发射式植入刺激器的研制及其在截瘫猗排尿功能障碍时的…

介绍一种体外发射式植入刺激器的结构和电路原理。该机不但体积较小,耗电少,且可选择较强刺激电压,其植入部分的生物相容性较好,并初步观察了用此刺激器刺激骶神经以恢复截瘫狗排尿功能的情况。     

无线遥测和刺激技术建立兔房颤模型的探索

目的探索一种在无线遥测和刺激技术基础上的兔房颤模型的制作。方法新西兰兔皮下植入自主研发的植入式遥测刺激器,植入式遥测刺激器的制作是以TI公司（德州仪器）的MSP单片机和TI公司的RF无线收发芯片CC2250为核心开发设计。优化植入系统设计以满足新西兰兔房颤模型建立的探索实验;植入子植入新西兰兔腹部皮下,采集电极留置于左上肢和右上肢腋下皮下,两个刺激电极分别缝合于左心耳和左心房上,通过无线收发采集和刺激信号;实现利用Powerlab生理记录仪连续监测体表I导联心电信号,并通过专用计算机程序刺激软件,发放间歇（刺激2 s,暂停2 s）高频（频率20 Hz）阈上（强度2 mA,脉宽1 ms）刺激,若间歇期内出现房颤,则人为干预中止刺激,若转为窦性心律,则继续刺激。结果植入式遥测刺激器在体内可稳定工作（包括采集模拟心电信号和发放刺激）30 d,植入新西兰兔体内刺激3周后可诱导出房颤,持续时间〉48 h。结论用新西兰兔代替比格犬建立基于无线遥测和刺激基础上的房颤模型是完全可行的,同时也体现了动物福利优化和替代原则。     

深部脑刺激的工作原理

深部脑刺激器是一种体内植入型治疗设备．它能连续不断地传送刺激脉冲到深部脑组织区域，这种作用称为深部脑刺激。神经外科医生通常会用深部脑刺激来治疗各种抗药性运动障碍疾病，如帕金森氏症、原发性震颤及肌张力异常等，但科学家们一直不清楚刺激作用改善疾病症状的机理。     

改进电子刺激器的使用方法

改进电子刺激器的使用方法电子刺激器或多用仪是动物生理学实验的常用仪器，然而使用时多使用刺激隔离器。有的利用变压器做隔离器，用变压器做隔离器，严重改变了电子刺激器的刺激强度和波形。一般刺激器或多用仪输出的是方波（也有锯齿波刺激器），而经隔离变压器输出后...     

世界植入式神经刺激器现状及发展趋势展望

本文介绍了目前世界各植入式神经刺激器厂家最新产品现状及植入式神经刺激器技术的发展趋势。     

小型遥控刺激器

刺激器是生理学及医学实验中广泛应用的一种电子仪器。近年来,随着针刺麻醉原理和临床研究的不断深入,广大科技工作者和医务人员研制了不少不同性能的刺激器,各有特点。为了适应慢性动物实验的需要,我们研制了一     

神经刺激仪的设计

目前电刺激器在医院麻醉和理疗科室的应用已十分普遍。本文介绍的神经刺激器是用于麻醉时神经定位和神经肌肉功能监测。微处理器产生电脉冲,经过D／A（数／模）转化输出强度可调的脉冲电流,针对不同病人采用不同刺激频率,同时显示刺激电流的大小。刺激器有两种功能：自动循环进行刺激和手动选择刺激频率挡。     

视觉假体的研究进展与面临的挑战

人工视觉假体是当今国际上对视网膜色素变性和老年性黄斑病变患者进行视觉修复的研究热点,该人工装置采集外界图像信息,并进行编码处理,通过微电流刺激器将刺激微电流信号加载到微电极阵列,对视觉神经系统进行作用,从而在视觉中枢产生光幻视,实现视觉功能修复。根据目前的国际研究现状,视觉假体可以对视觉通路的任意位置进行电刺激,以期产生视光感。按照植入位置的不同,视觉假体基本上可以分为视皮层假体、视网膜上假体、视网膜下假体和视神经假体。本文着重介绍了中国的C-Sight小组在视神经假体方面的工作进展和面临的挑战。     

