276 resultados para Ornamental pot plant


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Laser-induced breakdown spectroscopy (LIBS) as a powerful analytical technique is applied to analyze trace-elements in fresh plant samples. We investigate the LIBS spectra of fresh holly leaves and observe more than 430 lines emitted from 25 elements and molecules in the region 230-438 nm. The influence of laser wavelength on LIBS applied to semi-quantitative analysis of trace-element contents in plant samples is studied. The results show that the UV laser has lower relative standard deviations and better repeatability for semi-quantitative analysis of trace-element contents in plant samples. This work may be helpful for improving the quantitative analysis power of LIBS applied to plant samples.

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Plant cell cultures have been suggested as a feasible technology for the production of a myriad of plant-derived metabolites. However, commercial application of plant cell culture has met limited success with only a handful of metabolites produced at the pilot- and commercial-scales. To improve the production of secondary metabolites in plant cell cultures, efforts have been devoted predominantly to the optimization of biosynthetic pathways by both process and genetic engineering approaches. Given that secondary metabolism includes-the synthesis. metabolism and catabolism of endogenous compounds by the specialized proteins, this review intends to draw attention to the manipulation and optimization of post-biosynthetic events that follow the formation of core metabolite structures in biosynthetic pathways. These post-biosynthetic events-the chemical and enzymatic modifications, transport, storage/secretion and catabolism/degradation have been largely unexplored in the past. Potential areas are identified where further research is needed to answer fundamental questions that have implications for advanced bioprocess design. Anthocyanin production by plant cell cultures is used as a case study for this discussion, as it presents a good example of compounds for which there are extensive research publications but still no commercial bioprocess. It is perceived that research on post-biosynthetic processes may lead to future opportunities for significant advances in commercial plant cell cultures. (C) 2002 Elsevier Science Inc. All rights reserved.

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目的】研究水肥空间组合对冬小麦形态指标及生物量的影响,对指导旱地施肥具有一定理论和实践意义。【方法】以肥熟土垫旱耕人为土为供试土壤,在全生育期遮雨和人工控制土壤水分条件下,采用分层隔水土柱试验法研究与田间土层分布相同土柱不同土层水分、氮、磷组合对冬小麦叶面积、株高、分蘖数、生物量、根冠比和收获指数等指标的影响。【结果】与整体湿润水分处理相比,上干下湿水分处理(0~30cm土层干旱胁迫,30~90cm土层湿润)下,抽穗期小麦旗叶面积、株高分别降低7.03%和3.77%;小麦地上部和根系生物量及收获指数也不同程度降低,但根冠比增加。从肥料处理看,单施磷和氮磷配施处理,小麦叶面积、株高、有效分蘖数和总生物量均极显著高于单施氮和CK,这与供试土壤各土层严重缺磷,而氮素供应相对丰富有关。从不同土层施肥看,在两种水分处理下,单施氮时,以均匀施入0~90cm土层小麦叶面积、株高、有效分蘖数、地上部生物量和根系生物量最高,施入0~30cm土层最低;单施磷和氮磷配施时,0~90cm与0~30cm土层施肥间总叶面积、旗叶面积、株高、有效分蘖数以及总生物量差异不显著,但均显著高于30~60cm和60~90cm土层相应施肥处理。【...

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在封闭的植物培养箱中,通过盆栽实验,研究了红豆草和土壤氮含量对CO2浓度增加的响应.结果表明,与正常CO2浓度(355~370μmol·mol-1)相比,CO2浓度升高(700μmol·mol-1),植物生物量增加25·1%(P<0·01),但植物体氮浓度降低25·3%(P<0·001),植物全氮没有显著的变化.经3个月盆栽实验后,与原始土壤相比,两种CO2浓度处理土壤全N、NO3--N和NH4+-N都有所降低,而土壤微生物氮则显著增加,这可能与植物生长有关.不同CO2浓度处理土壤NH4+-N浓度基本一致,但在高CO2浓度下,土壤NO3--N浓度显著降低,而微生物生物氮显著增加.对整个土壤-植物系统而言,盆栽实验后,整个系统全氮有少量增加,但变化不显著,特别是在高CO2浓度条件下,土壤-植物系统全氮最大,这可能与培养材料红豆草为豆科植物,而且在高CO2浓度下生物量增加,导致氮的固定量增加有关.

