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1.
天然河道底部的障碍物形成了复杂的水流环境,洄游鱼类对复杂水流环境的响应行为对于鱼能否上行或下行通过障碍物并完成生活史至关重要。本研究在封闭水槽中采用递增流速法测试了鳙(Aristichthys nobilis)幼鱼在不同障碍物型式下的临界游泳速度,结果表明:鳙幼鱼在自由来流、圆柱和半圆柱下的临界游泳能力无显著性差异(P>0.05),而方柱下鳙幼鱼的临界游泳能力显著降低(P<0.05);鳙幼鱼受障碍物下游复杂流场影响表现出3个特征游泳姿态,依此划分出3个位置区间;为了分析方柱下游泳能力下降的原因,统计了不同流速下鳙幼鱼在3个位置区间所占的时间百分比,并提取了相应的游泳动力学指标,包括摆尾频率、摆尾幅度、鱼头侧向最大加速度、鱼身侧向最大加速度、身体波动速度、身体波长和鱼头最大转角速度;鳙幼鱼在近柱区(障碍物下游6~26 cm; A区)停留时间最长,时间百分比高达63.1%;其次是中区(障碍物下游26~46 cm; B区)为29.1%;远柱区(障碍物下游46~66 cm; C区)最低,为7.8%;不同水流速度下,鳙幼鱼在方柱下游3个位置区间的时间百分比分布也有明显差异,在流速为5...  相似文献   

2.
鳙(花鲢)在自然环境中分布于中国南部流域至阿穆尔河,是重要的经济性鱼类,具江湖生殖洄游特性。大坝建设阻碍了其洄游产卵繁殖通道,导致自然环境中其繁殖力的下降,需要有效的过鱼设施帮助鳙通过大坝等水流屏障。为了设计高效的鱼道引导鳙通过,本文通过自制密封的鱼类游泳实验装置,研究了鳙幼鱼游泳能力。测定了5个温度(5、10、15、20和25℃)下鳙幼鱼的临界游泳速度。通过测定不同温度下,疲劳前后血清总蛋白(TP)、血糖(GLU)和甘油三酯(TG)含量,评价疲劳运动引起的生理胁迫。结果表明,在试验温度范围内,随着温度的升高,临界游泳速度显著提高(P0.05)。25℃时临界游泳速度最大,为7.01 BL/s(1.19 m/s)。在疲劳运动后,血清总蛋白、血糖和甘油三酯含量显著升高(P0.05)。水温低于15℃与高于15℃相比,鳙疲劳运动后血清总蛋白、血糖和甘油三酯含量显著升高。以鳙幼鱼为研究对象,研究了非适宜温度环境和疲劳运动胁迫下鱼类的生理反应。以期为鱼类生理学研究和渔业保护管理等领域提供理论依据,为制定有效的鱼道提供数据参考。  相似文献   

3.
研究以具有下行洄游需求的鲢(Hypophthalmichthys molitrix)、鳙(Aristichthys nobilis)幼鱼为实验对象, 分别在2种不同流态加速流(Ⅰ: 22—55 cm/s, Ⅱ: 25—60 cm/s)中进行下行实验, 对实验鱼在2种加速流中的游泳行为(下行率、下行方式及各区域游泳时间)进行定量分析并利用游泳停留时间百分比Ft衡量其偏好水流速度。结果显示: 加速流下鲢、鳙均表现出了直接下行与非直接下行两种行为。其中加速流Ⅰ中鲢、鳙直接下行率分别为35.71%、30.00%, Ⅱ中分别为45.83%、59.09%。非直接下行的鲢在2种加速流中小于30 cm/s流速区域的停留时间显著高于其他区域(P<0.05), 即鲢在实验条件下的偏好水流速度范围为小于30 cm/s; 非直接下行的鳙在加速流Ⅰ中小于30 cm/s及50—55 cm/s流速区域的停留时间显著高于其他区域(P<0.05), Ⅱ中小于30 cm/s流速区域的停留时间显著高于其他区域(P<0.05), 即鳙本实验条件下偏好水流速度范围为小于30 cm/s。将2种加速流流速相同区域合并分析发现鲢、鳙在小于30 cm/s和50—55 cm/s流速区域的停留时间存在显著性差异(P<0.05), 中间及高流速区域无明显性差异(P>0.1)。研究表明: 加速流对鲢、鳙下行游泳行为产生了影响且2种鱼在下行通过方式和偏好流速选择上存在一定的种间差异性。  相似文献   