鸽子慢性电刺激用电极转接装置及其固定方法

慢性电极植入以及无线刺激技术被广泛应用于动物自由活动状态下的脑区功能研究。实现刺激器与脑内植入电极过渡连接的转接装置需固定在颅骨之上。鸟类特殊的骨质构造不利于转接装置的长期固定。以鸽子(Columba livia)为例设计制作了一种用于慢性运动诱导实验的9通道电极转接装置,长12.8 mm、宽9.5 mm、高5.5 mm,重0.42 g;根据鸽子颅骨特点在固定过程中对颅骨表面进行粗糙化处理增加固定时与牙科水泥的接触面积,并选取特定位点拧入螺钉进行固定,有效延长了转接装置的固定时间。经实验验证能够在鸽子头部稳定固定6个月以上,满足鸽子长期运动诱导研究的需求,未对动物正常活动产生影响。该装置及其固定方法亦可为其他小型动物的脑区功能研究提供借鉴。     

治疗失禁的刺激器

在美国大约有1300万人患有失禁症,他们不能控制膀胱的功能,排尿不能自制,常常令人窘迫,苦不堪言。据美国医疗保健政策研究机构报导,每年用于尿失禁的医疗费用高达110万美元。老年人的尿失禁是美国的托老所和敬老院获准入院最常见的理由和原因。 最近,美国Meditronic公司研制开发了一种植入式的神经刺激器,据称可以治疗这种疾病。这种刺激器使用电子信号超越控制促使失禁的脉冲,这种病症的特点是先突然感到马上     

Cuban Calisto (Lepidoptera, Nymphalidae, Satyrinae), a review based on morphological and DNA data

The Cuban species of Calisto are reviewed based on the morphology of adult and immature stages, as well as DNA sequences of six genes (COI, EF1α, wingless, GAPDH, RpS5, CAD). A new species, Calisto occultasp. n., is described from the northeastern Cuban mountains. Calisto smintheus Bates, 1935 and Calisto bruneri, Michener 1949 are revised and revalidated. A new status, the species level, is proposed for Calisto brochei, Torre 1973, Calisto muripetens, Bates 1939 and Calisto bradleyi, Munroe 1950. The immature stages of Calisto smintheus, Calisto brochei,and Calisto occulta are described for the first time, and those of Calisto herophile, Hübner 1823 are redescribed. Useful morphological characters for adults are the shape and conspicuousness of androconial patch, the number and relative size of white dots on underside of hindwing, the shape of aedeagus, the shape of digitiform projection of genitalia valve, the shape and relative size of tegumen and uncus, the relative size of female genitalia, the height of sterigmal ring dorsal crown of the latter, and the relative size of corpus bursae and ductus bursae. For the immature stages, the most important characters are the color pattern of head capsule, the number and width of longitudinal lines of body, in the larvae; and the color pattern and the absence or presence of dorsal ridges on the abdomen of pupae. The phylogenetic relationships between the Cuban Calisto species are quite robust and well-supported; however, conflict between mitochondrial and nuclear datasets was detected in Calisto brochei, Calisto muripetens and to a lesser degree in Calisto bradleyi.     

Areography of the Gymnosperms of China (1) Distribution of the Pinaceae of China

Nine of 10 genera and 119 of approximately 240 species of the Pinaceae occur in China, including 67 endemic species and two endemic genera. In this paper, the distributional maps of all the genera of the Pinaceae are presented (fig. 1-8). The horizontal and vertical distributions of species in each genus are discussed. The analysis of the distribution patterns of the genera indicates that some genera, such as Keteleeria, Tsuga, Pseudotsuga, Cathaya and Pseudolarix, are restricted to the area south of the Qinling Mountains and the Huaihe River, and the others, i. e. Picea, Abies, Larix and Pinus, extend northward to northeastern China. However, all of the genera except Keteleeria and Pinus are not found in very dry areas and tropical mountainous regions of China. The monotypic genera, Cathaya and Pseudolarix, are distributed in eastern and central China. The genus Keteleeria consists of 10 species, 7 of which are concentrated in southern Guizhou, northern Guangxi, southwestern Hunan and easternmost Yunnan. The distribution of the remaining 6 genera shows the maximum concentration in western Sichuan and northwestern Yunnan. (Figs. 2-8). Furthermore, more than third of species of the Pinaceae (37.8%) are also concentrated in western Sichuan and northwestern Yunnan. where a great variety of habitats and different topographic features occur. It is apparent that to conduct our systematic and evolutionary studies on this family in these region is especially needed. The relations between the areal size and the tolerance of species are discussed. The distributions of macrofossils and microfossils of the genera of the Pinaceae ia China are given, and it has been proved that areas of most genera of the family were considerably larger in the past. than at present.     

