不同流速下杂交鲟幼鱼游泳状态与活动代谢研究

为研究水流速度对杂交鲟幼鱼行为和代谢的影响,探讨游泳状态与活动代谢及相关游泳运动参数之间的关系,在26℃水温下,使用特制的鱼类游泳行为和活动代谢同步测定装置,测定了杂交鲟幼鱼在0.1、0.3、0.5 m/s三种流速和静水条件下的游泳状态、趋流率、摆尾频率和耗氧率。结果表明:随着流速的增大,杂交鲟幼鱼逆流前进和逆流静止游泳状态所占时间比例显著减少,而逆流后退所占时间比例显著增加,顺流而下时间比例有所上升。在0.0—0.3 m/s的流速范围内,杂交鲟幼鱼各个时段的平均趋流率、摆尾频率和耗氧率均随着流速的增加而增大,在0.3 m/s流速下分别达到100%﹑(2.53±0.34)Hz和(490.99±164.59)mg O2/(kg.h)。当流速增加至0.5 m/s时,在趋流率仍保持100%的情况下,其耗氧率相比0.3 m/s增加了21.86%,而摆尾频率却减小了6.70%。实验过程杂交鲟幼鱼趋流率与摆尾频率呈显著线性正相关,而摆尾频率与耗氧率在大部分时段却无相关性。随着时间的延长,各流速组杂交鲟幼鱼趋流率、摆尾频率和耗氧率呈现不同的变化趋势,其趋流率均相对稳定;但摆尾频率均随时间延长呈下降趋势,而耗氧率则在实验前9h随时间延长逐渐增加,随后趋于稳定。研究结果提示:杂交鲟幼鱼游泳状态的变化与流速有关,而反映运动强度大小的摆尾频率与活动代谢率的关系受到游泳状态的显著影响,同时也与运动代谢特征的时间变化有关。       

不同流速对鱇(鱼良)白鱼游泳行为的影响

在25℃水温下,采用特制的鱼类游泳行为测定装置对实验鱼在静水和0.1、0.2和0.25 m·s-1流速下的游泳状态、游泳速度、趋流率和摆尾频率等参数进行测定,研究水流速度对鱇(鱼良)白鱼(Anabarilius grahami)游泳行为的影响.结果表明:有流速组的趋流率显著高于静水组,但不同流速组间的趋流率无显著差别;在0 ～0.2 m·s-1流速范围内,摆尾频率随流速加快而显著增大,但在0.25 m·s-1流速下40 min后摆尾频率显著低于0.2m·s-1流速组;随着流速的增大,主要游泳状态由逆流前进变为逆流静止;在有流速组,顺流而下状态所占时间比例相对其他游泳状态都较少;在逆流游泳的3种状态中,游泳速度均随流速的增加而增大,在顺流而下状态中,游泳速度和水速间无显著相关;游泳速度、摆尾频率和水流速度两两之间均存在显著的线性相关.     

不同流速下红鳍银鲫趋流行为与耗氧率的变化

在28℃水温下,使用特制的鱼类游泳行为和活动代谢同步测定装置对红鳍银鲫(Barbodes schwanenfeldi)幼鱼在0 m/s、0.1 m/s、0.3 m/s、0.5 m/s 4种流速条件下的趋流行为和耗氧率进行了同步测定和统计分析.结果表明: 红鳍银鲫在静水下的游泳活动表现出随机而无特定的方向性,当流速达到0.3 m/s以上时则呈现很强的趋流性.和静水对照组相比,三个流速实验组在各个时间段的趋流率、摆尾频率和耗氧率均显著上升,其中多数时间段以0.3 m/s流速组最大,0.5 m/s流速组次之.低流速组(0,0.1 m/s)三个指标在90 min内随时间变化不显著,而高流速组(0.3,0.5 m/s)随时间变化明显.红鳍银鲫在90 min各个时间段摆尾频率(Tail beat frequency)与趋流率(Rheotaxis frequency)均呈显著的线性相关,其回归关系式为:RF=a bTBF,a值在41.13-55.02、b值在8.0 7-11.42、R在0.69-0.95之间;摆尾频率和耗氧率(Oxygen consumption rate)同样呈 显著的线性相关,其回归关系式为:OCR=a bTBF,a值在77.38-137.42, b值在10.85-59.36,R在0.87-0.96之间.0.3 m/s流速下红鳍银鲫趋流率、摆尾频率和耗氧率24 h的变化规律为:实验开始时三个指标均随时间延长而逐渐增大,在3 h达到最大值,然后开始下降并长时间维持在一定水平上,其中耗氧率在最初3 h的增幅显著大于趋流率和摆尾频率,而随后回落的幅度却小于前两者.在较高流速下,红鳍银鲫幼鱼不能长期保持趋流状态和维持较高的代谢水平     

