中国老工业城市能源消费碳排放的驱动力分析——以沈阳市为例

开展人为因素对区域生态环境影响作用的量化分析,是国际可持续发展领域的研究热点.本文以典型的老工业城市--沈阳市为例,基于IPCC能源消费碳排放计算方法,对1978-2009年城市能源消费碳排放进行核算,并应用基于Kaya等式和岭回归的STIRPAT模型,对影响碳排放量的人文驱动因素进行时间序列分析.结果表明： 研究期间,沈阳市碳排放变化经历了3个阶段,先缓升再略降随后快速增加,2009年的碳排放总量是1978年的46倍;人口规模是影响沈阳市碳排放量增加的主要驱动因子,碳排放量与人口数量呈同比例变化;城市化显著影响碳排放量,是仅次于人口数量的另一个主要驱动因子;人均GDP与碳排放量呈正相关关系,经济发展与碳排放之间不存在Kuznets曲线假说;能源强度降低即技术进步因素是碳排放量降低的主要因素.     

柑橘丛枝菌根真菌生长与根际有效磷和磷酸酶活性的相关性

通过观测田间国庆1号温州密柑/枳和国庆4号温州密柑/枳根系菌根侵染率、孢子密度、根际有效磷和磷酸酶活性的年变化,探讨丛枝菌根真菌生长与根际有效磷和磷酸酶活性的相关性.结果表明,2种柑橘菌根侵染率和孢子密度的年变化均呈 “Λ”形,2月和12月较低,4月和10月居中,6月和8月较高;有效磷和中性磷酸酶年变化呈“V”形.2种柑橘的菌根侵染率都与孢子密度呈极显著正相关,与有效磷呈极显著负相关,说明较高的孢子密度和较低的有效磷对菌根侵染率有促进作用;2种柑橘的孢子密度均与有效磷呈极显著负相关,与中性磷酸酶和总磷酸酶呈极显著正相关,表明中性磷酸酶和总磷酸酶对孢子密度有刺激作用,而有效磷对其有抑制作用.柑橘树下有机磷矿化主要以中性磷酸酶为主.     

菌根真菌对土壤呼吸以及凋落物分解的影响

土壤呼吸是植物固定的碳由陆地生态系统进入大气的主要途径之一; 凋落物分解是养分循环的重要环节。陆地植物的90%以上可同菌根真菌形成共生关系, 菌根真菌对于植物获取环境中的养分具有重要的作用。然而, 其对土壤呼吸和凋落物分解的影响却经常在生态系统对环境变化的响应研究中被忽视。本文系统地综述了国内外相关研究进展, 对菌根真菌如何影响土壤呼吸和凋落物分解这两个过程及这种影响如何受到环境变化的制约做了全面的分析, 并对以往研究中存在的问题以及未来的研究方向提出了展望。     

丛枝菌根真菌对西瓜嫁接苗生长和根系防御性酶活性的影响

在温室盆栽条件下,研究丛枝菌根(AM)真菌地表球囊霉(Glomus versiforme)对连作土壤中西瓜自根苗和嫁接苗生长、根系膜透性、丙二醛(MDA)含量和防御性酶活性的影响.结果表明： 接种AM真菌能显著增加西瓜自根苗和嫁接苗的生物量,提高根系活力,降低根系膜透性和MDA含量.接种AM真菌的自根苗地上部鲜质量、地上部干质量和根系活力分别增加了57.6%、60.0%和142.1%,而接种AM真菌的嫁接苗分别增加了26.7%、28.0%和11.0%;自根苗（C）、嫁接苗（G）、接种AM真菌自根苗（C+M）和接种AM真菌嫁接苗（G+M）的根系细胞膜透性为C>G>C+M>G+M,根系MDA含量为C>G>G+M>C+M.接种AM真菌能提高西瓜自根苗和嫁接苗根系的苯丙氨酸解氨酶(PAL)、过氧化氢酶(CAT)、过氧化物酶(POD)、几丁质酶和β 1,3 葡聚糖酶活性,而且接种AM真菌的西瓜自根苗和嫁接苗根系POD、PAL和β-1,3-葡聚糖酶活性的峰值比不接种的提前2周出现.接种AM真菌能激活西瓜自根苗和嫁接苗与抗逆性有关的防御性酶反应,使根系对逆境产生快速反应,从而提高其抗连作障碍的能力.     

