豆科植物及其在内蒙古锡林河流域放牧草原生态系统中作用的研究

内蒙古锡林河流域是我国典型温带草原分布地区，也是我国重点牧区之一。近年来，由于人口增加、过度放牧以及管理不善等原因导致草原退化加剧，草原生态系统养分输入输出失衡，草地生产力下降。 豆科植物不仅是高蛋白优质牧草，而且具有生物固氮能力，对维持草地生态系统中土壤-植物-动物之间的氮平衡有重要作用。本论文主要调查研究了内蒙古锡林河流域放牧草原生态系统中豆科植物的分布、固氮能力、微生物状况，并探讨了目前草原大量出现的豆科植物小叶锦鸡儿灌丛在养分供给上对草原生态系统的影响。 豆科植物的分布调查采用样线法在4 种草原植被类型7 个植物群落进行，包括典型草原（羊草群落、大针茅群落及小叶锦鸡儿群落和冷蒿群落2 个退化草原群落）、草甸草原（贝加尔针茅群落）、河漫滩草甸（灰脉苔草群落）及沙地（榆树疏林群落），除榆树疏林群落仅放牧处理外，其他群落均包括放牧和不放牧对照处理。结果显示，豆科植物共有12 属，16 种。放牧总体上降低了豆科植物种群在群落中的数量特征（平均高度、密度、频度）和种类组成，但在退化草原群落中有不同的变化趋势。小叶锦鸡儿在典型草原中分布广、密度大、出现频率高；尤其在小叶锦鸡儿群落放牧样地，出现频度为95%，密度近4 株•m-2。花苜蓿在4 种草原植被类型中均有分布。 典型草原4 个群落在放牧和不放牧条件下土壤微生物碳氮含量和微生物呼吸速率的测定结果显示，放牧影响了豆科植物根际土壤的微生物量和微生物呼吸速率，但各群落变化规律不一致。放牧后小叶锦鸡儿分布最为广泛的小叶锦鸡儿群落在放牧条件下微生物碳含量和微生物呼吸速率都显著增加。小叶锦鸡儿灌丛与其他草本豆科植物相比，根际土壤的微生物量和微生物呼吸速率较高。土壤水分对微生物呼吸速率以及微生物碳氮含量有重要作用，存在极显著的正相关关系。 采用15N 自然丰度法评估野外条件下小叶锦鸡儿和花苜蓿的固氮百分率，计算结果高于100%，这主要是由野外植物叶片δ15N 值低于室内无氮培养的B 值引起的。15N 自然丰度法是否适用于评估草原植物的固氮能力还有待深入研究，但从野外δ15N 测定中也得到了一些有趣的结果。优势豆科和非豆科植物之间的δ15N 差异很大。小半灌木木地肤δ15N 值最高，并在放牧后显著下降，杂类草、禾本科大针茅与之变化趋势相同；具有潜在固氮能力的豆科植物和禾本科羊草在放牧后无显著差异或显著增加；豆科植物小叶锦鸡儿、乳白花黄芪和花苜蓿的叶片δ15N 值均为偏低负值，显著低于非豆科植物。研究结果说明不同植物的氮利用方式不同，豆科植物和羊草的生物固氮可能同时为受氮限制的内蒙古草原提供氮源。 小叶锦鸡儿灌丛影响了周围土壤的有效氮含量。灌丛内部土壤硝态氮和氨态氮有高于外部土壤的趋势。土壤含水量与硝态氮浓度显著正相关。土壤有效氮含量变异系数平均高于50%，土壤资源表现出很强的空间异质性。灌丛内部植物体内全氮含量高于灌丛外，而灌丛斑块发育时间对植物化学元素没有显著影响。

