大熊猫臼齿釉质的超微结构和氨基酸组成

大熊猫臼齿釉质的超微结构特征主要是施氏明暗带的宽度一般由8—15条釉柱组成;釉柱的横切面一般呈六角形或四角形,由里向外,釉柱的直径逐渐增大。在靠近釉牙本质界处,釉柱数量逐渐减少,有时甚至完全缺失,形成无釉柱结构的釉质。大熊猫臼齿釉质的氨基酸组成主要以甘氨酸,丙氨酸,谷氨酸,天冬氨酸和亮氨酸的含量为最高,而蛋氨酸,胱氨酸和酪氨酸的含量为最低。另外,还含有少量的羟脯氨酸。这种组成模式一般与人类和其它哺乳动物牙齿釉质的氨基酸组成相类似。     

植物群落种群分布格局研究的新方法

本文给出一种研究植物群落种群分布格局的新方法。该方法与英国著名生态学家Greig-Smith提出的“邻接格子样方法”相比较,具有如下优点: 1.用计算机算出的结果,具有令人满意的精度。当计算完毕后,机器能打印输出植物种群斑块大小、斑块在样地平面上分布的状况,样地上某种植物斑块的总面积,种群个体的总数等有关信息。 2.适用于天然植物群落种群分布格局的研究。 本文讨论了处理数据时采用的计算公式,所依据的数学原理以及如何确定输出界限(舍入界限)等问题。 此外,文中还叙述了用该法对随机相嵌几何斑块图形,人工模拟草地样方进行处理的过程和计算结果分析。 源程序是用BASIC语言编制的。     

Histogenesis of the pituitary in rainbow trout (Salmo gairdneri) in different ambient salinities with particular reference to the rostral pars distalis

Summary The pituitary gland is first evident in rainbow trout two weeks before hatching. Differentiation of prolactin and ACTH cells is not marked until 3–4 days after hatching when the follicular arrangement of the prolactin cells become apparent. There is no difference in the time of development of either prolactin or ACTH cells in larvae reared in different ambient salinities despite marked changes in tissue ion and water content. This suggests that prolactin and ACTH do not play the osmo- and iono-regulatory roles in larval rainbow trout that they are considered to play in adult salmonids.The work was supported by a grant-in-aid of research from the National Research Council of Canada     

Regulation of the synthesis of human chorionic gonadotropin by strains of HeLa cells in culture

Summary Thirty-seven strains of HeLa cells were examined for their ability to synthesize human chorionic gonadotropin (hCG) and its alpha subunit (hCG-α) in culture. Synthesis of hCG-α and hCG also was investigated in the presence of sodium butyrate and 5-bromo-2′-deoxyuridine (BrdUrd). All HeLa strains synthesized hCG-α in culture. Sodium butyrate increased the synthesis of hCG-α in all HeLa cells; BrdUrd increased synthesis in 32 of the 37 strains examined. Although few HeLa strains synthesized hCG in the absence of inducers, hCG was detected in most strains in the presence of sodium butyrate. The synthesis of hCG and its alpha subunit is, therefore, a stable genetic characteristics of HeLa cells. Certain preparations of hCG and its subunits were generously provided through the Center for Population Research of the National Institute of Child Health and Human Development, NIH.     

The peritrophic membrane in adult simuliids (Diptera) before and after feeding on blood and blood-sucrose mixtures

A peritrophic membrane formed in the posterior midgut of female simuliids of seven species within 30 min of feeding on blood of various avian or mammalian hosts, and 6–12 hr thereafter it displayed up to seven concentric laminae. Within the first 48 hr of blood digestion, the posterior part of the peritrophic membrane (where digestion was most advanced) began to decompose and PM disappearance was complete at the end of blood digestion. In different species blood digestion at 18°–20° required 120–180 hr which was increased to over 200 hr by microsporidan infection. If a blood-sucrose mixture went directly to the midgut, a thin membrane formed around it, but not if it went indirectly by way of the crop. A prefeeding secretion in the anterior midgut is considered to be the peritrophic membrane of the pharate adult surrounding a small, but variable, amount of material, the meconium.

