武汉东湖水生植被及其恢复途径探讨

１９９２～１９９３年对武汉东湖三个主要湖区（郭郑湖、汤林湖和牛巢湖）水生植被的调查表明,该湖区共有水生植物３２种,优势种为大茨藻、狐尾藻、苦草和菱。金鱼藻呈不断扩大的趋势。植被类型可分为１１个群丛,植被面积约为０．６５ｋｍ￣２,总生物量为１２３６．３９ｔ（湿重）,植被带状分布仅见于汤林湖北部和其他部分湖汊。汤林湖和牛巢湖水生植被正处于自然恢复演替阶段。     

东湖围隔（栏）中的植被恢复对水中氮的影响

利用大型围隔研究自然水体的某些生态过程具有真实准确、易于控制等优点 ,2 0世纪 80年代以来 ,国内陆续开展了一些研究[1～ 4 ] 。水体富营养化是目前我国湖泊存在的普遍问题 ,恢复水生植被可有效改善水质 ,减轻富营养化程度。武汉东湖(Ｅ114°2 3’ ,Ｎ30°33’)是一个典型的浅水城郊湖泊 ,已严重富营养化 ,为重建其水生植被 ,恢复其良性生态系统 ,在东湖建立了两个大型围隔和一个围栏 ,对其中的水生植被恢复及水质变化等方面进行了定位研究 ,旨在为重建和优化东湖水生植被 ,改善其水质提供借鉴。1　研究方法实验区位于东湖的汤林湖区。设…     

东湖大型围隔及围栏内植物群落和水质的变化

为恢复湖泊水生植被,初步研究了建在武汉东湖的大型围隔、围栏中的植物群落和水质的季节动态以及两者间的关系,结果表明：围隔、围栏中,植物生物量明显增加,漂浮植物易定植,水绵和刚毛藻易发生,植物群落结构难以自然地得到优化;养鱼对水生维管束植物的生长和恢复不利;水中总氮与总磷的变化具一致性,它们与水生植物的生物量间关系密切,围隔中水生植物的良好生长使水的总氮、总磷浓度明显降低     

武汉东湖水生植被春恢复途径探讨

１９９２－１９９３年对武汉东湖三个主要湖区水生植被的调查表明,该湖区共有水一植 物３２种优势种为大茨藻、狐尾藻、苦草和菱。金鱼藻呈不断扩大的趋势。     

收割对穗花狐尾藻生长的影响

在水深为24 cm的桶中,以6、12和18 cm等3个收割强度对穗花狐尾藻（Myriophyllum spicatum）进行了连续4次收割实验,研究了收割强度、收割频次及收割季节对穗花狐尾藻生长恢复的影响。结果表明：8月下旬第1次收割18 cm后,植物在41 d恢复,但产生分枝较少,影响了植物的无性繁殖;9月下旬之前,前2次收割6 cm或12 cm后,穗花狐尾藻在55 d恢复,并能产生较多的分枝,而且条枝总长有明显的增加,表明穗花狐尾藻的无性繁殖没有受到抑制;10月初第2次收割18 cm,或11月下旬前第3次收割6或12 cm后,植物均能安全越冬,恢复时间至少4个月以上;各次收割后,穗花狐尾藻的新生枝条主要从切割处萌发（至少40%以上）,其次是从基部萌发（0～41.3%）;随着收割次数增加,干质量的相对增长率下降,而根冠比增加。     

武汉东湖水生植物群落演替的研究

 本文根据1992～1993年调查结果并结合前人研究资料,讨论了东湖水生植物群落30多年来的动态变化及其与富营养化和渔业养殖等因素的关系,提出了东湖水生植物群落的演替系列是从微齿眼子菜阶段→微齿眼子菜+大茨藻+金鱼藻+狐尾藻阶段→微齿眼子菜消失阶段→大茨藻阶段→大茨藻+狐尾藻+苦草阶段。同时,还从物种生理生态、补偿和再生能力、生活史及生殖对策、种间关系等方面探讨了水生植物群落演替的物种替代机制及其演替模式,为湖泊水生植被恢复、人工调控和优化提供理论依据。     

