桂西北喀斯特坡地典型生境不同植物叶片的碳同位素差异

通过测定7种典型植物的叶片δ13C值,比较了桂西北喀斯特坡地连片裸露石丛及其临近浅薄土层处植物叶片δ13C值及其季节性差异。结果表明:旱季(2008年11月、2009年3月)植物叶片δ13C值显著高于雨季(2009年7月)(P0.05);旱季和雨季菜豆树、铁线莲、黄荆的δ13C值无显著差异(P0.05),而盐肤木、红背山麻杆、蕨、肾蕨旱季显著高于雨季(P0.05);季节性降雨差异对乔木类菜豆树、藤本类的铁线莲以及根系较深灌木叶片δ13C值的影响较小,而对浅根系草本植物、浅根灌木影响较大;旱季和雨季2种生境下菜豆树叶片δ13C值差异均不大,旱季和雨季连片裸岩生境的红背山麻杆和黄荆叶片δ13C值与临近浅薄土层生境值的差异虽不显著(P0.05),但差异大于菜豆树,说明生境条件的差异对这2种灌木叶片δ13C值的影响较大。     

NaCl胁迫对大米草光合·蒸腾等生理特性的影响

研究了NaCl胁迫下大米草净光合速率(Pn)、蒸腾速率(Tr),叶片气孔导度(Gs)、细胞问CO_2浓度(Ci)、株高、叶长、叶宽、茎粗、叶绿素含量、气孔限制值和水分利用效率.结果表明:当NaCl浓度高于300mmol/L时,大米草Pn、Tr、Gs、株高、叶长以及叶绿素含量受到显著抑制(P＜0.05),叶宽及茎粗则无显著性差异.NaCl胁迫下,大米革光合速率的降低是气孔因素和非气孔因素综合导致的结果,Pn、Tr、Gs、株高以及叶绿素含量的降低可作为大米草受NaCl胁迫的症状,而WUE则保持在较高的水平,因此在防治大米草蔓延时,排水处理不是最佳选择.     

土壤水分状况对花生和早稻叶片气体交换的影响

通过田间测坑试验研究了长期处于不同土壤水分状况下花生和早稻叶片气体交换的一些特点.结果表明,花生分枝期轻度和中度水分胁迫使气孔导度(Gs)和蒸腾速率(Tr)略有下降,净光合速率(Pn)和叶片水分利用效率(WUE)减小,轻度水分胁迫Gs/Tr略有上升而中度胁迫Gs/Tr变小.花生结荚期轻度和中度水分胁迫都使Gs、Tr、Gs/Tr和Pn显著降低,WUE大幅度上升.花生结荚期明显受土壤水分胁迫影响.早稻灌浆期轻度和中度水分胁迫Gs、Tr和Gs/Tr变化不显著,Pn和WUE增加,并且轻度水分胁迫下籽粒产量增加.Gs和Gs/Tr变化情况相结合可以作为作物水分胁迫程度的一个参考指标,即如果Gs和Gs/Tr同时下降则作物已经受到水分胁迫影响.     

模拟光条件下禾本科植物和藜科植物蒸腾特性与水分利用效率比较

利用人工模拟光源研究了两种 C4 光合途径禾本科植物 (虎尾草、狗尾草 )和两种 C3光合途径藜科植物 (藜、绿藜 )的光合速率 ( Pn)、蒸腾速率 ( Tr)、水分利用率 ( WUE)、气孔导度 ( Gs)、胞间 CO2 浓度 ( Ci)及叶面饱和蒸气压亏缺 ( Vpdl)随模拟光辐射 ( SPR)增强的变化规律及 Gs、Ci、Vpdl对 Tr和 WUE的影响。结果表明 :( 1 ) 4种植物的 Pn和 Tr均随 SPR增强而增大 ,两种藜科植物最大净 Pn和 Tr均高于两种禾本科植物的最大净 Pn和 Tr。 ( 2 ) WUE随 SPR增强先增大后减小 ,两种禾本科植物和两种藜科植物分别在SPR为 40 0、1 2 0 0 μmol/( m2·s)时达到最大值 ,禾本科植物的最大 WUE明显高于藜科植物。 ( 3) 4种植物的 Gs、Ci均随 SPR的增强而减小 ,两种藜科植物的 Gs和 Ci均显著高于两种禾本科植物。4种植物的 Vpdl均随 SPR增强而增大 ,禾本科植物高于藜科植物。实验表明 ,在以水分为限制因素的半干旱草原区 ,禾本科植物具有更好的保水机制和更高的水分利用效率 ,与藜科植物相比 ,在水分生态上具有一定的竞争优势。     

