基于SRP模型的南雄丹霞梧桐自然保护区生态脆弱性评价

通过建立生态敏感性-生态恢复力-生态压力度（SRP）模型，利用主成分分析法确定指标权重，对南雄丹霞梧桐自然保护区进行生态脆弱性评价。结果表明:1）从生态敏感性角度，研究区高度脆弱和极度脆弱面积分别为756.50 hm²和773.58 hm²，占比之和>50%，主要集中分布于北部和中部，而主要影响要素为土壤侵蚀强度，其次为距水源距离；2）从生态恢复力角度，研究区不脆弱和轻度脆弱面积分别为777.71 hm²和676.73 hm²，占比之和>50%，主要集中分布于西部和西南部，主要影响要素为生物多样性，其次为植被覆盖度；3）从生态压力度角度，研究区不脆弱和轻度脆弱面积分别为551.33 hm²和1 205.12 hm²，占比之和>60%，主要集中分布于西部及东部，而主要影响要素为GDP密度和人口密度；4）研究区整体生态脆弱性较高，中度及以上脆弱性面积之和达到67.72%，主要集中于研究区的中部和北部，其中生态敏感性对生态脆弱性的影响最大，说明研究区整体生态脆弱性较强，应做好生态保护工作。     

Effects of Benzyl Adenine and Abscisic Acid on Grain Yield and Yield Components in Triticale and Wheat

Grain yield and yield components (grains per ear, grain weight, 1000-grain weight, ear weight, ear seed ratio and dry matter partitioning between ear and seed) were examined in a wheat genotype (PBW-343) with well-filled grains and a Triticale genotype (DT-46) with poorly filled grains (showing grain shrivelling) grown in pots. Six days after anthesis (DAA), benzyladenine (BA) @2 µg ear⁻¹ and abscisic acid (ABA) @4 µg ear⁻¹ were injected at the base of the mother shoot ear in both species. It was observed that, in both wheat and Triticale , BA increased the grain weight, grain number and partitioning of dry matter between ear and seed, whereas ABA decreased the grain weight, grain number and dry matter partitioning between ear and seed. However, these decreases were slower in Triticale than in wheat. BA treatment increased the grain dry matter accumulation, which in turn resulted in better filling of grains and increased the grain weight in both wheat and Triticale . The average grain weight of Triticale was lower than that of wheat. Thus, it appears that variation in grain weight between wheat and Triticale might be due to different availabilities of growth-promoting phytohormones such as cytokinins and assimilates.     

一种电流模式多功能滤波器结构

提出了一种简单的电流模式多功能滤波器结构，具有一个输入端和三个输出端，可以实现低通，高通，带通，全通和陷波功能，不需要任何严格匹配关系，该结构中使用了６个ＣＣ器件，两个接地电阻和两个接地电容，结构十分简单且无源灵敏度很低。     

Photosynthate Unloading from Seed Coats of Phaseolus vulgaris L. an Attempt to Define Conditions Required for Stimulation by Abscisic Acid and Benzylamino Purine

The instablity of the stimulation of photosynthate unloading from seed coats of Phaseolus vulgaris by abscisic acid (ABA ) and benzylamino purine ( BAP ) was studied in terms of experimental conditions. ABA stimulated photosynthate unloading at pH 6 and pH 8 without close dependence upon pH. ABA at a concentration range of 10-5-10-4 mol/L displayed stimulatory effect. However, BAP revealed no effect at a concentration range of 10-6-10-4 mol/L. Experiments designed with different transport time of 14C-photosynthate indicated that ABA might act at the plasma membrane of the unloading cells. Reducing endogenous ABA level by diminishing leaf area did not facilitate the manifestation of exogenous ABA function. Potassium ion stimulated photosynthate unloading from seed coats with highest promotion at 100 mmol/L K . However, no dependence of ABA stimulation of photosynthate unloading on K was found.     

