Ultrastructural immunogold localization of major sperm protein (MSP) in spermatogenic cells of the nematode Acrobeles complexus (Nematoda,Rhabditida)

The nematode spermatozoa represent a highly modified (aberrant) type of male gametes that lack a flagellum but for which the process of spermatogenesis culminates in the production of a crawling spermatozoon on the basis of the cytoskeletal component known as “major sperm protein”, or MSP. MSP is also known as an important hormone triggering oocyte maturation and ovulation in the model nematode Caenorhabditis elegans, where this protein was first identified. However, direct evidence of MSP localization and of its fate in nematode spermatogenic cells is rare. In this study, the spermatogenesis and sperm structure in the rhabditid nematode Acrobeles complexus (Rhabditida: Tylenchina: Cephalobomorpha: Cephaloboidea: Cephalobidae) has been examined with electron microscopy. Morphological observations were followed by high-pressure freezing and freeze-substitution fixation which allows post-embedding immunogold localization of MSP in all stages of sperm development using antibodies raised for MSP of C. elegans. In spermatocytes, synthetic activity results in the development of specific cellular components, fibrous bodies (FB) and membranous organelles (MO), which appear as FB-MO complexes where the filamentous matter of FB has been MSP-labeled. The spermatids subdivide into a residual body with superfluous cytoplasm, and a main cell body which contains nucleus, mitochondria and FB-MO complexes. These complexes dissociate into individual components, MO and FB, with the MSP being localized in FB. Immature spermatozoa from testes are opaque cells where a centrally located nucleus is surrounded by mitochondria, MO and FB clustered together, the MSP still being localized only in FB. Cytoplasm of mature spermatozoa from spermatheca is segregated into external pseudopods lacking organelles and a central cluster of mitochondria with intact MO surrounding the central nucleus. The FB ultimately disappear, and the MSP labeling becomes concentrated in the filamentous content of pseudopods and cytoplasm of the main cell body. Although the spermatogenesis and sperm structure of A. complexus is similar to that of many other rhabditid nematodes, their intact MO makes the morphology of the mature spermatozoa distinct from the “rhabditid pattern” and may be considered as a synapomorphy. The MSP localization in spermatogenic cells of A. complexus also follows the “rhabditid pattern” described in C. elegans and Ascaris spp. Our results and techniques of MSP labeling of A. complexus spermatogeneous cells reveal new possibilities to elucidate different research questions on MSP localization in nematodes related to C. elegans. Furthermore, the laboratory-cultured A. complexus strains can be used as a new and fascinating model to study MO and MSP functions in nematode reproduction.     

A Structure Theorem for Strong Immersions

A graph H is strongly immersed in G if H is obtained from G by a sequence of vertex splittings (i.e., lifting some pairs of incident edges and removing the vertex) and edge removals. Equivalently, vertices of H are mapped to distinct vertices of G (branch vertices) and edges of H are mapped to pairwise edge‐disjoint paths in G, each of them joining the branch vertices corresponding to the ends of the edge and not containing any other branch vertices. We describe the structure of graphs avoiding a fixed graph as a strong immersion. The theorem roughly states that a graph which excludes a fixed graph as a strong immersion has a tree‐like decomposition into pieces glued together on small edge cuts such that each piece of the decomposition has a path‐like linear decomposition isolating the high degree vertices.     

Optimization of ultrasound-assisted extraction of bioactive compounds from wild garlic (Allium ursinum L.)

Ultrasound-assisted extraction was used for extraction of bioactive compounds and for production of Allium ursinum liquid extract. The experiments were carried out according to tree level, four variables, face-centered cubic experimental design (FDC) combined with response surface methodology (RSM). Temperature (from 40 to 80 °C), ethanol concentration (from 30% to 70%), extraction time (from 40 to 80 min) and ultrasonic power (from 19.2 to 38.4 W/L) were investigated as independent variables in order to obtain the optimal conditions for extraction and to maximize the yield of total phenols (TP), flavonoids (TF) and antioxidant activity of obtained extracts. Experimental results were fitted to the second order polynomial model where multiple regression and analysis of variance were used to determine the fitness of the model and optimal condition for investigated responses. The predicted values of the TP (1.60 g GAE/100 g DW), TF (0.35 g CE/100 g DW), antioxidant activity, IC₅₀ (0.71 mg/ml) and EY (38.1%) were determined at the optimal conditions for ultrasound assisted extraction: 80 °C temperature, 70% ethanol, 79.8 min and 20.06 W/L ultrasonic power. The predicted results matched well with the experimental results obtained using optimal extraction conditions which validated the RSM model with a good correlation.     

