我国直翅目昆虫细胞分类学研究现状

从研究材料、研究方法、染色体研究在昆虫分类上的应用 3个方面对我国昆虫尤其是直翅目昆虫的细胞分类学研究情况作了简要的概述 ,并着重论述了直翅目昆虫的核型及带型的研究现状 ,同时对我国直翅目昆虫分类学的发展前景进行了展望     

昆虫标本馆建设与昆虫系统学的未来

昆虫标本馆是昆虫标本的保藏、研究和科学教育的实体,代表国家或者区域水平,致力于研究昆虫多样性、揭示昆虫进化规律,为国民经济建设持续发展服务。昆虫系统学研究是昆虫标本馆研究人员的主要任务,它的发展与昆虫标本馆的建设唇齿相依。本文阐述了昆虫标本馆的功能与作用,建设昆虫标本馆的重要性和迫切性;展望了昆虫系统学的未来以及昆虫系统学发展的机遇。     

食用昆虫的研究与应用进展

对食用昆虫的研究与应用进行综述,介绍了世界各地对食用昆虫的利用概况,分析了食用昆虫的营养价值,以及昆虫在有机废弃物生物转化方面、作为人类食品和作为动物饲料代替鱼粉方面的应用情况、产业化研究现状及存在问题,最后对食用昆虫的研究开发前景进行了展望.     

基于新一代测序技术的昆虫转录组学研究进展

新一代测序技术具有快速、 高通量和低成本的特点, 为“组学”研究带来了新方法、 新方案, 正在深刻地改变着当前生物学的研究模式。近年来, 新一代测序技术极大促进了昆虫特别是无参考基因组信息昆虫的转录组学研究。自2008年至今, 采用新一代测序技术已对7个目的68种昆虫进行了转录组测序, 其中由我国学者完成了6个目的22种昆虫的转录组测序。目前, 昆虫转录组学研究主要集中在基因挖掘、 分子标记开发、 基因表达分析等方面, 为全面揭示昆虫生命活动中相关基因功能、 系统发生与进化以及昆虫与其他生物相互作用等奠定了基础。本文总结了当前昆虫转录组学研究的已有成果, 分析了其今后的发展趋势, 讨论了采用新一代测序技术开展昆虫转录组学研究中存在的诸如研究对象相对局限、 测序准确性不够高等不足, 并指出开展昆虫转录组学研究时需充分思考所要回答的科学问题, 选择合适的研究策略, 评估性价比, 以及开发转录组信息高效利用的方法等。作者建议未来的研究方向侧重于： （1）大规模开展基于新一代测序技术的昆虫转录组学研究, 特别是对其他目以及独特生态环境中的代表性昆虫应予以重点关注; （2）开发昆虫转录组数据存储及分析的软硬件; （3）合理利用新一代测序技术研究昆虫转录组并充分挖掘已测昆虫转录组中的遗传信息。     

鳞翅目昆虫人工饲料的研究现状

鳞翅目昆虫为昆虫纲第二大目昆虫,其中大多数为农业害虫,以及可作为资源开发利用的资源昆虫。对鳞翅目人工饲料的研究是对其进行科学研究与资源利用的基础。本文阐述了目前鳞翅目昆虫人工饲料研究的现况,并提出了研究中存在的若干问题。     

昆虫数学形态学研究及其应用展望

数学形态学是用数学方法描述或分析一个物体图象的形状的理论和方法,是图象处理和图象识别技术的发展,但在生物学当中的应用还很有限。本文介绍了一个新的分支学科——昆虫数学形态学,包括三方面的内容：①昆虫数学形态学技术研究,涉及昆虫图象数字化技术和昆虫图象处理与识别技术;②昆虫数学形态学理论研究,主要以昆虫图象的解释和理解研究及昆虫数学形态学与分类学等学科的关系研究为主;③昆虫和昆虫数学形态学应用基础研究,涉及昆虫数学形态学数据库及其分析软件开发,昆虫图象的机器学习和计算机视觉等内容。昆虫数学形态学理论和方法与计算机视觉技术相结合,在害虫虫情监测、昆虫多媒体专家系统的构建等方面具有广阔的应用前景。     

中国昆虫表皮碳氢化合物与昆虫化学分类学的研究进展

基于表皮碳氢化合物的昆虫化学分类学已成为昆虫分类的一个重要工具。本文首先简述了世界范围内昆虫化学分类学的起源、发展及应用领域;其次在收集的大量文献基础上,综合分析了我国已开展昆虫表皮碳氢化合物组成研究的昆虫种类、研究内容、取样与进样技术、数据的统计分析、应用领域和存在的问题。针对我国昆虫表皮碳氢化合物研究进展及其在昆虫分类中应用的现状,提出了今后我国在昆虫化学分类领域的研究方向,并展望其应用前景。     