柑桔授粉处理和单性结实子房（幼果）内源IAA,ABA和ZT含量的变化

广橙在授粉后３天内即完成受精，与未授粉子房相比，授粉子房迅速膨大，授粉处理可使内源ＩＡＡ、ＡＢＡ和ＺＴ水平急剧上升，尤其是在处理后的前３天。至第４天趋平缓。以每子房ｎｇ含量计，至处理后第３天，ＩＡＡ、ＡＢＡ和ＺＴ含量分别是处理开始时的６．８、５．２和４．１倍，而未授粉的分别为２．５、２．６和１．２倍，这种变化与子房（幼果）的发育密切相关。试验还分析了广橙授粉处理与内源激素平衡关系，发现授粉处理ＡＢ     

福建土壤对酸沉降的相对敏感性评价与区划

选择母岩、土壤类型、土地利用和降雨量 4个生态因子 ,应用半定量化方法对其进行类目划分和权重 ,综合评价了福建省土壤对酸沉降的相对敏感性 ,并应用地理信息系统进行了区划 .由于福建省风化缓慢的硅质岩所占的比例较大 ,土壤大多呈酸性至微酸性反应 ,降水丰富 ,加之针叶林面积大 ,所以全省有 60 %以上面积的土壤显示出较大的敏感性等级 (5～ 7级 )     

Sensitivity,specificity, and predictive values of reagent test strip estimations of blood urea nitrogen

Azostix-reagent-tests(R) strips (Ames, Miles, Inc., Diagnostic Division, Elkhart, IN) were used to measure blood urea nitrogen values in blood samples from 125 dogs and cats at the North Carolina State University, College of Veterinary Medicine. Results of the tests were compared with standard serum urea nitrogen results. Sensitivity, specificity, and negative predictive values were high (86.4, 90.3, and 96.5%, respectively). Positive predictive value was low, 65.5% of the dogs and cats with elevated blood urea nitrogen values were correctly classified as abnormal The test performs well when the prevalence of abnormal values is near 50%.     

外源Ca2+ 和ABA 对高温下黄瓜花药中Ca2 + 、ABA及蛋白质合成的影响

 外源Ca^{2 +}能降低高温下黄瓜单核期花药的胞内Ca^{2 +}水平并提高花粉萌发率, 而ABA的作用与此相反。外源Ca^{2 +}和ABA处理能显著提高高温下黄瓜花药内源ABA的水平, 并产生新的蛋白质。以上结果表明, 高温下外源Ca^{2 +}可影响黄瓜花药内ABA信号系统, 继而可能改变基因表达, 并获得耐热性;外源ABA亦能影响黄瓜花药内Ca^{2 +}信号系统。     

苹果采前落果与内源激素的关系

为了探讨苹果采前落果与内源激素之间的关系,在采前8周间定期测定了不同苹果品种的果柄、果台和离层形成部位组织中IAA、ABA含量;在采收前20d内定期测定了离层部位组织中细胞壁分解酶(Cellulase)的活性;在收获期测定了果实乙烯的发生量。结果表明:不同品种果柄、果台和离层部位组织中IAA和ABA含量变化有差异,但它们变化的总趋势相似,都是随着果实成熟IAA含量下降,而ABA含量上升;不同品种的成熟果实中乙烯发生量有很大差异,以落果多的品种显著大于落果少的品种;采前落果重的品种离层部位组织中细胞壁分解酶的活性在果实成熟期急剧增加。由于果实进入成熟阶段后,IAA含量下降,ABA含量升高,ABA/IAA之间的相对平衡被打破,高ABA/IAA以及高乙烯会刺激离层组织中细胞壁分解酶的活性增高,进而促进离层形成,这可能是导致落果发生的原因。     

Bcl-2 antisense oligodeoxynucleotide increases the sensitivity of HL60 and K562 cells to daunorubicin

AIM:To investigate whether the bcl-2 antisense oligonucleotide increases the sensitivity of HL60 and K562 cell lines to daunorubicin.METHODS:IC50 for HL60 and K562 was determined with MTT method, the expression levels of Bcl-2 protein were assayed by immunofluorescence using fluoresce isothiocyanate labeling. In addition, apoptosis was detected by morphological observation and flow cytometric analysis of DNA fragmentation.RESULTS:It was found that the two oligonucleotides directed against the coding region and the translation initiation of bcl-2 mRNA, combined respectively with daunorubicin, inhibited expression of bcl-2 protein, increased apoptosis in HL60 and K562 cells, and decreased IC50 of daunorubicin significantly (P＜0.05). Compared to the antisense oligonucleotide directed against the translation initiation of bcl-2 mRNA, the antisense oligonucleotide directed against the coding region showed stronger effects in the aspects of increasing the sensitivity of HL60 cells to daunorubicin (P＜0.05).CONCLUSIONS:These two antisense sequences in the translation initiation and the coding region of bcl-2 mRNA increased the sensitivity of HL60 and K562 cell lines to daunorubicin in a sequence-specific manner.