Origin,Differentiation, and Geographic Distribution of the Chenopodiaceae

Numbers of species and genera,endemic genera,extant primitive genera,relationship and distribution patterns of presently living Chenopodiaceae(two subfamilies,12 tribes,and 118 genera)are analyzed and compared for eight distributional areas,namely central Asia,Europe,the Mediterranean region,Africa,North America,South America, Australia and East Asia． The Central Asia,where the number of genera and diversity of taxa are greater than in other areas,appears to be the center of distribution of extant Chenopodiaceae．North America and Australia are two secondary centers of distribution． Eurasia has 11 tribes out of the 12,a total of 70 genera of extant chenopodiaceous plants,and it contains the most primitive genera of every tribe． Archiatriplex of Atripliceae,Hablitzia of Hablitzeae,Corispermum of Corispermeae,Camphorosma of Camphorosmaea,Kalidium of Salicornieae,Polecnemum of Polycnemeae,Alexandra of Suaedeae,and Nanophyton of Salsoleae,are all found in Eurasia,The Beteae is an Eurasian endemic tribe,demonstrating the antiquity of the Chenopodiaceae flora of Eurasia．Hence,Eurasia is likely the place of origin of chenopodiaceous plants． The presence of chenopodiaceous plants is correlated with an arid climate．During the Cretaceous Period,most places of the continent of Eurasia were occupied by the ancient precursor to the Mediterranean,the Tethys Sea．At that time the area of the Tethys Sea had a dry and warm climate．Therefore,primitive Chenopodiaceae were likely present on the beaches of this ancient land．This arid climatic condition resulted in differentiation of the tribes Chenopodieae,Atripliceae,Comphorosmeae,Salicornieae,etc．,the main primitive tribes of the subfamily Cyclolobeae. Then following continental drift and the Laurasian and Gondwanan disintegration, the Chenopodiaceae were brought to every continent to propagate and develop, and experience the vicissitudes of climates, forming the main characteristics and distribution patterns of recent continental floras. The tribes Atripliceae, Chenopodieae, Camphorosmeae, and Salicornieae of recent Chenopodiaceae in Eurasia, North America, South America, southern Africa, and Australia all became strongly differentiated. However, Australia and South America, have no genera of Spirolobeae except for a few maritime Suaeda species. The Salsoleae and Suaedeae have not arrived in Australia and South America, which indicates that the subfamily Spirolobeae developed in Eurasia after Australia separated from the ancient South America-Africa continent, and South America had left Africa. The endemic tribe of North America, the tribe Sarcobateae, has a origin different from the tribes Salsoleae and Suaedeae of the subfamily Spirolobeae. Sarcobateae flowers diverged into unisexuality and absence of bractlets. Clearly they originated in North America after North America had left the Eurasian continent. North America and southern Africa have a few species of Salsola, but none of them have become very much differentiated or developed, so they must have arrived through overland migration across ancient continental connections. India has no southern African Chenopodiaceae floristic components except for a few maritime taxa, which shows that when the Indian subcontinent left Africa in the Triassic period, the Chenopodiaceae had not yet developed in Africa. Therefore, the early Cretaceous Period about 120 million years ago, when the ancient Gondwanan and Laurasian continents disintegrated, could have been the time of origin of Chenopodiaceae plants.The Chinese flora of Chenopodiaceae is a part of Chenopodiaceae flora of central Asia. Cornulaca alaschnica was discovered from Gansu, China, showing that the Chinese Chenopodiaceae flora certainly has contact with the Mediterranean Chenopodiaceae flora. The contact of southeastern China with the Australia Chenopodiaceae flora, however, is very weak.     