4.
张倩  康斌 《动物学研究》2013,34(4):429-436
为探讨团头鲂幼鱼(Megalobrama amblycephala)游泳行为对水流的响应规律,该文通过特制鱼类游泳行为测定装置,测定了团头鲂幼鱼在25℃,0、0.1、0.2、0.3、0.4m/s流速条件下的游速、游距、转角、至中心点的距离及游泳轨迹。结果表明:随着流速的增大,个体游速、游距及转角值均相应增大。0、0.1及0.2m/s流速组间的游速、游距及转角差异均不显著(P>0.05),但显著小于0.3和0.4m/s组别,且0.3和0.4m/s流速组之间差异均不显著(P>0.05);整个时间段内,个体至中心点的距离随流速增大并未呈现明显规律性,各流速间差异不显著(P>0.05),游速与游距呈显著线性正相关,而与转角呈显著线性负相关,与至中心点的距离则无相关性;游泳轨迹随水流增大趋向复杂化。  相似文献   

5.
胭脂鱼幼鱼的临界游泳速度   总被引:2,自引:0,他引:2  
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6.
五种淡水鱼类幼鱼游泳能力的比较   总被引:1,自引:0,他引:1  
付翔  付成  付世建 《生态学杂志》2020,(5):1629-1635
为了探讨栖息于不同生境中鱼类的游泳能力和偏好游泳速度及其生理机制,本研究以中华倒刺鲃(Spinibarbus sinensis)、异育银鲫(Carassius auratus gibelio)、岩原鲤(Procypris rabaudi)、青鱼(Mylopharyngodon piceus)和胭脂鱼(Myxocryprinus asiaticus) 5种鱼的幼鱼为对象,在(25±1)℃条件下测定了5种鱼类的标准代谢率(SMR)、最大代谢率(MMR)、有氧代谢范围(MS)、临界游泳速度(Ucrit)、最大匀加速游泳速度(Ucat)和偏好游泳速度(Upref)。结果发现:5种实验鱼中,中华倒刺鲃的游泳能力最强,游泳能力较差的为青鱼和胭脂鱼; 5种鱼之间的代谢和游泳能力差异显著,其偏好游泳速度主要集中在(10~24.5cm·s-1)区域。研究表明,鱼类游泳能力的种间差异可能主要由心鳃系统相关的呼吸能力和体型相关的游泳效率所决定。本研究提供的有关鱼类游泳能力、偏好游泳速度等资料对于鱼道设计等有一定的参考价值...  相似文献   

7.
以具有下行洄游需求的鳙(Aristichthys noblis)幼鱼为研究对象, 在自行设计制造加速流的装置中进行下行实验, 结果发现: 在实验设置的3个入口流速下(入口流速分别为: 0.018、0.034和0.053 m/s), 鳙幼鱼的通过率均为100%。在下行通过孔口的方式上, 以尾部先通过为主(即顶流通过), 尤其是在流速较高的时候, 头部先通过比例仅为6.25%。在通过总时间(从实验开始至通过孔口的时间)上, 鳙幼鱼在低流速条件下显著小于在中流速条件下(P<0.05), 而在高流速条件下与中低两个流速条件下均无显著性差异(P>0.1)。在通过时间(从实验鱼最后一次进入加速区域, 至通过孔口的时间)上, 鳙幼鱼在三种流速条件下没有显著差异性(P>0.1)。研究表明, 加速流会对鳙幼鱼下行的时间和方式产生影响。研究旨在为鱼类资源保护, 帮助鱼类安全高效过坝提供基础数据, 同时也为研究鱼类在下行过程中应对加速流的行为研究提供一种研究方法。  相似文献   