水流对团头鲂(Megalobrama amblycephala)幼鱼游泳行为的影响

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。     

不同体质量和饥饿程度对红鳍东方鲀幼鱼游泳能力的影响

为了考察不同体质量和饥饿程度红鳍东方鲀(Takifugu rubripes)幼鱼的游泳能力,利用行为生态学方法测定了不同体质量(0.22—3.31 g)和饥饿天数(1d、3d、6d和9d)下红鳍东方鲀幼鱼的绝对临界游速(U_crit,cm/s)、相对临界游速(U_crit’,体长/s,BL/s)、偏好游速(U_pref,cm/s)、6个流速区域(2—36 cm/s)下停留时间百分比(P_t,%)、偏好区域平均流速(V_mean,cm/s)和总游泳距离(D_1h,m)等游泳行为指标。结果显示,体质量和饥饿显著影响红鳍东方鲀幼鱼的U_crit、U_crit’、P_t、V_mean和D_1h。随体质量增加,实验鱼的U_crit、U_pref、V_mean和D_1h均逐渐升高,而U_crit...     

障碍物对鳙幼鱼游泳行为的影响

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...     

流速对细鳞裂腹鱼游泳行为及能量消耗影响的研究

通过自制密封的鱼类游泳实验装置, 研究了流速对细鳞裂腹鱼游泳行为和能量消耗的影响。结果显示,细鳞裂腹鱼的摆尾频率随游泳速度的变化有明显的变化规律, 摆尾频率随着流速的增加而显著性的增加,而摆尾幅度有减小趋势, 差异性不显著。结果还表明, (26±1) ℃时, (10.60±0.54) cm 细鳞裂腹鱼的相对临界游泳速度为(11.5±0.5) BL/s, 绝对临界游泳速度为(110.28±2.02) cm/s。测定的相对临界流速较其他的鲤科鱼大,是对生存水流环境(流速0.5—1.5m/s)适应性的表现。这一结果表明鱼类的游泳能力是能够训练的。运动代谢率与相对流速的关系为, AMR = 93.08e(0.307v) + 314.33, R2= 0.994; 单位距离能耗与流速的指数关系为COT =28e (-1.03V) +6.05, R2= 0.998。流速达到8 BL/s 时, 裂腹鱼耗氧率开始下降, 从流速7 BL/s 时, (1245.57±90.97 )mg O2/(kg·h)最大, 下降到(978.78±189.38) mg O2/(kg·h)。1—7 BL/s 流速范围内, 裂腹鱼单位时间内的耗氧率随着游泳速度的增加而增加, 而且随着游泳速度的增加, 单位距离能耗(COT)逐渐减少, 最小能耗在6 倍体长流速, 0.68 m/s 时, 为(6.00±1.57) J/(kg·m), 其能量利用效率最大。       

