Novel molecular markers of Chlamydia pecorum genetic diversity in the koala (Phascolarctos cinereus)

Background Chlamydia pecorum is an obligate intracellular bacterium and the causative agent of reproductive and ocular disease in several animal hosts including koalas, sheep, cattle and goats. C. pecorum strains detected in koalas are genetically diverse, raising interesting questions about the origin and transmission of this species within koala hosts. While the ompA gene remains the most widely-used target in C. pecorum typing studies, it is generally recognised that surface protein encoding genes are not suited for phylogenetic analysis and it is becoming increasingly apparent that the ompA gene locus is not congruent with the phylogeny of the C. pecorum genome. Using the recently sequenced C. pecorum genome sequence (E58), we analysed 10 genes, including ompA, to evaluate the use of ompA as a molecular marker in the study of koala C. pecorum genetic diversity. Results Three genes (incA, ORF663, tarP) were found to contain sufficient nucleotide diversity and discriminatory power for detailed analysis and were used, with ompA, to genotype 24 C. pecorum PCR-positive koala samples from four populations. The most robust representation of the phylogeny of these samples was achieved through concatenation of all four gene sequences, enabling the recreation of a "true" phylogenetic signal. OmpA and incA were of limited value as fine-detailed genetic markers as they were unable to confer accurate phylogenetic distinctions between samples. On the other hand, the tarP and ORF663 genes were identified as useful "neutral" and "contingency" markers respectively, to represent the broad evolutionary history and intra-species genetic diversity of koala C. pecorum. Furthermore, the concatenation of ompA, incA and ORF663 sequences highlighted the monophyletic nature of koala C. pecorum infections by demonstrating a single evolutionary trajectory for koala hosts that is distinct from that seen in non-koala hosts. Conclusions While the continued use of ompA as a fine-detailed molecular marker for epidemiological analysis appears justified, the tarP and ORF663 genes also appear to be valuable markers of phylogenetic or biogeographic divisions at the C. pecorum intra-species level. This research has significant implications for future typing studies to understand the phylogeny, genetic diversity, and epidemiology of C. pecorum infections in the koala and other animal species.

Do people gamble with their lives : The relationship between risky driving behaviour and other risky behaviours

General risky behaviour is explored for correlation with risky driving behaviour in light of two theories, self-control and cross-situational consistency. Identification of general risky behaviours associated with risky driving behaviour, and the theory that best predicts the behaviours, will enable better targeting of intervention and education strategies to reduce driving related fatalities and injuries. A correlational study using participants (N=152) drawn from first year university undergraduates and the public surveyed their lifestyle and behaviours. Relationships were found between risky driving behaviours and other risky behaviours such as alcohol consumption, cannabis use and performing unlawful activities. No significant differences were found between genders, with the exception that males were more likely to believe that they were at risk of injury from their employment, χ2 (1, N = 152) = 4.49, p = .03, were more likely to have performed an unlawful offence, χ2 (1, N = 152) = 11.77, p = .001 and were more likely to drink drive, t (55.41) = -3.87, p < .001, mean difference = -0.63, CI 95% (-0.9, -0.37). People engaged in risky driving behaviours were more likely to engage in other risky behaviours. The theories that were explored were unable to accurately predict an association between general risky behaviour and driving without a license or when disqualified. Cross-situational consistency explained 20% (R2adj = .16) of the variance in which people engaged in risky driving with low self-control theory explaining an additional 0.3% variance (R2change = .003), F (8,143) = 6.92, p < .001. Driving while under the influence of alcohol could be predicted by risky behaviours in lifestyle, health, smoking, cannabis use and alcohol consumption, F (8,143) = 6.92, p < .001. The addition of self-control was not significant.

