华南人颅骨上、下颌臼齿磨耗与年龄变化的关系

本文以华南人103例17—73岁男性颅骨的709个臼齿为材料,研究了上下颌臼齿磨耗度与年龄的关系。将磨耗度分为九级,统计分析结果表明,华南人臼齿的磨耗度与年龄关系是密切相关的,这种相关关系,能够作为估计华南人颅骨年龄的标准。第一臼齿与第二臼齿的磨耗平均年龄比率是M1∶M2=6∶6.9;磨耗度与年龄的相关系数M1为0.91,M2为0.90,均为高度相关。并得出磨耗度的平均年龄及95％置信区间(见表3)。华南人下颌臼齿的磨耗比上颌臼齿的磨耗稍大(61.5％)。     

军都山古代人群牙齿磨耗及其饮食

以军都山墓地为代表的"玉皇庙文化"系中国北方青铜时代的一支具有鲜明地方特色的少数部族文化。本文对军都山墓地出土人骨牙齿标本作牙齿磨耗状况分析,试图为其饮食结构和社会经济形态的探讨提供线索。结果显示:军都山古代人群中,相同年龄组的男女两性牙齿磨耗差异不大;前部牙齿磨耗轻于后部臼齿,第一臼齿磨耗最重;臼齿磨耗样式大多呈现"正常平匀"式,臼齿磨耗角度大多较小,两者均随年龄而变化但没有显著的性别差异。经与其他样本组的对比认为军都山古代人群牙齿磨耗的特点可能与其社会经济农牧兼营的性质有关,推测动物性食物(肉食)可能在军都山古代人群主要饮食结构中占据重要比例,并包含有一定的农业经济成分。不同游牧人群牙齿磨耗程度差异较大,只有结合了磨耗形态及其他信息才有可能更切实地反映其饮食状况。     

陶寺、上马、延庆古代人群臼齿磨耗速率的比较研究

本文采用Scott定义的臼齿磨耗级别系统,对陶寺、上马、延庆三组人牙的第一、第二臼齿磨耗情况进行观察,并通过主轴回归分析对其磨耗速率进行比较和讨论。在经济类型上,陶寺和上马属于农业经济,但陶寺的狩猎在其经济生活中占有一定地位;延庆畜牧业则比较发达。分析表明三组人牙均表现出臼齿磨耗速率下颌快于上颌的特点,而在性别上没有明显差异。在组间差别上,上马组的磨耗速率似略快于其他两组。磨耗速率的组内、组间差异与上下颌牙齿咬合关系、口腔咀嚼生理以及不同经济文化古人群的食物构成等差异有关。     

多元分析方法分辨细齿小塔塔鼠的下臼齿

啮齿类梳趾鼠科小塔塔鼠的下臼齿的形态非常接近。本文根据已有的一百多个牙齿,用齿冠的长度和宽度两个性状,在坐标系中画出了M_1、M_2和M_3的一系列椭圆,代表着这些牙齿一定比例的样本分布范围,并以此得出了细齿小塔塔鼠这三种牙齿的判别线。     

同口牙齿的磨耗级比较

本文比较和分析了同口同侧牙齿的相应的磨耗级,提供了除臼齿以外的牙齿磨耗年龄变化依据。同时还对上下对应牙、两侧对称牙的磨耗级作了比较和分析。     

新疆吐鲁番加依墓地青铜—早期铁器时代居民牙齿的磨耗北大核心CSCD

本文对新疆吐鲁番市加依墓地青铜—早期铁器时代居民的牙齿磨耗、口腔疾病和骨质隆起等特征进行了观察与研究,结果显示,加依墓地居民的牙齿磨耗较重,但前后部牙齿的磨耗程度差异不大,臼齿偏斜式磨耗现象显著,龋齿罹患率偏低。生前脱落、牙结石等口腔疾病在该人群中普遍流行,部分个体的下颌存在发育显著的骨质隆起现象。本文还通过臼齿磨耗方向指数(Wear Orientation)对加依墓地居民的偏斜式磨耗进行了量化研究,并参考相关民族学调查、考古发现以及现代医学研究成果对加依墓地居民复杂的牙齿磨耗形态和口腔疾病的成因进行了初步探讨。推测加依墓地居民的食物结构应以肉类为主,谷类亦占有一定地位;此外可能是受到恶劣生活环境及特殊谷物加工技术的影响,日常食物较为坚硬。     

