婴儿泪在室内生长的光照范围研究

研究了婴儿泪适宜生长的光照范围问题。通过测定试验房间光照的分布图 ,选择试验房间内具有代表性的光区进行栽培试验。实验环境温度为 15～ 2 5℃ ,湿度为 33%～ 6 9%。经栽培 4 0d后 ,用LI 6 4 0 0测定其不同光强下的光合特性 ,计算光补偿点、光饱和点、最大净光合速率。同时测定不同试验区植株的枝长与叶片数量的生长量。结果表明 :婴儿泪在 >8 5μmol·m-2 ·s-1～ <2 99 0 μmol·m-2 ·s-1(4 2 5～ 14 95 0lx ,RH33%～ 6 9% ,温度 15～ 2 5℃ )的光照条件下能够生长     

钝顶螺旋藻形态、生长及光合作用对不同波段太阳辐射的响应

为探讨中不同波段的光合有效辐射对钝顶螺旋藻(Arthrospira platensis)形态、生长及光合作用的影响,实验将钝顶螺旋藻D-0083藻液转入带塞的石英管中, 石英管水平置于阳光下并在其上覆盖不同的截止型和带通型滤光片, 以使藻丝接受不同波段的太阳辐射; 并检测其生长、形态与光合活动的变化。结果发现: 所有波段 (320500、395700、510700和610700 nm) 光合有效辐射下的藻丝均螺旋变紧且生物量增加。其中以包含少量紫外辐射A (Ultraviolet-A)的蓝光波段 (320500 nm)和红光波段(600700 nm) 对藻丝形态变化、生长及光合速率的诱发效率较高。在320500、395700、510700和 610700 nm波段上的单位能量光照引起钝顶螺旋藻螺距变化的效率分别为0.070、0.015、0.021、0.045 m/(Wm2)。 波段320500 nm虽然会轻微抑制钝顶螺旋藻D-0083的有效光化学效率(Fv'/Fm')、电子传递速率(ETR)和藻蓝蛋白的荧光发射, 但是却能够有效诱导其藻丝变紧促进生长。此外, 钝顶螺旋藻D-0083的藻丝变紧程度、比生长速率变化与不同波段太阳辐射下藻丝体的光合性能相一致。该研究表明任何波段的光合有效辐射都能使螺旋藻藻丝螺旋变紧并引发生长和光合作用, 其中以蓝光和红光的效率最高。     

Burkholderia xenovorans LB400联苯双加氧酶及突变体对DDTs的降解

DDTs（dichlorodiphenyltrichloroethane,1,1,1-三氯-2,2-双氯苯基乙烷）是一种典型的持久性有机污染物,曾在疟疾防治和农业除虫方面被广泛应用。虽然包括我国在内的很多国家已经禁止使用DDTs,但目前对环境中DDTs的检测发现它仍然广泛存在且具有新的输入源。DDTs的持续存在对近海生态系统和人类健康具有一定危害,因此它所造成的环境污染问题仍然值得关注。由于Rieske型芳香羟化双加氧酶能够起始多种持久性污染物的降解,过去的几十年里一直是芳香化合物降解领域的焦点。[目的] 为探讨联苯双加氧酶对DDTs的降解特性及机制,本研究选取了食异生素伯克霍尔德氏菌LB400（Burkholderia xenovorans）联苯双加氧酶及突变体对p,p''-DDT和o,p''-DDT的降解过程进行研究。[方法] 以BphAE_LB400为亲本,通过两步定点突变将283位的丝氨酸突变为蛋氨酸,获得突变体BphAE_S283M。通过比较亲本酶与突变体对DDTs的催化性能,模拟突变蛋白结构和分子对接等方法,探究其降解特性及机制。[结果] BphAE_LB400和突变体BphAE_S283M都无法降解对位的p,p''-DDT,但突变体BphAE_S283M可以代谢o,p''-DDT并产生2个立体异构体。对接p,p''-DDT的BphAE_LB400和BphAE_S283M的结构分析表明,BphAE_LB400和BphAE_S283M中p,p''-DDT的反应环均不与原晶体结构中的联苯反应环重合。而对接o,p''-DDT的BphAE_S283M的结构分析表明o,p''-DDT的反应环与晶体结构中的联苯反应环距离很近,且2、3位的碳原子与单核铁原子催化中心的距离在0.5 nm以内,此外,BphAE_S283M的催化腔表面积和体积比BphAE_LB400更大,这很可能有助于BphAE_S283M与o,p''-DDT的结合。[结论] 283位氨基酸是影响BphAE_LB400对DDTs的催化代谢能力的关键氨基酸残基,它可以通过调节反应碳原子与催化中心的距离以及催化腔的大小来影响底物特异性。本次研究进一步阐明了283位氨基酸残基的影响机理,为更有效修复DDTs污染提供理论依据和技术支持。     