药用野生稻复合体（稻属）的分子系统发育与进化研究

稻属（Oryza L.）隶属于禾本科（Gramineae）Ehrhartoideae亚科的稻族（Oryzeae），包括两个栽培种（亚洲栽培稻O. sativa和非洲栽培稻O. glaberrima）和大约20多个野生种，广布于热带亚洲、非洲、大洋洲、中美洲和南美洲。药用野生稻复合体（O. officinalis complex）是稻属中最大、也是最复杂的一个复合体，共包括9个种，含有5种染色体组类型（B、C、BC、CD 和E）。作为栽培稻品质改良的重要基因库，药用野生稻复合体在稻属中具有重要的地位。但是，相似的形态和重叠的地理分布使部分物种的分类和鉴定一直较为困难;种内染色体组构成和倍性的不同更增加了分类鉴定的复杂性。这种情况阻碍了对这些野生稻遗传优势的有效利用。另外，由于物种间断分布和缺乏明确的二倍体亲本等原因，药用野生稻复合体内的异源多倍体起源一直存在争议。本文通过细胞核乙醇脱氢酶基因（Adh）和nrDNA的内转录间隔区（ITS）限制性片段长度多态性（RFLP）分析;叶绿体matK 基因、trnL 内含子和trnL-trnF 基因间隔区、核基因Adh和GPA1以及核糖体DNA ITS片段等序列比较的方法，对药用野生稻复合体中染色体组和物种的鉴定、种间系统发育关系，以及异源多倍体CCDD物种的起源和多倍体ITS的分子进化等进行了研究。主要研究结果如下： 1． 利用核Adh 基因限制性片段长度多态性，检测了来自国际水稻研究所基因库的64份药用野生稻复合体的样品。结果证明，所有O. rhizomatis样品都是含C染色体组的二倍体，所有O. minuta样品都是含BC 染色体组的四倍体。但是，种子库中鉴定为O. officinalis、O. punctata和O. eichingeri的样品中，同时都发现了含C染色体组的二倍体和含BC染色体组的四倍体。四倍体的O. officinalis只在印度分布，而且曾被描述为另一个种O. malampuzhaensis。 四倍体的O. punctata，也被一些学者称为O. schweinfurthiana，被发现和其二倍体一样分布广泛。值得注意的是，有两个曾被作为O. officinalis 四倍体的样品实际上是含有CD染色体组的物种O. latifolia。我们的结果增进了对国际水稻研究所种子库中部分野生稻样品染色体组构成的理解, 纠正了以往对药用野生稻复合体样品的错误鉴定，为今后进一步研究和利用这部分资源提供了种质编目的重要基础。 2． 对稻属中代表不同地理分布区的、含CD染色体组的11个样品（包括77个克隆）的ITS片段进行了测序。基于这些ITS序列的限制性片段长度多态性，提出一个快速而可靠的区分稻属CD 染色体组物种的方法。这个方法的具体步骤是：（1）利用通用引物扩增ITS 片段;（2）利用限制性内切酶FokI和/或DraⅢ消化PCR扩增产物;（3）用1%的琼脂糖胶电泳并根据消化产物的片段长度多态性来区分不同物种。 3． 利用包括两个叶绿体片段（matK和 trnL-trnF）、nrDNA内转录间隔区（ITS）和三个核基因（Adh1、Adh2和GPA1）的同源序列分析，探讨了药用野生稻复合体中二倍体物种和它们所代表的染色体组之间的系统发育关系。