松嫩平原盐碱土饱和浸提液与土水比1∶5浸提液间化学参数的换算关系

采用饱和浸提液与土水比1∶5浸提液两种方法分析了松嫩平原94份盐碱土样品的电导率、钠吸附比、主要阳离子(Na⁺、K⁺、Ca²⁺、Mg²⁺)以及总阳离子浓度等化学参数,并对两种方法测定的盐碱化参数相关性进行了研究。结果表明：饱和浸提液电导率、钠吸附比、总阳离子浓度、Na⁺离子浓度与土水比1∶5浸提液相应参数存在极显著的相关关系,其关系方程可用于松嫩平原盐碱土饱和浸提液与1∶5浸提液间化学参数的换算;而K⁺、Ca²⁺、Mg²⁺离子浓度在两种浸提液间不存在相关性。     

祁连山西水林区土壤阳离子交换量及盐基离子的剖面分布

以祁连山西水林区分布的棕钙土、灰褐土、栗钙土和高山草甸土为对象,研究了阳离子交换量和盐基离子(K+、Na+、Ca2+、Mg2+)的剖面分布规律及其与土壤理化因子的关系。结果表明:土壤阳离子交换量(CEC,介于4.80—48.10 cmol/kg)和盐基总量(TEB,介于4.67—21.34 cmol/kg)随剖面深度的增加逐渐减小,不同土壤类型的大小顺序为:灰褐土>高山草甸土>栗钙土>棕钙土;土壤盐基组成以Ca2+、Mg2+为主(占TEB的比例平均为71.6%、22.9%),K+、Na+所占比例较低(占TEB的比例平均为3.3%、2.2%);棕钙土、灰褐土和栗钙土盐基离子的剖面分布由浅至深呈现:K+≈Ca2+>Na+≈Mg2+,高山草甸土盐基离子则呈现:K+>Na+>Mg2+>Ca2+。不同土壤类型间盐基离子的含量及饱和度随发生层次不同存在较大差异。土壤有机质是CEC的主要贡献因素,粉粒对CEC也有显著的促进作用,而砂粒、CaCO3对CEC有显著抑制作用。土壤生物复盐基作用弱于淋溶作用,造成盐基饱和度较大(BSP,介于44.4%—97.2%),并随剖面深度的增加逐渐增大。相关性分析表明,土壤交换性Na+、Mg2+的含量及饱和度均呈极显著正相关,交换性Na+、Mg2+饱和度与CaCO3含量呈极显著正相关;pH值与BSP呈极显著正相关;土壤速效P含量与CEC呈极显著正相关,速效K含量与交换性K+含量呈极显著正相关。     

不同pH 值土壤及其浸提液对羊草种子萌发和幼苗生长的影响

研究了不同pH值土壤以及重度盐碱土和非盐碱土浸提液对羊草(Leymus chinensis)种子萌发及幼苗生长的影响。不同pH值土壤由配土和调酸两种方式取得, 前者由重度盐碱土(pH = 10.24)与非盐碱土(pH = 7.49)按不同比例配制, 后者是由重度苏打盐碱土经硫酸调酸处理得到。配土发芽的实验结果表明, 当pH值在7.49-9.14时, 种子的发芽率均在50%以上, 且幼苗能够正常生长; pH = 9.53时, 羊草种子的发芽率低于50%, 仅部分幼苗个体能够成活; 当pH > 9.86时, 幼苗在萌发后50天左右全部枯死。说明羊草种子个体萌发期最大耐受pH值在9.14-9.53之间。重度苏打盐碱土调酸发芽实验结果表明, 当调酸后 的土壤pH值降至7.0-10.0时, 均能显著促进羊草种子的萌发, 且幼苗生长正常。确定了羊草种子萌发的最适pH值为8.0-8.5。土/水比为1: 1的非盐碱土浸提液能够显著提高羊草种子发芽率, 而重度苏打盐碱土浸提液对羊草种子萌发没有产生显著抑制。     