沉水植物重建对富营养水体氮磷营养水平的影响

利用富营养浅水湖泊(武汉东湖)中所建立的大型实验围隔系统,研究了沉水植物对水体N、P营养水平的影响．结果表明,沉水植物重建后N、P营养水平显著降低．在研究期间,水生植物围隔总N和总P水平均显著低于对照围隔和大湖水体,而且水生植物围隔的总P含量一般维持在0．1mg·L^-1左右。季节性波动远低于对照围隔和大湖水体．水生植物围隔水体中氨态氮和亚硝态氮含量较低．而硝态氮含量与对照围隔和和大湖水体差别不大．由此可见。恢复以沉水植物为主的水生植被,可以有效地降低N、P营养循环速度,控制浮游植物过度增长,是重建富营养湖泊生态系统的重要措施．     

沉水植物穗花狐尾藻耐盐性与生长

通过室内人工海水培养和杭州湾栽培实验,探究了穗花狐尾藻的耐盐能力及在低盐度水域中的生长情况。室内培养表明:穗花狐尾藻断枝可在盐度12以内的人工海水中正常生长;低盐度处理可促进不定根的生长;水体盐度达到15后,穗花狐尾藻叶绿素含量和最大光合效率Fv/Fm降低,生长停滞,大部分植株逐渐死亡。野外栽培表明:从2017年6月到2018年5月,穗花狐尾藻可在杭州湾水体盐度6.06～9.03,水温3.85～33.37℃条件存活,8—10月是穗花狐尾藻的快速生长期;穗花狐尾藻在杭州湾低盐度水体中可进行有性繁殖和无性繁殖,以无性繁殖为主。研究结果为穗花狐尾藻在低盐度水体中建立种群提供了依据。     

鄂东花马潮水生高等植物研究——Ⅱ.水生植被

花马湖位于湖北省鄂州市境内,面积约27.5km~2。湖中分布有水生高等植物82种2变种。花马湖水生植被可分为15个群丛,其中菱群丛、竹叶眼子菜群丛、金鱼藻+狐尾藻+菹草+苦草群丛较为重要。湖中水生植波呈不规则的环带状分布,并可划分为湿生、挺水、浮叶和沉水4个植被带,各带均有相应的群丛分布。     

水生植物对富营养水体水质净化作用研究

利用富营养浅水湖泊武汉东湖中所建立的大型实验围隔系统,对沉水植物的水质净化作用作了现场实验研究。重建后的沉水植物可以显著改善水质,水体透明度显著提高,水色降低。在研究期间,水生植物围隔CODcr和BOD5一般分别为20和5mg/L左右;对照围隔和大湖水体则分别约为40和10mg/L。水生植物围隔水体中检出的有机污染种类也较对照围和大湖水体柢。实验结果表明恢复以沉水植物为主的水生植被是改善营养湖泊水质和重建生态系统的有效措施。     

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.     

Growth and mitogenic effects of arylphorin in vivo and in vitro

In insects, developmental responses are organ- and tissue-specific. In previous studies of insect midgut cells in primary tissue cultures, growth-promoting and differentiation factors were identified from the growth media, hemolymph, and fat body. Recently, it was determined that the mitogenic effect of a Manduca sexta fat body extract on midgut stem cells of Heliothis virescens was due to the presence of monomeric alpha-arylphorin. Here we report that in primary midgut cell cultures, this same arylphorin stimulates stem cell proliferation in the lepidopterans M. sexta and Spodoptera littoralis, and in the beetle Leptinotarsa decemlineata. Studies using S. littoralis cells confirm that the mitogenic effect is due to free alpha-arylphorin subunits. In addition, feeding artificial diets containing arylphorin increased the growth rates of several insect species. When tested against continuous cell lines, including some with midgut and fat body origins, arylphorin had no effect; however, a cell line derived from Lymantria dispar fat body grew more rapidly in medium containing a chymotryptic digest of arylphorin.     