独立和合并的基因系统发育树都显示了一致的结果，即C染色体组和B染色体组的亲缘关系要比它们和E染色体组的近。三个含C染色体组的二倍体中，O. officinalis 和O. rhizomatis表现出较近的亲缘关系。值得注意的是，在O. eichingeri种内，尽管基于多基因的数据支持来自斯里兰卡的样品和来自非洲的样品聚成一个分支，但是较低的支持率表明, 两个地区的样品之间存在着较高的遗传分化。 4． 稻属中含CD染色体组的物种特产于拉丁美洲，包括O. alta、 O. grandiglumis 和O. latifolia。由于具有相同的染色体组类型、相似的形态特征和重叠的地理分布，这3个物种间的系统发育关系一直存在争论。另外，因为美洲大陆上没有含C和D染色体组的二倍体物种存在，对这些含CD染色体组物种的可能起源也有不同的假设被提出。使这个问题更具挑战性的是，尽管开展了世界范围的收集，至今仍没有找到含D 染色体组的二倍体物种。在本研究中，代表含C、CD和E染色体组以及含G染色体组的外类群共7个物种，共15份样品的2个叶绿体片段（matK和trnL-trnF）和3个核基因（Adh1，Adh2 和 GPA1）部分片段被测序。基于简约法、距离法和最大似然法的系统发育分析都充分支持含CD染色体组的物种起源于一次杂交事件的推论，并且显示，在物种形成时，含C染色体组的物种（O. officinalis 或O. rhizomatis 而非O. eichingeri）可能承担了母本，而含E染色体组的物种（O. australiensis）则可能承担了父本。另外，CCDD物种间非常一致的系统发育关系表明，非常大的分歧存在于 O. latifolia 和其它两个种（O. alta和O. grandiglumis）之间，这个结果倾向于将后两个种处理为同种或同种下不同分类群。 5． 基于178个克隆序列比较，探讨了ITS在稻属多倍体中的致同进化及其系统学意义。研究发现稻属异源四倍体的ITS存在不同形式的进化方式：首先，非洲BBCC四倍体O. eichingeri和O. punctata 的ITS片段同时保留了双亲拷贝，而且系统发育研究表明，二倍体的O. eichingeri和O. punctata 可能是这两个四倍体的直接祖先;其次，亚洲四倍体O. malampuzhaensis和O. minuta 的ITS仅定向保留母本ITS拷贝;另外，美洲CCDD四倍体的ITS序列发生了双向致同进化，即O. alta和O. grandiglumis的ITS位点一致化成C染色体组类型，而O. latifolia一致化成 D/E 染色体组类型。我们的研究进一步表明在利用ITS片段进行系统发育分析时，特别是涉及异源多倍体时必须慎重。 6． 利用栽培稻的微卫星引物，对含B/C染色体组的6个物种，157个体的SSR位点进行扩增。结果在这些亲缘关系稍远的野生稻中得到7个SSR位点，其中5个位点表现出多态性。比较BB、CC和BBCC物种SSR位点的每位点平均等位基因数A、多态位点百分率P和期望杂合度He ，3项指标发现，四倍体物种的遗传多样性，总体上要高于二倍体物种;二倍体物种内部，O. officnalis的遗传变异最大。另外，以遗传相关性为标准，讨论了B/C染色体组物种间的系统发育关系，同时推测了现存二倍体物种和4个BBCC四倍体物种的遗传关系。