香溪河库湾春季水华期间水体光学特征及相关分析

研究了香溪河库湾春季水华期间(2006年3月3日—4月16日)透明度水层可见光衰减系数KSd的时空特征,分析其与表层水叶绿素a浓度、DOC浓度和透明度Sd的相关关系。结果表明:香溪河库湾春季水华可见光衰减系数KSd时空变异很大;除峡口河段(样点X7—X8)外,可见光衰减系数KSd的变化特征取决于叶绿素a浓度和DOC浓度的时空变化,类似于深水湖泊;除峡口河段(样点X7—X8)外,香溪河库湾可见光衰减系数KSd和透明度之间呈反比的关系具有显著的相关,但它们之间的反比关系因水体叶绿素a和无机悬浮颗粒的空间差异而有所不同。       

Phytoplankton morphological response to the underwater light conditions in a vegetated wetland

This study analyses the influence of the underwater light climate on the morphometric characteristics of the phytoplankton at the population and community levels. The differences in light conditions across the floodplain were mainly defined by the patchiness of floating macrophytes and humic acids concentration. A morphometric response at the community level to the underwater PAR was registered. Sites with strong light constraints were characterised by non-flagellated organisms or with a small proportion of unicellular flagellates. Short organisms (<10 μm) with a unit volume of less than 1,000 μm³ and a high surface:volume ratio (S/V >2) were the morphotypes related to poorly illuminated environments. Moreover, the organisms showed forms more slender under these limiting conditions. This pattern was different to that registered in well-illuminated sites where longer and larger organisms, with a smaller S/V and frequently flagellated, coexisted with the previously mentioned organisms. The autotrophic picoplankton, the smallest phytoplankton fraction, revealed lower abundances at sites with higher humic substances. Short term morphological changes were additionally studied for the dominant species by means of mesocosm experiments simulating different light climates. Intraspecific morphological plasticity was observed with respect to the filament length and the vacuolization of cells. Electronic Supplementary Material Supplementary material is available for this article at and is available to authorized users.     

行距和播种量对冬小麦冠层光合有效辐射垂直分布、生物量和籽粒产量的影响

为明确行距和播种量对冬小麦冠层光合有效辐射(PAR)垂直分布、生物量和籽粒产量的影响,在不增加水肥等投入的基础上,设置等行距(R1,20 cm+20 cm)、宽窄行(R2,12 cm+12 cm+12 cm+24 cm)两种行距方式和低(D1,120 kg· hm-2)、中(D2,157.5 kg·hm-2)、高(D3...     

Phosphorylation of Dab2 is involved in inhibited VEGF‐VEGFR‐2 signaling induced by downregulation of syndecan‐1 in glomerular endothelial cell