昆虫的RNA干扰

RNA干扰(RNAi)是一种强有力的分子生物学技术, 在昆虫研究中得到了较多的应用。目前, RNAi技术主要应用于昆虫功能基因和功能基因组研究, 已在多个目的19种昆虫上实现了RNAi。在昆虫上实现RNAi的方法主要有注射、浸泡、喂食、转基因和病毒介导等方法, 这些方法各有特点, 其中喂食法因其简单而最有应用前景。昆虫RNAi的系统性较为复杂, 只有部分昆虫具有RNAi的系统性。昆虫中RNAi信号传导的基因可能是sid-1, 但昆虫RNAi的系统性机理还不是很清楚。转基因植物产生的dsRNA实现了对作物的保护, 证实了RNAi技术可用于害虫控制, 为害虫控制开辟了新领域。昆虫的RNAi研究处在起步阶段, 研究昆虫RNAi的机理, 特别是RNAi在昆虫体内的系统性扩散机理, 改进实现RNAi的方法, 提高RNAi技术在昆虫研究中的应用, 有利于昆虫基因功能鉴定和害虫控制, 促进昆虫学科的发展。     

昆虫学研究进入基因组学时代

自2000年果蝇(Drosophila melanogaster)基因组公布以来,昆虫基因组学得到了快速发展并为昆虫学的研究思路和方法带来了革命性转变.本文介绍了近年来DNA测序技术和生物信息学的发展及其对昆虫基因组学研究的促进作用,综述了模式昆虫、卫生害虫、社会性昆虫和农业昆虫的基因组学研究现状,并对昆虫基因组学研究的意义和发展趋势进行了总结和展望.     

昆虫听觉相关基因的研究进展

听觉对于昆虫的求偶、同种竞争、躲避天敌以及寄生昆虫寻找寄主等方面具有非常重要的作用。早年人们对昆虫听觉系统的形态学、生理学及行为学等方面进行了广泛研究。而近年来,研究人员对昆虫听觉分子机理开展了大量研究,对昆虫听觉相关基因包括Atonal(Ato)基因、Spalt(Sal)基因等十几种基因进行了结构分析和功能研究。本文综述了国内外昆虫听觉相关基因的研究进展。     

Dynamics of growth and the content of endogenous phytohormones during kidney bean scoto-and photomorphogenesis

The dynamics of growth and the contents of free and bound endogenous IAA, gibberellins (GA), cytokinins (zeatin and its riboside), and ABA in kidney bean plants (Phaseolus vulgaris L., cv. Belozernaya) grown in darkness or in the light was studied. Phytohormones were quantified in 5–15-day-old plants by the ELISA technique. Plant growth and phytohormone content were shown to depend on plant age and the conditions of illumination. During scotomorphogenesis, changes in the biomass and hypocotyl length were highly correlated with the content of GA, whereas during photomorphogeneses, these parameters were correlated with the content of zeatin. In darkness, epicotyl growth displayed a positive correlation with the content of GA, whereas in the light, the correlation was negative. Growth characteristics of the primary leaves were shown to correlate with IAA in darkness and with GA and zeatin in the light. At a low concentration of cytokinins in illuminated leaves, cell divisions occurred, whereas, at the higher cytokinin concentrations, cell expansion occurred. The highest content of GA was characteristic of leaves in the period of growth cessation. ABA accumulated during active leaf and root elongation and biomass increment in the light and during hypocotyl growth in darkness. After plant illumination, the ratio of auxins to cytokinins increased in bean roots and decreased in their epicotyls. Thus, light changed the developmental programs of bean plants, which was manifested in the changed rate and duration of growth of various organs (root, hypocotyl, epicotyl, and leaf). Some mechanisms of light action depended on the contents of IAA, ABA, GA, and cytokinins and the ratios between these phytohormones. Differences between scotonorphogenesis of mono-and dicotyledonous plants are discussed in relation to the levels of phytohormones in them.     

