草地尤其是高寒草原的放牧利用。4）放牧生态系统是一个环境-植物-家畜自适应系统。在放牧管理中不能仅通过控制载畜量缓解草地超载,还需要综合考虑生态系统的弹性及各营养级的适应性,合理配置放牧强度,控制季节性超载和局部超载。     

Eradication of Propionibacterium acnes by its endogenic porphyrins after illumination with high intensity blue light

Propionibacterium acnes is a Gram-positive, microaerophilic bacterium that causes skin wounds. It is known to naturally produce high amounts of intracellular porphyrins. The results of the present study confirm that the investigated strain of P. acnes is capable of producing endogenic porphyrins with no need for any trigger molecules. Extracts from growing cultures have demonstrated emission peaks around 612 nm when excited at 405 nm, which are characteristic for porphyrins. Endogenic porphyrins were determined and quantified after their extraction from the bacterial cells by fluorescence intensity and by elution retention time on high-performance liquid chromatography (HPLC). The porphyrins produced by P. acnes are mostly coproporphyrin, as shown by the HPLC elution patterns. Addition of delta-aminolevulinic acid (ALA) enhanced intracellular porphyrin synthesis and higher amounts of coproporphyrin have been found. Eradication of P. acnes by its endogenic porphyrins was examined after illumination with intense blue light at 407-420 nm. The viability of 24 h cultures grown anaerobically in liquid medium was reduced by less than two orders of magnitude when illuminated once with a light dose of 75 J cm(-2). Better photodynamic effects were obtained when cultures were illuminated twice or three times consecutively with a light dose of 75 J cm(-2) and an interval of 24 h between illuminations. The viability of the culture under these conditions decreased by four orders of magnitude after two illuminations and by five orders of magnitude after three illuminations. When ALA-triggered cultures were illuminated with intense blue light at a light dose of 75 J cm(-2) the viability of the treated cultures decreased by seven orders of magnitude. This decrease in viability can occur even after a single exposure of illumination for the indicated light intensity. X-ray microanalysis and transmission electron microscopy revealed structural damages to membranes in the illuminated P. acnes. Illumination of the endogenous coproporphyrin with blue light (407-420 nm) apparently plays a major role in P. acnes photoinactivation. A treatment protocol with a series of several illuminations or illumination after application of ALA may be suitable for curing acne. Treatment by both pathways may overcome the resistance of P. acnes to antibiotic treatment.     

Full-Length Recombinant Plasmodium falciparum VAR2CSA Binds Specifically to CSPG and Induces Potent Parasite Adhesion-Blocking Antibodies

Plasmodium falciparum malaria remains one of the world's leading causes of human suffering and poverty. Each year, the disease takes 1-3 million lives, mainly in sub-Saharan Africa. The adhesion of infected erythrocytes (IEs) to vascular endothelium or placenta is the key event in the pathogenesis of severe P. falciparum infection. In pregnant women, the parasites express a single and unique member of the P. falciparum erythrocyte membrane protein 1 (PfEMP1) family named VAR2CSA, which is associated with the ability of the IEs to adhere specifically to chondroitin sulphate A (CSA) in the placenta. Several Duffy-binding-like domains from VAR2CSA molecules have been shown in vitro to bind to CSA, but it has also been demonstrated that Duffy-binding-like domains from PfEMP1 proteins other than VAR2CSA can bind CSA. In addition, the specificity of the binding of VAR2CSA domains to glycosaminoglycans does not match that of VAR2CSA-expressing IEs. This has led to speculation that the domains of native VAR2CSA need to come together to form a specific binding site or that VAR2CSA might bind to CSA through a bridging molecule. Here, we describe the expression and purification of the complete extracellular region of VAR2CSA secreted at high yields from insect cells. Using surface plasmon resonance, we demonstrate that VAR2CSA alone binds with nanomolar affinity to human chondroitin sulphate proteoglycan and with significantly weaker affinity to other glycosaminoglycans, showing a specificity similar to that observed for IEs. Antibodies raised against full-length VAR2CSA completely inhibit recombinant VAR2CSA binding, as well as parasite binding to chondroitin sulphate proteoglycan. This is the first study to describe the successful production and functionality of a full-length PfEMP1. The specificity of the binding and anti-adhesion potency of induced IgG, together with high-yield production, encourages the use of full-length PfEMP1 in vaccine development strategies.