葛洲坝产卵场中华鲟繁殖群体数量与繁殖规模估算及其变动趋势分析

采用声学探测的方法,进行中华鲟(Acipenser sinensis)繁殖群体数量的估算。2005～2007年,第1次产卵前的资源量分别为235尾、217尾和203尾;第1次产卵后的资源量分别为157尾、157尾和102尾。采用食卵鱼解剖统计和股分析的方法对中华鲟的自然繁殖规模进行估算,其结果为,2005～2007年间中华鲟的产卵量分别为356万粒、119.6万粒和238.6万粒。结合历史相关研究数据,对近10年的中华鲟繁殖群体数量和繁殖规模的变动趋势进行分析,结果显示,在20世纪90年代中期,第1次产卵

武汉月湖水生植被重建的实践与启示

通过生物操纵、浮水植物和植物浮岛原位净化、岸边人工湿地净化和科学种植等措施,2—3年内,在长江中游地区、面积为0.66km2、水质为劣Ⅴ类的重富营养湖泊武汉月湖重建了以菹草和伊乐藻为优势种的沉水植物先锋群落,2005年春季的沉水植物盖度达到45%,提高了透明度。利用水位低、透明度相对高的冬季种植伊乐藻、菹草等适合冬春季生长的沉水植物是建立沉水植物先锋群落的一个有效途径。重污染水体过低的透明度是重建沉水植被的主要限制因子,在低水位或较高透明度时期,水生植物可以耐受相对较高的污染负荷,并且在有条件降低水位时,

利用脉冲场凝胶电泳测定东湖浮游病毒基因组的大小

采用脉冲场凝胶电泳,对东湖水样中的浮游病毒基因组大小进行了测定,显示5条主要核酸带,其大小分别为20、50、100、150和250 kb,以20~60 kb的核酸带为强,而这符合噬菌体和噬藻体的基因组主要范围,进一步证实东湖浮游病毒的优势类群为噬菌体和噬藻体.

银鲫ZP3的表达特征和卵壳ZP3蛋白的分离

克隆得到银鲫(Carassius auratus gibelio)ZP3基因全长cDNA,在体外表达出银鲫的ZP3融合蛋白,并制备出多抗血清;通过免疫印迹和RT-PCR分析,研究了银鲫ZP3在卵子发生过程中的表达特征和在早期发育胚胎中的状态变化。研究结果表明,银鲫ZP3的转录发生在卵黄发生以前,而ZP3蛋白的翻译起始于卵黄形成阶段,且随着卵母细胞进一步成熟,其含量不断增加。ZP3蛋白的存在状态在受精后和早期胚胎发育过程中发生了明显变化。在受精后5—30min期间,抽提液中原始的ZP3蛋白带迅速消失,取而代

中华鳖造血和免疫器官的个体发育

采用常规孵化的中华鳖胚胎为材料 ,对不同发育时期造血和免疫器官进行了组织学研究 ,描述了卵黄囊、胸腺、肝、脾、肾以及骨髓的形态结构变化。发现胚胎期首先出现的造血器官是卵黄囊。此后 ,卵黄囊的造血干细胞出现在胚体的血循环中 ,造血功能相继在胚胎胸腺、肝、脾、骨髓 (可能还包括肾 )中产生。胸腺是中华鳖免疫系统发育的第一个淋巴器官 ,来自卵黄囊的干细胞在此先分化成小淋巴细胞 ,然后再迁移至脾脏。脾脏发育中首先出现各发育阶段的红细胞、嗜酸性的细胞和少量粒细胞 ,淋巴细胞出现较晚 ,未发现淋巴小结。在胚胎期肝脏发

网湖似刺鳊鮈种群生长和死亡率研究

本文根据６６９尾标本，研究长江中游网湖小型经济鱼类似刺鳊的种群生长和死亡率，从理论推导证明，鱼类的生长拐点与其临界年龄是一致的，并据以对网湖似刺鳊等小型经济鱼类的合理渔业对策问题进行了初步分析讨论。

丝藻目的一新属——骈丝藻属

<正> 1976年6月至8月,中国科学院青藏高原综合科学考察队藏北分队对冈底斯山,念青唐古拉山以北,昆仑山以南的广大藏北地区进行了多学科的综合考察。我所陈宜瑜同志参加了这次考察,对该地区各种水体的水生生物进行了广泛地采集,在采得的标本中,藻类是十分丰富的。我们在鉴定该区振泉湖藻类标本时,发现一特殊类型的藻类。通过对液浸标本和固定染色标本的研究,确定它是绿藻门丝藻目的一新属。

Comparative Expression of Zebrafish Lats1 and Lats2 and Their Implication in Gastrulation Movements

Large tumor suppressor (Lats) is a Ser/Thr kinase, and it presents an important function in tumor suppression. lats was originally identified in Drosophila and recently in mammals. In mammals, it contains two homologues, lats1 and lats2. In the present study, lats1 and lats2 were characterized from zebrafish (Danio rerio), which is the first report of lats in a nonmammalian vertebrate. The primary structure, genomic organization, and phylogenesis of lats from different species were studied, and the results suggest that lats1 is the direct descendant of invertebrate lats, whereas lats2 is formed by genome duplication. In zebrafish, both lats genes are maternally expressed, while they show distinctly different expression profiles during gastrulation. lats1 is almost ubiquitously expressed through development, and lats2 is more prominently expressed in the non-neural ectoderm region of zebrafish gastrula. Most intriguingly, as revealed by cell tracing and gene expression analysis, morpholino-mediated knockdown of either lats1 or lats2 led to obvious defects of cell migration in gastrulation, indicating the functional significance of lats in gastrulation movements. Developmental Dynamics 238:28502859, 2009. (C) 2009 Wiley-Liss, Inc.

Effects of cyanobacterial toxin microcystin-LR on the transcription levels of immune-related genes in grass carp Ctenopharyngodon idella

Recent studies in mammals have revealed that the cyanobacterial toxin MC-LR suppresses immune functions. Nevertheless, immunotoxic effects of microcystins have been little studied in fish. In this paper, we present the profiles of the immune modulation of MC-LR in grass carp, and quantitative real-time PCR methodology was developed for the measurement of relative transcription changes of six immune-related genes in the spleen and head kidney of the grass carp Ctenopharyngodon idella, which were intraperitoneally injected with 50 mu g MC-LR center dot kg(-1) body weight in a three-week period. This study was focused exclusively on gene transcription level changes at different time points after MC-LR exposure, so, only one dose was given. The investigated genes were interleukin-1 beta (IL-1 beta), tumor necrosis factor-alpha (TNF-alpha), type I interferon (Type I IFN), peptidoglycan recognition protein-L (PGRP-L), immunoglobulin M (IgM) and major histocompatibility complex class I (MHC-I) genes. The results demonstrated that the transcription levels of the TNF-alpha, type I IFN, and PGRP-L genes in the spleen and head kidney were significantly low at all time points, and those of IL-1 beta were significantly low in the head kidney at different time points. In addition, IgM and MHC-I transcription levels were only significantly low in the spleen and head kidney at 21 d postinjection. The changes in the transcription levels of immune-related genes induced by MC-LR confirmed its effect on inhibiting immune function at the transcription level.