Dichloroacetate- and trichloroacetate-induced phagocytic activation and production of oxidative stress in the hepatic tissues of mice after acute exposure

Dichoroacetate (DCA) and trichloroacetate (TCA) are by-products formed during chlorination of the drinking water and were found to be hepatotoxic and hepatocarcinogenic in rodents. In this study, the abilities of the compounds to induce oxidative stress and phagocytic activation have been studied in B6C3F1 mice. Groups of mice were administered 300 mg/kg of either DCA or TCA, p.o, and were sacrificed after 6 or 12 h. Peritoneal lavage cells (PLCs) were isolated and assayed for superoxide anion (SA) production, and hepatic tissues were assayed for the production of SA, lipid peroxidation (LP), and DNA-single strand breaks (SSBs). TCA resulted in significant production of SA in the PLCs, and in the production of SA, LP, and DNA-SSBs in the hepatic tissues, 12 h after dosing, as compared with the control. DCA administration, on the other hand, resulted in significant increases in the productions of LP and DNA-SSBs in the hepatic tissues at both time points, and in SA production in PLCs and hepatic tissues, 6 h after dosing. However, DCA-induced increases in SA production in PLC and hepatic tissues declined at the 12-h time point, reaching control level in the hepatic tissues. These results may implicate the contribution of phagocytic activation to the induction of oxidative stress in the hepatic tissues and also the role of SA production in the induction of LP and/or DNA damage in those tissues, in response to the compounds. The results also suggest studying the involvement of these mechanisms in the long-term hepatotoxicity/hepatocarcinogencity of the compounds.     

Evolution of urate-degrading enzymes in animal peroxisomes

The end product of purine metabolism varies from species to species. The degradation of purines to urate is common to all animal species, but the degradation of urate is much less complete in higher animals. The comparison of subcellular distribution, intraperoxisomal localization forms, molecular structures, and some other properties of urate-degrading enzymes (urate oxidase, allantoinase, and allantoicase) among animals is described. Liver urate oxidase (uricase) is located in the peroxisomes in all animals with urate oxidase. On the basis of the comparison of intraperoxisomal localization forms, mol wt, and solubility of liver urate oxidase among animals, it is suggested that amphibian urate oxidase is a transition form in the evolution of aquatic animals to land animals. Allantoinase and allantoicase are different proteins in fish liver, but the two enzymes form a complex in amphibian liver. The subcellular localization of allantoinase and allantoicase varies among fishes. Hepatic allantoinase is located both in the peroxisomes and in the cytosol in saltwater fishes, and only in the cytosol in freshwater fishes. Hepatic allantoicase is located on the outer surface of the, peroxisomal membrane in the mackerel group and in the peroxisomal matrix in the sardine group. Amphibian hepatic allantoinase-allantoicase complex is probably located in the mitochondria. On the basis of previous data, changes of allantoinase and allantoicase in molecular structure and intracellular localization during animal evolution may be as follows: Fish liver allantoinase is a single peptide with a mol wt of 54,000, and is located both in the peroxisomes and in the cytosol, or only in the cytosol. Fish liver allantoicase consists of two identical subunits with a mol wt of 48,000, and is located in the peroxisomal matrix or on the outer surface of the peroxisomal membrane. The evolution of fishes to amphibia resulted in the dissociation of allantoicase into subunits, and in the association of allantoinase with the subunit of allantoicase. This amphibian enzyme was lost by further evolution.     

啮齿动物作用下退耕地山杏种子扩散与贮藏的季节变化

啮齿动物对植物种子的取食和扩散影响种子的时空分布,继而影响种子的萌发和幼苗建成,因而在森林更新中起着重要作用.在国有济源市愚公林场,选择退耕地生境,于春季、夏季、秋季分别释放人工标记的山杏种子,观察啮齿动物扩散与埋藏山杏种子的季节性差异.结果表明：1）退耕地中的啮齿动物主要包括大林姬鼠、社鼠、黑线姬鼠;2）山杏种子扩散速率在春季显著慢于夏季,夏季显著慢于秋季;3）种子搬运量受季节和种子状态交互作用影响,春季显著少于夏季,夏季显著少于秋季;4）不同季节种子平均搬运距离不同,秋季不同状态种子的搬运距离均大于春季和夏季;5）啮齿动物对山杏种子的贮藏点大小多为1粒种子,少量为2、3粒种子,且贮藏点大小与季节间存在显著的交互作用,春季单粒种子的贮藏点数量显著少于夏季和秋季,而夏季与秋季的贮藏点则倾向于多粒种子;6）在夏季和秋季各有5枚（共释放1800枚）被啮齿动物分散贮藏的山杏种子建成幼苗.     