8.
温度对鳊幼鱼临界游泳速度和代谢范围的影响   总被引:2,自引:0,他引:2  
杨阳  曹振东  付世建 《生态学杂志》2013,32(5):1260-1264
为了考查温度对鳊(Parabramis pekinensis)幼鱼有氧运动能力的影响并探讨有关代谢机制,本研究分别在不同温度(10、18、26和34℃)下测定实验鱼的静止耗氧率(RMR)、临界游泳速度(Ucrit)和运动过程中的最大耗氧率(MMR),并以MMR和RMR的差值分别计算各温度下的能量代谢范围(MS).结果表明:随着温度的上升,Ucrit呈现显著上升的趋势(P<0.05),温度由10℃升高至34℃,Ucrit由(6.01±0.32)升至(8.82±0.27) BL·s-1;RMR和MMR也随温度的升高呈现显著上升趋势(P<0.05),其测定值在温度由10℃升高至34 c℃时分别为(161.7±28.8)、(293.0±27.6) mg O2·kg-1·h-1和(558.6±20.4)、(1278.7±57.4) mgO2 ·kg-1 ·h-1,MMR在34℃与26℃相比有下降趋势;MS在10~26℃范围随温度的上升显著上升,26 ~ 34℃却出现显著下降(P<0.05).可见:Ucrit和MS在高温条件下的反应不尽一致;这可能与水的粘滞系数下降、进而导致鳊能量效率提升有关,还可能由于实验鱼无氧代谢能力提高所致.  相似文献   

9.
鲢幼鱼在不同水流速度下的暴发-滑行行为策略   总被引:1,自引:0,他引:1  
在水温(18±1)℃的条件下,以全长(11.70±0.57)cm的鲢(Hypophthalmichthys molitrix)幼鱼为研究对象,测定其不同流速(16.5、22.0、27.5、33.0、38.5、44.0、49.5和55.0 cm/s)下的持续游泳时间、调头百分比和暴发-滑行运动数据。结果表明,鲢的平均持续游泳时间先随流速的增加而减小,后随流速的增加而增加。当流速33.0 cm/s时,平均持续时间最短为118.6min,其中各组试验鱼的最大可持续游泳时间均可达到200min。调头百分比随流速的增加迅速减小,当流速≥44.0 cm/s时,不再出现调头行为。暴发-滑行游泳的平均暴发时间随流速的增加呈上升趋势(y=0.03x+2.64,R2=0.92,P<0.05)。平均对地暴发距离均在30-45 cm,没有显著性差异(P>0.05),平均绝对暴发距离存在极显著性差异,且随流速的增加而增加(y=4.98x-5.63,R2=0.98,P<0.001)。平均对地暴发速度没有显著性差异(平均对地平均速度和最大速度分别在9-12 cm/s、12-16 cm/s,P>0.05)。平均绝对暴发速度与水流速度之间存在线性正相关关系(平均绝对平均暴发速度:y=0.98x+10.74,R2=1.00,P<0.001;平均绝对最大暴发速度:y=1.02x+13.75,R2=0.99,P<0.001)。研究表明鲢在不同的流速下采取的暴发-滑行行为策略不同。  相似文献   

10.
两种温度条件下四种鱼类临界游泳速度的比较   总被引:2,自引:0,他引:2  
以鳜(Siniperca chuatsi)、瓦氏黄颡鱼(Pelteobagrus vachelli)、鲫(Carassius auratus)、鳙(Aristichthys nobilis)4种暖水性鱼类为研究对象,分别在(28±1)℃和(10±1)℃条件下测定它们的临界游泳速度,采用SPSS17.0统计软件进行数据的分析比较。体长相近的鱼类之间比较,鳜的绝对临界游泳速度和相对临界游泳速度均显著性低于鳙(P0.01),瓦氏黄颡鱼的绝对临界游泳速度和相对临界游泳速度均显著性低于鲫(P0.01)。通过比较两种温度条件下同种鱼的临界游泳速度,结果发现4种鱼在这两种温度条件下的临界游泳速度均有极显著性差异(P0.01),在(28±1)℃条件下4种鱼的临界游泳速度极显著性高于(10±1)℃条件下它们的临界游泳速度。  相似文献   

