田野蛛属（蜘蛛目：光盔蛛科）两种记述

本文记述光盔蛛科田野蛛属两种:蒙古田野蛛Agroeca mongolica Schenkel,1936和山田野蛛Agroeca montana Hayashi,1986。前一种的雄蛛为首次发现,后一种为中国新纪录。     

中国合狂蛛属一新种(蜘蛛目:平腹蛛科)

本文记述的平腹蛛科合狂蛛属系首次在中国发现,并报道了该属1新种,命名为大围合狂蛛,新种Synaphosus daweiensis sp. nov.     

台湾管巢蛛和樟木管巢蛛的雄性新发现(蜘蛛目,管巢蛛科)

作者在进行中国管巢蛛属系统学研究时,发现了管巢蛛科管巢蛛属2雄性新发现:台湾管巢蛛Clubiona taiwanica Ono,1994和樟木管巢蛛Clubiona zhangmuensis Hu et Li,1987.这两种以前描述时均只有雌性,在此予以补充描述.所有标本保存在河北大学生命科学学院.文中测量单位为mm.     

浙江猫蛛科一新种：蜘蛛目

在浙江三门发现猫蛛科一新种,暂归人哈猫蛛属,定名为三门哈猫蛛Hamataliwa sanmenensis sp.nov.本新种与三突哈猫蛛H.tricuspidata相近似,但有明显区别。本属为我国新纪录属。     

西藏和四川省管巢蛛属三新种记述(蜘蛛目,管巢蛛科)

在进行中国管巢蛛科系统学研究时,发现了产自西藏和四川的管巢蛛属3新种:波密管巢蛛Clubiona bomiensis sp.nov.,心形管巢蛛Clubiona cordata sp.nov.和指管巢蛛 Clubiona dactyla sp.nov,.这3新种均属于管巢蛛属的拟管巢蛛种组(group paraclubiona).所有标本均保存在河北大学生命科学学院.文中测量单位为mm.     

新疆肥蛛属（蜘蛛目：园蛛科）两种记述

本文记述园蛛科肥蛛属两种:华丽肥蛛Larinia eleqans Spassky,1939 和涅氏肥蛛L.nenilini Marusik,1986 为中国新纪录种。     

中国球蛛三新种和二新记录（蜘蛛目：球蛛科）

本文报道了蜘蛛目球蛛科3属3新种和1个中国新记录属2新记录种。新种为笠腹希蛛Achaearanea galeiforma sp.nov.,三斑丽蛛Chryssa trimaculata sp.nov.,奇异球蛛Theridion mirabilis sp.nov.。模式标本保存在河北教育学院生物系。     

湖南省隙蛛属两新种(蜘蛛目,暗蛛科)

记述了中国湖南省隙蛛属两新种,即联溯隙蛛,Coelotes liansui sp.nov.和桃源洞隙蛛,Coelotes taoyuandongsp.nov.模式标本保存于湖南师范大学生命科学学院.文中度量单位为mm.     

中国数种熊蛛研究(蜘蛛目:狼蛛科)

记述我国狼蛛科熊蛛属５种,其中２新种为：沟谷熊蛛,三齿熊蛛,１种雄性新发现：湄潭熊蛛１９９３,中国２新纪录种;掠熊蛛富士熊蛛。     

中国南方隅蛛属和漏斗蛛属新种记述：蜘蛛目：漏斗蛛科

本文记述隅蛛属一新种和漏斗蛛属两新种:刺隅蛛,新种Tegenaria aculeata sp.nov.三角漏斗蛛,新种Agelena triangulata sp.nov.,小斑漏斗蛛,新种Agelena micropunetulata sp.nov.。     

Leaf lipids of Ribes nigrum: a plant containing 16:3, alpha-18:3, gamma-18:3 and 18:4 fatty acids

The glycerolipid composition of Ribes nigrum (blackcurrant) leaves was determined. The total fatty acid composition was unusual in that alpha-linolenic acid (alpha-18:3) occurred together with cis-7,10,13-hexadecatrienoic acid (16:3) and lower amounts of stearidonic acid (18:4) and gamma-linolenic acid (gamma-18:3). Monogalactosyldiacylglycerol contained the highest proportion of 16:3 with less in digalactosyldiacylglycerol. gamma-18:3 and 18:4 were present in all lipids and 18:4 was always greater than gamma-18:3. The highest percentages of gamma-18:3 and 18:4 were in phosphatidylcholine, but phosphatidylglycerol was particularly low in these acids. In summary, the lipid composition was largely typical of 16:3 plants but there was a minor contribution typical of 18:4 plants. The possibility of three pathways for glycolipid biosynthesis is discussed.     