Distribution,ontogeny and ultrastructure of somatostatin immunoreactive cells in the pancreas and gut

Summary Somatostatin cells are numerous in the pancreas and digestive tract of mammals as well as birds. In the pancreas of chicken, cat and dog they occur in both the exocrine parenchyma and in the islets. In the rat and rabbit, somatostatin cells have a peripheral location in the islets, whereas in the cat, dog and man the cells are usually more randomly distributed. In the stomach of rabbits and pigs, somatostatin cells are more numerous in the oxyntic gland area than in the pyloric gland area, whereas the reverse is true for the cat, dog and man. In the cat, pig and man, somatostatin cells are fairly numerous in the duodenum, whereas in the rat, rabbit and dog they are few in this location. In the remainder of the intestines somatostatin cells are few but regularly observed. Somatostatin cells are numerous in the human fetal pancreas and gut. In the fetal rat, somatostatin cells first appear in the pancreas and duodenum (at about the 16–17th day of gestation) and subsequently in the remainder of the intestine. Somatostatin cells do not appear in the gastric mucosa until after birth. Three weeks after birth, somatostatin cells show the adult frequency of occurrence and pattern of distribution. In the chicken, somatostatin cells are numerous in the proventriculus, absent from the gizzard, abundant in the gizzard-duodenal junction (antrum), infrequent in the duodenum and virtually absent from the remainder of the intestines. No immunoreactive cells can be observed in the thyroid of any species nor in the ultimobranchial gland of the chicken. In the chick embryo, somatostatin cells are first detected in the pancreas and proventriculus (at about the 12th day of incubation). They appear in the remainder of the gut much later, in the duodenum at the 16th day, in the antrum at about the 19th day and still later in the lower small intestine. The ultrastructure of the somatostatin cells was studied in the chicken, rat, cat and man; the cells were identified by the consecutive semithin/ultrathin section technique. The somatostatin cells display the properties of the D cell. There was no difference in granule ultrastructure between somatostatin cells in the gut and the pancreas. The granules, which are the storage site of the peptide, are round, supplied with a tightly fitting membrane and have a moderately electron-dense, fine-granulated core. The mean diameter of the somatostatin granules is smallest in rat (155–170 nm) and largest in the chicken (270–290 nm).     

Nutrient relations in coppiced black cottonwood and red alder

Two-year-old coppice of black cottonwood and red alder, grown in pure culture and in mixture, were compared using terminal twigs and leafless shoots harvested in the winter. Terminal twigs were taken with buds intact; they were about 15 cm long. Leafless shoot samples included all above-ground components. In pure culture, dry weights of the leafless shoots per plant were similar for the two species. In mixture with alder, however, weight of the cottonwood plants was enhanced and that of alder was reduced, but neither response was statistically significant. Nutrient concentration, content per plant, and utilization varied by the plant tissues analyzed, cultural treatment (purevs. mixed), and species. In general, nutrient concentrations were higher in the terminal twigs than in the leafless shoots of both species. Cultural treatment did not significantly affect nutrient concentration in cottonwood twigs or in the leafless shoots of either species. Concentrations of N and Fe were significantly higher and those of Mn were lower in twigs of mixed alder than in twigs of pure alder. Twigs of cottonwood were significantly higher than those of alder in concentration of P and Zn, and lower in N, Mn, and Cu. Compared with alder, cottonwood leafless shoots were significantly higher in concentration of Ca, but lower in N, S, Cu, and Mn. With few exceptions, nutrient content was highest in the shoots of the large plants of mixed cottonwood, intermediate in medium-sized pure cottonwood and pure alder, and lowest in the small mixed alder. Cottonwood was significantly more efficient than alder in use of N, S, and Cu, and less efficient in use of Ca. Some of the differences between cultural treatments and species may be associated directly or indirectly with the N₂-fixing ability of red alder. Mixed culture of the two species appears promising because of the increased growth of cottonwood. Planted separately in pure culture, the choice between cottonwood and alder may be determined, in part, by the nutritional status of the soil where plantations are established.     