11.
鳙鱼同工酶发育遗传学研究   总被引:18,自引:3,他引:18  
采用淀粉或聚丙烯酰胺凝胶电泳法分析鳙鱼早期发育阶段(从未受精卵到卵黄吸尽期)及成体不同组织(脑、眼、心、肌、肾、肝)中六种同工酶(LDH,MDH,IDH,ADH,SDH,EST)的分化表达模式。鳙鱼同工酶基因的表达具有明显的组织特异性。早期发育阶段,ADH和SDH均无染色活性;LDH、MDH和IDH具有不同的发育变化谱式,而EST酶谱在整个早期发育阶段均无明显变化。与鲢、草鱼相比,鳙鱼早期发育过程中胚胎Ldh-A基因激活的时间被推迟。上述结果可为鳙鱼种群的生化遗传结构分析以及鳙鱼的人工育种提供基础资料。  相似文献   

12.
大鼠肝糖皮质激素受体的昼夜节律   总被引:1,自引:0,他引:1  
雄性成年大鼠102只,分自然光组、人工光组和明暗颠倒组,于不同时间处死,测定肝胞坡和胞核的糖皮质激素受体(GCR_c和GCR_o)。发现GCR_c和GCR_o都以23:00和O2:00为最高,中午最低。明暗颠倒组的GCR_c以23:00为最高,02:00—11:00都在低水平。同时还测定了肝的酪氨酸转氨酶活性和血浆皮质酮,讨论了三者昼夜节律的相互关系。  相似文献   

13.
研究表明, 哺乳动物脑中去甲肾上腺素(Norepinephrine, NE) 作为一种植物性神经信息传递的经典递质, 表现为水平波动的昼夜节律行为(李思嘉. 1982. 生理科学进展13 (2) : 189) , 该变化可能与机体生理机能改变相关。在低氧应激下, 脑内N E 的更新率升高, 可对脑中各脑区功能起到协调作用。根田鼠是青藏高原金露梅灌丛的优势小哺乳动物, 本文研究在自然光照下, 根田鼠大脑内去甲肾上腺素(NE) 水平的昼夜节律, 以及在模拟低氧5 000 m 和7 000 m 高度条件下的含量变化情况。  相似文献   

14.
为探讨树视交叉上核是否参与泌尿昼夜节律的调控,对正常树及视交叉上核损毁后的树排尿的昼夜时间规律进行了观测分析。结果表明,正常树排尿呈现明显的昼夜节律———白天尿量为全天尿量的(8852±1540)%;视交叉上核损毁后,树排尿的昼夜节律明显改变———白天尿量仅为全天尿量的(6286±1818)%,同时树的尿量(特别是夜间的尿量)明显憎多。以上结果说明视交叉上核在树体内也参与了泌尿昼夜节律的调节。  相似文献   

15.
In previous experiments, we found that rats raised in constant light (LL) manifested a more robust circadian rhythm of motor activity in LL and showed longer phase shifts after a light pulse in constant darkness (DD) than those raised under constant darkness. In addition, we observed that the effects produced by constant light differed depending on the time of postnatal development in which it was given. These results suggest that both sensitivity to light and the functioning of the circadian pacemaker of the rat could be affected by the environmental conditions experienced during postembryonic development. Thus, the present experiment aimed to study whether postnatal exposure to light could also affect the circadian system of the mouse. Three groups of mice were formed: One group was raised under constant darkness during lactation (DD group), the second under constant light (LL group), and the third under light-dark cycles (LD group). After lactation, the three groups were submitted first to constant light of high intensity, then to LD cycles, and finally to constant darkness. In the DD stage, a light pulse was given. Finally, mice were submitted to constant light of low intensity. We observed that the circadian rhythm of the DD group was more disturbed under constant light than the rhythm of the LL group, and that, when light intensity increased, the period of the rhythm of the DD group lengthened more than that of the LL group. No significant differences among the groups were found in the phase shift induced by the light pulse. Therefore, it appears that DD mice are more sensitive to light than their LL counterparts. However, at present there is no evidence to affirm that the light environment experienced by the mouse during postnatal development affects the circadian pacemaker. (Chronobiology International, 18(4), 683–696, 2001)  相似文献   