水肥耦合对汉源花椒幼苗叶片光合作用的影响

以汉源花椒幼苗为试验材料,通过盆栽试验研究了不同水肥耦合处理对汉源花椒叶片气孔导度(Gs)、胞间CO_2浓度(Ci)、净光合速率(Pn)、蒸腾速率(Tr)、水分利用效率(WUE)和叶面饱和水汽压亏缺(Vpdl)日变化的影响,并探讨了汉源花椒光合特性与土壤田间持水量(FWC)、施肥量(包括施全量NPK、1/2NPK和不施肥,其中全量NPK含尿素150 kg N/hm~2、过磷酸钙60kg P_2O_5/hm~2和硫酸钾150 kg K_2O/hm~2)和环境因子间的关系。结果表明:各处理汉源花椒叶片Gs、Pn、Tr和Vpdl日变化均呈"单峰"型曲线,其峰值分别出现在10:00—12:00、10:00—12:00、14:00和14:00左右,没有出现光合"午休"现象;Ci最低值出现在10:00—12:00左右;WUE日变化呈"双峰"型曲线,峰值分别出现在10:00和16:00左右,但第2个峰值明显低于第1个峰值。NPK+50%FWC和1/2NPK+50%FWC两处理叶片Pn日变化峰值出现在12:00左右,而其他处理均出现在10:00左右。叶片Gs、Pn、Tr和WUE平均值均随施肥量的增加而增加,而Ci和V_(pdl)平均值随施肥量的增加而降低。叶片Gs、Pn和Tr平均值随土壤水分含量的增加总体上呈先增加后降低的趋势变化;Ci平均值总体上随土壤水分含量的增加而增加;WUE平均值随土壤水分含量的增加而降低;V_(pdl)平均值随土壤水分含量的增加呈先降低后增加的趋势变化。叶片Pn与地径(D)、苗高(H)、D~2H、叶绿素含量和chla/chlb比值呈显著正相关。为了促进植株生长和获得较高的叶片Pn和WUE,土壤水分应控制在35.9%—46.7%FWC。叶片Gs、Pn和Tr与光合有效辐射强度(PAR)呈显著正相关,Tr与气温的相关系数高于它与其他环境因子的相关系数,提高叶片Pn的最佳PAR为1263.6μmol m~(-2)s~(-1)。说明适宜的土壤水分含量和肥料施用量能延长汉源花椒叶片Pn达到峰值的时间,对提高叶片Pn和WUE及促进植株生长具有重要作用;PAR是影响叶片Gs和Pn的主要环境因子,气温是影响叶片Tr的首要环境因子。     