崇左金花茶花朵和叶片类黄酮UPLC-Q-TOF-MS分析

以崇左金花茶（Camellia chuangtsoensis）为材料,利用超高效液相色谱-四极杆-飞行时间质谱（UPLC-Q-TOF-MS）联用技术定性定量分析其花朵（花瓣、雄蕊）和叶片（老叶、新叶）中类黄酮成分与含量。结果表明,崇左金花茶中共检测到14种类黄酮成分,木犀草素、木犀草素-7-O-芸香糖苷、槲皮素-3,7-O-二葡萄糖苷、芸香柚皮苷、圣草素和染料木苷为山茶属金花茶组植物中首次发现,其中槲皮素-3,7-O-二葡萄糖苷、芸香柚皮苷、圣草素和染料木苷主要存在于花朵中,木犀草素和木犀草素-7-O-芸香糖苷在花朵中含量高于叶片,雄蕊中高于花瓣;槲皮素-3-O-葡萄糖苷、槲皮素-7-O-葡萄糖苷、槲皮素-3-O-芸香糖苷和山柰酚-3-O-葡萄糖苷为金花茶组植物叶片中首次发现,其叶片中含量远低于花朵,老叶中远低于新叶,雄蕊中远低于花瓣;儿茶素和表儿茶素在花朵中含量高于叶片,雄蕊中高于花瓣;槲皮素和山萘酚在花朵和叶片中含量均较低。崇左金花茶花瓣和雄蕊中含量较高的类黄酮为儿茶素类、木犀草素类和槲皮素类,主要是表儿茶素、木犀草素和槲皮素-3-O-葡萄糖苷;叶片中为儿茶素类和木犀草素类,主要是表儿茶素、木犀草素和木犀草素-7-O-芸香糖苷。崇左金花茶花瓣和雄蕊中儿茶素类、木犀草素类及类黄酮总量均高于叶片,且雄蕊高于花瓣;花瓣和雄蕊中槲皮素类远高于叶片,且花瓣中远高于雄蕊。     

The substance P content of peripheral tissues in several mammals

Levels of substance P immunoreactivity (SPI) were determined in several skin and mucosal areas, in parts of the sympathetic nervous system, the urinary, biliary and respiratory systems of cats, rabbits and guinea-pigs, and in various skin and mucosal areas of humans by radioimmunoassay. Salient findings are (1) The general distribution pattern of SPI in rabbits was similar to that in rodents. (2) The highest SPI tissue levels were found in the sympathetic nervous system, notably in guinea-pigs. (3) The guinea-pig also had the highest SPI levels in ureter, urinary bladder and bile duct. (4) The aorta, pulmonary artery and portal vein of the rabbit contained very low amounts of SPI, the concentration in the carotid sinus being several fold higher. (5) Skin SPI content was generally highest in the cat, especially in the hindpaw-pad, and lowest in abdominal and back skin. (6) SPI levels found in postmortem human skin and mucosal samples are comparable to those found in other mammals. The observations are discussed in view of the sensory innervation of the various tissues.     

Distribution of galanin-like immunoreactivity in the gastro-intestinal tract of several mammalian species

Summary The distribution of galanin-immunoreactive (GAL-IR) neurons was mapped in detail in the gastro-intestinal tract of the rat, mouse, guinea-pig and pig by use of the indirect immunofluorescence technique. GAL-IR cell bodies were found in both the submucous and the myenteric plexus, with considerably higher numbers in the former ganglia. The largest number of GAL-IR perikarya was seen in the duodenal submucous plexus of the pig. With some (single) exceptions, GAL-IR cell somata were not observed in the myenteric plexus of the pig and guinea-pig, and in the submucous plexus of the esophagus and the stomach of the guinea-pig.GAL-IR fibers ocurred in most parts of the gastro-intestinal tract. In the lamina propria a few non-varicose, weakly fluorescent fibers were noted in the mouse and rat, whereas in the pig and guinea-pig were large numbers of GAL-IR fibers with a varicose appearance was observed. These fibers were in all species most numerous in the distal portion of the intestinal tract. In the submucosa GAL-IR fibers were detected in all four species, and in the pig and guinea-pig some fibers surrounded blood vessels. A large number of GAL-IR fibers was generally seen in the circular smooth muscle layer, except in the guinea-pig, which only seemed to contain a few fibers. In the longitudinal muscle layer only single fibers could be detected. However, the gastric fundus region of the pig contained a moderate number of fibers in the longitudinally and obliquely oriented layers.In general, in the rat, mouse and pig, the submucous and myenteric plexus contained moderate or large numbers of GAL-IR fibers. In the guinea-pig, no or only single fibers were observed in the plexus of the upper gastro-intestinal tract and the rectum, while moderate numbers were seen in the ileum and colon.Thin adjacent sections stained for vasoactive intestinal polypeptide (VIP) and GAL revealed the coexistence of these two peptides in cell bodies of the myenteric plexus in the pig duodenum and guinea-pig colon. In these two species the GALand VIP-nerve fiber networks also exhibited marked similarities. However, in the rat and mouse VIPand GAL-distribution patterns were in general different.The present findings indicate the presence of yet another neuropeptide or peptide family in the gastro-intestinal tract of several rodents and the pig.