荒漠草原不同植物根际与非根际土壤养分及微生物量分布特征

通过对宁夏荒漠草原6种地带性优势物种长芒草、蒙古冰草、甘草、牛心朴子、黑沙蒿和苦豆子植物根际与非根际土壤养分和微生物量分布特征进行研究,探讨不同植物根际养分的富集的相关性和差异性。研究结果表明:6种植物根际土壤养分和微生物量均表现出明显的富集效应,根际富集率大小依次为菊科(黑沙蒿)豆科(苦豆子、甘草)禾本科(长芒草、蒙古冰草)萝藦科(牛心朴子);全磷(TP)在根际和非根际中无显著差异(P0.05),其它土壤养分及理化指标在根际中均表现出显著富集(P0.05),土壤养分中以有机碳(SOC)的富集作用最为明显;土壤有效态养分较全量养分对植物根际微小的变化响应更为灵敏;不同荒漠植物根际与非根际SOC与全氮(TN)呈极显著线性关系(P0.01),TN与碱解氮之间呈极显著线性关系(P0.01),TP与有效磷(AP)没有显著的相关性(P0.05)。荒漠植物土壤有效养分在根际存在一定的富集,灌木和豆科植物的根际效应的大于禾本科植物,它们通过降低根际pH值可以提高根际养分,有利于在脆弱环境下对土壤养分的有效利用。     

青藏高原不同气候区高寒沙地两种优势植物及其根际土壤的养分特征

为了探究青藏高原寒冷沙地上优势植物及其根际土壤的养分对不同气候的响应过程, 选取半干旱和半湿润沙地上的优势植物中国沙棘(Hippophae rhamnoides subsp. sinensis)和沙蒿(Artemisia desertorum)为对象, 调查自然条件下青藏高原半干旱和半湿润沙地上两种植物枝叶和根的碳、氮、磷含量, 及其根际0-10 cm和10-20 cm土壤的有机碳、全氮、全磷、铵态氮、硝态氮、有效磷含量, 并探讨两种优势植物和根际土壤的养分含量的关系及其影响因子。结果表明, 半干旱和半湿润条件下中国沙棘和沙蒿及其根际土壤的养分差异明显。半干旱和半湿润气候条件下两种植物碳、氮、磷的积累差异显著。半湿润条件下, 沙蒿根际土壤中的有机碳、全氮、铵态氮、硝态氮、有效磷的含量高于半干旱条件, 而中国沙棘根际土壤养分的结果却相反。不同气候条件下, 沙蒿和沙棘的养分和根际土壤的养分显著相关, 两种植物的养分比差异显著, 沙蒿氮磷比与其根际土壤的氮磷比以及中国沙棘的碳氮比与其根际土壤的碳氮比显著负相关。     

樟子松林根际与非根际土壤碳氮磷化学计量特征

为揭示呼伦贝尔沙地樟子松根际与非根际土壤碳氮磷化学计量特征,以不同林龄(28、37、46年生)樟子松人工林为研究对象,以樟子松天然林为对照,研究根际与非根际土壤有机碳、全氮和全磷含量及其化学计量比,分析土壤性质与土壤化学计量特征间的相关性。结果表明：在樟子松人工林中,根际效应显著影响土壤N∶P,林龄显著影响土壤有机碳含量;各林龄人工林的土壤有机碳含量均显著低于天然林。人工林的根际与非根际土壤有机碳、全氮含量均随林龄增加先降低再升高;全磷含量在根际土壤中先升高再降低,在非根际土壤中先降低再升高。C∶N与C∶P在根际土壤中呈显著正相关,但在非根际土壤中不存在显著相关关系,说明根际土壤氮磷限制具有更高的协同性。根际与非根际土壤N∶P均值分别为4.98与8.40,表明樟子松人工林的生长受土壤N限制,且根际土壤受N限制程度更高。根际与非根际土壤碳氮磷化学计量特征受土壤性质的显著影响,其中,速效磷是最主要的驱动因子。呼伦贝尔沙地樟子松生长受N限制,其植物根系对土壤养分的富集与维持有明显作用,建议在樟子松生长阶段适当补充土壤氮素,并根据根际土壤氮磷限制的协同性适当补充磷素。     