火烧、施肥、刈割及其交互作用对草原土壤净氮矿化的影响

我国北方温带草原地处干旱半干旱区，是欧亚大陆草原生物区系的重要组成部分，也是我国重要的畜牧业生产基地。土壤氮素作为陆地植物生长和生态系统初级生产力的主要限制因子之一，了解其矿化和可利用性对各种人为干扰因素的响应，有助于我们充分认识草地退化机理，维持草场生产力并进一步促进畜牧业的可持续发展，为草地恢复、重建和维护提供理论依据。本实验在中国科学院内蒙古草原生态系统定位研究站的多年围封退化样地，分别实施了火烧、施肥、刈割及其交互作用的人为干扰处理，利用原状土野外培养的方法，在两年时间中，研究不同的人为干扰因素（火烧、施肥、刈割及其交互处理）对土壤净氮矿化作用的影响。 火烧显著影响草原的氮循环过程，季节和年际的气候变化参与调节氮循环对火烧处理的响应。多年围封后的初次人工火烧处理显著降低了第一个生长季（2006 年生长季）和其后冬季的土壤净氮矿化速率，但是，火烧处理仅在冬季对土壤无机氮含量产生显著降低作用；2007 年生长季，火烧处理对土壤净氮矿化速率和土壤无机氮含量没有显著作用，但是在个别月份，不同的火烧频率对土壤净氮矿化速率和无机氮含量的影响表现出差异。2006 年生长季，未火烧样地和火烧样地净氮矿化积累量分别为3.07±0.26 g N m-2 和2.18±0.21 g N m-2；冬季，未火烧样地和火烧样地净氮矿化积累量分别为1.18±0.25 g N m-2 和0.51±0.08 g N m-2；2007 年生长季，未火烧样地（BC）、每年火烧样地（B1）和两年一烧样地（B2）净氮矿化积累量分别为1.32±0.21 g N m-2、0.54±0.30 g N m-2 和 0.77±0.24 g N m-2。较为湿润的2006 年生长季的净氮矿化积累量显著高于较为干旱的2007 年生长季，冬季也存在相当丰富的净氮矿化积累量。我们推论，长时间围封后的单次火烧处理对土壤净氮矿化作用的影响可能是短效的，但是年际间气候变化对土壤净氮矿化作用影响显著。 施肥显著提高了土壤的无机氮含量，并且与施肥梯度呈显著正相关关系。施肥对土壤无机氮含量的影响具有累加效应，第一次施肥和第二次施肥后的首次取样，+N5.25 、+N17.5 、+N28.0 三个施肥梯度的样地土壤无机氮含量比未施肥样地分别高出56%、219%、1054%和514%、891%、1811%。施肥处理在2006 年和2007 年对土壤净氮矿化作用都没有显著影响，仅在2007 年的个别月份有一定效果。以上结果说明，无机氮肥的添加可以明显提高土壤中无机氮的含量，满足植物生长的需求，但对于土壤氮转化过程的影响可能还要受其它环境和生物因子的制约。 刈割对土壤无机氮含量和净硝化速率没有显著作用，对土壤净氮矿化速率仅在个别月份表现显著效果。2007 年生长季，未刈割样地和刈割样地净氮矿化积累量分别为1.32±0.21 g N m-2 和1.08±0.35 g N m-2，不存在显著差异。我们推论，长期围封后的单次刈割处理在短期内对生长季的土壤氮动态仅有微弱影响，并且这种效果还可能受水分因素的制约。 火烧、施肥、刈割的交互处理在2007 年生长季对土壤无机氮含量产生显著作用，但是，对土壤净氮矿化速率和净硝化速率没有显著效果，然而，在不同的取样时间，火烧、施肥、刈割的交互处理对土壤无机氮含量、净氮矿化速率和净硝化速率的影响存在显著差异，说明火烧、施肥、刈割的交互处理对土壤无机氮和净氮矿化作用的影响可能受各种环境因子的制约，尤其是在水分相对缺乏的半干旱内蒙古草原，非生物因子和生物因子可能共同影响着土壤中的氮平衡。 本研究初步分析了长期围封后火烧、施肥、刈割及其交互处理对土壤净氮矿化的影响，初步探究了人为干扰和环境气候变化对土壤可利用性氮的调节作用，为科学地进行禁牧、割草、人工养份添加等草原管理提供了数据支持。