鳊鱼和宽鳍鱲幼鱼流速选择与运动能量代谢特征的关联

为考察喜好激流环境的宽鳍鱲(Zacco platypus)和喜好缓流环境的鳊鱼(Parabramis pekinensis)的最适游泳速度和流速选择的关联以及运动能量代谢特征对流速选择的影响,在(25±0.5)℃条件下将实验鱼(n=13×2)单尾分别置于梯度流速选择仪(设定流速范围为18.6—102.7 cm/s,等距离划分为5个流速区域)中获取视频资料,采用Ethovision XT19软件分析视频资料并计算两种实验鱼在5个流速区域的平均停留时间百分比(P_t)和平均出入频率百分比(Pf);另外,使用游泳代谢仪测定两种实验鱼的临界游泳速度(U_(crit))和不同游泳速度下的运动耗氧率(M_(O2)),并计算出不同速度下单位位移耗能(COT)、最适游泳速度(U_(opt))、静止耗氧率(RMR)和净单位位移耗能(COTnet)。结果显示:鳊鱼的U_(crit)和RMR均显著小于宽鳍鱲(P0.05),但二者的最大耗氧率(MMR)无显著差异;随游泳速度的增加,两种实验鱼的M_(O2)均显著上升,尽管在较低游泳速度下,鳊鱼的M_(O2)和COT均小于宽鳍鱲,但在高游泳速度下则相反;两种实验鱼的U_(opt)分别为(6.20±1.29)体长(BL)/s和(11.56±1.57)BL/s,鳊鱼显著小于宽鳍鱲;两种实验鱼的COTnet随着游泳速度增加差异逐渐增大,鳊鱼显著高于宽鳍鱲(P0.05);两种实验鱼在最低流速区域(18.6—23.8 cm/s)的P_t和Pf显著大于其他速度区域(P0.05),由此可见两种实验鱼的偏好游泳速度(U_(perf))等于或小于(18.6—23.8 cm/s),然而鳊鱼在最低速度区域P_t和Pf均显著大于且在较高速度区域的P_t和Pf则均显著小于宽鳍鱲(P0.05)。结果表明:有别于过往研究的是两种实验鱼的U_(perf)均与U_(opt)偏离;在激流环境中生存的宽鳍鱲更加偏好较高的水流速度,生境水流对实验鱼的水流速度选择特征存在显著影响,这种影响的主要能量学机制与鱼类的运动能量效率有关。     

不同适应条件对细鳞鲑幼鱼游泳能力的影响

为了研究适应条件对鲑科鱼类幼鱼续航游泳能力的影响,在(16.0±0.2)℃和8 mg/L溶解氧条件下,以续航时间作为评定游泳能力的关键指标,通过适应时间、适应流速、加速时间以及测试流速对细鳞鲑幼鱼的续航游泳时间的影响进行了研究,试验采用4因素8水平的均匀设计方案。结果表明,最大适应流速应控制在1—1.5 BL/s为宜,相应的最佳适应时间应为1 h,在合理条件下适应流速和适应时间对续航游泳能力的影响可忽略不计;加速时间只在大流速条件下(0.5 m/s)对续航时间有极显著影响,其他情况的影响可以忽略不计;尽管长时间适应环境更有利于鱼类身体机能的充分调整,但适应时间仍建议控制在1—2 h以内,且受试鱼类要经过试验前的适应能力筛选;测试流速建议控制在3—4 BL/s以内,以避免超过鱼类的最大游泳耐受范围。测试流速对细鳞鲑幼鱼的续航时间有极为显著的影响,其续航时间随测试流速的增加呈幂函数规律衰减。     

亚成体巨须裂腹鱼游泳能力及活动代谢研究

以野生雅鲁藏布江巨须裂腹鱼(Schizothorax macropogon)为对象,通过自制的鱼类游泳实验装置,测定了4个温度(5、10、15和18℃)梯度下亚成体巨须裂腹鱼的临界游泳速度(Ucrit)及流速变化对耗氧率的影响,并通过摄像记录分析了不同游泳速度下的游泳行为。野生亚成体巨须裂腹鱼的临界游速随着温度的变化呈近似线性的递增趋势(P<0.001),4个温度下的绝对临界游速(Ucrit-a)分别为(0.88±0.07)、(1.09±0.07)、(1.24±0.15)和(1.49±0.15)m/s;若以单位时间内游过的体长倍数(BL/s)表示,相对临界游速(Ucrit-r)分别为(3.96±0.21)、(4.4±0.16)、(4.9±0.18)和(5.35±0.14)BL/s。根据不同温度及流速下耗氧率的变化情况,采用非线性拟合得到了4个温度梯度下耗氧率与游泳速度关系的幂函数模型(P<0.05)。模型表明耗氧率随游泳速度的增大而增加,且温度越高耗氧率随游泳速度的变化越显著。4个温度下的速度指数分别为2.4、2.6,2.8及3.1,表明有氧运动的效率随温度升高有所降低。在自然水温条件下(5—9℃),摆尾频率(TBF)与流速的关系呈线性正相关(P<0.001),而运动步长(Ls)的变化与流速没有显著关系,出现由高至低再升高的三个阶段。录像分析表明在流速逐渐增加的过程中,巨须裂腹鱼采用了三种不同的游泳方式,以实现降低能量消耗的目的。研究可为鱼道等过鱼设施的设计提供参考,对数量日益减少的巨须裂腹鱼保护具有较大的意义。     