Importance of biological and abiotic factors for geochemical cycling in a freshwater eutrophic lake

Here we report the results of a comprehensive biogeochemical monitoring of Rostherne Mere in 1998, including changes in dissolved oxygen, organic carbon and nitrogen, nitrate/nitrite, ammonia, Al, Na, S, K, Mg, Ca, Si, Fe, Mn, orthophosphate, particulate N & P, suspended solids, temperature, pH, chlorophyll-a and zooplankton. The results demonstrated the major influence of primary producers on the overall geochemical cycling of N, P and Si, and suggested that the significance of zooplankton might have been previously underestimated. For major anions and cations, however, the influence of biota on lake water concentrations appeared to be negligible, reflecting the fact that these chemicals were present far in excess of plankton requirements. Thus changes in concentrations of Ca, K, Na, Mg and S were rather limited and must have reflected changes in hydrological and meteorological parameters. K, however, demonstrated a transitional pattern, reflecting some influence of biological uptake. During the stratification period, the slow processes of bacterial decomposition in the hypolimnion gradually released chemicals contained in the materials accumulated in the bottom layer, remarkably increasing the concentrations of dissolved compounds of those elements present in amounts comparable with the pool stored in the sedimenting detritus (e.g. orthophosphate P, ammonia N, Si and DOC). The decomposition also resulted in a drop in the redox potential, followed by partial denitrification and chemical release from the sediments. The hypolimnion of the Mere was confirmed to remain at the stage of Mn release, characterised by accumulation of DOC, orthophosphates, ammonia and initial stages of denitrification. High levels of P released from the sediments during the stratification period suggest that the lake’s recovery after sewage diversion might be further delayed.     

Small Subunit rRNA Phylogenies Show that the Class Nassophorea is Not Monophyletic (Phylum Ciliophora)

ABSTRACT. The hypostome ciliates have been generally classified into two classes, Phyllopharyngea and Nassophorea. The status of Nassophorea and its relationship with Phyllopharyngea is one of the most controversial issues in ciliate systematics. Here we focus on the phylogenetic interrelationships of Nassophorea and Phyllopharyngea based on small subunit ribosomal RNA gene sequences. The three nassophorean subgroups, synhymeniids, microthoracids, and nassulids, each emerged as monophyletic, with synhymeniids as a sister group of Phyllopharyngea, and microthoracids as a sister of the synhymeniids+Phyllopharyngea clade in all phylogenies. The exact placement of the nassulids, however, remains uncertain. Following a detailed analysis of phenotypic characters, we hypothesize that: (1) the Phyllopharyngea could have evolved from synhymeniids, with the further development of their subkinetal microtubules as one of the major events; and (2) the development of monokinetid structures, as well as the reduction and specialization of the cyrtos and cortex, might have occurred during the diversifications of the microthoracids, synhymeniids, and Phyllopharyngea from a common ancestor. Expanding the class Phyllopharyngea to include the synhymeniids as a subclass, and designating a new subclass Subkinetalia n. subcl. for the group comprising cyrtophorians, chonotrichians, rhynchodians, and suctorians, are proposed.     