Salmonella enteritidis Serotype 501, 2, 3: z4, z24: -

Characteristics of a new Salmonella serotype, subgenus IV, are reported. Culture 5534-68 was recovered from the intestinal tract of Anolis biporcatus, an arboreal lizard found in deep forest tracts in Panama Province, Republic of Panama. The antigenic composition of this new serotype was found to be 50(1, 2, 3):z(4), z(24):-.     

浙江天童常绿阔叶林、常绿针叶林与落叶阔叶林的C:N:P化学计量特征

以浙江天童常绿阔叶林、常绿针叶林和落叶阔叶林为对象, 通过对叶片和凋落物C:N:P比率与N、P重吸收的研究, 揭示3种植被类型N、P养分限制和N、P重吸收的内在联系。结果显示: 1)叶片C:N:P在常绿阔叶林为758:18:1, 在常绿针叶林为678:14:1, 在落叶阔叶林为338:11:1; 凋落物C:N:P在常绿阔叶林为777:13:1, 常绿针叶林为691:14:1, 落叶阔叶林为567:14:1; 2)常绿阔叶林和常绿针叶林叶片与凋落物C:N均显著高于落叶阔叶林; 叶片C:P在常绿阔叶林最高, 常绿针叶林中等, 落叶阔叶林最低, 常绿阔叶林和常绿针叶林凋落物C:P显著高于落叶阔叶林; 叶片N:P比也是常绿阔叶林最高、常绿针叶林次之, 落叶阔叶林最低, 但常绿阔叶林凋落物N:P最低; 3)植被叶片N、P含量间(N为x, P为y)的II类线性回归斜率显著大于1 (p < 0.05), 表明叶片P含量的增加可显著提高叶片N含量; 凋落物N、P含量的回归斜率约等于1, 反映了凋落物中单位P含量与单位N含量间的等速损耗关系; 4)常绿阔叶林N重吸收率显著高于常绿针叶林与落叶阔叶林, 落叶阔叶林P重吸收率显著高于常绿阔叶林和常绿针叶林。虽然植被的N:P指示常绿阔叶林受P限制, 落叶阔叶林受N限制, 常绿针叶林受N、P的共同限制, 但是N、P重吸收研究结果表明: 受N素限制的常绿阔叶林具有高的N重吸收率, 受P限制的落叶阔叶林并不具有高的P重吸收率。可见, 较高的N、P养分转移率可能不是植物对N、P养分胁迫的一种重要适应机制, 是物种固有的特征。     

Characterization of uropathogenic E. coli O25b-B2-ST131, O15:K52:H1, and CGA: Neutrophils apoptosis,serum bactericidal assay,biofilm formation,and virulence typing

Pathogenic and drug-resistant strains of Escherichia coli (E. coli) O25b-B2-ST131, O15:H1-D-ST393, and CGA (clonal group A) clonal groups have spread worldwide. This study aimed at determining E. coli epidemic clonal groups, their virulence factors, biofilm formation, neutrophils apoptosis, and antimicrobial resistance pattern of uropathogenic E. coli. A total of 95 CTX-M-1-producing E. coli clinical isolates were enrolled. E. coli O25b-B2-ST131, CGA, and O15:K52:H1 were identified by serotyping and phylogrouping and allele-specific polymerase chain reaction-based assay. Antibiotic susceptibility, biofilm formation, hemolysis, and human serum bactericidal assay were performed. Neutrophil apoptosis was assayed by flow cytometry. Nine E. coli clonal groups including six O25b-B2-ST131 strains, two CGA, and one O15:K52:H1-D-ST393 strains were detected. One O25b-B2-ST131 isolate was a strong biofilm-producer. Three ST131 isolates had type I fimbriae. Furthermore, all the CGA and O15:K52:H1 and three of ST131 isolates harbored the P fimbriae. The virulence genes ompT, fimH, and traT were detected among all the clonal groups. The apoptosis was induced by O25b-B2-ST131, CGA, and O15:K52:H1 E. coli. There was no significant difference regarding apoptosis induction among clonal groups. Furthermore, the presence of the cdt, usp, and vat genes was significantly associated with the apoptosis of neutrophils by O25b-B2-ST131, CGA, and O15:K52:H1-D-ST393 clonal groups.     

