卵形鲳鲹幼鱼耗氧率和排氨率的初步研究

运用封闭流水式实验方法对不同体重和放养密度的卵形鲳鲹(Trachinoms ovatus)幼鱼耗氧率和排氨率进行了初步的研究。结果表明,卵形鲳鲹幼鱼的耗氧率随着鱼体重的增加而逐渐下降,排氨率总体上也呈降低的趋势,体重对卵形鲳鲹耗氧率、排氨率的影响均达到显著水平(P0.05);光照对卵形鲳鲹幼鱼的耗氧率和排氨率影响非常显著(P0.01),幼鱼在遮光条件下的耗氧率和排氨率分别比在自然光照条件下要低25.18%～40.76%和16.28%～40.28%;随着放养密度的增加,卵形鲳鲹幼鱼的耗氧率逐渐降低,排氨率随着密度的增加呈先上升后下降的趋势,放养密度对卵形鲳鲹耗氧率、排氨率的影响均达到显著水平(P0.05)。卵形鲳鲹的耗氧率和排氨率具有明显的昼夜变化,白天的耗氧率和排氨率均高于夜间值,耗氧率的低谷值为高峰值的69.68%,排氨率的低谷值为高峰值的30.91%。卵形鲳鲹幼鱼的窒息点溶解氧含量为(0.991±0.058)mg/L。     

三种流速对卵形鲳鲹幼鱼耗氧率和排氨率的影响

【摘要】采用实验生态学方法, 研究了饥饿态下平均体重分别为(2.54±1.09) g、(24.35±7.19) g、(233.79±26.00) g、(508.98±126.61) g的卵形鲳鲹幼鱼(Trachinotus ovatus)在静水、0.1 m·s -1、0.2 m·s -1三种流速下的耗氧率和排氨率的变化。结果表明, 卵形鲳鲹体重对耗氧率和排氨率影响显著(P < 0.05)。在同一流速下, 耗氧率和排氨率分别随体重的增加而下降, 体重与两者间的回归关系符合异速方程Y=aWb。卵形鲳鲹的耗氧率和排氨率随着流速的升高均出现升高的趋势, 流速对均重为24.35 g和233.79 g卵形鲳鲹的耗氧率和排氨率影响显著(P < 0.05)。在静水条件下, 卵形鲳鲹代谢氧氮比的范围为31.36-46.32, 表明卵形鲳鲹主要以脂肪和碳水化合物为能源, 蛋白质其次。在试验流速范围内, 均重为24.35 g卵形鲳鲹幼鱼的氧氮比随着流速的升高而升高, 其他两组的氧氮比则随着流速的升高而降低。     

鲻幼鱼耗氧率、排氨率和窒息点的研究

为探讨鲻幼鱼的耗氧率、排氨率和窒息点,采用封闭流水式实验方法,在不同体质量、光照、放养密度、水流速度以及昼夜更替的条件下,测定鲻幼鱼的耗氧率和排氨率,并且观测体质量对幼鱼窒息点和窒息时间的影响。实验期间水温为19℃±1℃,盐度30,pH7.7。研究结果显示:鲻幼鱼的耗氧率随体质量增加而上升,其变化趋势可用幂函数方程表达:Y=0.4759X0.1878(R2=0.9454);光照对耗氧率的影响较大,对排氨率无明显影响;放养密度对耗氧率的影响差异显著(P0.05),对排氨率的影响差异极显著(P0.01);幼鱼的呼吸代谢旺盛时段在中午11∶00至夜间23∶00;流速对耗氧率和排氨率的影响差异均极显著(P0.01);不同体质量幼鱼窒息点和窒息时间的差异极显著(P0.01)。     

温度对黑鱾幼鱼耗氧率和排氨率的影响

本文研究了温度对饱食和饥饿状态下黑纪(Girella melanichthys)幼鱼耗氧率和排氨率的影响.结果表明:在温度为15～30℃范围内,黑纪幼鱼在饱食状态下的耗氧率、饥饿状态下的耗氧率、饱食状态下的排氨率和摄食率均随温度的升高而增加(P＜0.01),30℃时达到最大,温度为32℃时,均下降;在温度为15～32℃范围内,黑鱾幼鱼在饥饿状态下的排氨率随温度升高而增加(P＜0.01),32℃时达到最大.多项指标表明黑纪幼鱼生长适温在30℃左右.     