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National Natural Science Foundation of China [40771205]; National Science Fund for Distinguished Young Scholars [40625002]; Chinese Academy of Sciences [KZCX2-YW-315]

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Plant traits and individual plant biomass allocation of 57 perennial herbaceous species, belonging to three common functional groups (forbs, grasses and sedges) at subalpine (3700 m ASL), alpine (4300 m ASL) and subnival (>= 5000 m ASL) sites were examined to test the hypothesis that at high altitudes, plants reduce the proportion of aboveground parts and allocate more biomass to belowground parts, especially storage organs, as altitude increases, so as to geminate and resist environmental stress. However, results indicate that some divergence in biomass allocation exists among organs. With increasing altitude, the mean fractions of total biomass allocated to aboveground parts decreased. The mean fractions of total biomass allocation to storage organs at the subalpine site (7%+/- 2% S.E.) were distinct from those at the alpine (23%+/- 6%) and subnival (21%+/- 6%) sites, while the proportions of green leaves at all altitudes remained almost constant. At 4300 m and 5000 m, the mean fractions of flower stems decreased by 45% and 41%, respectively, while fine roots increased by 86% and 102%, respectively. Specific leaf areas and leaf areas of forbs and grasses deceased with rising elevation, while sedges showed opposite trends. For all three functional groups, leaf area ratio and leaf area root mass ratio decreased, while fine root biomass increased at higher altitudes. Biomass allocation patterns of alpine plants were characterized by a reduction in aboveground reproductive organs and enlargement of fine roots, while the proportion of leaves remained stable. It was beneficial for high altitude plants to compensate carbon gain and nutrient uptake under low temperature and limited nutrients by stabilizing biomass investment to photosynthetic structures and increasing the absorption surface area of fine roots. In contrast to forbs and grasses that had high mycorrhizal infection, sedges had higher single leaf area and more root fraction, especially fine roots.

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A faccile and efficient one-pot synthesis of highly substituted thiophenes has been developed and employed for the preparation of a small focused library. Treatment of 1,3-dicarbonyl compounds 1 with CS2 in the presence of K2CO3 in DMF at room temperature, followed by stepwise addition of alkyl bromides 2 and methylene active bromides 3, provided via intramolecular cyclization 2,3,4,5-tetrasubstituted thiophenes 4 in yields of 77-94%. This protocol, combining construction and modification of the thiophene ring, increases the structural diversity of final products from readily available materials. A mechanism for the one-pot synthesis of thiophenes of type 4 has been proposed. A small focused library of thiophenes is prepared using the sequential addition of reagents to achieve unique substitution in the 2 and 5 position of the thiophene ring

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A facile and efficient one-pot synthesis of substituted pyridine-2,4(1H,3H)-diones has been developed. Subjected to N,N-dimethylformamide dimethyl acetal (DMFDMA) in N,N-dimethylformamide at 120 ˚C, a series of acyl(carbamoyl)ketene S,S-acetals were converted into the corresponding substituted pyridine-2,4(1H,3H)-diones in high yields.

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We describe a facile one-pot process to synthesize Ag nanoplates by reducing silver nitrate with 3,3',5,5'-tetramethylbenzidine (TMB) at room temperature. The silver nanoplates were highly oriented single crystals with (111) planes as the basal planes. TMB can be readily oxidized to charge-transfer (CT) complex between TMB, as a donor, and (TMB)(2+), as an acceptor. The pi-pi interaction of the neutral amine (TMB) and diiminium structure (dication, TMB2+) result in the formation of one-dimensional CT complex nanofiber.

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Here we present a simple wet-chemical approach to synthesize flower-like silver nanostrip assembling architecture at room temperature. Transmission electron microscopy (TEM) and scanning electron microscopy (SEM) images indicate that these microstructures with the diameter of similar to 500nm exhibit hietarchical characteristic. X-ray diffraction (XRD), energy-dispersed X-ray spectroscopy (EDX) and Raman spectroscopy indicate that poly (o-diaminobenzene) (PDB) also exists in the silver hierarchical microstructure.

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A convenient and cost-effective strategy for synthesis of hyperbranched poly(ester-amide)s from commercially available dicarboxylic acids (A(2)) and multihydroxyl secondary amine (CB2) has been developed. By optimizing the conditions of model reactions, the AB(2)-type intermediates were formed dominantly during the initial reaction stage. Without any purification, the AB(2) intermediate was subjected to thermal polycondensation in the absence of any catalyst to prepare the aliphatic and semiaromatic hyperbranched poly(ester-amide)s bearing multi-hydroxyl end-groups.