Proteomic Analysis of Proteins Involved in Spermiogenesis in Mouse

Spermiogenesis is a unique process in mammals during which haploid round spermatids mature into spermatozoa in the testis. Its successful completion is necessary for fertilization and its malfunction is an important cause of male infertility. Here, we report the high-confidence identification of 2116 proteins in mouse haploid germ cells undergoing spermiogenesis: 299 of these were testis-specific and 155 were novel. Analysis of these proteins showed many proteins possibly functioning in unique processes of spermiogenesis. Of the 84 proteins annotated to be involved in vesicle-related events, VAMP4 was shown to be important for acrosome biogenesis by in vivo knockdown experiments. Knockdown of VAMP4 caused defects of acrosomal vesicle fusion and significantly increased head abnormalities in spermatids from testis and sperm from the cauda epididymis. Analysis of chromosomal distribution of the haploid genes showed underrepresentation on the X chromosome and overrepresentation on chromosome 11, which were due to meiotic sex chromosome inactivation and expansion of testis-expressed gene families, respectively. Comparison with transcriptional data showed translational regulation during spermiogenesis. This characterization of proteins involved in spermiogenesis provides an inventory of proteins useful for understanding the mechanisms of male infertility and may provide candidates for drug targets for male contraception and male infertility.

Effect of glycerol and dimethyl sulfoxide on cryopreservation of rhesus monkey (Macaca mulatta) sperm

Glycerol and dimethyl sulfoxide (DMSO) are widely used as penetrating cryoprotectants in the freezing of sperm, and various concentrations are applied in different species and laboratories. The present study aimed to examine the effect of these two cryoprotectants at different concentrations (2%, 5%, 10%, and 15% glycerol or DMSO) on rhesus monkey sperm cryopreservation. The results showed that the highest recovery of post-thaw sperm motility, and plasma membrane and acrosome integrity was achieved when the sperm was frozen with 5% glycerol. Spermatozoa cryopreserved with 15% DMSO showed the lowest post-thaw sperm motility, and spermatozoa cryopreserved with 15% glycerol and 15% DMSO showed the lowest plasma membrane integrity among the eight groups. The results achieved with 5% glycerol were significantly better for all parameters than those obtained with 5% DMSO. The functional cryosurvival of sperm frozen with 5% glycerol was further assessed by in vitro fertilization (IVF). Overall, 85.7% of the oocytes were successfully fertilized, and 51.4% and 5.7% of the resulting zygotes developed into morulae and blastocysts, respectively. The results indicate that the type and concentration of the penetrating cryoprotectant used can greatly affect the survival of rhesus monkey sperm after it is frozen and thawed. The suitable glycerol level for rhesus monkey sperm freezing is 5%, and DMSO is not suitable for rhesus monkey sperm cryopreservation. (C) 2004 Wiley-Liss, Inc.

A novel disintegrin, jerdonatin, inhibits platelet aggregation and sperm-egg binding

A novel disintegrin, jerdonatin, was purified to homogeneity from Trimeresurus jerdonii venom by gel filtration and reversed-phase high-pressure liquid chromatography. We isolated the cDNA encoding jerdonatin from the snake venom gland. Jerdonatin cDNA precursor,;encoded pre-peptide, metalloprotease and disintegrin domain. Jerdonatin is composed of 72 amino acid residues including 12 cysteines and the tripeptide sequence Arg-Gly-Asp (RGD), a well-known characteristic of the disintegrin family. Molecular mass of jerdonatin was determined to be 8011 Da by matrix-assisted laser desorption ionization time of flight mass spectrometry (MALDI-TOF-MS). Jerdonatin inhibited ADP- and collagen-induced human platelet aggregation with IC50 of 123 and 135 nM, respectively. We also investigated the effect of jerdonatin on the binding of B6D2F1 hybrid mice spermatozoa to mice zona-free eggs and their subsequent fusion. Jerdonatin significantly inhibited sperm-egg binding in a concentration-dependent manner, but had no effect on the fusion of sperm-egg. These results indicate that integrins on the egg play a role in mammalian fertilization. (C) 2004 Elsevier Inc. All rights reserved.