Origin and Evolution of Rosaceae

Rosaceae. consisting of about 126 genera and 3200 species, is widely distributed in warm temperate and subtropical regions of the Northern Hemisphere, while more than half of the genera are Asiatic and more then 80% of the total number of Asiatic occur in China (Table 1). In this paper, the origin and evolution of Chinese genera is discussed mainly. The principal tendency of the whole family is also described from the point of view of evolution. First of all, the systematic position of Rosaceae in Angiospermae is reviewed. According to the records of paleobotany, rosaceous plants occurred first in the Tertiary, from the early period of Eocene (genera such as Spiraea and Prunus) to the late period of Miocene (e.g. Crataegus, Malus amd Rosa). They have quite a long history in geological data. Where has this big and old family originated and what steps does it stand in the long course of evolution of flowering plants? There are several opinions and explanations by different authors. In this paper, a general survey of the six prevailing classical systems (Table 2) is made to give a brief idea of the position of this family in the Angiospermae and of the relationships between the subfamilies and also the relationships between different genera in each subfamily. At the end of this paper, an attempt is made to analyse and sum up the major evolutionary tendency of the whole family. As generally condidered, Rosaceae originated from Magnoliales, and woody plants of the family still hold a dominant position. For instance, subfamily Spiraeoideae consists of only one herbaceous genus (i.e., Aruncus) and subfamily Rosoideae only a few herbaceous genera. All of these herbaceous genera are derived from the closely related woody genera of the same subfamily. In the course of evolution of Angiospermae, Rosaceae stands at the initial to the middle stages of development. All parts of plant body in this family are at the chang ing and developing stages, with carpels, fruits and inflorescences being the most active. The primitive types in this family, such as the members of subfamily Spiraeoideae, usually have 5 and free carpels, the number of which are either reduced to 2-1 or increased to 10-numerous. They have different levels of union and are either completely free from each other or coherent at base. The carpels usually occur on the upper part of the receptacle, because the shapes of receptacle are variable, sometimes disk-shaped, cupshaped, tube-shaped or even bottle-shaped. In the last case carpels grow inside the receptacle. Thus the position of carpels has changed from superior to inferior through halfsuperior. In accordance with the development of the carpels, various kinds of fruits are produced. The primitive types of fruit are follicles, with dry, dehiscent carpels opened along different sutures. The next step, the carpels have developed into an indehiscent, I-celled and l-seeded fruit, the so-caned achene. In different genera, the achenes have different coat types and appendages to facilitate dispersing the seeds. Some of the achenes grow upon the fleshy receptacle (like strawberry) and some of them inside the fleshy receptacle (like rose). Sometimes a few carpels are united with the receptacle and develop into a pome (like apple and pear). Another direction of the fruit development is the single carpel with fleshy exocarp and mesocarp, and a bony endocarp, then becoming a drupe (like peach and plum). In addition to fleshy receptacle of thickened fruit coats, they usually have showy colour, fragrant smell and also plenty of sugars, acids, vitamins, etc. which are edible and attract animals and human beings to assist the dispersion of seeds. In this family, there are various types of flower arrangements, both indefinite inflorescences including raceme, umbel, corymb and panicle, and the definite inflorescence, such as solitary flower, cyme and compound cyme. In the evolution course, they tend to change mostly from multiflowered compound inflorescence towards few-flowered simple inflorescence, and finally becoming a solitary flower: simultaneously with the decreasing of number of flowers on the inflorescence, the increasing of size of petals, which become very showy for attraction of insects so as to guarantee pollination and fertilization of the plants concerned. Another tendency, if the bisexual flowers change to unisexual, either monoecious- or dioecious-polygamous, then they form a dense spike which is beneficial to cross pollination. The abundance, diversity, and wide range of distribution of the species and genera of Rosaceae are considered mainly resulted from their highly developed reproductive organs.     

云南复叶耳蕨属的分类修订

研究了云南产复叶耳蕨属植物,提出了新的分类处理。云南共有本属植物２０种２变种,其中包括１新组,３个改级新组合,７个云南分布新记录,并清理出了５４个云南及其他省区种类的新异名。     

草鱼鳃上寄生毛管虫一新种——变异毛管虫的研究

吸管亚纲(Subclass suctoria)中,多数种类具有或长或短的炳,附着它物上营固着生活。寄生在鱼类体表、鳃丝内的毛管虫(Trichophrya)和簇管虫(Erastophrya)的种类中,至今未见报道有固着柄的代表。       

The impact of European Directives on estuarine and coastal science and management

Many recent developments in European marine and estuarine science have been against the demands of European Union legislation. The implementation of certain statutes, the role of scientists and the nature of the data required are discussed using examples from the UK, the Netherlands and Portugal. This includes the implementation of the EU Directives on Urban Waste-water Treatment, the control of Nitrates, the designation of Species and Habitats, the control of Dangerous Substances, the statutory requirement for Environmental Impact Assessments and the recently proposed Water Framework Directive. For these, the integration of physical, chemical and biological monitoring and investigation is discussed in relation to the science dictated by the legislative and administrative requirements. Each of these Directives requires the development of generic guidelines and protocols for implementation and the use of national enabling legislation. This indicates that, in several cases, the science should concentrate on monitoring and assessment in a well-structured and quality-controlled manner. The paper concludes by summarising developments based on similarities in the implementation of present and proposed Directives across Europe.