中条山油松人工林下物种对群落物种丰富度分布格局的贡献

该研究以中条山油松人工林群落为研究对象,研究林下不同大小的子群落对群落物种丰富度分布格局的贡献,并确定影响该区域群落物种丰富度分布格局的关键种,为区域物种多样性保护提供理论依据。结果表明:(1)该地区林下物种频度分布格局呈明显右偏,且不同样方物种丰富度存在明显差异。(2)常见种对群落丰富度分布格局的贡献大于稀有种。(3)最常见的物种解释了整个群落物种丰富度格局的88.4%(P0.01),而最稀有物种仅解释了24.5%(P0.05),去除最稀有物种后,最常见物种可以解释剩余物种的90.8%(P0.01),而去除最常见物种后,最稀有物种仅能解释剩余物种的48.6%(P0.01)。(4)当子群落中常见种越多时,子群落与整个群落的丰富度分布格局相关性越高。(5)连翘(Forsythia suspensa)、太平花(Philadelphus pekinensis)、鞘柄菝葜(Smilax stans)、多歧沙参(Adenophora wawreana)、金花忍冬(Lonicera chrysantha)等对群落物种丰富度分布格局的贡献最大,但并非越常见的物种对群落丰富度格局贡献越大。(6)与频度较高物种的种间关联度低的物种对于群落物种的分布格局贡献较大,但此解释并不适用于稀有种。研究发现,稀有种对中条山油松人工林群落物种丰富度分布格局存在较大的贡献,所以在油松人工林物种多样性保护过程中并不能只关注常见种而忽视稀有种。     

地塞美松中间体的C1,4脱氢和11α-羟基化

地塞美松 (Ｄｅｘａｍｅｔｈａｓｏｎｅ)为高效肾上腺皮质激素药物 ,临床上广泛使用。开拓用梯可吉宁 (Ｔｉｇｏｇｅｎｉｎ)为起始原料生产从化学结构和合成技术上讲较为合理 ,而且适合于资源综合利用[1] 。在合成过程中 ,除了Ａ环需引入Ｃ1,2 和Ｃ4 ,5两个双键 (含Ｃ-3 羟基氧化 )外 ,还需用微生物法在Ｃ-11位引入羟基。国外常采用化学法脱氢 ,然后再用霉菌 11α 羟基化[2 ,3 ] 。本文报道用两类微生物菌种 ,节杆菌 (Ａｒｔｈｒｏｂａｃｔｅｒｓｐ .)ＡＸ86和绿僵菌 (Ｍｅｔａｒｈｉｚｉｕｍｓｐ .)Ｍ 88,混合转化一步完成脱氢和羟基化反应…     

甾体1，4-脱氢和11α-羟基化反应的两种不同微生物转化

Two kinds of micro-organism, Arthrobacter sp. AX86(1,4-dehdrogenator)and Absidia sp. A28(11α-hydroxylator) were used in this experiment. Two different fermentation techniques were performed to accomplish the multiple conversional reactions for producing 16β-methyl-11α, 17α, 21-trihydroxy-1,4-pregnadiene-3,20-dione (Ⅲ) from 16β-methyl-3β, 17α,21-trihydroxy-5α-pregnane-20-one-21-acetate(1) 1)To produce product(Ⅲ)by means of a two-step fermentation method which were independently performed first by Arthrobacter and next by Abslaia, and 2)the product was obtained by a sequential fermentation system of aforesaid two micro-organisms in a single fermentor without isolation of the intermediates from the mixture. Our results showed that in both fermentation systems high yield of product was obtained. However, according to the technical simplicity, shorter duration of fermentation cycle and efficient yield of product, the second method is better than the first one.     

