我国2种微蟹蛛记述（蜘蛛目：蟹蛛科）

提出对前报道的蟹蛛科微蟹蛛属２种的修订：西安微蟹蛛ＬｙｓｔｉｅｌｅｓｘｉａｎｅｎｓｉｓＳｏｎｇｅｔＷａｎｇ,１９９１应为小微蟹蛛Ｌｙｓｔｅｌｅｓｍｉｎｉｕｍｕｓ（Ｓｃｈｅｎｋｅｌ１９５３）的异名,唐迎秋等（１９９５）报道的小微蟹蛛雌蛛,改订为１个新种－文微蟹蛛Ｌｙｓｔｅｌｅｓｗｅｎｅｎｓｉｓｓｐ．ｎｏｖ。     

中国栉足蛛科2新种（蛛形纲：蜘蛛目）

记述我国栉足蛛科（Ｃｔｅｎｉｄａｅ）２新种,命名为简安蛛,新种Ａｎａｈｉｔａ ｓａｎｐｌｅｘａ ｓｐ．ｎｏｖ．和道县弱栉蛛Ｌｅｐｔｏｃｔｅｎｕｓ ｄａｏｘｉａｎｅｎｓｉｓ ｓｐ．ｎｏｖ．。     

中国盾板蛛属一新种及一新纪录种：蜘蛛目：皿蛛科：微蛛亚科

本文记述我国皿蛛科微蛛亚种蜘蛛的一新纪录属盾板蛛属ＰｅｌｅｃｏｐｓｉｓＳｉｍｏｎ,１８６４,一新种黑突盾板蛛Ｐ．ｎｉｇｒｏｇｌｏｂａｓｐ．ｎｖｏ．,及一新纪录种平行盾板蛛Ｐ．ｐａｒａｌｌｅｌａ（Ｗｉｄｅｒ,１８３４）。     

湖北圆腹蛛一新种（蜘蛛目：球蛛科）

本文描述采自湖北省恩施和咸宁地区的球蛛科圆腹蛛属一新种－湖北圆腹蛛Ｄｉｐｏｅｎａ ｈｕｂｅｉｅｎｓｉｓ ｓｐ．ｎｏｖ．。     

湖南省5种皿蛛的记述（蜘蛛目：皿蛛科）

记述采自我国湖南省南岳、道县和双桥的皿蛛科皿蛛亚科蜘蛛５种,其中有４个新种：南岳斑皿蛛ｌｅｐｔｈｙｐｈａｎｔｅｓ ｎａｎｙｒｅｎｓｉｓ、衡山斑皿蛛Ｌｅｐｔｈｙｐｈａｎｔｅｓ ｈｅｎｈｓｈａｎｅｎｓｉｓ、双刺长指蛛Ｋａｅｓｔｎｅｒｉａ ｂｉｃｕｌｔｒａｔａ和双板指蛛Ｂａｔｈｙｐｈａｎｔｅｓ ｄｉｐｅｔａｌｕｓ,１个既有种：天目中指蛛Ｃｅｎｔｒｏｍｅｒｕｓ ｔｉａｎｍｕｓｈａｎｕｓ Ｃｈｅｎ ｅｔ Ｓ     

陕西蟹蛛科蜘蛛三新种记述

本文记述陕西秦岭山区蟹蛛科Ｔｈｏｍｉｓｉｄａｅ蜘蛛三新种：高寒花蟹蛛,新种Ｘｙｓｔｉｃｕｓ ａｌｓｕｓ ｓｐ．ｎｏｖ．,太白峭腹蛛,新种Ｔｍａｒｕｓ ｔａｉｂａｉｅｎｓｉｓ ｓｐ．ｎｏｖ．,秦岭峭腹蛛,新种Ｔｍａｒｕｓ ｑｉｎｌｉｎｇｅｎｓｉｓ ｓｐ．ｎｏｖ,。     

陕西蟹蛛科蜘蛛三新种记述──(蜘蛛目)

本文记述陕西秦岭山区蟹蛛科Ｔｈｏｎｄｓｉｄａｅ蜘蛛三新种：高寒花蟹蛛,新种Ｘｙｓｔｉｃｕｓａｌｓｕｓｓｐ．ｎｏｖ,太白峭腹蛛,新种Ｔｍａｒｕｓｔａｉｂａｉｅｎｓｉｓｓｐ．ｎｏｖ．,秦岭峭腹蛛,新种Ｔｍａｒｕｓｑｉｎｌｉｎｇｅｎｓｉｓｓｐ．ｎｏｖ．．     