温度和盐度突变对菲律宾蛤仔斑马蛤耗氧率和排氨率的影响

为研究温度和盐度对蛤仔新品种斑马蛤耗氧排氨的影响,以野生蛤仔为对照,实验设置15、20、25、30和35℃五个温度梯度和20、25、30、35和40五个盐度梯度,结果表明:温度和盐度对斑马蛤的耗氧率和排氨率影响显著（P < 0.05）。在温度15-35℃内,随着温度的增加,耗氧率和排氨率整体上呈增加的趋势。在20-40盐度内,耗氧率随着盐度的升高先减少后增加,排氨率随着盐度的升高先增加后减少,在盐度为30时达到最高值。在水温为15℃,盐度20-40内,斑马蛤的O:N为9.534-62.008;在盐度为35,水温在15-35℃内,斑马蛤的O:N是20.700-74.138。与野生蛤仔比较,斑马蛤的耐高温能力要强于野生蛤仔,从Q₁₀的变化反映出斑马蛤对温度的敏感性相对较弱,适应温度变化的能力比较强;斑马蛤的耐低盐和耐高盐能力强于野生蛤仔。研究结果为进一步完善蛤仔斑马蛤的人工养殖技术提供参考。     

盐度和温度对不同规格虎斑乌贼幼体的耗氧率、排氨率和窒息点的影响

为探究体重、盐度和温度对不同规格的虎斑乌贼(Sepia pharaonis)幼体耗氧率、排氨率以及其窒息点的影响。采用单因子试验设计和密闭静水法, 对不同体重下(0.212、0.385、0.476、0.597、0.754和0.946 g)虎斑乌贼幼体的耗氧率和排氨率, 以及不同体重(0.476、0.673、1.341、3.873和4.205 g)幼体的窒息点进行了测定, 同时研究了不同盐度(19‰、22‰、25‰、28‰和31‰)和温度(18、21、24、27和30℃)对不同规格[A: 体重(0.366±0.042) g, B: 体重(0.556±0.038) g, C: 体重(0.844±0.051) g]的虎斑乌贼幼体耗氧率(R_O)和排氨率(R_N)的影响。结果表明: (1)虎斑乌贼幼体体重对耗氧率和排氨率均影响显著(P<0.05)。随着幼体体重的增长, 耗氧率和排氨率显著下降, 个体越小耗氧率和排氨率越大; (2)盐度对幼体的耗氧率和排氨率有显著影响(P<0.05), 均随着盐度的增加呈先下降后上升的趋势, 其中, A规格和B规格的幼体在盐度25‰时, 耗氧率和排氨率显著低于盐度19‰、22‰和31‰时的3个试验组(P<0.05), 而与盐度28‰时无显著差异(P>0.05); C规格幼体的耗氧率在盐度28‰时显著低于盐度19‰组(P<0.05), 而排氨率在盐度25‰时显著低于盐度19‰和31‰两组(P<0.05)。盐度对A规格幼体的氧氮比(O/N)值有显著影响(P<0.05), 而对B规格和C规格的幼体无显著影响(P>0.05)。(3)温度对不同规格幼体的耗氧率和排氨率有显著影响(P<0.05), 均随温度的增长, 呈先上升后下降的趋势。其中, A规格和C规格幼体的耗氧率在27℃时, 显著高于18和30℃两组(P<0.05), B规格的在水温24℃时显著高于18和30℃(P<0.05); A规格和B规格幼体的排氨率分别在24和27℃时, 显著高于其他温度组(P<0.05), C规格的在温度27℃时, 显著高于18和30℃两组(P<0.05); 温度对A规格幼体的O/N值有显著影响(P<0.05), 而对B规格和C规格的幼体无显著影响(P>0.05)。(4)虎斑乌贼幼体的窒息点为0.84—1.62 mg/L, 随着体重的增加而逐渐降低。     

