柳树对水体氮素的去除率及其吸收动力学

在水培条件下,研究了2种柳树(Salix integra)无性系(“一支笔”和“微山湖”)对模拟富营养化水体中氮素的吸收状况,并采用常规耗竭法探讨了柳树幼苗根系对NH4+-N、NO3--N的吸收动力学特征.结果表明:2种柳树无性系对低浓度模拟富营养化水体中总氮的去除率均达90％以上,是高浓度情况下的2倍;对低浓度模拟污水中总磷的去除率达80％,高浓度下则达92％,且“一支笔”对总氮、总磷的吸收效果优于“微山湖”;2种柳树无性系对氮素的吸收均表现为水体中营养物质浓度越高,去除效果越好;只有NH4+-N或NO3--N存在时,“微山湖”的最大吸收速率和亲和力高于“一支笔”;当有其他氮源影响时,2种柳树无性系对NH4+-N和NO3--N的吸收效率则下降至50％;研究表明,柳树对富营养化水体的生态修复作用较强,是进行面源污染生态修复的优良树种.     

鲎的分布及生活习性

鲎是一种古老的节肢动物,现存的鲎分为二亚科三属四种,本文对鲎在世界上的分布及其生活习性做了概述。     

Gill microsomal (Na+,K+)-ATPase from the blue crab Callinectes danae: Interactions at cationic sites

Euryhaline crustaceans tolerate exposure to a wide range of dilute media, using compensatory, ion regulatory mechanisms. However, data on molecular interactions occurring at cationic sites on the crustacean gill (Na⁺,K⁺)-ATPase, a key enzyme in this hyperosmoregulatory process, are unavailable. We report that Na⁺ binding at the activating site leads to cooperative, heterotropic interactions that are insensitive to K⁺. The binding of K⁺ ions to their high affinity sites displaces Na⁺ ions from their sites. The increase in Na⁺ ion concentrations increases heterotropic interactions with the K⁺ ions, with no changes in K_0.5 for K⁺ ion activation at the extracellular sites. Differently from mammalian (Na⁺,K⁺)-ATPases, that from C. danae exhibits additional NH₄⁺ ion binding sites that synergistically activate the enzyme at saturating concentrations of Na⁺ and K⁺ ions. NH₄⁺ binding is cooperative, and heterotropic NH₄⁺ ion interactions are insensitive to Na⁺ ions, but Na⁺ ions displace NH₄⁺ ions from their sites. NH₄⁺ ions also displace Na⁺ ions from their sites. Mg²⁺ ions modulate enzyme stimulation by NH₄⁺ ions, displacing NH₄⁺ ion from its sites. These interactions may modulate NH₄⁺ ion excretion and Na⁺ ion uptake by the gill epithelium in euryhaline crustaceans that confront hyposmotic media.     

锯缘青蟹卵黄发生期卵母细胞和卵泡细胞之间的结构变化

通过电镜研究了锯缘青蟹二次卵巢发育过程中卵黄发生期（分为初期和后期）卵母细胞表面的结构和胞质的变化。卵黄发生初期分为：内源性卵黄发生阶段和有卵泡细胞直接参与的外源性卵黄合成阶段,前者特征为：在卵母细胞中充满了内质网泡,在泡内有不同程度的卵黄物质合成,此时在卵母细胞的表面区域,可见很多卵泡细胞向卵母细胞表面迁移,并包围卵母细胞。后者其特征是在卵母细胞的表面,有大量的胞饮小泡出现在卵膜的内面,随着两细胞表面膜的逐步融合和胞饮作用加强最后形成链锁状结构,胞质中靠近卵质周围有卵黄体的积极合成和大更换 脂肪滴积累,在此阶段的后期,卵泡细胞质已基本吸收完毕,卵泡细胞膜和卵母细胞膜融合,某些界面已无膜结构。卵黄发生后期在亲蟹孵出幼体后的第11d至第27d基本结束,此期也主要以外源性卵黄发生为主,在卵母细胞的周围,卵泡细胞迅速扩大,其间分布着大量的大小不同的囊泡和线粒体,在接近卵母细胞表面,还常可见大量的脂肪滴存在。卵泡细胞与卵母细胞间其膜结构完全消失,从而可使滤泡大片细胞质直接融入卵母细胞中,以后随着卵黄发生的进一步发展,卵母细胞与卵泡细胞的交界面逐步形成一个网状的膜结构屏障,同时在卵巢中可见正在降解的卵母细胞,在卵黄发生近结束以后,在卵母细胞的表面,逐步形成两层卵膜,这时的卵母细胞质中几乎充满了卵黄体和脂肪滴。     