丛枝菌根真菌对西瓜嫁接苗生长和根系防御性酶活性的影响

在温室盆栽条件下,研究丛枝菌根(AM)真菌地表球囊霉(Glomus versiforme)对连作土壤中西瓜自根苗和嫁接苗生长、根系膜透性、丙二醛(MDA)含量和防御性酶活性的影响.结果表明： 接种AM真菌能显著增加西瓜自根苗和嫁接苗的生物量,提高根系活力,降低根系膜透性和MDA含量.接种AM真菌的自根苗地上部鲜质量、地上部干质量和根系活力分别增加了57.6%、60.0%和142.1%,而接种AM真菌的嫁接苗分别增加了26.7%、28.0%和11.0%;自根苗（C）、嫁接苗（G）、接种AM真菌自根苗（C+M）和接种AM真菌嫁接苗（G+M）的根系细胞膜透性为C>G>C+M>G+M,根系MDA含量为C>G>G+M>C+M.接种AM真菌能提高西瓜自根苗和嫁接苗根系的苯丙氨酸解氨酶(PAL)、过氧化氢酶(CAT)、过氧化物酶(POD)、几丁质酶和β 1,3 葡聚糖酶活性,而且接种AM真菌的西瓜自根苗和嫁接苗根系POD、PAL和β-1,3-葡聚糖酶活性的峰值比不接种的提前2周出现.接种AM真菌能激活西瓜自根苗和嫁接苗与抗逆性有关的防御性酶反应,使根系对逆境产生快速反应,从而提高其抗连作障碍的能力.     

溶磷细菌和丛枝菌根真菌接种对南方红豆杉生长及根际微生物和土壤酶活性的影响

以南方红豆杉实生苗为材料,采用盆栽实验探讨了高效溶磷细菌草木樨中华根瘤菌(Sinorhizobium meliloti)CHW10B与丛枝菌根真菌缩球囊霉(Glomus constrictum)单独和双接种条件下,其植株生长、根际土壤可培养微生物数量、土壤酶活和土壤微生物功能多样性变化,在微生态水平揭示接种对南方红豆杉生长的影响及其机制。结果表明:(1)各接种处理对南方红豆杉幼苗均有促生长作用,接种处理苗高、地径和生物量均较对照显著增加,并以双接种促进效果最好。(2)各接种处理提高了南方红豆杉根际土壤可培养细菌、真菌和放线菌含量,增加了土壤微生物碳源利用率,改变了土壤中物种的丰富度和均一度,增加了土壤中的生物多样性。(3)各接种处理促进了南方红豆杉根际重要土壤酶(酸性磷酸酶、脱氢酶、转化酶)活力的增加,且双接种的促进作用最为明显。可见,溶磷细菌(草木樨中华根瘤菌CHW10B)和丛枝菌根真菌(缩球囊霉)具有协同作用,两者同时接种可显著提高南方红豆杉根际土壤微生物数量及土壤酶活力,提高土壤微生物碳源利用率和土壤肥力,增加土壤中的生物多样性,从而达到间接促进宿主植物南方红豆杉生长的目的。     