Energy savings in sea bass swimming in a school: measurements of tail beat frequency and oxygen consumption at different swimming speeds

Tail beat frequency of sea bass, Dicentrarchus labrax (L.) (23.5 ± 0·5 cm, L_T ), swimming at the front of a school was significantly higher than when swimming at the rear, for all water velocities tested from 14·8 to 32 cm s⁻¹. The logarithm of oxygen consumption rate, and the tail beat frequency of solitary swimming sea bass (28·8 ± 0·4 cm, L_T ), were each correlated linearly with swimming speed, and also with one another. The tail beat frequency of individual fish was 9–14% lower when at the rear of a school than when at the front, corresponding to a 9–23% reduction in oxygen consumption rate.     

Anomalies in the motion dynamics of long-flagella mutants of Chlamydomonas reinhardtii

Chlamydomonas reinhardtii has long been used as a model organism in studies of cell motility and flagellar dynamics. The motility of the well-conserved ‘9+2’ axoneme in its flagella remains a subject of immense curiosity. Using high-speed videography and morphological analyses, we have characterized long-flagella mutants (lf1, lf2-1, lf2-5, lf3-2, and lf4) of C. reinhardtii for biophysical parameters such as swimming velocities, waveforms, beat frequencies, and swimming trajectories. These mutants are aberrant in proteins involved in the regulation of flagellar length and bring about a phenotypic increase in this length. Our results reveal that the flagellar beat frequency and swimming velocity are negatively correlated with the length of the flagella. When compared to the wild-type, any increase in the flagellar length reduces both the swimming velocities (by 26–57%) and beat frequencies (by 8–16%). We demonstrate that with no apparent aberrations/ultrastructural deformities in the mutant axonemes, it is this increased length that has a critical role to play in the motion dynamics of C. reinhardtii cells, and, provided there are no significant changes in their flagellar proteome, any increase in this length compromises the swimming velocity either by reduction of the beat frequency or by an alteration in the waveform of the flagella.     

The swimming performance of brown trout and whitefish: the effects of exercise on Ca2 + handling and oxidative capacity of swimming muscles

The swimming performance of two fish species, the brown trout and whitefish, having initially different swimming strategies, was measured after nine different training programs in order to relate the effects of exercise on Ca²⁺ handling and oxidative capacity of swimming muscles. The time to 50% fatigue was measured during the training period, and compared with the density of dihydropyridine (DHP) and ryanodine (Ry) receptors and succinate dehydrogenase (SDH) and phosphorylase activity determined by histochemical analysis of the swimming muscles. Overall, both trained brown trout and whitefish had superior swimming performance as compared to control ones. Interestingly, the training programs had different effect on the two species studied since brown trout achieved the highest swimming performance, swimming against the water flow velocity of 2 BL s⁻¹ while among whitefish the best efficiency was seen after training with lower swimming velocities. Training also induced a significant increase in DHP and Ry receptor density in both species. Generally, in brown trout the most notable increase in the receptor densities was observed in red muscle sections from the fish swimming for 6 weeks against water currents of 1 BL s⁻¹ (DHPR 176.5 ± 7.7% and RyR 231.4 ± 11.8%) and white muscle sections against 2 BL s⁻¹ (DHPR 129.6 ± 12.4% and RyR 161.9 ± 15.5%). In whitefish the most prominent alterations were noted in samples from both muscle types after 6 weeks of training against water current of 1.5 BL s⁻¹ (DHPR 167.1 ± 16.9% and RyR 190.4 ± 19.4%). Finally, after all the training regimens the activity of SDH increased but the phosphorylase activity decreased significantly in both the species. To conclude, our findings demonstrate an improved swimming performance and enhanced Ca²⁺ regulation and oxidative capacity after training. Moreover, there seems to be a connection between the swimming performance and receptor levels, especially in white swimming muscles of different fish species, regardless of their initially deviant swimming behaviours. However, depending on the training regimen the divergent swimming behaviours do cause a different response, resulting in the most prominent adaptational changes in the receptor levels of red muscle samples with lower swimming velocities in brown trout and with higher ones in whitefish.     