不同pH值土壤及其浸提液对羊草种子萌发和幼苗生长的影响

研究了不同pH值土壤以及重度盐碱土和非盐碱土浸提液对羊草(Leymus chinensis)种子萌发及幼苗生长的影响。不同pH值土壤由配土和调酸两种方式取得,前者由重度盐碱土(pH=10．24)与非盐碱土(pH=7．49)按不同比例配制,后者是由重度苏打盐碱土经硫酸调酸处理得到。配土发芽的实验结果表明,当pH值在7．49-9．14时,种子的发芽率均在50％以上,且幼苗能够正常生长;pH=9．53时,羊草种子的发芽率低于50％,仅部分幼苗个体能够成活;当pH>9．86时,幼苗在萌发后50天左右全部枯死。说明羊草种子个体萌发期最大耐受pH值在9．14-9．53之间。重度苏打盐碱土调酸发芽实验结果表明,当调酸后的土壤pH值降至7．0-10．0时,均能显著促进羊草种子的萌发,且幼苗生长正常。确定了羊草种子萌发的最适pH值为8．0-8．5。土／水比为1:1的非盐碱土浸提液能够显著提高羊草种子发芽率,而重度苏打盐碱土浸提液对羊草种子萌发没有产生显著抑制。     

毛竹各器官和根际土浸提液对杉木种子萌发的化感作用

随着毛竹杉木混交林面积的不断扩大,它们之间既会产生促进作用,又会产生抑制作用。本研究对比分析了不同浓度毛竹各器官(鲜叶、干叶、枝条、竹杆、竹鞭和鞭根)的浸提液及枯落物、根际土浸提液对杉木种子发芽率的影响,探讨了毛竹各器官浸提液及枯落物、根际土浸提液对杉木种子萌发的化感作用。结果表明:(1)处理前期,毛竹各器官浸提液对杉木种子萌发具有抑制作用,且当浸提液浓度为1∶25和1∶50的高浓度时,相对于低浓度浸提液对杉木种子萌发的抑制作用更为持久;(2)处理后期,低浓度的毛竹各器官浸提液对杉木种子萌发促进作用较快,而高浓度的浸提液仍呈现抑制作用,促进作用出现较为缓慢;(3)枯落叶浸提液总体上对杉木种子萌发具有抑制作用,在整个实验过程中低于对照组的发芽率,仅在1∶50浓度时略高对照组实验;而根际土浸提液对杉木种子萌发自始至终都具有促进作用,其中低浓度的促进作用十分显著。故在实际的毛竹杉木混交林生产营林过程中可选用毛竹根际土制备浸提液,促进杉木种子萌发,为毛竹杉木混交林的生产经营提供参考。     

桑叶营养对家蚕血淋巴阳离子水平的调节作用

调查了取食不同品种桑树（M-5, S-36和V-1）叶片的家蚕（多化性品种Pure Mysore、 二化性品种NB4D2和CSR2）5龄幼虫血淋巴中阳离子的变化。结果表明: 家蚕幼虫血淋巴中Na+浓度低, K+和Mg2+浓度很高, Ca2+浓度较高。在幼虫活跃取食期间, 血淋巴中阳离子水平显著提高。血淋巴中阳离子水平与排泄物的量呈负相关。血淋巴中阳离子水平受阳离子外泌的控制。与非取食阶段相比, 取食阶段的阳离子清除速率低。家蚕二化性品种的血淋巴阳离子水平比多化性品种PM高出30%。结果说明家蚕品种对家蚕血淋巴阳离子变化的影响显著大于桑树品种或家蚕个体发育的影响。     

3种药赏两用植物对滨海盐碱土改良效应的比较

为比较种植药赏两用植物对滨海盐碱土的改良效应,采用实生栽培方法种植了薄荷(Mentha haplocalyxBriq.)、地榆(Sanguisorba officinalis L.)和枸杞(Lycium chinense Mill.)1年生植株,对不同土层的pH值以及可溶性盐和主要离子含量的变化进行了比较分析。结果表明:种植3种植物后,0～10、10～20和20～30 cm土层的pH值以及可溶性盐、K+、Na+、Ca2+、Mg2+、Cl-和SO42-含量均有不同程度的变化,且以0～10 cm土层的变化相对明显,并且各土层的离子组成也有所改变。种植3种植物后,0～10和10～20 cm土层的pH值以及0～10 cm土层的可溶性盐含量均低于对照,其中,地榆种植土壤pH值及枸杞种植土壤可溶性盐含量的降低效应最明显。种植3种植物后,各土层的Ca2+含量及10～20和20～30 cm土层的K+和Mg2+含量均极显著高于对照,各土层的Na+含量及0～10 cm土层的Cl-含量、10～20和20～30 cm土层的SO42-含量均极显著低于对照;不同土层的K+/Na+值均高于对照、(K++Na+)/(Ca2++Mg2+)值均低于对照、主要阳离子(Ca2+、K+和Mg2+)的交换量总和均明显增加。总体上,地榆和枸杞对土壤中K+及Ca2+和Mg2+含量、K+/Na+值、主要阳离子(Ca2+、K+和Mg2+)交换量总和的提高效应以及对Na+含量、(K++Na+)/(Ca2++Mg2+)值的降低作用均较强,而薄荷的作用均较弱。研究结果显示:供试的3种药赏两用植物对盐碱地均具有明显的改良作用,其中枸杞和地榆的改良效果较好。     