Antiplatelet and antithrombotic activities of purpurogallin in vitro and in vivo

Enzymatic oxidation of pyrogallol was efficiently transformed to an oxidative product, purpurogallin (PPG). Here, the anticoagulant activities of PPG were examined by monitoring activated partial thromboplastin time (aPTT), prothrombin time (PT), and the activities of thrombin and activated factor X (FXa). And, the effects of PPG on expression of plasminogen activator inhibitor type 1 (PAI-1) and tissue-type plasminogen activator (t-PA) were evaluated in tumor necrosis factor (TNF)-α activated human umbilical vein endothelial cells (HUVECs). Treatment with PPG resulted in prolonged aPTT and PT and inhibition of the activities of thrombin and FXa, as well as inhibited production of thrombin and FXa in HUVECs. In addition, PPG inhibited thrombin-catalyzed fibrin polymerization and platelet aggregation. PPG also elicited anticoagulant effects in mice. In addition, treatment with PPG resulted in significant reduction of the PAI-1 to t-PA ratio. Collectively, PPG possesses antithrombotic activities and offers a basis for development of a novel anticoagulant. [BMB Reports 2014; 47(7): 376-381]     

Growth and reproduction of Arabidopsis thaliana in relation to storage of starch and nitrate in the wild-type and in starch-deficient and nitrate-uptake-deficient mutants

We have investigated the interactions between resource assimilation and storage in rosette leaves, and their impact on the growth and reproduction of the annual species Arabidopsis thaliana. The resource balance was experimentally perturbed by changing (i) the external nutrition, by varying the nitrogen supply; (ii) the assimilation and reallocation of resources from rosette leaves to reproductive organs, by cutting or covering rosette leaves at the time of early flower bud formation, and (iii) the internal carbon and nitrogen balance of the plants, by using isogenic mutants either lacking starch formation (PGM mutant) or with reduced nitrate uptake (NU mutant). When plants were grown on high nitrogen, they had higher concentrations of carbohydrates and nitrate in their leaves during the rosette phase than during flowering. However, these storage pools did not significantly contribute to the bulk flow of resources to seeds. The pool size of stored resources in rosette leaves at the onset of seed filling was very low compared to the total amount of carbon and nitrogen needed for seed formation. Instead, the rosette leaves had an important function in the continued assimilation of resources during seed ripening, as shown by the low seed yield of plants whose leaves were covered or cut off. When a key resource became limiting, such as nitrogen in the NU mutants and in plants grown on a low nitrogen supply, stored resources in the rosette leaves (e.g. nitrogen) were remobilized, and made a larger contribution to seed biomass. A change in nutrition resulted in a complete reversal of the plant response: plants shifted from high to low nutrition exhibited a seed yield similar to that of plants grown continuously on a low nitrogen supply, and vice versa. This demonstrates that resource assimilation during the reproductive phase determines seed production. The PGM mutant had a reduced growth rate and a smaller biomass during the rosette phase as a result of changes in respiration caused by a high turnover of soluble sugars ( Caspar et al. 1986 ; W. Schulze et al. 1991 ). During flowering, however, the vegetative growth rate in the PGM mutant increased, and exceeded that of the wild-type. By the end of the flowering stage, the biomass of the PGM mutant did not differ from that of the wild-type. However, in contrast to the wild-type, the PGM mutant maintained a high vegetative growth rate during seed formation, but had a low rate of seed production. These differences in allocation in the PGM mutant result in a significantly lower seed yield in the starchless mutants. This indicates that starch formation is not only an important factor during growth in the rosette phase, but is also important for whole plant allocation during seed formation. The NU mutant resembled the wild-type grown on a low nitrogen supply, except that it unexpectedly showed symptoms of carbohydrate shortage as well as nitrogen deficiency. In all genotypes and treatments, there was a striking correlation between the concentrations of nitrate and organic nitrogen and shoot growth on the one hand, and sucrose concentration and root growth on the other. In addition, nitrate reductase activity (NRA) was correlated with the total carbohydrate concentration: low carbohydrate levels in starchless mutants led to low NRA even at high nitrate supply. Thus the concentrations of stored carbohydrates and nitrate are directly or indirectly involved in regulating allocation.     

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.