A possible general mechanism for ultrasound-assisted extraction (UAE) suggested from the results of UAE of chlorogenic acid from Cynara scolymus L. (artichoke) leaves

The use of ultrasound-assisted extraction (UAE) for the extraction of chlorogenic acid (CA) from Cynara scolymus L., (artichoke) leaves using 80% methanol at room temperature over 15 min gave a significant increase in yield (up to a 50%) compared with maceration at room temperature and close to that obtained by boiling over the same time period. A note of caution is introduced when comparing UAE with Soxhlet extraction because, in the latter case, the liquid entering the Soxhlet extractor is more concentrated in methanol (nearly 100%) that the solvent in the reservoir (80% methanol) due to fractionation during distillation. The mechanism of UAE is discussed in terms of the effects of cavitation on the swelling index, solvent diffusion and the removal of a stagnant layer of solvent surrounding the plant material.     

Application of Solid Immersion Lens to Submicron Resolution Imaging of Nano-Scale Quantum Wells

We have discussed the resolution of submicron photoluminescence (PL) imaging using a solid immersion lens (SIL), which collects an evanescent light field. We apply the SIL microscope to measure PL image of a strip-line-patterned GaAs quantum well structure at low temperature. An improved resolution beyond diffraction limit and high collection efficiency of PL are realized.This paper was originally presented at the 5th International Conference on NEAR FIELD OPTICS and RELATED TECHNOLOGIES (NFO-5), which was held on December 6–10, 1998 at Coganoi Bay Hotel, Shirahama, Japan, in cooperation with the Japan Society of Applied Physics and Mombusho Grant-in Aid for Scientific Research on Priority Areas “Nearfield Nano-optics” Project, sponsored by Japan Society for the Promotion of Science.     

Dynamic Systems Analysis and Control Based on a Configuration Manifold Model

This paper presents a configuration manifold model for the analysis of dynamic systems and the development of control algorithms from both geometrical and topological points of view. The fundamental theory of surfaces and differential manifolds endowed with Riemannian metrics is overviewed. The concepts of configuration manifolds (C-manifolds) and their immersions and embeddings are then introduced and applied to dynamic systems modeling. An explicit form of the smooth embedding for a given dynamic system with its C-manifold is derived. In an open serial-chain robotic system, a topological equivalence, i.e. a homeomorphism, is found and shown to be useful for dynamic model reduction. With topology being viewed as the structure of geometry, we discover and prove that the kinematics of a dynamic system determines its topology so that the kinematics is virtually a structure of the system's dynamics. This key point of view is further extended to the development of an adaptive control strategy. A computer simulation study is finally performed to verify the proposed model and adaptive control scheme.     

基于纳米压痕试验的混凝土微观耐久性表征

利用纳米压痕和扫描电镜研究了不同冻融循环下混凝土的微观性能,揭示了冻融循环所导致混凝土退化的机理．纳米压痕结果显示,混凝土浆体的压痕模量与硬度的相关系数很大,并且都不满足正态分布．本文利用核密度估计来计算浆体微观性能的概率密度函数．根据浆体和骨料的性能差异,用阶跃函数来拟合界面过渡区的微观力学性能,同时利用扫描电镜观察界面过渡区的形貌．采用以上两种方法研究不同冻融循环下的混凝土,发现在不同的尺度下,冻融循环对混凝土的影响不同：在纳米尺度下,由于水的参与,高密度水凝胶会进一步形成;而在微米尺度下,由于冻融循环中水结冰膨胀和材料多相性,微裂纹进一步扩展,导致断裂能量降低,混凝土表现出宏观退化．     

Modulation of the PGE2-Mediated Pathway in the Eclosion Blocking Effect of Flumethrin and Terpenoid Subfraction Isolated from Artemesia nilagirica in Rhipicephalus annulatus