茂兰喀斯特地区森林降水分配的水化学特征

于2007年9月—2009年8月对中国西南茂兰喀斯特地区亚热带常绿落叶阔叶混交林大气降水、林冠穿透雨和树干茎流进行观测,分析了各降水分配中的养分离子(Ca2+、Mg2+、K+、Na+、NH4+、SO42-、NO3-、Cl-)浓度动态变化规律及年养分元素输入量。结果表明:7—9月,林外雨、林冠穿透雨和树干茎流中各养分离子浓度相对较低,12月—翌年2月,各降水分配中各养分离子浓度相对较高;降水通过林冠或树干后,除了Na+浓度无显著变化外,NH4+浓度表现下降趋势,Ca2+、Mg2+、K+、Cl-、NO3-和SO42-均表现增加趋势;林外雨的养分元素输入量顺序为Ca2+SO42--SNH4+-NCl-K+Na+Mg2+NO3--N。在林冠穿透雨+树干茎流中的养分元素输入量顺序为K+Ca2+Cl-SO42--SMg2+NH4+-NNO3--NNa+。与非喀斯特地区相比,林外雨中的各养分离子浓度较低,林冠穿透雨、树干茎流中的K+、Ca2+、Mg2+增加幅度较大。总体来看,独特的立地特征决定了该地区Ca2+、Mg2+的积极参与生态系统养分循环和K+高效循环的特征。     

外源EBR对NaCl胁迫下燕麦幼苗无机离子吸收、运输和分配的影响

为了探讨外源2,4-表油菜素内酯(2,4-epibrassinolide,EBR)诱导燕麦(Avena sativa L.)幼苗抗盐性的效果及其生理调节机制,以"青引2号"和"加燕2号"燕麦为材料,研究NaCl胁迫下施用外源EBR对燕麦幼苗无机离子吸收、运输和分配的影响。结果表明:100mmol·L-1NaCl胁迫下,"青引2号"和"加燕2号"燕麦幼苗叶片和根系中的Na+、Cl-含量均显著升高,对阳离子的吸收产生了拮抗作用,导致燕麦幼苗叶片和根系中的K+、Ca2+、Mg2+、Mn2+、Fe2+、Zn2+、Cu2+含量显著降低,离子稳态平衡被打破;100 mmol·L-1NaCl胁迫下,施用0.01μmol·L-1外源EBR后,"青引2号"和"加燕2号"燕麦幼苗叶片和根系中的Na+和Cl-含量显著降低,促进了燕麦幼苗根系对K+、Ca2+、Mg2+、Fe2+、Mn2+、Cu2+和Zn2+的吸收,叶片和根系中K+/Na+、Cl-/Na+、Ca2+/Na+、Mg2+/Na+、Fe2+/Na+、Mn2+/Na+、Cu2+/Na+和Zn2+/Na+显著升高,并且有效调控燕麦幼苗体内无机离子的运输比和阳离子的运输选择性比率,离子稳态重新达到平衡状态;说明外源EBR能够缓解NaCl胁迫下Na+和Cl-对燕麦幼苗所造成的离子毒害作用,有效调控燕麦幼苗对无机离子的选择性吸收、运输和分配,对维持燕麦幼苗体内的离子稳态平衡具有正向调控作用。     

青钱柳种皮甲醇浸提液的生物测定

通过对青钱柳[Cyclocarya paliurus (Batal.) Iljinskaja]种皮甲醇浸提液的生物测定,探讨青钱柳种子休眠与种皮内源抑制物质的关系.结果表明,青钱柳种皮不同浓度的甲醇浸提液(10%、20%、25%、30%和40%)对白菜(Brassica campestris L. ssp. chinensis)种子发芽率和种子活力以及幼苗的高生长、根生长均有抑制作用,浓度越高抑制作用越明显.用30%和40%浸提液处理, 白菜种子不能萌发;用10%、 20%和25%浸提液处理, 白菜种子的萌发率分别为98.6%、 75.0%和9.0%;苗高和根长分别比对照降低了31.6%、 48.1%、 79.7%和21.3%、 70.8%、 90.2%.表明青钱柳种子的种皮中含有抑制种子萌发和幼苗生长的成分.     