冠层高度对毛竹叶片光合生理特性的影响

借助LI-6400便携式光合作用系统,研究了冠层高度对不同林龄毛竹(Phyllostachys pubescens)叶片光合生理特性和水分利用效率(WUE)的季节性影响,为促进毛竹林碳汇能力和生产力提升的林分结构调整等可持续栽培技术提供理论依据。结果表明:(1)出笋期,不同竹龄毛竹叶片净光合速率(Pn)和蒸腾速率(Tr)的日均值呈现出冠层上部小于冠层下部的梯度变化趋势,且2a生毛竹不同冠层Pn日均值大于3a生毛竹;孕笋行鞭期,不同林龄毛竹各时间点Pn值和日均值、以及2年生毛竹各时间点的Tr值均为冠层上部大于冠层下部。各生长季节,不同林龄毛竹个体叶片的气孔导度(Gs)均与Tr的变化趋势一致。(2)2年生毛竹各季节仅冠层上部叶片会出现"光合午休",而3年生毛竹仅于出笋期时各冠层叶片出现"光合午休"现象。(3)出笋期毛竹叶片WUE日均值随着冠层高度增加而增加,这种变化趋势不受竹龄影响;而孕笋行鞭期,仅2年生毛竹叶片WUE日均值随着冠层高度增加而下降。不同冠层高度的孕笋行鞭期毛竹叶片WUE日均值都显著高于出笋期;冠层高度对毛竹叶片气体交换特性和WUE的影响受生长发育关键期的季节因素影响,且毛竹叶片WUE与Gs之间存在负相关关系,其不受毛竹个体年龄和叶片冠层高度影响。(4)不同生长季节各冠层叶绿素a/b值均随着冠层高度下降而降低,不同林龄毛竹叶片叶绿素含量基本随着冠层自上而下呈逐渐增加的趋势。各生长季节,不同林龄个体叶片氮素含量、比叶重随冠层高度垂直变化趋势与叶片Pn日均值的垂直变化趋势一致。研究认为,毛竹不同冠层部位叶片通过改变形态、氮素含量来适应不同生长季节生长环境的变化,以便充分利用光能提高光合能力。     

铝胁迫对蓼科植物生长和光合、蒸腾特性的影响

采用水培试验,设置5种铝处理浓度,研究了铝对3种蓼科植物酸模叶蓼、杠板归和辣蓼叶片光合、蒸腾和叶绿素荧光参数的影响。结果表明,高铝处理(400μmol.L-1)显著抑制3种蓼科植物地上部和根系生长,并且导致3种蓼科植物叶片叶绿素含量、Chla/Chlb、净光合速率(Pn)、水分利用效率(WUE)、PSII光合电子传递量子效率(φPSII)和光化学猝灭系数(qP)显著下降。中低铝处理(25~100μmol.L-1)时,与对照相比,酸模叶蓼生物量显著增加,杠板归显著减少,辣蓼先增加后减少。其中,酸模叶蓼和辣蓼叶绿素含量、Chla/Chlb、Pn、蒸腾速率(Tr)、胞间CO2浓度(Ci)、PSII最大光化学效率(Fv/Fm)、qP均未发生显著变化,但辣蓼WUE、φPSII和非光化学猝灭系数(NPQ)显著下降,酸模叶蓼无显著变化;而杠板归除Ci、Fv/Fm外,其余叶片光合、蒸腾及叶绿素荧光参数均出现显著下降。上述结果表明,酸模叶蓼在中低铝处理条件下可通过保持较高的叶绿素含量、Chla/Chlb、WUE、Pn、PSII反应中心光化学反应效率以及提高非辐射能量耗散来增强其对铝的耐性。     

正常和环割条件下不同形态氮素添加对红椎幼苗光合特性的影响

采用盆栽试验和韧皮部环割方法研究了碳水化合物供应、氮素形态及其交互作用对红椎幼苗叶片光合特性的影响。无机氮源采用硝酸铵(AN)、铵态氮(NH_4~+-N)、硝态氮(NO_3~--N),有机氮源采用尿素(Urea)、精氨酸(Arg)和甘氨酸(Gly),氮素施用量均为10g N/m~2,处理时间为10 d。研究结果表明,环割、氮素形态及其交互作用均显著影响了红椎幼苗叶片的净光合速率(Pn);单一环割处理显著降低了红椎幼苗叶片Pn、气孔导度(Gs)、胞间CO_2浓度(Ci)、蒸腾速率(Tr)、相对叶绿素含量和CO2利用效率(CUE),但显著提高了叶片水分利用效率(WUE)和气孔限制值(Ls),其叶片Pn降低主要是由气孔限制和叶绿素含量降低所导致的。正常条件下,所有氮素形态处理均显著降低了红椎幼苗叶片的Pn、Gs、Ci和Tr,但显著升高了叶片Ls和WUE,其叶片Pn降低的主要原因是供氮过高引起的叶片气孔限制。正常条件下,除Arg处理外,其他氮素形态均显著升高了红椎幼苗叶片的CUE,其中以Gly处理的促进作用最大。环割条件下,3种有机态氮素的添加均显著缓解了单一环割处理对红椎幼苗叶片Pn的抑制作用,尤其以精氨酸最为明显,供应精氨酸的叶片Pn值从单一环割处理的强烈抑制中恢复到了对照水平,而无机态氮的供应均未显著改变这种抑制。结果表明短期碳水化合物供应的阻断会显著抑制红椎幼苗叶片的光合能力,适量供应精氨酸、甘氨酸和尿素等有机态氮会有效缓解这种抑制作用,其中以精氨酸的作用最为明显。     