氮沉降及菌根真菌对长白落叶松苗木根系构型及根际酶活性的影响

为探究氮沉降和接种菌根真菌对长白落叶松苗木根系构型和根际土壤酶活性的影响,以1年生长白落叶松(Larix olgensis)的盆栽菌根苗(简称+M,混合接种8种外生菌根真菌)和非菌根苗(简称-M,未接种处理)为研究对象,设置4个氮沉降处理(不施氮(0N,0 kg·N·hm^-1·yr^-1)、低氮(LN,15 kg·N·hm^-1·yr^-1)、中氮(MN,30 kg·N·hm^-1·a^-1)和高氮(HN,60 kg·N·hm^-1·a^-1)),测定直径0~0.5 mm根系的总根长、总表面积、总体积和根尖数等根系形态指标,对比分析氮沉降和接种菌根真菌处理对苗木根际土壤酶(β-1,4葡萄糖苷酶(BG)、亮氨酸氨基肽酶(LAP)、β-1,4-N-乙酰-氨基葡糖氨糖苷酶(NAG)、酸性磷酸酶(ACP)和碱性磷酸酶(ALP))活性的影响。结果表明:①长白落叶松苗木直径0~0.5 mm根系的总根长、总表面积、总体积和根尖数均随氮浓度的递增呈下降的趋势;在0N、LN和MN处理下,-M处理的根系形态指标均高于+M处理。②随氮浓度增加,+M和-M处理苗木根际土壤中BG、LAP、ACP和ALP活性均呈先增加后下降的趋势,而NAG活性呈下降的趋势。③+M和-M处理下,长白落叶松直径0~0.5 mm根系的形态指标与根际土壤BG活性均呈显著负相关关系(P<0.05);除根尖数外,其它根系形态指标与NAG活性相关性均为正相关(P<0.05)。综上所述,苗木菌根化处理削弱了氮沉降对落叶松苗木根系构型的影响;而低氮处理下,+M处理对苗木根际土壤酶的活化程度高于-M处理。     

丛枝菌根真菌对辣椒光合特性及根际微生物多样性和酶活性的影响

在育苗和栽培基质中添加具有生物活性的微生物群体是改善无土栽培有机基质性状和提高应用效果的重要途径。该试验通过在辣椒育苗和栽培基质中添加丛枝菌根真菌制剂恩益碧(NEB-F),研究了AMF对辣椒生长、果实产量、光合特性以及根际微生物多样性和酶活性的影响。结果显示:(1)基质添加AMF显著促进了辣椒植株生长,并明显提高了产量。(2)AMF处理显著提高了辣椒植株叶片的净光合速率(Pn)、气孔导度(Gs)、蒸腾速率(Tr)、水分利用效率(WUE),而使胞间二氧化碳浓度(Ci)显著降低,同时对辣椒叶片最大光化学效率(Fv/Fm)的影响不大,而使实际光化学效率(ФPSⅡ)、光化学猝灭(qP)和表观光合电子传递效率(ETR)显著提高。(3)基质添加AMF显著增加基质中细菌、放线菌数量,而降低真菌数量,并明显提高了根际微生物多样性指数以及过氧化氢酶、碱性磷酸酶和尿酶活性;添加AMF基质中的细菌、真菌、放线菌数量均与其过氧化氢酶、脲酶、碱性磷酸酶之间呈显著或极显著正相关关系。研究表明,基质添加AMF不仅增大了辣椒叶片气孔导度,而且促进电子传递速率,提高CO2同化利用效率和净光合速率;同时促使辣椒根际微生物区系从低肥力的"真菌型"向高肥力的"细菌型"转化,提高根际微生物多样性和酶活性,有助于维持辣椒根际生态系统的稳定性与和谐性,从而促进辣椒幼苗生长,并提高产量。基质中添加AMF是提高有机基质应用效果的有效途径。     

泡囊丛枝(VA)菌根对玉米根际磷酸酶活性的影响

以玉米为材料,利用三室隔网培养方法,研究了缺P土壤上施用植酸和卵磷脂时接种几种菌根真菌(Glomus mosseae, Glmous versiformea, Gigaspora margarita)对根际土壤酸性磷酸酶和碱性磷酸酶活性的影响.玉米生长70d后,收获测定距根表不同距离土壤中的磷酸酶活性.结果表明,接种菌根真菌增加了根际土壤酸性和碱性磷酸酶活性,Gigaspora margarita菌根菌的作用大于其它2个菌根菌.不同P源对磷酸酶活性有明显影响.     