CORRELATION OF ZONA-BINDING WITH OOCYTE MATURATION AND SPERM MOTILITY IN RHESUS-MONKEYS BY HEMIZONA ASSAY

The hemizona assay (HZA) in Rhesus monkeys was employed to study the correlation of zona-binding ability with sperm motility or with naturally developing oocytes at various maturational stages. Oocytes from unstimulated ovaries were retrieved within 2 hr from monkeys sacrificed for vaccine production (in reproductive season, but with their menstrual cycles not determined). Oocytes were divided into four groups based on their morphological maturation: 1) Oocytes surrounded by more than one cumulus layer (MC); 2) Oocytes retaining intact germinal vesicle nuclei (GV); 3) Oocytes with germinal vesicle breakdown showing distinct perivitelline space (PVS); and 4) Oocytes extruding the first polar body (PB1). The mean numbers of sperm bound to hemizona for PBI, PVS, GV, and MC groups were 132.9 +/- 12.0, 71.5 +/- 10.1, 36.1 +/- 4.0, and 20.1 +/- 2.9 (Mean +/- SE), respectively. The four groups showed significant differences from each other in sperm/egg binding ability (P < 0.01). The number of bound sperm significantly increased with oocyte maturation. The present study also showed that zona-binding ability was also affected by sperm motility. For sperm with 67.7% motility and sperm with 31.2% motility, the average numbers of bound sperm were 43.5 +/- 2.2 and 25.3 +/- 2.9 (Mean +/- SE), respectively. There was significantly higher binding ability for sperm with higher motility (P < 0.01). The results suggest that: 1)The rhesus monkey model can serve as a very sensitive model for studying sperm/egg interaction by HZA; 2) Sperm motility positively correlated with sperm/egg binding; and 3) Sperm/egg binding ability increases with oocyte maturation. The binding ability is highest when oocytes matured to the PB1 stage, which is also the best opportunity for fertilization. This is strong evidence for the ''zona maturation'' hypothesis. (C) 1994 Wiley-Liss, Inc.

Cryopreservation of Kunming mouse oocytes using slow cooling, ultrarapid cooling and vitrification protocols

The cryopreservation of oocytes has been only marginally successful with any of the current protocols, including slow cooling, rapid cooling and vitrification. We wished to test the hypothesis that oocytes from a single mouse strain would freeze successfully by 1 of the 3 mentioned protocols. Unfertilized Kunming mouse oocytes obtained 14 h after PMSG/hCG administration were randomly assigned to be cryopreserved after slow cooling, ultra rapid cooling and vitrification. Oocytes were thawed by straws being placed into 37 degrees C water, and their morphological appearance and in vitro fertilization capability were compared with that of oocytes that had not undergone cryopreservation. Survival of oocytes was indicated by the absence of darkened ooplasm or by broken membranes or zona pellucida. Functional integrity was evaluated by the formation of a 2-cell embryo after IVF. Survival rate of slow cooled oocytes did not differ from that seen in vitrified oocytes (55.1 vs 65.9%) but was significantly lower in the rapidly cooled oocytes (24.2%; P<0.01). The results of NF of slow cooled and vitrified oocytes were similar to those of the control group (72 and 73 vs 77%; P>0.05). It appears that Kunming mouse oocytes can be successfully cryopreserved using the slow cooling method with 1,2-propanediol and vitrification, which contains both permeating and nonpermeating cryoprotectants. (C) 1997 by Elsevier Science Inc.

Development of zona-free hamster ova to blastocysts in vitro

The zona pellucida (ZP) enclosing the mammalian ovum is important for its protection and for initial stages of fertilization, but the role of the ZP during embryo development is less clear. This study was designed to investigate if the hamster ZP is needed for embryo development from 1-cell to blastocyst in vitro, and to compare methods for removing the ZP. A total of 395 hamster pronucleate ova were collected 10 h post activation from superovulated, mated female hamsters. The ZP was removed from some ova using either 0.05% pronase, 0.05% trypsin or acid Tyrode's solution. To prevent ZP-free ova from sticking together, they were cultured singly in 30-50 muL drops of HECM-6 culture medium together with ZP-intact ova as controls. There was no significant difference among treatment groups in embryo development to blastocyst: 36/87 (42%) in the ZP intact group; 35/75 (47%) in the pronase-treated ZP-free group; 37/74 (50%) in the trypsin-treated ZP-free group; and 37/71 (52%) in the acid-treated ZP-free group. These results indicate that 1) the ZP is unnecessary for hamster embryo development in vitro from the pronucleate ovum stage to blastocyst; 2) none of the three ZP-removal methods was detrimental to embryo development; 3) embryos do not need to be cultured in groups during in vitro development from 1-cell to blastocyst. (C) 2000 by Elsevier Science Inc.