遮荫处理对臭柏幼苗光合特性的影响

为了探明臭柏幼苗在不同遮荫处理下的光合特性和色素含量,通过盆栽实验,测定了0%、25%、50%、75%和90%四个遮荫处理下臭柏光合特性日变化和色素含量。结果表明:(1)随着遮荫率增加,臭柏净光合速率(Pn)、气孔导度(Gs)及蒸腾速率(Tr)随之减小,而胞间CO2浓度(Ci)随之增大,非气孔制限因素是臭柏光合速率下降的主要原因,且90%遮荫会影响臭柏幼苗的正常生长;(2)叶绿素a(Chl a)、叶绿素b(Chl b)和叶绿素总量(Chl a+b)均随着遮荫率增加而增大,Chl a/b则随着遮荫率的增大而呈下降趋势;(3)几乎所有遮荫处理组Gs均与Tr表现出不同程度的相关性,而Gs与Pn的相关性较差;所有遮荫处理组水分利用效率(WUE)与Pn均呈极显著相关,而与Tr相关性不显著,说明臭柏是通过较高的光合速率来实现高的水分利用效率以适应不同的光照条件。同时WUE和Ci也表现出不同程度的相关性。     

干旱胁迫下油橄榄品种光合特性研究

为揭示油橄榄(Olea europaea L.)耐旱性与光合特性之间的关系,以筛选出的适宜于半干旱川西南地区种植的7个引进油橄榄品种为供试材料,采用盆栽模拟干旱胁迫的方法,研究持续干旱胁迫对其光合特性的影响。结果表明:(1)随着干旱胁迫程度加剧,7个油橄榄品种叶片相对含水量均显著降低,至干旱胁迫后期(25d),各品种叶片均出现大幅失水,其中品种‘科拉蒂’失水率最高(45.79%),而品种‘小苹果’失水率最低(25.52%),说明‘小苹果’叶片在干旱胁迫下较其他油橄榄品种具有更高保水能力。(2)随着干旱胁迫程度加剧,7个油橄榄品种叶片光合色素含量均不同程度降低,表明光合色素分解量大于合成量;干旱胁迫持续25d时,品种‘豆果’的叶绿素a和叶绿素b含量下降幅度最大(P0.05),品种‘皮削利’类胡萝卜素含量下降幅度最大(P0.05),而品种‘小苹果’叶绿素a含量下降幅度最小。(3)随着干旱胁迫的持续进行,各油橄榄品种叶片净光合速率(Pn)、蒸腾速率(Tr)、气孔导度(Gs)和胞间CO2浓度(Ci)均不同程度降低,而水分利用效率(WUE)则呈上升趋势;干旱胁迫期间,品种‘佛奥’的Pn、Tr和Ci以及‘皮削利’的Gs降幅均高于其他品种,而‘小苹果’的Pn、Gs和Ci降幅均为最小且WUE上升幅度最大。研究发现,在持续干旱胁迫条件下,油橄榄幼苗叶片均大幅失水,光合色素结构被破坏、色素分解、含量降低,同时气孔关闭蒸发减少,光合作用减弱,而供试油橄榄品种中‘小苹果’对干旱胁迫的适应性最强,适宜于在半干旱的川西地区种植。     

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.     

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.     

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.     

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.     

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.