Facial duplication: case, review, and embryogenesis

The craniofacial anatomy of an infant with facial duplication is described. There were four eyes, two noses, two maxillae, and one mandible. Anterior to the single pituitary the brain was duplicated and there was bilateral arhinencephaly. Portions of the brain were extruded into a large frontal encephalocele. Cases of symmetrical facial duplication reported in the literature range from two complete faces on a single head (diprosopus) to simple nasal duplication. The variety of patterns of duplication suggests that the doubling of facial components arises in several different ways: Forking of the notochord, duplication of the prosencephalon, duplication of the olfactory placodes, and duplication of maxillary and/or mandibular growth centers around the margins of the stomatodeal plate. Among reported cases, the female:male ratio is 2:1.     

Serine: glyoxylate, alanine:glyoxylate, and glutamate:glyoxylate aminotransferase reactions in peroxisomes from spinach leaves

Two different aminotransferases, that have glyoxylate as the amino acceptor, have specific activities of 1 to 2 mumol . min-1 . mg of protein-1 in the isolated peroxisomal fraction from spinach leaves. Their properties were evaluated after separation on a hydroxylapatite column. Both enzymes had a Km for glyoxylate of 0.15 mM and an amino acid Km of 2 to 3 mM. Reactions proceeded by a Ping Pong Bi Bi mechanism. Serine:glyoxylate aminotransferase was relatively specific for both substrates and could only be slightly reversed with 100 mM glycine, although the Ki of glycine was 33 mM. The glutamate:glyoxylate amino-transferase protein was equally active in catalyzing an alanine:glyoxylate aminotransferase reaction, but the reverse reactions with 100 mM glycine were hardly measureable, although the Ki (glycine) was 8.7 mM. Protection against hydroxylamine inhibition from reaction with pyridoxal phosphate was used to investigate the specificity of amino acid binding. Substrate amino acids protected at about the same concentration as their Km, while glycine protected at its Ki concentration. Thus, the nearly irreversible catalysis with glycine is not due to a failure to bind glycine. The significance of a peroxisomal alanine:glyoxylate aminotransferase activity has not been incorporated into schemes for the oxidative photosynthetic carbon cycle.     

Analysis of Erwinia chrysanthemi EC16 pelE::uidA, pelL::uidA, and hrpN::uidA mutants reveals strain-specific atypical regulation of the Hrp type III secretion system

The plant pathogen Erwinia chrysanthemi produces a variety of factors that have been implicated in its ability to cause soft-rot diseases in various hosts. These include HrpN, a harpin secreted by the Hrp type III secretion system; PelE, one of several major pectate lyase isozymes secreted by the type II system; and PelL, one of several secondary Pels secreted by the type II system. We investigated these factors in E. chrysanthemi EC16 with respect to the effects of medium composition and growth phase on gene expression (as determined with uidA fusions and Northern analyses) and effects on virulence. pelE was induced by polygalacturonic acid, but pelL was not, and hrpN was expressed unexpectedly in nutrient-rich King's medium B and in minimal salts medium at neutral pH. In contrast, the effect of medium composition on hrp expression in E. chrysanthemi CUCPB1237 and 3937 was like that of many other phytopathogenic bacteria in being repressed in complex media and induced in acidic pH minimal medium. Northern blot analysis of hrpN and hrpL expression by the wild-type and hrpL::omegaCmr and hrpS::omegaCmr mutants revealed that hrpN expression was dependent on the HrpL alternative sigma factor, whose expression, in turn, was dependent on the HrpS putative sigma54 enhancer binding protein. The expression of pelE and hrpN increased strongly in late logarithmic growth phase. To test the possible role of quorum sensing in this expression pattern, the expI/expR locus was cloned in Escherichia coli on the basis of its ability to direct production of acyl-homoserine lactone and then used to construct expI mutations in pelE::uidA, pelL::uidA, and hrpN::uidA Erwinia chrysanthemi strains. Mutation of expI had no apparent effect on the growth-phase-dependent expression of hrpN and pelE, or on the virulence of E. chrysanthemi in witloof chicory leaves. Overexpression of hrpN in E. chrysanthemi resulted in approximately 50% reduction of lesion size on chicory leaves without an effect on infection initiation.     