鲢幼鱼通过水流速度障碍的模拟

鱼类能否通过水流速度障碍直接影响过鱼设施的过鱼效果。利用计算机技术,综合水力因素、鱼类行为、地理特征及环境因子,展开鱼类通过水流速度障碍的模拟,有助于过鱼设施的优化设计。以国外涵洞式鱼道模拟软件Fish Xing为切入点,结合主要模块和关键因子,对我国特有鱼类鲢幼鱼进行模拟,得到鲢通过不同水流速度障碍的成功率;对比鲢在物理模型中的游泳表现,从模型主要模块和影响鱼类游泳表现的关键因子角度,分析影响鱼类通过水流速度障碍模拟的因素。结果表明,Fish Xing软件不能精确模拟鲢通过水流速度障碍的表现。分析表明,该软件在地理要素、管道特征和水力信息等参数方面具备独特的优势,但对我国鱼类有一定局限性,主要体现在鱼类的生物学信息如鱼类游泳特征等方面存在不足;进行鱼过障碍的模拟需要深入研究目标鱼类的生理特征、游泳能力及其与水力环境因子的响应关系。     

鲢幼鱼在不同水流速度下的暴发-滑行行为策略

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。     

Swimming response of goldfish,Carassius auratus,and the tetra,Hemigrammus caudovittatus,larvae to individual food items and patches

Synopsis Swimming speed and swimming path of goldfish and tetra larvae were studied in aquaria containing food patches composed of decapsulated cysts and immobilized nauplii of Artemia salina or sparsely distributed prey. The mean swimming speed of starved larvae in the medium without food was about four times higher than the speed of larvae feeding in a patch. Satiated larvae swam about 1.5 times slower than hungry fish. Consumption of single prey items by starved larvae caused the following sequence of swimming responses: handling pause (cessation of swimming), slow swimming in a restricted area, and fast swimming (approximately twice as fast as hungry larvae before encountering food) accompanied by a widening of the area searched (area increased searching). Mean swimming speed was constant over a broad range (10¹–10³ ind·1^–1 of food density, although at extreme (high or low) values of food density it depended on swimming responses of the predator. Frequency of visits to the different parts of the aquarium strongly depended on encounters of hungry fish with food particles or patches.     

A model for switching between particulate-feeding and filter-feeding in the common bream,Abramis brama

Synopsis A model has been developed to describe the process of switching between particulate- and filter-feeding in common bream, Abramis brama, in relation to fish size and zooplankton density. The model assumes that the encounter rate of fish and zooplankton is determined by the density of zooplankton and the swimming speed of fish. However, if zooplankton density is so high as to allow at least one prey to be engulfed per random snap, the encounter rate is determined by the volume of the buccal cavity and by zooplankton density, but is independent of swimming speed. The snapping frequency will be maximal at the time of switching, decreasing with increasing zooplankton density because of the extra time needed for intra-oral prey handling. The model predicted switching from particulate- to filter-feeding only for bream> 15 cm standard length at zooplankton densities < 500 l^-1. The snap frequency of six size classes of bream (7.5, 10.4, 12.5, 15, 24 and 29.5 cm) was measured at varying densities of Daphnia. The model predictions for snap frequencies of all size classes corresponded to the highest values observed. The average of the observed snap frequencies was only 50% of the predicted values, probably because the calculated average distance between prey animals assumed an ideal swimming route of the fish and error-free vision for particulate-feeding, and the handling time was ignored.