Vitrification of Yunnan Yellow Cattle oocytes: work in progress

The objective of this study was to provide a simple cryopreservation method for oocytes from Yunnan Yellow Cattle and facilitate preservation efforts in this native Chinese breed, which is threatened by agricultural modernization. Cumulus-oocyte complexes (COCs) were collected from slaughterhouse ovaries and matured in vitro for 22-24 h, then selected for cryopreservation. Vitrification in open pulled straws (OPS) or in microdrops on a cooled metal surface (solid surface vitrification, SSV) was compared. The OPS vitrification solution consisted of 20% ethylene glycol (EG) and 20% DMSO. The SSV solution was a mixture of 35% EG, 5% polyvinyl-pyrrolidon (PVP) and 0.4 M trehalose. Vitrified and warmed oocytes were either fertilized in vitro or parthenogenetically activated. The rates of cleavage and development to blastocysts of fertilized oocytes following OPS versus SSV were not statistically different (38.3 and 12.5% versus 35.8 and 6.0%, respectively). The corresponding rates of parthenogenetic development to blastocysts were also not different (8.2 versus 3.5%, respectively). Development to blastocysts of non-vitrified controls following fertilization was significantly higher than that of the vitrified oocytes (22.6%, P < 0.05). These results demonstrate for the first time, that although both OPS and SSV procedures reduced embryonic development, Yunnan Yellow Cattle oocytes are capable of developing to blastocysts following cryopreservation. (C) 2002 Elsevier Science Inc. All rights reserved.

Amino acid requirements for maturation of rhesus monkey (Macacca mulatta) oocytes in culture

This study evaluated the effects of different amino acid formulations on supporting meiotic and cytoplasmic maturation of rhesus monkey (Macacca mulatta) oocytes in vitro. Five hundred and forty-six cumulus-oocyte complexes (COCs) aspirated from unstimulated adult monkey follicles (greater than or equal to 1000 mum in diameter) were cultured in either modified Connaught Medical Research Laboratories 1066 medium (mCMRL-1066) or in one of eight chemically defined media (modified basic medium 5 supplemented with 5.5 mmol glucose l(-1), 0.003 mmol pantothenic acid l(-1) and different amino acid formulations) as below: (1) modified basic medium 5 (mBM5) containing no amino acid; (2) mBM5 + 0.2 mmol glutamine l(-1); (3) mBM5 + 11 amino acids from hamster embryo culture medium 6 (HECM-6) (11 AA); (4) mBM5 + Eagle's non-essential amino acids (NEA); (5) mBM5 + NEA + 0.2 mmol glutamine l(-1); (6) mBM5 + Eagle's essential amino acids (EA) without glutamine; (7) mBM5 + EA + 0.2 mmol glutamine l(-1); (8) mBM5 + Eagle's 20 amino acids (20 AA) + 0.2 mmol glutamine l(-1); and (9) mCMRL-1066 (control). All media contained FSH, LH, oestradiol and progesterone. After maturation, mature oocytes were subjected to the same fertilization and embryo culture procedures. COCs matured in treatment 5 had greater potential to progress to metaphase II (66%; P < 0.05) than did those in treatments 1 (37.3%), 2 (48.3%)f 3 (41%), 6 (41%) and 9 (43%). Oocytes matured in treatment 8 had the best morula (53%) and blastocyst (18%) developmental responses (P<0.05). The lowest (P<0.05) morula and blastocyst developmental responses were obtained from COCs matured in treatments 1 (0%) and 6 (8%). The other media supported intermediate embryonic development (range 11-38% of morula and blastocyst). These results indicate that the choice of amino acids affects the competence of oocyte maturation and that Eagle's 20 AA with 0.2 mmol glutamine l(-1) is more efficient than the other amino acid formulations for maturation of rhesus monkey oocytes.

Developmental potential of vitrified holstein cattle embryos fertilized in vitro with sex-sorted sperm

In vitro fertilization (IVF) is a feasible way to utilize sex-sorted sperm to produce offspring of a predetermined sex in the livestock industry. The objective of the present study was to examine the effects of various factors on bovine IVF and to systema

