Processes involved in formation and emission of methane in rice paddies

The seasonal change of the rates of production and emission of methane were determined under in-situ conditions in an Italian rice paddy in 1985 and 1986. The contribution to total emission of CH₄ of plant-mediated transport, ebullition, and diffusion through the flooding water was quantified by cutting the plants and by trapping emerging gas bubbles with funnels. Both production and emission of CH₄ increased during the season and reached a maximum in August. However, the numbers of methanogenic bacteria did not change. As the rice plants grew and the contribution of plant-mediated CH₄ emission increased, the percentage of the produced CH₄ which was reoxidized and thus, was not emitted, also increased. At its maximum, about 300 ml CH₄ were produced per m² per hour. However, only about 6% were emitted and this was by about 96% via plant-mediated transport. Radiotracer experiments showed that CH, was produced from H₂/CO₂. (30–50%) and from acetate. The pool concentration of acetate was in the range of 6–10 mM. The turnover time of acetate was 12–16 h. Part of the acetate pool appeared to be not available for production of CH₄ or CO₂     

一个光子能量的非连续分布方程

在假设光子的波长是最小波长的整数倍的基础上,给出一个光子能量的非连续分布方程。从方程得到以下结果,光子的最大能量为1/4(J),光的最高频率为1/πh(Hz),光的最小波长为πhc(m)。我们认为光的最小波长就是Planck长度,也是超弦的长度。     

利用荧光寿命变化定量分子内和分子间相互作用的方法

荧光寿命是指荧光分子在回到基态前在激发态停留的平均时间.本文发展了基于荧光寿命测量来定量分子内和分子间相互作用的方法:通过G碱基猝灭对于荧光寿命的影响定量DNA二级结构的形成;通过荧光共振能量传递(FRET)中荧光寿命的变化来定量分子间的相互作用.第一种方法巧妙利用了G碱基会猝灭临近的染料分子的性质,结合荧光寿命的变化...     

The site of regulation of light capture in Symbiodinium: Does the peridinin–chlorophyll a–protein detach to regulate light capture?

Dinoflagellates from the genus Symbiodinium form symbiotic associations with cnidarians including corals and anemones. The photosynthetic apparatuses of these dinoflagellates possess a unique photosynthetic antenna system incorporating the peridinin–chlorophyll a–protein (PCP). It has been proposed that the appearance of a PCP-specific 77 K fluorescence emission band around 672–675 nm indicates that high light treatment results in PCP dissociation from intrinsic membrane antenna complexes, blocking excitation transfer to the intrinsic membrane-bound antenna complexes, chlorophyll a–chlorophyll c₂–peridinin–protein-complex (acpPC) and associated photosystems (Reynolds et al., 2008 Proc Natl Acad Sci USA 105:13674–13678).We have tested this model using time-resolved fluorescence decay kinetics in conjunction with global fitting to compare the time-evolution of the PCP spectral bands before and after high light exposure. Our results show that no long-lived PCP fluorescence emission components appear either before or after high light treatment, indicating that the efficiency of excitation transfer from PCP to membrane antenna systems remains efficient and rapid even after exposure to high light. The apparent increased relative emission at around 675 nm was, instead, caused by strong preferential exciton quenching of the membrane antenna complexes associated with acpPC and reaction centers. This strong non-photochemical quenching (NPQ) is consistent with the activation of xanthophyll-associated quenching mechanisms and the generally-observed avoidance in nature of long-lived photoexcited states that can lead to oxidative damage. The acpPC component appears to be the most strongly quenched under high light exposure suggesting that it houses the photoprotective exciton quencher.     

Multiphoton imaging of the dentine‐enamel junction

Multiphoton microscopy has been used to reveal structural details of dentine and enamel at the dentin‐enamel junction (DEJ) based on their 2‐photon excited fluorescence (2PEF) emission and second harmonic generation (SHG). In dentine tubule 2PEF intensity varies due to protein content variation. Intertubular dentin produces both SHG and 2PEF signals. Tubules are surrounded by a thin circular zone with a lower SHG signal than the bulk dentine and the presence of collagen fibers perpendicular to the tubule longitudinal axis is indicated by strong SHG responses. The DEJ appears as a low intensity line on the 2PEF images and this was never previously reported. The SHG signal is completely absent for enamel and aprismatic enamel shows a homogeneous low 2PEF signal contrary to prismatic enamel. The SHG intensity of mantle dentine is increasing from the dentine‐enamel junction in the first 12 μm indicating a progressive presence of fibrillar collagen and corresponding to the more external part of mantle dentine where matrix metallo‐proteases accumulate. The high information content of multiphoton images confirms the huge potential of this method to investigate tooth structures in physiological and pathological conditions. (© 2013 WILEY‐VCH Verlag GmbH & Co. KGaA, Weinheim)     