CRANIODENTAL VARIATION OF MACAQUES ( Macaca ): SIZE,FUNCTION AND PHYLOGENY

为了研究猕猴属的颅骨差异性, 从而探 讨种间在形态、功能和系统分化方面的相互联系, 测定了11 个猕猴种类的77 个颅骨变量, 用于主成 分分析和判别分析。应用巢式分析方法, 分析过程 包括3 个步骤。所有变量根据功能和部位的不同首 先分为7 个单位: 下颌、下颌齿、上颌齿、上面 颅、下面颅、面颅后部和颅腔。第2 步根据它们所 揭示的相似性(具有相同的种间及种内差异性类 型) 合并为3 个解剖区域: 咀嚼器官(下颌、下颌 齿、上颌齿) , 面颅(上面颅和下面颅) 和整个面 颅后(面颅后和颅腔) 。第3 步从3 个解剖区域筛 选出27 个变量代表整个颅骨的形态结构。除了寻 找不同的功能单位, 解剖区域及总的颅骨具有不同 的种间和种内差异类型外, 此过程对筛出研究意义 不大的变量起很重要的作用。上述分析过程分别用 于对雌、雄性和两性的研究。所研究的11 个猕猴 种类间形成了3 聚类。第1 类包括食蟹猴(Macaca f ascicularis) 、戴帽猴( M1 sinica) 和头巾猴( M1 radiata) ; 第2 类包括猕猴( M1 mulatta ) 、熊猴 (M1 assensis ) 、平顶猴( M1 nemestrina ) 和黑猿 (M1 nigra) ; 第3 类包括蛮猴( M1 sylvanus ) 、日 本猴( M1 f uscata) 、短尾猴( M1 arctoides ) 和藏 酋猴(M1 thibetana) 。分别从两性差异、食物、生态、分类和系统分化方面进行了差异性讨论, 结果 认为猕猴种间颅骨的差异性主要是由于系统分化不 同而引起个体差异所致, 即种间和种内存在的个体 差异。在主成分分析中, 这些差异在不同的区域表 现在不同的成分上。在咀嚼器官上种间的差异在第 1 主成分上, 种内的差异则在第2 主成分上。面颅 的情况则刚好相反。这两种差异在面颅后及颅腔上 则被第1 和第2 主成分所平分。这样, 种间的差异 在咀嚼器官上大于种内的差异。种内的差异在面颅 上则大于种间的差异。这两种差异在面颅后和颅腔 上则几乎大小相等。这一研究结果表明, 与传统的 概念不同, 第2 主成分不仅仅表现形态、形状的差 异, 而如同第1 主成分一样, 也表现形态的大小成 分。此研究所揭示的猕猴种间关系部分与Foden (1976 , 1980) 和Delson (1980) 相同。如平顶猴 与黑猿、短尾猴、藏酋猴和熊猴的关系。食蟹猴、 头巾猴和戴帽猴的关系则不同, 并已得到有关分子 生物学的支持, 此3 种可能来自同一祖先并经历相 同的扩散过程。此研究所设计的巢式分析过程提供 了一种很好的差异性研究手段。最终结果暗示在形 态学研究中仅仅考虑某一区域的形态结构是很不够 的, 因为不同的部分具有不同的种间及种内差异类 型。这在化石研究中尤其要注意。

滇西鸡足山蝴蝶考察

在滇西鸡足山共采到蝶类100种, 隶属于8科58属。其中, 凤蝶科4属10种, 粉蝶科9属15种, 斑蝶科4属4种, 眼蝶科6属17种, 蛱蝶科14属23种, 蚬蝶科2属3 种, 厌蝶科13属17种, 弄蝶 科6属11种。表1参7

人工湿地组合系统除磷的净化空间研究

通过小试试验研究了由塘系统、垂直流、推流床单元组成的人工湿地工艺系统组合在内部不同空间上除磷的净化效应。结果发现,在高水力负荷下运行一段时间后,各套组合工艺系统对磷的净化效率均出现了不同程度的下降,其中下行池单元表层对磷的去除效率下降得最为显著;在各种组合中,塘单元对磷的净化效果并不理想。但是好氧塘单元与湿地的联用却可以有效地避免正磷酸盐释放的问题。

不育转基因鱼研制方法获发明专利

<正>日前,中国科学院水生生物研究所鱼类基因工程学科组关于不育的转基因鱼研制的方法获得美国发明专利。此前,该研究已获中国发明专利。

田块尺度下土壤磷素的空间变异性

采用经典统计学与地统计学相结合的方法,对中国科学院沈阳生态实验站30 m×42 m样地进行网格法分层(0~10和10~20 cm)取样,研究了田块尺度下土壤全P和Olsen-P的空间变异特征.结果表明,49对样本土壤Olsen-P的变异系数(46.56%~56.42%)远高于全P(11.68%~13.33%);全P和Olsen-P具有较好的空间结构且具有较相近的空间相关距离.最佳理论模型的参数显示各变量空间变异主要受结构性因素的影响,各变量半方差变异函数的C/(C0+C)均高于66%.全P和Olsen-P之间及在2个土层之间均具有较相似的空间分布格局.变异系数结合空间格局分析可以大大降低试验取样的数量.

Breviarium Strigoniense.

