中国典型草原放牧草场蝗虫为害损失及经济阈值的估算(英语)

传统上估算蝗虫在放牧草场为害损失的方法几乎都是用来测定对牧草秋季产量的影响,而实际上,在估算放牧草场蝗虫为害损失及经济阈值时,牧草的现存量而非秋季产量是更应考虑的因素.本文提出了一种适合测定蝗虫对牧草现存生物量影响的新方法,即野外挂笼饲养与蝗虫种群动态相结合的估算方法,并在此基础上组建了放牧草场蝗虫种群经济阈值模型;α_0 α_1M_1_α_2M_2_ α_3S_1 α_4S_2=C其中,M_1:狭翅雏蝗生物量;M_2:宽须蚁蝗生物量;S_1:狭翅雏蝗平均个体重量,S_2:宽须蚁蝗平均个体重量;α_0-α_4:常数.同时引入蝗虫种群数量和生物量两项参数来表达蝗虫种群的发生程度.     

野生紫斑牡丹和四川牡丹种子萌发特性及与其致濒的关系

野生牡丹种子一般较小,而且不同产地之间形状、大小差异较大。其萌发特性与栽培牡丹相比也有较大差异：萌发期长达半年以上,且萌发温度在１０～１５℃为宜,超过２０℃则明显不利于生根及上胚轴生长。四个不同分布地的四川牡丹种子萌发率较一致,均在６０～７７％之间。三个不同产地的紫斑牡丹种子萌发率则相差甚远,分布于甘肃文县的萌发率达７６％,而分布于陕西略阳和湖北神农架的萌发率则分别只有１２％和４．４％,出苗率则更低。本文认为紫斑牡丹的种子特性是其在自然界处于濒危状态的重要原因之一。     

杉木、台湾杉、香杉逐步判别分析

通过对杉木、台湾杉、香杉２２个种源的叶长、叶宽、叶厚、维管束的宽与厚、栅栏组织厚、机械组织厚、表皮厚和气孔数等９个叶性状进行逐步判别分析,选取栅栏组织厚（Ｘ＿６）、叶长（Ｘ＿１）和叶厚（Ｘ＿３）三个重要因子,建立优化判别方程：Ｆ＿１（台湾杉）＝－２３５．８７１４＋１７．３１０４Ｘ＿６＋２６．３５８７Ｘ＿１＋５．９０４６Ｘ＿３Ｆ＿２（杉木）＝－５６４．９２５９＋７８．４２５４Ｘ＿６＋９３．１９２３Ｘ＿１＋０．６２９５Ｘ＿３Ｆ＿３（香杉）＝－３４９．４２０５＋６４．１９２６Ｘ＿６＋６２．６４７９Ｘ＿１＋０．８９６９Ｘ＿３定量地区分这三个树种,旨在对逐步判别分析法在树种分类上的应用进行探讨。     

Nanometric design of extraordinary hydrophobic-induced pKa shifts for aspartic acid: Relevance to protein mechanisms

Commonly a key element enabling proteins to function is an amino acid residue or residues with functional side chains having shifted pKa values. This article reports the results on a set of protein-based polymers (model proteins) that exhibit hydrophobic folding and assembly transitions, and that have been designed for the purpose of achieving large hydrophobic-induced pKa shifts by selectively replacing Val residues by Phe residues. The high molecular weight polypentapeptides, actually poly (tricosapeptides) with six varied pentamers in fixed sequence, were designed and synthesized to have the same amino acid compositions but different proximities between a single aspartic acid residue and 5 Phe residues per 30 residues. With the 5 Phe residues distal from the Asp residue, the observed pKa shift was 2.9 when compared to the Val-containing reference. With the 5 Phe residues within 1 nm of the Asp residue, the pKa shift was 6.2. This represents a free energy of interaction of 8 kcal/moles. To our knowledge, this is the largest pKa shift documented for an Asp residue in a polypeptide– or protein–water system. Data are reviewed that do not support the usual electrostatic arguments for pKa shifts of charge–charge repulsion and/or unfavorable ion self-energies arising from displacement of water by hydrophobic moieties, but rather the data are interpreted to indicate the presence of an apolar–polar repulsive free energy of hydration, which results from a potentially highly cooperative competition between apolar and polar species for hydration. © 1994 John Wiley & Sons, Inc.     

Differential expression inArabidopsis ofLhca2, a PSI cab gene

A cDNA clone of the geneLhca2 encoding a photosystem I (PSI) type II chlorophylla/b-binding protein was isolated fromArabidopsis thaliana. The isolation of this, the fourth PSI cab gene fromArabidopsis, confirms a previous report [1] that indicatedArabidopsis may contain all four PSI cab genes identified in other plant species.Lhca2 is a single-copy gene as are the other knownArabidopsis PSI cab genes. The patterns of developmental expression and tissue-specific regulation ofLhca2 are similar to those of other PSI and PSII cab genes, but the light induction pattern and the steady-state mRNA level ofLhca2 are distinct. This suggests that a different mechanism may be employed to regulate the expression ofLhca2.     

Expression and characterization of virus-like particles containing rubella virus structural proteins.

Rubella virus (RV) virions contain two envelope glycoproteins (E1 and E2) and a capsid protein (C). Noninfectious RV-like particles (VLPs) containing three structural proteins were expressed in a BHK cell line (BHK-24S) by using an inducible promoter. These VLPs were found to resemble RV virons in terms of their size, their morphology, and some biological activities. In immunoblotting studies, VLPs were found to bind similarly to native RV virions with 10 of a panel of 12 RV-specific murine monoclonal antibodies. Immunization of mice with VLPs induced specific antibody responses against RV structural proteins as well as virus-neutralizing and hemagglutination-inhibiting antibodies. After immunization of mice with VLPs, in vitro challenge of isolated lymphocytes with inactivated RV and individual RV structural proteins stimulated proliferation. Our data suggest the possibility of using VLPs as immunogens for serodiagnostic assays and RV vaccines.