铅对鲫鱼碱性磷酸酶和酸性磷酸酶活性的影响

在实验条件下,将鲫鱼置于1、10、40 mg/L的Pb2 溶液中静态染毒,分别在24 h、48 h、96 h、144 h测定鳃、肝、胰、肾、脑组织的碱性磷酸酶(AKP)和酸性磷酸酶(ACP)活性.结果 表明,鲫鱼鳃、肝、胰、肾、脑组织中碱性磷酸酶和酸性磷酸酶的活性随着铅浓度的升高和染毒时间的延长均呈下降趋势,其中以肾脏和脑下降最明显.     

接种AM真菌对PAEs污染土壤中微生物和酶活性的影响

土壤灭菌条件下 ,添加 5 0mg·kg-1DEHP和 5 0mg·kg-1DBP ,在温室进行盆栽试验 ,观察土壤施加DEHP与DBP和接种AM真菌 (Acaulosporalavis,光壁无梗球囊霉 ,菌号 :34)后菌根际 (简称A)、菌丝际 (简称B)和常规土 (简称C)中土壤微生物和部分土壤酶活性的变化。结果表明 ,土壤施加DEHP和DBP后 ,A、B和C层土中土壤微生物数量和土壤酶含量下降 ;接种AM真菌后 ,受AM直接影响的A和B层土中细菌、放线菌和真菌数量比不接种低 ,而C层土中三菌数量比不接种高 ;A和B层土中中性磷酸酶和脲酶含量下降 ,脱氢酶含量在A、C层土中下降 ,在B层土中稍有增加 ,AM对土壤脱氢酶活性影响不大。接种AM真菌没有降低DEHP和DBP对土壤微生物生长和土壤酶活性不利影响的程度     

Vertical distribution of arbuscular mycorrhizal fungi under corn (Zea mays L.) in no-till and conventional tillage systems

 We compared the vertical distribution (0–25 cm) of arbuscular mycorrhizae, extraradical hyphae, and glomalean spores at grain-filling of corn under conventional tillage versus no tillage. Root colonization, total hyphae density, and spore density were correlated, and were highest at a depth of 0–15 cm in soil. Tillage significantly reduced total hypha density and spore density at 0–5 cm depth, but did not affect root colonization. Plowing below 15 cm is likely to diminish AM fungus inocula in the rooting zone of establishing seedlings. Accepted: 19 April 1998     

AM真菌对紫花苜蓿茎点霉叶斑病及豌豆蚜为害的影响

苜蓿茎点霉(Phoma medicaginis)叶斑病和豌豆蚜(Acyrthosiphon pisum)是紫花苜蓿(Medicago sativa)生产中重要的病虫害,在自然条件下常混合发生。本研究以紫花苜蓿为植物材料,探究接种AM真菌后,紫花苜蓿被苜蓿茎点霉侵染时,植物自身的防御机制,以及对后续豌豆蚜为害的影响,以期明确AM真菌对其调控机制。结果表明:AM真菌可显著降低植株茎点霉叶斑病病情指数(P<0.05); AM真菌促进了紫花苜蓿生长(P<0.05),改变了植株抗氧化酶(超氧化物歧化酶(SOD)和过氧化氢酶(CAT))活性以及植物激素信号物质(水杨酸(SA))含量(P<0.05);病原菌侵染会诱导植物抗氧化防御系统活性增强,包括过氧化物酶(POD)、SOD、CAT和多酚氧化酶(PPO)(P<0.05),从而增加植物对后续虫害的抗性; AM真菌在植物受到病原菌胁迫时会发挥积极作用,显著提高植株的SOD和CAT活性(P<0.05),有效抑制病原菌侵染对植株造成的危害;而蚜虫为害则进一步加重了植物受到的损害,抑制了AM真菌对植物抗病性的正向调控。研究结果对...     