Degradation and conversion of somatostatin in normal and diabetic rats in vivo and in vitro

Plasma somatostatin-like immunoreactivity in the portal and jugular veins of streptozotocin diabetic rats was compared with that in normal control rats. In the diabetic group, somatostatin levels in the portal (p less than 0.05) and jugular (p less than 0.01) veins were both elevated compared with those in the control group. Moreover, the degree of elevation was greater in the jugular vein than in the portal vein. To further investigate the role of the liver in the clearance of somatostatin-28 in vivo, 2 micrograms of somatostatin-28 was administered as a bolus into the external jugular vein of intact and functionally hepatectomized rats. The mean half-time of somatostatin-28 was significantly longer in intact diabetic rats than in controls (p less than 0.05). The functional hepatectomy did not cause a significant difference in the half-time in diabetic rats but made it longer in control rats. These results suggest that the longer half-time of somatostatin-28 in diabetic rats in vivo is due to its slower hepatic clearance. The hepatic clearance of somatostatin-28 and somatostatin-14 was further studied in vitro using a recirculating liver perfusion method. The hepatic clearance of 1.2 nM of either somatostatin-28 or somatostatin-14 was significantly lower in diabetic rats than in controls (p less than 0.01). This indicates that elevated plasma somatostatin levels in diabetic rats are caused at least in part by decreased hepatic clearance of somatostatin.(ABSTRACT TRUNCATED AT 250 WORDS)     

Production of arsine and methylarsines in soil and in culture

Arsenate, arsenite, monomethylarsonate, and dimethylarsinate were added to different soils, and evolution of gaseous arsenical products was determined over 3 weeks. Arsine was produced in all three soils from all substrates, whereas methylarsine and dimethylarsine were produced only from methylarsonate and dimethylarsinate, respectively. At least three times more arsine than dimethylarsine was produced in soil incubated with dimethylarsinate. Resting cell suspensions of Pseudomonas and Alcaligenes produced arsine as the sole product when incubated anaerobically in the presence of arsenate or arsenite. In all instances, no trimethylarsine was observed, nor could any evidence be shown for the methylation of any arsenical substrate in soil or in culture. It was concluded that reduction to arsine, not methylation to trimethylarsine, was the primary mechanism for gaseous loss of arsenicals from soil.     

Development and comparison of in vivo and in vitro models for endometritis in cows and mares

In order to investigate pathogenic mechanisms of acute endometritis in cows and mares, we established an in vivo model in both species. Based on the results of an in vitro transmigration system, human recombinant interleukin-8 (rhIL-8; 1.25 microg per mare and 5 microg per cow in 50 ml phosphate-buffered saline) was used to attract polymorphonuclear neutrophil granulocytes (PMNs) into the uteri. Peak numbers of uterine neutrophils were attracted after 6h, in both cows and mares. On average, mares responded more sensitively than cows, with 15 times higher numbers of rhIL-8-attracted uterine neutrophils (72+/-8 x 10(7)cells). In contrast to in vitro studies, in vivo migrated neutrophils (uterine neutrophils) of both species displayed a significantly reduced MHC class I expression. Expression of the CD11a molecule was significantly enhanced on equine uterine neutrophils but downregulated on bovine cells. Compared with untreated autologous peripheral neutrophils, both uterine and in vitro migrated neutrophils showed no alteration of phagocytic capacity. The ability to generate reactive oxygen species (ROS) was significantly upregulated in bovine and equine uterine neutrophils. This was also observed after in vitro migration of equine neutrophils, whereas ROS generation by bovine neutrophils was significantly depressed. In summary, the concept of inducing endometritis directly by local application of human interleukin-8 has been reliably successful in cows and mares. The model permits the analysis of PMN migration into the uterus under defined and controlled conditions. The observed differences between cows and mares with respect to phenotypical and functional characteristics of in vivo attracted uterine cells point to species-related features of neutrophil migration. In vitro transmigrated bovine and equine cells partially differ in phenotype and function from uterine neutrophils. Therefore, the in vitro transmigration assay cannot completely represent the in vivo endometritis model described here.     

