黑荆树单宁浸取技术的研究

采用分段浸取新工艺是黑荆树皮单宁提取的关键技术。即以平转型连续最提为常压段、以水平渗滤（进、出）垂直釜为加压段，经生产考核，其工艺先进、运行可靠、经济合理、操作简便，产品质量稳定。     

一种新型微生态保健品在兽医临床中的应用研究

利用一种微生态保健品和3种抗菌素药物，即氟哌酸、氯霉素、庆大霉素在兽医临床上用于治疗仔猪黄白痢，断奶猪的应激性腹泻，肥猪及母猪的腹泻作了对比试验，结果表明：微生态保健品对仔猪黄痢的治愈率为93％，对仔猪白痢的治愈率为95％，对断奶仔猪的应激性腹泻治愈率为94％，对肥猪及母猪的腹泻治愈率为100％。与氟哌酸、庆大霉素的疗效比较，差异显著（P＜0．05）；与氯霉素比较差异极显著（P＜0．01）．     

桃需冷量遗传特性的研究

对桃的９个杂交组合４６３株杂种实生苗需冷量进行测定,统计结果表明：桃需冷量是由多基因控制的,Ｆ＿１需冷量平均值较亲中值短,不同组合偏离程度不同,南山甜桃、红日、玛丽维拉、白凤、大久保需冷量育种值分别为１５９、２１６、３１９、８３１、８３４ｈ,遗传传递力分别为７９%、５４%、９２%、８３%、９３%。需冷量的遗传力为８９．６９%。萌芽开花与需冷量密切相关。     

大肠杆菌耐热性肠毒素ST1—K99／LacZ基因重组的研究

将构建的ｐＢＳＴ２～６工程菌质粒用限制性内切酶ＢａｍＨＩ／ＢｇｌⅡ酶切，经琼脂糖凝胶电泳和电洗脱，回收１４７ｂｐ的目的ＳＴ１基因。随之将该基因分别重组到能有效表达Ｋ９９菌毛抗原和ＬａｃＺ酶的ｐＧＫ９９之Ｋ９９基因ＢｇｌⅡ位点和ｐＵＣ１８的ＢａｍＨＩ位点中。通过ＳＴ１基因探针菌落原位杂交、特定酶切分析及ＤＮＡ序列分析，筛选并鉴定出了理想重组子，从而构建出了能分别表达ＳＴ１融合基因产物的工程菌株ｐＳＫ２１９和ｐＸＳＴ１。     

犬瘟热的微生物学诊断研究

对临床诊断为犬瘟热的１４例病犬，取其脑组织，运用细胞培养、合胞体检查、包涵体检查、免疫荧光试验、电镜观察等５种检测方法，就犬瘟热的微生物学诊断进行了系统的研究。结果表明，犬脑组织块与猫胚（ＦＥ）细胞或非洲绿猴肾（Ｖｅｒｏ）细胞共同培养，盲传的培养物出现不稳定的细胞病变，通过对不同代次的培养物检查包涵体，并作超薄切片或负染，电镜观察犬瘟热病毒（ＣＤＶ）粒子，证实分离到ＣＤＶ野毒。病犬脑组织切片经ＨＥ染色检查包涵体及用ＣＤＶ荧光抗体直接法检测脑抹片及接种犬脑的细胞培养物，均获得一定的阳性结果。建立的改良离子捕获电镜法，用于检测犬脑匀浆和犬脑接种细胞培养物，与离子捕获电镜法、免疫电镜法及直接电镜法相比，效果更为理想。１４例临床诊断为犬瘟热的病犬，综合运用上述微生物学手段检测，结果为１２例阳性，２例疑似。     

溶剂法制歧化松香

将松脂或松香溶于溶剂中，Ｃ Ｐｄ／Ｃ为催化剂，≤２００℃反应，可得色泽浅与不皂化物含理低的歧化松香。对该歧化松香组成研究后表明，在上条件下除含有通常的少量脱羧产物外，尚有降解产物，它带羧基，分子量为２７６，没有其它小分子降解产物，因而收率较高，不皂化物少。     

用紫外分光法测定鱼藤中异黄酮类的总含量

根据鱼藤中异黄酮类化合物在紫外光２１０～２４５ｎｍ及２９０～３０５ｎｍ处具有吸收峰这一特性，提出了用紫外分光法测定鱼藤中异黄酮类总含量的方法．在３００ｎｍ波长处，浓度低于６×２．６１８×１０－３／ｍｏｌ·Ｌ－１时，测定了标准系列的吸光值，结果表明吸光值与浓度近乎直线相关，相关系数为０．９９７７；标准系列吸光值准确性高；加样回收率达９９％以上；测定样品时，重现性好．     

Factors influencing decline in soil pH in Hawaiian Eucalyptus and Albizia plantations

Soil pH declined from 5.9 to 5.0 in 8 years beneath plantations of Eucalyptus saligna (Sm.) in Hawaii. In stands of Albizia falcataria, (L.) Fosberg, the soil pH change was more dramatic, declining from 5.9 to 4.6. We measured several components of soil acidity beneath four mixtures of the two tree species to gain insight on the processes responsible for the decline in soil pH. These components were studied using an empirical method of comparing acid quantity, degree of neutralization (depletion of base cations), and acid strength. The decline in soil pH differed between species as a result of differences in the degree of neutralization of the soil exchange complex; the larger decrease in soil pH under Albizia was produced by greater acidification of the exchange complex. Empirical titration curves suggested that differences in acid strength moderated the divergence in soil pH beneath the species. Had the acids accumulating in the soil under Albizia been as strong as those in the Eucalyptus soil, the difference in soil pH would have been greater. Though the two species had contrasting effects on soil pH, the differences in degree of neutralization, responsible for the pH decline, were small compared with differences in the amount of cations stored in tree biomass. Continued supply of nutrient cations (from weathering or fertilization) will ultimately control both the extent of soil pH decline and the level of productivity sustained by the forest.     

茶树种质资源抗茶云纹叶枯病鉴定

 茶云纹叶枯病(Guignardia camelliae,无性时代为Colletotrichum camelliae)在我国各产茶省(区)均有发生和为害。对该病的发生规律及防治研究有过报导,但对茶树种质资源的抗病性研究报导甚少,本文简要报道30份茶种质资源抗茶云纹叶枯病的鉴定试验研究结果。     

Monoclonal antibodies to bovine viral diarrhea virus: cross-reactivities to field isolates and hog cholera virus strains.

Monoclonal antibodies to bovine viral diarrhea virus (BVDV) were examined for binding with a large number of North American BVDV isolates and eight strains of the serologically related pestivirus, hog cholera virus (HCV). No single BVDV monoclonal antibody reacted with all BVDV isolates. The most cross-reactive monoclonal antibody was an anti-p80/p125 antibody which showed a positive reaction with 173 of 180 (96%) North American isolates. From a fewer number of isolates tested, one anti-gp53 monoclonal antibody also showed a high cross-reactivity (94%). All BVDV isolates showed a positive reaction with at least one of the seven monoclonal antibodies in the panel. Thus, the results indicated that a pool of these monoclonal antibodies may be used in place of polyclonal antisera for the detection of BVDV contamination of cell lines or for virus isolation. For HCV, all three anti-p80/p125 monoclonal antibodies reacted positively with all eight virus strains. In contrast, none of the anti-gp53 monoclonal antibodies were reactive to HCV strains. Thus, the anti-gp53 monoclonal antibodies may be useful for distinguishing between usually innocuous BVDV infections and the highly significant HCV infections in swine for foreign animal disease surveillance.