干旱荒漠区不同灌木根际与非根际土壤氮素的含量特征

选取广泛分布于阿拉善干旱荒漠区的白刺、霸王、红砂、沙冬青、沙木蓼、梭梭和驼绒藜7种不同的旱生灌木,研究其根际与非根际土壤各种形态氮素、有机碳的含量特征及土壤pH的变化.结果表明,相对于非根际土壤,根际土壤全氮、铵态氮、硝态氮分别平均高24.9%、24.5%和65.1%,土壤有机碳平均高出18.5%,土壤pH值平均低0.14个单位.根际与非根际土壤的全氮、铵态氮、硝态氮、有机碳和pH之间都呈现出了极显著差异(p<0.01).7种灌木根际土壤全氮、硝态氮和有机碳含量均比非根际土壤含量高.除沙冬青根际铵态氮含量较非根际低以外,其余6种灌木根际土壤铵态氮含量均高于非根际土壤.梭梭的根际土壤pH高于非根际,其它6种灌木均是根际pH低于非根际土壤.在根际与非根际,土壤有机碳与土壤全氮之间均呈显著相关,二者表现为线性关系.而土壤全氮与铵态氮在根际与非根际则均无相关性,全氮与硝态氮在根际和非根际土壤均显著相关,且二者也呈线性相关.     

不同立地铁杆蒿化学计量特征及其与土壤养分的关系

以陕西吴起杨青川流域铁杆蒿群落为研究对象,结合坡向、坡位及土壤养分变化探究不同立地铁杆蒿群落化学计量特征及其与土壤养分的关系.结果表明:从峁顶、阳坡、半阴坡到阴坡,铁杆蒿地上部分和根有机碳、全氮、全磷含量、碳氮比均逐渐增大;地上部分碳磷比和根氮磷比呈减小趋势;地上部分氮磷比、根碳磷比先减小后增大.从峁顶、上坡位、中坡位到下坡位,地上部分有机碳、全氮、全磷含量以及根有机碳含量先增加后减小;地上部分碳氮比、氮磷比先减小后增大.铁杆蒿群落植物化学计量特征一般与土壤化学计量特征呈正相关,但碳氮比、碳磷比、氮磷比及根全磷与土壤相应指标呈负相关,且植物地上部分与土壤的相关性大于根.综上,不同立地铁杆蒿群落植物在阴坡中坡位生长状态最佳,其化学计量特征与土壤养分状况具有明显的相关关系.坡向和坡位在铁杆蒿群落植物和土壤的化学计量特征中具有重要影响,适宜的铁杆蒿群落将有利于土壤养分的恢复.     

黄土高原典型植物根际对土壤微生物生物量碳、氮、磷和基础呼吸的影响

选择黄土高原7种典型植物的根际与非根际土壤为研究对象,对土壤的养分含量、微生物生物量碳、氮、磷和基础呼吸的影响进行了初步研究。结果表明,7种不同植物根际土壤与非根际土壤的养分含量、微生物生物量和基础呼吸均存在显著差异;除冷蒿的土壤微生物生物量磷以外,其他各种植物的根际土壤的养分含量、微生物生物量和基础呼吸均比非根际土壤的高;土壤有机碳、全氮与土壤微生物生物量碳、氮及基础呼吸之间均具有极显著或显著相关关系,表明了土壤微生物生物量碳、氮可以作为判断土壤肥力状况的生物学指标,同时也可为提高土壤肥力水平和土壤培肥效果提供依据。     

黄土丘陵区不同植被根际土壤微量元素含量特征

为了解黄土高原不同植被土壤微量元素的根际效应,分析了该地区柠条、沙棘、沙打旺、柳枝稷、阿尔泰狗娃花和茵陈蒿6种植被根际与非根际土壤中有机碳、全氮、Mn、Cu、Fe、Zn含量.结果表明： 6种植被中,柠条、阿尔泰狗娃花和茵陈蒿根际土壤的有机碳、全氮含量高于非根际土壤;除柠条和沙棘外,其余4种植被非根际土壤pH值均显著高于根际土壤.6种植被根际土壤有效Mn含量均低于非根际;柠条、沙打旺和柳枝稷根际有效Cu含量显著高于非根际,表现出强烈根际富集现象.除沙打旺外,其他5种植被根际有效Fe含量均略高于非根际.沙打旺、柳枝稷、茵陈蒿和阿尔泰狗娃花表现出强烈的有效Zn根际富集现象.根际与非根际土壤有机碳、全氮与有效Mn、有效Zn,以及有效Mn与有效Zn呈极显著正相关.根际土壤pH值与有效Mn和有效Zn呈显著负相关.由于不同植物根系的生长特征、根际pH值及微生物种类等的差异,不同植被根际的微量元素含量不同,茵陈蒿根际4种微量元素含量高于其他植被.     