温度和个体大小对单齿螺耗氧率和排氨率的影响

采用静水法测定了不同温度、不同个体大小的单齿螺耗氧率和排氨率。结果表明:在16-33℃的实验温度范围内单齿螺的耗氧率(R_O)和排氨率(R_N)与软体部干重(W)都呈负相关,它们之间关系可以分别用幂函数R_O=aW^-b和R_N=a₁W^-b1表示。16～29℃温度范围内单齿螺的耗氧率和排氨率均随温度的升高而增加,29℃时耗氧率和排氨率达到最大值,当温度继续升高超过29℃后,耗氧率和排氨率则随温度的升高而下降,耗氧率、排氨率与温度之间呈显著的指数函数关系R_O=ce^dT和R_N=c₁e^d1T;不同个体大小单齿螺的O:N比在16～20℃时较大,Q₁₀取值范围0.56-3.74,平均值为1.64。方差分析表明,温度、软体部干重对单齿螺的耗氧率和排氨率均有极显著的影响(P<0.01)。     

栉孔扇贝耗氧率和排氨率的研究

1999年 4～ 6月 ,采用室内实验生态学方法对栉孔扇贝的耗氧率和排氨率进行了研究 .结果表明 ,在适宜的温度范围内 ,栉孔扇贝的耗氧率和排氨率均与温度成正比 ,而与体重呈负相关关系 .在实验室温度 (8～ 2 8℃ )条件下 ,栉孔扇贝的耗氧率为 0 .48～ 9.0 9mg·g-1·h-1,排氨率为 0 .0 5～ 1 0 1mg·g-1·h-1.其中耗氧率在 2 3℃时达到最高值 ,2 8℃时开始下降 ,而排氨率则呈持续升高趋势 .栉孔扇贝的日常代谢明显高于标准代谢 ,耗氧率和排氨率平均值分别提高约 35 .8%和 75 .9% .     

温度、盐度及交互作用对僧帽牡蛎(Saccostrea cucullata)呼吸排泄的影响

采用实验生态学方法研究了温度(13、18、23、28、31、34℃)和盐度(18、23、28、33)对僧帽牡蛎(Saccostrea cueullata)耗氧率和排氨率的影响,并分析了二者交互作用对呼吸排泄的影响。结果表明,不同温度条件下,僧帽牡蛎的耗氧率变化范围为0.43-3.15mg g~(-1)h~(-1),排氨率的变化范围为72.62-1245.77μg g~(-1)h~(-1),方差分析显示,温度和盐度对僧帽牡蛎耗氧率(F=60.440,P0.01)和排氨率(F=61.083,P0.01)的影响均极显著;二者的交互作用对僧帽牡蛎耗氧率(F=4.907,P0.01)和排氨率(F=11.412,P0.01)影响也极显著,耗氧率(Y)、排氨率(Y)与温度(T)和盐度(S)之间的二元线性回归方程为y=a+bT+cS+dT×S。在一定温度范围内(13-31℃)僧帽牡蛎单位体重耗氧率(Y)与温度(T)呈正相关符合指数方程Y=ae~(bT),其中a的取值范围为0.1378-0.2117,b的取值范围为0.0757-0.0912;单位体重排氨率也与温度呈正相关,符合上述指数方程,其中a的取值范围为20.364-30.634,b的取值范围为0.1004-0.1341。不同温度和盐度条件下,僧帽牡蛎呼吸排泄的氧氮比在2.20-7.78之间,平均值为3.81。     