Nitrous oxide fluxes from corn fields: on-farm assessment of the amount and timing of nitrogen fertilizer

Nitrogen fertilization is considered as an important source of atmospheric N₂O emission. A seven site‐year on‐farm field experiment was conducted at Ottawa and Guelph, ON and Saint‐Valentin, QC, Canada to characterize the affect of the amount and timing of N fertilizer on N₂O emission in corn (Zea mays L.) production. Using the static chamber method, gas samples were collected for 28‐days after preplant and 28‐days after sidedress fertilization at the seven site‐year, resulting in 14 monitoring periods. For both methods of fertilization, peak N₂O flux and cumulative emission increased with the amount of N applied, with rates ranging from 30 to 900 μg N m^?2 h^?1. Depending on N amount and time of application, cumulative emission varied from 0.05 to 2.42 kg N ha^?1, equivalent to 0.03% to 1.45% of the N fertilizer applied. Differences in N₂O emission peaks among fertilizer treatments were clearly separated in 13 out of 14 monitoring periods. Total N₂O emissions may have been underestimated compared with annual monitoring in 10 out of the 49 cases because the monitoring period ended before N₂O efflux returned to the baseline level. The flux of N₂O was negligible when soil mineral N in the 0–15 cm layer was < 20 mg N kg^?1. While rainfall stimulated emission, soil temperature > 15 °C was likely the driving force responsible for the higher levels of N₂O found for sidedress than preplant application methods. However, caution must be taken when interpreting these later results as preplant fertilization may have continuously stimulated N₂O emissions after the 28‐days monitoring period, especially in situations where N₂O effluxes have not fallen back to their baseline levels. Increasing fertilizer rates from 90 to 150 kg N ha^?1 resulted in slight increases in yields, but doubled cumulative N₂O emissions.     

遗传变异与修复机制的量子观点

根据一种使得量子可以完全克隆的机制——量子半保留克隆机制,并以量子相干态可以半保留克隆为基础,作了推广到研究生物DNA分子克隆上的尝试,提出了量子半保留克隆、量子涨落与量子压缩相干态可以作为分别研究生物的遗传、变异与修复机制的可行性基础.研究指出:细胞分裂事件或者细胞死亡事件服从泊松分布;DNA复制的过程中存在着自发的、不可避免的出错几率,相对大小为平均的基因数乘以4π之后的倒数(该公式的计算与实验结果十分吻合);存在修复机制,由此导致了生物体的特殊基因座不同的自发突变频率.     

Optimization of heterocyclic 4-hydroxystyryl derivatives for histological localization of endogenous and immunobound peroxidase activity

Assisted by the development of light excitation and measuring techniques and the commercial availability of highly sensitive equipment, luminescent labels are sensitive detection tools for life sciences research. By contrast to a wide variety of well established chromogenic techniques, fluorescent labels for detecting peroxidase (PO) have been confined to only a few substrates. We describe here novel fluorescent substrates of PO derived from heterocyclic 4-hydroxy styrenes as useful tools for detecting endogenous and exogenous targets in fixed cells and tissues. Excellent localization, high staining sensitivity, outstanding photostability, and exceptionally low background staining were achieved by optimizing the substrate through chemical synthesis. Structure/staining behavior relationships are discussed. By contrast to tyramine-fluorochrome conjugates employed in the catalyzed reporter deposition (CARD) technique, reporting and anchoring functions are no longer separated. Consequently, enzymatic cross-linking of the substrate yields an altered fluorochrome with different properties. Spectral properties and anchoring capability are interdependent and influenced by environmental effects and pH. We screened overall staining capability of 4-hydroxy styryl derivatives using an iterative semi-empirical approach, and ascertained optimal substitution patterns for high PO staining specificity and high fluorescence response. Reliable staining performance was achieved with alkyl chains of short or medium length at the positively charged nitrogen, whereas introducing polar groups often impaired the staining specificity of PO. Catalytic cross-linking of heterocyclic 4-hydroxy-styryl derivatives is a promising approach for permanent fluorescent staining of PO in fixed cells and tissues, and complements the CARD technique. Histochemical and immunohistochemical applications are presented using conventional and confocal fluorescence microscopes with different excitation sources. Spectral properties of selected stains are discussed. Novel stains also are of potential interest as “reactive-tracers” for living cells under multi-photon laser excitation conditions, because they exhibit pronounced nonlinear optical properties.