Loss of myocardial capillary endothelial-cell alkaline phosphatase (ALP) activity in primary endothelial cell culture

Primary cultures of rat myocardial capillary endothelial cells were established and characterized. A range of typical endothelial cell-specific markers were retained in vitro. Cell kinetic studies in confluent endothelial-cell cultures in vitro revealed a roughly 50-fold increase in the proportion of cells in s-phase, indicating a very considerable shortening of cell turnover time, compared to in vivo conditions. Alkaline phosphatase enzyme activity and encoding mRNA are strongly expressed in myocardial capillary endothelial cells in vivo, but were not detectable in vitro. This was true in cell cultures from two strains of rat, which revealed significantly different enzyme expression levels in vivo. In co-cultures of pericytes and endothelial cells, positive ALP enzyme reaction was detected in pericytes, which in vivo show only very weak enzyme reactivity. Treatment of cell cultures with ≤10 M retinoic acid had no effect in pure endothelial cell cultures, but did increase ALP expression of pericytes in co-cultures. The observation of a loss of endothelial ALP expression in vitro supports other in vitro as well as our own in vivo observations, indicating a negative correlation of ALP expression and proliferative activity of endothelial cells.     

Comparison of phosphatase localization in the intraradical hyphae of arbuscular mycorrhizal fungi,Glomus spp. and Gigaspora spp.

The localization of acid and alkaline phosphatases in the intraradical hyphae of the arbuscular mycorrhizal fungi, Glomus mosseae (Nicol. and Gerd.) Gerd. and Trappe (Gm), Gl. etunicatum Becker and Gerd. (Ge) and Gigaspora rosea Nicol. and Schenck (Gir) were compared. Marigold (Tagetes patula L.) and leek (Allium porrum L.) were inoculated with each of the three fungi. The mycorrhizal roots were harvested at 3, 4, 5 and 6 weeks after sowing (WAS), treated with a digestion solution containing cellulase and pectinase, and then stained for phosphatase activities at pH 5.0 and pH 8.5. The development of fungal structures in the host root was also examined. Gm formed fine-branched (mature) arbuscules only at the early phase of infection (3 to 4 WAS). Mature arbuscules of Ge and Gir were observed from the early phase (4 WAS) up to the end of experiment. At pH 5.0, the localization of the phosphatase activities of the three fungi were similar irrespective to host plant species. The activity appeared in mature arbuscules and intercellular hyphae, whereas the collapsed arbuscules were inactive. Ten millimolar NaF, an acid phosphatase inhibitor, inhibited the phosphatase activities of Gm and Ge but did not affect that of Gir. At pH 8.5, a difference among the fungal species was found in the localization of phosphatase activity while that between host species was not. The mature arbuscules were also the active sites in all three species. Only Gir showed the activity in the intercellular hyphae while the two Glomus spp. did not. Five millimolar EDTA inhibited the activity of Gir at pH 8.5 while the activities of Ge and Gm were not affected by either 5 mM EDTA or 10 mM KCN (both are alkaline phosphatase inhibitors).     

泡囊丛枝（VA）菌根对玉米际磷酸酶活性的影响

以玉米为材料,利用三室隔网培养方法,研究了缺P土壤上施用植酸和卵磷脂时接种几种菌根真菌（Glomus mosseae,Glmous versiformea,Gigaspora margarita)对根际土壤酸性磷酸酶和碱性磷酸酶活性的影响,玉米生长70d后,收获测定距根表不同距离土壤中的磷酸酶活性,结果表明,接种菌根真菌增加了根际土壤酸性和碱性磷酸酶活性,Gigaspora margarita菌根菌的作用大于其它2个菌极菌,不同P源对磷酸酶活性有明显影响。     