温度、盐度、pH和麻醉剂对长鳍篮子鱼幼鱼耗氧率的影响

采用Winkler法研究了温度、盐度、pH和麻醉剂对长鳍篮子鱼幼鱼(体长(3.325±0.205) cm,体质量(0.706±0.155) g)耗氧率的影响。结果表明：长鳍篮子鱼幼鱼耗氧率随着温度升高而增加,其回归关系可用对数函数Y=1.3819lnX-3.55(r=0.9475,P<0.01)表示,其生长的适宜温度为24 ℃～32 ℃;幼鱼耗氧率随着盐度的降低而逐渐增加,其回归关系可用线性函数Y=-0.1802X+1.7551(r=0.9837,P<0.01)来表示;在不同的pH下耗氧率有显著性差异(P<0.01),pH值在6.0时耗氧率最低,9.0时耗氧率最高;耗氧率随着丁香酚、MS-222的浓度升高而逐渐降低,各实验组的耗氧率要显著低于对照组,丁香酚和MS-222可以作为长鳍篮子鱼幼鱼运输过程中的麻醉剂。     

卵形鲳鲹胚胎及早期仔鱼耗氧量的研究

运用SKW-3微量呼吸仪对卵形鲳鲹(Trachinotus ovatus)胚胎和早期仔鱼的耗氧量进行测定,研究温度、盐度及pH的变化对胚胎耗氧量和Cu²⁺、Cd²⁺等重金属离子对早期仔鱼的耗氧量的影响。结果表明:在(25±0.5)℃条件下,卵形鲳鲹胚胎和早期仔鱼的耗氧量均随着发育时间的延长总体上呈上升的趋势,胚胎耗氧量在出膜前达到最大值,其中以原肠期和出膜期耗氧量变化最为显著。胚胎耗氧量随着温度、盐度、pH的增大而逐渐升高,在水温25℃、盐度35和pH为8时耗氧量到达最大值,随后逐渐减小。随着Cu²⁺浓度的升高,早期仔鱼耗氧量呈先增大后减小,在0.01mg·L^-1时耗氧率最大:胚胎耗氧量随着Cd²⁺浓度的升高而逐渐降低。     

温度和摄食对溪红点鲑幼鱼呼吸代谢的影响

在不同水温［(5.5±0.5) ℃、(8.5±0.5) ℃、(11.5±0.5) ℃、(14.5±0.5) ℃、(17.5±0.) ℃］条件下,分别测定了饱食和空腹状态下溪红点鲑幼鱼的耗氧率和排 氨率,分析了温度和摄食对溪红点鲑幼鱼呼吸代谢的影响.结果表明：饱食后,5个温度梯度组溪红点鲑幼鱼的耗氧率和排氨率均迅速上升,达最大值后缓慢下降,并逐渐恢复到初始水平;饱食状态下,溪红点鲑幼鱼耗氧率（OR）和排氨率（NR）与温度（t）的回归方程分别为OR=-0.0601t⁴+2.5542t³-39.256t²+276.26t-598.75(n=650,R²=1,4.5 ℃4+0.0826t³-1.2318t²+8.6186t-18.838(n=650,R²=1,4.5 ℃0.9738(n=650,R²=0.9974,4.5 ℃1.0896( n=650,R²=0.9977,4.5 ℃相似文献   

Effects of salinity on physiological conditions in juvenile common snook Centropomus undecimalis

This study describes the effects of different salinities on oxygen consumption, ammonia excretion, osmotic pressure, apparent heat increment, postprandial nitrogen excretion, and oxygen:nitrogen ratio in juvenile common snook Centropomus undecimalis. Oxygen consumption of fish fasting and fish feeding was statistically different in relation with salinity. Fish maintained at 0, 25, and 35 ppt invested more energy processing feed than fish maintained at 12 ppt. Fasting fish had lower ammonia excretion than feeding fish and excretion was reduced at high salinities. Snook can change the energetic substrate in function with salinity, from a mixture of protein and lipids and carbohydrates at 35 ppt to a more acute preference for proteins at lower salinities. This species changes osmotic plasma concentrations at extreme experimental salinities. The different salinities were the snook inhabits (0-36 ppt), have a direct effect on the physiology, inducing changes on the oxygen consumption, nitrogen excretion, changes on the energetic substrate and plasma osmotic pressure.     