Cf. notice du ms. par Leroquais, Bréviaires, III, 182-185 n° 591 et pl. XCIX; P. Radó, Libri liturgici manuscripti bibliothecarum Hungariae et limitropharum regionum, Budapest, 1973. Un bréviaire d'Esztergom a été imprimé en 1524 à Venise. F. 2-8v Calendrier à l'usage d'Esztergom, avec un grand nombre de saints d'origines diverses (2-7v); cf. Leroquais, op. cit., 182. À noter les saints non mentionnés dans les Acta sanctorum, ou du moins pas pour la date correspondante; ne sont pas relevés les saints hongrois considérés comme classiques par Radó, op. cit., passim : 4 févr., «Victoris m.»; 8 févr., «Juliani m.»; 13 févr., «Adalberti m.», signalé une fois dans Radó, op. cit., 96 d'après ms. Budapest, B. N. Hung., c. l. m. ae. 395; 15févr., «Faustiani m.»; 21 févr., «Septuaginta mm.», non signalé sous cette forme pour cette date dans Radó, op. cit.; 15 mars, «Hilarii conf. et pont.», non signalé sous cette forme pour cette date dans Radó, op. cit.; 17 mars, «Bernardi conf.»; 26mars, «Eustachii abb.», signalé une fois dans Radó, op. cit., 96 d'après ms. Budapest, B.N. Hung., c. l. m. ae. 395; 28 mars, «Gastuli m.», non signalé dans Radó, op. cit.; 3 juill., «Bonifacii ep.», non signalé dans Radó, op. cit.; 5 juill., «Dominici m.»; 4 août, «Gaudentii ep. et conf.», signalé une fois dans Radó, op. cit., 329 d'après ms. Budapest, B. N. Hung., c. l. m. ae. 408; 8 août, «Adventus sanguinis D. N. J. C.»; 31 août, «Pauli ep. et m.», non signalé dans Radó, op. cit.; 12 oct., «Quatuor milium mm.», non signalé dans Radó, op. cit., à rapprocher de quatuor mille octingenti septuaginta mm., cf. Radó, op. cit., 167 d'après ms. Esztergom, B. metropolitana Strigoniensis I. 20; 14 oct., «Cerbonii conf.»; 27 oct., «Vedasti m.»; 15 nov., «Martini conf.», non signalé pour cette date dans Radó, op. cit; 20 nov., «Aniani ep. [Aurelianensis] et conf.». Pour plusieurs saints du calendrier on ne trouve pas d'office dans le sanctoral, et vice versa. — «Sequitur tabula impositionis historiarum...» (8-8v). F. 11-76 Psautier férial (11-72). — Office des défunts à l'usage d'Esztergom (72v-76); cf. K. Ottosen, The responsories and versicles of the latin office of the dead, Aarhus 1993, 127 (description des ff.74v-75v = «BN8879B») et 180 (description des ff.72v-74v = «BN8879A»). F. 77-528v Temporal : «Incipit breviarium secundum chorum alme ecclesie Strigoniensis. Dominica prima in adventu Domini...» (77-282v). Sanctoral : «Incipit secunda pars breviarii scilicet de festivitatibus. De s. Silvestro...» (286-486). À noter : office de l'Immaculée Conception composé par Léonard Nogarolo (480v). Commun des saints : «Incipit commune de sanctis et primo in vigilia unius apostoli...» (486v-513v). — «Sequitur de b. Virgine sabbatis diebus per estatem. Ad vesperas...» (513v-516v). «In quotidianis horis b. Virginis...» (516v-525). — «Sequuntur preces in quadragesima...» (525-526v). — «Sequuntur suffragia sabbatis diebus per estatem...» (526v-528), dont suffrages des ss. [Stephani regis Hungariae; Emerici ducis] (527), [Ladislai regis Hungariae; Adalberti ep. Pragensis et m.] (527v). — «Absolutio excommunicati...» (528-528v). 106 hymnes mentionnées dans la table des incipit, dont une non répertoriée dans Chevalier, Repert. hymn. ni dans les A. H., pour les confesseurs : «Christe lucis splendor vere fabrice mundi semper nobis parcens miserere confessorum precibus//...» (506v); cf. P. Radó, Répertoire hymnologique des mss. liturgiques dans les bibliothèques publiques de Hongrie, Budapest 1945, n° 111, relevée une fois dans le ms. Budapest, Bibl. nat. Hung. c. l. m. ae. 132, ms. décrit par Radó, Libri liturgici..., op. cit., 395-400.