Prostaglandins are a group of important cell-signaling molecules involved in the regulation of ovarian maturation, oocyte development, egg laying and associated behaviors in invertebrates. However, the presence of prostaglandin E₂ (PGE₂), the key enzymes for PGE₂ biosynthesis and its interference by drugs were not investigated previously in the ovary of ticks. The present study was undertaken to assess the modulation of the PGE₂-mediated pathway in the eclosion blocking effect of flumethrin and terpenoid subfraction isolated from Artemisia nilagirica in Rhipicephalus annulatus ticks. The acaricidal activities and chemical profiling of the terpenoid subfraction were performed. The localization of the cyclooxygenase1 (COX1) and prostaglandin E synthase (PGES) enzymes and the quantification of PGE₂ in the ovaries of the ticks treated with methanol (control), flumethrin and terpenoid subfraction were also undertaken. In addition, the vitellogenin concentration in hemolymph was also assayed. Both flumethrin and the terpenoid subfraction of A. nilagirica elicited a concentration-dependent inhibition of fecundity and blocking of hatching of the eggs. The COX1 could not be detected in the ovaries of treated and control ticks, while there was no significant difference observed in the concentration of vitellogenin (Vg) in them. The presence of PGES in the oocytes of control ticks was confirmed while the immunoreactivities against PGES were absent in the vitellogenic oocytes of ticks treated with flumethrin and terpenoid subfraction. The levels of PGE₂ were below the detection limit in the ovaries of the flumethrin-treated ticks, while it was significantly lower in the ovaries of the terpenoid subfraction-treated ticks. Hence, the prostaglandin E synthase and PGE₂ were identified as very important mediators for the signaling pathway for ovarian maturation and oviposition in ticks. In addition, the key enzyme for prostaglandin biosynthesis, PGES and the receptors for PGE₂ can be exploited as potential drug targets for tick control. The detection of PGES by immunohistochemistry and quantification of PGE₂ by LC-MSMS can be employed as valuable tools for screening newer compounds for their eclosion blocking acaricidal effects.     

A simplified version of the total kjeldahl nitrogen method using an ammonia extraction ultrasound-assisted purge-and-trap system and ion chromatography for analyses of geological samples

The total Kjeldahl nitrogen (TKN) method was simplified by using a manifold connected to a purge-and-trap system immersed into an ultrasonic (US) bath for simultaneous ammonia (NH₃) extraction from many previously digested samples. Then, ammonia was collected in an acidic solution, converted to ammonium (NH₄⁺), and finally determined by ion chromatography method. Some variables were optimized, such as ultrasonic irradiation power and frequency, ultrasound-assisted NH₃ extraction time, NH₄⁺ mass and sulfuric acid concentration added to the NH₃ collector flask. Recovery tests revealed no changes in the pH values and no conversion of NH₄⁺ into other nitrogen species during the irradiation of NH₄Cl solutions with 25 or 40 kHz ultrasonic waves for up to 20 min. Sediment and oil free sandstone samples and soil certified reference materials (NCS DC 73319, NCS DC 73321 and NCS DC 73326) with different total nitrogen concentrations were analysed. The proposed method is faster, simpler and more sensitive than the classical Kjeldahl steam distillation method. The time for NH₃ extraction by the US-assisted purge-and-trap system (20 min) was half of that by the Kjeldahl steam distillation (40 min) for 10 previously digested samples. The detection limit was 9 μg g⁻¹ N, while for the Kjeldahl classical/indophenol method was 58 μg g⁻¹ N. Precision was always better than 13%. In the proposed method, carcinogenic reagents are not used, contrarily to the indophenol method. Furthermore, the proposed method can be adapted for fixed-NH₄⁺ determination.     

Ultrasound-assisted emulsification-microextraction combined with flame atomic absorption spectrometry for determination of trace cadmium in water samples

The process of ultrasound-assisted emulsification-microextraction (USAEME) was successfully applied for the first time for the extraction and pre-concentration of trace cadmium from water samples, followed by flame atomic absorption spectrometry (FAAS). In the proposed approach, sodium diethyldithiocarbamate trihydrate solution (NaDDTC·3H₂O) was used as a chelating agent and carbon tetrachloride was selected as extraction solvent. Some effective parameters on the microextraction and the complex formation were selected and optimized. These parameters included extraction solvent type as well as extraction volume, time, temperature, and pH, the amount of the chelating agent, and salt effect. Under optimum conditions, an enrichment factor of 95 was obtained from only 5.0 mL of water sample. The calibration graph was linear in the range of 10-600 μg L⁻¹ with a detection limit of 0.91 μg L⁻¹. The relative standard deviation (R.S.D) for ten replicate measurements of 50 and 500 μg L⁻¹ of cadmium were 2.56 and 1.62%. This proposed method was successfully applied in the analysis of four real environmental water samples and good spiked recoveries over the range of 96.5-101.7% were obtained.