中国尖腹蛛属一新种记述：蜘蛛目：园蛛科

本文记述分布于我国陕西太白山的园蛛科Ａｒａｎｅｉｄａｅ尖腹蛛属Ａｃｕｌｅｐｅｒｉａ一新种,太白尖腹蛛Ａｃｕｌｅｐｅｒｉａｔａｉｂａｉｓｈａｎｅｎｓｉｓｓｐ．ｎｏｖ．,模式标本分别保存河北教育学院和西安师范学院。     

中国蟹蛛科（蜘蛛目）新种记述

记述我国蟹蛛科花蟹蛛属６新种和蟹蛛属２新种,共计８新种,金林花蟹蛛Ｘｙｓｔｉｃｕｓｊｉｎｌｉｎ,玛纳斯花蟹蛛Ｘ．ｍａｎａｓ,林芝花蟹蛛Ｘ．ｎｙｉｎｇｃｈｉｅｎｓｉｓ,拟斑花蟹蛛Ｘ．ｐａｒａｐｕｎｃｔａｔｕｓ,似旋花蟹蛛Ｘ．ｔｏｒｓｉｖｏｉｄｅｓ,吴氏花蟹蛛Ｘ．ｗｕａｅ,广西蟹蛛Ｔｈｏｍｉｓｕｓｇｕａｎｇｘｉｃｕｓ和胡氏蟹蛛Ｔ．ｈｕｉ。     

海南小遁蛛属1新种（蜘蛛目：巨蟹蛛科）

记述采自海南省乐东县尖峰岭国家自然保护区的巨蟹蛛科小遁蛛属１新种,海南小遁蛛Ｍｉｃｒｏｍｍａｔａ ｈａｉｎａｎｅｎｓｉｓ ｓｐ．ｎｏｖ．。     

Localization of Escherichia coli RNA polymerase binding sites on bacteriophage S13 and 0X174 DNAs by electron microscopy.

Complexes between Escherichia coli RNA polymerase and bacteriophage S13 and phage phiX174 replicative form III DNAs have been shown to form at specific locations on the phage genomes. The major locations on S13 have been mapped at 8 to 10 and 92 to 96% of the genome length, starting from the unique Pst I cleavage site. The locations correspond to the beginnings of genes D and B, respectively. Four minor locations map at 18 to 22, 28 to 32, 50 to 56, and 70 to 74% of the genome. The 70 to 74% site corresponds to the beginning of the A gene. The major locations on phiX174 are at 8 to 10, 50 to 54, and 92 to 94% of the genome. The 50 to 54% site is at the start of the H gene and has an equivalent minor site on S13, but it is not a promoter site. Three minor sites on phiX174, at 20 to 24, 26 to 32, and 68 to 74% of the genome, correspond to sites on S13. The data confirm the locations of sites identified by restriction fragment binding experiments (E. Rassart and J. H. Spencer, J. Virol. 27:677--687, 1978) and the assignment of putative promoters at the start of genes A, B and D.     

西双版纳热带雨林蚁科昆虫区系分析

在西双版纳热带雨林已鉴定蚊科昆虫９亚科７６属２６７种。西双版纳地区的蚂蚁区系以热带至亚热带分布的东洋界成分最为丰富。在属级水平上,与马来西亚界关系最为密切。与澳洲界关系较密切;与非洲界和马拉加西界的关系知中。与新北界,新热带界和古北界的关系最为疏远。可见西双版纳的蚂蚁区系具有典型的热带亚洲起源特征,同时与澳洲和非洲的热带区系有一定的渊源关系。     

Specificity of the binding of trifluoperazine to the calcium-dependent activator of phosphodiesterase and to a series of other calcium-binding proteins

Trifluoperazine inhibits the activation of phosphodiesterase by binding to the calcium-dependent activator. To determine further the specificity by which trifluoperazine binds to activator, we compared the binding of trifluoperazine to activator prepared from several species and tissues and to a number of other calcium-binding proteins devoid of activator activity.Trifluoperazine binds to activator prepared from human, bovine, rat and rabbit brain and from chick embryo fibroblasts. In each case, the binding of trifluoperazine to activator was qualitatively similar and related quantitatively to the ability of the preparation to activate phosphodiesterase.Of the other calcium-binding proteins examined, namely, troponin-C, S-100 protein, phospholipase A, phospholipase B and myosin light chain, only troponin-C displayed any significant calcium-specific binding of trifluoperazine. The binding to troponin-C, however, appeared to be different from the binding to activator; whereas the binding of trifluoperazine to actovator showed no cooperativity, the binding to troponin-C showed positive cooperatively.These results and earlier data showing that trifluoperazine fails to bind to a variety of other proteins, indicate that the binding of trifluoperazine to the calcium-dependent activator of phosphodiesterase is selective and suggest that this binding may explain some of the biochemical and pharmacological actions of this antipsychotic agent.     