Breviarium Strigoniense.

Cf. notice du ms. par Leroquais, Bréviaires, III, 182-185 n° 591 et pl. XCIX; P. Radó, Libri liturgici manuscripti bibliothecarum Hungariae et limitropharum regionum, Budapest, 1973. Un bréviaire d'Esztergom a été imprimé en 1524 à Venise. F. 2-8v Calendrier à l'usage d'Esztergom, avec un grand nombre de saints d'origines diverses (2-7v); cf. Leroquais, op. cit., 182. À noter les saints non mentionnés dans les Acta sanctorum, ou du moins pas pour la date correspondante; ne sont pas relevés les saints hongrois considérés comme classiques par Radó, op. cit., passim : 4 févr., «Victoris m.»; 8 févr., «Juliani m.»; 13 févr., «Adalberti m.», signalé une fois dans Radó, op. cit., 96 d'après ms. Budapest, B. N. Hung., c. l. m. ae. 395; 15févr., «Faustiani m.»; 21 févr., «Septuaginta mm.», non signalé sous cette forme pour cette date dans Radó, op. cit.; 15 mars, «Hilarii conf. et pont.», non signalé sous cette forme pour cette date dans Radó, op. cit.; 17 mars, «Bernardi conf.»; 26mars, «Eustachii abb.», signalé une fois dans Radó, op. cit., 96 d'après ms. Budapest, B.N. Hung., c. l. m. ae. 395; 28 mars, «Gastuli m.», non signalé dans Radó, op. cit.; 3 juill., «Bonifacii ep.», non signalé dans Radó, op. cit.; 5 juill., «Dominici m.»; 4 août, «Gaudentii ep. et conf.», signalé une fois dans Radó, op. cit., 329 d'après ms. Budapest, B. N. Hung., c. l. m. ae. 408; 8 août, «Adventus sanguinis D. N. J. C.»; 31 août, «Pauli ep. et m.», non signalé dans Radó, op. cit.; 12 oct., «Quatuor milium mm.», non signalé dans Radó, op. cit., à rapprocher de quatuor mille octingenti septuaginta mm., cf. Radó, op. cit., 167 d'après ms. Esztergom, B. metropolitana Strigoniensis I. 20; 14 oct., «Cerbonii conf.»; 27 oct., «Vedasti m.»; 15 nov., «Martini conf.», non signalé pour cette date dans Radó, op. cit; 20 nov., «Aniani ep. [Aurelianensis] et conf.». Pour plusieurs saints du calendrier on ne trouve pas d'office dans le sanctoral, et vice versa. — «Sequitur tabula impositionis historiarum...» (8-8v). F. 11-76 Psautier férial (11-72). — Office des défunts à l'usage d'Esztergom (72v-76); cf. K. Ottosen, The responsories and versicles of the latin office of the dead, Aarhus 1993, 127 (description des ff.74v-75v = «BN8879B») et 180 (description des ff.72v-74v = «BN8879A»). F. 77-528v Temporal : «Incipit breviarium secundum chorum alme ecclesie Strigoniensis. Dominica prima in adventu Domini...» (77-282v). Sanctoral : «Incipit secunda pars breviarii scilicet de festivitatibus. De s. Silvestro...» (286-486). À noter : office de l'Immaculée Conception composé par Léonard Nogarolo (480v). Commun des saints : «Incipit commune de sanctis et primo in vigilia unius apostoli...» (486v-513v). — «Sequitur de b. Virgine sabbatis diebus per estatem. Ad vesperas...» (513v-516v). «In quotidianis horis b. Virginis...» (516v-525). — «Sequuntur preces in quadragesima...» (525-526v). — «Sequuntur suffragia sabbatis diebus per estatem...» (526v-528), dont suffrages des ss. [Stephani regis Hungariae; Emerici ducis] (527), [Ladislai regis Hungariae; Adalberti ep. Pragensis et m.] (527v). — «Absolutio excommunicati...» (528-528v). 106 hymnes mentionnées dans la table des incipit, dont une non répertoriée dans Chevalier, Repert. hymn. ni dans les A. H., pour les confesseurs : «Christe lucis splendor vere fabrice mundi semper nobis parcens miserere confessorum precibus//...» (506v); cf. P. Radó, Répertoire hymnologique des mss. liturgiques dans les bibliothèques publiques de Hongrie, Budapest 1945, n° 111, relevée une fois dans le ms. Budapest, Bibl. nat. Hung. c. l. m. ae. 132, ms. décrit par Radó, Libri liturgici..., op. cit., 395-400.