Prevalence of Carriage of Shiga Toxin-Producing Escherichia coli Serotypes O157:H7, O26:H11, O103:H2, O111:H8, and O145:H28 among Slaughtered Adult Cattle in France

The main pathogenic enterohemorrhagic Escherichia coli (EHEC) strains are defined as Shiga toxin (Stx)-producing E. coli (STEC) belonging to one of the following serotypes: O157:H7, O26:H11, O103:H2, O111:H8, and O145:H28. Each of these five serotypes is known to be associated with a specific subtype of the intimin-encoding gene (eae). The objective of this study was to evaluate the prevalence of bovine carriers of these “top five” STEC in the four adult cattle categories slaughtered in France. Fecal samples were collected from 1,318 cattle, including 291 young dairy bulls, 296 young beef bulls, 337 dairy cows, and 394 beef cows. A total of 96 E. coli isolates, including 33 top five STEC and 63 atypical enteropathogenic E. coli (aEPEC) isolates, with the same genetic characteristics as the top five STEC strains except that they lacked an stx gene, were recovered from these samples. O157:H7 was the most frequently isolated STEC serotype. The prevalence of top five STEC (all serotypes included) was 4.5% in young dairy bulls, 2.4% in young beef bulls, 1.8% in dairy cows, and 1.0% in beef cows. It was significantly higher in young dairy bulls (P < 0.05) than in the other 3 categories. The basis for these differences between categories remains to be elucidated. Moreover, simultaneous carriage of STEC O26:H11 and STEC O103:H2 was detected in one young dairy bull. Lastly, the prevalence of bovine carriers of the top five STEC, evaluated through a weighted arithmetic mean of the prevalence by categories, was estimated to 1.8% in slaughtered adult cattle in France.     

Early-weaned sows: altrenogest therapy, estrus, ovulation, and reproductive performance

Early weaning is a technique used to increase swine health status, and may cause consequences in reproductive performance of sows. An experiment was performed to evaluate these effects in a herd of sows, with weaning at 9 or 10 days post-farrowing, located in west of Minas Gerais, Brazil. Large-White sows (n=102), with three or four previous parturitions were randomly allocated to three treatment groups: T1: artificial insemination (AI) at first post-weaning estrus of the sows; T2: AI at second post-weaning estrus, T3: AI at first estrus, after an administration of a daily individual dose of 20 mg of altrenogest from 5 to 8 days post-weaning. The duration of the first post-weaning estrus did not differ among treatment groups; however, the second estrus of the T2 group was of shorter duration relative to the other treatment groups (P< or =0.035). Ovulation occurred earlier at the second estrus of the T2 group, compared with the T1 and T3 groups (P< or =0.027), being similar to that at the first estrus of T2 group (P=0.177). The relationship of the timing between ovulation and estrus was similar among treatment groups (P> or =0.221). There was no difference in farrowing rate among treatment groups (P> or =0.313). The T2 group produced a mean of 2.5 more piglets per litter (P=0.002). In conclusion, the use of altrenogest did not increase the reproductive performance of early-weaned sows.     

Differences in sleep, light, and circadian phase in offshore 18:00-06:00 h and 19:00-07:00 h shift workers

Complaints concerning sleep are high among those who work night shifts; this is in part due to the disturbed relationship between circadian phase and the timing of the sleep-wake cycle. Shift schedule, light exposure, and age are all known to affect adaptation to the night shift. This study investigated circadian phase, sleep, and light exposure in subjects working 18:00-06:00 h and 19:00-07:00 h schedules during summer (May-August). Ten men, aged 46+/-10 yrs (mean+/-SD), worked the 19:00-07:00 h shift schedule for two or three weeks offshore (58 degrees N). Seven men, mean age 41+/-12 yrs, worked the 18:00-06:00 h shift schedule for two weeks offshore (61 degrees N). Circadian phase was assessed by calculating the peak (acrophase) of the 6-sulphatoxymelatonin rhythm measured by radioimmunoassay of sequential urine samples collected for 72 h at the end of the night shift. Objective sleep and light exposure were assessed by actigraphy and subjective sleep diaries. Subjects working 18:00-06:00 h had a 6-sulphatoxymelatonin acrophase of 11.7+/-0.77 h (mean+/-SEM, decimal hours), whereas it was significantly later, 14.6+/-0.55 h (p=0.01), for adapted subjects working 19:00-07:00 h. Two subjects did not adapt to the 19:00-07:00 h night shift (6-sulphatoxymelatonin acrophases being 4.3+/-0.22 and 5.3+/-0.29 h). Actigraphy analysis of sleep duration showed significant differences (p=0.03), with a mean sleep duration for those working 19:00-07:00 h of 5.71+/-0.31 h compared to those working 18:00-06:00 h whose mean sleep duration was 6.64+/-0.33 h. There was a trend to higher morning light exposure (p=0.07) in the 19:00-07:00 h group. Circadian phase was later (delayed on average by 3 h) and objective sleep was shorter with the 19:00-07:00 h than the 18:00-06:00 h shift schedule. In these offshore conditions in summer, the earlier shift start and end time appears to favor daytime sleep.