Role of the adaptor protein CIKS in the activation of the IKK complex

Nuclear factor kappaB (NF-kappaB) plays a pivotal role in numerous cellular processes, including stress response, inflammation, and protection from apoptosis. Therefore, the activity of NF-kappaB needs to be tightly regulated. We have previously identified a novel gene, named CIKS (connection to IkappaB-kinase and SAPK), able to bind the regulatory sub-unit NEMO/IKKgamma and to activate NF-kappaB. Here, we demonstrate that CIKS forms homo-oligomers, interacts with NEMO/IKKgamma, and is recruited to the IKK-complex upon cell stimulation. In addition, we identified the regions of CIKS responsible for these functions. We found that the ability of CIKS to oligomerize, and to be recruited to the IKK-complex is not sufficient to activate the NF-kappaB. In fact, a deletion mutant of CIKS able to oligomerize, to interact with NEMO/IKKgamma, and to be recruited to the IKK-complex does not activate NF-kappaB, suggesting that CIKS needs a second level of regulation to efficiently activate NF-kappaB.     

Surface topology of the Escherichia coli K-12 ferric enterobactin receptor.

Monoclonal antibodies (MAb) were raised to the Escherichia coli K-12 ferric enterobactin receptor, FepA, and used to identify regions of the polypeptide that are involved in interaction with its ligands ferric enterobactin and colicins B and D. A total of 11 distinct FepA epitopes were identified. The locations of these epitopes within the primary sequence of FepA were mapped by screening MAb against a library of FepA::PhoA fusion proteins, a FepA deletion mutant, and proteolytically modified FepA. These experiments localized the 11 epitopes to seven different regions within the FepA polypeptide, including residues 2 to 24, 27 to 37, 100 to 178, 204 to 227, 258 to 290, 290 to 339, and 382 to 400 of the mature protein. Cell surface-exposed epitopes of FepA were identified and discriminated by cytofluorimetry and by the ability of MAb that recognize them to block the interaction of FepA with its ligands. Seven surface epitopes were defined, including one each in regions 27 to 37, 204 to 227, and 258 to 290 and two each in regions 290 to 339 and 382 to 400. One of these, within region 290 to 339, was recognized by MAb in bacteria containing intact (rfa+) lipopolysaccharide (LPS); all other surface epitopes were susceptible to MAb binding only in a strain containing a truncated (rfaD) LPS core, suggesting that they are physically shielded by E. coli K-12 LPS core sugars. Antibody binding to FepA surface epitopes within region 290 to 339 or 382 to 400 inhibited killing by colicin B or D and the uptake of ferric enterobactin. In addition to the FepA-specific MAb, antibodies that recognized other outer membrane components, including Cir, OmpA, TonA, and LPS, were identified. Immunochemical and biochemical characterization of the surface structures of FepA and analysis of its hydrophobicity and amphilicity were used to generate a model of the ferric enterobactin receptor's transmembrane strands, surface peptides, and ligand-binding domains.     

Specificity of the binding of trifluoperazine to the calcium-dependent activator of phosphodiesterase and to a series of other calcium-binding proteins.

Trifluoperazine inhibits the activation of phosphodiesterase by binding to the calcium-dependent activator. To determine further the specificity by which trifluoperazine binds to activator, we compared the binding of trifluoperazine to activator prepared from several species and tissues and to a number of other calcium-binding proteins devoid of activator activity. Trifluoperazine binds to activator prepared from human, bovine, rat and rabbit brain and from chick embryo fibroblasts. In each case, the binding of trifluoperazine to activator was qualitatively similar and related quantitatively to the ability of the preparation to activate phosphodiesterase. Of the other calcium-binding proteins examined, namely, troponin-C, S-100 protein, phospholipase A, phospholipase B and myosin light chain, only troponin-C displayed any significant calcium-specific binding of trifluoperazine. The binding to troponin-C, however, appeared to be different from the binding to activator; whereas the binding of trifluoperazine to actovator showed no cooperativity, the binding to troponin-C showed positive cooperatively. These results and earlier data showing that trifluoperazine fails to bind to a variety of other proteins, indicate that the binding of trifluoperazine to the calcium-dependent activator of phosphodiesterase is selective and suggest that this binding may explain some of the biochemical and pharmacological actions of this antipsychotic agent.     

