柴达木盆地第四系介形类化石带与磁性柱

柴达木盆地东部晚上新世－全新世湖相沉积巨厚,无明显间断,微体化石丰富。区内已建厚度超过２０００ｍ的第四系磁性柱中,记录了布容、松山和高斯极性时带。由于有剖面上部的同位素测年数据和剖面中、下部的介形类化石带序列的对比成果配合验证,布容、松山极性时下限的确定和布拉克、莫纳、琵琶湖、奥尔杜威、马默思等亚极性时的鉴别依据充足可信。据此极性年表标定的晚上新世－第四纪介形类化石带序列中１２个标准化石的时限得以识别。古生态研究与壳体元素分析的资料表明,始见于距今３０５万年的Ｍｉｃｒｏｌｉｍｎｏｃｙｔｈｅｒｅｓｉｎｅｎｓｉｓ指示低温水体,该化石带的出现标志着中新世以来柴达木盆地古气候的首次明显变冷。     

Zn、Cd在太原工业区和紫金山非工业区环颈雉不同组织中的分布及比较研究

为了探讨Zn、Cd在环颈雉（Phasianuscolchicus）体内的积累和分布规律,对太原工业区环颈雉体内不同组织的Zn、Cd进行了分析,并以紫荆山区为对照区（相对非污染区）,对两区环颈雉体内不同组织的Zn、Cd进行了比较。研究结果表明：Zn在环颈雉体内的分布规律为：股骨＞胸骨＞心＞肝＞肾＞肺＞股肌＞胸肌;Cd在环颈雉体内的分布规律为：肾＞胸骨＞股骨＞肝＞肺＞胸肌＞心＞股肌。两区环颈雉各组织中,Zn的含量没有明显差异,而肾脏中的Cd含量差异显著。     

大兴安岭北部地区原始林火干扰历史的研究

在大兴安岭阿龙山林业局的一个集水区,通过样地法（９６个样地）,调查了大量的火疤木,研究了景观水平上的火状况。结果表明,由１８２５至１９９３年间样区共发生１４次火灾,火烧种类主要是地表火,但也有少量树冠火;火烧强度主要为弱度火;火场面积通常很大;火烧平均间隔期为３７ａ,火烧轮回期的约３０ａ。这些指标对大于大兴安岭北部林区有一定的代表意义。大兴安岭北部林区的火状况主要决定于兴安落叶松的抗火特性和森林群     

国产前原鹅观草的订正

对我国文献中记载的前原鹅观草（Ｒｏｅｇｎｅｒｉａｍａｙｅｂａｒａｎａ（Ｈｏｎｄａ）Ｏｈｗｉ）的标本和植物,与原产于日本的该种进行了比较形态学、细胞学研究,二者差异显著。作者认为我国所记载的该种种名应是山东鹅观草（Ｒｏｅｇｎｅｒｉａｓｈａｎｄｏｎｇｅｎｓｉｓ（Ｂ．Ｓａｌｏｍｏｎ）Ｊ．Ｌ．Ｙａｎｇ,Ｙ．Ｈ．ＺｈｏｕｅｔＹｅｎ）,其内稃先端钝圆,长为外稃的３／４,染色体数为２ｎ＝４ｘ＝２８,具ＳＹ染色体组,结实率达９０％以上,过去被错定为Ｒ．ｍａｙｅｂａｒａｎａ。而Ｒ．ｍａｙｅｂａｒａｎａ在日本系一天然杂种,其内稃先端尖,与外稃等长或稍短,染色体数为２ｎ＝６ｘ＝４２,具ＨＳＹ染色体组,结实率极低,仅０．２％～０．４％。     

甘蔗和烟草幼叶原生质体的核酸含量与核酸酶活性及其影响因素

与幼叶组织相比,酶法新鲜分离的甘蔗和烟草幼叶原生质体内的ＲＮＡ、ＤＮＡ及总核酸含量均降低。其原因可能是刚游离的原生质体内酸性和碱性ＲＮＡ酶与ＤＮＡ酶等活性提高所致。甘蔗叶原生质体内的核酸降低量和ＲＮＡ酶与ＤＮＡ酶活性的增加程度均高于烟草。随用作渗透压稳定剂的甘露醇浓度增加,甘蔗和烟草叶原生质体的ＲＮＡ酶和ＤＮＡ酶活性均相应提高。其中以甘蔗叶原生质体的核酸酶活性增加水平较明显。在细胞壁降解产物的作用下,除了甘蔗原生质体内的ＲＮＡ酶活性略被促进外,其ＤＮＡ酶和烟草叶原生质体内的核酸酶均不受影响     

黄鳝食性的初步研究

通过对不同产地的２７１尾野生黄鳝的食性研究表明,全长小于１００ｍｍ的稚鱼,其食性随着全长的生长而变化,稚鱼前期以摄食轮虫,枝角类为主,后期则以水生寡毛类,摇蚊幼虫为主,而全长１０１ｍｍ－２００ｍｍ的幼鳝及全长大于２００ｍｍ的成鳝的食性,随全长变化相对稳定,且细鳝和成鳝的食谱基本相同,其主要食物组成均包括摇蚊幼虫,水生寡毛类,蚯蚓,昆虫幼虫,枝角类和桡足类等。其肠内含物中的饵料生物种类含量均在季节变     

nfi, the gene for endonuclease V in Escherichia coli K-12.

Endonuclease V is specific for single-stranded DNA or for duplex DNA that contains uracil or that is damaged by a variety of agents (B. Demple and S. Linn, J. Biol. Chem. 257:2848-2855, 1982). Thus, it may be a versatile DNA repair enzyme. The protein was purified to apparent homogeneity, and from its N-terminal sequence, its gene, nfi, was identified. nfi is immediately downstream of hemE, at kb 4208 (90.4 min) on the current chromosomal map of Escherichia coli K-12. This region was cloned, and plasmid insertion and deletion mutants were used to study its molecular organization. Although nfi is the third of four closely spaced, codirectional genes, it is expressed independently.     

Characterization of the oriC region of Mycobacterium smegmatis.

A 3.5-kb DNA fragment containing the dnaA region of Mycobacterium smegmatis has been hypothesized to be the chromosomal origin of replication or oriC (M. Rajagopalan et al., J. Bacteriol. 177:6527-6535, 1995). This region included the rpmH gene, the dnaA gene, and a major portion of the dnaN gene as well as the rpmH-dnaA and dnaA-dnaN intergenic regions. Deletion analyses of this region revealed that a 531-bp DNA fragment from the dnaA-dnaN intergenic region was sufficient to exhibit oriC activity, while a 495-bp fragment from the same region failed to exhibit oriC activity. The oriC activities of plasmids containing the 531-bp sequence was less than the activities of those containing the entire dnaA region, suggesting that the regions flanking the 531-bp sequence stimulated oriC activity. The 531-bp region contained several putative nine-nucleotide DnaA-protein recognition sequences [TT(G/C)TCCACA] and a single 11-nucleotide AT-rich cluster. Replacement of adenine with guanine at position 9 in five of the putative DnaA boxes decreased oriC activity. Mutations at other positions in two of the DnaA boxes also decreased oriC activity. Deletion of the 11-nucleotide AT-rich cluster completely abolished oriC activity. These data indicate that the designated DnaA boxes and the AT-rich cluster of the M. smegmatis dnaA-dnaN intergenic region are essential for oriC activity. We suggest that M. smegmatis oriC replication could involve interactions of the DnaA protein with the putative DnaA boxes as well as with the AT-rich cluster.