新疆吐鲁番加依墓地青铜—早期铁器时代居民牙齿的磨耗

本文对新疆吐鲁番市加依墓地青铜—早期铁器时代居民的牙齿磨耗、口腔疾病和骨质隆起等特征进行了观察与研究,结果显示,加依墓地居民的牙齿磨耗较重,但前后部牙齿的磨耗程度差异不大,臼齿偏斜式磨耗现象显著,龋齿罹患率偏低。生前脱落、牙结石等口腔疾病在该人群中普遍流行,部分个体的下颌存在发育显著的骨质隆起现象。本文还通过臼齿磨耗方向指数(Wear Orientation)对加依墓地居民的偏斜式磨耗进行了量化研究,并参考相关民族学调查、考古发现以及现代医学研究成果对加依墓地居民复杂的牙齿磨耗形态和口腔疾病的成因进行了初步探讨。推测加依墓地居民的食物结构应以肉类为主,谷类亦占有一定地位;此外可能是受到恶劣生活环境及特殊谷物加工技术的影响,日常食物较为坚硬。     

东胡林4号人牙齿形态特征观察

北京门头沟区斋堂镇东胡林遗址是重要的新石器时代早期遗址。本文描述了东胡林4号人(14C年龄约为8540aBP., 树轮校正年龄约为7500aBC.) 的上颌牙、下颌牙21枚。多数牙齿重度磨耗, 意味着当时人类处于狩猎—采集经济时代, 食物结构可能主要以坚硬食物(如朴树果核) 或高纤维食物为主。上第三臼齿退化缩小, X光透视检查为东胡林人下第三臼齿阻生提供了确凿无疑的证据。在4枚牙齿上发现龋洞, 其中左上第一臼齿、第二臼齿的龋蚀已破坏牙本质全层。严重的龋齿病揭示了东胡林4号人的口腔状态, 在一定程度上可能与经常性地摄取富含碳水化合物的食物有关。     

郑州汪沟遗址仰韶文化居民的牙齿磨耗及口腔健康状况

对汪沟遗址出土的174例仰韶文化居民的2816枚牙齿进行统计与分析,计算出牙齿的平均磨耗等级和前后部牙齿磨耗差别指数,统计特殊磨耗、龋齿、骨质隆起在样本中的出现率。结果显示,汪沟组牙齿平均磨耗等级为3.403262级,男性牙齿平均磨耗等级为3.63级,女性为3.61级;男女两性牙齿磨耗差异不显著（p>0.05);前后部牙齿磨耗差别指数比达到1:1;出现26例由于深覆牙合导致的特殊磨耗;臼齿咬合面凹坑式磨耗出现率为2.50%;龋齿患病率68.97%,龋齿率26.56%,龋均4.30;骨质隆起的出现率为5.20%,颌骨粗壮程度不显著。汪沟人群的牙齿磨耗程度总体偏轻,牙齿磨耗程度与河南下王岗组居民接近。基于以上特点,我们认为中原地区仰韶文化人群在饮食结构和用牙习惯上存在一定的共性。     

甘肃结沟保德期Agriotherium的发现及其意义

本文记述了郊熊的一个新种: Agriotherium inexpetans sp. nov..这是 Agriotherium 与保德期三趾马动物群共生的首次可靠记录.新种个体小,下臼齿具有若干近祖性状:如 M_2 的下前尖和 M_3 各主尖尚可辨认等.A. inexpetans 在形态上与内蒙古通古尔中中新统发现的 Dinocyon (=Hemicyon) teilhardi 有许多相近之处.它们很可能有最直接的系统关系.作者还就这一发现对熊科分类的含义进行了讨论.     

The effect of pollen irradiation on segregation in spring barley crosses

Observations on the Ml, M2 and M3 generations from three barley crosses confirmed that pollen irradiation can cause deviations from expected segregation ratios for certain characters. The reduced fertility observed in the Ml and M2 generations of these crosses could be problematical in breeding programmes. It was of particular interest that at the highest dose rate used for the cross TS117 × Scots Bere there was no expression of the 6-row character, which is controlled by a recessive paternal factor.     

Replication of double-stranded RNA in mycovirus from the plant pathogenic fungus, Fusarium solani

Abstract A mycovirus (named FusoV) from the plant pathogenic fungus Fusarium solani possessed two types of double-stranded (ds) RNA genome, designated Ml and M2. RNA-dependent RNA polymerase activity was detected in FusoV particle fractions. An in vitro RNA polymerase reaction using purified FusoV particles that was supplemented with NTPs revealed the synthesis of single-stranded (ss) RNA species and a subsequent formation of dsRNAs having the same size as Ml and M2. The ssRNA species synthesized in the first stage were proved to be of positive polarity (coding strand) for both M1 and M2 by dot blot hybridization analysis. These results suggest that FusoV genomic dsRNA replicates in a conservative manner.     