Interactions of cadmium and selenium in rat plasma in vivo and in vitro

⁷⁵Se and ¹⁰⁹Cd tracers were used to study the binding of Se and Cd to plasma proteins at various SeO₃^2? doses and times up to 24 h after the simultaneous subcutaneous administration of SeO₃^2? and CdCl₂ to adult male rats. The simultaneous injection of CdCl₂ and SeO₃^2? markedly increased both Se and Cd plasma levels over that in control animals. Gel permeation chromatography of plasma indicated that at all times up to 24 h Cd and Se were bound in an atomic ratio of approx. 1 : 1 in 330 000 and 130 000 dalton fractions. From 4 to 24 h, Cd and Se appeared in the 420 000 dalton fraction, also with an atomic ratio of approx. 1 : 1. The 330 000 dalton molecules appeared to have a maximal binding capacity for the Cd-Se complex at a concentration of approx. 30 μmol/ml of plasma, while the 130 000 and 420 000 dalton molecules show a higher binding capacity. Studies in vitro revealed that SeO₃^2? does not interact directly with Cd and plasma proteins. It is metabolized by erythrocytes to a form that interacts in an atomic ratio of 1 : 1 with Cd to form a protein-bound complex of 130 000 daltons.     

Activity of native and dextran-modified hyaluronidase in in vitro and in vivo systems

Modified hyaluronidase derivatives have been obtained. Covalent coupling of the enzyme with aldehyde dextran results in 65-85% protein binding to the carrier, residual catalytic activity accounting for 90-100% of the baseline. Modified hyaluronidase is more thermostable than the native enzyme. The data on intravenous drug distribution in the mouse organs are promising and ensure effective use of modified hyaluronidase for the treatment of pulmonary diseases.     

Importance of guanine nitration and hydroxylation in DNA in vitro and in vivo

Guanine (Gua) modification by nitrating and hydroxylating systems was investigated in DNA. In isolated calf thymus DNA, 8-NO(2)-Gua and 8-oxo-Gua were dose-dependently formed with peroxynitrite, and 8-NO(2)-Gua was released in substantial amounts. Myeloperoxidase (MPO) with H(2)O(2) and NO(2)(-) reacted with calf thymus DNA to form 8-NO(2)-Gua dose dependently without release of 8-NO(2)-Gua. The frequency of strand breaks was higher than the sum of 8-NO(2)-Gua and 8-oxo-Gua, particularly in the MPO-treated DNA, indicating the importance of other types of damage. The activation of human neutrophils and lymphocytes with phorbol ester did not induce 8-NO(2)-Gua and 8-oxo-Gua in their nuclear DNA. However, 8-NO(2)-Gua was found in calf thymus DNA co-incubated with activated neutrophils in the presence of NO(2)(-). No significant formation of 8-NO(2)-Gua was found in liver DNA from mice treated with Escherichia coli lipopolysaccharide. The incubation of peroxynitrite or MPO-H(2)O(2)-NO(2)(-)-treated DNA with formamidopyrimidine glycosylase (Fpg) released 8-oxo-Gua, but not 8-NO(2)-Gua, indicating that 8-NO(2)-Gua is not a substrate for Fpg. Although 8-NO(2)-Gua was generated in isolated DNA by different nitrating systems, other types of damage were formed in abundance, and the lesion could not be found reliably in nuclear DNA, suggesting that the biological importance is limited.     

Biosynthesis of beta-glucuronides of retinol and of retinoic acid in vivo and in vitro

After the intraportal injection of retinol-6,7-(14)C to rats, the O-ether derivative of retinol, retinyl -glucosiduronate, appears in the bile. Both retinoyl -glucuronide and retinyl -glucosiduronate are also synthesized in vitro when washed rat liver microsomes are incubated with uridine diphosphoglucuronic acid (UDPGA) and either retinoic acid or retinol, respectively. The synthesis of retinoyl -glucuronide was also demonstrated in microsomes of the kidney and in particulate fractions of the intestinal mucosa. The glucuronides were characterized by their UV absorption spectra, by their quenching of UV light or fluorescence under it, by their thin-layer chromatographic behavior in two solvent systems, and by the identification of products released during their hydrolysis by -glucuronidase. With retinoic acid as the substrate, the UDP glucuronyl transferase of rat liver microsomes had a pH optimum of 7.0, a temperature optimum of 38 degrees C, and a marked dependence on the concentrations of both retinoic acid and UDPGA, but was unaffected by a number of possible inhibitors, protective agents, and competitive substrates. The conversion of retinal to retinoic acid and the synthesis of retinoyl -glucuronide from retinoic acid could not be detected in whole homogenates, cell fractions, or outer segments of the bovine retina.