The air distribution index as an indicator for energy consumption and performance of ventilation systems

This paper deals with the energy consumption and the evaluation of the performance of air supply systems for a ventilated room involving high- and low-level supplies. The energy performance assessment is based on the airflow rate, which is related to the fan power consumption by achieving the same environmental quality performance for each case. Four different ventilation systems are considered: wall displacement ventilation, confluent jets ventilation, impinging jet ventilation and a high level mixing ventilation system. The ventilation performance of these systems will be examined by means of achieving the same Air Distribution Index (ADI) for different cases. The widely used high-level supplies require much more fan power than those for low-level supplies for achieving the same value of ADI. In addition, the supply velocity, hence the supply dynamic pressure, for a high-level supply is much larger than for low-level supplies. This further increases the power consumption for high-level supply systems. The paper considers these factors and attempts to provide some guidelines on the difference in the energy consumption associated with high and low level air supply systems. This will be useful information for designers and to the authors' knowledge there is a lack of information available in the literature on this area of room air distribution. The energy performance of the above-mentioned ventilation systems has been evaluated on the basis of the fan power consumed which is related to the airflow rate required to provide equivalent indoor environment. The Air Distribution Index (ADI) is used to evaluate the indoor environment produced in the room by the ventilation strategy being used. The results reveal that mixing ventilation requires the highest fan power and the confluent jets ventilation needs the lowest fan power in order to achieve nearly the same value of ADI.

Biology and fertility life table of the South American fruit fly Anastrepha fraterculus on grape

Conselho Nacional de Desenvolvimento Científico e Tecnológico (CNPq)

Exercise training attenuates acute hyperalgesia in streptozotocin-induced diabetic female rats

Fundação de Amparo à Pesquisa do Estado de São Paulo (FAPESP)

Influence of Er,Cr: YSGG laser on bond strength of self-adhesive resin cement

The purpose of this study was to investigate the bond strength of fiber post previously laser treated root canals. Forty single-rooted bovine teeth were endodontically treated, randomly and equally divided into two main groups according to the type of pretreatment: G1: 2.5% NaOCl (control group); and G2: Er,Cr:YSGG laser. Each group was further subdivided into 2 groups based on the category of adhesive systems/ luting materials used: a: an etch-and-rinse resin cement (Single Bond/RelyX ARC; 3M ESPE), and b: a self-adhesive resin cement (Rely X Unicem; 3M ESPE). Three 1.5 mm thick slabs were obtained per root and the push-out test was performed at a crosshead speed of 0.5 mm/min until post dislodgement occurred. Data were analyzed by ANOVA and post-hoc Tukey's test at a pre-set alpha of 0.05. Analysis of variance showed no statistically significant difference (p > 0.05) among the groups G1a (25.44 ± 2.35) and G1b (23.62 ± 3.48), G2a (11.77 ± 2.67) and G2b (9.93 ± 3.37). Fractures were observed at the interface between the dentin and the resin in all groups. The Er,Cr:YSGG laser irradiation did not influence on the bond strength of the resin cements and the etch-and-rinse resin cement had better results on bond strength than self-adhesive resin cement.