宁南山区典型草本植物茎叶分解对土壤酶活性及微生物多样性的影响

采用凋落物分解袋法,以宁南山区典型草本植物长芒草、铁杆蒿、百里香为研究对象,分析了3种植物茎叶分解过程中土壤酶活性变化特征和分解后期微生物多样性特征,以及土壤酶活性与初始土壤化学性质的关系.结果表明: 植物茎叶分解480 d后,各处理土壤酶活性均有不同程度的增加,且长芒草处理土壤蔗糖酶活性和碱性磷酸酶活性最高,分别为32.40和1.99 mg·g^-1·24 h^-1,百里香处理土壤脲酶活性最高(2.66 mg·g^-1·24 h^-1),铁杆蒿处理土壤纤维素酶活性最高(1.42 mg·g^-1·72 h^-1).分解末期土壤纤维素酶活性与土壤初始微生物生物量碳呈显著正相关;分解末期土壤纤维素酶活性与土壤初始硝态氮含量呈显著负相关.添加植物茎叶处理土壤细菌和真菌的Ace指数、Chao指数和Shannon指数均显著大于对照,Simpson指数显著小于对照.植物茎叶的分解显著提高了土壤细菌和真菌的丰度及多样性,进而提高了植物茎叶的分解速率,促进了生态系统营养物质的循环与转化.     

氮添加对盐渍化草地根际土壤理化性质的影响

为探究氮输入和根际效应对盐渍化草地土壤理化性质的影响,对8个水平氮添加处理下(0、1、2、4、8、16、24和32 g N·m^-2·a^-1)晋北盐渍化草地根际和非根际土壤理化性质进行研究。结果表明: 氮添加显著降低根际土壤pH,显著增加根际和非根际土壤Ca²⁺、NO₃^--N和无机氮含量;随氮添加量的增加,根际和非根际土壤Ca²⁺、NO₃^--N、无机氮含量以及根际土壤全氮含量呈逐渐升高的趋势,而根际土壤Na⁺、K⁺、Mg²⁺、NH₄⁺-N和氨基酸含量以及非根际土壤全氮含量呈先升高后降低的趋势。主成分分析表明,根际土壤理化性质对低氮(≤8 g·m^-2·a^-1)和高氮添加(>8 g·m^-2·a^-1)的响应具有明显差异。根际土壤pH、有机酸和氨基酸含量分别比非根际土壤低0.71、44.3%和9.8%,而K⁺、Ca²⁺、Mg²⁺、NH₄⁺-N、无机氮、全碳和全氮含量分别比非根际土壤高51.0%、47.6%、20.8%、215.5%、139.3%、31.7%和65.3%,表明根际效应对盐渍化草地土壤理化性质的影响大于氮输入的影响。     

氮素添加和CO2浓度升高对白羊草根际和非根际土壤水溶性有机碳、氮的影响

采用盆栽控制试验对黄土丘陵区白羊草在不同CO₂浓度(400和800 μmol·mol^-1)和施氮水平(0、2.5、5.0 g N·m^-2·a^-1)条件下根际和非根际土壤水溶性有机碳(DOC)和水溶性有机氮(DON)的变化特征进行研究.结果表明: CO₂浓度升高对白羊草根际和非根际土壤DOC、水溶性总氮(DTN)、DON、水溶性铵态氮(NH₄⁺-N)、水溶性硝态氮(NO₃^--N)含量均无显著影响.施氮显著提高了根际和非根际土壤DTN、NO₃^--N含量和根际土壤DON含量,显著降低了根际土壤DOC/DON.在各处理条件下,根际土壤DTN、NO₃^--N和DON含量均显著低于非根际土壤,根际土壤DOC/DON显著高于非根际土壤.短期CO₂浓度升高对黄土丘陵区土壤水溶性有机碳、氮含量无显著影响,而氮沉降的增加在一定程度上改善了土壤中水溶性氮素缺乏的状况,但并不足以满足植被对水溶性氮素的需求.     

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.     

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)     

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.     

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.     

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.     

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.     

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.