Changes in myosin during differentiation of myeloid leukemia cells

Changes in cellular myosin were followed during the differentiation into macrophages of a myeloid leukemia cell line (Ml) which can be induced by conditioned medium (CM) from a rat embryo culture. To extract the myosin, we used three different procedures, all of which gave a lower yield of myosin for the differentiated than for the undifferentiated Ml cells. This low extractability we attributed to increased binding of the myosin to the plasma membrane. Taking the different extractabilities into consideration, we calculated the myosin contents in the total cellular protein from the densitometry of SDS-polyacrylamide electrophoresis, 0.6% for the untreated Ml cells and 1.0% for the differentiated ones. The three ATPase activities of the Ml cell myosin were in the order, K+-EDTA-=Ca2+- much greater than Mg2+-ATPase in the presence of 0.6 M KCl, whether or not there was treatment with CM. Myosin was purified through fractionation with 25-55% saturated ammonium sulfate, then gel filtration with Sepharose 4B followed by affinity chromatography on F actin-Sepharose 4B. The Ml cell myosin consists of 1 heavy chain (H) and 3 light chains (L1, L2, L3), with molecular ratios of L1 + L2/H not equal to and L3/H not equal to 1. The ratio of L1/L2 was about 1.2 for the untreated Ml cells, but it decreased to about 0.7 after differentiation.     

A phosphorylated light-chain component of myosin from skeletal muscle

1. The low-molecular-weight components of myosin from rabbit skeletal muscle migrated as four bands on polyacrylamide-gel electrophoresis in 8m-urea but only as three in systems containing sodium dodecyl sulphate. The two bands of intermediate mobility in 8m-urea (Ml(2) and Ml(3)) had identical mobilities in sodium dodecyl sulphate. 2. The isolation of pure samples of all four low-molecular-weight components by DEAE-Sephadex chromatography is described. 3. The amino acid compositions of components Ml(2) and Ml(3) were identical. Further analyses showed the presence of 1 mol of phosphate/18500g of component Ml(2) and less than 10% of this amount in component Ml(3). Neither light component contained ribose. 4. Alkaline phosphatase from Escherichia coli converted component Ml(2) into Ml(3). Incubation with crude preparations of phosphorylase b kinase or protein kinase in the presence of ATP converted component Ml(3) into Ml(2). 5. Phosphorylation of component Ml(3) with the kinases isolated from skeletal muscle and [gamma-(32)P]ATP gave incorporation of (32)P only into component Ml(2) whether whole myosin or separated low-molecular-weight components were used. 6. High-voltage electrophoresis at pH6.5 and pH1.8 of a chymotryptic digest of (32)P-labelled component Ml(2) yielded one major radioactive peptide containing serine phosphate. 7. The amino acid sequence of this peptide was shown to be: Arg-Ala-Ala-Ala-Glu-Gly-Gly-(Ser,Ser(P))-Asn-Val-Phe. This sequence shows no obvious similarity to the site phosphorylated in the conversion of phosphorylase b into phosphorylase a by phosphorylase b kinase. 8. Evidence suggests that in vivo all the 18500-molecular-weight light chain is in the phosphorylated form. The extent of dephosphorylation that occurred during myosin extraction depended on the conditions employed.     

The porcine M blood group system: evidence to suggest assignment of its Ml factor to a new system (P)

A new allele M^aejm and a more precise genetic analysis of the Ml factor previously assigned to the M system are described after screening three generation families (Wild Boar × Pietrain, Meishan × Pietrain) for the M blood group system using a complete set of 13 M reagents. From informative families with proven parental M genotypes it was shown that the Ml antigen is controlled by an allele from another system. We propose to designate this new system P and to change the factor designation from Ml to Pa.     

记陕西蓝田晚中新世灞河组4种跳鼠(Dipodidae,Rodentia)化石

描述了陕西蓝田晚中新世早期灞河组的4属4种跳鼠:蓝田原跳鼠(新种)(Protalacta- ga lantianensis sp.nov.)、副跳鼠(未定种)(Paralactaga sp.)、原始三趾心颅跳鼠(新种)(Sal- pingotus primitivus sp.nov.)和小五趾心颅跳鼠(新种)(Cardiocranius pusillus sp.nov.)。蓝田原跳鼠兼有原跳鼠和副跳鼠的特征,可能是原跳鼠向副跳鼠进化过程中产生的一种过渡类型。副跳鼠和原始三趾心颅跳鼠及小五趾心颅跳鼠分别代表了副跳鼠属在中国的最早记录和心颅跳鼠亚科(Cardiocraniinae)在地史上的首次出现。4种跳鼠指示了蓝田地区当时的自然环境可能比现代更加干旱。     

Expression of the nucleotide sequence for the M2e peptide of avian influenza virus in transgenic tobacco plants