应用碳、氮稳定同位素研究鄱阳湖枯水末期水生食物网结构

稳定碳、氮同位素比值分析技术是研究生态系统中物质循环与能量流动的有效技术。δ13C值常用来分析消费者食物来源,δ15N值常用来确定生物在食物网中的营养位置。应用稳定同位素技术分析了鄱阳湖北部湖口县、都昌县、星子县、吴城镇4个采样点95条鱼和其他食物网成分样品的碳、氮稳定同位素比值,构建了鄱阳湖枯水期末期水生食物网。结果表明,不同水域颗粒有机物(POM)的δ13C值不同,范围为-27.5‰～-24.6‰可以区分赣江、修水、鄱阳湖、长江和鄱阳湖湖交汇处水体的颗粒有机物特征。江西鄱阳湖国家级自然保护区受人类活动

罗氏沼虾卵子在授精时的变化(英文)

<正> The freshwater giant prawn, Macrobrachium rosenbergii is of great economic importance in many coun-tries. It's farmed production is recorded globally. We examine the fertilization cytology in the hope that theymay serve to augment the previous reports

Waterborne exposure to PFOS causes disruption of the hypothalamus-pituitary-thyroid axis in zebrafish larvae

Thyroid hormones (THs) play an important role in the normal development and physiological functions in fish. Environmental chemicals may adversely affect thyroid function by disturbing gene transcription. Perfluorooctane sulfonate (PFOS), a persistent compound, is widely distributed in the aquatic environment and wildlife. In the present study, we investigated whether PFOS could disrupt the hypothalamic-pituitary-thyroid (HPT) axis. Zebrafish embryos were exposed to various concentrations of PFOS (0, 100, 200 and 400 mu g L-1) and gene expression patterns were examined 15 d post-fertilization. The expression of several genes in the HIPT system, i.e., corticotropin-releasing factor (CRF), thyroid-stimulating hormone (TSH), sodium/iodide symporter (NIS), thyroglobulin (TG), thyroid peroxidase (TPO), transthyretin (TTR), ioclothyronine deiodinases (Dio1 and Dio2) and thyroid receptor (TR alpha and TR beta), was quantitatively measured using real-time PCR. The gene expression levels of CRF and TSH were significantly up-regulated and down-regulated, respectively, upon exposure to 200 and 400 mu g L-1 PFOS. A significant increase in NIS and Diol gene expression was observed at 200 mu g L-1 PFOS exposure, while TG gene expression was down-regulated at 200 and 400 mu g L-1 PFOS exposure. TTR gene expression was down-regulated in a concentration-dependent manner. Up-regulation and down-regulation of TR alpha and TR beta gene expression, respectively, was observed upon exposure to PFOS. The whole body thyroxine (T-4) content remained unchanged, whereas triiodothyronine (T-3) levels were significantly increased, which could directly reflect disrupted thyroid hormone status after PFOS exposure. The overall results indicated that PFOS exposure could alter gene expression in the HPT axis and that mechanisms of disruption of thyroid status by PFOS could occur at several steps in the synthesis, regulation, and action of thyroid hormones. (C) 2009 Elsevier Ltd. All rights reserved.

Using drift nets to capture early life stages and monitor spawning of the Yangtze River Chinese sturgeon (Acipenser sinensis)

P>A sampling system for capturing sturgeon eggs using a D-shaped bottom anchored drift net was used to capture early life stages (ELS) of Chinese sturgeon, Acipenser sinensis, and monitor annual spawning success at Yichang on the Yangtze River, 1996-2004, before and just after the Three Gorges Dam began operation. Captured were 96 875 ELS (early life stages: eggs, yolk-sac larvae = eleuthero embryos, and larvae); most were eggs and only 2477 were yolk-sac larvae. Most ELS were captured in the main river channel and inside the bend at the Yichang spawning reach. Yolk-sac larvae were captured for a maximum of 3 days after hatching began, indicating quick dispersal downstream. The back-calculated day of egg fertilization over the eight years indicated a maximum spawning window of 23 days (20 October-10 November). Spawning in all years was restricted temporally, occurred mostly at night and during one or two spawning periods, each lasting several days. The brief temporal spawning window may reduce egg predation by opportunistic predators by flooding the river bottom with millions of eggs. During 1996-2002, the percentage of fertilized eggs in an annual 20-egg sample was between 63.5 to 94.1%; however, in 2003 the percentage fertilized was only 23.8%. This sudden decline may be related to the altered environmental conditions at Yichang caused by operation of the Three Gorges Dam. Further studies are needed to monitor spawning and changes in egg fertilization in this threatened population.