16.
17.
大麝鼩是一种夜行性动物,其夜间(19:00—6:00)的活动频次占全天活动总频次的88.67%;夜间活动呈双峰型曲线,前峰在19:00—24:00,后峰在2:00—5:00。其夜行性指数为6.31,但各季节不同:春季5.94,夏季4.01,秋季6.56,冬季8.71,比其他鼩鼱科动物高。每日活动总额次雄性高于雌性,雄性的夜行性指数亦比雌性高。在人工倒置光周期的条件下,其最初几天的活动节律极度紊乱,至第7天后才稳定地回到自然光周期的日活动次数水平。  相似文献   

18.
Although extraocular light can entrain the circadian rhythms of invertebrates and nonmammalian vertebrates, almost all studies show that the mammalian circadian system can only be affected by light to the eyes. The exception is a recent study by Campbell and Murphy that reported phase shifts in humans to bright light applied with fiber-optic pads behind the knees (popliteal region). We tested whether this extraocular light stimulus could accelerate the entrainment of circadian rhythms to a shift of the sleep schedule, as occurs in shift work or jet lag. In experiment 1, the sleep/dark episodes were delayed 8h from baseline for 2 days, and 3h light exposures were timed to occur before the temperature minimum to help delay circadian rhythms. There were three groups: (1) bright (about 13,000 lux) extraocular light from fiber-optic pads, (2) control (dim light, 10–20 lux), and (3) medium-intensity (about 1000 lux) ocular light from light boxes. In experiment 2, the sleep/dark episodes were inverted, and extraocular light was applied either before the temperature minimum to help delay circadian rhythms or after the temperature minimum to help advance rhythms. Circadian phase markers were the salivary dim light melatonin onset (DLMO) and the rectal temperature minimum. There was no evidence that the popliteal extraocular light had a phase-shifting effect in either experiment. Possible reasons for phase shifts in the Campbell and Murphy study and not the current study include the many differences between the protocols. In the current study, there was substantial sleep deprivation before the extraocular light was applied. There was a large shift in the sleep/dark schedule, rather than allowing subjects to sleep each day from midnight to noon, as in the Campbell and Murphy study. Also, when extraocular light was applied in the current protocol, subjects did not experience a change from sleeping to awake, a change in posture (from lying in bed to sitting in a chair), or a change in ocular light (from dark to dim light). Further research is necessary to determine the conditions under which extraocular light might produce phase shifts in human circadian rhythms. (Chronobiology International, 17(6), 807–826, 2000).  相似文献   

19.
In order to study circadian rhythms and decompression sickness (DCS), we determined: 1) the baseline circadian time structure in noncompressed rats of potential response variables to compression/decompression (C/D), and 2) whether rats subjected to C/D display a circadian time-dependent difference in inflammatory response intensity and biological tolerance. Subgroups of male rats, standardized to a 12?h light/12?h dark schedule, were evaluated every 4?h over 24?h after they were either compressed to 683?kPa (group E) or remained at sea level (group C). During 60?min recovery, evaluation included gross DCS symptoms and pulmonary edema in all E rats, and cell counts, nitric oxide, protein, thromboxane B2, and leukotriene E4 levels in survivors. Chi-square, ANOVA, and 24?h cosinor analyses were used to test for time-of-day effects. C/D exposures near the end of dark/activity or during light/resting were generally better tolerated, with lowest signs of DCS symptoms and lowest responses by most of the variables monitored. More deaths were observed in the first half of the dark/activity span. Of the 16 subsets of inflammatory-associated variables, overall increases were observed in 13 and decreases in 2. Significant or borderline significant circadian time effects were found in 14 variables in group C, 12 variables in group E, and 13 variables in response (E%C). Thus, nearly all baseline indices of DCS demonstrated circadian time-dependencies in the sea-level exposed control rats (group C), and nearly all were modified by the circadian time of C/D. Such time-of-day effects of DCS are potentially relevant to the operational concerns of occupations involving decompression exposures and the investigation of prevention and treatment intervention strategies of DCS. (Author correspondence: ).  相似文献   

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