The M2e peptide of the H5N1 A/Chicken/Kurgan/05/2005 avian influenza virus was successfully synthesized in transgenic tobacco plants. The amino-terminal segment of the M2 protein, comprised of 22, 30, or 43 amino acids, including the M2e peptide (M122, M130, and M143 variants, respectively), was translationally fused with the N-terminus of β-glucuronidase in the pBI121 plant expression vector. The nucleotide sequence of the target fragment was synthesized by ligation from synthetic oligonucleotides; its codon composition was adapted for expression in plants. Tobacco plants were successfully transformed with the obtained vectors (pBIM122, pBIM130, and pBIM143, respectively). In the plants transformed with pBIM143, the Ml43-β-glucuronidase fusion protein was not produced, probably due to the presence of the M2 protein transmembrane domain (25–43 aa of M2) in this construct. In the pBIM122- and pBIMl30-transformed plants, the target M2e peptide was expressed as a component of the Ml22-β-glucuronidase and M130-β-glucuronidase fusion proteins, respectively, as was detected by Western blot analysis. These proteins were detected as bands of the expected size without apparent degradation. As a result, the M2e peptide of the H5N1 avian influenza virus was successfully synthesized for the first time in nuclear-transformed transgenic plants. The results obtained in this study will be used for developing a transgenic plant-based edible antiinfluenza vaccine.     

球孢白僵菌对油桐尺蛾的生物效力（英文）

分别在2005年和2006年的5、6月份,在Kamalpur和Hunterpara茶园、孟加拉西部以及印度地区对一种昆虫致病真菌球孢白僵菌对油桐尺蛾Buzura (=Biston) suppressaria Guen.的生物效力进行了评估。以农场主常用的化学杀虫剂40% SP灭多虫和25% EC氯氰菊酯作为标准检测物。试验中球孢白僵菌浓度为1.50 g,2.00 g和2.5 g/lit. of water;灭多虫和氯氰菊酯浓度分别为0.75 mL,1.00 mL和1.50 mL,和0.50 mL,1.00 mL和1.50 mL/lit. of water。在喷洒2.5 g/lit. of water 球孢白僵菌3天后,Kamalpur和Hunterpara茶园中油桐尺蛾种群个体数分别降低了88.00%和84.00%。死的毛虫变成黑色,垂悬在叶片上。并且发现球孢白僵菌的杀虫活性与高剂量的灭多虫和氯氰菊酯的相当。     

Acetylation of a fucosyl residue at the reducing end of Mesorhizobium loti nod factors is not essential for nodulation of Lotus japonicus

NodMl-V(C(18:1), Me, Cb, AcFuc) is a major component of lipo-chitin oligosaccharides (LCOs), or Nod factors, produced by Mesorhizobium loti. The presence of a 4-O-acetylated fucosyl residue (AcFuc) at the reducing end has been thought to be essential for symbiotic interactions with the compatible host plant, Lotus japonicus. We generated an M. loti mutant in which the nolL gene is disrupted; nolL has been shown to encode acetyltransferase that is responsible for acetylation of the fucosyl residue. The nolL disruptant Ml107 produced LCOs that lacked acetylation of fucosyl residues as expected, but exhibited nodulation performance on L. japonicus as efficiently as the wild-type M. loti strain MAFF303099. We show that LCOs without acetylation of a fucosyl residue purified from Ml107 are also able to induce abundant root hair deformation and nodule primordium formation. These results indicate that NolL-dependent acetylation of a fucosyl residue at the reducing end of M. loti LCOs is not essential for nodulation of L. japonicus.     

Regulation of prostaglandin synthesis during differentiation of cultured mouse myeloid leukemia cells

Mouse myeloid leukemia cells (Ml) were induced to differentiate into mature macrophages and granulocytes by various inducers. The differentiated Ml cells synthesized and released prostaglandins, whereas untreated Ml cells did not. When the cells were prelabelled with [¹⁴C]arachidonate, the major prostaglandins released into the culture media were found to be prostaglandin E₂, D₂, and F_2α in an early stage of differentiation, but the mature cells produced predominantly prostaglandin E₂. The synthesis and release of prostaglandins were completely inhibited by indomethacin. Dexamethasone, a potent inducer of differentiation of Ml cells, did not induce production of prostaglandins in resistant Ml cells that could not differentiate even with a high concentration of dexamethasone. These results suggest that production of prostaglandins in Ml cells is closely associated with differentiation of the cells. Homogenates of dexamethasone-treated Ml cells converted arachidonate to prostaglandins, but this conversion was scarcely observed with homogenates of untreated Ml cells. Dexamethasone and the other inducers stimulated the release of arachidonate from phospholipids. Therefore, induction of prostaglandin synthesis during differentiation of Ml cells may result from induction of prostaglandin synthesis activity and stimulation of the release of arachidonate from cellular lipids. Lysozyme activity, which is a typical biochemical marker of macrophages, was induced in Ml cells by prostaglandin E₂ or D₂ alone, as well as by inducers of differentiation of the cells, but it was not induced by arachidonate or prostaglandin F_2α. These results suggest that prostaglandin synthesis is important in differentiation of myeloid leukemia cells.