不同产地冬虫夏草及不同厂家虫草发酵菌丝的可溶性蛋白比较

冬虫夏草〔Ｃｏｒｄｙｃｅｐｓｓｉｎｅｎｓｉｓ (Ｂｅｒｋ .)Ｓａｃｃ.〕为我国滋补名贵出口中药 ,主产于青海、西藏、四川、云南、甘肃等省。因野生资源有限 ,严重脱销。为解决药源问题 ,近年来我国已开发出了虫草菌丝体发酵产品[1] 。由于虫草系真菌寄生在昆虫体上的复合体     

Effects of amines and aminoalcohols on bovine intestine alkaline phosphatase activity

Bovine intestine alkaline phosphatase (BIALP) is widely used as a signaling enzyme in sensitive assays such as enzyme immunoassay (EIA). In this study, we evaluated the effects of various aminoalcohols and amines on the activity of BIALP in the hydrolysis of p-nitrophenyl phosphate (pNPP) at pH 9.8, at 20 °C. The k_cat values at 0.05 M diethanolamine, 0.1 M triethanolamine, and 0.2 M N-methylethanolamine were 190 ± 10, 840 ± 30, and 500 ± 10 s⁻¹, respectively. The k_cat values increased with increasing concentrations of diethanolamine, triethanolamine, and N-methylethanolamine and reached 1240 ± 60, 1450 ± 30, and 2250 ± 80 s⁻¹, respectively, at 1.0 M. On the other hand, the k_cat values at 0.05-1.0 M ethanolamine, ethylamine, methylamine, and dimethylamine were in the range of 100-600 s⁻¹. These results indicate that diethanolamine, triethanolamine and N-methylethanolamine highly activate BIALP and might be suitable as a dilution buffer of BIALP in EIA. Interestingly, the K_m values increased with increasing concentrations of diethanolamine and N-methylethanolamine, but not triethanolamine: the K_m value at 1.0 M diethanolamine (0.83 ± 0.15 mM) was 12-fold higher than that at 0.05 M (0.07 ± 0.01 mM), and that at 1.0 M N-methylethanolamine (2.53 ± 0.20 mM) was 14-fold higher than that at 0.2 M (0.18 ± 0.02 mM), while that at 1.0 M triethanolamine (0.31 ± 0.01 mM) was similar as that at 0.2 M (0.25 ± 0.01 mM), suggesting that the mechanisms of BIALP activation are different between the aminoalcohols.     

hPTH-fragments (53-84) and (28-48) antagonize the stimulation of calcium release and repression of alkaline phosphatase activity by hPTH-(1-34) in vitro

Different C-terminal fragments of parathyroid hormone (PTH)-(1-84) in blood participate in the regulation of calcium homeostasis by PTH-(1-84), and an antagonizing effect for the large carboxyl-terminal parathyroid hormone (C-PTH)-fragment (7-84) on calcium release has been described in vivo and in vitro. In this study the smaller C-PTH-fragment (53-84) and mid-regional PTH fragment (28-48), which represent discrete areas of activity in the PTH-(7-84) molecule, were assayed for their effects on calcium release and alkaline phosphatase (ALP) activity in a chick bone organ culture system. Neither PTH-(28-48) nor PTH-(53-84) had any effect on calcium release into the medium and both fragments stimulated ALP activity in the bone tissue, suggesting that the cAMP/PKA signalling pathway was not affected by these fragments. However they suppressed the calcium release induced by PTH-(1-34) and attenuated the down regulation of ALP activity caused by PTH-(1-34), suggesting that the effect on the cAMP/PKA signalling pathway may be indirectly. In conclusion, the study shows that the PTH-fragments (53-84) and (28-48) antagonize the PTH-(1-34) induced effects on calcium release and inhibition of ALP activity in a chick bone organ culture system.