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Résumé Sept espèces de simulies ont été étudiées: 5 ornithophiles, 2 mammalophiles. Trente minutes après un repas de sang sur divers oiseaux (poulet, canard) ou mammifères (homme, cerf, élan d'Amérique) on constate qu'une membrane péritrophique est sécrétée par toute le surface épithéliale dans la région moyenne de l'intestin moyen postérieur dilaté des femelles. Six à douze heures après le repas cette membrane comporte jusqu'à sept lamelles concentriques. Une sécrétion moins importante se forme autour de la petite quantité de sang que l'on trouve dans l'estomac antérieur, non dilaté et étroit; cette sécrétion glisse vers l'arrière et forme une capsule recouvrant le pôle antérieur du bol alimentaire sanguin dans la partie postérieure de l'intestin moyen, ceci pendant le premier jour. La digestion commence à la périphérie et à l'extrémité postérieure de la masse sanguine et se poursuit enfin à l'extrémité antérieure, où la membrane péritrophique conserve le plus longtemps sa structure en contact avec le sang non digéré. Dans les premières 48 heures de la digestion du sang, la région postértieure de la membrane péritrophique (là où la digestion est la plus avancée) commence à se décomposer, et sa disparition est complète quand la digestion du sang est achevée. Chez les différentes espèces étudiées, la digestion du sang à 18–20° exige 120–180 heures, pouvant demander plus de 200 heures chez des insectes atteints d'une infection par des microsporidies. Si un mélange de sang et sucrose parvient directement dans la région moyenne de l'intestin moyen, une membrane mince se forme autour, mais non si cet aliment passe par le jabot. Une sécrétion précédant l'alimentation s'observe dans l'intestin moyen antérieur des mouches non nourries et doit représenter, chez l'adulte venant d'éclore, la membrane péritrophique entourant le méconium: petite quantité de matière d'importance variable. Cette matière se retrouve souvent au centre de la masse sanguine après alimentation et est lente à digérer.

     

A four-iron, four-sulfide ferredoxin with high thermostability from Clostridium thermoaceticum.

A ferredoxin containing only one [Fe4S4] cluster was purified from Clostridium thermoaceticum. It has a molecular weight of about 7,300, a partial specific volume of 0.67, and an isoelectric point of 3.25. Its absorption spectrum has two maxima at 390 nm (epsilon = 16.8 X 10(3)M-1cm-1) and at 280 nm (epsilon = 24.2 X 10(3)M-1cm-1). The absorption at 390 nm is almost half that of other clostridial ferredoxins, which have two [Fe4S4] clusters, and is similar to other ferredoxins with only one [Fe4S4] cluster. The ferredoxin had high thermal stability and retained over 50% of its activity after treatment at 80 degrees C. It functions in the transfer of electrons from pyruvate to nicotinamide adenine dinucleotide phosphate (NADP), which indicates the presence of pyruvate:ferredoxin oxidoreductase and reduced ferredoxin-NADP reductase in C, thermoaceticum. NADPH is used in the synthesis of acetate from CO2 in this organism.     

Suppression of IgE antibody production in SJL mice. II. Expression of Ly-1 antigen on helper and nonspecific suppressor T cells.

Under appropriate conditions of immunization combined with irradiation, SJL/J mice show a high and persistent anti-DNP IgE antibody response. Spleen cells transferred from normal untreated SJL mice suppress this response. Elimination of Ly-1+ cells, but not of Ly-2+ cells, abolished the capacity of spleen cells to suppress the IgE response. Thus of the three T cell Ly subclasses presently identified, Ly-1, Ly-2,3, and Ly-1,2,3, the normal SJL spleen cell which suppresses the IgE response of irradiated-immunized SJL mice belongs to the Ly-1 set. It is not known whether this Ly-1 cell suppresses the IgE response directly or by helping another cell in the recipient. The carrier-specific helper cell activity for IgE and probably IgG1 antibody response belongs to Ly-1 subclass in the SJL strain also.     

Select growth of human T lymphocytes in single phase semisolid culture.

Selective growth and clonal proliferation of human T lymphocytes can be achieved by using a single-phase semi-solid methylcellulose system without the requirement of preincubation with lectins. Significant proliferation, however, depends upon the continued presence of Con A or PHA, but not pokeweed mitogen or lipopolysaccharide within the methylcellulose. This procedure eliminates nonspecific agglutination by lectins and allows for direct visualization of colonies and their specific removal and subsequent cloning in liquid phase. Optimal growth and production of colonies greater than 40-cell size require 3 to 9 days. Individual cells can be identified on the basis of E rosette formation and absence of surface immunoglobulin or ability to phagocytize latex particles. Moreover, proliferation is inhibited by antithymocyte but not anti-B cell sera and can be demonstrated with peripheral blood T and MOLT-4 cells, but not with B or Raji cells. Finally, colony formation is not enhanced by the presence of 2-mercaptoethanol. The clonal proliferation of human T lymphocytes has wide application in the study of both antigen recognition and lymphocyte alterations in specific diseases.