Disabled‐2 (Dab2) and PAR‐3 (partitioning defective 3) are reported to play critical roles in maintaining retinal microvascular endothelial cells biology by regulating VEGF‐VEGFR‐2 signaling. The role of Dab2 and PAR‐3 in glomerular endothelial cell (GEnC) is unclear. In this study, we found that, no matter whether with vascular endothelial growth factor (VEGF) treatment or not, decreased expression of Dab2 could lead to cell apoptosis by preventing activation of VEGF‐VEGFR‐2 signaling in GEnC, accompanied by reduced membrane VEGFR‐2 expression. And silencing of PAR‐3 gene expression caused increased apoptosis of GEnC by inhibiting activation of VEGF‐VEGFR‐2 signaling and membrane VEGFR‐2 expression. In our previous research, we found that the silencing of syndecan‐1 gene expression inhibited VEGF‐VEGFR‐2 signaling by modulating internalization of VEGFR‐2. And our further research demonstrated that downregulation of syndecan‐1 lead to no significant change in the expression of Dab2 and PAR‐3 both at messenger RNA and protein levels in GEnC, while phosphorylation of Dab2 was significantly increased in GEnC transfected with Dab2 small interfering RNA (siRNA) compared with control siRNA. Atypical protein kinase C (aPKC) could induce phosphorylation of Dab2, thus negatively regulating VEGF‐VEGFR‐2 signaling. And we found that decreased expression of syndecan‐1 lead to activation of aPKC, and aPKC inhibitor treatment could block phosphorylation of Dab2 in GEnC. Besides, aPKC inhibitor treatment could activate VEGF‐VGEFR‐2 signaling in GEnC transfected with syndecan‐1 siRNA in a dose‐dependent manner. In conclusion, we speculated that phosphorylation of Dab2 is involved in preventing activation of VEGF‐VEGFR‐2 signaling in GEnC transfected with syndecan‐1 siRNA. This provides a new target for the therapy of GEnC injury and kidney disease.     

Introduction: International conference on forest ecosystems: Ecology,conservation and sustainable management

Abstract

A pollen diagram from a small lake, Kutulahdenlampi, in northern Finland is interpreted in terms of the development of forest vegetation during the Holocene. The abundance of each of the forest taxa is considered independently by means of pollen accumulation rates (PARs), using as the reference material, long term average pollen deposition values monitored by a network of pollen traps. Particular attention is paid to the arrival of spruce and to the species in the original forests that this newcomer replaces. A model of pollen dispersal and deposition developed by Sugita is used to estimate the area around the lake that the pollen assemblage is most clearly reflecting. This relevant source area of pollen (RSAP), for the present day situations is c. 1,500 m. Pollen loadings calculated for a simulated landscape that mimics (i) that of the present day and (ii) for the situation at 8,000 BP (as deduced from the PARs) are compared with the pollen assemblages from the diagram at those points in time, and are seen to be compatible. The advantages of combining PAR and modelling to look at the spatial scale of vegetation reconstructions are discussed.     

Identification and molecular cytogenetic characterization of a novel complex Y chromosome rearrangement in a boy with disorder of sexual development

Ambiguous genitalia or disorder of the sexual development is a birth defect where the external genitals do not have the typical appearance of either a male or female. Here we report a boy with ambiguous genitalia and short stature. The cytogenetic analysis by G-banding revealed a small Y chromosome and an additional material on the 15p arm. Further, molecular cytogenetic analysis by Fluorescence in situ hybridization (FISH) using whole chromosome paint probes showed the presence of Y sequences on the 15p arm, confirming that it is a Y;15 translocation. Subsequent, FISH with centromere probe Y showed two signals depicting the presence of two centromeres and differing with a balanced translocation. The dicentric nature of the derivative 15 chromosome was confirmed by FISH with both 15 and Y centromeric probes. Further, the delineation of the Y chromosomal DNA was also done by quantitative real time PCR. Additional Y-short tandem repeat typing was performed to find out the extent of deletion on small Y chromosome. Fine mapping was carried out with 8 Y specific BAC clones which helped in defining the breakpoint regions. MLPA was performed to check the presence or absence of subtelomeric regions and SHOX regions on Y. Finally array CGH helped us in confirming the breakpoint regions. In our study we identified and characterized a novel complex Y chromosomal rearrangement with a complete deletion of the Yq region and duplication of the Yp region with one copy being translocated onto the15p arm. This is the first report of novel and unique Y complex rearrangement showing a deletion, duplication and a translocation in the same patient. The possible mechanism of the rearrangement and the phenotype–genotype correlation are discussed.