Oxygen consumption and ammonia excretion of juvenile pink shrimp (Farfantepenaeus paulensis) in culture: temperature effects

We evaluated oxygen consumption and ammonia excretion by juveniles of the pink shrimp Farfantepenaeus paulensis at three different temperatures (15, 20 and 25 °C). The shrimp were collected in the coastal region of Cananéia, São Paulo State, Brazil. The selected temperatures are the limits recorded in aquaculture tanks in the coastal region of Cananéia. We measured oxygen consumption and ammonia excretion as proxies for metabolic activity. Oxygen consumption and ammonia excretion increased with increasing temperature, but no change was observed at 15 and 20 °C. It is possible that within this temperature range, there is thermal independence in juvenile F. paulensis do not need to allocate additional energy to compensate for temperature changes because they are physiologically adapted for this range.     

Oxygen consumption, ammonia excretion and protein use in response to thermal changes in juvenile Atlantic salmon Salmo salar

Experiments were designed to examine the effects of various temperature challenges on oxygen consumption and ammonia excretion rates and protein utilization in juvenile Atlantic salmon Salmo salar . Fish acclimated to 15° C were acutely and abruptly exposed to either 20 or 25° C for a period of 3 h. To simulate a more environmentally relevant temperature challenge, a third group of fish was exposed to a gradual increase in temperature from 15 to 20° C over a period of 3 h ( c. 1·7° C h⁻¹). Oxygen consumption and ammonia excretion rates were monitored before, during and after the temperature shift. From the ammonia excretion and oxygen consumption rates, protein utilization rates were calculated. Acute temperature changes (15–20° C or 15–25° C) caused large and immediate increases in the oxygen consumption rates. When the temperature was gradually changed ( i.e. 1·7° C h⁻¹), however, the rates of oxygen consumption and ammonia excretion were only marginally altered. When fish were exposed to warmer temperatures ( i.e. 15–20° C or 15–25° C) protein use generally remained at pre-exposure (15° C) levels. A rapid transfer back to 15° C (20–15° C or 25–15° C) generally increased protein use in S. salar . These results indicate that both the magnitude and the rate of temperature change are important in describing the physiological response in juvenile salmonids.     

Changes in the composition of the urine of yellow-vented bulbuls (Pycnonotus xanthopygos): the effects of ambient temperature, nitrogen, and water intake.

Uricotely (uric acid >50% of urinary nitrogen) in birds was once considered ubiquitous. However, Anna's hummingbirds (Calypte anna) have been shown to be an exception to this rule; under conditions of low ambient temperature (T(a)) and on a nitrogen-free diet, they increased their water intake and often became ammonotelic (ammonia >50% of urinary nitrogen). Our aim was to identify the effects of nitrogen intake, water intake, and T(a) on the ammonia excretion of yellow-vented bulbuls (Pycnonotus xanthopygos). We chose this predominantly frugivorous species because many of the characteristics of nectarivores that were used to explain increased ammonia excretion by C. anna are also characteristics of frugivorous birds. We assayed ureteral urine composition in eight yellow-vented bulbuls (P. xanthopygos), each randomly allocated a diet of 20% (0.6 M) sucrose solution supplemented by either 1.03 g/L or 7.23 g/L soy protein and held at a T(a) of either 28 degrees C or 10 degrees C. Food, and therefore water, intake rates varied with nitrogen intake but not with T(a). Food intake increased significantly with decreased nitrogen intake, while concentrations of all the excretory compounds in the urine (P<0.05) decreased; yet their proportions in the urine did not change significantly. The lower T(a) had no significant effect on food intake or on the concentration of uric acid. However, at 10 degrees C, the ammonia and urea concentrations increased (P<0.05), and this led to a significant increase in the proportion of ammonia in the urine. Our results demonstrate that, when bulbuls are exposed to low T(a), they are able to save energy by increasing the proportion of the ammonia in their urine.