细菌抵抗消毒剂及其对抗生素共耐药

消毒剂是一种可杀灭物体表面、器材设备、皮肤、空气和水源等传播媒介上携带的病原微生物的有机分子。它在体外能杀灭病原微生物,切断其传播途径,进而达到控制污染的目的,在生命安全防控中起着重要的作用。但是不合理地使用消毒剂导致细菌对消毒剂产生耐药。消毒剂耐药基因在不同种属间的水平转移加剧其传播风险,使消毒剂耐药情况进一步恶化。更令人担忧的是,细菌对消毒剂的耐药可能会导致对抗生素产生共耐药,给公共安全带来巨大的威胁。但目前为止,对消毒剂耐药以及共耐药的认识还不够全面。本文总结了关于细菌对消毒剂耐药的研究报道,对消毒剂的作用机制、细菌对消毒剂的耐药机制进行了论述,另外针对消毒剂耐药基因的传播以及细菌对消毒剂和抗生素的共耐药进行了综述,为减少消毒剂耐药性的产生和制定合理的消毒剂使用规范奠定基础。     

Quantitative data on training new world primates to urinate

This study assessed the effectiveness of operant conditioning in training three species of captive callitrichid primates (Leontopithecus rosalia, Callithrix geoffroyi, and Saguinus imperator) to urinate on demand. There were three goals to the study: 1) to develop a system for quantitatively assessing positive reinforcement training; 2) to ascertain whether or not positive reinforcement techniques can be used to train callitrichid monkeys to urinate on demand, and if so, how many training sessions are required; and 3) to determine the effect on urination behavior of the trainer entering the cage to collect a urine sample. Positive reinforcement with a continuous reinforcement schedule was used to capture a natural behavior: urination. Training sessions (30 min each) were conducted at dawn thrice weekly during five consecutive phases: habituation, control, training (animals were rewarded for urinating), maintenance (animals had reached a defined training criteria and continued to be rewarded for urinating), and collection (animals were rewarded for urinating, and the trainer entered the cage to collect the sample). The numbers of 30-min training sessions required to train the three monkey species (L. rosalia, C. geoffroyi, and S. imperator) were five, six, and eight, respectively. For the three species, the mean number of urinations per animal was significantly greater during the training, maintenance, and collection phases compared to the control phase. However, the three species differed significantly in the manner in which the rates of urination changed across the five phases. A higher proportion of subjects urinated during the training, maintenance, and collection phases compared to the control phase. Latency to first urination varied significantly across the five phases, with significantly reduced latencies to urinate during the training, maintenance, and collection phases compared to the control phase. The entry of the trainer into the cage to collect the urine sample did not appear to alter urination behavior. We demonstrate that operant conditioning techniques, which typically incur minimal cost, time investment, and disturbance, can be used to increase the quantity of urine samples collected for physiological analysis, the proportion of animals that urinate, and the speed of sample collection.     

Fluorescence location of RVLM kainate microinjections that alter the control of breathing

Kainic acid (4.7 mM) applied to the rostral ventrolateral medulla (RVLM) surface decreases phrenic output, CO2 sensitivity, and blood pressure in chloralose-urethan-anesthetized, vagotomized, paralyzed, glomectomized, servoventilated cats. In this study using the same preparation, bilateral 50- to 100-nl kainate injections just below the RVLM surface better localized these responses topographically. The physiological responses to unilateral 10-nl kainate injections were then correlated with anatomic location determined by fluorescent microbeads (0.5 micron diam). Many sites were associated with no effect, a few rostral and caudal sites with increased phrenic activity, and cluster of sites with decreased phrenic activity often to apnea, decreased CO2 sensitivity, and decreased responses to carotid sinus nerve stimulation. Blood pressure was unaffected. These sites, within 400 microns of the surface, were ventral to the facial nucleus, ventrolateral to the nucleus paragigantocellularis lateralis, caudal to the superior olive, and rostral to the retrofacial nucleus. They appeared to be within the recently described retrotrapezoid nucleus, which contains cells with respiratory-related activity and projections to the dorsal and ventral respiratory groups. Cells within this site appear able to provide tonic input to respiration and to affect peripheral and central chemoreception.     

宁波沿海平原Z02孔第四纪地层及古环境演变

宁波沿海平原第四纪沉积物属于海陆交互沉积,记录了良好的古气候变化信息,是研究古气候冷暖变化、沉积物沉积特征的良好载体.对位于宁波沿海平原东南部的Z02孔进行14C和古地磁测年,根据钻孔岩性、孢粉组合、有孔类和介形类组合、粒度等环境替代指标特征,确定了 Z02孔第四纪地层划分,揭示了研究区第四纪以来的古环境演变信息.结果...