Characterization of IL-2 receptor expression and function on murine macrophages

This study was designed to examine the expression and function of IL-2R on murine macrophages. We used a model system of murine macrophage cell lines (ANA-1 and GG2EE) that was established by infecting normal murine bone marrow-derived cells with the J2 (v-raf/v-myc) recombinant murine retrovirus. ANA-1 macrophages did not constitutively express detectable levels of mRNA for the p55, IL-2R alpha. However, a brief exposure to IFN-gamma was sufficient to induce IL-2R alpha mRNA in ANA-1 macrophages. Flow cytometric analysis indicated that ANA-1 macrophages expressed low constitutive levels of IL-2R alpha on their cell surface that were augmented after treatment of the cells with IFN-gamma. Affinity binding and cross-linking of [125I]IL-2 to ANA-1 macrophages demonstrated that IL-2R alpha and the p70-75, IL-2R beta were both present on ANA-1 macrophages constitutively. IFN-gamma increased the expression of IL-2R alpha on ANA-1 macrophages but did not increase the expression of IL-2R beta on these macrophages. Although IL-2 alone did not induce the tumoricidal activity of ANA-1 macrophages, IL-2 acted synergistically with IFN-gamma to induce macrophage tumoricidal activity. These data demonstrate the expression of IL-2R on murine macrophage cell lines and establish the role of IL-2 as a costimulator of macrophage-mediated tumoricidal activity.     

MORPHOLOGICAL VARIATION WITHIN AND BETWEEN NATURAL POPULATIONS OF NON-TIDE POOL FUCUS DISTICHUS (PHAEOPHYTA) IN NEW ENGLAND1,2

The sources of morphological variation in natural populations of Fucus distichus L. ssp. edentatus (De la Pyiaie) Powell and F. distichus L. ssp, evanescens (C. Agardh) Powell from New England were evaluated. Individuals from different populations were morphologically distinct as judged by population means and analysis of variance. A correlation between the plant's form and its habitat was established by field observation. The broadest material grows in calm estuarine habitats, while the narrowest plants occur in exposed, open coastal areas. Major differences in morphology also appear seasonally. In addition, microhabitat factors such as exposure to wave action and elevation explain some morphological variation. Cultured germlings from distinct populations of “evanescens” and “edentatus” type plants were outplanted to an experimental garden in order to ascertain whether the variation was heritable or environmentally induced. The latter experiments indicate that major differences in morphology are genetically determined.     

The growth,reproductive phenology,and longevity of non-tide-pool Fucus distichus (L.) powell in New England

The growth, reproductive phenology, and longevity of in situ populations of Fucus distichus L. ssp. edentatus (De la Pylaie) Powell and F. distichus L. ssp. evanescens (C. Agardh) Powell were evaluated in New England. Both subspecies exhibited maximum growth during early summer, a slight decline in late summer, and a brief resurgence in the early fall. The maximum growth rates (in terms of elongation) for F. distichus ssp. edentatus and ssp. evanescens were 3.5 and 3.7 cm/28 days, respectively. Populations of both subspecies showed a distinct bimodal reproductive periodicity, with maxima in the spring and fall. Even so, individuals were either reproductive in the spring or fall but never in both seasons. After reproduction, receptacles dehisced and plants either became vegetative or died. Higher rates of plant attrition were observed during periods of reproduction than during non-reproductive periods.     

The interaction of calcium and magnesium ions with deoxyribonucleic acid.

Conductance and equilibrium dialysis studies are reported for the aqueous systems (native calf thymus) DNA-CaCl₂ and DNA-MgCl₂ at various pH values and ionic strengths at 25 °C. Discontinuities occur in the conductance curves at mole ratios of Ca²⁺ and Mg²⁺ to nucleate phosphorus of 0.125, 0.30, and 0.50. The dialysis results show the formation of complexes of stoichiometry 0.50 and 1.00 mol Ca²⁺ or Mg²⁺/mol nucleate phosphorus (2:1 and 1:1 complexes), the latter only in neutral or alkaline solutions, in agreement with the conductance discontinuity at 0.50. The other discontinuities may be due to preferential binding in the formation of the 2:1 complex. Binding constants for the 2:1 complexes are evaluated. Absorption-temperature profiles have been determined for “native” and dialysed DNA in the presence of NaCl, CaCl₂, and MgCl₂. For dialysed DNA at 26 ° C and 260 nm the decrease of absorbance with increased salt concentration was halted for MgCl₂ and CaCl₂ at a concentration corresponding to the formation of the 2:1 complex. The absorbance of “native” DNA did not decrease. T_m and the reciprocal of the hypochromic rise ($\text{1}\text{h}$) increased linearly with log (salt concn). Values of T_m were the same at 230, 260, and 280 nm, but h was greater at 230 and 280 than at 260 nm, which may be due to the existence of alternating blocks of (A + T) and (G ? C) pairs. The entropy of transition was in the order Ca > Mg ? Na.