Walking speed and area utilization of red king crab (<Emphasis Type="Italic">Paralithodes camtschaticus</Emphasis>) introduced to the Barents Sea coastal ecosystem

The red king crab (Paralithodes camtschaticus) was introduced in the Barents Sea in the 1960s and soon established a viable population. Proper management and exploitation of the Barents Sea king crab stock require better understanding of the spatial dynamics at different scales. This study examines the small-scale movement patterns of seven adult male crabs tracked for a period of up to one month from mid July to mid August at 150 m depth in a semi-enclosed fjord on the Russo-Norwegian border. The crabs were tagged with acoustic transmitters and their movements monitored with an acoustic positioning system. Low walking speeds (<0.01 m s⁻¹) were most frequent but the crabs could move at a maximum speed of 0.15 m s⁻¹ and walk an actual distance of up to 270 m over a period of one hour. However, the crabs usually moved within a relatively restricted area with mean hourly longest rectilinear distance varying from 26 to 64 m. The crabs alternated between periods of low and high activity, which could reflect feeding in and movements between food patches. The lack of a diel activity rhythm may be due to high light levels during the polar summer night, or a chemically mediated food search strategy.     

Auditory stimulation dishabituates anti-predator escape behavior in hermit crabs (Coenobita clypeatus)

Responses to innocuous stimuli often habituate with repeated stimulation, but the mechanisms involved in dishabituation are less well studied. Chan et al. (2010b) found that hermit crabs were quicker to perform an anti-predator withdrawal response in the presence of a short-duration white noise relative to a longer noise stimulus. In two experiments, we examined whether this effect could be explicable in terms of a non-associative learning process. We delivered repeated presentations of a simulated visual predator to hermit crabs, which initially caused the crabs to withdraw into their shells. After a number of trials, the visual stimulus lost the ability to elicit the withdrawal response. We then presented the crabs with an auditory stimulus prior to an additional presentation of the visual predator. In Experiment 1, the presentation of a 10-s, 89-dB SPL noise produced no significant dishabituation of the response. In Experiment 2 we increased the duration (50 s) and intensity (95 dB) of the noise, and found that the crabs recovered their withdrawal response to the visual predator. This finding illustrates dishabituation of an antipredator response and suggests two distinct processes—distraction and sensitization—are influenced by the same stimulus parameters, and interact to modulate the strength of the anti-predator response.     

黄河口邻近海域生态系统能量流动与三疣梭子蟹增殖容量估算

增殖放流是渔业资源养护的重要手段, 生态系统与放流种类能流格局的变化研究,是进行增殖容量评估的研究基础.根据2012和2013年黄河口邻近海域的资源调查数据,构建了黄河口邻近海域6、8、10月的Ecopath模型,比较分析了3个月份该海域生态系统能量流动的变化,初步评估了三疣梭子蟹的增殖容量.结果表明： 黄河口邻近海域生态系统的能量流动主要在营养级I～III之间进行,营养级IV以及以上的能量流动较小.6月第I营养级整合系统流动的比例最高,8月最低.第II营养级整合系统流动的比例8月最高,6月最低.三疣梭子蟹相对能量流动和绝对能量流动均是第III营养级最高,三疣梭子蟹的营养级3月平均为3.28.黄河口邻近海域生态系统有较高的剩余生产量,6月最高、8月最低,系统的总初级生产量/总呼吸(TPP/TR) 3个月份分别为5.49、2.47、3.01,总初级生产量/总生物量(TPP/B)分别为47.61、33.30、29.78,同时具有较低的循环指数(FCI：0.03～0.06),黄河口邻近海域生态系统处于脆弱的不稳定期.系统的能量转换效率为7.3%～11.5%;渔获物的平均营养级8月和10月有所下降,3个月份分别为3.23、2.97和2.82;总捕捞效率8月最高,6月最低.在黄河口邻近海域8月Ecopath模型基础上,初步评估三疣梭子蟹的增殖容量为1.5115 t·km^-2.     

中国鲎精子发生的研究:Ⅱ.精子形成

应用电技术研究中国鲎精子形成过程和特点,早期精子细胞核圆,染色质呈网状分布,胞质中有许多线粒体和高尔基液泡,精子形成期间,出现合胞体现象,核分裂而胞质不分裂,细胞通过胞质桥相联系,随后出现隔板,逐渐将细胞核分开。细胞随访核向后移动而呈现极化现象。核的顶部出现一个高尔基－线粒体区,顶体由高在液泡演变而。精子形成期间,核中央位置形成贯穿整个的中央通道,并在核中形成植入窝,中心粒位于其中,成熟精子胞质极